Podcasts about genetic research

In this episode of the Boost Your Biology podcast, Lucas Aoun interviews Dr. Tyler Panzner, a specialist in supplements and genetics. They discuss Dr. Panzner's journey into the world of supplements, the evolution of genetic testing, and the importance of understanding methylation and its impact on health. The conversation also covers common mistakes people make with supplements, the role of glutathione, and the benefits of lithium orotate. In this conversation, Dr. Tyler Panzner and Lucas Aoun delve into the complexities of brain chemistry, the role of lithium in mental health, and the benefits of creatine as a supplement. They discuss the importance of understanding individual responses to supplements, the interactions between various compounds, and the need for more genetic research in health optimization. The dialogue emphasizes a holistic approach to health, considering both natural and synthetic substances as pharmacological tools.Relevant links:Cell Signaling Model of Disease Course: Begin to learn how Dr. Tyler Panzner views health, one pathway at a time. This free course shows an entirely new way of viewing your external world, whether it be foods, supplements, or lifestyle habits. Once you see life like this, you can NOT unsee it!https://drtylerpanzner.com/cell-signaling1:1 Deep Dive Genetic Analysis: Pinpoint precisely which foods, vitamins, supplements, and lifestyle habits your cells do (and don't) need to feel their best with a personal analysis and consult with Dr. Panzner.https://drtylerpanzner.com/startyourjourneyEmail Newsletter: Subscribe to Dr. Panzner's free email newsletter for weekly emails about cellular health, supplement science, and other quirky science to enhance your human experience of life.https://drtylerpanzner.com/email-newsletterGet Lucas' New Supplement Here: https://www.inb4supps.com/ Chapters:00:00 Introduction to the Podcast and Guest02:53 Dr. Tyler Panzner's Journey into Supplements and Genetics06:09 The Evolution of Genetic Testing and Its Implications08:55 Understanding Methylation and Its Impact on Health12:11 The Role of Glutathione and Sulfur in Health14:59 Common Supplement Mistakes and Overstimulation17:49 The Benefits and Risks of Lithium Orotate30:56 Understanding Brain Chemistry and Anxiety36:05 The Role of Lithium in Mental Health41:02 Exploring Creatine and Its Benefits49:00 Navigating Supplement Interactions57:01 The Importance of Genetic Research in HealthDisclaimer:The information provided in this podcast episode is for entertainment purposes and is NOT MEDICAL ADVICE. If you have any questions about your health, contact a medical professional. This content is strictly the opinions of Lucas Aoun and is for informational and entertainment purposes only. It is not intended to provide medical advice or to take the place of medical advice or treatment from a personal physician. All viewers of this content are advised to consult with their doctors or qualified health professionals regarding specific health questions. Neither Lucas Aoun nor the publisher of this content takes responsibility for possible health consequences of any person or persons reading or following the information in this content. All consumers of this content especially taking prescription or over-the-counter medications should consult their physician before beginning any nutritional, supplement or lifestyle program. Hosted on Acast. See acast.com/privacy for more information.

Parent-specific epigenetic marks (imprints) leading to parent-specific gene expression are crucial for normal growth and development, yet their mechanisms of establishment and maintenance are not fully understood. In humans, approximately 200 imprinted genes have been discovered, and improper imprinting can manifest in growth restriction, obesity, intellectual disabilities, behavioral abnormalities, and an increased risk of certain cancers. While the use of pluripotent stem cells, especially those in the naïve state, have advanced aspects of modeling early development, a persistent issue hampering bona fide naïve hPSCs is the erosion of imprints. Our guests on today's episode will discuss genomic imprinting, its function, impact, and a new reporter system of imprinted gene expression in hPSCs that enables real-time visualization of loss-of-imprinting at single-cell resolution. This assay provides an important tool to help discover how to improve the imprint fidelity of naïve hPSCs and hence their application for studies of human development and regeneration. Guests Thorold Theunissen, PhD, Department of Developmental Biology, Washington University in St Louis, USA Gal Keshet, The Azrieli Center for Stem Cells and Genetic Research, The Hebrew University of Jerusalem, IsraelSupporting ContentTracking and mitigating imprint erasure during induction of naïve human pluripotency at single-cell resolutionHostJanet Rossant, Editor-in-Chief, Stem Cell Reports and The Gairdner FoundationAbout Stem Cell ReportsStem Cell Reports is the open access, peer-reviewed journal of the International Society for Stem Cell Research (ISSCR) for communicating basic discoveries in stem cell research, in addition to translational and clinical studies. Stem Cell Reports focuses on original research with conceptual or practical advances that are of broad interest to stem cell biologists and clinicians.X: @StemCellReportsAbout ISSCRWith nearly 5,000 members from more than 80 countries, the International Society for Stem Cell Research (@ISSCR) is the preeminent global, cross-disciplinary, science-based organization dedicated to stem cell research and its translation to the clinic. The ISSCR mission is to promote excellence in stem cell science and applications to human health.ISSCR StaffKeith Alm, Chief Executive OfficerYvonne Fisher, Managing Editor, Stem Cell ReportsKym Kilbourne, Director of Media and Strategic CommunicationsMegan Koch, Senior Marketing ManagerJack Mosher, Scientific AdvisorHunter Reed, Senior Marketing CoordinatorVoice WorkBen Snitkoff

For decades, we've been told that our DNA is a fixed blueprint—an unchangeable code that dictates our health and lifespan. But what if that's only half the story? Sharon Hausman-Cohen, a physician, researcher, and genomics expert at IntellxxDNA, joins Dave to reveal the cutting-edge science of genetic optimization—how understanding your DNA can unlock longer life, better brain function, and even protection from chronic disease. Forget the old-school genetic reports that left you with useless percentages. The new frontier of precision genomics goes beyond risk factors to actionable insights, showing you exactly how to turn on your body's most powerful longevity genes and turn off the pathways driving inflammation, cognitive decline, and disease. What You'll Learn in This Episode: • Why genetics alone don't determine your future—and how to use epigenetics to control your health • The truth about MTHFR, APOE4, and other “bad” genes—are they actually harming you? • How genetic reports can predict and eliminate brain fog, fatigue, and pain • The hidden genetic reasons behind ADHD, depression, and anxiety—and how to fix them • Why some people age faster—and the one longevity gene that determines your biological age • Cutting-edge breakthroughs in DNA-based biohacking—is it possible to edit your genes for peak performance? This is the future of personalized medicine. By understanding your own genetic blueprint, you can stop guessing and start making the precise changes that will optimize your energy, brainpower, and lifespan! ** Visit IntellxxDNA at https://intellxxdna.com/asprey/ When you go to the website to find a clinician please select “human upgrade/longevity” as the type of consult to get specialized biohacking clinicians! ** SPONSORS -Timeline | Head to https://www.timeline.com/dave to get 10% off your first order. -Leela Quantum Tech | Head to https://leelaq.com/DAVE for 10% off. Resources: • Dave Asprey's New Book - Heavily Meditated: https://daveasprey.com/heavily-meditated/ • IntellxxDNA Website: https://intellxxdna.com/asprey/ • 2025 Biohacking Conference: https://biohackingconference.com/2025 • Danger Coffee: https://dangercoffee.com • Dave Asprey's Website: https://daveasprey.com • Dave Asprey's Linktree: https://linktr.ee/daveasprey • Upgrade Collective – Join The Human Upgrade Podcast Live: https://www.ourupgradecollective.com • Own an Upgrade Labs: https://ownanupgradelabs.com • Upgrade Labs: https://upgradelabs.com • 40 Years of Zen – Neurofeedback Training for Advanced Cognitive Enhancement: https://40yearsofzen.com Timestamps: • 00:00 – Intro • 02:00 – The Role of Genetics in Longevity • 03:37 – Gene Variants & Cognitive Health • 05:58 – Epigenetics vs. Genetics • 08:21 – Genomics & Pain Management • 09:26 – Breakthroughs in Genetic Research • 12:33 – The Future of Genomic Medicine • 14:27 – How to Use Genomic Reports • 38:25 – Mitochondria & Longevity • 42:40 – BH4 & Mental Health • 43:42 – Folinic Acid & Brain Function • 44:37 – Genomics & Autism • 46:06 – Personalized Medicine • 56:00 – APOE4 & Alzheimer's Risk • 59:44 – Genetics & Heart Health • 01:04:54 – The Future of Precision Medicine • 01:20:23 – Conclusion & Next Steps See Privacy Policy at https://art19.com/privacy and California Privacy Notice at https://art19.com/privacy#do-not-sell-my-info.

We're experimenting and would love to hear from you!In this episode of 'Discover Daily', we begin with the unexpected shutdown of Humane's AI Pin. The much-discussed wearable device's discontinuation and subsequent $116 million acquisition by HP marks a significant shift in the wearable AI landscape, highlighting the challenges of introducing new device categories in today's competitive market.We also delve into the launch of Protector, an innovative app revolutionizing personal security in major US cities. This "Uber for armed guards" service offers on-demand access to professional security details and motorcades, bringing high-end protection services to a broader audience through a user-friendly platform in Los Angeles and New York City.The episode's main focus examines a fascinating breakthrough in human evolution research: the NOVA1 gene's role in speech development. Scientists at Rockefeller University have identified this crucial protein variant, present in virtually all modern humans, as a potential key to understanding how we developed our unique capacity for complex speech. Through groundbreaking experiments with genetically modified mice, researchers have demonstrated NOVA1's significant impact on vocalization patterns, opening new possibilities for treating communication disorders and understanding human evolution.From Perplexity's Discover Feed: https://www.perplexity.ai/page/humane-shuts-down-ai-pin-QYaGHA_mRQaNJYpvrVc3.whttps://www.perplexity.ai/page/uber-for-armed-guards-climbs-a-3vMrFSDqQ5ududobBxbgzAhttps://www.perplexity.ai/page/human-speech-gene-identified-lk71mFheSMqALlOPuwVOgQ**Introducing Perplexity Deep Research:**https://www.perplexity.ai/hub/blog/introducing-perplexity-deep-research Perplexity is the fastest and most powerful way to search the web. Perplexity crawls the web and curates the most relevant and up-to-date sources (from academic papers to Reddit threads) to create the perfect response to any question or topic you're interested in. Take the world's knowledge with you anywhere. Available on iOS and Android Join our growing Discord community for the latest updates and exclusive content. Follow us on: Instagram Threads X (Twitter) YouTube Linkedin

A Daily Chronicle of AI Innovations on February 20th 2025

Will genetic therapies revolutionize hearing loss treatment? Dr. Christo Bester, Head of Implant Innovation at Ear Science Institute Australia, discusses the emerging role of gene therapy and personalized medicine in hearing restoration. He highlights the Aussie Earbank initiative, a pioneering effort to collect genetic samples and audiometric data, helping researchers develop targeted treatments. With over 155 genes linked to hearing loss, this presents both challenges and opportunities for targeted interventions. He emphasizes the importance of global collaboration in advancing gene therapy, as large-scale research efforts are needed to bring these treatments from the lab to clinical practice. The discussion sheds light on how biobanking plays a crucial role in identifying patients who may benefit from emerging genetic treatments, offering new hope beyond traditional hearing aids and cochlear implants.Looking ahead, gene therapy and personalized medicine are set to reshape hearing care by complementing existing solutions. While still in its early stages, genetic research is paving the way for a future where treatments are tailored to an individual's unique genetic profile, potentially restoring hearing function in ways never before possible.Be sure to subscribe to our YouTube channel for the latest episodes each week, and follow This Week in Hearing on LinkedIn and X (formerly Twitter):https://www.linkedin.com/company/this-week-in-hearing/https://twitter.com/WeekinHearing

Scientists are working to breed drought- and heat-tolerance traits into common beans from tepary beans, which are native to the Sonoran desert in Mexico and the U.S. Learn more at https://www.yaleclimateconnections.org/ 

Madeline Oudin, Ph.D., is a scientist and mother on a groundbreaking mission to help her daughter, Margot, who has two de novo mutations in the SCN8A gene, which causes epilepsy. Margot's condition causes frequent seizures and developmental challenges. Determined to make a difference, Madeleine and her team are pioneering a cutting-edge genetic therapy that could one day transform treatment for Margot and others like her. In this heartfelt talk, Madeleine shares how her scientific expertise and personal journey intersect, revealing the highs and lows of developing life-changing treatments. From innovative approaches using Antisense Oligonucleotides (ASOs) to the unexpected success of a ketogenic diet, this story is about resilience, hope, and the power of community. Series: "Autism Tree Project Annual Neuroscience Conference" [Health and Medicine] [Science] [Show ID: 40210]

Madeline Oudin, Ph.D., is a scientist and mother on a groundbreaking mission to help her daughter, Margot, who has two de novo mutations in the SCN8A gene, which causes epilepsy. Margot's condition causes frequent seizures and developmental challenges. Determined to make a difference, Madeleine and her team are pioneering a cutting-edge genetic therapy that could one day transform treatment for Margot and others like her. In this heartfelt talk, Madeleine shares how her scientific expertise and personal journey intersect, revealing the highs and lows of developing life-changing treatments. From innovative approaches using Antisense Oligonucleotides (ASOs) to the unexpected success of a ketogenic diet, this story is about resilience, hope, and the power of community. Series: "Autism Tree Project Annual Neuroscience Conference" [Health and Medicine] [Science] [Show ID: 40210]

Madeline Oudin, Ph.D., is a scientist and mother on a groundbreaking mission to help her daughter, Margot, who has two de novo mutations in the SCN8A gene, which causes epilepsy. Margot's condition causes frequent seizures and developmental challenges. Determined to make a difference, Madeleine and her team are pioneering a cutting-edge genetic therapy that could one day transform treatment for Margot and others like her. In this heartfelt talk, Madeleine shares how her scientific expertise and personal journey intersect, revealing the highs and lows of developing life-changing treatments. From innovative approaches using Antisense Oligonucleotides (ASOs) to the unexpected success of a ketogenic diet, this story is about resilience, hope, and the power of community. Series: "Autism Tree Project Annual Neuroscience Conference" [Health and Medicine] [Science] [Show ID: 40210]

Madeline Oudin, Ph.D., is a scientist and mother on a groundbreaking mission to help her daughter, Margot, who has two de novo mutations in the SCN8A gene, which causes epilepsy. Margot's condition causes frequent seizures and developmental challenges. Determined to make a difference, Madeleine and her team are pioneering a cutting-edge genetic therapy that could one day transform treatment for Margot and others like her. In this heartfelt talk, Madeleine shares how her scientific expertise and personal journey intersect, revealing the highs and lows of developing life-changing treatments. From innovative approaches using Antisense Oligonucleotides (ASOs) to the unexpected success of a ketogenic diet, this story is about resilience, hope, and the power of community. Series: "Autism Tree Project Annual Neuroscience Conference" [Health and Medicine] [Science] [Show ID: 40210]

Madeline Oudin, Ph.D., is a scientist and mother on a groundbreaking mission to help her daughter, Margot, who has two de novo mutations in the SCN8A gene, which causes epilepsy. Margot's condition causes frequent seizures and developmental challenges. Determined to make a difference, Madeleine and her team are pioneering a cutting-edge genetic therapy that could one day transform treatment for Margot and others like her. In this heartfelt talk, Madeleine shares how her scientific expertise and personal journey intersect, revealing the highs and lows of developing life-changing treatments. From innovative approaches using Antisense Oligonucleotides (ASOs) to the unexpected success of a ketogenic diet, this story is about resilience, hope, and the power of community. Series: "Autism Tree Project Annual Neuroscience Conference" [Health and Medicine] [Science] [Show ID: 40210]

Madeline Oudin, Ph.D., is a scientist and mother on a groundbreaking mission to help her daughter, Margot, who has two de novo mutations in the SCN8A gene, which causes epilepsy. Margot's condition causes frequent seizures and developmental challenges. Determined to make a difference, Madeleine and her team are pioneering a cutting-edge genetic therapy that could one day transform treatment for Margot and others like her. In this heartfelt talk, Madeleine shares how her scientific expertise and personal journey intersect, revealing the highs and lows of developing life-changing treatments. From innovative approaches using Antisense Oligonucleotides (ASOs) to the unexpected success of a ketogenic diet, this story is about resilience, hope, and the power of community. Series: "Autism Tree Project Annual Neuroscience Conference" [Health and Medicine] [Science] [Show ID: 40210]

Madeline Oudin, Ph.D., is a scientist and mother on a groundbreaking mission to help her daughter, Margot, who has two de novo mutations in the SCN8A gene, which causes epilepsy. Margot's condition causes frequent seizures and developmental challenges. Determined to make a difference, Madeleine and her team are pioneering a cutting-edge genetic therapy that could one day transform treatment for Margot and others like her. In this heartfelt talk, Madeleine shares how her scientific expertise and personal journey intersect, revealing the highs and lows of developing life-changing treatments. From innovative approaches using Antisense Oligonucleotides (ASOs) to the unexpected success of a ketogenic diet, this story is about resilience, hope, and the power of community. Series: "Autism Tree Project Annual Neuroscience Conference" [Health and Medicine] [Science] [Show ID: 40210]

What would you like to see more of? Let us know!In today's episode of Discover Daily, we explore how Niantic, the creator of Pokémon Go, is using player-generated data to develop a sophisticated Large Geospatial Model. With over 30 billion processed images and 10 million scanned locations worldwide, this AI system is creating detailed 3D maps of the real world, raising important questions about data privacy and user consent in the age of augmented reality gaming.We also examine the recent sabotage of two critical undersea telecommunications cables in the Baltic Sea. The incident, which affected connections between Finland-Germany and Lithuania-Sweden, has reduced bandwidth capacity by one-third for some users and could cost up to $12 million per cable to repair. German Defense Minister Boris Pistorius has explicitly labeled this as an act of sabotage, prompting NATO to strengthen protection of vital undersea infrastructure.Our deep dive focuses on a fascinating discovery that might finally resolve the age-old chicken-or-egg paradox. Scientists studying Chromosphaera perkinsii, a single-celled organism found near Hawaii, have revealed that the genetic toolkit for multicellular development existed over a billion years before animals evolved. This tiny organism forms embryo-like structures and uses genes similar to those found in animal development, suggesting that the egg's fundamental mechanisms predated complex animals by hundreds of millions of years.From Perplexity's Discover Feed:https://www.perplexity.ai/page/pokemon-data-creates-ai-model-ANxDd7eARIe6c7UTG1OfrQhttps://www.perplexity.ai/page/baltic-sea-cable-sabotage-ZPHHtKJkQQuT_t3DykHcsAhttps://www.perplexity.ai/page/chicken-or-egg-paradox-solved-BBSzMjmKQtOtl8R9AGbKEwPerplexity is the fastest and most powerful way to search the web. Perplexity crawls the web and curates the most relevant and up-to-date sources (from academic papers to Reddit threads) to create the perfect response to any question or topic you're interested in. Take the world's knowledge with you anywhere. Available on iOS and Android Join our growing Discord community for the latest updates and exclusive content. Follow us on: Instagram Threads X (Twitter) YouTube Linkedin

How does primate genetic research tie into forensic science? How is collecting blood, saliva, and hair at crime scenes used for DNA typing? Professor Sreetharan Kanthaswamy, an expert in biomedicine, genetics, and forensics, joins the Good Question Podcast to share his insights. Sreetharan is a professor in the School of Mathematical and Natural Sciences at Arizona State University's West campus. He is also a Research Geneticist at the California National Primate Research Center, University of California, Davis. His unique perspective, spanning both primate genetics and forensic science, allows him to cover everything from primates living in the wild to the complex world of DNA typing… In this episode, we dive into: How studying wildlife can shed light on human social structures.  Fascinating facts about the behavioral patterns of orangutans. What genetic markers can indicate the origins of species. Ready to learn how Sreetharan applies his population, forensic, and conservation genetics knowledge for the greater good? Tune in now!     Click here to follow along with Sreetharan's groundbreaking work at ASU! Episode also available on Apple Podcasts: https://apple.co/38oMlMr

Learn about Columnar Apple Trees for Small Gardens in this episode of the Orchard People radio show. Our guests are: Kenong Xu, Associate Professor, and Laura Dougherty of Cornell University in Geneva New York and Angela Palmer, Founder and Co-Owner of Plants Nouveau in Alabama. The host of the Orchard People radio show and podcast is Susan Poizner of the fruit tree care education website www.orchardpeople.com.  FOUR WAYS TO TUNE INJoin our live show on the last Tuesday of every month at 1:00 PM ET and submit your questions and comments! Can't make it live? No worries—catch the podcast later.Here's how:Live Audio: Listen on RealityRadio101 at 1:00 PM on TuesdayLive Video: Watch live on the Orchard People YouTube page at 1:00 PM on TuesdayAudio Podcast: Download the podcast after the showVideo Podcast: Watch the recorded video on our YouTube Podcast Playlist Do you want to learn to grow organic fruit trees successfully? Sign up for OrchardPeople.com's free monthly newsletter at https://orchardpeople.com/sign-up/For premium fruit tree care education visit: https://learn.orchardpeople.com/. (00:00) - Introduction to Apple Trees (00:17) - Exploring Dwarfing and Columnar Apple Trees (01:14) - Meet the Experts: Cornell University Researchers and Horticulturalist from Plants Nouveau (03:01) - History of Columnar Apple Trees (06:14) - Audience Interaction and Questions (07:01) - Why Columnar Apple Trees are Unique (08:34) - Columnar Apple Tree Rootstocks (09:20) - Can Columnar Trees be Tip Bearing (12:16) - Genetic Research and Breeding Columnar Apple Trees for Small Gardens (16:17) - How long before a Wijcik columnar apple tree bears fruit? (17:12) - What do the apples from a Wijcik apple tree taste like? (18:21) - Do Columnar Apple Trees need Cross Pollination? (20:22) - Challenges and Benefits of Columnar Apple Trees (23:34) - Variations in the Columnar Shape (26:24) - What does Columnar Growing Habit Mean and What do Columnar Apple Trees Look Like? (29:01) - Do Columnar Apple Trees Produce as Much Fruit as Conventional Apple Trees? (29:45) - Do Columnar Apple Trees Get Canker More Frequently than Conventional Apple Trees? (32:05) - Commercial Break (35:11) - Show Resumption and Guest Introduction (35:58) - Do Columnar Apple Trees Need Pruning and Special Care? (38:00) - Marketing and Cultivars of Columnar Apple Trees (45:36) - Can Columnar Apple Trees be Used for Espalier Plantings? (47:22) - Columnar Apple Tree Rootstocks and Growing Conditions (49:15) - Columnar Apple Trees and Chill Hours for Cold and Warm Climates (51:29) - Growing Columnar Apple Trees in Pots (56:16) - Future of Columnar Apple Trees - In Outer Space??? (57:58) - Conclusion and Farewell

Dr. Jonathan Hill, VP of Science and Technology and co-founder of Wasatch Biolabs joins the podcast today to talk about the future of genetic testing technology. Dr. Hill shares his journey in genetics, starting from his undergraduate days to co-founding multiple biotech companies. They discuss the cutting-edge genomic and bioinformatic methods being developed at Wasatch Biolabs, including targeted DNA methylation sequencing and its significant implications for personalized medicine and early disease detection. Dr. Hill also elaborates on the integration of lab work and data analysis in genetic research, partnerships in diagnostic advancements, the role of AI in the future of genetic testing, and the importance of quality management in product development. Additionally, he speaks about the challenges faced in implementing these technologies and how they are being addressed. The conversation concludes with Dr. Hill's vision for the future of genetic testing and his approach to preparing students for the industry's evolving landscape.00:00 Introduction to the Episode00:25 Meet Dr. Jonathan Hill01:45 Dr. Hill's Journey in Genetics03:27 Understanding DNA Methylation Sequencing06:15 Applications in Personalized Medicine15:06 Challenges in Implementing Assays18:40 Future of Genetic Testing Technology23:14 Importance of Collaborations and Partnerships26:58 Fun and Personal Insights27:43 Conclusion and Contact InformationMore about Dr. Hill:Dr. Hill is the VP of Science and Technology and a co-founder of Wasatch BioLabs, a biotechnology company committed to transforming the field of diagnostics. The company delivers reliable laboratory services, offering transparent testing and accurate results for biotech firms, patients, and research institutions.https://www.wasatchbiolabs.com/ https://www.linkedin.com/in/jonathon-t-hill/  Qualio website:https://www.qualio.com/ Previous episodes:https://www.qualio.com/from-lab-to-launch-podcast Apply to be on the show:https://forms.gle/uUH2YtCFxJHrVGeL8 Music by keldez

En este episodio de El Siglo 21 es Hoy, te llevamos a un análisis profundo de la película Gattaca: Experimento Genético y su impacto en el contexto actual de la genética y la bioética. Capítulos:00:00 Episodio 154504:20 La Revolución Genética en la Sombra05:36 Gattaca08:15 Doctor Cantillo10:38 Prevención Genética: Tratando Enfermedades Antes de que Aparezcan12:47 El Destino en el ADN: Predicciones de Vida y Muerte Desde el Nacimiento16:01 Andrew Niccol: La Mente Detrás de Gattaca y su Compleja Visión del Futuro19:15 Diseñando el Futuro: La Selección de Rasgos en los Hijos22:54 Cuando la Perfección Falla: Cómo un Accidente Abre Nuevas Oportunidades28:31 La Ciencia Oculta en las Letras33:31 Elegir Pareja en Gattaca: La Ciencia Reemplaza al Corazón37:04 Meritocracia y Determinismo Genético en Gattaca44:37 Simbolismo Visual en Gattaca: La Escalera en Espiral y la Doble Hélice del ADN48:58 Bioética y Discriminación Genética en Gattaca52:21 El ADN Bajo Lupa: La Privacidad Genética en Riesgo56:00 CréditosGattaca, una obra maestra de la ciencia ficción, nos transporta a un futuro donde la manipulación genética no solo es posible, sino que define la vida de los individuos desde el momento en que nacen. Exploramos cómo en este mundo distópico, la selección de rasgos genéticos predice capacidades, enfermedades, y hasta la expectativa de vida, desafiando los límites de la ética en la ciencia.Conectamos estos conceptos con los avances reales en la tecnología de los cromosomas artificiales, un tema que ha generado gran expectación en la comunidad científica. Abordamos preguntas cruciales como: ¿Hasta dónde debería llegar la intervención genética en los seres humanos? ¿Es posible tratar enfermedades antes de que aparezcan? ¿Qué implicaciones tiene la pérdida de la privacidad genética en un mundo donde el ADN se convierte en el nuevo "currículum"?¿Por qué temas como la inteligencia artificial dominan las conversaciones actuales, mientras que la revolución genética, que tiene el potencial de transformar radicalmente nuestras vidas, permanece en la sombra? También analizamos el simbolismo y los elementos visuales de Gattaca, como la escalera en espiral que recuerda a una doble hélice de ADN, y cómo estos detalles enriquecen la narrativa.Este episodio es una invitación a reflexionar sobre los dilemas bioéticos que Gattaca plantea, y que cada vez se acercan más a nuestra realidad. ¿Es la ciencia ficción realmente ficción, o estamos viendo los primeros pasos hacia un futuro donde la genética lo dicta todo? Acompáñanos en esta exploración de cómo la película Gattaca no solo anticipa futuros escenarios genéticos, sino que también nos advierte sobre los peligros de una sociedad obsesionada con la perfección genética y el control total del ADN.Bibliografía"Gattaca (1997) - Película completa," OK.RU."Gattaca: The Impact of Science Fiction on Genetic Research," David A. Kirby: The New Eugenics in Cinema."The New Eugenics in Cinema: Genetic Determinism and Gene Therapy in GATTACA," Science Magazine."French Anderson, El Pionero de la Terapia Génica," Voz de América.Groer, Annie, y Debra Gerhart. "Father of Gene Therapy, W. French Anderson, on Science and Scandal," STAT News.Conviértete en un seguidor de este podcast: https://www.spreaker.com/podcast/el-siglo-21-es-hoy--880846/support.

En este episodio de El Siglo 21 es Hoy, te llevamos a un análisis profundo de la película Gattaca: Experimento Genético y su impacto en el contexto actual de la genética y la bioética. Capítulos:00:00 Episodio 154504:20 La Revolución Genética en la Sombra05:36 Gattaca08:15 Doctor Cantillo10:38 Prevención Genética: Tratando Enfermedades Antes de que Aparezcan12:47 El Destino en el ADN: Predicciones de Vida y Muerte Desde el Nacimiento16:01 Andrew Niccol: La Mente Detrás de Gattaca y su Compleja Visión del Futuro19:15 Diseñando el Futuro: La Selección de Rasgos en los Hijos22:54 Cuando la Perfección Falla: Cómo un Accidente Abre Nuevas Oportunidades28:31 La Ciencia Oculta en las Letras33:31 Elegir Pareja en Gattaca: La Ciencia Reemplaza al Corazón37:04 Meritocracia y Determinismo Genético en Gattaca44:37 Simbolismo Visual en Gattaca: La Escalera en Espiral y la Doble Hélice del ADN48:58 Bioética y Discriminación Genética en Gattaca52:21 El ADN Bajo Lupa: La Privacidad Genética en Riesgo56:00 CréditosGattaca, una obra maestra de la ciencia ficción, nos transporta a un futuro donde la manipulación genética no solo es posible, sino que define la vida de los individuos desde el momento en que nacen. Exploramos cómo en este mundo distópico, la selección de rasgos genéticos predice capacidades, enfermedades, y hasta la expectativa de vida, desafiando los límites de la ética en la ciencia.Conectamos estos conceptos con los avances reales en la tecnología de los cromosomas artificiales, un tema que ha generado gran expectación en la comunidad científica. Abordamos preguntas cruciales como: ¿Hasta dónde debería llegar la intervención genética en los seres humanos? ¿Es posible tratar enfermedades antes de que aparezcan? ¿Qué implicaciones tiene la pérdida de la privacidad genética en un mundo donde el ADN se convierte en el nuevo "currículum"?¿Por qué temas como la inteligencia artificial dominan las conversaciones actuales, mientras que la revolución genética, que tiene el potencial de transformar radicalmente nuestras vidas, permanece en la sombra? También analizamos el simbolismo y los elementos visuales de Gattaca, como la escalera en espiral que recuerda a una doble hélice de ADN, y cómo estos detalles enriquecen la narrativa.Este episodio es una invitación a reflexionar sobre los dilemas bioéticos que Gattaca plantea, y que cada vez se acercan más a nuestra realidad. ¿Es la ciencia ficción realmente ficción, o estamos viendo los primeros pasos hacia un futuro donde la genética lo dicta todo? Acompáñanos en esta exploración de cómo la película Gattaca no solo anticipa futuros escenarios genéticos, sino que también nos advierte sobre los peligros de una sociedad obsesionada con la perfección genética y el control total del ADN.Bibliografía"Gattaca (1997) - Película completa," OK.RU."Gattaca: The Impact of Science Fiction on Genetic Research," David A. Kirby: The New Eugenics in Cinema."The New Eugenics in Cinema: Genetic Determinism and Gene Therapy in GATTACA," Science Magazine."French Anderson, El Pionero de la Terapia Génica," Voz de América.Groer, Annie, y Debra Gerhart. "Father of Gene Therapy, W. French Anderson, on Science and Scandal," STAT News.Conviértete en un seguidor de este podcast: https://www.spreaker.com/podcast/el-siglo-21-es-hoy--880846/support.

En este episodio de El Siglo 21 es Hoy, te llevamos a un análisis profundo de la película Gattaca: Experimento Genético y su impacto en el contexto actual de la genética y la bioética. Capítulos:00:00 Episodio 154504:20 La Revolución Genética en la Sombra05:36 Gattaca08:15 Doctor Cantillo10:38 Prevención Genética: Tratando Enfermedades Antes de que Aparezcan12:47 El Destino en el ADN: Predicciones de Vida y Muerte Desde el Nacimiento16:01 Andrew Niccol: La Mente Detrás de Gattaca y su Compleja Visión del Futuro19:15 Diseñando el Futuro: La Selección de Rasgos en los Hijos22:54 Cuando la Perfección Falla: Cómo un Accidente Abre Nuevas Oportunidades28:31 La Ciencia Oculta en las Letras33:31 Elegir Pareja en Gattaca: La Ciencia Reemplaza al Corazón37:04 Meritocracia y Determinismo Genético en Gattaca44:37 Simbolismo Visual en Gattaca: La Escalera en Espiral y la Doble Hélice del ADN48:58 Bioética y Discriminación Genética en Gattaca52:21 El ADN Bajo Lupa: La Privacidad Genética en Riesgo56:00 CréditosOye el episodio en Spotify.Gattaca, una obra maestra de la ciencia ficción, nos transporta a un futuro donde la manipulación genética no solo es posible, sino que define la vida de los individuos desde el momento en que nacen. Exploramos cómo en este mundo distópico, la selección de rasgos genéticos predice capacidades, enfermedades, y hasta la expectativa de vida, desafiando los límites de la ética en la ciencia.Conectamos estos conceptos con los avances reales en la tecnología de los cromosomas artificiales, un tema que ha generado gran expectación en la comunidad científica. Abordamos preguntas cruciales como: ¿Hasta dónde debería llegar la intervención genética en los seres humanos? ¿Es posible tratar enfermedades antes de que aparezcan? ¿Qué implicaciones tiene la pérdida de la privacidad genética en un mundo donde el ADN se convierte en el nuevo "currículum"?¿Por qué temas como la inteligencia artificial dominan las conversaciones actuales, mientras que la revolución genética, que tiene el potencial de transformar radicalmente nuestras vidas, permanece en la sombra? También analizamos el simbolismo y los elementos visuales de Gattaca, como la escalera en espiral que recuerda a una doble hélice de ADN, y cómo estos detalles enriquecen la narrativa.Este episodio es una invitación a reflexionar sobre los dilemas bioéticos que Gattaca plantea, y que cada vez se acercan más a nuestra realidad. ¿Es la ciencia ficción realmente ficción, o estamos viendo los primeros pasos hacia un futuro donde la genética lo dicta todo? Acompáñanos en esta exploración de cómo la película Gattaca no solo anticipa futuros escenarios genéticos, sino que también nos advierte sobre los peligros de una sociedad obsesionada con la perfección genética y el control total del ADN.Bibliografía"Gattaca (1997) - Película completa," OK.RU."Gattaca: The Impact of Science Fiction on Genetic Research," David A. Kirby: The New Eugenics in Cinema."The New Eugenics in Cinema: Genetic Determinism and Gene Therapy in GATTACA," Science Magazine."French Anderson, El Pionero de la Terapia Génica," Voz de América.Groer, Annie, y Debra Gerhart. "Father of Gene Therapy, W. French Anderson, on Science and Scandal," STAT News.Conviértete en un seguidor de este podcast: https://www.spreaker.com/podcast/el-siglo-21-es-hoy--880846/support.

Christa Lafayette, the innovative CEO of Etalon Equine Genetics, returns to the podcast, this time with the results of the genetic tests that her company ran on two of Russell True's horses. He's learning the results in real time, as are you. Christa shares her insights on how genetic information can enhance breeding programs, improve horse health, and even predict performance traits. Whether you're a horse lover or a science geek, this episode is an enlightening journey into the genetic blueprint of our equine companions and how genetic research is shaping the future of the horse industry.

Children's genetic disorders and the non-profit Cool Cars for Kids were discussed by Sarah E. Raible, MS, LCGC, a genetic counselor and the clinical director of the Center for Cornelia de Lange Syndrome (CdLS), and rare disease core leader in the Roberts Individualized Medical Genetics Center (IMGC) at Children's Hospital of Philadelphia  and the Chief Operating Officer of Cool Cars for Kids, and Lainey Moseley, an Emmy® award winning journalist working for CBS and NBC News,  founder of CHOPS Syndrome Global; an organization raising awareness for her daughter Leta's rare disease CHOPS Syndrome, and Cool Cars for Kids Board Member.  We talked about how ‘rare' is rare?  One in 11 families are affected by some form of genetic disorder, ranging from clef lip, spina bifida, to heart malformations and other identifiable conditions.  Othe genetic mutations can be so rare that – as in the case of Leta, the exact cause can take decades to discover.  Her disorder was identified by a CHOP test when she was 18, her genetic condition named CHOPS Syndrome in honor of the hospital that discovered it.  Today there are some 40 patients found in Italy, Texas and around the globe, now connected by Lainey's organization.    We spoke about the extra roles the parents of these children must take on, caregiver, advocate and researcher.  Lainey is currently in post-production on her documentary RARE, an essay-style documentary in three acts, each delving into the lives of families grappling with rare diseases, the immense challenges they face, and the remarkable scientific progress they drive in the quest for cures. She has also organized their 2nd CHOPS Syndrome symposium in Philadelphia this summer, July 19th and 20th where Unravel Bioscience will be discussing their results for potential FDA repurposed drugs that may be treatment options for their kids.   Fundraising is vital to these families and to the research that helps identify their conditions.  Cool Cars for Kids was founded by former CHOP geneticist Ian Krantz , Sarah and others to provide help and hope to children with rare genetic diagnoses and their families, and to support research that will identify the best possible treatments and cures.  Their annual fundraiser, the Seventh Annual Philadelphia Concours d'Elegance kicks off with a Preview Gala on Saturday, June 22, followed by the main event on Sunday, June 23 at the Simeone Foundation Automotive Museum.  Tis year's featured model is the Jaguar, with special displays and a panel discussion about the vehicle.  There will again be the Cool Car Corral, an outdoor space where anyone can display their ‘cool' car, classic, rare or just beloved.  Kids activities, music, food trucks and admission to the Simeon racing car collection are part of the day's fun.   Tickets and corral registration available by visiting philadelphiaconcours.com or coolcarsforkids.org.  Walk-ins and drive-ins are welcome that day.

Professor Parry Guilford is known for successfully in identifying the first known genetic mutations in the CDH1 gene, leading to the description of a new cancer syndrome Hereditary Diffuse Gastric Cancer (HDGC). This discovery has conservatively saved 27,000 people from developing a severe form of stomach cancer. Parry is determined to continue to change the course of HDGC stomach cancer patients outcomes, he is invested in the CDH1 mutation families and feels their trials as if they were his own. We discuss genetic counselling, the age at which we test our children for hereditary cancers, his work on lobular breast cancer, bowel cancer and funding research. 

Join us in this inspiring episode of the Living the Dream podcast with Curveball, where we sit down with the multifaceted Doctor Cindy Starke. With her compelling story of overcoming childhood trauma and her journey through medicine, Dr. Starke shares her insights on mindset, relationships, and personal growth. Discover how she brings out the champion in others through her work in Soul Circle Academy and her transition from full-time medicine to entrepreneurship. Plus, delve into her experience with Ironman triathlons and her book, "From Fear and Failure to the Finish Line." Don't miss Dr. Starke's powerful message on breaking generational patterns and creating a fulfilling life.www.drcindystarke.com

In this episode of ATP, Shambhavi Naik and Saurabh Todi discuss the recent completion of the 10,000 Genome Project and the importance of collecting such data for medical research. Do check out Takshashila's public policy courses: https://school.takshashila.org.in/courses We are @‌IVMPodcasts on Facebook, Twitter, & Instagram. https://twitter.com/IVMPodcasts https://www.instagram.com/ivmpodcasts/?hl=en https://www.facebook.com/ivmpodcasts/ You can check out our website at https://shows.ivmpodcasts.com/featured Follow the show across platforms: Spotify, Google Podcasts, Apple Podcasts, JioSaavn, Gaana, Amazon Music .Do share the word with your folks  See omnystudio.com/listener for privacy information.

Arafaat Valiani (University of Oregon) has a conversation with the Infectious Historians about genomic and genetic research with indigenous communities. Arafaat goes over what is genomic research, then describes how tests work and the bioethical debate surrounding them. He describes some of the different approaches among biomedical researchers that approach marginalized communities. The conversation moves on to discuss some of the practicalities of working with and within these communities, followed by a reflection about whether other communities should adopt similar practices as well. The interview finishes with a discussion of the role of AI within genomic research.

In this captivating episode, I'm joined by Elena Buglo. Elena's background is a PhD in neurogenetics from the University of Miami Miller School of Medicine. She now works supporting a rare disease biotech company in medical affairs, and she leads with great passion for neuroscience, genetics and genetic editing technologies. In her research work she utilized CRISPR technology to model and study various rare disease genes. She recently started her podcast on gene therapies and precision medicines. Check it out and support her by subscribing and giving a 5-star review at : https://podcasters.spotify.com/pod/show/gene-therapy-insightsElena discusses the significance of genetic diversity, advocating for a personalized approach to health that celebrates our unique genetic makeup. She explores neurodiversity, challenging conventional views on cognitive and physiological differences, and emphasizes the holistic interconnectedness of our biological systems. Her expertise illuminates the critical role of mitochondria and other cellular components in overall health, highlighting the need for comprehensive health strategies.This episode is a must-listen for those interested in genetic science, personalized medicine, and the future of healthcare. Elena's perspectives encourage a deeper understanding of our biological uniqueness and the potential of gene editing technologies to revolutionize health and wellness. Whether you're in the medical field, facing genetic health challenges, or simply fascinated by science, Elena's insights offer valuable guidance on navigating the complexities of human biology and the promise of tailored healthcare solutions.Key Points From This Episode:Sleep and Overall Health [00:01:53]Introduction to Neurogenetics Discussion [00:03:53]Explaining Neurogenetics in Simple Terms [00:05:0]The Impact of Debilitating Genetic Diseases [00:07:13]Genetics vs. Epigenetics [00:09:01]Personal Genetic Insights and Lifestyle Adjustments [00:14:05]The Complexity of Genetic Influence on Health [00:27:10]The Risks of Over-Optimizing Health [00:29:57]The Role of Geneticists in Healthcare [00:37:45]Genetic Testing and Personalized Medicine [00:42:50]BDNF Levels and Genetic Variability [00:44:46]Genetic Compensation and Physiological Adaptation [00:47:59]Analogy for Genetic Function and Adaptation [00:53:52]The benefits of gene editing [00:56:35] Neurodiversity and unique phenotypes. [01:03:17] Living with ADD and medication [01:05:39]Genetic dating app. [01:11:40]  Reproduction and genetic optimization. [01:13:23]Attraction to different genetic backgrounds. [01:18:23]Genetic attraction and relationships. [01:22:37] Lysosomal storage disorders. [01:29:57] Unique backgrounds and accepting differences. [01:33:17] Genetics and intuition. [01:39:05] Looking to discover your science and optimize your life?APPLY FOR HEALTH OPTIMIZATION COACHINGhttps://calendly.com/andrespreschel/intro-call-with-andresLinks Mentioned in Today's Episode:Click HERE to save on BiOptimizers MagnesiumPeopleElena Buglo LinkedinGeorge Church:WikiTwitter: @geochurchBen Greenfield: Ben Greenfield FitnessSupport the show

Today's Episode Dr. Raj talks with Dr. Rudy Tanzi about his work in Alzheimer's Disease research, his acronym SHIELD for evading its progression, and how his background as a musician has intersected with this work.  Today's Guest Dr. Tanzi is the Vice-Chair of Neurology, Director of the Genetics and Aging Research Unit, Co-Director of the Henry and Allison McCance Center for Brain Health, and Co-Director of the MassGeneral Institute for Neurodegenerative Disease at Massachusetts General Hospital. He also serves as the Joseph P. and Rose F. Kennedy Professor of Neurology at Harvard Medical School. Dr. Tanzi received his BS (microbiology) and BA (history) at the University of Rochester in 1980 and his PhD (neurobiology) at Harvard Medical School in 1990. Dr. Tanzi co-discovered the first Alzheimer's disease (AD) gene, the amyloid precursor protein (APP) gene, and the two other early-onset familial AD genes, presenilin 1 and presenilin 2. As leader of the Cure Alzheimer's Fund Alzheimer's Genome Project, Dr. Tanzi identified several other AD genes, including CD33, the first AD gene shown to regulate neuroinflammation. He also discovered the Wilson's disease gene and other neurological disease genes. Dr. Tanzi's team was the first to use human stem cells to create three-dimensional neural-glial; cell culture organoids of AD, dubbed “Alzheimer's-in-a-Dish”. This model was the first to recapitulate all three key AD pathological hallmarks in vitro, and first to definitively show that amyloid plaques directly cause neurofibrillary tangles - and also made drug screening for AD faster and more cost-effective. Using this system, Dr. Tanzi has developed several novel therapies for AD including gamma secretase modulators targeting amyloid pathology and AMX0035, which was already successful in a clinical trial of ALS and now seeking FDA approval. Dr. Tanzi also discovered that beta-amyloid plays a functional role in the brain as an anti-microbial peptide, supporting a role for infection in AD pathology. Dr. Tanzi serves as Chair of the Cure Alzheimer's Fund Research Leadership Group and numerous advisory and editorial boards. He has been named to TIME magazine's list of TIME100 Most Influential People in the World. Dr. Tanzi is a New York Times bestselling author who has co-authored the books Decoding Darkness, and the bestsellers Super Brain, Super Genes, and The Healing Self with Dr. Deepak Chopra. Dr. Tanzi has hosted several shows on public television, regularly appears on television news programs, and has testified to Congress on both Alzheimer's disease and brain health. About Dr. Raj Dr Raj is a quadruple board certified physician and associate professor at the University of Southern California. He was a co-host on the TNT series Chasing the Cure with Ann Curry, a regular on the TV Show The Doctors for the past 7 seasons and has a weekly medical segment on ABC news Los Angeles. Want more Dr. Raj? Check out the Beyond the Pearls lecture series! The Ultimate High Yield Bundle: The complete review of high-yield clinical medicine topics necessary for graduate medical education board exams including NBME, USMLE Steps 1/2/3, ITE and ABIM Boards. You can also listen to the Beyond the Pearls podcast. Check out our other shows: Physiology by Physeo Step 1 Success Stories The InsideTheBoards Study Smarter Podcast The InsideTheBoards Podcast Produced by Ars Longa Media To learn more about us and this podcast, visit arslonga.media. You can leave feedback or suggestions at arslonga.media/contact or by emailing info@arslonga.media. Produced by: Christopher Breitigan and Erin McCue. Executive Producer: Patrick C. Beeman, MD Legal Stuff The information presented in this podcast is intended for educational purposes only and should not be construed as professional or medical advice. Learn more about your ad choices. Visit megaphone.fm/adchoices

We're joined by Dr. Rebecca Foran, who currently leads research & development at Wisdom Panel. Learn about how canine health research is conducted, and how breeders play a crucial part in this process. Dr. Foran also discusses the details of some genetic disorders including CDDY and IVDD in addition to the results of recent genetic research.

Robert Joseph Plomin CBE FBA is an American/British psychologist and geneticist best known for his work in twin studies and behavior genetics. A Review of General Psychology survey, published in 2002, ranked Plomin as the 71st most cited psychologist of the 20th century. Newsletter sign up (new and exciting developments) https://learningwithlowell.us12.list-manage.com/subscribe?u=08ed8a56013d8b3a3c01e27fc&id=6ecaa9189b Join this channel to get access to perks: https://www.youtube.com/channel/UCzri06unR-lMXbl6sqWP_-Q/join Over 321 books from 170 plus interviews over 5 years https://www.learningwithlowell.com/over-321-books-from-170-interviews-over-5-years-for-autodidacts/ https://youtu.be/i4i69UhtqQg PODCAST INFO: The Learning With Lowell show is a series for the everyday mammal. In this show we'll learn about leadership, science, and people building their change into the world. The goal is to dig deeply into people who most of us wouldn't normally ever get to hear. The Host of the show – Lowell Thompson- is a lifelong autodidact, serial problem solver, and founder of startups. LINKS Spotify: https://open.spotify.com/show/66eFLHQclKe5p3bMXsCTRH RSS: https://www.learningwithlowell.com/feed/podcast/ Youtube: https://www.youtube.com/channel/UCzri06unR-lMXbl6sqWP_-Q Youtube clips: https://www.youtube.com/channel/UC-B5x371AzTGgK-_q3U_KfA Website: https://www.learningwithlowell.com/ Robert Plomin links https://www.amazon.com/Blueprint-How-DNA-Makes-Press/dp/0262039168 https://www.kcl.ac.uk/people/robert-plomin https://en.wikipedia.org/wiki/Robert_Plomin Timestamps 00:00 Introduction to Psychological Concepts and Genetics 00:19 Debunking the Concept of Jungian Archetypes and Typologies 01:02 The Misconceptions of Genetics and Dichotomies 01:56 The Shift from Determinism to Probability in Genetics 02:19 The Problem with Typologies and Psychiatric Classifications 03:03 The Myth of Myers Briggs and Other Personality Tests 04:58 The Role of Genetics in Predicting Job Performance 05:50 The Shift from Treatment to Prevention in Medicine 09:18 The Impact of DNA Testing on Insurance Policies 19:55 The Future of DNA Testing in Dating and Relationships 36:32 The Role of Genetics in Child Rearing and Obesity Prevention 40:06 Motivation and Environment Management 40:30 The Problem with Parenting Industry 40:49 The Influence of Talent and Parenting 41:16 The Misconceptions about Parenting 41:56 The Impact of Genetics on Mental Health 42:34 The Role of Genetics in Personality and Behavior 43:08 The Influence of Parenting Styles on Children's Development 43:58 The Importance of Genetics in Parenting 46:04 The Role of Genetics in Intelligence and Achievement 51:09 The Impact of Genetics on Generational Trauma 55:53 The Future of Genetic Testing and Its Implications 58:23 The Intersection of Genetics and Social Constructs 01:08:11 The Future of Genetic Research and Its Potential Impact 01:17:52 The Role of Genetics in Longevity and Health 01:18:42 The Future of Genetic Research and Its Potential Impact

David Whitehead joins Brendan to discuss the hidden networks of globalist power that seek to retain control over the masses from behind the scenes (mostly). Who are the would-be powers ruling the world? What circles do they move in? What are the nexus points between these shadowy networks and visible geopolitical activity and known figureheads? David talks about the esoteric knowledge base held and protected by these "elites" for many years now. This episode touches on the divine right to rule, Black Nobility, royal connections to the occult, child trafficking, Vatican involvement, freemasonry, occult symbolism (like the all-seeing eye), divide and conquer tactics, how old traditions became corrupted over time, the private religions and practices of public figures, John of God, and much more. Special Guest: David Whitehead.

Dr Marta Di Forti is a Clinical Reader in Psychosis Research at the Dept of Social, Developmental and Genetic Research, KCL. She leads the first Cannabis Clinic for patients with Psychotic disorders in UK. In 2021 she awarded the Royal College of Psychiatrist Researcher of the year prize. In 2020 she was granted a MRC Senior Research Fellowship to expand her research in the role of cannabis use in psychosis and its underlying biology. Today on the show we discuss: why cannabis is more dangerous than ever today, what Marta's research reveals about the link between cannabis and psychosis, why edibles can lead to an overdose, risk factors for developing psychosis and the role that your age plays in this, how to recover from psychosis and cannabis addiction, does the dosage actually make the poison and much more. ⚠ WELLNESS DISCLAIMER ⚠ Please be advised; the topics related to health and mental health in my content are for informational, discussion, and entertainment purposes only. The content is not intended to be a substitute for professional advice, diagnosis, or treatment. Always seek the advice of your health or mental health professional or other qualified health provider with any questions you may have regarding your current condition. Never disregard professional advice or delay in seeking it because of something you have heard from your favorite creator, on social media, or shared within content you've consumed. If you are in crisis or you think you may have an emergency, call your doctor or 911 immediately. If you do not have a health professional who is able to assist you, use these resources to find help: Emergency Medical Services—911 If the situation is potentially life-threatening, get immediate emergency assistance by calling 911, available 24 hours a day. National Suicide Prevention Lifeline, 1-800-273-TALK (8255) or https://suicidepreventionlifeline.org. SAMHSA addiction and mental health treatment Referral Helpline, 1-877-SAMHSA7 (1-877-726-4727) and https://www.samhsa.gov Learn more about your ad choices. Visit megaphone.fm/adchoices

This podcast is a commentary and does not contain any copyrighted material of the reference source. We strongly recommend accessing/buying the reference source at the same time. ■Reference Source https://www.ted.com/talks/keolu_fox_why_genetic_research_must_be_more_diverse ■Post on this topic (You can get FREE learning materials!) https://englist.me/101-academic-words-reference-from-keolu-fox-why-genetic-research-must-be-more-diverse-ted-talk/ ■Youtube Video https://youtu.be/5YMOTXJszxQ (All Words) https://youtu.be/eLdj-4LZGm4 (Advanced Words) https://youtu.be/6RmMLZlwVTU (Quick Look) ■Top Page for Further Materials https://englist.me/ ■SNS (Please follow!)

Evidence is growing that China is experimenting with genetic manipulation to create super soldiers, human-animal hybrids, bioweapons, and other horrors. But are the Chinese using genetic information from the millions of Americans who have handed over their DNA to corporations like 23andMe and AncestryDNA to fuel their disturbing experiments? James Poulos is joined by geneticist and thought leader Razib Khan to discuss the shocking developments in genetic research, the woke ideological capture of America's research institutions, whether obesity is feminizing men and contributing to the current gender madness, and much more.

I have never wanted a “cure” for my albinism and corresponding visual impairment, but only recently found the words to explain why. Research regarding treatments for and the genetic origins of disabilities raises complex ethical questions. Does studying albinism in a laboratory genuinely improve people's lives, or does it merely satisfy the curiosity of medical professionals? In “I'm Not Broken,” I argue that albinism should be viewed as part of one's identity and a source of community rather than an undesirable mutation. I consider the emotional, social, and political impacts of seeking to reverse or cure blindness. I then argue how redirecting these funds towards developing assistive technology, advocating for legislative changes, and providing necessities (sunscreen, UV protective gear, etc.) to people with albinism would have a stronger impact. Keep in mind that this is a deeply personal subject. My goal is to share my perspective and lived experience—not speak on behalf of the entire albinism community.  “I think it is very important to center lived experience and the voices of people with albinism when discussing research about our condition. Because when it's only parents and medical professionals making these decisions, they miss part of the picture.” Connect with Legally Blonde & Blind! Website  - https://www.legallyblondeblind.com/  Instagram - https://www.instagram.com/legallybb_/?hl=en  Facebook - https://www.facebook.com/legallybb/  LinkedIn - https://www.linkedin.com/company/legally-blonde-blind/ Key Points: 0:00 - Intro 2:30 - Why is genetic research such a complex issue in the disability community? 5:30 - NOAH and Albinism Research  7:20 - Personal and Emotional Experiences with Albinism Research  13:30 - Does focusing on albinism at the molecular level meaningfully improve people's lives? 14:25 - The “Vision” Component - Does sight equal quality of life? 19:10 - The “Appearance” Component and Beauty of Biodiversity   21:05 - Final Thoughts  Resources:  “Should ‘Broken' Genes be Fixed? My Daughter Changed the way I think about that Question” - https://www.statnews.com/2020/02/21/should-broken-genes-be-fixed-my-daughter-changed-the-way-i-think-about-that-questi “‘Curing Blindness:' Why we Need a new Perspective on Sight Rehabilitation” - https://theconversation.com/curing-blindness-why-we-need-a-new-perspective-on-sight-rehabilitation-145276  “Is a ‘Cure' for Blindness Worth $1 Million?” - https://www.theatlantic.com/science/archive/2017/12/gene-therapy-blindness-luxturna/549059/  “Blind YouTube Star Molly Burke Doesn't Want a Cure - SHe Wants a Voice” - https://www.msnbc.com/know-your-value/blind-youtube-star-molly-burke-doesn-t-want-cure-she-n1040376 “Stop Trying to ‘Fix' My Disability” - https://youtu.be/ZPeH43XI4vA  “Do I Want to be Cured and get my Sight  back?” - https://youtu.be/IpyHoO2Q-Jk  “NOAH Research Program” - https://www.albinism.org/research/  “Nitisinone Increases Melanin in People with Albinism” - https://www.nih.gov/news-events/news-releases/nitisinone-increases-melanin-people-albinism  Transcript - https://www.legallyblondeblind.com/post/27-i-m-not-broken-why-albinism-advocacy-is-more-valuable-than-genetic-research 

In today's episode, we discuss genetic research as it pertains to the African genome. Joining us today to talk about this topic is world-renowned geneticist, Ambroise Wonkam.  Ambroise Wonkam is a Professor of Genetic Medicine and director of the McKusick-Nathans Institute of Genetic Medicine at Johns Hopkins University. Professor Wonkam received medical training from the Faculty of Medicine and Biomedical Sciences at the University of Yaoundé I. He completed a thesis in Medical Sciences from the University of Geneva in Switzerland, and a Ph.D. in Human Genetics from the University of Cape Town in South Africa. He has also received training as a specialist medical geneticist from the University of Switzerland. Professor Wonkam is a well-seasoned researcher, with more than 190 peer-reviewed publications. His research interests hone in on 1) Genomics modifiers of sickle cell disease (SCD); 2) Genetics of hearing loss, and 3) Ethical and educational issues in human genetics in Africa. Over the past 10 years, Prof. Wonkam has successfully led numerous NIH- and Wellcome Trust–funded projects, accounting for about 20 million USD. His research projects span several countries across Africa including Tanzania, Cameroon, Nigeria, Zimbabwe, Zambia, Uganda, Mali, Sudan, Rwanda, and Ghana.Additionally, Professor Wonkam serves as president of the African Society of Human Genetics, the chair of the steering committee of H3 Africa, a board member of the International Federation of Human Genetics Societies, a steering committee member of the Global Genetic Medicine Collaborative (G2MC), and a faculty scholar of the Human Genome Organization (HUGO). Furthermore, he is the associate editor of the American Journal of Human Genetics, the American Journal of Medical Genetics, and the Journal of Community Genetics, the academic editor of PLoS One, and a member of the editorial board of Human Genetics.Links/References:Five Priorities of African Genomics Research: The Next FrontierAmbroise Wonkam, Nchangwi S. Munung, Collet Dandara, Kevin K. Esoh, Neil A. Hanchard, Guida LandoureAnnual Review of Genomics and Human Genetics 2022 23:1, 499-521https://www.annualreviews.org/doi/abs/10.1146/annurev-genom-111521-102452 Follow us on Twitter (@unfiltered_gh), LinkedIn (Global Health Unfiltered!), and Instagram (@ghunfiltered).Keep up with us on Twitter: @desmondtanko @ulricksidney and @DrellaamoakoContact us: unfilteredgh@gmail.comAudio editing and social media marketing: Diana NkhomaResearch intern: Chisomo MwaleTheme music: Antidote by KetsaArtwork: Chidiebere Ibe

Emerging Genetic Research with Chad Cruchley #89 Over the last few decades a number of strains have come to market with huge success. MyfloraDNA is a genetics company. In this interview we meet Analytical Consultant, Chad Cruchley. Chad is a professional in the field with more than 15 years of experience in cannabis material, testing, and development. In this episode we discuss why it's important to test our plants, why the current mandates COAs need improvement and the risks consumers face when consuming untested and poorly tested cannabis products? What can be done to mitigate these risks? That's the topic for today. The Cannabis Advocate podcast advocates for businesses in the cannabis industry and explores the unique challenges they face. Despite hurdles in legislation, regulation, and culture, there are tremendous opportunities for growers, manufacturers and retail sellers of cannabis products. Many of these issues are unique to the cannabis industry. This podcast speaks to these common concerns and shares stories of success. This is a production of Habanero Media.  https://habaneromedia.net To subscribe to the podcast go to  https://cannabisadvocatepodcast.com/listen/ If you have a question or comment, https://cannabisadvocatepodcast.com/contact We would love to hear from you!

Diversity in genetic research is a key part of health careNeil Hanchard, senior investigator, and section head at the National Human Genome Research Institute, discusses genetic diversity in research. Chinese surveillance balloon elevates US-China tensions Bryan Clark, senior fellow at the Hudson Institute, discusses how the U.S. took down the Chinese surveillance balloon. American satisfaction with the government increases for first time in years Forrest Morgeson, director of research at the American Customer Satisfaction Index, discusses the increase in American satisfaction with the government.See Privacy Policy at https://art19.com/privacy and California Privacy Notice at https://art19.com/privacy#do-not-sell-my-info.

This episode, our Partnerships Lead, Lindsey Wahlstrom-Edwards dove into the importance of representation in genetic research, covering the techniques used by leading organisations to make research more accessible and representative. Lindsey is joined by Listen to speakers Natasha Ratcliffe of COUCH Health, Del Smith of Acclinate and Ebony Scott of Lupus Research Alliance to learn how to make sure your precision medicine study is inclusive by design.

This episode, our Partnerships Lead, Lindsey Wahlstrom-Edwards dove into the importance of representation in genetic research, covering the techniques used by leading organisations to make research more accessible and representative. Lindsey is joined by Listen to speakers Natasha Ratcliffe of COUCH Health, Del Smith of Acclinate and Ebony Scott of Lupus Research Alliance to learn how to make sure your precision medicine study is inclusive by design.

In this week's episode, GOLD speaks to Patrick Short, CEO, Sano Genetics, about the challenges and opportunities in genetic medicine today. He discusses his personal connection to tackling genetic diseases, the top reasons behind research participation hesitancy and the therapy areas in which he believes genomic testing and medicine could be most impactful. Plus, news from the World Health Summit. If you're interested in learning more about the topic areas discussed in this episode, check out the following content: Tackling the trust gap in genomic medicine https://www.emg-gold.com/post/tackling-the-trust-gap-in-genomic-medicine The rare disease disparity https://www.emg-gold.com/post/the-rare-disease-disparity Davidek Herron on embracing pharma's digital transformation https://www.emg-gold.com/post/embracing-pharma-s-digital-transformation

Dr. Nathaniel Jeanson, research biologist at Answers in Genesis, joins the Master Books podcast to share his breakthrough research of human DNA and how it has proven the authority of the Bible. In his book, Traced: Human DNA's Big Surprise, Dr. Jeanson shows that genetically we can all trace our ancestry back to the family on Noah's Ark. This information puts Creation Science on the offensive and evolutionists on the defense when debating the biblical timeline. It also disproves racial superiority theories and demolishes the idea of white surpremacy.  Homeschool families with this new brand new research will be able to add the facts to their student's history and bible curriculum. Save an additional 20% on Traced: Human DNA's Big Surprise by Dr. Nathaniel Jeanson at MasterBooks.com between 10/17 - 10/23/22 using Coupon Code: TRACED20 Purchase Traced: http://masterbooks.com/traced Show Highlights: 1:55 - Dr Jeanson's homeschool background 3:39 - Human DNA's Big Surprise 4:00 – Tracing your ancestry back to Noah's family 5:53 – The Rosetta stone of human history 6:55 – DNA research gives the indigenous people their history back 7:05 – Traced offers this amazing new discovery before it is incorporated in homeschool history curriculum 8:28 – A new phase of Creation Science 9:35 – Dr. Jeanson homeschools his children 9:42 – Know which descendant of Noah you came from 11:12 – How this DNA Research impacts the age of the earth debate 16:03 – Creation Scientists have met the standard of science that evolutionist have demanded 17:16 – Evolutionists' response to the DNA research presented in Traced 21:56 – New DNA research disproves racial biases and could resolve racial conflicts 25:40 – How can anyone claim racial superiority (white supremacy for example) with these facts? 27:46 – Traced is a readable history book tracing humanity's DNA

Hosted by Andrew Keen, Keen On features conversations with some of the world's leading thinkers and writers about the economic, political, and technological issues being discussed in the news, right now. In this episode, Andrew is joined by Alice Wexler, author of The Analyst: A Daughter's Memoir. Alice Wexler is the author of a two-volume biography of Emma Goldman as well as Mapping Fate: A Memoir of Family, Risk, and Genetic Research (1995) and The Woman Who Walked Into the Sea: Huntington's and the Making of a Genetic Disease (2008). She is a former Guggenheim fellow and is active on the board of the Hereditary Disease Foundation. Learn more about your ad choices. Visit megaphone.fm/adchoices

--{ "Sentience in the Balance - Treasure or Trash? - Your Choice."}-- System of commerce based on creating unhappiness - Maximizing profit, cheapening product. New religion of State-Earth worship - Happy sterilization volunteers to save Gaia. Culture Creation - Mimicry of what is seen on stage - Military music for war. Britain-Europe Merger - Karl Marx: 3 Trading Blocs, Most Favoured Nation status. San Francisco U.N. Charter. Australia, New Zealand - Royal Institute for International Affairs - Royal Charter on behalf of London Elite. Genetic Research, Engineering - Complete Predictability of Every Individual - Active ID Card - "Defective" genes. "Changing of the Age" - Pisces out, Aquarius in - "Heavenly Plan" explained. "What group is doing this?"-All competing top groups have been amalgamated. Computer to Cell-Phone to Brain-Chip - Public seeking "relief" - Tranquilizers and sedative drugs. John Stuart Mill (father and son) - Eradication of certain races, peoples, creeds - Hitler - Eugenics - Nobility Genealogies - Inbred Psychopaths. Pyramid from Capstone down to Wasteland (General Public) - MATRIX=Mother, World of MATTER. 800 B.C.: Coined Money - Phoenicians - Existence to Serve Economic System. Free Trade Negotiations - NAFTA - Preamble Terminology - Integration of US-Canada-Mexico, then Chile. New Feudal Overlords: International Corporations - British East India Co. - Royal Shareholders. Adam Weishaupt, Illuminati. Philanthropic Foundations under guise of Charity. Knowing what is happening - Transcending Worry - Sense of Peace from Knowing. (BOOK: "The Next Million Years" by Charles Galton Darwin)

In this third pandemic summer, it's difficult to say anything about Covid that hasn't been said before. More than two years into this transformative event, we've pretty much heard it all. But that doesn't mean we've reached a state of peaceful coexistence with the virus, or an acceptance of pandemic life. In spite of all that's unfolded since news of a novel respiratory virus emerged out of Wuhan, China in late 2019, the infection has continued to surprise us and catch us off guard. Even at this late stage, with many effective vaccines and therapies and a near global consensus from authorities that it's time to roll back measures and learn to “live with the virus”, we continue to struggle with new variants, massive numbers of infections and, in spite of the many effective means of prevention and treatment at our disposal, illness and death. While many of you have probably had Covid, or at the very least know someone who has, we are by no means done with this pandemic. I've been hesitant to dedicate an episode to Covid and uncertain of the point of expending yet more energy on what is certainly the most talked about subject of the last two years. But faced with the virus's persistent and ever-changing impact on our lives, and having so many unanswered and nagging questions about our response to it, I decided it needed to be done. I chose Donald Vinh, an infectious disease clinician and researcher, as my guest for this conversation. Don is an experienced medical communicator, and a measured, rigorous voice on Covid. I came to know of him because of his vocal and unflinching but always factual assessments of our local response to Covid here in Quebec. He's also actively engaged in research on Covid, and contributed to an international study on severe Covid that was published in the prestigious journal Science in 2020 and was named one of 2020's 10 remarkable scientific discoveries by the equally prestigious journal Nature. So, he seemed like the ideal person to have on for a deep dive on Covid. Donald Vinh is an Infectious Disease specialist and Medical Microbiologist at the McGill University Health Centre. He is Director of the Centre of Excellence for Genetic Research in Infection and Immunity, and Fonds de recherche du Québec Santé Senior Scholar with a translational research program on human immunodeficiencies and genetic susceptibility to infectious diseases at the Research Institute of the McGill University Health Centre. His frequent media appearances have earned him a reputation as a trusted voice on infectious diseases, such as Covid-19, monkeypox, and the rare diseases he studies. He has been interviewed on many occasions by such outlets as CBC, BBC, and NPR. Don and I talked about what his research has to teach us about Covid and how it shifts the paradigm for understanding infectious diseases, his evolution as a medical and scientific communicator, and the benefits and pitfalls of Covid Twitter. ***Links: Don's selected publicationsNature's 10 Remarkable Discoveries 2020Inborn errors of type I IFN immunity in patients with life-threatening COVID-19, Science***Recorded July 19, 2022Music: Mr Smith  Art: Jeff Landman

Rachel Chaikof was one week old when her mother, Melissa, suspected that something was wrong: she didn't startle at the sound of a slamming car door. Rachel was diagnosed with Usher Syndrome, a genetic condition which causes either inherent or progressive deafness.  But being deaf was not an absolute: as a child, Rachel became one of the first children to receive a Cochlear Implant by way of an FDA trial. Because of medical innovation, Rachel could now experience the world for how it was meant to be experienced.  But later, Rachel also began to lose her sight. At the age of 19, Rachel was diagnosed with Usher Type 1, more specifically categorized by progressive blindness in addition to loss of hearing. This time, there was no medical innovation currently available, and Melissa, an experienced advocate in the network of nonprofits dedicated to hearing loss, devoted herself to a new goal: finding a cure for Usher's Type 1.  The Chaikof's have seen all that medical innovation is capable of. That's why Melissa and her husband started the Usher 1F Collaborative, a nonprofit devoted to funding such research. And while their daughter remains optimistic about all that she is capable of, her loss of sight has compromised what she loves most about the world: seeing its beauty in color and having the freedom to navigate on her own.  While Rachel is thankful for all of the modern innovations that have allowed people with disabilities to navigate society, she also believes that sometimes, that can distract from the commitment to finding a cure for genetic conditions like Usher Syndrome. Instead of pushing for our environments to adapt to us, how can we push for new research that will instead allow us to access the world for all that it is–beautiful, colorful, and full of possibilities?  Melissa Chaikof is the Board Chair for Usher 1F Collaborative, Inc. Interested in contributing? Find them here: https://www.usher1f.org/

Dr. Di Forte is world renowned expert in cannabis induced psychosis research and risk factors for schizophrenia. Dr Marta Di Forti is a Clinical Reader in Psychosis Research at the Dept of Social, Developmental and Genetic Research, Institute of Psychiatry, and Honorary Consultant Adult Psychiatrist, Lambeth EI Community team, South London and Maudsley NHS foundation Trust. She leads the first Cannabis Clinic for patients with Psychotic disorders in UK. She was recently awarded the Royal College of Psychiatrist Researcher of the year prize.  In 2020 she was granted a MRC Senior Research Fellowship to expand her research in the role of cannabis use in psychosis and its underlying biology. With her team she showed for the first time that use of high potency types of cannabis e.g. "skunk" carries a higher risk of psychosis than use of traditional types and that it affects rates of Psychotic disorders across Europe. Though it still remains unclear who are those cannabis use most at risk. Her future work aims to investigate the interaction between cannabis use and genes predisposing to schizophrenia, and how cannabis changes the epigenome. Lancet Article: Daily High Potency (10%) Cannabis Use is associated with nearly 5 fold increased odds of Psychotic Disorder

Dr. Nathaniel Jeanson talks about his newest book, Traced, and how it confirms the Biblical timeline and what the response has been from the skeptics.To take the Genetics test:https://www.23andme.com/dna-health-ancestry/?ad=true&utm_source=google&utm_medium=search_generic&utm_campaign=US_mothers_sales_prs_generic_roas&gclid=CjwKCAjwtIaVBhBkEiwAsr7-czhHcDlrW_a8Ip9MDvotVwv4bL9bbppvo-hrbmmG34SvEqUrt6MVrRoCM_kQAvD_BwE&gclsrc=aw.ds To send Dr. Jeanson your genetic test results:Answersingenesis.org/go/traced Get the book in hardcover, ebook, and audiobook form:Answers in Genesis: https://answersingenesis.org/.../traced-human-dnas-big.../Master Books:https://www.masterbooks.com/tracedAmazon:https://www.amazon.com/Traced-Human-DNAs.../dp/1683442911Follow Him onGab:Nathaniel_Jeansonhttps://gab.com/Nathaniel_JeansonParler:Nathanieljeansonhttps://parler.com/user/NathanieljeansonMeWe:Nathaniel Jeansonhttps://mewe.com/i/nathanieljeansonTelegram:Nathaniel_JeansonGETTRNathan Jeansonhttps://gettr.com/user/nathanjeansonSupport the show

​Dr. Adriana Humanes is a coral reef scientist from Venezuela. She completed her Ph.D. in Australia, and now is pursuing a postdoc with the @Coralassist_Lab through Newcastle University in the UK….I met her on the ship to Antarctica in 2018.For the last four years Adriana, and her colleagues have conducted field work in Palau, which is an archipelago of more than 300 islands situated in the Pacific Ocean between Indonesia and the Philippines.As Adriana explains, coral reefs are facing and unprecedented decline due to marine heatwaves, and also because of mass coral bleaching events. In the last decade, there have been five large scale coral bleaching and mortality events which have affected hundreds of reefs around the world.During the last massive bleaching event, on the Great Barrier Reef of Australia, almost half of the coral cover lost. Over the last 30 years, worldwide, coral cover has decreased by an alarming 20 per cent.The research at the Coralassist lab (as well as Adriana's) focuses on testing the feasibility of assisting evolution by identifying coral colonies that have a high tolerance to heat stress, and then, sexually breeding them. The goal is to create next generation corals that have inherited heat tolerance from their parents.Adriana first went to Palau in 2018, which was not long after I met her, in Antarctica. Although the pandemic has restricted her ability to travel there to continue her onw field research, by coincidence, one lone Ph.D student working with the  Coralassist lab  flew to Palau on March 7, 2020 … which turned out to be a long stay for her, 18 months, to be exact, where she became the lone student there tasked with keeping the Lab research project going.Adriana and her colleagues hope to returned this year, for their final leg of field research...after being away for years. And good news! They found corals spawning! Hopefully this is one more step towards the goal to use these sexually produced corals to help increase their future resilience, and hopefully even restore some vreefs that have been damaged or degraded from heat waves. Who knows, maybe they could even restore some reefs that have endured massive bleaching events, which are predicted to be more frequent in future climate change scenarios.Only science will tell.This episode was brought to you by the newsletter Audio Love, where I share unforgettable stories, with sound and word. To subscribe, go here:https://bit.ly/Audio-love