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Browsing Tag

Gene Expression

22 posts
GGenetics
Further phenotypical delineation of DLG3-related neurodevelopmental disorders
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Further phenotypical delineation of DLG3-related neurodevelopmental disorders

  • September 22, 2025
Elias GM, Elias LAB, Apostolides PF, Kriegstein AR, Nicoll RA. Differential trafficking of AMPA and NMDA receptors by…
GGenetics
Diversity challenges and reconciles genetics in facioscapulohumeral muscular dystrophy
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Diversity challenges and reconciles genetics in facioscapulohumeral muscular dystrophy

  • September 16, 2025
Wang LH, Tawil R. Facioscapulohumeral dystrophy. Curr Neurol Neurosci Rep. 2016;16:66. Article  PubMed  Google Scholar  Mul K, Lassche…
GGenetics
News18
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Expert Explains How Love Heals Body Through DNA, Internet Says, ‘It Can Damage Too’ | Viral News

  • September 7, 2025
Last Updated:September 07, 2025, 06:30 IST Dr Niraj Rai explained how love doesn’t just make you feel good,…
GGenetics
New method advances RNA velocity analysis with spatial and multi batch integration
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New method advances RNA velocity analysis with spatial and multi batch integration

  • September 6, 2025
Essentially all cells in an organism’s body have the same genetic blueprint, or genome, but the set of…
GGenetics
Clinical exome sequencing efficacy and phenotypic expansions involving non-isolated congenital anomalies of kidney and urinary tract (CAKUT+)
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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
A novel MCMDC2 variant causes meiotic arrest and non-obstructive azoospermia in a consanguineous Chinese family
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A novel MCMDC2 variant causes meiotic arrest and non-obstructive azoospermia in a consanguineous Chinese family

  • September 2, 2025
Cerván-Martín M, Castilla JA, Palomino-Morales RJ, Carmona FD. Genetic landscape of nonobstructive azoospermia and new perspectives for the…
GGenetics
MYH2-associated myopathy caused by novel compound heterozygous mutations: a case report and literature review
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MYH2-associated myopathy caused by novel compound heterozygous mutations: a case report and literature review

  • September 1, 2025
Morales PN, Coons AN, Koopman AJ, Patel S, Chase PB, Parvatiyar MS, et al. Post-translational modifications of vertebrate…
GGenetics
Next-gen sequencing reveals the regulatory potential of the non-coding genome
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Next-gen sequencing reveals the regulatory potential of the non-coding genome

  • August 24, 2025
The non-coding genome, once dismissed as “junk DNA”, is now recognized as a fundamental regulator of gene expression…
GGenetics
A Japanese familial spastic paraplegia associated with a missense UBQLN2 variant
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A Japanese familial spastic paraplegia associated with a missense UBQLN2 variant

  • August 22, 2025
Statland JM, Barohn RJ, McVey AL, Katz JS, Dimachkie MM. Patterns of weakness, classification of motor neuron disease,…
GGenetics
Early lipid genetics: identification of common and rare genetic variants for lipid traits in Indian adolescents
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Early lipid genetics: identification of common and rare genetic variants for lipid traits in Indian adolescents

  • August 21, 2025
Heller DA, de Faire U, Pedersen NL, Dahlen G, McClearn GE. Genetic and environmental influences on serum lipid…
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