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CRYGS
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
Congenital Eye Disorders Gene Panel
Divalent Cations and the Divergence of Βγ-Crystallin Function Kyle W
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
Research Article Complex and Multidimensional Lipid Raft Alterations in a Murine Model of Alzheimer’S Disease
A Novel Nonsense Mutation in CRYGC Is Associated with Autosomal Dominant Congenital Nuclear Cataracts and Microcornea
A Novel Mutation in CRYAA Is Associated with Autosomal Dominant Suture Cataracts in a Chinese Family
High-Throughput Genetic Screening of 51 Pediatric Cataract Genes Identifies Causative Mutations in Inherited Pediatric Cataract in South Eastern Australia
Lens Adaptation to Glutathione Deficiency
A New Locus for Autosomal Dominant Congenital Cataracts Maps to Chromosome 3
High-Throughput Genetic Screening of 51 Pediatric Cataract Genes Identifies Causative Mutations in Inherited Pediatric Cataract in South Eastern Australia
Molecular and Genetic Mechanism of Non-Syndromic Congenital Cataracts
A Missense Mutation in CRYBA4 Associated with Congenital Cataract and Microcornea
A Meta-Analysis of the Effects of High-LET Ionizing Radiations in Human Gene Expression
Top View
Photoreceptor-Induced RPE Phagolysosomal
Molecular and Structural Analysis of Genetic Variations in Congenital Cataract
Microarray Analysis of Iris Gene Expression in Mice with Mutations Influencing Pigmentation
A Novel T→G Splice Site Mutation of CRYBA1/A3 Associated with Autosomal Dominant Nuclear Cataracts in a Chinese Family
Proteomic Landscape of the Human Choroid–Retinal Pigment Epithelial Complex
The Human Crystallin Gene Families Graeme Wistow
Congenital Cataract and Its Genetics: the Era of Next-Generation Sequencing
Genetic and Allelic Heterogeneity of Cryg Mutations in Eight Distinct Forms of Dominant Cataract in the Mouse
1 Supplementary Table 1. List (Akronym and Description) Of
Identification of a Missense Mutation in MIP Gene Via Mutation Analysis of a Guangxi Zhuang Ethnic Pedigree with Congenital Nuclear Cataracts
CRYGS Rabbit Pab
Structure of the Crysta II I Ns
Partial Duplication of the CRYBB1-CRYBA4 Locus Is Associated with Autosomal Dominant Congenital Cataract
A Novel Mutation in CRYBB2 Responsible for Inherited Coronary
Gene Expression in the Mouse Eye: an Online Resource for Genetics Using 103 Strains of Mice
Epidemiology and Molecular Genetics of Congenital Cataracts
CRYGB, CRYGC, and CRYGS) As Candidates for Hereditary Cataracts in the Dachshund
CRYBB1) Associated with Autosomal Recessive Nuclear Pulverulent Cataract