Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Francis Jolivette"'
Autor:
Véronique Dorval, Wim Mandemakers, Francis Jolivette, Laetitia Coudert, Rachid Mazroui, Bart De Strooper, Sébastien S Hébert
Publikováno v:
PLoS ONE, Vol 9, Iss 1, p e85510 (2014)
Mutations in leucine-rich repeat kinase 2 (LRRK2) are the most frequent cause of genetic Parkinson's disease (PD). The biological function of LRRK2 and how mutations lead to disease remain poorly defined. It has been proposed that LRRK2 could functio
Externí odkaz:
https://doaj.org/article/e58ecffaf8174c4486532ec434b85745
Autor:
Sepideh Parsi, Cynthia Lecours, Francisco-Jose Fernandez-Gomez, Françoise Morin, Kanchan Bisht, Claudia Goupil, Francis Jolivette, Frédéric Calon, Julia Hernandez-Rapp, Sébastien S. Hébert, Marie-Ève Tremblay, Véronique Dorval, Luc Buée, Nicolas Sergeant, David A. Bennett, Emmanuel Planel, Pascal Y. Smith
Publikováno v:
Human molecular genetics. 24(23)
Alzheimer's disease (AD) and related tauopathies comprise a large group of neurodegenerative diseases associated with the pathological aggregation of tau protein. While much effort has focused on understanding the function of tau, little is known abo
Autor:
Emmanuel Planel, Francis Jolivette, Julia Hernandez-Rapp, Marie-Ève Tremblay, Sébastien S. Hébert, Pascal Y. Smith
Publikováno v:
Alzheimer's & Dementia. 11
Autor:
Laetitia Coudert, Véronique Dorval, Sébastien S. Hébert, Francis Jolivette, Bart De Strooper, Wim Mandemakers, Rachid Mazroui
Publikováno v:
PLoS ONE, Vol 9, Iss 1, p e85510 (2014)
PLoS ONE
PLoS ONE
Mutations in leucine-rich repeat kinase 2 (LRRK2) are the most frequent cause of genetic Parkinson’s disease (PD). The biological function of LRRK2 and how mutations lead to disease remain poorly defined. It has been proposed that LRRK2 could funct