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Gap junction protein
A Rare Missense Mutation in GJB3 (Cx31g45e) Is Associated with a Unique Cellular Phenotype Resulting in Necrotic Cell Death Easton, J
GJA4/Connexin 37 Mutations Correlate with Secondary Lymphedema Following Surgery in Breast Cancer Patients
Localized Calcium Signaling and the Control of Coupling at Cx36 Gap Junctions
Characterization of a Variant of Gap Junction Protein Α8 Identified in a Family with Hereditary Cataract
In Silico Analysis of Non-Synonymous Single Nucleotide Polymorphisms (Nssnps) in the Human GJA3 Gene Associated with Congenital
Restoration of Desmosomal Junction Protein Expression and Inhibition Of
Evidence of Decreased Gap Junction Coupling Between Astrocytes and Oligodendrocytes in the Anterior Cingulate Cortex of Depresse
Pannexins and Connexins: Their Relevance for Oocyte Developmental Competence
Structure and Function of Gap Junction Proteins: Role of Gap Junction Proteins in Embryonic Heart Development BHAVESH K
The Impact of GJA8 Snps on Susceptibility to Age-Related Cataract
Connexins in the Heart: Regulation, Function and Involvement in Cardiac Disease
Connexin in Lens Physiology and Cataract Formation Mauricio A
Gap Junction Enhancer As an Anti-Cancer Agent Via Gjic-Independent and -Dependent Pathways
The Complex and Critical Role of Glycine 12 (G12) in Beta-Connexins of Human Skin
A Novel Missense Mutation in the Gene for Gap-Junction Protein α3 (GJA3) Associated with Autosomal Dominant •Œnuclear Pu
The Connexin 46 Mutant (V44M) Impairs Gap Junction Function Causing Congenital Cataract
Connexin Genes Variants Associated with Non-Syndromic Hearing Impairment: a Systematic Review of the Global Burden
Identification and Functional Analysis of a Novel Missense Mutation in GJA8, P.Ala69thr Dandan Li1†, Chenjia Xu2†, Dandan Huang3, Ruru Guo2, Jian Ji2 and Wei Liu2*
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Gap Junction-Mediated Cell-To-Cell Communication in Oral Development and Oral Diseases: a Concise Review of Research Progress
Whole Genome Sequencing Reveals a Recurrent Missense Mutation in the Connexin 46 (GJA3) Gene Causing Autosomal Dominant Lamellar Cataract
Connexin Mutations Associated with Palmoplantar Keratoderma and Profound Deafness in a Single Family
New GJA8 Variants and Phenotypes Highlight Its Critical Role in a Broad Spectrum of Eye Anomalies
Evaluation of the Pathogenicity of GJB3 and GJB6 Variants Associated with Nonsyndromic Hearing Loss
Intercellular Communication and Its Role in Cancer
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Delineation of Novel Autosomal Recessive Mutation in GJA3 and Autosomal Dominant Mutations in GJA8 in Pakistani Congenital Cataract Families
Atrial Fibrillation-Linked GJA5/Connexin40 Mutants Impaired
GJB3 Gene Gap Junction Protein Beta 3