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PRX (gene)
Inherited Neuropathies
A Case Report on Charcot-Marie-Tooth Disease with a Novel Periaxin Gene Mutation
(12) Patent Application Publication (10) Pub. No.: US 2008/0057509 A1 Lupski Et Al
Prediction of Tissue-Specific Cis-Regulatory Sequences: Application to the Ascidian Ciona Intestinalis and the Anterior Neurectoderm Maximilian Häussler
In This Table Protein Name, Uniprot Code, Gene Name P-Value
Peroxiredoxins: Guardians Against Oxidative Stress and Modulators of Peroxide Signaling
Mouse Prx Knockout Project (CRISPR/Cas9)
Expression of Periaxin (PRX) Specifically in the Human
Genome-Scale Analysis of DNA Methylation in Lung Adenocarcinoma and Integration with Mrna Expression
A Yeast-Based Model for Hereditary Motor and Sensory Neuropathies: a Simple System for Complex, Heterogeneous Diseases
A Polymorphism in the Nuclear Receptor Coactivator 7 Gene and Breast Cancer Susceptibility
The Dystrobrevin-Binding Protein 1 Gene
Direct Binding of the Flexible C-Terminal Segment of Periaxin to Β4 Integrin Suggests 2 a Molecular Basis for CMT4F 3 4 Arne Raasakka1, Helen Linxweiler1, Peter J
Gene Ontology Analysis of Arthrogryposis (Multiple Congenital Contractures)
The Glomerular Transcriptome and a Predicted Protein–Protein Interaction Network
Transcriptomic Comparison of Human and Mouse Brain Microvessels Hannah W
Proteome Profile of Peripheral Myelin in Healthy Mice and in a Neuropathy
Atlas Journal
Top View
Charcot-Marie-Tooth Disease: Seventeen Causative Genes
Regulatory Divergence Modifies Limb Length Between Mammals
Local Regulation of Fat Metabolism in Peripheral Nerves
Term Matrix: a Novel Gene Ontology Annotation Quality Control System Based on Ontology Term Co-Annotation Patterns
View of the Peroxiredoxin Family………………………
Dataset S2. Change-Of-Function Mutations in the C. Elegans Candidate Regions
Periaxin Mutations Cause Recessive Dejerine-Sottas Neuropathy Cornelius F
Supplemental Table S1. the 38 BMD GWA Studies Used for This Analysisa First Author Study BMD Region/Typeb Ancestry Population Ye