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BFSP2
Isyte: Integrated Systems Tool for Eye Gene Discovery
A New Mutation in BFSP2 (G1091A) Causes Autosomal Dominant Congenital Lamellar Cataracts
Variants in PAX6, PITX3 and HSF4 Causing Autosomal Dominant Congenital Cataracts ✉ ✉ Vanita Berry 1,2 , Alex Ionides2, Nikolas Pontikos 1,2, Anthony T
Avian Binocularity and Adaptation to Nocturnal Environments: Genomic Insights Froma Highly Derived Visual Phenotype Rui Borges Universidade Do Porto - Portugal
Duke University Dissertation Template
Cytoskeletal Proteins in Neurological Disorders
Novel Recessive BFSP2 and PITX3 Mutations: Insights Into Mutational Mechanisms from Consanguineous Populations Mohammed A
Foraging Shifts and Visual Pre Adaptation in Ecologically Diverse Bats
(BFSP1) Gene Mutation Associated with Autosomal Dominant
Report a Juvenile-Onset, Progressive Cataract Locus on Chromosome
Robles JTO Supplemental Digital Content 1
Lens Differentiation Is Characterized by Stage-Specific Changes In
A Novel Mutation in CRYAA Is Associated with Autosomal Dominant Suture Cataracts in a Chinese Family
A Robust Transcriptional Program in Newts 5 Undergoing Multiple Events of Lens Regeneration 6 Throughout Their Lifespan
Inherited Cataracts: Molecular Genetics, Clinical Features, Disease Mechanisms and Novel Therapeutic Approaches
Detection of H3k4me3 Identifies Neurohiv Signatures, Genomic
A Locus for Isolated Cataract on Human Xp P J Francis, V Berry, a J Hardcastle, E R Maher, a T Moore, S S Bhattacharya
Molecular and Genetic Mechanism of Non-Syndromic Congenital Cataracts
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Cataract and Optic Disk Drusen in a Patient with Glycogenosis and Di George Syndrome: Clinical and Molecular Report D
Diplomarbeit Sabrina Sibitz
A Novel Locus for Autosomal Dominant Nuclear Cataract Mapped to Chromosome 2P12 in a Pakistani Family
DNA-Binding and Transcriptional Activities of Human HSF4 Containing
Progressive Sutural Cataract Associated with a BFSP2 Mutation in a Chinese Family
A Novel Locus of Coralliform Cataract Mapped to Chromosome 2P24-Pter
Integrated Systems Tool for Eye Gene Discovery Salil A. Lachke,1,2,9
Identification of Novel Transcripts and Peptides in Developing Murine Lens
CRYAA Antibody(Center) Affinity Purified Rabbit Polyclonal Antibody (Pab) Catalog # Ap19751c
Functions of the Intermediate Filament Cytoskeleton in the Eye Lens
BFSP2 Mouse Monoclonal Antibody [Clone ID: OTI2G2] Product Data
Expression of the Type VI Intermediate Filament Proteins CP49 and Filensin in the Mouse Lens Epithelium
A Novel P.G112E Mutation in BFSP2 Associated with Autosomal Dominant Pulverulent Cataract with Sutural Opacities
BFSP2 Mouse Monoclonal Antibody [Clone ID: OTI4D3] Product Data
Phenotype Loss Is Associated with Widespread Divergence of the Gene Regulatory Landscape in Evolution
Investigation of Crystallin Genes in Familial Cataract, and Report of Two
Cell Death Triggered by a Novel Mutation in the Alphaa-Crystallin Gene Underlies Autosomal Dominant Cataract Linked to Chromosome 21Q
A Novel Mutation in CRYBB2 Responsible for Inherited Coronary