Animal models of Huntington's disease for translation to the clinic: best practices.
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Cognitive Training at a Young Age Attenuates Deficits in the zQ175 Mouse Model of HD.Advances in Stem Cell Research- A Ray of Hope in Better Diagnosis and Prognosis in Neurodegenerative DiseasesComprehensive Analysis of the 16p11.2 Deletion and Null Cntnap2 Mouse Models of Autism Spectrum Disorder.Motivational, proteostatic and transcriptional deficits precede synapse loss, gliosis and neurodegeneration in the B6.HttQ111/+ model of Huntington's disease.The expanded CAG repeat in the huntingtin gene as target for therapeutic RNA modulation throughout the HD mouse brain.Altered excitatory and inhibitory inputs to striatal medium-sized spiny neurons and cortical pyramidal neurons in the Q175 mouse model of Huntington's disease.Correlations of Behavioral Deficits with Brain Pathology Assessed through Longitudinal MRI and Histopathology in the HdhQ150/Q150 Mouse Model of Huntington's Disease.RAN Translation in Huntington Disease.Allelic series of Huntington's disease knock-in mice reveals expression discorrelates.Enhanced mitochondrial biogenesis ameliorates disease phenotype in a full-length mouse model of Huntington's disease.Stem and Progenitor Cell-Based Therapy of the Central Nervous System: Hopes, Hype, and Wishful Thinking.Induced Pluripotent Stem Cells in Huntington's Disease: Disease Modeling and the Potential for Cell-Based Therapy.AAV5-miHTT gene therapy demonstrates suppression of mutant huntingtin aggregation and neuronal dysfunction in a rat model of Huntington's disease.Cognitive dysfunction in Huntington's disease: mechanisms and therapeutic strategies beyond BDNF.Huntington Disease: Linking Pathogenesis to the Development of Experimental Therapeutics.Neurofilament light protein in CSF and blood is associated with neurodegeneration and disease severity in Huntington's disease R6/2 mice.Towards an Understanding of Energy Impairment in Huntington's Disease Brain.Progress in developing transgenic monkey model for Huntington's disease.Early Detection of Apathetic Phenotypes in Huntington's Disease Knock-in Mice Using Open Source Tools.A novel ex vivo Huntington's disease model for studying GABAergic neurons and cell grafts by laser microdissection.Translation of MicroRNA-Based Huntingtin-Lowering Therapies from Preclinical Studies to the Clinic.Population-specific genetic modification of Huntington's disease in Venezuela.Adeno-Associated Viral Vector Serotype DJ-Mediated Overexpression of N171-82Q-Mutant Huntingtin in the Striatum of Juvenile Mice Is a New Model for Huntington's Disease.
P2860
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P2860
Animal models of Huntington's disease for translation to the clinic: best practices.
description
2014 nî lūn-bûn
@nan
2014年の論文
@ja
2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
2014年论文
@zh
2014年论文
@zh-cn
name
Animal models of Huntington's disease for translation to the clinic: best practices.
@en
type
label
Animal models of Huntington's disease for translation to the clinic: best practices.
@en
prefLabel
Animal models of Huntington's disease for translation to the clinic: best practices.
@en
P2860
P356
P1433
P1476
Animal models of Huntington's disease for translation to the clinic: best practices.
@en
P2093
Daniela Brunner
Liliana Menalled
P2860
P304
P356
10.1002/MDS.26006
P407
P577
2014-09-01T00:00:00Z