A Novel Autosomal Recessive GJA1 Missense Mutation Linked to Craniometaphyseal Dysplasia | PLOS ONE
GJA1 Gene - GeneCards | CXA1 Protein | CXA1 Antibody
GJA1 gene polymorphism is a genetic predictor of recurrence after pulmonary vein isolation in patients with paroxysmal atrial fibrillation - ScienceDirect
Biomolecules | Free Full-Text | An Alternatively Translated Connexin 43 Isoform, GJA1-11k, Localizes to the Nucleus and Can Inhibit Cell Cycle Progression
Dynamic UTR Usage Regulates Alternative Translation to Modulate Gap Junction Formation during Stress and Aging
In silico analysis of the Cx43 gene (GJA1) and its correlation with the... | Download Scientific Diagram
GJA1 Depletion Causes Ciliary Defects by Affecting Rab11 Trafficking to the Ciliary Base | bioRxiv
GJA1 (connexin43) is a key regulator of Alzheimer's disease pathogenesis | Acta Neuropathologica Communications | Full Text
GJA1 (connexin43) is a key regulator of Alzheimer's disease pathogenesis | Acta Neuropathologica Communications | Full Text
Expression of Gja1 correlates with the phenotype observed in oculodentodigital syndrome/type III syndactyly | Journal of Medical Genetics
GJA1 (connexin43) is a key regulator of Alzheimer's disease pathogenesis | Acta Neuropathologica Communications | Full Text
GJA1 Gene - GeneCards | CXA1 Protein | CXA1 Antibody
Overexpression of Astrocytes-Specific GJA1-20k Enhances the Viability and Recovery of the Neurons in a Rat Model of Traumatic Brain Injury | ACS Chemical Neuroscience
GJA1 (connexin43) is a key regulator of Alzheimer's disease pathogenesis | Acta Neuropathologica Communications | Full Text
A heterozygous mutation in GJA1 gene in Chinese family with serious erythrokeratodermia variabilis et progressive | Chinese Medical Journal
GJA1 Gene - GeneCards | CXA1 Protein | CXA1 Antibody
Protective mitochondrial fission induced by stress responsive protein GJA1-20k | bioRxiv
Biomolecules | Free Full-Text | An Alternatively Translated Connexin 43 Isoform, GJA1-11k, Localizes to the Nucleus and Can Inhibit Cell Cycle Progression
GJA1 Depletion Causes Ciliary Defects by Affecting Rab11 Trafficking to the Ciliary Base | bioRxiv
Addgene: AICSDP-43: GJA1-mEGFP
Alternatively translated isoforms of Connexin 43 (Cx43). Schematic... | Download Scientific Diagram
Two de novo GJA1 mutation in two sporadic patients with erythrokeratodermia variabilis et progressiva - Li - 2019 - Molecular Genetics & Genomic Medicine - Wiley Online Library
