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注意:仅列出部分参考文献,下载原文获取全部文献信息。Mutation analysis of GLT8D1 and ARPP21 genes in amyotrophic lateral sclerosis patients from mainland China
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Aude Nicolas et al.
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SDM: a server for predicting effects of mutations on protein stability
Arun Prasad Pandurangan et al.
NUCLEIC ACIDS RESEARCH (2017)
The Hsp70/Hsp90 Chaperone Machinery in Neurodegenerative Diseases
Rachel E. Lackie et al.
FRONTIERS IN NEUROSCIENCE (2017)
Mutation spectrum of Chinese patients with familial and sporadic amyotrophic lateral sclerosis
Qing Liu et al.
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY (2016)
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Karissa C. Arthur et al.
NATURE COMMUNICATIONS (2016)
A revision of the El Escorial criteria-2015
Albert Ludolph et al.
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration (2015)
mCSM: predicting the effects of mutations in proteins using graph-based signatures
Douglas E. V. Pires et al.
BIOINFORMATICS (2014)
State of play in amyotrophic lateral sclerosis genetics
Alan E. Renton et al.
NATURE NEUROSCIENCE (2014)
Identification of C9orf72 repeat expansions in patients with amyotrophic lateral sclerosis and frontotemporal dementia in mainland China
Bin Jiao et al.
NEUROBIOLOGY OF AGING (2014)
Identification of PRRT2 as the causative gene of paroxysmal kinesigenic dyskinesias
Jun-Ling Wang et al.
BRAIN (2011)
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Mariely DeJesus-Hernandez et al.
NEURON (2011)
Structural basis of J cochaperone binding and regulation of Hsp70
Jianwen Jiang et al.
MOLECULAR CELL (2007)
Hsp70 chaperones: Cellular functions and molecular mechanism
MP Mayer et al.
CELLULAR AND MOLECULAR LIFE SCIENCES (2005)