Association between novel TARDBP mutations and Chinese patients with amyotrophic lateral sclerosis
Published 2010 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Association between novel TARDBP mutations and Chinese patients with amyotrophic lateral sclerosis
Authors
Keywords
-
Journal
BMC Medical Genetics
Volume 11, Issue 1, Pages -
Publisher
Springer Nature
Online
2010-01-19
DOI
10.1186/1471-2350-11-8
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- TARDBP(TDP-43) sequence analysis in patients with familial and sporadic ALS: identification of two novel mutations
- (2009) R. Del Bo et al. EUROPEAN JOURNAL OF NEUROLOGY
- High frequency ofTARDBPgene mutations in Italian patients with amyotrophic lateral sclerosis
- (2009) Lucia Corrado et al. HUMAN MUTATION
- TDP-43 M311V mutation in familial amyotrophic lateral sclerosis
- (2009) R Lemmens et al. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
- Screening for TARDBP mutations in Japanese familial amyotrophic lateral sclerosis
- (2009) Masaki Kamada et al. JOURNAL OF THE NEUROLOGICAL SCIENCES
- Mutations in FUS, an RNA Processing Protein, Cause Familial Amyotrophic Lateral Sclerosis Type 6
- (2009) C. Vance et al. SCIENCE
- A novel mutation in thesenataxingene identified in a Chinese patient with sporadic amyotrophic lateral sclerosis
- (2008) Zhen-hua Zhao et al. Amyotrophic Lateral Sclerosis
- TDP-43mutation in familial amyotrophic lateral sclerosis
- (2008) Akio Yokoseki et al. ANNALS OF NEUROLOGY
- TDP-43A315T mutation in familial motor neuron disease
- (2008) Michael A. Gitcho et al. ANNALS OF NEUROLOGY
- Two German Kindreds With Familial Amyotrophic Lateral Sclerosis Due to TARDBP Mutations
- (2008) Peter Kühnlein et al. ARCHIVES OF NEUROLOGY
- TARDBP mutations in amyotrophic lateral sclerosis with TDP-43 neuropathology: a genetic and histopathological analysis
- (2008) Vivianna M Van Deerlin et al. LANCET NEUROLOGY
- TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis
- (2008) Edor Kabashi et al. NATURE GENETICS
- Neuronal inclusion protein TDP-43 has no primary genetic role in FTD and ALS
- (2008) Ilse Gijselinck et al. NEUROBIOLOGY OF AGING
- Genetics of familial amyotrophic lateral sclerosis
- (2008) P. N. Valdmanis et al. NEUROLOGY
- TDP-43 Is Not a Common Cause of Sporadic Amyotrophic Lateral Sclerosis
- (2008) Rita J. Guerreiro et al. PLoS One
- TDP-43 Mutations in Familial and Sporadic Amyotrophic Lateral Sclerosis
- (2008) J. Sreedharan et al. SCIENCE
- Novel Mutations in TARDBP (TDP-43) in Patients with Familial Amyotrophic Lateral Sclerosis
- (2008) Nicola J. Rutherford et al. PLoS Genetics
- Multiple roles of TDP-43 in gene expression, splicing regulation, and human disease
- (2007) Emanuele Buratti Frontiers in Bioscience-Landmark
Find Funding. Review Successful Grants.
Explore over 25,000 new funding opportunities and over 6,000,000 successful grants.
ExploreCreate your own webinar
Interested in hosting your own webinar? Check the schedule and propose your idea to the Peeref Content Team.
Create Now