Profilin-1 mutations are rare in patients with amyotrophic lateral sclerosis and frontotemporal dementia
Published 2013 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Profilin-1 mutations are rare in patients with amyotrophic lateral sclerosis and frontotemporal dementia
Authors
Keywords
-
Journal
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration
Volume 14, Issue 5-6, Pages 463-469
Publisher
Informa UK Limited
Online
2013-05-02
DOI
10.3109/21678421.2013.787630
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- How do the RNA-binding proteins TDP-43 and FUS relate to amyotrophic lateral sclerosis and frontotemporal degeneration, and to each other?
- (2012) Robert H. Baloh CURRENT OPINION IN NEUROLOGY
- How do C9ORF72 repeat expansions cause amyotrophic lateral sclerosis and frontotemporal dementia
- (2012) Marka van Blitterswijk et al. CURRENT OPINION IN NEUROLOGY
- Evidence for an oligogenic basis of amyotrophic lateral sclerosis
- (2012) Marka van Blitterswijk et al. HUMAN MOLECULAR GENETICS
- Mutations in the profilin 1 gene cause familial amyotrophic lateral sclerosis
- (2012) Chi-Hong Wu et al. NATURE
- Apolipoprotein E ε4 and age effects on florbetapir positron emission tomography in healthy aging and Alzheimer disease
- (2012) Adam S. Fleisher et al. NEUROBIOLOGY OF AGING
- Phenotypic signatures of genetic frontotemporal dementia
- (2011) Jonathan D. Rohrer et al. CURRENT OPINION IN NEUROLOGY
- The spinal muscular atrophy disease protein SMN is linked to the rho-kinase pathway via profilin
- (2011) Anna Nölle et al. HUMAN MOLECULAR GENETICS
- FMRP Regulates the Transition from Radial Glial Cells to Intermediate Progenitor Cells during Neocortical Development
- (2011) R. Saffary et al. JOURNAL OF NEUROSCIENCE
- Amyotrophic lateral sclerosis
- (2011) Matthew C Kiernan et al. LANCET
- SMN deficiency attenuates migration of U87MG astroglioma cells through the activation of RhoA
- (2011) Víctor Caraballo-Miralles et al. MOLECULAR AND CELLULAR NEUROSCIENCE
- Clinical genetics of amyotrophic lateral sclerosis: what do we really know?
- (2011) Peter M. Andersen et al. Nature Reviews Neurology
- Expanded GGGGCC Hexanucleotide Repeat in Noncoding Region of C9ORF72 Causes Chromosome 9p-Linked FTD and ALS
- (2011) Mariely DeJesus-Hernandez et al. NEURON
- A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD
- (2011) Alan E. Renton et al. NEURON
- Clinical, genetic and pathological heterogeneity of frontotemporal dementia: a review
- (2010) H. Seelaar et al. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
- RNA processing pathways in amyotrophic lateral sclerosis
- (2010) Marka van Blitterswijk et al. NEUROGENETICS
- How depolymerization can promote polymerization: the case of actin and profilin
- (2009) Elena G. Yarmola et al. BIOESSAYS
- Aberrant cleavage of TDP-43 enhances aggregation and cellular toxicity
- (2009) Y.-J. Zhang et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Nomenclature for neuropathologic subtypes of frontotemporal lobar degeneration: consensus recommendations
- (2008) Ian R. A. Mackenzie et al. ACTA NEUROPATHOLOGICA
- Phosphorylation of Profilin by ROCK1 Regulates Polyglutamine Aggregation
- (2008) J. Shao et al. MOLECULAR AND CELLULAR BIOLOGY
Create your own webinar
Interested in hosting your own webinar? Check the schedule and propose your idea to the Peeref Content Team.
Create NowBecome a Peeref-certified reviewer
The Peeref Institute provides free reviewer training that teaches the core competencies of the academic peer review process.
Get Started