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CRYAA
A Comprehensive Analysis of the Expression of Crystallins in Mouse Retina Jinghua Xi Washington University School of Medicine in St
Related Macular Degeneration and Cutis Laxa
Congenital Cataracts Due to a Novel 2‑Bp Deletion in CRYBA1/A3
Transgenic Zebrafish Models Reveal Distinct Molecular Mechanisms for Cataract-Linked Αa-Crystallin Mutants
Supplementary Materials
Alpha a Crystallin (CRYAA) Mouse Monoclonal Antibody [Clone ID: OTI3B12] Product Data
Congenital Polymorphic Cataract Associated with a G to a Splice Site Mutation in the Human Beta-Crystallin Gene Cryβa3/A1
Alpha-Crystallin Mutations Alter Lens Metabolites in Mouse Models of Human Cataracts
A Recurrent Mutation in CRYGD Is Associated with Autosomal Dominant Congenital Coralliform Cataract in Two Unrelated Chinese Families
Rescue of Retinal Degeneration by Intravitreally Injected Adult Bone Marrow–Derived Lineage-Negative Hematopoietic Stem Cells
Novel Mutation in the Γ-S Crystallin Gene Causing Autosomal Dominant Cataract
Competing Endogenous RNA Regulatory Network in Papillary Thyroid Carcinoma
CRISPR/Cas9–Mediated Mutation of Aa-Crystallin Gene Induces Congenital Cataracts in Rabbits
Effects of Maternal Immune Activation on Gene Expression Patterns in the Fetal Brain
Dynamic Aspects of the Human Eye Lens Molecular Chaperones Alphaa- and Alphab- Crystallin Studied by NMR Spectroscopy
Mutation Analysis of CRYAA, CRYGC, and Crygdassociated With
(12) Patent Application Publication (10) Pub. No.: US 2003/0198970 A1 Roberts (43) Pub
A Novel Mutation in CRYAA Is Associated with Autosomal Dominant Suture Cataracts in a Chinese Family
Top View
Clinical Characteristics of Congenital Lamellar Cataract and Myopia in a Chinese Family
High-Throughput Genetic Screening of 51 Pediatric Cataract Genes Identifies Causative Mutations in Inherited Pediatric Cataract in South Eastern Australia
High-Throughput Genetic Screening of 51 Pediatric Cataract Genes Identifies Causative Mutations in Inherited Pediatric Cataract in South Eastern Australia
A Missense Mutation in CRYBA4 Associated with Congenital Cataract and Microcornea
Supplementary Tables Supplementary Table S1. a List of 3,039 Genes
STAT3 Targets Suggest Mechanisms of Aggressive Tumorigenesis in Diffuse Large B Cell Lymphoma
New Phenotype Associated with an Arg116cys Mutation in the CRYAA Gene Nuclear Cataract, Iris Coloboma, and Microphthalmia
Genomic Analysis of Cryaa-R49C and Cryab-R120G Knockin Mutant
Supplementary Data
Mechanism of Action of VP1-001 in Cryab(R120G)- Associated and Age-Related Cataracts
Neonatal Eye Defects and Stem Cell Therapeutics Introduction
Microarray Analysis of Iris Gene Expression in Mice with Mutations Influencing Pigmentation
Proteomic Landscape of the Human Choroid–Retinal Pigment Epithelial Complex
Supplementary Material - Tables and Figures
Retinoic Acid Signaling Regulates Differential Expression of the Tandemly-Duplicated Long Wavelength-Sensitive Cone Opsin Genes in Zebrafish
The Human Crystallin Gene Families Graeme Wistow
Human/Mouse/Rat Alphab Crystallin/CRYAB Antibody
Osteocrin, a Peptide Secreted from the Heart and Other Tissues, Contributes