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。MicroRNA editing patterns in Huntington's disease
Shiyong Guo et al.
SCIENTIFIC REPORTS (2022)
The distribution and density of Huntingtin inclusions across the Huntington disease neocortex: regional correlations with Huntingtin repeat expansion independent of pathologic grade
Richard A. Hickman et al.
ACTA NEUROPATHOLOGICA COMMUNICATIONS (2022)
Transcriptional Dysregulation in Huntington's Disease: The Role in Pathogenesis and Potency for Pharmacological Targeting
Aleksandra Pogoda et al.
CURRENT MEDICINAL CHEMISTRY (2021)
Shedding a new light on Huntington's disease: how blood can both propagate and ameliorate disease pathology
Marie Rieux et al.
MOLECULAR PSYCHIATRY (2021)
MicroRNAs in Huntington's Disease: Diagnostic Biomarkers or Therapeutic Agents?
Xiaoyu Dong et al.
FRONTIERS IN CELLULAR NEUROSCIENCE (2021)
Altered microRNA expression in animal models of Huntington's disease and potential therapeutic strategies
Bridget Martinez et al.
NEURAL REGENERATION RESEARCH (2021)
High-Throughput Sequencing of BACHD Mice Reveals Upregulation of Neuroprotective miRNAs at the Pre-Symptomatic Stage of Huntington's Disease
Isabella G. Olmo et al.
ASN NEURO (2021)
MicroRNAs as major regulators of the autophagy pathway
Yunus Akkoc et al.
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH (2020)
On the Number of Functional microRNA Targets
Herve Seitz
MOLECULAR BIOLOGY AND EVOLUTION (2019)
The Role of MicroRNAs in Spinocerebellar Ataxia Type 3
Sybille Krauss et al.
JOURNAL OF MOLECULAR BIOLOGY (2019)
Platelet abnormalities in Huntington's disease
Helena L. Denis et al.
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY (2019)
MicroRNA signatures of endogenous Huntingtin CAG repeat expansion in mice
Peter Langfelder et al.
PLOS ONE (2018)
Supplemental Treatment for Huntington's Disease with miR-132 that Is Deficient in Huntington's Disease Brain
Masashi Fukuoka et al.
MOLECULAR THERAPY-NUCLEIC ACIDS (2018)
Converging pathways in neurodegeneration, from genetics to mechanisms
Li Ga et al.
NATURE NEUROSCIENCE (2018)
Huntingtin Aggregation Impairs Autophagy, Leading to Argonaute-2 Accumulation and Global MicroRNA Dysregulation
Karolina Pircs et al.
CELL REPORTS (2018)
Overview of MicroRNA Biogenesis, Mechanisms of Actions, and Circulation
Jacob O'Brien et al.
FRONTIERS IN ENDOCRINOLOGY (2018)
Co-occurrence of mixed proteinopathies in late-stage Huntington's disease
Isabelle St-Amour et al.
ACTA NEUROPATHOLOGICA (2018)
Dicer and microRNAs protect adult dopamine neurons
Piotr Chmielarz et al.
CELL DEATH & DISEASE (2017)
RNAi mechanisms in Huntington's disease therapy: siRNA versus shRNA
Sebastian Aguiar et al.
TRANSLATIONAL NEURODEGENERATION (2017)
microRNA-132/212 deficiency enhances Aβ production and senile plaque deposition in Alzheimer's disease triple transgenic mice
Julia Hernandez-Rapp et al.
SCIENTIFIC REPORTS (2016)
Memory formation and retention are affected in adult miR-132/212 knockout mice
Julia Hernandez-Rapp et al.
BEHAVIOURAL BRAIN RESEARCH (2015)
miR-10b-5p expression in Huntington's disease brain relates to age of onset and the extent of striatal involvement
Andrew G. Hoss et al.
BMC MEDICAL GENOMICS (2015)
Dysregulated miRNA biogenesis downstream of cellular stress and ALS-causing mutations: a new mechanism for ALS
Anna Emde et al.
EMBO JOURNAL (2015)
The biological functions of miRNAs: lessons from in vivo studies
Joana A. Vidigal et al.
TRENDS IN CELL BIOLOGY (2015)
The complexity of miRNA-mediated repression
A. Wilczynska et al.
CELL DEATH AND DIFFERENTIATION (2015)
Transcriptional dysregulation in Huntington's disease: a failure of adaptive transcriptional homeostasis
Amit Kumar et al.
DRUG DISCOVERY TODAY (2014)
Regulation of microRNA biogenesis
Minju Ha et al.
NATURE REVIEWS MOLECULAR CELL BIOLOGY (2014)
MicroRNAs Located in the Hox Gene Clusters Are Implicated in Huntington's Disease Pathogenesis
Andrew G. Hoss et al.
PLOS GENETICS (2014)
miR-196a Ameliorates Phenotypes of Huntington Disease in Cell, Transgenic Mouse, and Induced Pluripotent Stem Cell Models
Pei-Hsun Cheng et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2013)
Relationship between BDNF expression in major striatal afferents, striatum morphology and motor behavior in the R6/2 mouse model of Huntington's disease
P. Samadi et al.
GENES BRAIN AND BEHAVIOR (2013)
Sequestration of DROSHA and DGCR8 by Expanded CGG RNA Repeats Alters MicroRNA Processing in Fragile X-Associated Tremor/Ataxia Syndrome
Chantal Sellier et al.
CELL REPORTS (2013)
Interrogation of brain miRNA and mRNA expression profiles reveals a molecular regulatory network that is perturbed by mutant huntingtin
Jing Jin et al.
JOURNAL OF NEUROCHEMISTRY (2012)
Gene Network and Pathway Analysis of Mice with Conditional Ablation of Dicer in Post-Mitotic Neurons
Veronique Dorval et al.
PLOS ONE (2012)
TDP-43 promotes microRNA biogenesis as a component of the Drosha and Dicer complexes
Yukio Kawahara et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2012)
Altered microRNA regulation in Huntington's disease models
Soon-Tae Lee et al.
EXPERIMENTAL NEUROLOGY (2011)
MicroRNA-132 loss is associated with tau exon 10 inclusion in progressive supranuclear palsy
Pascal Y. Smith et al.
HUMAN MOLECULAR GENETICS (2011)
Huntington's disease: from molecular pathogenesis to clinical treatment
Christopher A. Ross et al.
LANCET NEUROLOGY (2011)
The Ataxin-2 protein is required for microRNA function and synapse-specific long-term olfactory habituation
Cathal McCann et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2011)
Nuclear factor TDP-43 can affect selected microRNA levels
Emanuele Buratti et al.
FEBS JOURNAL (2010)
Genetic ablation of Dicer in adult forebrain neurons results in abnormal tau hyperphosphorylation and neurodegeneration
Sebastien S. Hebert et al.
HUMAN MOLECULAR GENETICS (2010)
A Role for Huntington Disease Protein in Dendritic RNA Granules
Jeffrey N. Savas et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2010)
A myriad of miRNA variants in control and Huntington's disease brain regions detected by massively parallel sequencing
Eulalia Marti et al.
NUCLEIC ACIDS RESEARCH (2010)
Mutant Huntingtin N-terminal Fragments of Specific Size Mediate Aggregation and Toxicity in Neuronal Cells
Tamara Ratovitski et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2009)
Dicer loss in striatal neurons produces behavioral and neuroanatomical phenotypes in the absence of neurodegeneration
Trinna L. Cuellar et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2008)
Huntington's disease protein contributes to RNA-mediated gene silencing through association with Argonaute and P bodies
Jeffrey N. Savas et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2008)
Role of brain-derived neurotrophic factor in Huntington's disease
Chiara Zuccato et al.
PROGRESS IN NEUROBIOLOGY (2007)
Huntingtin forms toxic NH2-terminal fragment complexes that are promoted by the age-dependent decrease in proteasome activity
H Zhou et al.
JOURNAL OF CELL BIOLOGY (2003)
The selective vulnerability of nerve cells in Huntington's disease
KA Sieradzan et al.
NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY (2001)