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GJA8
A Computational Approach for Defining a Signature of Β-Cell Golgi Stress in Diabetes Mellitus
Genes in Eyecare Geneseyedoc 3 W.M
Human Gene Copy Number Spectra Analysis in Congenital Heart Malformations Aoy Tomita-Mitchell Medical College of Wisconsin
Supplementary Materials
Ion Channels
Altered Physiological Functions and Ion Currents in Atrial Fibroblasts From
Curriculum Vitae
Strand Breaks for P53 Exon 6 and 8 Among Different Time Course of Folate Depletion Or Repletion in the Rectosigmoid Mucosa
In Silico Analysis of Non-Synonymous Single Nucleotide Polymorphisms (Nssnps) in the Human GJA3 Gene Associated with Congenital
1 1 2 3 Cell Type-Specific Transcriptomics of Hypothalamic
A Novel Missense Mutation of GJA8 Causes Congenital Cataract in A
Table S3. RAE Analysis of Well-Differentiated Liposarcoma
(12) Patent Application Publication (10) Pub. No.: US 2003/0198970 A1 Roberts (43) Pub
A Novel Mutation in the GJA1 Gene in a Family with Oculodentodigital Dysplasia
Connexins and Disease
Calcium Regulation of Cell-Cell Communication and Extracellular Signaling
A Novel Missense Mutation in the Gene Encoding Major Intrinsic Protein (MIP) in a Giant Panda with Unilateral Cataract Formation
Inherited Cataracts: Molecular Genetics, Clinical Features, Disease Mechanisms and Novel Therapeutic Approaches
Top View
The Impact of GJA8 Snps on Susceptibility to Age-Related Cataract
Investigation on Genetic Modifiers of Age at Onset of Major Depressive Disorder
Alsaai Udel 0060D 14351.Pdf
Analysis of Rare Copy Number Variation in Absence Epilepsies
Congenital Progressive Polymorphic Cataract Caused by a Mutation in the Major Intrinsic Protein of the Lens, MIP (AQP0)
RNA-Sequencing Analysis of Shell Gland Shows Differences in Gene Expression Profile at Two Time-Points of Eggshell Formation In
Snapshot: Connexins and Disease Dale W
In GJA1 (Connexin 43)
Transcript Length Frequency 0 0 50 0 100 9 200 20 300 33 400 89 500
Gene OMIM Subgroup GJA8 600897 Abnormality of the Lens
Exome Sequencing Enhanced Package Department of Pathology and Laboratory Medicine Feb 2012 UCLA Molecular Diagnostics Laboratories Page:1
1 Imipramine Treatment and Resiliency Exhibit Similar
Ion Channel Expression in Human Melanoma Samples: in Silico Identification and Experimental Validation of Molecular Targets
Signaling Between TRPV1/TRPV4 and Intracellular Hydrostatic Pressure in the Mouse Lens
Modified Recombinant Vaccinia Viruses, Uses Thereof
A Novel Connexin46 (GJA3) Mutation in Autosomal Dominant Con- Genital Nuclear Pulverulent Cataract
You Can Check If Genes Are Captured by the Agilent Sureselect V5 Exome
Gap Junction Channelopathies and Calmodulinopathies. Do Disease-Causing Calmodulin Mutants Affect Direct Cell–Cell Communication?