DOCSLIB.ORG
Explore
Sign Up
Log In
Upload
Search
Home
» Tags
» GJC2
GJC2
A Computational Approach for Defining a Signature of Β-Cell Golgi Stress in Diabetes Mellitus
Clinical Vignette Novel Bi-Allelic Variants in GJC2 Associated
Caracterización De Las Bases Genéticas De Ataxias Hereditarias
Chr Start End Size Gene Exon 1 69482 69600 118 OR4F5 1 1 877520
A Translaminar Genetic Logic for the Circuit Identity of Intracortically-Projecting Neurons
Insurance and Advance Pay Test Requisition
Ion Channels
Comparative Transcriptome Profiling of the Human and Mouse Dorsal Root Ganglia: an RNA-Seq-Based Resource for Pain and Sensory Neuroscience Research
Download Positional Information of Genomic Sequence (Refseq Gene: Hg38) and Common Snps (Snp147common: Hg38) in the Region of Interest
UC San Diego UC San Diego Electronic Theses and Dissertations
1 1 2 3 Cell Type-Specific Transcriptomics of Hypothalamic
Integrative Analysis of Disease Signatures Shows Inflammation Disrupts Juvenile Experience-Dependent Cortical Plasticity
Table S3. RAE Analysis of Well-Differentiated Liposarcoma
Diagnostic Test: MALATTIE CEREBELLARI
An Investigation of the Properties and Functions of Connexins in the Mammalian Inner Ear
GJC2 Gene Gap Junction Protein Gamma 2
Download CGT Exome V2.0
GJC2 Missense Mutations Cause Human Lymphedema
Top View
Connexins and Disease
NGS Panel Portfolio Bene T from Our Medical Expertise and Streamlined Genetic Testing
Literature Revision and Description of a Novel GJC2 Mutation in an Unusually Severe Form
Autocrine IFN Signaling Inducing Profibrotic Fibroblast Responses By
Murine Perinatal Beta Cell Proliferation and the Differentiation of Human Stem Cell Derived Insulin Expressing Cells Require NEUROD1
Title Evaluation of Seizure Foci and Genes in the Lgi1(L385R/+) Mutant
After a Review of the Current Available Literature, CGS Administrators Has Determined That Testing for the Following Genes/Gene
Autocrine IFN Signaling Inducing Profibrotic Fibroblast Responses by a Synthetic TLR3 Ligand Mitigates
NGS in Hereditary Ataxia: When Rare Becomes Frequent
The Effects of BCG Vaccination in COVID-19 Pandemic
Exome Sequencing Enhanced Package Department of Pathology and Laboratory Medicine Feb 2012 UCLA Molecular Diagnostics Laboratories Page:1
Regionally Specified Human Pluripotent Stem Cell-Derived Astrocytes Exhibit Different Molecular Signatures and Functional Properties Robert A
Ion Channel Expression in Human Melanoma Samples: in Silico Identification and Experimental Validation of Molecular Targets
Supplementary Online Content
Somatic Mutations
You Can Check If Genes Are Captured by the Agilent Sureselect V5 Exome
Early Colorectal Cancers Provide New Evidence for a Lynch Syndrome-To-CMMRD Phenotypic Continuum
Gap Junction Channelopathies and Calmodulinopathies. Do Disease-Causing Calmodulin Mutants Affect Direct Cell–Cell Communication?