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CRYBB2
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
Rescue of Retinal Degeneration by Intravitreally Injected Adult Bone Marrow–Derived Lineage-Negative Hematopoietic Stem Cells
82314791.Pdf
Novel Mutation in the Γ-S Crystallin Gene Causing Autosomal Dominant Cataract
(12) Patent Application Publication (10) Pub. No.: US 2003/0198970 A1 Roberts (43) Pub
Aey2, a New Mutation in the ßb2-Crystallin–Encoding Gene Of
Bidirectional Analysis of Cryba4-Crybb1 Nascent Transcription and Nuclear Accumulation of Crybb3 Mrnas in Lens Fibers
A Novel Mutation in CRYAA Is Associated with Autosomal Dominant Suture Cataracts in a Chinese Family
Alterations in Energy Metabolism, Neuroprotection and Visual Signal Transduction in the Retina of Parkinsonian, MPTP-Treated Monkeys
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
Autocrine IFN Signaling Inducing Profibrotic Fibroblast Responses By
Novel Mutation in CRYBB3 Causing Pediatric Cataract and Microphthalmia
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
Top View
Photoreceptor-Induced RPE Phagolysosomal
17Β-Estradiol Delivered in Eye Drops: Evidence of Impact on Protein Networks and Associated Biological Processes in the Rat Retina Through Quantitative Proteomics
Table Legend
Microarray Analysis of Iris Gene Expression in Mice with Mutations Influencing Pigmentation
The Human Crystallin Gene Families Graeme Wistow
This Thesis Has Been Submitted in Fulfilment of the Requirements for a Postgraduate Degree (E.G
Identification of a Missense Mutation in MIP Gene Via Mutation Analysis of a Guangxi Zhuang Ethnic Pedigree with Congenital Nuclear Cataracts
CRYAA Nucleotide Variants to a Complex Presentation of Anterior Segment Dysgenesis Andrey V
Partial Duplication of the CRYBB1-CRYBA4 Locus Is Associated with Autosomal Dominant Congenital Cataract
Investigation of Crystallin Genes in Familial Cataract, and Report of Two
A Novel Mutation in CRYBB2 Responsible for Inherited Coronary
Proteomic Analysis of the Aqueous Humour in Eyes with Pseudoexfoliation Syndrome Amelie Botling Taube,1,2 Anne Konzer,3 Albert Alm,1 Jonas Bergquist 3
Sigma Receptor 1 Modulates Endoplasmic Reticulum Stress in Retinal Neurons
Long-Term Neuroprotective Effects of NT-4–Engineered Mesenchymal Stem Cells Injected Intravitreally in a Mouse Model of Acute Retinal Injury
Analyzing the Association of Polymorphisms in the CRYBB2 Gene with Prostate Cancer Risk in African Americans
(CRYGD) Associated with Autosomal Dominant "Coral-Like" Cataract Linked to Chromosome 2Q Donna S
CRYBB1) Associated with Autosomal Recessive Nuclear Pulverulent Cataract
A Novel CRYBB2 Stopgain Mutation Causing Congenital Autosomal