Abnormalities of neurogenesis in the R6/2 mouse model of Huntington's disease are attributable to the in vivo microenvironment.
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Mood disorders in Huntington's disease: from behavior to cellular and molecular mechanismsModeling Huntington's disease with induced pluripotent stem cellsNeurodegenerative disease and adult neurogenesisThe subependymal zone neurogenic niche: a beating heart in the centre of the brain: How plastic is adult neurogenesis? Opportunities for therapy and questions to be addressedMicroRNAs in Experimental Models of Movement Disorders.Impaired adult olfactory bulb neurogenesis in the R6/2 mouse model of Huntington's disease.Huntington disease models and human neuropathology: similarities and differencesExercise is not beneficial and may accelerate symptom onset in a mouse model of Huntington's diseaseThe latent stem cell population is retained in the hippocampus of transgenic Huntington's disease mice but not wild-type mice.BDNF signaling and survival of striatal neurons.Small-molecule TrkB receptor agonists improve motor function and extend survival in a mouse model of Huntington's diseaseNeurotransmitters couple brain activity to subventricular zone neurogenesisTherapeutic application of neural stem cells and adult neurogenesis for neurodegenerative disorders: regeneration and beyondReduction in subventricular zone-derived olfactory bulb neurogenesis in a rat model of Huntington's disease is accompanied by striatal invasion of neuroblasts.Properties of doublecortin-(DCX)-expressing cells in the piriform cortex compared to the neurogenic dentate gyrus of adult mice.HD iPSC-derived neural progenitors accumulate in culture and are susceptible to BDNF withdrawal due to glutamate toxicity.Sleep Physiology Alterations Precede Plethoric Phenotypic Changes in R6/1 Huntington's Disease MiceAll in the Family: How the APPs Regulate NeurogenesisHippocampal neurogenesis, cognitive deficits and affective disorder in Huntington's diseaseProgenitor cells and adult neurogenesis in neurodegenerative diseases and injuries of the basal ganglia.Increased Olfactory Bulb BDNF Expression Does Not Rescue Deficits in Olfactory Neurogenesis in the Huntington's Disease R6/2 Mouse.Sertraline slows disease progression and increases neurogenesis in N171-82Q mouse model of Huntington's disease.Striatal oligodendrogliogenesis and neuroblast recruitment are increased in the R6/2 mouse model of Huntington's diseasePhysiological, pathological, and engineered cell identity reprogramming in the central nervous system.Stem cell-based cell therapy for Huntington disease: a review.Exosome-Based Delivery of miR-124 in a Huntington's Disease Model.Postnatal neurogenesis: from neuroblast migration to neuronal integration.Adult neurogenesis in neurodegenerative diseases.Adult neurogenesis and neurodegenerative diseases: A systems biology perspective.Mutant Ataxin-1 Inhibits Neural Progenitor Cell Proliferation in SCA1.Epigenetic mechanisms in neurogenesis.Hippocampal dysfunction defines disease onset in Huntington's disease.Stem cell quiescence in the hippocampal neurogenic niche is associated with elevated transforming growth factor-beta signaling in an animal model of Huntington disease.Sustained induction of neuronal addition to the adult rat neostriatum by AAV4-delivered noggin and BDNF.Transforming Growth Factor-Beta Signaling in the Neural Stem Cell Niche: A Therapeutic Target for Huntington's Disease.Expanded CAG repeats in the murine Huntington's disease gene increases neuronal differentiation of embryonic and neural stem cells.The antidepressant sertraline improves the phenotype, promotes neurogenesis and increases BDNF levels in the R6/2 Huntington's disease mouse model.Microglia-derived IL-1β triggers p53-mediated cell cycle arrest and apoptosis in neural precursor cells.Neurogenesis in the R6/1 transgenic mouse model of Huntington's disease: effects of environmental enrichment.Concise Review: The Use of Stem Cells for Understanding and Treating Huntington's Disease.
P2860
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P2860
Abnormalities of neurogenesis in the R6/2 mouse model of Huntington's disease are attributable to the in vivo microenvironment.
description
2005 nî lūn-bûn
@nan
2005年の論文
@ja
2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
2005年论文
@zh
2005年论文
@zh-cn
name
Abnormalities of neurogenesis ...... the in vivo microenvironment.
@en
Abnormalities of neurogenesis ...... the in vivo microenvironment.
@nl
type
label
Abnormalities of neurogenesis ...... the in vivo microenvironment.
@en
Abnormalities of neurogenesis ...... the in vivo microenvironment.
@nl
prefLabel
Abnormalities of neurogenesis ...... the in vivo microenvironment.
@en
Abnormalities of neurogenesis ...... the in vivo microenvironment.
@nl
P1476
Abnormalities of neurogenesis ...... o the in vivo microenvironment
@en
P2093
Wendy Phillips
P304
11564-11576
P356
10.1523/JNEUROSCI.3796-05.2005
P407
P577
2005-12-01T00:00:00Z