The ALS gene FUS regulates synaptic transmission at the Drosophila neuromuscular junction
出版年份 2014 全文链接
标题
The ALS gene FUS regulates synaptic transmission at the Drosophila neuromuscular junction
作者
关键词
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出版物
HUMAN MOLECULAR GENETICS
Volume 23, Issue 14, Pages 3810-3822
出版商
Oxford University Press (OUP)
发表日期
2014-02-26
DOI
10.1093/hmg/ddu094
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注意:仅列出部分参考文献,下载原文获取全部文献信息。- The Molecular Basis of Self-Avoidance
- (2013) S. Lawrence Zipursky et al. Annual Review of Neuroscience
- 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
- ALS mutant FUS disrupts nuclear localization and sequesters wild-type FUS within cytoplasmic stress granules
- (2013) Caroline Vance et al. HUMAN MOLECULAR GENETICS
- Mutations in the 3′ untranslated region of FUS causing FUS overexpression are associated with amyotrophic lateral sclerosis
- (2013) Mario Sabatelli et al. HUMAN MOLECULAR GENETICS
- The Bruchpilot cytomatrix determines the size of the readily releasable pool of synaptic vesicles
- (2013) Tanja Matkovic et al. JOURNAL OF CELL BIOLOGY
- Defects in Synapse Structure and Function Precede Motor Neuron Degeneration in Drosophila Models of FUS-Related ALS
- (2013) M. Shahidullah et al. JOURNAL OF NEUROSCIENCE
- The changing scene of amyotrophic lateral sclerosis
- (2013) Wim Robberecht et al. NATURE REVIEWS NEUROSCIENCE
- Early Changes of Neuromuscular Transmission in the SOD1(G93A) Mice Model of ALS Start Long before Motor Symptoms Onset
- (2013) Mariana C. Rocha et al. PLoS One
- ALS-Associated FUS Mutations Result in Compromised FUS Alternative Splicing and Autoregulation
- (2013) Yueqin Zhou et al. PLoS Genetics
- Misregulated RNA processing in amyotrophic lateral sclerosis
- (2012) Magdalini Polymenidou et al. BRAIN RESEARCH
- Evaluating the role of the FUS/TLS-related gene EWSR1 in amyotrophic lateral sclerosis
- (2012) Julien Couthouis et al. HUMAN MOLECULAR GENETICS
- Regulation of Fasciclin II and Synaptic Terminal Development by the Splicing Factor Beag
- (2012) E. S. Beck et al. JOURNAL OF NEUROSCIENCE
- Drosophila Neuroligin 2 is Required Presynaptically and Postsynaptically for Proper Synaptic Differentiation and Synaptic Transmission
- (2012) Y.-C. Chen et al. JOURNAL OF NEUROSCIENCE
- Motor neuron apoptosis and neuromuscular junction perturbation are prominent features in a Drosophila model of Fus-mediated ALS
- (2012) Ruohan Xia et al. Molecular Neurodegeneration
- Expression of Fused in sarcoma mutations in mice recapitulates the neuropathology of FUS proteinopathies and provides insight into disease pathogenesis
- (2012) Christophe Verbeeck et al. Molecular Neurodegeneration
- Divergent roles of ALS-linked proteins FUS/TLS and TDP-43 intersect in processing long pre-mRNAs
- (2012) Clotilde Lagier-Tourenne et al. NATURE NEUROSCIENCE
- The p150Glued CAP-Gly Domain Regulates Initiation of Retrograde Transport at Synaptic Termini
- (2012) Thomas E. Lloyd et al. NEURON
- 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
- Structural and energetic basis of ALS-causing mutations in the atypical proline–tyrosine nuclear localization signal of the Fused in Sarcoma protein (FUS)
- (2012) Zi Chao Zhang et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- FET proteins in frontotemporal dementia and amyotrophic lateral sclerosis
- (2011) Ian R.A. Mackenzie et al. BRAIN RESEARCH
- Understanding the role of TDP-43 and FUS/TLS in ALS and beyond
- (2011) Sandrine Da Cruz et al. CURRENT OPINION IN NEUROBIOLOGY
- TDP-43: new aspects of autoregulation mechanisms in RNA binding proteins and their connection with human disease
- (2011) Emanuele Buratti et al. FEBS Journal
- ALS mutations in FUS cause neuronal dysfunction and death in Caenorhabditis elegans by a dominant gain-of-function mechanism
- (2011) Tetsuro Murakami et al. HUMAN MOLECULAR GENETICS
- A Drosophila model of FUS-related neurodegeneration reveals genetic interaction between FUS and TDP-43
- (2011) N. A. Lanson et al. HUMAN MOLECULAR GENETICS
- 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
- Neuroligin 2 Is Required for Synapse Development and Function at the Drosophila Neuromuscular Junction
- (2011) M. Sun et al. JOURNAL OF NEUROSCIENCE
- Accumulation of insoluble forms of FUS protein correlates with toxicity in Drosophila
- (2011) Laetitia Miguel et al. NEUROBIOLOGY OF AGING
- A yeast functional screen predicts new candidate ALS disease genes
- (2011) J. Couthouis et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- FUS Transgenic Rats Develop the Phenotypes of Amyotrophic Lateral Sclerosis and Frontotemporal Lobar Degeneration
- (2011) Cao Huang et al. PLoS Genetics
- Expression of human FUS protein in Drosophila leads to progressive neurodegeneration
- (2011) Yanbo Chen et al. Protein & Cell
- TDP-43 regulates its mRNA levels through a negative feedback loop
- (2010) Youhna M Ayala et al. EMBO JOURNAL
- ALS-associated fused in sarcoma (FUS) mutations disrupt Transportin-mediated nuclear import
- (2010) Dorothee Dormann et al. EMBO JOURNAL
- Mutant FUS proteins that cause amyotrophic lateral sclerosis incorporate into stress granules
- (2010) Daryl A. Bosco et al. HUMAN MOLECULAR GENETICS
- TDP-43 and FUS/TLS: emerging roles in RNA processing and neurodegeneration
- (2010) C. Lagier-Tourenne et al. HUMAN MOLECULAR GENETICS
- Fused in sarcoma/translocated in liposarcoma: A multifunctional DNA/RNA binding protein
- (2010) Shu Yang et al. INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY
- TheDrosophilaLarval Neuromuscular Junction as a Model for Scaffold Complexes at Glutamatergic Synapses: Benefits and Limitations
- (2010) Ulrich Thomas et al. JOURNAL OF NEUROGENETICS
- Nuclear localization sequence of FUS and induction of stress granules by ALS mutants
- (2010) Jozsef Gal et al. NEUROBIOLOGY OF AGING
- Increased vesicular glutamate transporter expression causes excitotoxic neurodegeneration
- (2010) Richard W. Daniels et al. NEUROBIOLOGY OF DISEASE
- Drosophila Neuroligin 1 Promotes Growth and Postsynaptic Differentiation at Glutamatergic Neuromuscular Junctions
- (2010) Daniel Banovic et al. NEURON
- Neurexin in Embryonic Drosophila Neuromuscular Junctions
- (2010) Kaiyun Chen et al. PLoS One
- Assaying Locomotor Activity to Study Circadian Rhythms and Sleep Parameters in Drosophila
- (2010) Joanna C. Chiu et al. Jove-Journal of Visualized Experiments
- CNTNAP2 and NRXN1 Are Mutated in Autosomal-Recessive Pitt-Hopkins-like Mental Retardation and Determine the Level of a Common Synaptic Protein in Drosophila
- (2009) Christiane Zweier et al. AMERICAN JOURNAL OF HUMAN GENETICS
- A Drosophila Resource of Transgenic RNAi Lines for Neurogenetics
- (2009) Jian-Quan Ni et al. GENETICS
- Genetic interaction between Neurexin and CAKI/CMG is important for synaptic function in Drosophila neuromuscular junction
- (2009) Mingkuan Sun et al. NEUROSCIENCE RESEARCH
- 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
- Activity-dependent site-specific changes of glutamate receptor composition in vivo
- (2008) Andreas Schmid et al. NATURE NEUROSCIENCE
- 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
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