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HSPB3
Proteomic and Metabolomic Analyses of Mitochondrial Complex I-Deficient
Consequences of Disease-Causing Small Heat Shock Protein Mutations on ARE-Mediated
Burden of Rare Variants in ALS and Axonal Hereditary Neuropathy Genes Influence Survival In
High Resolution Physical and Comparative Maps of Horse
Autosomal Dominant Late-Onset Spinal Motor Neuronopathy Is Linked to a New Locus on Chromosome 22Q11.2-Q13.2
Prediction of Human Disease Genes by Human-Mouse Conserved Coexpression Analysis
Double Homeobox 4 Activates Germline Genes, Endogenous Retroelements and Immune Modulators: Implications for Facioscapulohumeral Muscular Dystrophy
Transcriptome Profiling Reveals the Complexity of Pirfenidone Effects in IPF
A Yeast-Based Model for Hereditary Motor and Sensory Neuropathies: a Simple System for Complex, Heterogeneous Diseases
Gnomad Lof Supplement
Systematic Detection of Brain Protein-Coding Genes Under Positive Selection During Primate Evolution and Their Roles in Cognition
Junl;G.~~ Assistant Professor Department of Mechanical Engineering Rice University
HSPB3 Protein Is Expressed in Motoneurons and Induces Their Survival After Lesion-Induced Degeneration
View and Expressed As the Number of Mhspb1 Positive Cells Over Total Cells
Characterization of a Small Heat Shock Protein B3 (Hspb3)
Small Heat Shock Proteins, Big Impact on Protein Aggregation in Neurodegenerative Disease
Table S1. Complete List of Up- and Down-Regulated Genes in C1 Cells
Downloaded from the Gtex Portal Ones Can Give Rise to Non-Specific Effects and Has Therapeutic (Version 7)
Top View
Novel Extracellular and Nuclear Caspase-1 and Inflammasomes
A New Perspective of Genetic Associations to the Cause of Multiple Sclerosis
Using Massively Parallel Sequencing to Determine the Genetic Basis of Leigh Syndrome, the Most Common Mitochondrial Disorder Affecting Children
Transcriptional Response to Stress in the Dynamic Chromatin Environment of Cycling and Mitotic Cells
Structural and Functional Principles of the Small Heat Shock Protein Α-Crystallin
Distant Cis-Regulatory Elements in Human Skeletal Muscle Differentiation
The 2020 Version of the Gene Table of Neuromuscular Disorders (Nuclear Genome) Louise Benarroch, Gisèle Bonne, Francois Rivier, Dalil Hamroun
Design Principles of Gene Evolution for Niche Adaptation Through Changes
Neuromuscular Diseases Due to Chaperone Mutations: a Review and Some New Results
Supplementary Information
Inflammatory Leiomyosarcoma Is a Distinct Tumor Characterized by Near-Haploidization, Few Somatic Mutations, and a Primitive
BAG3-Mediated Proteostasis at a Glance Christina Klimek, Barbara Kathage, Judith Wördehoff and Jörg Höhfeld*