Cdc42-interacting protein 4 binds to huntingtin: neuropathologic and biological evidence for a role in Huntington's disease
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The palmitoyl acyltransferase HIP14 shares a high proportion of interactors with huntingtin: implications for a role in the pathogenesis of Huntington's diseaseAKAP350 interaction with cdc42 interacting protein 4 at the Golgi apparatusDisruption of axonal transport perturbs bone morphogenetic protein (BMP)--signaling and contributes to synaptic abnormalities in two neurodegenerative diseasesNormal huntingtin function: an alternative approach to Huntington's diseaseGene-environment interactions: neurodegeneration in non-mammals and mammalsF-BAR family proteins, emerging regulators for cell membrane dynamic changes-from structure to human diseases.The F-BAR protein CIP4 inhibits neurite formation by producing lamellipodial protrusions.The BAR Domain Superfamily Proteins from Subcellular Structures to Human DiseasesThe proposed functions of membrane curvatures mediated by the BAR domain superfamily proteins.Inactivation of Drosophila Huntingtin affects long-term adult functioning and the pathogenesis of a Huntington's disease model.Genetic aspects of behavioral neurotoxicologyIn vivo expression of polyglutamine-expanded huntingtin by mouse striatal astrocytes impairs glutamate transport: a correlation with Huntington's disease subjects.Large-scale functional RNAi screen in C. elegans identifies genes that regulate the dysfunction of mutant polyglutamine neurons.General structural motifs of amyloid protofilaments.Functional characterization of Trip10 in cancer cell growth and survival.Similar striatal gene expression profiles in the striatum of the YAC128 and HdhQ150 mouse models of Huntington's disease are not reflected in mutant Huntingtin inclusion prevalence.Cdc42-interacting protein-4 promotes TGF-Β1-induced epithelial-mesenchymal transition and extracellular matrix deposition in renal proximal tubular epithelial cells.BAR proteins in cancer and blood disordersCaenorhabditis elegans: an emerging model in biomedical and environmental toxicology.The BMP signaling pathway at the Drosophila neuromuscular junction and its links to neurodegenerative diseases.Attachment of rod-like (BAR) proteins and membrane shape.Barfly: sculpting membranes at the Drosophila neuromuscular junction.Stem cell therapy and cellular engineering for treatment of neuronal dysfunction in Huntington's disease.Dynamic shaping of cellular membranes by phospholipids and membrane-deforming proteins.The F-BAR protein family Actin' on the membrane.Wild-type huntingtin participates in protein trafficking between the Golgi and the extracellular space.Evidence for a Pan-Neurodegenerative Disease Response in Huntington's and Parkinson's Disease Expression Profiles.Neurodegenerative Diseases: Regenerative Mechanisms and Novel Therapeutic Approaches
P2860
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P2860
Cdc42-interacting protein 4 binds to huntingtin: neuropathologic and biological evidence for a role in Huntington's disease
description
2003 nî lūn-bûn
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2003 թուականի Մարտին հրատարակուած գիտական յօդուած
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2003 թվականի մարտին հրատարակված գիտական հոդված
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2003年の論文
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2003年論文
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2003年論文
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2003年論文
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2003年論文
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2003年論文
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Cdc42-interacting protein 4 bi ...... a role in Huntington's disease
@ast
Cdc42-interacting protein 4 bi ...... a role in Huntington's disease
@en
Cdc42-interacting protein 4 bi ...... a role in Huntington's disease
@nl
type
label
Cdc42-interacting protein 4 bi ...... a role in Huntington's disease
@ast
Cdc42-interacting protein 4 bi ...... a role in Huntington's disease
@en
Cdc42-interacting protein 4 bi ...... a role in Huntington's disease
@nl
prefLabel
Cdc42-interacting protein 4 bi ...... a role in Huntington's disease
@ast
Cdc42-interacting protein 4 bi ...... a role in Huntington's disease
@en
Cdc42-interacting protein 4 bi ...... a role in Huntington's disease
@nl
P2860
P50
P356
P1476
Cdc42-interacting protein 4 bi ...... a role in Huntington's disease
@en
P2093
Sébastien Holbert
P2860
P304
P356
10.1073/PNAS.0437967100
P407
P577
2003-02-25T00:00:00Z