Furthermore, the team discovered that an X-linked transcriptional activator called ZFX, which escapes X-chromosome inactivation and is expressed at higher levels in females, acts as a master regulator of this convergent network—uncovering the molecular machinery underlying the female protective…
OncLive The panelists recommend germline and somatic testing for every patient with metastatic prostate cancer and germline testing for more aggressive localized disease, where results primarily inform cascade testing of relatives rather than treatment They acknowledge ongoing disagreement over testing…
CHAMPAIGN, Ill. — A particular signaling protein in the brain could be a therapeutic target for neurological disorders arising from the deletion of the autism-linked gene MEF2C, University of Illinois Urbana-Champaign researchers found in a new mouse study. Deletions or mutations to MEF2C are…
Molecular Psychiatry (2026) Cite this article Given that multiple proteins coordinate functionally in a cell, there are logical bottlenecks where distinct clusters interact utilizing minimal proteins. These connector proteins were analyzed based on participation coefficient, impact score, and degree: The impact…
Scientists at Boston Children’s Hospital have found that the ZFX gene regulates the activity of many autism-related genes and may be one of the factors behind women’s relative protection from severe symptoms of this condition. The results of the study,…
Genetic interaction networks, such as the one pictured here, allowed researchers to predict functions for previously uncharacterized genes. Newswise — Rockefeller scientists have created the most comprehensive map to date of how essential genes interact in Mycobacterium tuberculosis (Mtb), the bacterium…
The brain is an intricate puzzle, and its development is even more convoluted. Neural cells need to properly organize and divide in the many layers that will give rise to the different human brain regions. When there are malformations in…
Senior study author Christopher Walsh, MD, PhD, chief of the Division of Genetics and Genomics and Investigator of the Howard Hughes Medical Institute, and lead authors Rebecca Andersen, PhD and Maya Talukdar, PhD, along with colleagues studied a number of…
The field of hereditary genetic testing is rapidly evolving driven by technological advances and an increasing awareness of genetic conditions As this market expands it offers promising opportunities for improved healthcare outcomes through early diagnosis and personalized treatment options Below...
Cells soften and massage their nucleus to encourage the repair of broken DNA, research led by Barts Cancer Institute, Queen Mary University of London, has discovered. Using cells grown in the laboratory, the researchers uncovered a previously unknown role for…
Orphan conditions, registries, gene testing, and family support networks.
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