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HSPB8
Identification of the Binding Partners for Hspb2 and Cryab Reveals
Inherited Neuropathies
Prognostic Significance of Autophagy-Relevant Gene Markers in Colorectal Cancer
HSPB8 Gene Heat Shock Protein Family B (Small) Member 8
Autosomal Dominant Late-Onset Spinal Motor Neuronopathy Is Linked to a New Locus on Chromosome 22Q11.2-Q13.2
A High-Throughput Approach to Uncover Novel Roles of APOBEC2, a Functional Orphan of the AID/APOBEC Family
Small Heat Shock Proteins and Neurodegeneration: Recent Developments
Table S1. 103 Ferroptosis-Related Genes Retrieved from the Genecards
Exome Sequencing in Amyotrophic Lateral Sclerosis Implicates a Novel Gene, DNAJC7, Encoding a Heat-Shock Protein
The Small Heat Shock Protein B8 (HSPB8) Modulates Proliferation and Migration of Breast Cancer Cells
Primepcr™Assay Validation Report
The Heterooligomerization of Human Small Heat Shock Proteins Is Controlled by Conserved Motif Located in the N-Terminal Domain
The Role of HSPB8, a Component of the Chaperone-Assisted Selective Autophagy Machinery, in Cancer
Downloaded from the Gtex Portal Ones Can Give Rise to Non-Specific Effects and Has Therapeutic (Version 7)
Tyrosine Hydroxylase and HSPB8 Interact with the Prion Protein
Analysis of Breast Cancer Subtypes by AP-ISA Biclustering Liying Yang1*, Yunyan Shen1, Xiguo Yuan1, Junying Zhang1 and Jianhua Wei2*
Autosomal Dominant Distal Hereditary Motor Neuropathy Type II: a Korean Family Without Sequence Variation in HSPB1 and HSPB8
Charcot-Marie-Tooth Disease: Seventeen Causative Genes
Top View
Distal Hereditary Motor Neuropathy in Korean Patients with a Small Heat Shock Protein 27 Mutation
The Role of HSPB8, a Component of the Chaperone-Assisted Selective Autophagy Machinery, in Cancer
Clinical and Electrophysiological Aspects of Charcot-Marie-Tooth Disease
Overlapping Molecular Pathological Themes Link Charcot–Marie–Tooth Neuropathies and Hereditary Spastic Paraplegias
BAG3-Mediated Proteostasis at a Glance Christina Klimek, Barbara Kathage, Judith Wördehoff and Jörg Höhfeld*
Hot-Spot Residue in Small Heat-Shock Protein 22 Causes Distal Motor Neuropathy
Hot-Spot Residue in Small Heat-Shock Protein 22 Causes Distal Motor Neuropathy
Exome Sequencing Reveals HINT1 Mutations As a Cause of Distal Hereditary Motor Neuropathy
RNA Structure Drives Interaction with Proteins
The BAG3-Dependent and -Independent Roles of Cardiac Small Heat Shock Proteins