Zobrazeno 1 - 10
of 75
pro vyhledávání: '"Yuanyun Xie"'
Autor:
Stefan Bartl, Yuanyun Xie, Nalini Potluri, Ratnesh Kesineni, Katlin Hencak, Louisa Dal Cengio, Katja Balazs, Abid Oueslati, Michela Parth, Nina Salhat, Alberto Siddu, Oskar Smrzka, Francesca Cicchetti, Günther Staffler, Michael R. Hayden, Amber L. Southwell
Publikováno v:
Neurobiology of Disease, Vol 193, Iss , Pp 106444- (2024)
Externí odkaz:
https://doaj.org/article/9f127a6b6c0642d8b90cf4f316b4916a
Autor:
Stefan Bartl, Yuanyun Xie, Nalini Potluri, Ratnesh Kesineni, Katlin Hencak, Louisa Dal Cengio, Katja Balazs, Abid Oueslati, Michela Parth, Nina Salhat, Alberto Siddu, Oskar Smrzka, Francesca Cicchetti, Günther Straffler, Michael R. Hayden, Amber L. Southwell
Publikováno v:
Neurobiology of Disease, Vol 190, Iss , Pp 106376- (2024)
In Huntington disease (HD), the mutant huntingtin (mtHTT) protein is the principal cause of pathological changes that initiate primarily along the cortico-striatal axis. mtHTT is ubiquitously expressed and there is, accordingly, growing recognition t
Externí odkaz:
https://doaj.org/article/4d07a71b09d34d4a99a06f94d8778757
Autor:
Nicholas S. Caron, Raul Banos, Amirah E. Aly, Yuanyun Xie, Seunghyun Ko, Nalini Potluri, Christine Anderson, Hailey Findlay Black, Lisa M. Anderson, Benjamin Gordon, Amber L. Southwell, Michael R. Hayden
Publikováno v:
Neurobiology of Disease, Vol 166, Iss , Pp 105652- (2022)
Huntington disease (HD) is a neurodegenerative disease caused by a trinucleotide repeat expansion in the HTT gene encoding an elongated polyglutamine tract in the huntingtin (HTT) protein. Expanded mutant HTT (mHTT) is toxic and leads to regional atr
Externí odkaz:
https://doaj.org/article/60744919d1f14be893b4b7443dbd2e49
Publikováno v:
Frontiers in Earth Science, Vol 10 (2022)
Understanding the heavy mineral composition of the Songhua River basin in NE China and the influencing factors (e.g., provenance, transport processes and chemical weathering) is crucial for the study of both the source-to-sink processes and the drain
Externí odkaz:
https://doaj.org/article/d49c8ed4a2454c3b8d2234bfc68881ae
Autor:
Lei Sun, Yuanyun Xie, Chunguo Kang, Yunping Chi, Peng Wu, Zhenyu Wei, Siqi Li, Qian Zhao, Shuo Liu
Publikováno v:
PLoS ONE, Vol 17, Iss 10 (2022)
Comprehending heavy mineral composition of the sandy land in Northeast China (NESL) is of great significance for interpreting generation, pathways, source and geochemistry of sediments in this area. To this end, the fine-grained (
Externí odkaz:
https://doaj.org/article/d13603b54f0b4222b33618713065e445
Autor:
Emily Machiela, Ritika Jeloka, Nicholas S. Caron, Shagun Mehta, Mandi E. Schmidt, Helen J. E. Baddeley, Colton M. Tom, Nalini Polturi, Yuanyun Xie, Virginia B. Mattis, Michael R. Hayden, Amber L. Southwell
Publikováno v:
Frontiers in Aging Neuroscience, Vol 12 (2020)
Huntington disease (HD) is a fatal, inherited neurodegenerative disorder caused by a mutation in the huntingtin (HTT) gene. While mutant HTT is present ubiquitously throughout life, HD onset typically occurs in mid-life. Oxidative damage accumulates
Externí odkaz:
https://doaj.org/article/927e14de01344da3b997cbcf2b24e178
Autor:
Amber L. Southwell, Sonia Franciosi, Erika B. Villanueva, Yuanyun Xie, Laurie A. Winter, Janaki Veeraraghavan, Alan Jonason, Boguslaw Felczak, Weining Zhang, Vlad Kovalik, Sabine Waltl, George Hall, Mahmoud A. Pouladi, Ernest S. Smith, William J. Bowers, Maurice Zauderer, Michael R. Hayden
Publikováno v:
Neurobiology of Disease, Vol 76, Iss , Pp 46-56 (2015)
Huntington disease (HD) is an inherited, fatal neurodegenerative disease with no disease-modifying therapy currently available. In addition to characteristic motor deficits and atrophy of the caudate nucleus, signature hallmarks of HD include behavio
Externí odkaz:
https://doaj.org/article/99a93dc1282c4cf6b5dc56f2438c4a79
Autor:
Mahmoud A. Pouladi, Elsa Brillaud, Yuanyun Xie, Paola Conforti, Rona K. Graham, Dagmar E. Ehrnhoefer, Sonia Franciosi, Weining Zhang, Patrick Poucheret, Elsa Compte, Jean-Claude Maurel, Chiara Zuccato, Elena Cattaneo, Christian Néri, Michael R. Hayden
Publikováno v:
Neurobiology of Disease, Vol 48, Iss 3, Pp 282-289 (2012)
Huntington disease (HD), a neurodegenerative disorder caused by an expanded CAG repeat in the HTT gene, remains without a treatment to modify the course of the illness. Lithium, a drug widely used for the treatment of bipolar disorder, has been shown
Externí odkaz:
https://doaj.org/article/a662945d3163413c9b1c8e5189ed755b
Autor:
Jessica M. Simpson, Joana Gil-Mohapel, Mahmoud A. Pouladi, Mohamed Ghilan, Yuanyun Xie, Michael R. Hayden, Brian R. Christie
Publikováno v:
Neurobiology of Disease, Vol 41, Iss 2, Pp 249-260 (2011)
Perturbations in neurogenesis in the adult brain have been implicated in impaired learning and memory. In the present study, we investigated which stages of the neurogenic process are affected in the transgenic YAC128 mouse model of Huntington diseas
Externí odkaz:
https://doaj.org/article/41e68437097a457b898bbc4609b4e210
Autor:
Rachel J Harding, Yuanyun Xie, Nalini Potluri, Cheryl H Arrowsmith, Blair R Leavitt, Douglas Langbehn, Amber L Southwell
Publikováno v:
D: Wet biomarkers.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a0f9c7d0776b1a8e31d5099b7df8d8b7
https://doi.org/10.1136/jnnp-2022-ehdn.60
https://doi.org/10.1136/jnnp-2022-ehdn.60