GGenetics Read More Further phenotypical delineation of DLG3-related neurodevelopmental disordersSeptember 22, 2025 Elias GM, Elias LAB, Apostolides PF, Kriegstein AR, Nicoll RA. Differential trafficking of AMPA and NMDA receptors by…
GGenetics Read More Diversity challenges and reconciles genetics in facioscapulohumeral muscular dystrophySeptember 16, 2025 Wang LH, Tawil R. Facioscapulohumeral dystrophy. Curr Neurol Neurosci Rep. 2016;16:66. Article PubMed Google Scholar Mul K, Lassche…
GGenetics Read More Expert Explains How Love Heals Body Through DNA, Internet Says, ‘It Can Damage Too’ | Viral NewsSeptember 7, 2025 Last Updated:September 07, 2025, 06:30 IST Dr Niraj Rai explained how love doesn’t just make you feel good,…
GGenetics Read More New method advances RNA velocity analysis with spatial and multi batch integrationSeptember 6, 2025 Essentially all cells in an organism’s body have the same genetic blueprint, or genome, but the set of…
GGenetics Read More Clinical exome sequencing efficacy and phenotypic expansions involving non-isolated congenital anomalies of kidney and urinary tract (CAKUT+)September 6, 2025 Capone VP, Morello W, Taroni F, Montini G. Genetics of congenital anomalies of the kidney and urinary tract:…
GGenetics Read More A novel MCMDC2 variant causes meiotic arrest and non-obstructive azoospermia in a consanguineous Chinese familySeptember 2, 2025 Cerván-Martín M, Castilla JA, Palomino-Morales RJ, Carmona FD. Genetic landscape of nonobstructive azoospermia and new perspectives for the…
GGenetics Read More MYH2-associated myopathy caused by novel compound heterozygous mutations: a case report and literature reviewSeptember 1, 2025 Morales PN, Coons AN, Koopman AJ, Patel S, Chase PB, Parvatiyar MS, et al. Post-translational modifications of vertebrate…
GGenetics Read More Next-gen sequencing reveals the regulatory potential of the non-coding genomeAugust 24, 2025 The non-coding genome, once dismissed as “junk DNA”, is now recognized as a fundamental regulator of gene expression…
GGenetics Read More A Japanese familial spastic paraplegia associated with a missense UBQLN2 variantAugust 22, 2025 Statland JM, Barohn RJ, McVey AL, Katz JS, Dimachkie MM. Patterns of weakness, classification of motor neuron disease,…
GGenetics Read More Early lipid genetics: identification of common and rare genetic variants for lipid traits in Indian adolescentsAugust 21, 2025 Heller DA, de Faire U, Pedersen NL, Dahlen G, McClearn GE. Genetic and environmental influences on serum lipid…