A 16-month-old boy, KJ Muldoon, takes his first steps after receiving a first-ever personalized CRISPR therapy for a rare genetic disorder at Children's Hospital of Philadelphia. A medical miracle just in time for Christmas.
Over 75 students from Varanasi schools participated in a science outreach workshop at BHU's Centre for Genetic Disorders, exploring DNA, chronotypes, and herbarium techniques.
Kallmann Syndrome, a rare genetic disorder, delays puberty due to hormone deficiency. Learn about its causes, diagnosis, and treatment options in India. Seek expert advice for early intervention.
BrowserStack unveils Test Failure Analysis Agent, an AI-powered tool that automates debugging, reducing analysis time from hours to minutes. Discover how it boosts developer productivity.
Indira Gandhi Govt Medical College's Daga Hospital in Nagpur introduces compulsory sickle cell screening for newborns and mothers as patient count nears 2,900. Learn about free treatment and awareness initiatives.
Angelina Jolie opens up about her 2013 preventive double mastectomy, revealing scars to advocate for global access to genetic testing and healthcare. Her story continues to empower women.
Bengaluru is set to receive a central drug testing laboratory, significantly reducing wait times for sample analysis reports. Approval from the Centre is pending. Read more.
Dr Abhijit Dixit highlights India's genetic medicine revolution, gaps in infrastructure, and urgent need for newborn screening and data privacy laws. Read more.
Groundbreaking genetic research reveals ancient southern Africans lived in near-total isolation for 100,000 years, developing unique traits. Discover how this reshapes our understanding of human evolution. Read the full story.
A couple in China welcomed a blonde, blue-eyed daughter, sparking a DNA mystery. The paternity test confirmed she's theirs, unveiling a recessive gene from a Slavic great-grandfather. A heartwarming tale of genetic surprise.
A landmark genetic study reveals modern humans first arrived in Australia around 60,000 years ago via two distinct migration routes, aligning with Aboriginal oral histories and archaeology. Discover the full story of this ancient journey.
Haryana dairy farmer Shiv Kumar Redhu donates a genetically elite Murrah buffalo calf to GADVASU, Ludhiana. The calf, from a high-yield lineage, will aid university's genetic improvement and semen production programs.
Guru Angad Dev Veterinary University receives a high-value Murrah bull donation from a Haryana farmer, set to transform buffalo genetics in North India. Discover how this collaboration accelerates breed improvement.
Bengaluru's inStem discovers a distinct genetic cause for Hypertrophic Cardiomyopathy in South Indians, challenging global data and paving the way for personalized cardiac care. Read more.
A new women-centric study from Kolar, Karnataka, identifies key genetic mutations like CASP8 driving aggressive oral cancer in female tobacco chewers, paving the way for personalised treatment. Read more.
Tata Memorial Centre study identifies genetic factors that make Indians, especially from northeast, more vulnerable to oral cancer. Tobacco users develop cancer in just 10 years.
Tata Memorial Centre research identifies genetic markers explaining why some tobacco users develop oral cancer a decade earlier. Discover the groundbreaking findings and their implications for prevention.
Lucknow's KGMU achieves breakthrough in critical care, reducing ICU mortality from 26% to 18% through precision medicine. Learn how genetic profiling saves lives.
Bharathidasan University in Trichy hosted a 5-day ICMR-sponsored national workshop on advanced genetic diagnostics, offering hands-on training in DNA analysis and precision medicine techniques.
Indian neurologists report alarming rise in Parkinson's patients in their 30s-40s. New genetic research reveals South Asian-specific risk factors. Early detection crucial for treatment.
Learn about Wilson's Disease, a rare genetic disorder causing copper accumulation. Discover symptoms, inheritance patterns, and why early diagnosis prevents organ damage.
Discover how Stranger Things actor Gaten Matarazzo raises awareness about cleidocranial dysplasia, a rare genetic condition affecting bones and teeth. Learn about symptoms and treatment.
Indian researchers discover how HOXA10 and TWIST2 genes regulate embryo implantation. This breakthrough could transform fertility treatments and pregnancy success rates.
Discover how S Sanika carries forward her family's weightlifting legacy with genetic talent and determination. Learn about her journey in Indian sports and future aspirations.
Groundbreaking research reveals Neanderthals didn't go extinct but were gradually absorbed into human populations through interbreeding over millennia. Discover how genetics proves this evolutionary merger.
BrowserStack unveils AI-powered self-healing agent that automatically fixes test failures, reducing maintenance by 70%. Discover how this innovation transforms software testing workflows.
BrowserStack unveils groundbreaking AI-powered self-healing agent that automatically fixes test scripts, reducing maintenance by 70%. Discover how this innovation transforms software testing.
Discover how addiction runs in families and learn actionable strategies to break the cycle. Expert insights on genetic risks and effective prevention methods.
Scientists extract 39,000-year-old RNA from 'Yuka' the woolly mammoth, rewriting our understanding of RNA survival and offering unprecedented insights into extinct species.
Groundbreaking DNA analysis reveals Hitler had Kallmann syndrome affecting sexual development and carried neurodiverse traits. Discover the scientific findings shaping historical understanding.