$27.9 million from NIH to support Baylor’s Knockout Mouse Project
Nearly $28 million has been awarded to Baylor College of Medicine’s Knockout Mouse Project led by Dr. Arthur Beaudet, professor of molecular and human genetics,
Read MoreNearly $28 million has been awarded to Baylor College of Medicine’s Knockout Mouse Project led by Dr. Arthur Beaudet, professor of molecular and human genetics,
Read MoreDealing with the diagnosis of a developmental or genetic disorder can be a difficult and often confusing time for both parents and their children. Since
Read MoreA couple’s fertility depends on both the female’s and male’s ability to reproduce, which relies on thousands of genes working properly. Around the world, infertility
Read MoreFemales have two X chromosomes in each of their cells. Fully unfolded, each copy is two inches long. One of these two X chromosomes is
Read MoreAn international team of researchers has identified a new rare genetic condition – a chromosome breakage syndrome associated with severe infections and lung disease in
Read MoreWhen she was nine years old, Andersson Dyke, a cat lover, began imagining an idea for a story; the journey of an abandoned lion cub
Read MoreBearing fraternal twins, or dizygotic (DZ) twinning, runs in families, is potentially influenced by more than one gene and is linked to a maternal factor.
Read MoreOn April 1, 2016, the European Medicines Agency (EMA) approved the first ex-vivo (outside the body) gene therapy in the Western Hemisphere. Diseased stem cells
Read MoreAna María Rodríguez, Ph.D. In one of the largest studies on the genes involved in human behavior, a group of more than 190 researchers has
Read MoreBy Ana María Rodríguez, Ph.D. Missing the tip of chromosome 1, a region called 1p36, is a relatively common cause of intellectual disability affecting one in
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