Clinical and Molecular Aspects of Senataxin Mutations in Amyotrophic Lateral Sclerosis 4
Published 2020 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Clinical and Molecular Aspects of Senataxin Mutations in Amyotrophic Lateral Sclerosis 4
Authors
Keywords
-
Journal
ANNALS OF NEUROLOGY
Volume -, Issue -, Pages -
Publisher
Wiley
Online
2020-01-20
DOI
10.1002/ana.25681
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Refining the spinobulbar muscular atrophy phenotype by quantitative MRI and clinical assessments
- (2019) Julia R. Dahlqvist et al. NEUROLOGY
- Canonical TGF-β Signaling Negatively Regulates Neuronal Morphogenesis through TGIF/Smad Complex-Mediated CRMP2 Suppression
- (2018) Hideyuki Nakashima et al. JOURNAL OF NEUROSCIENCE
- Senataxin Mutation Reveals How R-Loops Promote Transcription by Blocking DNA Methylation at Gene Promoters
- (2018) Christopher Grunseich et al. MOLECULAR CELL
- Genetics of Amyotrophic Lateral Sclerosis
- (2017) Mehdi Ghasemi et al. Cold Spring Harbor Perspectives in Medicine
- Creatine kinase enzyme level correlates positively with serum creatinine and lean body mass, and is a prognostic factor for survival in amyotrophic lateral sclerosis
- (2016) M. K. Rafiq et al. EUROPEAN JOURNAL OF NEUROLOGY
- Human Senataxin Modulates Structural Plasticity of the Neuromuscular Junction in Drosophila through a Neuronally Conserved TGFβ Signalling Pathway
- (2016) Zeeshan Mushtaq et al. Neurodegenerative Diseases
- Biological follow-up in amyotrophic lateral sclerosis: decrease in creatinine levels and increase in ferritin levels predict poor prognosis
- (2015) F. Patin et al. EUROPEAN JOURNAL OF NEUROLOGY
- Astrocyte-Derived TGF-β1 Accelerates Disease Progression in ALS Mice by Interfering with the Neuroprotective Functions of Microglia and T Cells
- (2015) Fumito Endo et al. Cell Reports
- Mutations in prion-like domains in hnRNPA2B1 and hnRNPA1 cause multisystem proteinopathy and ALS
- (2013) Hong Joo Kim et al. NATURE
- Longitudinal changes of outcome measures in spinal and bulbar muscular atrophy
- (2012) Atsushi Hashizume et al. BRAIN
- Mutation in the senataxin gene found in a patient affected by familial ALS with juvenile onset and slow progression
- (2011) Francesca Avemaria et al. Amyotrophic Lateral Sclerosis
- Human Senataxin Resolves RNA/DNA Hybrids Formed at Transcriptional Pause Sites to Promote Xrn2-Dependent Termination
- (2011) Konstantina Skourti-Stathaki et al. MOLECULAR CELL
- Senataxin mutations and amyotrophic lateral sclerosis
- (2010) Michio Hirano et al. Amyotrophic Lateral Sclerosis
- Dual Energy X-Ray Absorptiometry Body Composition Reference Values from NHANES
- (2009) Thomas L. Kelly et al. PLoS One
- Mutations in the FUS/TLS Gene on Chromosome 16 Cause Familial Amyotrophic Lateral Sclerosis
- (2009) T. J. Kwiatkowski et al. SCIENCE
- TDP-43A315T mutation in familial motor neuron disease
- (2008) Michael A. Gitcho et al. ANNALS OF NEUROLOGY
Publish scientific posters with Peeref
Peeref publishes scientific posters from all research disciplines. Our Diamond Open Access policy means free access to content and no publication fees for authors.
Learn MoreBecome a Peeref-certified reviewer
The Peeref Institute provides free reviewer training that teaches the core competencies of the academic peer review process.
Get Started