Endangered marine mammals — seals, dolphins, whales, and otters — are almost as vulnerable as humans in becoming infected from
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The ongoing pandemic of coronavirus disease 2019 (COVID-19), caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), has led
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VEXAS syndrome in men is more common than previously thought
A rare disease first identified in 2020 is much more common than first thought, say researchers at the University of
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Placenta is a dumping ground for genetic defects
In the first study of the genomic architecture of the human placenta, scientists at the Wellcome Sanger Institute, the University
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Korea Brain Research Institute (KBRI, President Suh Pann-ghill) announced that the research team led by Dr. Jae-Yeol Joo discovered new
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Study provides new insight into the genetics of coronary artery disease
According to a new study published in The American Journal of Human Genetics, more than one third of genetic variants
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Study lays the groundwork for developing novel strategies to treat neurological diseases
A research team from the School of Life Sciences at The Chinese University of Hong Kong (CUHK) has recently discovered
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Spina bifida can be caused by uninherited genetic mutations
Genetic mutations which occur naturally during the earliest stages of an embryo’s development can cause the severe birth defect spina
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While the human brain has over 400 miles of total vasculature, little is known about the tiny capillaries that make
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Study sheds light on pathological characteristics behind sudden cardiac death
Nearly a half-million people a year die from sudden cardiac death (SCD) in the U.S. — the result of malfunctions
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