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33 results for "genetic mutation"
Scientists in West Michigan are creating breakthrough treatments that attack the root causes of ALS rather than just managing symptoms. Their work focuses on fixing the genetic mutations that trigger this devastating disease.
Scientists analyzed nearly 500 cat tumors and found striking genetic similarities to human cancers, potentially leading to better treatments for both species. The discovery marks a major breakthrough in understanding how cancers develop across different mammals.
Scientists analyzed nearly 500 cat tumors and discovered they share the same dangerous genetic mutations found in human cancers, opening doors to better treatments for both species. The breakthrough could transform cancer care through shared medical research.
A daily pill called daraxonrasib helped control cancer in 90% of pancreatic cancer patients during early trials, offering new hope for a disease that has had few effective treatments. The drug targets genetic mutations found in over 90% of pancreatic cancers.
A breakthrough drug that targets the genetic mutation driving 90% of pancreatic cancers has been authorized for expanded access by the FDA. Patients are seeing their cancer stabilized for months longer than expected, with some feeling better within days.
Scientists created a breakthrough gene-editing tool that can seek out and eliminate only diseased cells, including cancer, while leaving healthy cells untouched. The technology could transform how doctors treat diseases caused by specific genetic mutations.
A groundbreaking therapy is showing real promise against cancers long considered impossible to treat, shrinking tumors in patients who'd run out of options. The experimental drug targets a genetic mutation affecting thousands of lung and pancreatic cancer patients each year.
Children born deaf from a genetic mutation can now hear naturally thanks to a groundbreaking gene therapy just approved by the FDA. The one-time treatment restores a missing protein in the inner ear, allowing sound signals to reach the brain.
A breakthrough medication targeting a previously "undruggable" genetic mutation could transform treatment for one of the deadliest cancers. Patients in late-stage trials lived nearly twice as long when taking the new drug alongside chemotherapy.
A genetic mutation that helps yaks survive thin mountain air could offer a breakthrough treatment for multiple sclerosis and other nerve diseases. The discovery points to a natural molecule already in our bodies that can repair damaged brain tissue.
A 63-year-old Norwegian man became just the tenth person worldwide to achieve long-term HIV remission after a stem cell transplant from his brother. The procedure worked because his sibling carried a rare genetic mutation that blocks the virus from entering cells.
A 63-year-old Norwegian man appears completely cured of HIV after receiving stem cells from his brother during cancer treatment. The brother unknowingly carried a rare genetic mutation that grants natural resistance to the virus.
A 63-year-old Norwegian man has become only the tenth person ever functionally cured of HIV, thanks to a stem cell transplant from his brother who carried a rare genetic mutation. After five years off medication, doctors found zero traces of functioning HIV in his body.
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.
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