Liliana B Menalled, Andrea E Kudwa, Sam Miller, Jon Fitzpatrick, Judy Watson-Johnson, Nicole Keating, Melinda Ruiz, Richard Mushlin, William Alosio, Kristi McConnell, David Connor, Carol Murphy, Steve Oakeshott, Mei Kwan, Jose Beltran, Afshin Ghavami, Dani Brunner, Larry C Park, Sylvie Ramboz, David Howland. PLoS One 2012
Times Cited: 230
Times Cited: 230
Times Cited
Times Co-cited
Similarity
48
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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Characterization of neurophysiological and behavioral changes, MRI brain volumetry and 1H MRS in zQ175 knock-in mouse model of Huntington's disease.
Taneli Heikkinen, Kimmo Lehtimäki, Nina Vartiainen, Jukka Puoliväli, Susan J Hendricks, Jack R Glaser, Amyaouch Bradaia, Kristian Wadel, Chrystelle Touller, Outi Kontkanen,[...]. PLoS One 2012
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Full-length human mutant huntingtin with a stable polyglutamine repeat can elicit progressive and selective neuropathogenesis in BACHD mice.
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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.
Liliana B Menalled, Jessica D Sison, Ioannis Dragatsis, Scott Zeitlin, Marie-Françoise Chesselet. J Comp Neurol 2003
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Integrated genomics and proteomics define huntingtin CAG length-dependent networks in mice.
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22
Aggregation of huntingtin in neuronal intranuclear inclusions and dystrophic neurites in brain.
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Selective striatal neuronal loss in a YAC128 mouse model of Huntington disease.
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18
Characterization of HTT inclusion size, location, and timing in the zQ175 mouse model of Huntington's disease: an in vivo high-content imaging study.
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Neuropathological classification of Huntington's disease.
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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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Systematic behavioral evaluation of Huntington's disease transgenic and knock-in mouse models.
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The corticostriatal pathway in Huntington's disease.
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14
Aberrant splicing of HTT generates the pathogenic exon 1 protein in Huntington disease.
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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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Neuronal targets for reducing mutant huntingtin expression to ameliorate disease in a mouse model of Huntington's disease.
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12
Neurological abnormalities in a knock-in mouse model of Huntington's disease.
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12
Formation of neuronal intranuclear inclusions underlies the neurological dysfunction in mice transgenic for the HD mutation.
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12
Meso scale discovery-based assays for the detection of aggregated huntingtin.
Wolfgang Reindl, Barbara Baldo, Jana Schulz, Isabell Janack, Ilka Lindner, Markus Kleinschmidt, Yalda Sedaghat, Christina Thiede, Karsten Tillack, Christina Schmidt,[...]. PLoS One 2019
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Disrupted striatal neuron inputs and outputs in Huntington's disease.
Anton Reiner, Yun-Ping Deng. CNS Neurosci Ther 2018
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27
Quantification of mutant huntingtin protein in cerebrospinal fluid from Huntington's disease patients.
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11
Intranuclear inclusions and neuritic aggregates in transgenic mice expressing a mutant N-terminal fragment of huntingtin.
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11
Corticostriatal synaptic adaptations in Huntington's disease.
Joshua L Plotkin, D James Surmeier. Curr Opin Neurobiol 2015
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15
Characterization of Behavioral, Neuropathological, Brain Metabolic and Key Molecular Changes in zQ175 Knock-In Mouse Model of Huntington's Disease.
Qi Peng, Bin Wu, Mali Jiang, Jing Jin, Zhipeng Hou, Jennifer Zheng, Jiangyang Zhang, Wenzhen Duan. PLoS One 2016
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Differential loss of striatal projection neurons in Huntington disease.
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10
Expression of mutant huntingtin in mouse brain astrocytes causes age-dependent neurological symptoms.
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Jennifer Bradford, Ji-Yeon Shin, Meredith Roberts, Chuan-En Wang, Xiao-Jiang Li, Shihua Li. Proc Natl Acad Sci U S A 2009
10
Nuclear and neuropil aggregates in Huntington's disease: relationship to neuropathology.
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10
Quantification assays for total and polyglutamine-expanded huntingtin proteins.
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28
An enhanced Q175 knock-in mouse model of Huntington disease with higher mutant huntingtin levels and accelerated disease phenotypes.
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30
Loss of huntingtin-mediated BDNF gene transcription in Huntington's disease.
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10
Phenotype onset in Huntington's disease knock-in mice is correlated with the incomplete splicing of the mutant huntingtin gene.
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Loss of corticostriatal and thalamostriatal synaptic terminals precedes striatal projection neuron pathology in heterozygous Q140 Huntington's disease mice.
Y P Deng, T Wong, C Bricker-Anthony, B Deng, A Reiner. Neurobiol Dis 2013
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12
Unravelling and Exploiting Astrocyte Dysfunction in Huntington's Disease.
Baljit S Khakh, Vahri Beaumont, Roger Cachope, Ignacio Munoz-Sanjuan, Steven A Goldman, Rosemarie Grantyn. Trends Neurosci 2017
Baljit S Khakh, Vahri Beaumont, Roger Cachope, Ignacio Munoz-Sanjuan, Steven A Goldman, Rosemarie Grantyn. Trends Neurosci 2017
10
Reversal of neuropathology and motor dysfunction in a conditional model of Huntington's disease.
A Yamamoto, J J Lucas, R Hen. Cell 2000
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9
Huntingtin-encoded polyglutamine expansions form amyloid-like protein aggregates in vitro and in vivo.
E Scherzinger, R Lurz, M Turmaine, L Mangiarini, B Hollenbach, R Hasenbank, G P Bates, S W Davies, H Lehrach, E E Wanker. Cell 1997
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9
Huntington disease: natural history, biomarkers and prospects for therapeutics.
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9
Alterations in cortical excitation and inhibition in genetic mouse models of Huntington's disease.
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Damian M Cummings, Véronique M André, Besim O Uzgil, Steven M Gee, Yvette E Fisher, Carlos Cepeda, Michael S Levine. J Neurosci 2009
9
Network organization of the huntingtin proteomic interactome in mammalian brain.
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9
Multiple sources of striatal inhibition are differentially affected in Huntington's disease mouse models.
Carlos Cepeda, Laurie Galvan, Sandra M Holley, Shilpa P Rao, Véronique M André, Elian P Botelho, Jane Y Chen, Joseph B Watson, Karl Deisseroth, Michael S Levine. J Neurosci 2013
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11
Pathophysiology of Huntington's disease: time-dependent alterations in synaptic and receptor function.
L A Raymond, V M André, C Cepeda, C M Gladding, A J Milnerwood, M S Levine. Neuroscience 2011
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9
The Neuropathology of Huntington's Disease.
Henry J Waldvogel, Eric H Kim, Lynette J Tippett, Jean-Paul G Vonsattel, Richard L M Faull. Curr Top Behav Neurosci 2015
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11
Regional and cellular gene expression changes in human Huntington's disease brain.
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9
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.