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20 results for "genetic mutation"
A 63-year-old Norwegian man has been living without HIV medication for three years after receiving stem cells from his brother who carried a rare genetic mutation. His case offers crucial clues for researchers working toward an HIV cure.
A 63-year-old man became the first person to achieve HIV remission through a bone marrow transplant from his sibling, opening new possibilities for HIV treatment. His brother carried a rare genetic mutation that makes cells resistant to the virus.
Scientists at Yale University discovered that an inexpensive prescription drug already on pharmacy shelves could ease autism symptoms for people with specific genetic mutations. While it won't help everyone with autism, the breakthrough opens doors for more targeted treatments.
Researchers screened 774 FDA-approved drugs using zebrafish to create a precision medicine map for autism, identifying levocarnitine as a compound that reverses brain deficits caused by specific genetic mutations. The breakthrough could help doctors match treatments to individual patients based on their unique genetic profile.
A breakthrough gene editing treatment has achieved what doctors call a "functional cure" for sickle cell disease, with 27 out of 28 patients experiencing zero painful crises after receiving the therapy. The one-time treatment edits patients' own blood cells to correct the genetic mutation, offering new hope for 100,000 Americans living with this painful disease.
Yale researchers created a groundbreaking database of 520 FDA-approved drugs by studying tiny zebrafish, revealing potential personalized treatments for people with specific autism-related genetic mutations. One drug candidate successfully reversed disrupted behaviors in both fish and human brain cells.
A medical student who inherited the genetic mutation that killed her father is now leading eleven research projects to cure ALS before it affects her. Yentli Soto Albrecht has a 95% chance of developing the fatal disease, but she's turning her fate into fuel for breakthrough research.
A new drug combination could help prostate cancer patients earlier in their fight, reducing the risk of tumor growth by more than expected in a major clinical trial. The treatment targets a specific genetic mutation found in 1 in 4 metastatic prostate cancer cases.
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Scientists discovered that a genetic mutation helping yaks survive at extreme altitudes could lead to treatments for multiple sclerosis and cerebral palsy. The breakthrough reveals how nature's adaptations might repair damaged nerve cells in people.
Scientists discovered a rare genetic mutation that directly causes fatty liver disease, potentially affecting millions worldwide. The breakthrough could lead to new targeted treatments for a condition that strikes one in three adults.
Scientists discovered that cats develop cancer through the same genetic mutations as humans, opening new paths for treatments that could save both pets and people. Nearly 500 cats helped create a "cancer map" that might lead to personalized therapies for families and their felines.
After decades of slow progress, breakthrough drugs targeting a genetic mutation found in 90% of pancreatic cancers are nearing FDA approval in 2026. The KRAS inhibitors now in late-stage trials could transform treatment for one of medicine's deadliest diseases.
A pit bull named Theodore has a rare genetic mutation that gives him a fluffy, teddy bear coat on a classic pit bull face. After being rehomed six times, he finally found his perfect match with Joanna Meadows.
Scientists have developed a one-time CRISPR treatment that fixes the genetic mutation causing the most common inherited kidney disease. Early tests show it could replace lifelong medication for 12 million people worldwide.
Mayo Clinic scientists corrected a genetic mutation causing the most common inherited kidney disease with one injection. The treatment extended survival and stopped organ damage in mice, offering hope for 12 million people worldwide.
Google DeepMind's new AI can analyze a million DNA letters at once to identify genetic mutations driving disease. Scientists are already using AlphaGenome to unlock cancer mysteries and design targeted gene therapies.
Scientists discovered a way to use tiny zebrafish to quickly test if a newborn's genetic mutation will actually cause a deadly disease. The breakthrough helps doctors avoid giving babies unnecessary $2 million treatments while still protecting those who truly need help.
Scientists have developed a topical treatment that corrects disease-causing genetic mutations directly in the skin, offering hope for a lasting cure to conditions previously managed for life. The breakthrough could transform treatment for rare disorders and common conditions like eczema.
Scientists discovered why opposite genetic mutations both cause brain diseases like Alzheimer's and Parkinson's, solving a puzzle that has stumped researchers for decades. The breakthrough could help millions living with neurodegenerative conditions.
Scientists just proved that two harmful genetic mutations can actually restore normal function when combined, confirming a 60-year-old hypothesis. This breakthrough could transform how doctors diagnose and treat thousands of rare genetic diseases.