In a recent study published in the journal PLOS ONE, researchers from Japan compared phylogenetic trees based on proteomic data of microbiota with dendrograms of environmental factors to determine the ...
Non-protein-coding genes have been linked to a hereditary condition, retinitis pigmentosa, that causes progressive blindness.
The human genome may contain more protein-coding genes than prior analyses suggested. A study published last month (May 29) on BioRxiv provides an expanded database of approximately 5,000 novel ...
Almost 1,500 genes have been implicated in intellectual disabilities; yet for most people with such disabilities, genetic causes remain unknown. Perhaps this is in part because geneticists have been ...
For millennia, evolution has intrigued many great thinkers, prompting questions about how new traits emerge as species adapt over time. Then, attention shifted to natural selection and the inheritance ...
The human genome has to be carefully organized so it will fit inside of the nuclei of cells, while also remaining accessible ...
Thousands of previously “invisible” microproteins—tiny chains of fewer than 100 amino acids—can profoundly change human biology when mutated. A fundamental discovery is overturning decades of ...
A research team led by Zhiping Weng, Ph.D., and Jill Moore, Ph.D."18, at UMass Chan Medical School, has nearly tripled the ...
AZoLifeSciences on MSN
Replacing large mouse gene regions with human DNA
Humanized mouse models are essential for investigating human gene function; however, the complete replacement of mouse genes ...
News-Medical.Net on MSN
Non-coding RNA mutations unveiled as new cause of retinitis pigmentosa
Retinitis pigmentosa (RP) is a genetic eye disorder affecting around one in 5,000 people worldwide. It typically begins with ...
In patients with retinitis pigmentosa (RP), crucial cells in the retina known as rods and cones die over time; night ...
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