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Hemophilia, a rare inherited bleeding disorder, is primarily caused by mutations in specific genes that impair the body’s ...
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AZoLifeSciences on MSNComplete Reference Genomes Unlocked for Six Ape SpeciesComprehensive reference genomes have now been assembled for six ape species: siamang (a Southeast Asian gibbon), Sumatran ...
Understanding the material basis of adaptive evolution has been a central goal in biology dating back to at least the time of ...
A new study from Weill Cornell Medicine provides insights into how cells maintain the tiny end caps of chromosomes as they ...
Researchers from the Department of Pathology, School of Clinical Medicine at the LKS Faculty of Medicine of the University of ...
Colorectal cancer (CRC), a type of cancer that affects the large intestine and rectum, is one of the leading causes of cancer ...
12h
News-Medical.Net on MSNResearchers use algorithm to pinpoint disease risk mutations in noncoding DNAResearchers from Children's Hospital of Philadelphia (CHOP) and the Perelman School of Medicine at the University of ...
Most cancer genome studies have focused on mutations in the tumor itself and how such gene variants allow a tumor to grow unchecked. A new study takes a deep dive into inherited cancer mutations ...
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News Medical on MSNInherited mutations in healthy cells may contribute to cancer developmentMost cancer genome studies have focused on mutations in the tumor itself and how such gene variants allow a tumor to grow unchecked.
Researchers have uncovered a surprising mechanism by which a single genetic mutation in the BCL11B gene causes both immune dysfunction and brain development issues.
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