A potential approach to correct the FMR1 gene defect underlying fragile X syndrome (FXS) relies on the body’s own DNA repair mechanisms. This is described by researchers in the journal Cell. FXS [...]
Heterozygous variants in POLR1A resulting in a reduced protein function underlie a more variable phenotype than previously known. A study published in the American Journal of Human Genetics [...]
The role of DYRK1A might be a starting point for developing a molecular strategy to pharmacologically influence genomic instability. DYRK1A encodes the dual specificity tyrosine [...]
Specific heterozygous variants in HMGB1 cause an extremely rare congenital disorder, called BPTAS, which is characterized mainly by limb malformations including smaller-than-normal or extra [...]
A deep intronic GAA repeat expansion in the gene FGF14 causes a form of cerebellar ataxia manifesting in adulthood. In a study published in the New England Journal of Medicine, scientists [...]
New insights into how senescent cells play a role in wound healing not only through its secretory action but also by impacting on cell mechanics have been provided by a study performed at Charité [...]
Dominantly or recessively inherited variants in COL7A1 cause dystrophic epidermolysis bullosa (DEB), a devastating skin disorder. A gene therapy approach to treat DEB on a molecular basis has now [...]
Variants in a regulatory region of the gene HK1 result in the rare disorder of congenital hyperinsulinism. This has been reported in a study published in Nature Genetics. Coding HK1 variants have [...]
