Gene expression profiling of R6/2 transgenic mice with different CAG repeat lengths reveals genes associated with disease onset and progression in Huntington's disease.
about
The LRR and RING domain protein LRSAM1 is an E3 ligase crucial for ubiquitin-dependent autophagy of intracellular Salmonella TyphimuriumLoss of the E3 ubiquitin ligase LRSAM1 sensitizes peripheral axons to degeneration in a mouse model of Charcot-Marie-Tooth diseaseA novel LRSAM1 mutation is associated with autosomal dominant axonal Charcot-Marie-Tooth diseaseA frameshift mutation in LRSAM1 is responsible for a dominant hereditary polyneuropathyTransgenic animal models for study of the pathogenesis of Huntington's disease and therapyMouse models of polyglutamine diseases: review and data table. Part IComputational deconvolution of genome wide expression data from Parkinson's and Huntington's disease brain tissues using population-specific expression analysis.Huntington's disease mouse models online: high-resolution MRI images with stereotaxic templates for computational neuroanatomyTranscription, epigenetics and ameliorative strategies in Huntington's Disease: a genome-wide perspectiveA critical window of CAG repeat-length correlates with phenotype severity in the R6/2 mouse model of Huntington's disease.A LRSAM1 mutation links Charcot-Marie-Tooth type 2 to Parkinson's disease.DNA methylation in Huntington's disease: Implications for transgenerational effectsPrefoldin protects neuronal cells from polyglutamine toxicity by preventing aggregation formationVaccinia-related kinase 2 mediates accumulation of polyglutamine aggregates via negative regulation of the chaperonin TRiC.Mitochondrial and metabolic-based protective strategies in Huntington's disease: the case of creatine and coenzyme Q.Role of androgen receptor polyQ chain elongation in Kennedy's disease and use of natural osmolytes as potential therapeutic targets.Motor phenotype is not associated with vascular dysfunction in symptomatic Huntington's disease transgenic R6/2 (160 CAG) miceForkhead box protein p1 is a transcriptional repressor of immune signaling in the CNS: implications for transcriptional dysregulation in Huntington disease.Reduced Expression of Foxp1 as a Contributing Factor in Huntington's Disease.Early pridopidine treatment improves behavioral and transcriptional deficits in YAC128 Huntington disease mice.A novel relationship for schizophrenia, bipolar and major depressive disorder Part 3: Evidence from chromosome 3 high density association screen.Endoplasmic reticulum protein 29 protects cortical neurons from apoptosis and promoting corticospinal tract regeneration to improve neural behavior via caspase and Erk signal in rats with spinal cord transection.MicroRNA-939 inhibits cell proliferation via targeting LRSAM1 in Hirschsprung's disease.Epigenetic profiles in polyglutamine disorders.LRSAM1-mediated ubiquitylation is disrupted in axonal Charcot-Marie-Tooth disease 2P.
P2860
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P2860
Gene expression profiling of R6/2 transgenic mice with different CAG repeat lengths reveals genes associated with disease onset and progression in Huntington's disease.
description
2011 nî lūn-bûn
@nan
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
2011年论文
@zh
2011年论文
@zh-cn
name
Gene expression profiling of R ...... ssion in Huntington's disease.
@en
Gene expression profiling of R ...... ssion in Huntington's disease.
@nl
type
label
Gene expression profiling of R ...... ssion in Huntington's disease.
@en
Gene expression profiling of R ...... ssion in Huntington's disease.
@nl
prefLabel
Gene expression profiling of R ...... ssion in Huntington's disease.
@en
Gene expression profiling of R ...... ssion in Huntington's disease.
@nl
P2093
P2860
P1476
Gene expression profiling of R ...... ssion in Huntington's disease.
@en
P2093
Alexandre Kuhn
Daniel H Geschwind
Elizabeth A Thomas
Giovanni Coppola
P2860
P304
P356
10.1016/J.NBD.2011.02.008
P577
2011-02-18T00:00:00Z