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Gene conversion and evolution of Xq28 duplicons involved in recurring inversions causing severe hemophilia ABinding specificity of Toll-like receptor cytoplasmic domainsNeuroblastoma and pre-B lymphoma cells share expression of key transcription factors but display tissue restricted target gene expressionThe structure of a polyQ-anti-polyQ complex reveals binding according to a linear lattice modelHuntington's diseaseNovel variant of neuronal intranuclear rodlet immunoreactive for 40 kDa huntingtin associated protein and ubiquitin in the mouse brainHuntingtin-HAP40 complex is a novel Rab5 effector that regulates early endosome motility and is up-regulated in Huntington's disease.The Chapel Hill hemophilia A dog colony exhibits a factor VIII gene inversion.Huntingtin protein interactions altered by polyglutamine expansion as determined by quantitative proteomic analysis.Network organization of the huntingtin proteomic interactome in mammalian brain.A compact beta model of huntingtin toxicity.Cysteine proteases bleomycin hydrolase and cathepsin Z mediate N-terminal proteolysis and toxicity of mutant huntingtin.Phosphorylation of mutant huntingtin at serine 116 modulates neuronal toxicity.Eighteen years of molecular genotyping the hemophilia inversion hotspot: from southern blot to inverse shifting-PCR.Transgenic mouse model expressing the caspase 6 fragment of mutant huntingtin.Identification of novel potentially toxic oligomers formed in vitro from mammalian-derived expanded huntingtin exon-1 protein.Haemophilia A: from mutation analysis to new therapies.Synergistic roles of amelogenin and ameloblastin.Gene expression profile linked to p53 status in hepatitis C virus-related hepatocellular carcinoma.The Ubiquitin Receptor ADRM1 Modulates HAP40-Induced Proteasome Activity.Mutant huntingtin N-terminal fragments of specific size mediate aggregation and toxicity in neuronal cells.Characterization of huntingtin pathologic fragments in human Huntington disease, transgenic mice, and cell models.Multivariate eQTL mapping uncovers functional variation on the X-chromosome associated with complex disease traits.Adhesion Regulating Molecule 1 Mediates HAP40 Overexpression-Induced Mitochondrial Defects.Huntingtin spheroids and protofibrils as precursors in polyglutamine fibrilization.The cryo-electron microscopy structure of huntingtinEarly pathogenic events associated with Sjögren's syndrome (SjS)-like disease of the NOD mouse using microarray analysis.
P2860
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P2860
description
2000 nî lūn-bûn
@nan
2000 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2000 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2000年の論文
@ja
2000年論文
@yue
2000年論文
@zh-hant
2000年論文
@zh-hk
2000年論文
@zh-mo
2000年論文
@zh-tw
2000年论文
@wuu
name
Isolation of a 40-kDa Huntingtin-associated protein.
@ast
Isolation of a 40-kDa Huntingtin-associated protein.
@en
type
label
Isolation of a 40-kDa Huntingtin-associated protein.
@ast
Isolation of a 40-kDa Huntingtin-associated protein.
@en
prefLabel
Isolation of a 40-kDa Huntingtin-associated protein.
@ast
Isolation of a 40-kDa Huntingtin-associated protein.
@en
P2860
P356
P1476
Isolation of a 40-kDa Huntingtin-associated protein.
@en
P2093
P2860
P304
P356
10.1074/JBC.M008099200
P407
P577
2000-10-16T00:00:00Z