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Astrocyte Kir4.1 ion channel deficits contribute to neuronal dysfunction in Huntington's disease model miceTong, Xiaoping ; Ao, Yan ; Faas, Guido C ; Nwaobi, Sinifunanya E ; Xu, Ji ; Haustein, Martin D ; Anderson, Mark A ; Mody, Istvan ; Olsen, Michelle L ; Sofroniew, Michael V ; Khakh, Baljit SNature neuroscience, 2014-05, Vol.17 (5), p.694-703 [Periódico revisado por pares]United States: Nature Publishing GroupTexto completo disponível |
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The Biology of HuntingtinSaudou, Frédéric ; Humbert, SandrineNeuron (Cambridge, Mass.), 2016-03, Vol.89 (5), p.910-926 [Periódico revisado por pares]United States: Elsevier IncTexto completo disponível |
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Chromosomal profiles of gene expression in Huntington's diseaseAnderson, Alexander N. ; Roncaroli, Federico ; Hodges, Angela ; Deprez, Manuel ; Turkheimer, Federico E.Brain (London, England : 1878), 2008-02, Vol.131 (2), p.381-388 [Periódico revisado por pares]Oxford: Oxford University PressTexto completo disponível |
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Proteotoxic stress induces phosphorylation of p62/SQSTM1 by ULK1 to regulate selective autophagic clearance of protein aggregatesLim, Junghyun ; Lachenmayer, M Lenard ; Wu, Shuai ; Liu, Wenchao ; Kundu, Mondira ; Wang, Rong ; Komatsu, Masaaki ; Oh, Young J ; Zhao, Yanxiang ; Yue, Zhenyu Yang, WilliamPLoS genetics, 2015-02, Vol.11 (2), p.e1004987 [Periódico revisado por pares]United States: Public Library of ScienceTexto completo disponível |
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Choosing an animal model for the study of Huntington's diseasePouladi, Mahmoud A ; Morton, A Jennifer ; Hayden, Michael RNature reviews. Neuroscience, 2013-10, Vol.14 (10), p.708-721 [Periódico revisado por pares]England: Nature Publishing GroupTexto completo disponível |
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Cystathionine γ-lyase deficiency mediates neurodegeneration in Huntington's diseasePaul, Bindu D ; Sbodio, Juan I ; Xu, Risheng ; Vandiver, M Scott ; Cha, Jiyoung Y ; Snowman, Adele M ; Snyder, Solomon HNature (London), 2014-05, Vol.509 (7498), p.96-100 [Periódico revisado por pares]England: Nature Publishing GroupTexto completo disponível |
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Identification of Genetic Factors that Modify Clinical Onset of Huntington’s DiseaseLee, Jong-Min ; Wheeler, Vanessa C. ; Chao, Michael J. ; Vonsattel, Jean Paul G. ; Pinto, Ricardo Mouro ; Lucente, Diane ; Abu-Elneel, Kawther ; Ramos, Eliana Marisa ; Mysore, Jayalakshmi Srinidhi ; Gillis, Tammy ; MacDonald, Marcy E. ; Gusella, James F. ; Harold, Denise ; Stone, Timothy C. ; Escott-Price, Valentina ; Han, Jun ; Vedernikov, Alexey ; Holmans, Peter ; Jones, Lesley ; Kwak, Seung ; Mahmoudi, Mithra ; Orth, Michael ; Landwehrmeyer, G. Bernhard ; Paulsen, Jane S. ; Dorsey, E. Ray ; Shoulson, Ira ; Myers, Richard H.Cell, 2015-07, Vol.162 (3), p.516-526 [Periódico revisado por pares]United States: Elsevier IncTexto completo disponível |
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Mutant Huntingtin promotes autonomous microglia activation via myeloid lineage-determining factorsCrotti, Andrea ; Benner, Christopher ; Kerman, Bilal E ; Gosselin, David ; Lagier-Tourenne, Clotilde ; Zuccato, Chiara ; Cattaneo, Elena ; Gage, Fred H ; Cleveland, Don W ; Glass, Christopher KNature neuroscience, 2014-04, Vol.17 (4), p.513-521 [Periódico revisado por pares]United States: Nature Publishing GroupTexto completo disponível |
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The regulation of autophagosome dynamics by huntingtin and HAP1 is disrupted by expression of mutant huntingtin, leading to defective cargo degradationWong, Yvette C ; Holzbaur, Erika L FThe Journal of neuroscience, 2014-01, Vol.34 (4), p.1293-1305 [Periódico revisado por pares]United States: Society for NeuroscienceTexto completo disponível |
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Huntington's disease: from molecular pathogenesis to clinical treatmentRoss, Christopher A, Dr ; Tabrizi, Sarah J, FRCPLancet neurology, 2011, Vol.10 (1), p.83-98 [Periódico revisado por pares]England: Elsevier LtdTexto completo disponível |