MeSH tree: C19.642.482.500
Researchers at Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU) have identified a mechanism that protects the female brain from genetic diseases. Although one of the two X chromosomes is switched off in female cells ...
7 hours ago
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A team of researchers led by Professor Yoko Hamazaki and Assistant Professor Yann Pretemer (Department of Life Science Frontiers) has developed an in vitro model that faithfully recapitulates human thymic epithelial cell ...
Aug 26, 2025
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Researchers have found that mitochondrial dysfunction in the blood-brain barrier (BBB) may lead to neuropsychiatric disease in some patients with DiGeorge syndrome.
Aug 20, 2025
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Researchers have identified a promising strategy to improve memory and brain cell function in models of 22q11.2 Deletion Syndrome.
May 27, 2025
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Changes in brain connectivity before and after puberty may explain why some children with a rare genetic disorder have a higher risk of developing autism or schizophrenia, according to a UCLA Health study.
Apr 11, 2025
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The chromosomal disorder 22q11.2 deletion syndrome (22q) has emerged as one of the strongest risks for schizophrenia. Scientists at St. Jude Children's Research Hospital identified malformed regions of the cerebellum in laboratory ...
Dec 5, 2024
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A recent study published in Frontiers in Genetics demonstrates that combining copy number variants sequencing (CNVs-seq) and whole exome sequencing (WES) is effective in detecting congenital heart disease (CHD). CHDs are ...
Sep 4, 2024
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Is it possible to assess an individual's risk of psychosis? Identifying predictive markers is a key challenge in psychiatry. A team from the University of Geneva (UNIGE), part of the Synapsy Center for Neuroscience and Mental ...
Jul 22, 2024
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A group of researchers at the University of California San Diego School of Medicine have led an investigation that offers new insight into the causes of spina bifida, the most common structural disorder of the human nervous ...
May 8, 2024
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A recent study led by UC Davis Health researchers provides new insights into the molecular changes linked to the rare genetic condition 22q11.2 deletion syndrome, or 22q. It found unique biomarkers that could identify patients ...
Apr 26, 2024
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