Sqstm1 knock-down causes a locomotor phenotype ameliorated by rapamycin in a zebrafish model of ALS/FTLD
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Title
Sqstm1 knock-down causes a locomotor phenotype ameliorated by rapamycin in a zebrafish model of ALS/FTLD
Authors
Keywords
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Journal
HUMAN MOLECULAR GENETICS
Volume 24, Issue 6, Pages 1682-1690
Publisher
Oxford University Press (OUP)
Online
2014-11-20
DOI
10.1093/hmg/ddu580
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Note: Only part of the references are listed.- Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration
- (2014) Julie van der Zee et al. ACTA NEUROPATHOLOGICA
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- (2014) Sarah L. Rea et al. EXPERIMENTAL CELL RESEARCH
- Autophagy induction enhances TDP43 turnover and survival in neuronal ALS models
- (2014) Sami J Barmada et al. Nature Chemical Biology
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- (2013) Hiroshi Shimizu et al. ACTA NEUROPATHOLOGICA
- Mutations in SQSTM1 encoding p62 in amyotrophic lateral sclerosis: genetics and neuropathology
- (2013) Elisa Teyssou et al. ACTA NEUROPATHOLOGICA
- Behavioral effects of SQSTM1/p62 overexpression in mice: Support for a mitochondrial role in depression and anxiety
- (2013) M. Lamar Seibenhener et al. BEHAVIOURAL BRAIN RESEARCH
- Sequestosome-1 (SQSTM1) sequence variants in ALS cases in the UK: prevalence and coexistence of SQSTM1 mutations in ALS kindred with PDB
- (2013) Chun T Kwok et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Loss and gain of FUS function impair neuromuscular synaptic transmission in a genetic model of ALS
- (2013) Gary A.B. Armstrong et al. HUMAN MOLECULAR GENETICS
- Investigating the contribution of VAPB/ALS8 loss of function in amyotrophic lateral sclerosis
- (2013) Edor Kabashi et al. HUMAN MOLECULAR GENETICS
- Mutations in prion-like domains in hnRNPA2B1 and hnRNPA1 cause multisystem proteinopathy and ALS
- (2013) Hong Joo Kim et al. NATURE
- SQSTM1 mutations in Han Chinese populations with sporadic amyotrophic lateral sclerosis
- (2013) YongPing Chen et al. NEUROBIOLOGY OF AGING
- Pharmacological reduction of ER stress protects against TDP-43 neuronal toxicity in vivo
- (2013) Alexandra Vaccaro et al. NEUROBIOLOGY OF DISEASE
- Mutations in the gene encoding p62 in Japanese patients with amyotrophic lateral sclerosis
- (2013) M. Hirano et al. NEUROLOGY
- Gain-of-function mutations in the ALS8 causative gene VAPB have detrimental effects on neurons and muscles
- (2013) M. Sanhueza et al. Biology Open
- Early interneuron dysfunction in ALS: Insights from a mutantsod1zebrafish model
- (2012) Alexander McGown et al. ANNALS OF NEUROLOGY
- Autophagy activation ameliorates neuronal pathogenesis of FTLD-U mice
- (2012) I-Fang Wang et al. Autophagy
- p62/sequestosome 1 binds to TDP-43 in brains with frontotemporal lobar degeneration with TDP-43 inclusions
- (2012) Kunikazu Tanji et al. JOURNAL OF NEUROSCIENCE RESEARCH
- Neuromuscular effects of G93A-SOD1 expression in zebrafish
- (2012) Stacey A Sakowski et al. Molecular Neurodegeneration
- SQSTM1 mutations in frontotemporal lobar degeneration and amyotrophic lateral sclerosis
- (2012) E. Rubino et al. NEUROLOGY
- Methylene Blue Protects against TDP-43 and FUS Neuronal Toxicity in C. elegans and D. rerio
- (2012) Alexandra Vaccaro et al. PLoS One
- Autophagy activators rescue and alleviate pathogenesis of a mouse model with proteinopathies of the TAR DNA-binding protein 43
- (2012) I.-F. Wang et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Zebrafish: A See-Through Host and a Fluorescent Toolbox to Probe Host–Pathogen Interaction
- (2012) David M. Tobin et al. PLoS Pathogens
- p62 positive, TDP-43 negative, neuronal cytoplasmic and intranuclear inclusions in the cerebellum and hippocampus define the pathology of C9orf72-linked FTLD and MND/ALS
- (2011) Safa Al-Sarraj et al. ACTA NEUROPATHOLOGICA
- SQSTM1 Mutations in Familial and Sporadic Amyotrophic Lateral Sclerosis
- (2011) Faisal Fecto ARCHIVES OF NEUROLOGY
- A point mutation in the ubiquitin-associated domain of SQSMT1 is sufficient to cause a Paget's disease-like disorder in mice
- (2011) Anna Daroszewska et al. HUMAN MOLECULAR GENETICS
- Regulation of Autophagy by Neuropathological Protein TDP-43
- (2011) Jayarama Krishnan Bose et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- p62 Is a Key Regulator of Nutrient Sensing in the mTORC1 Pathway
- (2011) Angeles Duran et al. MOLECULAR CELL
- 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
- An MND/ALS phenotype associated withC9orf72repeat expansion: Abundant p62-positive, TDP-43-negative inclusions in cerebral cortex, hippocampus and cerebellum but without associated cognitive decline
- (2011) Claire Troakes et al. NEUROPATHOLOGY
- FUS and TARDBP but Not SOD1 Interact in Genetic Models of Amyotrophic Lateral Sclerosis
- (2011) Edor Kabashi et al. PLoS Genetics
- A genetic model of amyotrophic lateral sclerosis in zebrafish displays phenotypic hallmarks of motoneuron disease
- (2010) T. Ramesh et al. Disease Models & Mechanisms
- Mutant FUS proteins that cause amyotrophic lateral sclerosis incorporate into stress granules
- (2010) Daryl A. Bosco et al. HUMAN MOLECULAR GENETICS
- Regulation of TDP-43 aggregation by phosphorylation andp62/SQSTM1
- (2010) Owen A. Brady et al. JOURNAL OF NEUROCHEMISTRY
- Exome Sequencing Reveals VCP Mutations as a Cause of Familial ALS
- (2010) Janel O. Johnson et al. NEURON
- In the swim of things: recent insights to neurogenetic disorders from zebrafish
- (2010) Edor Kabashi et al. TRENDS IN GENETICS
- Zebrafish survival motor neuron mutants exhibit presynaptic neuromuscular junction defects
- (2009) Kum-Loong Boon et al. HUMAN MOLECULAR GENETICS
- Gain and loss of function of ALS-related mutations of TARDBP (TDP-43) cause motor deficits in vivo
- (2009) Edor Kabashi et al. HUMAN MOLECULAR GENETICS
- White matter lesions in the brain with frontotemporal lobar degeneration with motor neuron disease: TDP-43-immunopositive inclusions co-localize with p62, but not ubiquitin
- (2008) Masanori Hiji et al. ACTA NEUROPATHOLOGICA
- Als2 mRNA splicing variants detected in KO mice rescue severe motor dysfunction phenotype in Als2 knock-down zebrafish
- (2008) Francois Gros-Louis et al. HUMAN MOLECULAR GENETICS
- Genetic inactivation of p62 leads to accumulation of hyperphosphorylated tau and neurodegeneration
- (2008) J. Ramesh Babu et al. JOURNAL OF NEUROCHEMISTRY
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