Scientists discovered that the first 100 base pairs of human genes are unusually prone to mutations, especially during the ...
This study presents a large, systematically curated catalog of non-canonical open reading frames (ncORFs) in human and mouse by reanalyzing nearly 400 Ribo-seq datasets using a standardized pipeline; ...
Scientists at The Hospital for Sick Children (SickKids) have revealed a previously overlooked layer of genetic variation that could help explain why people experience disease differently, and why some ...
A new analysis in Biological Psychiatry identifies distinct epigenetic signatures in cord blood linked to an increased susceptibility to schizophrenia and other neurodevelopmental conditions.
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Scientists discover tiny parts of DNA that explain why diseases hit people differently
Tiny repeated stretches of DNA in your genome may quietly shape how your body works, how your brain develops and how you ...
This study presents a valuable tool named TSvelo, a computational framework for RNA velocity inference that models transcriptional regulation and gene-specific splicing. The evidence supporting the ...
Nobel Prize-winning American scientist James Watson, one of the co-discoverers of the structure of DNA, has died aged 97. In one of the greatest breakthroughs of the 20th Century, he identified the ...
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