Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Allison Citro"'
Autor:
Tara Vanderweyde, Daniel J. Apicco, Katherine Youmans-Kidder, Peter E.A. Ash, Casey Cook, Edroaldo Lummertz da Rocha, Karen Jansen-West, Alissa A. Frame, Allison Citro, John D. Leszyk, Pavel Ivanov, Jose F. Abisambra, Martin Steffen, Hu Li, Leonard Petrucelli, Benjamin Wolozin
Publikováno v:
Cell Reports, Vol 15, Iss 7, Pp 1455-1466 (2016)
Summary: Dendritic mislocalization of microtubule associated protein tau is a hallmark of tauopathies, but the role of dendritic tau is unknown. We now report that tau interacts with the RNA-binding protein (RBP) TIA1 in brain tissue, and we present
Externí odkaz:
https://doaj.org/article/221ecb1228fa44a68f43fcab96d83b55
Autor:
Liqun Liu-Yesucevitz, Aylin Bilgutay, Yong-Jie Zhang, Tara Vanderweyde, Allison Citro, Tapan Mehta, Nava Zaarur, Ann McKee, Robert Bowser, Michael Sherman, Leonard Petrucelli, Benjamin Wolozin
Publikováno v:
PLoS ONE, Vol 6, Iss 9 (2011)
Externí odkaz:
https://doaj.org/article/9aa962f272ee4acfb7c4a2ef5614541f
Autor:
Liqun Liu-Yesucevitz, Aylin Bilgutay, Yong-Jie Zhang, Tara Vanderweyde, Allison Citro, Tapan Mehta, Nava Zaarur, Ann McKee, Robert Bowser, Michael Sherman, Leonard Petrucelli, Benjamin Wolozin
Publikováno v:
PLoS ONE, Vol 5, Iss 10, p e13250 (2010)
Tar DNA Binding Protein-43 (TDP-43) is a principle component of inclusions in many cases of frontotemporal lobar degeneration (FTLD-U) and amyotrophic lateral sclerosis (ALS). TDP-43 resides predominantly in the nucleus, but in affected areas of ALS
Externí odkaz:
https://doaj.org/article/b2853d19afbe421789925766096920e7
Autor:
Benjamin Wolozin, Pavel Ivanov, Allison Citro, Hu Li, Alissa A. Frame, Leonard Petrucelli, Martin Steffen, Tara Vanderweyde, Jose F. Abisambra, Casey Cook, Daniel J. Apicco, Karen Jansen-West, Edroaldo Lummertz da Rocha, Peter E.A. Ash, John D. Leszyk, Katherine Youmans-Kidder
Publikováno v:
Cell Reports, Vol 15, Iss 7, Pp 1455-1466 (2016)
Summary: Dendritic mislocalization of microtubule associated protein tau is a hallmark of tauopathies, but the role of dendritic tau is unknown. We now report that tau interacts with the RNA-binding protein (RBP) TIA1 in brain tissue, and we present
Publikováno v:
Journal of Biological Chemistry. 286:16140-16149
Mutations in leucine-rich repeat kinase 2 (LRRK2) are currently the most common genetic cause of familial late-onset Parkinson disease, which is clinically indistinguishable from idiopathic disease. The most common pathological mutation in LRRK2, G20
Autor:
Shamol Saha, Klodjan Stafa, Allison Citro, Hu Li, Patrick Aebischer, Rina Bandopadhyay, Joon Y. Boon, Maria Guillily, Marcie A. Glicksman, Benjamin Wolozin, Claudio Derada Troletti, Zhenyu Yue, Adamantios Mamais, Min Liu, James J. Collins, Katherine L. Youmans, Julien Dusonchet, Darren J. Moore, Li Qun Liu, Bernard L. Schneider, Liliane Glauser
Publikováno v:
Human molecular genetics
Mutations in LRRK2 are one of the primary genetic causes of Parkinson's disease (PD). LRRK2 contains a kinase and a GTPase domain, and familial PD mutations affect both enzymatic activities. However, the signaling mechanisms regulating LRRK2 and the
Autor:
Tara Vanderwyde, Michael Y. Sherman, Yong Jie Zhang, Robert Bowser, Nava Zaarur, Tapan Mehta, Allison Citro, Liqun Liu-Yesucevitz, Ann C. McKee, Benjamin Wolozin, Leonard Petrucelli, Aylin Bilgutay
Publikováno v:
PLoS ONE, Vol 5, Iss 10, p e13250 (2010)
PLoS ONE
PLoS ONE
Tar DNA Binding Protein-43 (TDP-43) is a principle component of inclusions in many cases of frontotemporal lobar degeneration (FTLD-U) and amyotrophic lateral sclerosis (ALS). TDP-43 resides predominantly in the nucleus, but in affected areas of ALS
Publikováno v:
Experimental Gerontology. 48:699-700