A rare recessive distal hereditary motor neuropathy with HSJ1 chaperone mutation

Molecular Genetics and Mechanisms of Disease in Distal Hereditary Motor Neuropathies: Insights Directing Future Genetic Studies

(2011) A. P. Drew et al.   CURRENT MOLECULAR MEDICINE

DNAJB2 Expression in Normal and Diseased Human and Mouse Skeletal Muscle

(2010) Kristl G. Claeys et al.   AMERICAN JOURNAL OF PATHOLOGY

Levels of DNAJB family members (HSP40) correlate with disease onset in patients with spinocerebellar ataxia type 3

(2010) M. P. Zijlstra et al.   EUROPEAN JOURNAL OF NEUROSCIENCE

Molecular chaperone-mediated rescue of mitophagy by a Parkin RING1 domain mutant

(2010) Johanna M. Rose et al.   HUMAN MOLECULAR GENETICS

A DNAJB Chaperone Subfamily with HDAC-Dependent Activities Suppresses Toxic Protein Aggregation

(2010) Jurre Hageman et al.   MOLECULAR CELL

Chaperone networks: Tipping the balance in protein folding diseases

(2010) Cindy Voisine et al.   NEUROBIOLOGY OF DISEASE

Mutant small heat shock protein B3 causes motor neuropathy: Utility of a candidate gene approach

(2010) S. J. Kolb et al.   NEUROLOGY

The role of the ubiquitin proteasome system in synapse remodeling and neurodegenerative diseases

(2009) Mei Ding et al.   BIOESSAYS

Roles of ubiquitination at the synapse

(2008) Kevin F. Haas et al.   Biochimica et Biophysica Acta-Gene Regulatory Mechanisms

Guidelines for the nomenclature of the human heat shock proteins

(2008) Harm H. Kampinga et al.   CELL STRESS & CHAPERONES

HSP90β Regulates Rapsyn Turnover and Subsequent AChR Cluster Formation and Maintenance

(2008) Shiwen Luo et al.   NEURON

Amyotrophic lateral sclerosis: Protein chaperone dysfunction revealed by proteomic studies of animal models

(2008) Mohit Raja Jain et al.   Proteomics Clinical Applications