Alteration of protein folding and degradation in motor neuron diseases: Implications and protective functions of small heat shock proteins-Reference-Cited by-同舟云学术

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Alteration of protein folding and degradation in motor neuron diseases: Implications and protective functions of small heat shock proteins

Published:2012-05 Issue:2 Volume:97 Page:83-100
ISSN:0301-0082
Container-title:Progress in Neurobiology
language:en
Short-container-title:Progress in Neurobiology

Author:

Carra Serena,Crippa Valeria,Rusmini Paola,Boncoraglio Alessandra,Minoia Melania,Giorgetti Elisa,Kampinga Harm H.,Poletti Angelo

Funder

Telethon

Italian Ministry of University and Research

Italian Ministry of Labour, Health and Social Affairs

Convenzione Fondazione Mondino/UNIMI

Universita’ degli Studi di Milano; Fondazione CARIPLO

Fondation Thierry Latran, France

Marie Curie International Reintegration Grant

Prinses Beatrix Fonds/Dutch Huntington Association

Association Française contre les Myopathies Trampoline Grant

Publisher

Elsevier BV

Subject

General Neuroscience

Reference239 articles.

1. Expression of expanded repeat androgen receptor produces neurologic disease in transgenic mice;Abel;Hum. Mol. Genet.,2001

2. A mutation in the small heat-shock protein HSPB1 leading to distal hereditary motor neuronopathy disrupts neurofilament assembly and the axonal transport of specific cellular cargoes;Ackerley;Hum. Mol. Genet.,2006

3. Heat shock protein 70 chaperone overexpression ameliorates phenotypes of the spinal and bulbar muscular atrophy transgenic mouse model by reducing nuclear-localized mutant androgen receptor protein;Adachi;J. Neurosci.,2003

4. Widespread nuclear and cytoplasmic accumulation of mutant androgen receptor in SBMA patients;Adachi;Brain,2005

5. Transgenic mice with an expanded CAG repeat controlled by the human AR promoter show polyglutamine nuclear inclusions and neuronal dysfunction without neuronal cell death;Adachi;Hum. Mol. Genet.,2001

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