Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Aurore Voisin"'
Autor:
Nicolas Giguère, Benoît Delignat-Lavaud, Freja Herborg, Aurore Voisin, Yuan Li, Vincent Jacquemet, Madhu Anand-Srivastava, Ulrik Gether, Bruno Giros, Louis-Éric Trudeau
Publikováno v:
PLoS Genetics, Vol 15, Iss 8, p e1008352 (2019)
Parkinson's disease (PD) is a neurodegenerative disorder characterized by the loss of dopamine (DA) neurons in the substantia nigra pars compacta (SNc). Rare genetic mutations in genes such as Parkin, Pink1, DJ-1, α-synuclein, LRRK2 and GBA are foun
Externí odkaz:
https://doaj.org/article/f0618051b02541699df966c28c410d7e
Autor:
Romain Cayrol, Diana Matheoud, Samantha Gruenheid, Marie-Josée Bourque, Annie Laplante, Michel Desjardins, Lei Zhu, Heidi M. McBride, Charles Ducrot, Anna-Maija Penttinen, Lauriane Ramet, Aurore Voisin, Ahmed M. Fahmy, Armelle Le Campion, Tyler Cannon, Louis-Eric Trudeau
Publikováno v:
Nature. 571:565-569
Parkinson’s disease is a neurodegenerative disorder with motor symptoms linked to the loss of dopaminergic neurons in the substantia nigra compacta. Although the mechanisms that trigger the loss of dopaminergic neurons are unclear, mitochondrial dy
Autor:
Diana, Matheoud, Tyler, Cannon, Aurore, Voisin, Anna-Maija, Penttinen, Lauriane, Ramet, Ahmed M, Fahmy, Charles, Ducrot, Annie, Laplante, Marie-Josée, Bourque, Lei, Zhu, Romain, Cayrol, Armelle, Le Campion, Heidi M, McBride, Samantha, Gruenheid, Louis-Eric, Trudeau, Michel, Desjardins
Publikováno v:
Nature. 571(7766)
Parkinson's disease is a neurodegenerative disorder with motor symptoms linked to the loss of dopaminergic neurons in the substantia nigra compacta. Although the mechanisms that trigger the loss of dopaminergic neurons are unclear, mitochondrial dysf
Autor:
Ulrik Gether, Freja Herborg, Madhu B. Anand-Srivastava, Nicolas Giguère, Bruno Giros, Aurore Voisin, Louis-Eric Trudeau, Yuan Li, Benoît Delignat-Lavaud, Vincent Jacquemet
Publikováno v:
Giguère, N, Delignat-Lavaud, B, Herborg, F, Voisin, A, Li, Y, Jacquemet, V, Anand-Srivastava, M, Gether, U, Giros, B & Trudeau, L-E 2019, ' Increased vulnerability of nigral dopamine neurons after expansion of their axonal arborization size through D2 dopamine receptor conditional knockout ', PLOS Genetics, vol. 15, no. 8, e1008352 . https://doi.org/10.1371/journal.pgen.1008352
PLoS Genetics, Vol 15, Iss 8, p e1008352 (2019)
PLoS Genetics
PLoS Genetics, Vol 15, Iss 8, p e1008352 (2019)
PLoS Genetics
Parkinson’s disease (PD) is a neurodegenerative disorder characterized by the loss of dopamine (DA) neurons in the substantia nigra pars compacta (SNc). Rare genetic mutations in genes such as Parkin, Pink1, DJ-1, α-synuclein, LRRK2 and GBA are fo
Autor:
Diana Matheoud, Tyler Cannon, Aurore Voisin, Anna-Maija Penttinen, Lauriane Ramet, Ahmed Fahmy, Charles Ducrot, Annie Laplante, Marie-Josée Bourque, Lei Zhu, Armelle Le Campion, Heidi McBride, Samantha Gruenheid, Louis-Eric Trudeau, Michel Desjardins
Publikováno v:
The Journal of Immunology. 202:177.27-177.27
Parkinson’s disease (PD) is a neurodegenerative disorder linked to the loss of dopaminergic neurons (DN) in the substantia nigra. Although the mechanisms triggering the loss of DN are unclear, mitochondrial dysfunction and inflammation are viewed a