Identification of ter94, Drosophila VCP, as a strong modulator of motor neuron degeneration induced by knockdown of Caz, Drosophila FUS
Published 2014 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Identification of ter94, Drosophila VCP, as a strong modulator of motor neuron degeneration induced by knockdown of Caz, Drosophila FUS
Authors
Keywords
-
Journal
HUMAN MOLECULAR GENETICS
Volume 23, Issue 13, Pages 3467-3480
Publisher
Oxford University Press (OUP)
Online
2014-02-05
DOI
10.1093/hmg/ddu055
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- dNF-YB plays dual roles in cell death and cell differentiation during Drosophila eye development
- (2013) Luong Linh Ly et al. GENE
- Fused in sarcoma (FUS): An oncogene goes awry in neurodegeneration
- (2013) Dorothee Dormann et al. MOLECULAR AND CELLULAR NEUROSCIENCE
- A functional deficiency of TERA/VCP/p97 contributes to impaired DNA repair in multiple polyglutamine diseases
- (2013) Kyota Fujita et al. Nature Communications
- Emerging functions of the VCP/p97 AAA-ATPase in the ubiquitin system
- (2012) Hemmo Meyer et al. NATURE CELL BIOLOGY
- Knockdown of the Drosophila Fused in Sarcoma (FUS) Homologue Causes Deficient Locomotive Behavior and Shortening of Motoneuron Terminal Branches
- (2012) Hiroshi Sasayama et al. PLoS One
- TDP-43 and FUS/TLS: cellular functions and implications for neurodegeneration
- (2011) Fabienne C. Fiesel et al. FEBS Journal
- The ALS-associated proteins FUS and TDP-43 function together to affect Drosophila locomotion and life span
- (2011) Ji-Wu Wang et al. JOURNAL OF CLINICAL INVESTIGATION
- FUS and TARDBP but Not SOD1 Interact in Genetic Models of Amyotrophic Lateral Sclerosis
- (2011) Edor Kabashi et al. PLoS Genetics
- Novel FUS/TLS Mutations and Pathology in Familial and Sporadic Amyotrophic Lateral Sclerosis
- (2010) Christopher Hewitt et al. ARCHIVES OF NEUROLOGY
- p97/VCP at the intersection of the autophagy and the ubiquitin proteasome system
- (2010) Jeong-Sun Ju et al. Autophagy
- Imbalances in p97 co-factor interactions in human proteinopathy
- (2010) Vanesa Fernández-Sáiz et al. EMBO REPORTS
- Drosophila Syntrophins are involved in locomotion and regulation of synaptic morphology
- (2010) Rika Nagai et al. EXPERIMENTAL CELL RESEARCH
- TDP-43 and FUS/TLS: emerging roles in RNA processing and neurodegeneration
- (2010) C. Lagier-Tourenne et al. HUMAN MOLECULAR GENETICS
- Amyotrophic Lateral Sclerosis-associated Proteins TDP-43 and FUS/TLS Function in a Common Biochemical Complex to Co-regulate HDAC6 mRNA
- (2010) Sang Hwa Kim et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- TDP-43 Mediates Degeneration in a Novel Drosophila Model of Disease Caused by Mutations in VCP/p97
- (2010) G. P. Ritson et al. JOURNAL OF NEUROSCIENCE
- TDP-43 and FUS in amyotrophic lateral sclerosis and frontotemporal dementia
- (2010) Ian RA Mackenzie et al. LANCET NEUROLOGY
- Fusgene mutations in familial and sporadic amyotrophic lateral sclerosis
- (2010) Rosa Rademakers et al. MUSCLE & NERVE
- RNA processing pathways in amyotrophic lateral sclerosis
- (2010) Marka van Blitterswijk et al. NEUROGENETICS
- Exome Sequencing Reveals VCP Mutations as a Cause of Familial ALS
- (2010) Janel O. Johnson et al. NEURON
- ALS-associated mutations in TDP-43 increase its stability and promote TDP-43 complexes with FUS/TLS
- (2010) S.-C. Ling et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- RNA metabolism and the pathogenesis of motor neuron diseases
- (2010) Robin Lemmens et al. TRENDS IN NEUROSCIENCES
- Depletion of TDP-43 affectsDrosophila motoneuronsterminal synapsis and locomotive behavior
- (2009) Fabian Feiguin et al. FEBS LETTERS
- Mutations in TDP-43 link glycine-rich domain functions to amyotrophic lateral sclerosis
- (2009) G. S. Pesiridis et al. HUMAN MOLECULAR GENETICS
- Mutations in FUS, an RNA Processing Protein, Cause Familial Amyotrophic Lateral Sclerosis Type 6
- (2009) C. Vance et al. SCIENCE
- Mutations in the FUS/TLS Gene on Chromosome 16 Cause Familial Amyotrophic Lateral Sclerosis
- (2009) T. J. Kwiatkowski et al. SCIENCE
- 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
- Roles of VCP in human neurodegenerative disorders
- (2008) Akira Kakizuka BIOCHEMICAL SOCIETY TRANSACTIONS
- Mechanisms of Cdc48/VCP-mediated cell death — from yeast apoptosis to human disease
- (2008) Ralf J. Braun et al. BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH
- Structural determinants of the cellular localization and shuttling of TDP-43
- (2008) Y. M. Ayala et al. JOURNAL OF CELL SCIENCE
- TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis
- (2008) Edor Kabashi et al. NATURE GENETICS
- Modeling Spinal Muscular Atrophy in Drosophila
- (2008) Howard Chia-Hao Chang et al. PLoS One
- TDP-43 Mutations in Familial and Sporadic Amyotrophic Lateral Sclerosis
- (2008) J. Sreedharan et al. SCIENCE
Discover Peeref hubs
Discuss science. Find collaborators. Network.
Join a conversationFind the ideal target journal for your manuscript
Explore over 38,000 international journals covering a vast array of academic fields.
Search