Selective discrimination learning impairments in mice expressing the human Huntington's disease mutation.
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Asialoerythropoietin is not effective in the R6/2 line of Huntington's disease miceDopamine Receptors and NeurodegenerationMouse models of polyglutamine diseases: review and data table. Part IDisruption of axonal transport perturbs bone morphogenetic protein (BMP)--signaling and contributes to synaptic abnormalities in two neurodegenerative diseasesResponses to environmental enrichment differ with sex and genotype in a transgenic mouse model of Huntington's diseasePhosphodiesterases as therapeutic targets for Alzheimer's disease.Oral administration of the pimelic diphenylamide HDAC inhibitor HDACi 4b is unsuitable for chronic inhibition of HDAC activity in the CNS in vivoHigh-Throughput Automated Phenotyping of Two Genetic Mouse Models of Huntington's DiseaseReversal learning and associative memory impairments in a BACHD rat model for Huntington diseaseDeficits in a Simple Visual Go/No-go Discrimination Task in Two Mouse Models of Huntington's DiseaseTemporal separation of aggregation and ubiquitination during early inclusion formation in transgenic mice carrying the Huntington's disease mutationGenetic knock-down of HDAC3 does not modify disease-related phenotypes in a mouse model of Huntington's diseaseOnset and progression of behavioral and molecular phenotypes in a novel congenic R6/2 line exhibiting intergenerational CAG repeat stability.Genetic deletion of the Histone Deacetylase 6 exacerbates selected behavioral deficits in the R6/1 mouse model for Huntington's disease.The power of automated high-resolution behavior analysis revealed by its application to mouse models of Huntington's and prion diseases.Systematic behavioral evaluation of Huntington's disease transgenic and knock-in mouse models.Up-regulating BDNF with an ampakine rescues synaptic plasticity and memory in Huntington's disease knockin mice.Alterations in cortical excitation and inhibition in genetic mouse models of Huntington's disease.Direct evidence of progressive cardiac dysfunction in a transgenic mouse model of Huntington's disease.Neurodevelopmental impairment following neonatal hyperoxia in the mouse.Cognitive flexibility and long-term depression (LTD) are impaired following β-catenin stabilization in vivo.Studies on the Q175 Knock-in Model of Huntington's Disease Using Functional Imaging in Awake Mice: Evidence of Olfactory DysfunctionGlial A30P alpha-synuclein pathology segregates neurogenesis from anxiety-related behavior in conditional transgenic mice.Genetic knock-down of HDAC7 does not ameliorate disease pathogenesis in the R6/2 mouse model of Huntington's diseaseRoles of tau protein in health and disease.A potent small molecule inhibits polyglutamine aggregation in Huntington's disease neurons and suppresses neurodegeneration in vivo.CalDAG-GEFI down-regulation in the striatum as a neuroprotective change in Huntington's disease.Circadian Abnormalities in Motor Activity in a BAC Transgenic Mouse Model of Huntington's DiseaseAlterations in striatal synaptic transmission are consistent across genetic mouse models of Huntington's disease.Differential vulnerability of neurons in Huntington's disease: the role of cell type-specific features.Transplantation of induced pluripotent stem cells improves functional recovery in Huntington's disease rat model.Somatostatin receptor 1 and 5 double knockout mice mimic neurochemical changes of Huntington's disease transgenic miceHD mouse models reveal clear deficits in learning to perform a simple instrumental response.Skeletal muscle pathology in Huntington's diseaseAbnormal motor cortex plasticity in premanifest and very early manifest Huntington diseaseComprehensive behavioral and molecular characterization of a new knock-in mouse model of Huntington's disease: zQ175.Huntington's disease mouse models online: high-resolution MRI images with stereotaxic templates for computational neuroanatomyHuman umbilical cord plasma proteins revitalize hippocampal function in aged mice.Adaptation to experimental jet-lag in R6/2 mice despite circadian dysrhythmia.Early retinal function deficit without prominent morphological changes in the R6/2 mouse model of Huntington's disease.
P2860
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P2860
Selective discrimination learning impairments in mice expressing the human Huntington's disease mutation.
description
1999 nî lūn-bûn
@nan
1999年の論文
@ja
1999年学术文章
@wuu
1999年学术文章
@zh
1999年学术文章
@zh-cn
1999年学术文章
@zh-hans
1999年学术文章
@zh-my
1999年学术文章
@zh-sg
1999年學術文章
@yue
1999年學術文章
@zh-hant
name
Selective discrimination learn ...... Huntington's disease mutation.
@en
Selective discrimination learn ...... Huntington's disease mutation.
@nl
type
label
Selective discrimination learn ...... Huntington's disease mutation.
@en
Selective discrimination learn ...... Huntington's disease mutation.
@nl
prefLabel
Selective discrimination learn ...... Huntington's disease mutation.
@en
Selective discrimination learn ...... Huntington's disease mutation.
@nl
P2093
P50
P1476
Selective discrimination learn ...... Huntington's disease mutation
@en
P2093
P304
10428-10437
P356
10.1523/JNEUROSCI.19-23-10428.1999
P407
P577
1999-12-01T00:00:00Z