Protein binding of a DRPLA family through arginine-glutamic acid dipeptide repeats is enhanced by extended polyglutamine
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HSpin1, a transmembrane protein interacting with Bcl-2/Bcl-xL, induces a caspase-independent autophagic cell deathAtrophin recruits HDAC1/2 and G9a to modify histone H3K9 and to determine cell fatesFunctional architecture of atrophinsHistone deacetylase-associating Atrophin proteins are nuclear receptor corepressorsOf Fighting Flies, Mice, and Men: Are Some of the Molecular and Neuronal Mechanisms of Aggression Universal in the Animal Kingdom?Mouse model reveals the role of RERE in cerebellar foliation and the migration and maturation of Purkinje cellsAn allelic series of mice reveals a role for RERE in the development of multiple organs affected in chromosome 1p36 deletions.Mutation of the atrophin2 gene in the zebrafish disrupts signaling by fibroblast growth factor during development of the inner ear.Functional Profiling of Human MeCP2 by Automated Data Comparison Analysis and Computerized Expression Pathway ModelingModification of gene duplicability during the evolution of protein interaction networkInteraction of expanded polyglutamine stretches with nuclear transcription factors leads to aberrant transcriptional regulation in polyglutamine diseases.A screen for genes that interact with the Drosophila pair-rule segmentation gene fushi tarazuNeurological proteins are not enriched for repetitive sequences.Functional interactions between Fat family cadherins in tissue morphogenesis and planar polarity.Remarkable selective constraints on exonic dinucleotide repeats.Mutations in NR2E3 can cause dominant or recessive retinal degenerations in the same familyAtrophin proteins: an overview of a new class of nuclear receptor corepressorsMicroRNAs and neurodegeneration: role and impact.Small non-coding RNAs add complexity to the RNA pathogenic mechanisms in trinucleotide repeat expansion diseases.Modulation at age of onset in tunisian huntington disease patients: implication of new modifier genes1p36 is a preferential target of chromosome 1 deletions in astrocytic tumours and homozygously deleted in a subset of glioblastomas.Sodium butyrate ameliorates histone hypoacetylation and neurodegenerative phenotypes in a mouse model for DRPLA.Tailless and Atrophin control Drosophila aggression by regulating neuropeptide signalling in the pars intercerebralis.
P2860
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P2860
Protein binding of a DRPLA family through arginine-glutamic acid dipeptide repeats is enhanced by extended polyglutamine
description
2000 nî lūn-bûn
@nan
2000 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2000 թվականի մայիսին 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
Protein binding of a DRPLA fam ...... nced by extended polyglutamine
@ast
Protein binding of a DRPLA fam ...... nced by extended polyglutamine
@en
Protein binding of a DRPLA fam ...... nced by extended polyglutamine
@nl
type
label
Protein binding of a DRPLA fam ...... nced by extended polyglutamine
@ast
Protein binding of a DRPLA fam ...... nced by extended polyglutamine
@en
Protein binding of a DRPLA fam ...... nced by extended polyglutamine
@nl
prefLabel
Protein binding of a DRPLA fam ...... nced by extended polyglutamine
@ast
Protein binding of a DRPLA fam ...... nced by extended polyglutamine
@en
Protein binding of a DRPLA fam ...... nced by extended polyglutamine
@nl
P2093
P3181
P356
P1476
Protein binding of a DRPLA fam ...... nced by extended polyglutamine
@en
P2093
H Yanagisawa
K Tadokoro
K Tokunaga
T Miyashita
Y Okamura-Oho
P304
P3181
P356
10.1093/HMG/9.9.1433
P407
P577
2000-05-22T00:00:00Z