相关参考文献
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
Wanzhen Li et al.
NEUROBIOLOGY OF AGING (2020)
Long-read sequencing identified intronic repeat expansions in SAMD12 from Chinese pedigrees affected with familial cortical myoclonic tremor with epilepsy
Sheng Zeng et al.
JOURNAL OF MEDICAL GENETICS (2019)
Genetics of amyotrophic lateral sclerosis: A review
Stephane Mathis et al.
JOURNAL OF THE NEUROLOGICAL SCIENCES (2019)
Exome sequencing in amyotrophic lateral sclerosis implicates a novel gene, DNAJC7, encoding a heat-shock protein
Sali M. K. Farhan et al.
NATURE NEUROSCIENCE (2019)
Novel genes associated with amyotrophic lateral sclerosis: diagnostic and clinical implications
Ruth Chia et al.
LANCET NEUROLOGY (2018)
LRP10 genetic variants in familial Parkinson's disease and dementia with Lewy bodies: a genome-wide linkage and sequencing study
Marialuisa Quadri et al.
LANCET NEUROLOGY (2018)
Mutation analysis of the TIA1 gene in Chinese patients with amyotrophic lateral sclerosis and frontotemporal dementia
Zhenhua Yuan et al.
NEUROBIOLOGY OF AGING (2018)
Genome-wide Analyses Identify KIF5A as a Novel ALS Gene
Aude Nicolas et al.
NEURON (2018)
Genetic epidemiology of amyotrophic lateral sclerosis: a systematic review and meta-analysis
Zhang-Yu Zou et al.
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY (2017)
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)
Projected increase in amyotrophic lateral sclerosis from 2015 to 2040
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)
Expanded GGGGCC Hexanucleotide Repeat in Noncoding Region of C9ORF72 Causes Chromosome 9p-Linked FTD and ALS
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)
分享论文
