相关参考文献
注意：仅列出部分参考文献，下载原文获取全部文献信息。Human ESC-Derived Chimeric Mouse Models of Huntington's Disease Reveal Cell-Intrinsic Defects in Glial Progenitor Cell Differentiation
Mikhail Osipovitch et al.
CELL STEM CELL (2019)
Laquinimod Treatment Improves Myelination Deficits at the Transcriptional and Ultrastructural Levels in the YAC128 Mouse Model of Huntington Disease
Marta Garcia-Miralles et al.
MOLECULAR NEUROBIOLOGY (2019)
Complex spatial and temporally defined myelin and axonal degeneration in Huntington disease
H. D. Rosas et al.
NEUROIMAGE-CLINICAL (2018)
Subcortical volume and white matter integrity abnormalities in major depressive disorder: findings from UK Biobank imaging data
Xueyi Shen et al.
SCIENTIFIC REPORTS (2017)
Structural and molecular myelination deficits occur prior to neuronal loss in the YAC128 and BACHD models of Huntington disease
Roy Tang Yi Teo et al.
HUMAN MOLECULAR GENETICS (2016)
Targeting EZH2 in cancer
Kimberly H. Kim et al.
NATURE MEDICINE (2016)
Postnatal and adult consequences of loss of huntingtin during development: Implications for Huntington's disease
Eduardo E. Arteaga-Bracho et al.
NEUROBIOLOGY OF DISEASE (2016)
The transcriptome of mouse central nervous system myelin
Sudhir Thakurela et al.
SCIENTIFIC REPORTS (2016)
Genetic and Stress-Induced Loss of NG2 Glia Triggers Emergence of Depressive-like Behaviors through Reduced Secretion of FGF2
Fikri Birey et al.
NEURON (2015)
Mutant Huntingtin Downregulates Myelin Regulatory Factor-Mediated Myelin Gene Expression and Affects Mature Oligodendrocytes
Brenda Huang et al.
NEURON (2015)
An RNA-Sequencing Transcriptome and Splicing Database of Glia, Neurons, and Vascular Cells of the Cerebral Cortex
Ye Zhang et al.
JOURNAL OF NEUROSCIENCE (2014)
White matter connectivity reflects clinical and cognitive status in Huntington's disease
Govinda R. Poudel et al.
NEUROBIOLOGY OF DISEASE (2014)
Myelination and Oligodendrocyte Functions in Psychiatric Diseases
Klaus-Armin Nave et al.
JAMA PSYCHIATRY (2014)
The neuroanatomy of subthreshold depressive symptoms in Huntington's disease: a combined diffusion tensor imaging (DTI) and voxel-based morphometry (VBM) study
R. Sprengelmeyer et al.
PSYCHOLOGICAL MEDICINE (2014)
Selective Roles of Normal and Mutant Huntingtin in Neural Induction and Early Neurogenesis
Giang D. Nguyen et al.
PLOS ONE (2013)
Marked differences in neurochemistry and aggregates despite similar behavioural and neuropathological features of Huntington disease in the full-length BACHD and YAC128 mice
Mahmoud A. Pouladi et al.
HUMAN MOLECULAR GENETICS (2012)
Myelin Gene Regulatory Factor Is Required for Maintenance of Myelin and Mature Oligodendrocyte Identity in the Adult CNS
Matthias Koenning et al.
JOURNAL OF NEUROSCIENCE (2012)
A putative functional role for oligodendrocytes in mood regulation
N. Edgar et al.
TRANSLATIONAL PSYCHIATRY (2012)
The RE1 Binding Protein REST Regulates Oligodendrocyte Differentiation
Lisa Evans DeWald et al.
JOURNAL OF NEUROSCIENCE (2011)
Peroxisome-Proliferator-Activated Receptor Gamma Coactivator 1 α Contributes to Dysmyelination in Experimental Models of Huntington's Disease
Zhongmin Xiang et al.
JOURNAL OF NEUROSCIENCE (2011)
The Polycomb complex PRC2 and its mark in life
Raphael Margueron et al.
NATURE (2011)
White matter lesions in Parkinson disease
Nicolaas I. Bohnen et al.
NATURE REVIEWS NEUROLOGY (2011)
Natural history of disease in the YAC128 mouse reveals a discrete signature of pathology in Huntington disease
Jeffrey B. Carroll et al.
NEUROBIOLOGY OF DISEASE (2011)
The Sequence Read Archive
Rasko Leinonen et al.
NUCLEIC ACIDS RESEARCH (2011)
ChEA: transcription factor regulation inferred from integrating genome-wide ChIP-X experiments
Alexander Lachmann et al.
BIOINFORMATICS (2010)
Is Huntington disease a developmental disorder?
Sandrine Humbert
EMBO REPORTS (2010)
Huntingtin facilitates polycomb repressive complex 2
Ihn Sik Seong et al.
HUMAN MOLECULAR GENETICS (2010)
Simple Combinations of Lineage-Determining Transcription Factors Prime cis-Regulatory Elements Required for Macrophage and B Cell Identities
Sven Heinz et al.
MOLECULAR CELL (2010)
Myelination and support of axonal integrity by glia
Klaus-Armin Nave
NATURE (2010)
Human oligodendrocytes from embryonic stem cells: conserved SHH signaling networks and divergent FGF effects
Bao-Yang Hu et al.
DEVELOPMENT (2009)
Biological and clinical manifestations of Huntington's disease in the longitudinal TRACK-HD study: cross-sectional analysis of baseline data
Sarah J. Tabrizi et al.
LANCET NEUROLOGY (2009)
Detection of Huntington's disease decades before diagnosis: the Predict-HD study
J. S. Paulsen et al.
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY (2008)
Full-length human mutant huntingtin with a stable polyglutamine repeat can elicit progressive and selective neuropathogenesis in BACHD mice
Michelle Gray et al.
JOURNAL OF NEUROSCIENCE (2008)
Differentiation of Neural Stem Cells into Oligodendrocytes: Involvement of the Polycomb Group Protein Ezh2
Falak Sher et al.
STEM CELLS (2008)
Myelin breakdown and iron changes in Huntington's disease: Pathogenesis and treatment implications
George Bartzokis et al.
NEUROCHEMICAL RESEARCH (2007)
Diffusion tensor imaging in presymptomatic and early Huntington's disease: Selective white matter pathology and its relationship to clinical measures
H. Diana Rosas et al.
MOVEMENT DISORDERS (2006)
Regional white matter change in pre-symptomatic Huntington's disease: A diffusion tensor imaging study
SAJ Reading et al.
PSYCHIATRY RESEARCH-NEUROIMAGING (2005)
Functional diversity and specificity of neostriatal interneurons
JM Tepper et al.
CURRENT OPINION IN NEUROBIOLOGY (2004)
Progressive abnormalities in skeletal muscle and neuromuscular junctions of transgenic mice expressing the Huntington's disease mutation
RR Ribchester et al.
EUROPEAN JOURNAL OF NEUROSCIENCE (2004)
Huntingtin interacts with REST/NRSF to modulate the transcription of NRSE-controlled neuronal genes
C Zuccato et al.
NATURE GENETICS (2003)
The AN2 protein is a novel marker for the Schwann cell lineage expressed by immature and nonmyelinating Schwann cells
S Schneider et al.
JOURNAL OF NEUROSCIENCE (2001)
分享论文
