Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Celine Desseille"'
Autor:
Robert Barouki, Manolis Kogevinas, Karine Audouze, Kristine Belesova, Ake Bergman, Linda Birnbaum, Sandra Boekhold, Sebastien Denys, Celine Desseille, Elina Drakvik, Howard Frumkin, Jeanne Garric, Delphine Destoumieux-Garzon, Andrew Haines, Anke Huss, Genon Jensen, Spyros Karakitsios, Jana Klanova, Iida-Maria Koskela, Francine Laden, Francelyne Marano, Eva Franziska Matthies-Wiesler, George Morris, Julia Nowacki, Riikka Paloniemi, Neil Pearce, Annette Peters, Aino Rekola, Denis Sarigiannis, Katerina Šebková, Remy Slama, Brigit Staatsen, Cathryn Tonne, Roel Vermeulen, Paolo Vineis
Publikováno v:
Environment International, Vol 146, Iss , Pp 106272- (2021)
The outbreak of COVID-19 raised numerous questions on the interactions between the occurrence of new infections, the environment, climate and health. The European Union requested the H2020 HERA project which aims at setting priorities in research on
Externí odkaz:
https://doaj.org/article/5b7e4a64e4bc4949baf6c4af6f01ad4b
Autor:
Léo Houdebine, Domenico D’Amico, Jean Bastin, Farah Chali, Céline Desseille, Valentin Rumeau, Judy Soukkari, Carole Oudot, Thaïs Rouquet, Bruno Bariohay, Julien Roux, Delphine Sapaly, Laure Weill, Philippe Lopes, Fatima Djouadi, Cynthia Bezier, Frédéric Charbonnier, Olivier Biondi
Publikováno v:
Frontiers in Physiology, Vol 10 (2019)
Spinal Muscular Atrophy (SMA), an autosomal recessive neurodegenerative disease characterized by the loss of spinal-cord motor-neurons, is caused by mutations on Survival-of-Motor Neuron (SMN)-1 gene. The expression of SMN2, a SMN1 gene copy, partial
Externí odkaz:
https://doaj.org/article/0b7e68d9487c4a4d90e01f37457cf285
Autor:
Céline Desseille, Séverine Deforges, Olivier Biondi, Léo Houdebine, Domenico D’amico, Antonin Lamazière, Cédric Caradeuc, Gildas Bertho, Gaëlle Bruneteau, Laure Weill, Jean Bastin, Fatima Djouadi, François Salachas, Philippe Lopes, Christophe Chanoine, Charbel Massaad, Frédéric Charbonnier
Publikováno v:
Frontiers in Molecular Neuroscience, Vol 10 (2017)
Amyotrophic Lateral Sclerosis is an adult-onset neurodegenerative disease characterized by the specific loss of motor neurons, leading to muscle paralysis and death. Although the cellular mechanisms underlying amyotrophic lateral sclerosis (ALS)-indu
Externí odkaz:
https://doaj.org/article/93e08f1473ec471cac23c066507b727c