Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Tina De Wit"'
Autor:
Matthieu Drouyer, Marc F. Bolliger, Evy Lobbestael, Chris Van den Haute, Marco Emanuele, Réginald Lefebvre, William Sibran, Tina De Wit, Coline Leghay, Eugénie Mutez, Nicolas Dzamko, Glenda M. Halliday, Shigeo Murayama, Alain Martoriati, Katia Cailliau, Jean-François Bodart, Marie-Christine Chartier-Harlin, Veerle Baekelandt, R. Jeremy Nichols, Jean-Marc Taymans
Publikováno v:
Neurobiology of Disease, Vol 157, Iss , Pp 105426- (2021)
LRRK2 is a highly phosphorylated multidomain protein and mutations in the gene encoding LRRK2 are a major genetic determinant of Parkinson's disease (PD). Dephosphorylation at LRRK2's S910/S935/S955/S973 phosphosite cluster is observed in several con
Externí odkaz:
https://doaj.org/article/1fd99d9a1cef4426b7f99882df3c1bd9
Autor:
Katia Cailliau, Réginald Lefebvre, Alain Martoriati, R. Jeremy Nichols, Glenda M. Halliday, Tina De Wit, Chris Van den Haute, Marco Emanuele, William Sibran, Coline Leghay, Matthieu Drouyer, Shigeo Murayama, Marc Bolliger, Jean-François Bodart, Jean-Marc Taymans, Veerle Baekelandt, Evy Lobbestael, Nicolas Dzamko, Marie-Christine Chartier-Harlin, Eugénie Mutez
Publikováno v:
Neurobiology of Disease
Neurobiology of Disease, Elsevier, 2021, 157, pp.105426. ⟨10.1016/j.nbd.2021.105426⟩
Neurobiology of Disease, Vol 157, Iss, Pp 105426-(2021)
Neurobiology of Disease, 2021, 157, pp.105426. ⟨10.1016/j.nbd.2021.105426⟩
Neurobiology of Disease, Elsevier, 2021, 157, pp.105426. ⟨10.1016/j.nbd.2021.105426⟩
Neurobiology of Disease, Vol 157, Iss, Pp 105426-(2021)
Neurobiology of Disease, 2021, 157, pp.105426. ⟨10.1016/j.nbd.2021.105426⟩
LRRK2 is a highly phosphorylated multidomain protein and mutations in the gene encoding LRRK2 are a major genetic determinant of Parkinson's disease (PD). Dephosphorylation at LRRK2's S910/S935/S955/S973 phosphosite cluster is observed in several con
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7a8ddafe9dc8af16d33dd86a9887abcb
https://lirias.kuleuven.be/handle/123456789/679568
https://lirias.kuleuven.be/handle/123456789/679568
Mutations in the gene encoding leucine-rich repeat kinase 2 (LRRK2) are known today as the most common genetic cause of Parkinson's disease (PD). LRRK2 is a large protein that is hypothesized to regulate other proteins as a scaffold in downstream sig
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6719835a201ff8b0771499fd73f2ac8e
https://lirias.kuleuven.be/handle/123456789/610293
https://lirias.kuleuven.be/handle/123456789/610293
Autor:
Jean-Marc Taymans, Veerle Baekelandt, Evy Lobbestael, Laura Civiero, Tina De Wit, Elisa Greggio
Publikováno v:
Frontiers in Neuroscience. 11
Autor:
Matthieu Drouyer, Marc Böllliger, Tina De Wit, R. Jeremy Nichols, Marie-Christine Chartier-Harlin, Jean-Marc Taymans, Veerle Baekelandt, Evy Lobbestael
Publikováno v:
Frontiers in Neuroscience. 11