A null mutation in VAMP1/synaptobrevin is associated with neurological defects and prewean mortality in the lethal-wasting mouse mutant.
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VAMP1 mutation causes dominant hereditary spastic ataxia in Newfoundland familiesUbiquitin-Synaptobrevin Fusion Protein Causes Degeneration of Presynaptic Motor Terminals in MicePatterned neuroprotection in the Inpp4a(wbl) mutant mouse cerebellum correlates with the expression of Eaat4Homozygous mutations in VAMP1 cause a presynaptic congenital myasthenic syndromeWidespread sequence variations in VAMP1 across vertebrates suggest a potential selective pressure from botulinum neurotoxins.Exocytosis at the hair cell ribbon synapse apparently operates without neuronal SNARE proteins.The role of insulin-like growth factor-I in the physiopathology of hearing.An insertion of intracisternal A-particle retrotransposon in a novel member of the phosphoglycerate mutase family in the lew allele of mutant miceAlcohol induces synaptotagmin 1 expression in neurons via activation of heat shock factor 1.Genetically-controlled Vesicle-Associated Membrane Protein 1 expression may contribute to Alzheimer's pathophysiology and susceptibility.Unique biological activity of botulinum D/C mosaic neurotoxin in murine species.A novel mutation in Prph2, a gene regulated by Nr2e3, causes retinal degeneration and outer-segment defects similar to Nr2e3 ( rd7/rd7 ) retinas.Exocytosis and synaptic vesicle function.Organization of organelles and VAMP-associated vesicular transport systems in differentiating skeletal muscle cells.Molecular mechanisms governing Ca(2+) regulation of evoked and spontaneous release.Using the shared genetics of dystonia and ataxia to unravel their pathogenesis.Gene network of a phosphoglycerate mutase in muscle wasting in mice.Syntaxin 1B is important for mouse postnatal survival and proper synaptic function at the mouse neuromuscular junctions.Novel synaptobrevin-1 mutation causes fatal congenital myasthenic syndrome.HSF1 transcriptional activity mediates alcohol induction of Vamp2 expression and GABA releaseIndication for differential sorting of the rat v-SNARE splice isoforms VAMP-1a and -1b.The presynaptic machinery at the synapse of C. elegans.Animal Models of the Neuromuscular Junction, Vitally Informative for Understanding Function and the Molecular Mechanisms of Congenital Myasthenic Syndromes.
P2860
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P2860
A null mutation in VAMP1/synaptobrevin is associated with neurological defects and prewean mortality in the lethal-wasting mouse mutant.
description
2006 nî lūn-bûn
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2006年の論文
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2006年学术文章
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2006年学术文章
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2006年学术文章
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2006年学术文章
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2006年学术文章
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2006年学术文章
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2006年學術文章
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2006年學術文章
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name
A null mutation in VAMP1/synap ...... e lethal-wasting mouse mutant.
@en
A null mutation in VAMP1/synap ...... e lethal-wasting mouse mutant.
@nl
type
label
A null mutation in VAMP1/synap ...... e lethal-wasting mouse mutant.
@en
A null mutation in VAMP1/synap ...... e lethal-wasting mouse mutant.
@nl
prefLabel
A null mutation in VAMP1/synap ...... e lethal-wasting mouse mutant.
@en
A null mutation in VAMP1/synap ...... e lethal-wasting mouse mutant.
@nl
P2093
P1433
P1476
A null mutation in VAMP1/synap ...... e lethal-wasting mouse mutant.
@en
P2093
Andrew J Sachs
Andy W Yang
Arne M Nystuen
Jamie K Schwendinger
Neena B Haider
P2860
P2888
P356
10.1007/S10048-006-0068-7
P577
2006-11-11T00:00:00Z