Scientists identify infectious monkeypox virus mutations November 7, 2022 -- University of Missouri researchers have identified the specific mutations in the monkeypox virus that make it so infectious. The results could lead to modified versions of existing drugs or the development of new ones.Read More
Scientist use roundworms to identify genes relevant to the aging process November 1, 2022 -- Researchers from North Carolina State University have developed a new method for determining which genes are relevant to the aging process. Their findings could have broader applications for research into the genetics of aging.Read More
NIH scientists reveal workings of Stargardt disease October 31, 2022 -- National Institutes of Health (NIH) scientists have a new understanding of Stargardt disease, a rare disorder that causes progressive loss of central and night vision. The discovery suggests a therapeutic pathway to treat the disease, which may help lead to gene therapy.Read More
Scientists discover what causes nuclear envelope repair October 31, 2022 -- An international team of researchers has identified the precise role of key components in the nuclear envelope repair process, which could potentially lead to a better understanding of various rare genetic disorders such as laminopathies.Read More
Certain gene enables glioblastoma multiforme: study October 20, 2022 -- The gene P300 may be the one to tackle to support patients with treatment-resistant brain cancer glioblastoma multiforme, University of California, Los Angeles researchers have found.Read More
Low phosphate levels linked with CAR T neurological toxicity October 20, 2022 -- Patients with hypophosphatemia had higher incidences and more severe neurological side effects on chimeric antigen receptor (CAR) T-cell therapy than those with normal blood phosphate levels, according to a study published October 19 in the journal Cancer Immunology Research.Read More
Gene mutation protects the heart, study finds October 20, 2022 -- New research led by scientists from Germany partially explains why patients with hypertension and brachydactyly syndrome don't experience cardiac hypertrophy: a gene mutation.Read More