Zobrazeno 1 - 10
of 920
pro vyhledávání: '"Farrer Matthew J"'
Autor:
Gustavsson, Emil K, Follett, Jordan, Trinh, Joanne, Barodia, Sandeep K, Real, Raquel, Liu, Zhiyong, Grant-Peters, Melissa, Fox, Jesse D, Appel-Cresswell, Silke, Stoessl, A Jon, Rajput, Alex, Rajput, Ali H, Auer, Roland, Tilney, Russel, Sturm, Marc, Haack, Tobias B, Lesage, Suzanne, Tesson, Christelle, Brice, Alexis, Vilariño-Güell, Carles, Ryten, Mina, Goldberg, Matthew S, West, Andrew B, Hu, Michele T, Morris, Huw R, Sharma, Manu, Gan-Or, Ziv, Samanci, Bedia, Lis, Pawel, Periñan, Maria Teresa, Amouri, Rim, Ben Sassi, Samia, Hentati, Faycel, Tonelli, Francesca, Alessi, Dario R, Farrer, Matthew J *
Publikováno v:
In The Lancet Neurology June 2024 23(6):603-614
Autor:
Hinkle Kelly M, Yue Mei, Behrouz Bahareh, Dächsel Justus C, Lincoln Sarah J, Bowles Erin E, Beevers Joel E, Dugger Brittany, Winner Beate, Prots Iryna, Kent Caroline B, Nishioka Kenya, Lin Wen-Lang, Dickson Dennis W, Janus Christopher J, Farrer Matthew J, Melrose Heather L
Publikováno v:
Molecular Neurodegeneration, Vol 7, Iss 1, p 25 (2012)
Abstract Mutations in the LRRK2 gene are the most common cause of genetic Parkinson’s disease. Although the mechanisms behind the pathogenic effects of LRRK2 mutations are still not clear, data emerging from in vitro and in vivo models suggests rol
Externí odkaz:
https://doaj.org/article/6c25dd1f24ef43c6948b6a69831ef927
Autor:
Potts Lisa F, Cambon Alex C, Ross Owen A, Rademakers Rosa, Dickson Dennis W, Uitti Ryan J, Wszolek Zbigniew K, Rai Shesh N, Farrer Matthew J, Hein David W, Litvan Irene
Publikováno v:
BMC Medical Genetics, Vol 13, Iss 1, p 16 (2012)
Abstract Background There are no known causes for progressive supranuclear palsy (PSP). The microtubule associated protein tau (MAPT) H1 haplotype is the major genetic factor associated with risk of PSP, with both oxidative stress and mitochondrial d
Externí odkaz:
https://doaj.org/article/c1665e251b854490ac1348e77a8155dc
Autor:
Charisse Klaus, Toudjarska Ivanka, Kent Caroline, Hinkle Kelly, Ogholikhan Sina, He Zhen, Braithwaite Adam, Lincoln Sarah, Zehr Cynthia, Hope Andrew, Bumcrot David, Melrose Heather, Lewis Jada, Braich Ravi, Pandey Rajendra K, Heckman Michael, Maraganore Demetrius M, Crook Julia, Farrer Matthew J
Publikováno v:
Molecular Neurodegeneration, Vol 3, Iss 1, p 19 (2008)
Abstract Background Overexpression of α-synuclein (SNCA) in families with multiplication mutations causes parkinsonism and subsequent dementia, characterized by diffuse Lewy Body disease post-mortem. Genetic variability in SNCA contributes to risk o
Externí odkaz:
https://doaj.org/article/d7ed7967de974e5db11d3336f05e0163
Publikováno v:
BMC Medical Genetics, Vol 9, Iss 1, p 19 (2008)
Abstract Background Post-mortem Lewy body and Lewy neuritic inclusions are a defining feature of Parkinson's disease (PD) and dementia with Lewy bodies (DLB). With the discovery of missense and multiplication mutations in the alpha-synuclein gene (SN
Externí odkaz:
https://doaj.org/article/d5249bcda63d4c2a8c79e7e4c5008213
Publikováno v:
In Neuroscience Letters 10 August 2022 785
Autor:
Candido, Tara, Christilaw, Jan, Dragojlovic, Nick, Souich, Christèle du, Elliott, Alison M., Evans, Daniel M., Farrer, Matthew J., Friedman, Jan M., Guella, Ilaria, Lehman, Anna, Lynd, Larry D., Osiovich, Horacio, Tooman, Leah, Rodriguez Llorian, Elisabet, Campbell, Teresa M.
Publikováno v:
In Genetics in Medicine August 2022 24(8):1675-1683
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Akademický článek
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