Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Christina, Mo"'
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-13 (2024)
Abstract Perception is largely supported by cortical processing that involves communication among multiple areas, typically starting with primary sensory cortex and then involving higher order cortices. This communication is served in part by transth
Externí odkaz:
https://doaj.org/article/7aeea8854e9f48bb9afbbafa7e94b42c
Akademický článek
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Publikováno v:
Neurobiology of Disease, Vol 71, Iss , Pp 81-94 (2014)
Huntington's disease (HD) is a neurodegenerative disease caused by a tandem repeat mutation encoding an expanded polyglutamine tract. Our previous work showed that memory deficits in HD transgenic mice could be accelerated by increased levels of stre
Externí odkaz:
https://doaj.org/article/780a259d79d8434e902dda1956f913a5
High stress hormone levels accelerate the onset of memory deficits in male Huntington's disease mice
Autor:
Christina Mo, Terence Y. Pang, Mark I. Ransome, Rachel A. Hill, Thibault Renoir, Anthony J. Hannan
Publikováno v:
Neurobiology of Disease, Vol 69, Iss , Pp 248-262 (2014)
Huntington's disease (HD) is a neurodegenerative disorder caused by a tandem repeat mutation in the huntingtin gene. Lifestyle factors, such as lack of activity may contribute to the variability in the age of disease onset. Therefore, better understa
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https://doaj.org/article/76a86c29ebeb44b49b89493ad1e58adf
Akademický článek
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Akademický článek
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Autor:
S. Murray Sherman, Christina Mo
We now know that sensory processing in cortex occurs not only via direct communication between primary to secondary areas, but also via their parallel cortico-thalamo-cortical (i.e.,trans-thalamic) pathways. Both corticocortical andtrans-thalamic pat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b2eeef2425962cb50774ad6caaf6feeb
https://europepmc.org/articles/PMC6343647/
https://europepmc.org/articles/PMC6343647/
Huntington's disease (HD) is a neurodegenerative disorder largely governed by genetics. The cause of this tandem repeat disorder is a fully penetrant trinucleotide (CAG), inherited via autosomal dominant transmission. The length of this expanded tand
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c14fc973af8d89b07535c4005eebeebb
https://doi.org/10.1016/b978-0-12-813146-6.00020-5
https://doi.org/10.1016/b978-0-12-813146-6.00020-5
Autor:
Tamas Bartfai, Sarah L. Berga, Sondra T. Bland, Enrrico Bloise, Jenna E. Boyd, Brandy A. Briones, Maria Alexandra Brito, Wilson C.J. Chung, Iain J. Clarke, Daemon L. Cline, Everly Conway de Macario, R.A.L. Dampney, Clémence Disdier, Klaus P. Ebmeier, Elizabeth Gould, Sarah L. Gray, Matthew W. Hale, Robert J. Handa, Anthony J. Hannan, Belinda A. Henry, Holger Jahn, Naomi Kakoschke, Hagar Kandel, Ruth A. Lanius, Sonia J. Lupien, Alberto J.L. Macario, Nicola Maggio, Marie-France Marin, Cristina Martin-Perez, Stephen G. Matthews, M.P. Mattson, Anthony L. McCall, Bruce S. McEwen, Michael J. McKinley, Margaret C. McKinnon, Christina Mo, Donald W. Pfaff, Daniela Rabellino, Catherine Raymond, Thibault Renoir, Philip J. Ryan, Mathias V. Schmidt, Menahem Segal, Helmut Sies, Robert L. Spencer, Gregg D. Stanwood, Barbara S. Stonestreet, Nigel A.S. Taylor, Maarten van den Buuse, Antonio Verdejo-Garcia, Annamaria Vezzani, Enikő Zsoldos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::69d8c9547a9c758b41a0207e9e86e478
https://doi.org/10.1016/b978-0-12-813146-6.01002-x
https://doi.org/10.1016/b978-0-12-813146-6.01002-x
Publikováno v:
Behavioural Brain Research. 276:17-27
Huntington's disease (HD) is an autosomal dominant, neurodegenerative disorder with a characteristic triad of cognitive, affective and motor symptoms. Transgenic HD mice show excellent construct and face validity for many of these symptoms, however t