Forward Genetic Screen in Caenorhabditis elegans Suggests F57A10.2 and acp-4 As Suppressors of C9ORF72 Related Phenotypes
Published 2016 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Forward Genetic Screen in Caenorhabditis elegans Suggests F57A10.2 and acp-4 As Suppressors of C9ORF72 Related Phenotypes
Authors
Keywords
-
Journal
Frontiers in Molecular Neuroscience
Volume 9, Issue -, Pages -
Publisher
Frontiers Media SA
Online
2016-11-08
DOI
10.3389/fnmol.2016.00113
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Increased expression of the frontotemporal dementia risk factor TMEM106B causes C9orf72-dependent alterations in lysosomes
- (2016) Johanna I. Busch et al. HUMAN MOLECULAR GENETICS
- Genetic Variants of Microtubule Actin Cross-linking Factor 1 (MACF1) Confer Risk for Parkinson’s Disease
- (2016) Xin Wang et al. MOLECULAR NEUROBIOLOGY
- Autophagic down-regulation in motor neurons remarkably prolongs the survival of ALS mice
- (2016) Kuo-Wei Hsueh et al. NEUROPHARMACOLOGY
- C9orf72 is required for proper macrophage and microglial function in mice
- (2016) J. G. ORourke et al. SCIENCE
- Chitotriosidase and lysosomal enzymes as potential biomarkers of disease progression in amyotrophic lateral sclerosis: A survey clinic-based study
- (2015) Veronica Pagliardini et al. JOURNAL OF THE NEUROLOGICAL SCIENCES
- GGGGCC repeat expansion in C9orf72 compromises nucleocytoplasmic transport
- (2015) Brian D. Freibaum et al. NATURE
- Modifiers of C9orf72 dipeptide repeat toxicity connect nucleocytoplasmic transport defects to FTD/ALS
- (2015) Ana Jovičić et al. NATURE NEUROSCIENCE
- Lysosomal and phagocytic activity is increased in astrocytes during disease progression in the SOD1 G93A mouse model of amyotrophic lateral sclerosis
- (2015) David J. Baker et al. Frontiers in Cellular Neuroscience
- Network Analyses Reveal Novel Aspects of ALS Pathogenesis
- (2015) Mario Sanhueza et al. PLoS Genetics
- C9ORF72, implicated in amytrophic lateral sclerosis and frontotemporal dementia, regulates endosomal trafficking
- (2014) Manal A. Farg et al. HUMAN MOLECULAR GENETICS
- C9orf72 nucleotide repeat structures initiate molecular cascades of disease
- (2014) Aaron R. Haeusler et al. NATURE
- Antisense Proline-Arginine RAN Dipeptides Linked to C9ORF72-ALS/FTD Form Toxic Nuclear Aggregates that Initiate In Vitro and In Vivo Neuronal Death
- (2014) Xinmei Wen et al. NEURON
- C9orf72 repeat expansions cause neurodegeneration in Drosophila through arginine-rich proteins
- (2014) S. Mizielinska et al. SCIENCE
- Loss of function of C9orf72 causes motor deficits in a zebrafish model of Amyotrophic Lateral Sclerosis
- (2013) Sorana Ciura et al. ANNALS OF NEUROLOGY
- The product of C9orf72, a gene strongly implicated in neurodegeneration, is structurally related to DENN Rab-GEFs
- (2013) Timothy P. Levine et al. BIOINFORMATICS
- Promoter- and RNA polymerase II–dependenthsp-16gene association with nuclear pores inCaenorhabditis elegans
- (2013) Sabine Rohner et al. JOURNAL OF CELL BIOLOGY
- Deletion of C9ORF72 Results in Motor Neuron Degeneration and Stress Sensitivity in C. elegans
- (2013) Martine Therrien et al. PLoS One
- The C9orf72 GGGGCC Repeat Is Translated into Aggregating Dipeptide-Repeat Proteins in FTLD/ALS
- (2013) K. Mori et al. SCIENCE
- A Genome-Wide RNAi Screen in Caenorhabditis elegans Identifies the Nicotinic Acetylcholine Receptor Subunit ACR-7 as an Antipsychotic Drug Target
- (2013) Taixiang Saur et al. PLoS Genetics
- Amyotrophic lateral sclerosis-associated mutant VAPBP56S perturbs calcium homeostasis to disrupt axonal transport of mitochondria
- (2012) G. M. Morotz et al. HUMAN MOLECULAR GENETICS
- Rapamycin treatment augments motor neuron degeneration in SOD1G93Amouse model of amyotrophic lateral sclerosis
- (2011) Xiaojie Zhang et al. Autophagy
- 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
- OrthoList: A Compendium of C. elegans Genes with Human Orthologs
- (2011) Daniel D. Shaye et al. PLoS One
- A neurodegenerative disease mutation that accelerates the clearance of apoptotic cells
- (2011) A. W. Kao et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Characterization of the Properties of a Novel Mutation in VAPB in Familial Amyotrophic Lateral Sclerosis
- (2010) Han-Jou Chen et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- Clozapine Interaction with Phosphatidyl Inositol 3-Kinase (PI3K)/Insulin-Signaling Pathway in Caenorhabditis elegans
- (2009) Rakesh Karmacharya et al. NEUROPSYCHOPHARMACOLOGY
- A novel HSP90 chaperone complex regulates intracellular vesicle transport
- (2008) G. P. Lotz et al. JOURNAL OF CELL SCIENCE
Find Funding. Review Successful Grants.
Explore over 25,000 new funding opportunities and over 6,000,000 successful grants.
ExploreAdd your recorded webinar
Do you already have a recorded webinar? Grow your audience and get more views by easily listing your recording on Peeref.
Upload Now