Zobrazeno 1 - 10
of 58
pro vyhledávání: '"Yoon H. Cho"'
Autor:
Zhuowei Du, Margot Tertrais, Gilles Courtand, Thierry Leste-Lasserre, Laura Cardoit, Frédérique Masmejean, Christophe Halgand, Yoon H. Cho, Maurice Garret
Publikováno v:
Frontiers in Molecular Neuroscience, Vol 10 (2017)
Huntington’s disease (HD) is a neurodegenerative disorder characterized by progressive motor symptoms that are preceded by cognitive deficits and is considered as a disorder that primarily affects forebrain striatal neurons. To gain a better unders
Externí odkaz:
https://doaj.org/article/cc59dde7c5364244bf3fa852e675ef18
Publikováno v:
Neurobiology of Disease, Vol 48, Iss 3, Pp 409-417 (2012)
The pathophysiology of Huntington's disease (HD) is primarily associated with striatal degeneration and a number of behavioral symptoms such as involuntary movements, cognitive decline, psychiatric disorders, and in the most juvenile-onset cases with
Externí odkaz:
https://doaj.org/article/02beb78e247b46c6b59c5eb2efde0935
Publikováno v:
PLoS ONE, Vol 12, Iss 9, p e0184580 (2017)
Hereditary Huntington's disease (HD) is associated with progressive motor, cognitive and psychiatric symptoms. A primary consequence of the HD mutation is the preferential loss of medium spiny projection cells with relative sparing of local interneur
Externí odkaz:
https://doaj.org/article/90510fca95d9418b8e8f56d4452e62f8
Publikováno v:
Bone & Joint Research, Vol 13, Iss 7, Pp 315-320 (2024)
Aims: Achilles tendon re-rupture (ATRR) poses a significant risk of postoperative complication, even after a successful initial surgical repair. This study aimed to identify risk factors associated with Achilles tendon re-rupture following operative
Externí odkaz:
https://doaj.org/article/6253b7285f6f478dafe199f5e1b0de85
Autor:
Marianne Husson, Léa Tochon, Inés Ibañez-Tallon, Lauriane Harrington, Yoon H. Cho, Uwe Maskos, Vincent David
Publikováno v:
Journal of Neuroscience
Journal of Neuroscience, 2020, 40 (17), pp.3465-3477. ⟨10.1523/JNEUROSCI.0356-19.2020⟩
J Neurosci
Journal of Neuroscience, Society for Neuroscience, 2020, 40 (17), pp.3465-3477. ⟨10.1523/JNEUROSCI.0356-19.2020⟩
Journal of Neuroscience, 2020, 40 (17), pp.3465-3477. ⟨10.1523/JNEUROSCI.0356-19.2020⟩
J Neurosci
Journal of Neuroscience, Society for Neuroscience, 2020, 40 (17), pp.3465-3477. ⟨10.1523/JNEUROSCI.0356-19.2020⟩
Nicotine addiction, through smoking, is the principal cause of preventable mortality worldwide. Human genome-wide association studies have linked polymorphisms in theCHRNA5-CHRNA3-CHRNB4gene cluster, coding for the α5, α3, and β4 nicotinic acetylc
Autor:
Syndelle Arnaud, Marion Piquemal, Maurice Garret, Yoon H. Cho, Cristiana Pistono, Divyangana Rakesh, Elodie Poinama, Magali Cabanas, Jean-Louis Guillou
Publikováno v:
Journal of Huntington's Disease. 9:33-45
BACKGROUND Huntington's disease (HD) is a neurodegenerative disorder caused by the expansion of the trinucleotide CAG in the HD gene. While the presence of nuclear aggregates of mutant huntingtin (mHtt) in neurons is a hallmark of HD, the reason behi
Publikováno v:
PLoS ONE, Vol 8, Iss 11, p e79509 (2013)
STUDY OBJECTIVES: To search for early abnormalities in electroencephalogram (EEG) during sleep which may precede motor symptoms in a transgenic mouse model of hereditary neurodegenerative Huntington's disease (HD). DESIGN: In the R6/1 transgenic mous
Externí odkaz:
https://doaj.org/article/8aa6d16518ce4663aedbe56dd5c850e6
Autor:
Sylvain Miraux, Benjamin J.A. Robert, Jerome Ezan, Maïté M. Moreau, Nathalie Sans, Yoon H. Cho, Mireille Montcouquiol, Susanna Pietropaolo, Marlène Maitre, Wim E. Crusio
Social behavior is a basic domain affected in several neurodevelopmental disorders. Indeed, deficits in social interest, interactions and recognition represent core symptoms of Autism Spectrum Disorder but are also found associated with a heterogeneo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fd76ffe0b785cff37bd2a8e7b3e54a7e
https://hal.archives-ouvertes.fr/hal-03029888/file/2020.09.10.289397v1.full.pdf
https://hal.archives-ouvertes.fr/hal-03029888/file/2020.09.10.289397v1.full.pdf
Autor:
Elodie Mansour, Béatrice Alescio-Lautier, Yoon H. Cho, Veronique Paban, Sylvie Gory-Fauré, Susanna Pietropaolo, David Blum, Claude Villard, Béatrice Loriod, Ali Gharbi, Luc Buée
Publikováno v:
Gene
Gene, Elsevier, 2016, 600, pp.90-100. ⟨10.1016/j.gene.2016.11.022⟩
Gene, 2016, 600, pp.90-100. ⟨10.1016/j.gene.2016.11.022⟩
Gene, Elsevier, 2016, 600, pp.90-100. ⟨10.1016/j.gene.2016.11.022⟩
Gene, 2016, 600, pp.90-100. ⟨10.1016/j.gene.2016.11.022⟩
International audience; The identification of common gene/protein profiles related to brain alterations, if they exist, may indicate theconvergence of the pathogenic mechanisms driving brain disorders. Six genetically engineered mouse linesmodelling
Autor:
Yoon H. Cho, Philippe De Deurwaerdère, Rahul Bharatiya, Abdeslam Chagraoui, Emilie Puginier, Maurice Garret, Julien Manem
Publikováno v:
Neurochemistry International
Neurochemistry International, Elsevier, 2019, 128, pp.186-195. ⟨10.1016/j.neuint.2019.05.001⟩
Neurochemistry International, Elsevier, 2019, 128, pp.186-195. ⟨10.1016/j.neuint.2019.05.001⟩
Huntington's disease (HD) is a rare, autosomal neurodegenerative disease characterized by motor and cognitive impairments appearing in adults. The R6/1 mouse model of the disease recapitulates the adult onset of motor symptoms preceded by cognitive a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8387406edb27273327207625169ae511
https://hal.archives-ouvertes.fr/hal-02362066
https://hal.archives-ouvertes.fr/hal-02362066