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GIPC3
PLATFORM ABSTRACTS Abstract Abstract Numbers Numbers Tuesday, November 6 41
A Computational Approach for Defining a Signature of Β-Cell Golgi Stress in Diabetes Mellitus
Noninvasive Sleep Monitoring in Large-Scale Screening of Knock-Out Mice
Review of Hair Cell Synapse Defects in Sensorineural Hearing Impairment
Whole Exome Sequencing in Families at High Risk for Hodgkin Lymphoma: Identification of a Predisposing Mutation in the KDR Gene
Integrative Bulk and Single-Cell Profiling of Premanufacture T-Cell Populations Reveals Factors Mediating Long-Term Persistence of CAR T-Cell Therapy
1 Supplemental Table 1. Demographics, Clinicopathological
Whole Exome Sequencing Identified Mutations Causing Hearing Loss In
Whole Exome Sequencing Identified Mutations
Gipc3 Mutations Associated with Audiogenic Seizures and Sensorineural Hearing Loss in Mouse and Human
GIPC Proteins Negatively Modulate Plexind1 Signaling During Vascular Development
Molecular Characterization and Ligand Binding Specificity of the PDZ Domain-Containing Protein GIPC3 from Schistosoma Japonicum
The GIPC1‐Akt1 Pathway Is Required for the Specification of The
Supplementary Data
Table S1. 103 Ferroptosis-Related Genes Retrieved from the Genecards
An Integrative Genomic Analysis of the Longshanks Selection Experiment for Longer Limbs in Mice
In GIPC3 Gene Is a Frequent Cause of Hereditary Nonsyndromic Sensorineural Hearing Loss in Chuvash Population
Genomic Profiling of Primary Histiocytic Sarcoma Reveals Two Molecular
Top View
Gipc3 Mutations Associated with Audiogenic Seizures and Sensorineural Hearing Loss in Mouse and Human
Low Incidence of GIPC3 Variants Among the Prelingual Hearing Impaired from Southern India
Effects of Genetic Background on Susceptibility and the Acceleration of Hearing Loss in Mice 5 Effect
Hair Cells Use Active Zones with Different Voltage Dependence Of
A Canonical Splice Site Mutation in GIPC3 Causes Sensorineural Hearing Loss in a Large Pakistani Family
Gipc1 Has a Dual Role in Vangl2 Trafficking and Hair Bundle Integrity in the Inner Ear Arnaud P
Allicin Inhibits SARS-Cov-2 Replication and Abrogates The
Hereditary Hearing Loss
Complement Activation in Peritoneal Dialysis–Induced Arteriolopathy
Whole Exome Sequencing Identi Ed Mutations Causing Hearing Loss In
Table S1. Loci and Genes Underlying Non-Syndromic Hearing Loss That Are Grouped Into Several Functional Categories
GWAS Identi Es Candidate Susceptibility Loci and Microrna Biomarkers for Acute Encephalopathy with Biphasic Seizures and Late Re
1 KLF2 and KLF4 Control Endothelial Identity and Vascular Integrity
Supplementary Table 1A 1647 Genes Selected by the ANOVA Analyses
Gipc3 Mutations Associated with Audiogenic Seizures and Sensorineural Hearing Loss in Mouse and Human
Survival of BRCA2-Deficient Cells Is Promoted by GIPC3, a Novel Genetic
Functional Proteomics, Human Genetics and Cancer Biology of GIPC Family Members