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Zacks Small Cap Research on MSNDWTX: Phase 2b Trial in Chemotherapy Induced Neuropathic Pain Underway…DWTX READ THE FULL DWTX RESEARCH REPORT Business Update Phase 2b Trial of Halneuron® in CINP underway; Interim Results ...
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Live Science on MSNRare genetic mutation lets some people thrive on just 4 hours of shut-eyeA newly identified mutation helps super-sleepers get by on just four to six hours of shut-eye per night, while the rest of us ...
Not everyone needs 8 hours of sleep to function properly. Some people can feel well-rested and show no negative effects of ...
Fanconi anemia is an aggressive, life-threatening disorder. Most individuals living with this rare genetic condition, ...
However, a new study is challenging these guidelines, suggesting that a rare mutation in the SIK3 gene might allow the brain to function on less sleep than the average person needs. The study ...
Researchers have now found that a mutation in people with NSS, within the gene salt-induced kinase 3 (SIK3), also plays a key role in human sleep duration. A mutation called N783Y was found to alter ...
A newly identified mutation helps super-sleepers get by on just four to six hours of shut-eye per night, while the rest of us need around eight hours. Researchers described the SIK3-N783Y mutation ...
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ScienceAlert on MSNScientists Discover Genetic Mutation Linked to Needing Less SleepThe answer to the question 'how much sleep do I need each night?' depends on a variety of factors, and we just found a new ...
28, 2025 — To help achieve more precise control of gene therapy, engineers have designed ... of inherited deafness called DFNA50 caused by mutations in microRNA, by using a novel in vivo CRISPR ...
Scientists now believe these “super sleepers” owe their unique sleep pattern to a rare genetic mutation. Researchers at the University of California, San Francisco, have identified a mutation ...
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News-Medical.Net on MSNScientists link specific gene variants to post-vaccine myocarditis and pericarditisA genome-wide association study in Sweden identified rare genetic variants near the SCAF11 and LRRC4C genes that may be ...
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