America's Most Inbred Family: The Whittaker Story
An investigative journey into the lives of the Whittakers, known as America's most inbred family, uncovering their isolated existence and the genetic consequences of generations of intermarriage.
Category : Search result: genetic modification
Dolly the Sheep cloning pioneer Sir Ian Wilmut dies aged 92
Sir Ian Wilmut, the pioneering scientist who failed biology at Eton but went on to lead the team that cloned Dolly the Sheep, has passed away aged 92. Discover the remarkable journey of the man once told his scientific dreams were 'ridiculous'.
Pig Liver Filters Human Blood in Medical Breakthrough
Chinese scientists achieve revolutionary medical breakthrough as modified pig liver sustains brain-dead human body for 72 hours, potentially solving organ transplant shortages
Pig liver successfully filters human blood in transplant trial
Revolutionary xenotransplantation procedure offers new hope for thousands on organ waiting lists as scientists achieve unprecedented success with genetically engineered pig liver supporting human patient.
Pig liver successfully connected to human in transplant first
In a world-first medical breakthrough, surgeons have successfully attached a genetically modified pig liver to a human patient, potentially revolutionising organ transplantation and tackling donor shortages.
New Alzheimer's Gene Discovered in High-Risk Americans
Groundbreaking research reveals a previously unknown gene variant that dramatically increases Alzheimer's risk, offering new hope for early detection and treatment strategies.
Ancient DNA Rewrites Aztec Origins Story
Groundbreaking genetic research reveals the astonishing origins of the Aztec civilization, tracing their ancestors' epic 1,000-mile migration from Mexican deserts to their eventual empire.
Britain's only patient with ultra-rare disease
Exclusive story of Dean Sims, the solitary UK case of Mandibuloacral Dysplasia, and his extraordinary journey through the healthcare system.
Study: Intense Exercise May Increase MND Risk
Groundbreaking research from the University of Sheffield suggests vigorous exercise may accelerate motor neurone disease onset in those with predisposing genes, challenging fitness norms.
DNA Database Controversy Sparks Privacy Concerns
Conservative commentator Charlie Kirk's alarming claim about Utah's DNA collection practices sparks debate over genetic privacy rights and government overreach in criminal investigations.
Diabetes gene breakthrough could transform treatment
Groundbreaking research reveals how a specific gene disrupts insulin production in the pancreas, offering new hope for millions living with diabetes worldwide.
MAFS Emma Barnes reveals heartbreaking IVF journey
Married at First Sight favourite Emma Barnes opens up about her devastating fertility struggles and genetic condition discovery while trying for a baby with husband Matt.
Women genetically more vulnerable to depression - study
Groundbreaking research uncovers significant genetic differences that make women more vulnerable to depression, challenging long-held assumptions about mental health gender disparities.
EastEnders Star Reveals Son's Rare Condition Struggle
EastEnders actress Kellie Bright opens up about her family's emotional journey navigating her son's rare genetic disorder and the daily challenges they face.
Alien DNA Found in Humans? Study Reveals Genetic Evidence
Shocking new scientific research proposes that humanity's genetic blueprint contains evidence of extraterrestrial manipulation, challenging everything we know about human evolution.
46-year Florida kidnapping cold case solved
After nearly five decades of silence, Florida authorities have finally identified the perpetrator in Susan Perkins' shocking 1978 kidnapping case, bringing long-awaited closure to her grieving family.
Cousin marriages and substance abuse drive infant deaths
Groundbreaking ONS statistics expose how parental consanguinity and substance abuse are contributing to tragic infant deaths across Britain, with experts calling for urgent public health intervention.
Baby's rare disease battle: Family's 5-month diagnosis wait
A UK family shares their emotional journey as their newborn son battles a rare neonatal disease, facing months of uncertainty and fighting for answers in the NHS system.
Mark and Rebecca Black: The Siblings Who Married
Exclusive investigation reveals how Mark and Rebecca Black, raised as brother and sister in Scotland, discovered they were biological parents and entered into a secret marriage that stunned their community.
Scientists create human eggs from skin cells in fertility breakthrough
Groundbreaking research from UK scientists revolutionises fertility treatment by transforming skin cells into viable human eggs, offering new hope for infertility and genetic disorders.
Toddler's mystery illness diagnosed as rare genetic disorder
The emotional journey of a family who fought for answers after noticing developmental delays in their son, culminating in a rare MICPCH syndrome diagnosis.
NHS expands cancer screening for Angelina Jolie gene women
Thousands of British women carrying the BRCA1 gene mutation face increased ovarian cancer risk. New NHS programme offers regular blood tests to detect early signs.
DNA on snack wrapper helps police identify bike thief
Austin police employ groundbreaking DNA technology to identify alleged bicycle thief who left genetic evidence on snack wrapper at crime scene
Mother's battle against daughter's ultra-rare GRIN1 disease
Exclusive: The heart-wrenching story of a mother's battle to save her daughter, Arianna, from the ultra-rare GRIN1 gene mutation, a condition so uncommon it affects just a handful of people globally.
Huntington's Disease: New Drug Slows Progression in Trial
A revolutionary new drug, pridopidine, has shown significant promise in slowing the progression of Huntington's disease, offering new hope to UK families affected by the genetic condition.
Huntington's Disease Breakthrough: Revolutionary Therapy Offers Cure Hope
Groundbreaking medical research from UCL and University College London Hospitals has successfully lowered levels of the toxic protein that causes Huntington's disease using an innovative genetic therapy injected into the spinal fluid.
Coroner's urgent restaurant warning after pensioner chokes
A coroner issues a critical warning to UK restaurants after a pensioner with Parkinson's chokes on unmodified food, highlighting a widespread safety oversight.
Baby Born Without Eyes in Ultra-Rare Genetic Condition
The parents of a baby girl born without eyes due to an incredibly rare genetic condition share their emotional journey and determination to give their daughter the best life possible.
Ancient Irish DNA Study Rewrites History Books
Groundbreaking research from Queen's University Belfast uncovers the true genetic origins of the Irish people, tracing ancient DNA back to mass migrations from the Middle East and Eastern Europe.
Son's Rare Disorder Destroys Home: Mother's Plea for Help
An East Sussex mother's heart-wrenching account of her son's ultra-rare GRIN2B condition, which causes extreme violence, property destruction, and a desperate fight for support.
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