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RP9
Telomere Biology and Aging
Clinical Features of Autosomal Dominant Retinitis Pigmentosa Associated with a Rhodopsin Mutation
Genes and Mutations Causing Autosomal Dominant Retinitis Pigmentosa
Supplementary Figure 1. Network Map Associated with Upregulated Canonical Pathways Shows Interferon Alpha As a Key Regulator
Rp9 (NM 018739) Mouse Tagged ORF Clone – MG218146 | Origene
Targeted RP9 Ablation and Mutagenesis in Mouse Photoreceptor Cells by CRISPR-Cas9
A Collection of 1814 Human Chromosome 7-Specific Stss
Review Pre-Mrna Splicing and Retinitis Pigmentosa
Gnomad Lof Supplement
Swiss Rna Workshop
Genome Editing As a Treatment for the Most Prevalent Causative Genes of Autosomal Dominant Retinitis Pigmentosa
MOL #82305 TITLE PAGE Title: Induced CYP3A4 Expression In
CRISPR-Cas Genome Surgery in Ophthalmology
Benchmarking Exomiser on Real Patient Whole-Exome Data
A Large-Scale RNA Interference Screen Identifies Genes That
Association of a Novel Mutation in the Retinol Dehydrogenase 12 (RDH12) Gene with Autosomal Dominant Retinitis Pigmentosa
Immunity Resolution of Inflammation and Airway Diversity in Expression with Critical Roles in Macrophage Populations Reveals
Mpdz Null Allele in an Avian Model of Retinal Degeneration and Mutations in Human Leber Congenital Amaurosis and Retinitis Pigmentosa
Top View
Data Set 1. Biological Analysis of the Genes Found to Be Significant in the Endotoxin Study
Curriculum Vitae
Gene Expression and Coexpression Alterations Marking Evolution of Bladder Cancer
II ESERCITAZIONE Ricerca in Omim, Entrez Genes, Genecards, Human
Spaceflight Influences Gene Expression, Photoreceptor
(A) Hippocampal Neurons (B) Pre-LCM (C) Post-LCM
Molecular Genetics of Autosomal Dominant Retinitis Pigmentosa (ADRP): a Comprehensive Study of 43 Italian Families
Application of CRISPR Tools for Variant Interpretation and Disease Modeling in Inherited Retinal Dystrophies
Perspective on Genes and Mutations Causing Retinitis Pigmentosa
Pigmentosa Families: Frequencies of the Nine Known Loci and Evidence for Further Heterogeneity
Molecular Genetic Analysis of Human Inherited Retinal Degeneration
Transcription Coactivators P300 and CBP Are Necessary for Photoreceptor-Specific Chromatin Organization and Gene Expression Anne K
Physical and Transcriptional Mapping Studies Within the Retinitis
Transcription of Three C-Myc Exons Is Enhanced in Chicken Bursal
Functional and In-Silico Interrogation of Rare Genomic Variants Impacting RNA Splicing for the Diagnosis of Genomic Disorders
Whole-Genome Sequencing Is More Powerful Than Whole-Exome Sequencing for Detecting Exome Variants
Mutations in a Protein Target of the Pim-1 Kinase Associated with the RP9 Form of Autosomal Dominant Retinitis Pigmentosa
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