Results 141 to 150 of about 15,686 (159)
The Dual Role of Connexins in Stroke, Neurotrauma, Neurodegenerative and Psychiatric Disorders: A Global Systematic Review. [PDF]
MoleculesRodkin S +6 more
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Intercellular Mitochondrial Transfer as Endogenous Neuroprotection: Mechanisms and Therapeutic Implications in Ischemic Stroke. [PDF]
Transl Stroke ResZhang YF +9 more
europepmc +1 more source
A novel GJA1 mutation causes oculodentodigital dysplasia without syndactyly
American Journal of Medical Genetics, Part A, 2005 Oculodentodigital dysplasia (ODDD) is a rare autosomal dominant pleiotropic disorder, caused by mutations in the Connexin 43 gene (GJA1) [Paznekas et al. (2003): Am J Hum Genet 72:408-418], which is localized to human chromosome 6q22-q23.
Sandro Banfi, Enzo Maria Vingolo
exaly +2 more sources
GJA1mutations, variants, and connexin 43 dysfunction as it relates to the oculodentodigital dysplasia phenotype [PDF]
Human Mutation, 2009 peer reviewedThe predominantly autosomal dominant disorder, oculodentodigital dysplasia (ODDD) has high penetrance with intra- and interfamilial phenotypic variability. Abnormalities observed in ODDD affect the eye, dentition, and digits of the hands and
Lionel van Maldergem +2 more
exaly +2 more sources
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GJA1 reverses arsenic-induced EMT via modulating MAPK/ERK signaling pathway
Toxicology and Applied Pharmacology, 2022Linqing Wu
exaly