Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Mylène Gilleron"'
Autor:
Marie Joncquel, Julie Labasque, Julie Demaret, Marie-Adélaïde Bout, Aghilès Hamroun, Benjamin Hennart, Mathieu Tronchon, Magali Defevre, Isabelle Kim, Alain Kerckhove, Laurence George, Mylène Gilleron, Anne-Frédérique Dessein, Farid Zerimech, Guillaume Grzych
Publikováno v:
Antioxidants, Vol 12, Iss 7, p 1412 (2023)
Tacrolimus (FK506) is an immunosuppressant that is experiencing a continuous rise in usage worldwide. The related side effects are known to be globally dose-dependent. Despite numerous studies on FK506, the mechanisms underlying FK506 toxicity are st
Externí odkaz:
https://doaj.org/article/984d6e22f4c44b10a8238bdd0ccb1327
Autor:
Virginia Guarani, Claude Jardel, Dominique Chrétien, Anne Lombès, Paule Bénit, Clémence Labasse, Emmanuelle Lacène, Agnès Bourillon, Apolline Imbard, Jean-François Benoist, Imen Dorboz, Mylène Gilleron, Eric S Goetzman, Pauline Gaignard, Abdelhamid Slama, Monique Elmaleh-Bergès, Norma B Romero, Pierre Rustin, Hélène Ogier de Baulny, Joao A Paulo, J Wade Harper, Manuel Schiff
Publikováno v:
eLife, Vol 5 (2016)
Previously, we identified QIL1 as a subunit of mitochondrial contact site (MICOS) complex and demonstrated a role for QIL1 in MICOS assembly, mitochondrial respiration, and cristae formation critical for mitochondrial architecture (Guarani et al., 20
Externí odkaz:
https://doaj.org/article/c2eb5d8eb5b14293a741ed6e1db3525a
Autor:
Abdelhamid Slama, Anne Lombès, Sandra T. Cooper, Heni Abida, Chen-Hsien Su, Manuel Schiff, Alexander Tzagoloff, Kym Mina, Minal Menezes, Padma Sivadorai, Richard J.N. Allcock, Hélène Ogier de Baulny, Mylène Gilleron, John Christodoulou, Malgorzata Rak, David R. Thorburn, Nina Kresoje, Lisa G. Riley, Nigel G. Laing, Pierre Rustin, Mark R. Davis, Aurélien Bayot, Pauline Gaignard
Publikováno v:
The American Journal of Human Genetics. 93(2):384-389
Many individuals with abnormalities of mitochondrial respiratory chain complex III remain genetically undefined. Here, we report mutations (c.288G>T [p.Trp96Cys] and c.643C>T [p.Leu215Phe]) in CYC1, encoding the cytochrome c1 subunit of complex III,
Autor:
Laurence Jonard, Xiaowu Gai, Hongbo Xie, Valérie Desquiret-Dumas, Claude Jardel, Gaëlle Hardy, Patrizia Amati-Bonneau, Catherine Florentz, Marni J. Falk, Nadia Aoutil, Agnès Rötig, Marc Ferré, Isabelle Durand-Zaleski, Annabelle Chaussenot, Hassani Maoulida, Delphine Martinez, Sylvie Bannwarth, Claire Hoarau, Anne-Sophie Lebre, Brigitte Chabrol, Konstantina Fragaki, Abdelhamid Slama, Bénédicte Mousson de Camaret, Vincent Procaccio, Pauline Gaignard, Jennifer Ceresuela, Jean-Paul Bonnefont, Véronique Paquis-Flucklinger, Kim-Hanh Le Quan Sang, Mylène Gilleron, Pascal Reynier, Claire Marie Dhaenens, Christophe Rocher, Nathanaël Charrier, Aurore Devos, Sandrine Marlin, Caroline Espil-Taris
Publikováno v:
Journal of Medical Genetics
Journal of medical genetics
Journal of medical genetics, 2013, 50 (10), pp.704-14. ⟨10.1136/jmedgenet-2013-101604⟩
Journal of Medical Genetics, 2013, 50 (10), pp.704-14. ⟨10.1136/jmedgenet-2013-101604⟩
Journal of medical genetics
Journal of medical genetics, 2013, 50 (10), pp.704-14. ⟨10.1136/jmedgenet-2013-101604⟩
Journal of Medical Genetics, 2013, 50 (10), pp.704-14. ⟨10.1136/jmedgenet-2013-101604⟩
International audience; BACKGROUND: Mitochondrial DNA (mtDNA) diseases are rare disorders whose prevalence is estimated around 1 in 5000. Patients are usually tested only for deletions and for common mutations of mtDNA which account for 5-40% of case
Autor:
Emmanuelle Lacène, Mylène Gilleron, Manuel Schiff, Joao A. Paulo, Eric S. Goetzman, Virginia Guarani, Monique Elmaleh-Bergès, Hélène Ogier de Baulny, Anne Lombès, Clémence Labasse, J. Wade Harper, P. Rustin, Norma B. Romero, Apolline Imbard, Abdelhamid Slama, Pauline Gaignard, Dominique Chrétien, Agnès Bourillon, Paule Bénit, Jean-François Benoist, Imen Dorboz, Claude Jardel
Publikováno v:
eLife, Vol 5 (2016)
eLife
eLife, 2016, ⟨10.7554/eLife.17163⟩
eLife, eLife Sciences Publication, 2016, ⟨10.7554/eLife.17163⟩
eLife, eLife Sciences Publication, 2016, 〈10.7554/eLife.17163〉
eLife
eLife, 2016, ⟨10.7554/eLife.17163⟩
eLife, eLife Sciences Publication, 2016, ⟨10.7554/eLife.17163⟩
eLife, eLife Sciences Publication, 2016, 〈10.7554/eLife.17163〉
Previously, we identified QIL1 as a subunit of mitochondrial contact site (MICOS) complex and demonstrated a role for QIL1 in MICOS assembly, mitochondrial respiration, and cristae formation critical for mitochondrial architecture (Guarani et al., 20
Autor:
Clémence Labasse, J. Wade Harper, Anne Lombès, Jean-François Benoist, Mylène Gilleron, Monique Elmaleh-Bergès, Emmanuelle Lacène, Hélène Ogier de Baulny, Eric S. Goetzman, P. Rustin, Manuel Schiff, Joao A. Paulo, Norma B. Romero, Paule Bénit, Abdelhamid Slama, Dominique Chrétien, Agnès Bourillon, Virginia Guarani, Imen Dorboz, Pauline Gaignard, Claude Jardel, Apolline Imbard
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6972e8a8cc23348390c1fd1136dff586
https://doi.org/10.7554/elife.17163.012
https://doi.org/10.7554/elife.17163.012
Autor:
Pierre Lesimple, Neji Tebib, Tim M. Strom, Thomas Meitinger, Holger Prokisch, Guy Touati, Anne Lombès, Claude Jardel, Mylène Gilleron, Tobias B. Haack, Caroline L’hermitte-Stead, Hélène Ogier de Baulny, Sandrine Filaut, Laura S. Kremer, Hatem Azzouz
Publikováno v:
Journal of Hepatology
Journal of Hepatology, 2016, 65 (2), pp.377-85. ⟨10.1016/j.jhep.2016.04.017⟩
Journal of Hepatology, Elsevier, 2016, 65 (2), pp.377-85. ⟨10.1016/j.jhep.2016.04.017⟩
Journal of Hepatology, Elsevier, 2016, 65 (2), pp.377-85. 〈10.1016/j.jhep.2016.04.017〉
Journal of Hepatology, 2016, 65 (2), pp.377-85. ⟨10.1016/j.jhep.2016.04.017⟩
Journal of Hepatology, Elsevier, 2016, 65 (2), pp.377-85. ⟨10.1016/j.jhep.2016.04.017⟩
Journal of Hepatology, Elsevier, 2016, 65 (2), pp.377-85. 〈10.1016/j.jhep.2016.04.017〉
Next generation sequencing approaches have tremendously improved the diagnosis of rare genetic diseases. It may however be faced with difficult clinical interpretation of variants. Inherited enzymatic diseases provide an invaluable possibility to eva
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bac57137d8e07670b2d7e389689d19ed
https://www.hal.inserm.fr/inserm-01321215
https://www.hal.inserm.fr/inserm-01321215
Publikováno v:
Biochimie
Biochimie, 2014, 100, pp.171-6. ⟨10.1016/j.biochi.2013.08.012⟩
Biochimie, Elsevier, 2014, 100, pp.171-6. 〈10.1016/j.biochi.2013.08.012〉
Biochimie, Elsevier, 2014, 100, pp.171-6. ⟨10.1016/j.biochi.2013.08.012⟩
Biochimie, 2014, 100, pp.171-6. ⟨10.1016/j.biochi.2013.08.012⟩
Biochimie, Elsevier, 2014, 100, pp.171-6. 〈10.1016/j.biochi.2013.08.012〉
Biochimie, Elsevier, 2014, 100, pp.171-6. ⟨10.1016/j.biochi.2013.08.012⟩
19 pages; International audience; : Human mitochondrial diseases, defined as the diseases due to a mitochondrial oxidative phosphorylation defect, represent a large group of very diverse diseases with respect to phenotype and genetic causes. They pre
Autor:
Mylène Gilleron, Remi Neviere, Steve Lancel, Jessica Franczak, David Montaigne, Xavier Marechal
Publikováno v:
Biochemical and biophysical research communications. 388(4)
Cumulative doses of doxorubicin, a potent anticancer drug, lead to serious myocardial dysfunction. Numerous mechanisms including apoptosis have been proposed to account for its cardiotoxicity. Cardiac apoptosis induced by doxorubicin has been related
Autor:
Didier Périsse, Clement A. Gautier, Guillaume Huguet, Anne Faudet, Claudine Laurent, C Dupuits, Christopher Gillberg, Delphine Bouteiller, Cyril Mignot, Delphine Héron, Sandra Whalen, David Cohen, Mylène Gilleron, Marion Leboyer, Boris Keren, Thomas Bourgeron, Marion Gérard, Alexis Brice, C. Depienne, Alexandra Afenjar, Agnès Rastetter, Foudil Lamari, Richard Delorme, Aurélia Jacquette, Caroline Nava, S Caillet, Bruno Leheup
Publikováno v:
Translational Psychiatry
The striking excess of affected males in autism spectrum disorders (ASD) suggests that genes located on chromosome X contribute to the etiology of these disorders. To identify new X-linked genes associated with ASD, we analyzed the entire chromosome