DOCSLIB.ORG
Explore
Sign Up
Log In
Upload
Search
Home
» Tags
» FSCN2
FSCN2
Molecular Effects of Isoflavone Supplementation Human Intervention Studies and Quantitative Models for Risk Assessment
Null Mutation of the Fascin2 Gene by TALEN Leading to Progressive Hearing Loss and Retinal Degeneration in C57BL/6J Mice
Fascin (55Kd Actin-Bundling Protein, Singed-Like Protein, P55)
Fascin 2 (FSCN2) Goat Polyclonal Antibody – AP31070PU-N | Origene
The R109H Variant of Fascin-2, a Developmentally Regulated Actin Crosslinker in Hair-Cell Stereocilia, Underlies Early-Onset Hearing Loss of DBA/2J Mice
Characterizing Epigenetic Regulation in the Developing Chicken Retina Bejan Abbas Rasoul James Madison University
Using an Atlas of Gene Regulation Across 44 Human Tissues to Inform Complex Disease- and Trait-Associated Variation
Autosomal Dominant Macular Degeneration Associated with 208Delg Mutation in the FSCN2 Gene
Targeted RP9 Ablation and Mutagenesis in Mouse Photoreceptor Cells by CRISPR-Cas9
Mouse Models of Inherited Retinal Degeneration with Photoreceptor Cell Loss
Allelic Copy Number Variation in FSCN2 Detected Using Allele-Specific Genotyping and Multiplex Real-Time Pcrs
Using an Atlas of Gene Regulation Across 44 Human Tissues to Inform Complex Disease- and Trait-Associated Variation
Genetic Analysis of Rare Eye Disorders in Pakistani Families
Mrna Expression in Human Leiomyoma and Eker Rats As Measured by Microarray Analysis
Identification of Photoreceptor Genes Affected by PRPF31 Mutations Associated with Autosomal Dominant Retinitis Pigmentosa
Pathway and Network Analysis for Mrna and Protein Profiling Data
PDZD7-MYO7A Complex Identified in Enriched Stereocilia Membranes
Determining the Causes of Recessive Retinal Dystrophy
Top View
Molecular Composition of Vestibular Hair Bundles
The Role of Small In-Frame Insertions/Deletions in Inherited Eye
ABSTRACT Using a Bioinformatics Approach to Identify Genes That
Association of a Novel Mutation in the Retinol Dehydrogenase 12 (RDH12) Gene with Autosomal Dominant Retinitis Pigmentosa
Mouse Fscn2 Conditional Knockout Project (CRISPR/Cas9)
Text Mining Applied to Molecular Biology
PRODUCT SPECIFICATION Product Datasheet
Null Mutation of the Fascin2 Gene by TALEN Leading to Progressive Hearing Loss and Retinal Degeneration in C57BL/6J Mice
1 Supplementary Material Figure S1. Volcano Plot of Differentially
V11a110-Gamundi Pgmkr
Prognosticating Retinal Dystrophies in the Postgenomic Era Inheritance Patterns of Retinal Diseases
Mouse Fscn2 Knockout Project (CRISPR/Cas9)
Unravelling the Genetic Basis of Simplex Retinitis Pigmentosa Cases
A Genome-Wide Association Study Identifies Five Novel Genetic Markers for Trastuzumab-Induced Cardiotoxicity in Japanese Population
Epigenomewide Scan Identifies a Treatmentresponsive Pattern Of
Clinical Utility Gene Card For: Autosomal Recessive Cone-Rod Dystrophy
Global Analysis of Protein Expression of Inner Ear Hair Cells
Epigenome-Wide DNA Methylation Profiling in Progressive