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Times Cited
Times Co-cited
Similarity
44
Regional and cellular gene expression changes in human Huntington's disease brain.
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Exon 1 of the HD gene with an expanded CAG repeat is sufficient to cause a progressive neurological phenotype in transgenic mice.
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Comprehensive behavioral and molecular characterization of a new knock-in mouse model of Huntington's disease: zQ175.
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Time course of early motor and neuropathological anomalies in a knock-in mouse model of Huntington's disease with 140 CAG repeats.
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Characterization of neurophysiological and behavioral changes, MRI brain volumetry and 1H MRS in zQ175 knock-in mouse model of Huntington's disease.
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Decreased expression of striatal signaling genes in a mouse model of Huntington's disease.
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11
Differential loss of striatal projection neurons in Huntington disease.
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10
Neuronal identity genes regulated by super-enhancers are preferentially down-regulated in the striatum of Huntington's disease mice.
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19
Full-length human mutant huntingtin with a stable polyglutamine repeat can elicit progressive and selective neuropathogenesis in BACHD mice.
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10
Mutant huntingtin's effects on striatal gene expression in mice recapitulate changes observed in human Huntington's disease brain and do not differ with mutant huntingtin length or wild-type huntingtin dosage.
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10
Cell Type-Specific Transcriptomics Reveals that Mutant Huntingtin Leads to Mitochondrial RNA Release and Neuronal Innate Immune Activation.
Hyeseung Lee, Robert J Fenster, S Sebastian Pineda, Whitney S Gibbs, Shahin Mohammadi, Jose Davila-Velderrain, Francisco J Garcia, Martine Therrien, Hailey S Novis, Fan Gao,[...]. Neuron 2020
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Systematic behavioral evaluation of Huntington's disease transgenic and knock-in mouse models.
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Targeting H3K4 trimethylation in Huntington disease.
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Selective striatal neuronal loss in a YAC128 mouse model of Huntington disease.
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9
Early alteration of epigenetic-related transcription in Huntington's disease mouse models.
Irati Hervás-Corpión, Deisy Guiretti, Manuel Alcaraz-Iborra, Román Olivares, Antonio Campos-Caro, Ángel Barco, Luis M Valor. Sci Rep 2018
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Altered excitatory and inhibitory inputs to striatal medium-sized spiny neurons and cortical pyramidal neurons in the Q175 mouse model of Huntington's disease.
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9
Neuronal targets for reducing mutant huntingtin expression to ameliorate disease in a mouse model of Huntington's disease.
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8
Electrophysiological and morphological changes in striatal spiny neurons in R6/2 Huntington's disease transgenic mice.
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Length-dependent gametic CAG repeat instability in the Huntington's disease knock-in mouse.
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Oxidative damage and metabolic dysfunction in Huntington's disease: selective vulnerability of the basal ganglia.
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8
Progressive axonal transport and synaptic protein changes correlate with behavioral and neuropathological abnormalities in the heterozygous Q175 KI mouse model of Huntington's disease.
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13
Molecular insights into cortico-striatal miscommunications in Huntington's disease.
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Integrative Characterization of the R6/2 Mouse Model of Huntington's Disease Reveals Dysfunctional Astrocyte Metabolism.
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16
RNA Sequence Analysis of Human Huntington Disease Brain Reveals an Extensive Increase in Inflammatory and Developmental Gene Expression.
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8
Phenotype onset in Huntington's disease knock-in mice is correlated with the incomplete splicing of the mutant huntingtin gene.
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A YAC mouse model for Huntington's disease with full-length mutant huntingtin, cytoplasmic toxicity, and selective striatal neurodegeneration.
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8
Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.