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CRYGB
Appendix 4. Top 50 Highest Expressed Genes in Epithelial Cells Based on RPKM Values
CRYGB Rabbit Pab
Related Macular Degeneration and Cutis Laxa
Congenital Eye Disorders Gene Panel
Supplementary Materials
V13a25-Kamphuis Pgmkr
CRYGB (NM 005210) Human Tagged ORF Clone – RC214533L1
Novel Mutation in the Γ-S Crystallin Gene Causing Autosomal Dominant Cataract
Effects of Maternal Immune Activation on Gene Expression Patterns in the Fetal Brain
A Mutation in the Start Codon of C-Crystallin D Leads to Nuclear Cataracts in the Dahl SS/Jr-Ctr Strain
Mouse Models of Congenital Cataract
A Novel Nonsense Mutation in CRYGC Is Associated with Autosomal Dominant Congenital Nuclear Cataracts and Microcornea
Downloaded from Public Repository (Massive, MSV000078532) and the Numbers of MS/MS Spectra
Lens Adaptation to Glutathione Deficiency
A Component of Retinal Light Adaptation Mediated by the Thyroid Hormone Cascade
Autocrine IFN Signaling Inducing Profibrotic Fibroblast Responses By
GENE LIST ANTI-CORRELATED Systematic Common Description
CRYGB (NM 005210) Human Tagged ORF Clone – RC214533
Top View
Mrna Expression in Human Leiomyoma and Eker Rats As Measured by Microarray Analysis
Inherited Cataracts: Molecular Genetics, Clinical Features, Disease
A Mutation in GJA8 (P.P88Q) Is Associated with “Balloon-Like” Cataract with Y-Sutural Opacities in a Family of Indian Origin
New Phenotype Associated with an Arg116cys Mutation in the CRYAA Gene Nuclear Cataract, Iris Coloboma, and Microphthalmia
17Β-Estradiol Delivered in Eye Drops: Evidence of Impact on Protein Networks and Associated Biological Processes in the Rat Retina Through Quantitative Proteomics
Microarray Analysis of Iris Gene Expression in Mice with Mutations Influencing Pigmentation
Functions of the Intermediate Filament Cytoskeleton in the Eye Lens
Rabbit Anti-CRYGB/FITC Conjugated Antibody
The Human Crystallin Gene Families Graeme Wistow
Retinal Genomic Fabric Remodeling After Optic Nerve Injury
Genetic and Allelic Heterogeneity of Cryg Mutations in Eight Distinct Forms of Dominant Cataract in the Mouse
Novel Mutations Associated with Autosomal Dominant Congenital
Gene Expression in the Mouse Eye: an Online Resource for Genetics Using 103 Strains of Mice
Appendix 4. Differentially Regulated Genes in Mouse Retina Between
Cataract-Associated New Mutants S175G/H181Q of Βb2-Crystallin and P24S/S31G of Γd-Crystallin Are Involved in Protein Aggregation by Structural Changes
Sigma Receptor 1 Modulates Endoplasmic Reticulum Stress in Retinal Neurons
CRYGB, CRYGC, and CRYGS) As Candidates for Hereditary Cataracts in the Dachshund
Crystalline Cataract Caused by a Heterozygous Missense Mutation in Γd-Crystallin (CRYGD)