Bidirectional expression of CUG and CAG expansion transcripts and intranuclear polyglutamine inclusions in spinocerebellar ataxia type 8.
about
Autosomal dominant cerebellar ataxia type I: a review of the phenotypic and genotypic characteristicsSystematic analysis of compositional order of proteins reveals new characteristics of biological functions and a universal correlate of macroevolutionA noncoding expansion in EIF4A3 causes Richieri-Costa-Pereira syndrome, a craniofacial disorder associated with limb defectsLong non-coding RNAs in nervous system function and diseaseA natural antisense transcript at the Huntington's disease repeat locus regulates HTT expressionExpanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALSPrecision medicine in spinocerebellar ataxias: treatment based on common mechanisms of diseaseRAN translation and frameshifting as translational challenges at simple repeats of human neurodegenerative disordersInvolvement of long noncoding RNAs in diseases affecting the central nervous systemMechanisms of RNA-induced toxicity in CAG repeat disordersConverging mechanisms in ALS and FTD: disrupted RNA and protein homeostasisIntegration of modeling with experimental and clinical findings synthesizes and refines the central role of inositol 1,4,5-trisphosphate receptor 1 in spinocerebellar ataxiaLong non-coding RNAs and complex human diseasesThe unstable repeats--three evolving faces of neurological diseaseAtaxin-2 regulates RGS8 translation in a new BAC-SCA2 transgenic mouse modelTriplet repeat-derived siRNAs enhance RNA-mediated toxicity in a Drosophila model for myotonic dystrophyMultiple knockout mouse models reveal lincRNAs are required for life and brain developmentMotor Dysfunctions and Neuropathology in Mouse Models of Spinocerebellar Ataxia Type 2: A Comprehensive ReviewParkinsonism in spinocerebellar ataxiaRNA-mediated pathogenic mechanisms in polyglutamine diseases and amyotrophic lateral sclerosisRNA toxicity is a component of ataxin-3 degeneration in DrosophilaGeneration and characterisation of Friedreich ataxia YG8R mouse fibroblast and neural stem cell modelsStructure prediction of polyglutamine disease proteins: comparison of methods.Systems biology analysis of Drosophila in vivo screen data elucidates core networks for DNA damage repair in SCA1.The ubiquitin proteasome system in Huntington's disease and the spinocerebellar ataxiasSpinocerebellar ataxia type 8 larger triplet expansion alters histone modification and induces RNA foci.RNA gain-of-function in spinocerebellar ataxia type 8.Convergent transcription through a long CAG tract destabilizes repeats and induces apoptosisRNA metabolism in neurodegenerative disease.Oligonucleotide-based strategies to combat polyglutamine diseases.Repeat associated non-ATG translation initiation: one DNA, two transcripts, seven reading frames, potentially nine toxic entities!Brain, blood, and iron: perspectives on the roles of erythrocytes and iron in neurodegeneration.Brain pathology of spinocerebellar ataxias.Ubiquitous expression of CUG or CAG trinucleotide repeat RNA causes common morphological defects in a Drosophila model of RNA-mediated pathologyThe C9orf72 GGGGCC repeat is translated into aggregating dipeptide-repeat proteins in FTLD/ALS.Indole and synthetic derivative activate chaperone expression to reduce polyQ aggregation in SCA17 neuronal cell and slice culture models.Nucleotide excision repair, mismatch repair, and R-loops modulate convergent transcription-induced cell death and repeat instabilityPhosphorodiamidate morpholino oligomers suppress mutant huntingtin expression and attenuate neurotoxicity.Bidirectional transcription stimulates expansion and contraction of expanded (CTG)*(CAG) repeats.Non-ATG-initiated translation directed by microsatellite expansions.
P2860
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P2860
Bidirectional expression of CUG and CAG expansion transcripts and intranuclear polyglutamine inclusions in spinocerebellar ataxia type 8.
description
2006 nî lūn-bûn
@nan
2006 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2006 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
name
Bidirectional expression of CU ...... spinocerebellar ataxia type 8.
@ast
Bidirectional expression of CU ...... spinocerebellar ataxia type 8.
@en
Bidirectional expression of CU ...... spinocerebellar ataxia type 8.
@nl
type
label
Bidirectional expression of CU ...... spinocerebellar ataxia type 8.
@ast
Bidirectional expression of CU ...... spinocerebellar ataxia type 8.
@en
Bidirectional expression of CU ...... spinocerebellar ataxia type 8.
@nl
prefLabel
Bidirectional expression of CU ...... spinocerebellar ataxia type 8.
@ast
Bidirectional expression of CU ...... spinocerebellar ataxia type 8.
@en
Bidirectional expression of CU ...... spinocerebellar ataxia type 8.
@nl
P2093
P2860
P356
P1433
P1476
Bidirectional expression of CU ...... spinocerebellar ataxia type 8.
@en
P2093
Anne K Mosemiller
H Brent Clark
John W Day
Laura P W Ranum
Marcy R Weatherspoon
Melinda L Moseley
Randy S Daughters
Timothy J Ebner
P2860
P2888
P304
P356
10.1038/NG1827
P407
P577
2006-06-25T00:00:00Z