Torthaí cuardaigh - Arnaud Chevrollier

  • 1 - 18 toradh as 18 á dtaispeáint
Beachtaigh na torthaí
  1. 1
    Super-resolution microscopies, technological breakthrough to decipher mitochondrial structure and dynamic.

    Super-resolution microscopies, technological breakthrough to decipher mitochondrial structure and dynamic. de réir Pauline Teixeira, Rémi Galland, Arnaud Chevrollier

    Foilsithe / Cruthaithe 2024
    Faigh an téacs iomlán
    Revisão
    Cuir le mo chuid Ceanán
    Sábháilte in:
  2. 2
    Adenine nucleotide translocase 2 is a key mitochondrial protein in cancer metabolism

    Adenine nucleotide translocase 2 is a key mitochondrial protein in cancer metabolism de réir Arnaud Chevrollier, Dominique Loiseau, Pascal Reynier, Georges Stepien

    Foilsithe / Cruthaithe 2010
    Faigh an téacs iomlán
    Revisão
    Cuir le mo chuid Ceanán
    Sábháilte in:
  3. 3
    Improved Locus-Specific Database for<i>OPA1</i>Mutations Allows Inclusion of Advanced Clinical Data

    Improved Locus-Specific Database for<i>OPA1</i>Mutations Allows Inclusion of Advanced Clinical Data de réir Marc Ferré, Angélique Caignard, Dan Miléa, Stéphanie Leruez, Julien Cassereau, Arnaud Chevrollier, Patrizia Amati‐Bonneau, Christophe Verny, Dominique Bonneau, Vincent Procaccio, Pascal Reynier

    Foilsithe / Cruthaithe 2014
    Faigh an téacs iomlán
    Artigo
    Cuir le mo chuid Ceanán
    Sábháilte in:
  4. 4
    Mitochondrial F0F1-ATP synthase governs the induction of mitochondrial fission

    Mitochondrial F0F1-ATP synthase governs the induction of mitochondrial fission de réir Charlène Lhuissier, Valérie Desquiret‐Dumas, Anaïs Girona, Jennifer Alban, Justine Faure, Julien Cassereau, Philippe Codron, Guy Lenaers, Olivier R. Baris, Naïg Guéguen, Arnaud Chevrollier

    Foilsithe / Cruthaithe 2024
    Faigh an téacs iomlán
    Artigo
    Cuir le mo chuid Ceanán
    Sábháilte in:
  5. 5
    Autophagy controls the pathogenicity of <i><scp>OPA</scp>1</i> mutations in dominant optic atrophy

    Autophagy controls the pathogenicity of <i><scp>OPA</scp>1</i> mutations in dominant optic atrophy de réir Mariame Selma Kane, Jennifer Alban, Valérie Desquiret‐Dumas, Naïg Guéguen, Layal Ishak, Marc Ferré, Patrizia Amati‐Bonneau, Vincent Procaccio, Dominique Bonneau, Guy Lenaers, Pascal Reynier, Arnaud Chevrollier

    Foilsithe / Cruthaithe 2017
    Faigh an téacs iomlán Faigh an téacs iomlán
    Artigo
    Cuir le mo chuid Ceanán
    Sábháilte in:
  6. 6
    The MFN2 gene is responsible for mitochondrial DNA instability and optic atrophy 'plus' phenotype

    The MFN2 gene is responsible for mitochondrial DNA instability and optic atrophy 'plus' phenotype de réir Cécile Rouzier, Sylvie Bannwarth, Annabelle Chaussenot, Arnaud Chevrollier, Annie Verschueren, Nathalie Bonello‐Palot, Konstantina Fragaki, A. Caño, Jean Pouget, J.-F. Pellissier, Vincent Procaccio, B. Chabrol, Véronique Paquis‐Flucklinger

    Foilsithe / Cruthaithe 2011
    Faigh an téacs iomlán
    Artigo
    Cuir le mo chuid Ceanán
    Sábháilte in:
  7. 7
    Resveratrol Induces a Mitochondrial Complex I-dependent Increase in NADH Oxidation Responsible for Sirtuin Activation in Liver Cells

    Resveratrol Induces a Mitochondrial Complex I-dependent Increase in NADH Oxidation Responsible for Sirtuin Activation in Liver Cells de réir Valérie Desquiret‐Dumas, Naïg Guéguen, Géraldine Leman, Stéphanie Baron, Valérie Nivet‐Antoine, Stéphanie Chupin, Arnaud Chevrollier, Emilie Vessières, Audrey Ayer, Marc Ferré, Dominique Bonneau, Daniel Henrion, Pascal Reynier, Vincent Procaccio

    Foilsithe / Cruthaithe 2013
    Faigh an téacs iomlán
    Artigo
    Cuir le mo chuid Ceanán
    Sábháilte in:
  8. 8
    Idebenone increases mitochondrial complex I activity in fibroblasts from LHON patients while producing contradictory effects on respiration

    Idebenone increases mitochondrial complex I activity in fibroblasts from LHON patients while producing contradictory effects on respiration de réir Claire Angebault, Naïg Guéguen, Valérie Desquiret‐Dumas, Arnaud Chevrollier, Virginie Guillet, Christophe Verny, Julien Cassereau, Marc Ferré, Dan Miléa, Patrizia Amati‐Bonneau, Dominique Bonneau, Vincent Procaccio, Pascal Reynier, Dominique Loiseau

    Foilsithe / Cruthaithe 2011
    Faigh an téacs iomlán Faigh an téacs iomlán
    Artigo
    Cuir le mo chuid Ceanán
    Sábháilte in:
  9. 9
    The addition of ketone bodies alleviates mitochondrial dysfunction by restoring complex I assembly in a MELAS cellular model

    The addition of ketone bodies alleviates mitochondrial dysfunction by restoring complex I assembly in a MELAS cellular model de réir Samuel Frey, Guillaume Geffroy, Valérie Desquiret‐Dumas, Naïg Guéguen, Céline Bris, Sophie Belal, Patrizia Amati‐Bonneau, Arnaud Chevrollier, Magalie Barth, Daniel Henrion, Guy Lenaers, Dominique Bonneau, Pascal Reynier, Vincent Procaccio

    Foilsithe / Cruthaithe 2016
    Faigh an téacs iomlán
    Artigo
    Cuir le mo chuid Ceanán
    Sábháilte in:
  10. 10
    Molecular screening of 980 cases of suspected hereditary optic neuropathy with a report on 77 novel<i>OPA1</i>mutations

    Molecular screening of 980 cases of suspected hereditary optic neuropathy with a report on 77 novel<i>OPA1</i>mutations de réir Marc Ferré, Dominique Bonneau, Dan Miléa, Arnaud Chevrollier, Christophe Verny, Hélène Dollfus, Carmen Ayuso, Sabine Defoort, Catherine Vignal, Xavier Zanlonghi, Jean-François Charlin, Josseline Kaplan, Sylvie Odent, Christian P. Hamel, Vincent Procaccio, Pascal Reynier, Patrizia Amati‐Bonneau

    Foilsithe / Cruthaithe 2009
    Faigh an téacs iomlán Faigh an téacs iomlán
    Artigo
    Cuir le mo chuid Ceanán
    Sábháilte in:
  11. 11
    Increase in Cardiac Ischemia-Reperfusion Injuries in Opa1+/- Mouse Model

    Increase in Cardiac Ischemia-Reperfusion Injuries in Opa1+/- Mouse Model de réir Sophie Le Page, Marjorie Niro, Jérémy Fauconnier, Laura Cellier, Sophie Tamareille, Abdallah Gharib, Arnaud Chevrollier, Laurent Loufrani, Céline Grenier, Rima Kamel, Emmanuelle Sarzi, Alain Lacampagne, Michel Ovize, Daniel Henrion, Pascal Reynier, Guy Lenaers, Delphine Mirebeau‐Prunier, Fabrice Prunier

    Foilsithe / Cruthaithe 2016
    Faigh an téacs iomlán Faigh an téacs iomlán
    Artigo
    Cuir le mo chuid Ceanán
    Sábháilte in:
  12. 12
    OPA1 R445H mutation in optic atrophy associated with sensorineural deafness

    OPA1 R445H mutation in optic atrophy associated with sensorineural deafness de réir Patrizia Amati‐Bonneau, Agnès Guichet, Aurélien Olichon, Arnaud Chevrollier, Frédérique Viala, Stéphanie Miot, Carmen Ayuso, Sylvie Odent, Catherine Arrouet, Christophe Verny, M. Calmels, Gilles Simard, Pascale Belenguer, Jing Wang, Jean‐Luc Puel, Christian Hamel, Yves Malthièry, Dominique Bonneau, Guy Lenaers, Pascal Reynier

    Foilsithe / Cruthaithe 2005
    Faigh an téacs iomlán Faigh an téacs iomlán
    Artigo
    Cuir le mo chuid Ceanán
    Sábháilte in:
  13. 13
    Early-onset Behr syndrome due to compound heterozygous mutations in OPA1

    Early-onset Behr syndrome due to compound heterozygous mutations in OPA1 de réir Dominique Bonneau, Estelle Colin, Florine Oca, Marc Ferré, Arnaud Chevrollier, Naïg Guéguen, Valérie Desquiret‐Dumas, Sylvie Nguyen, Magalie Barth, Xavier Zanlonghi, Marlène Rio, Isabelle Desguerre, Christine Barnérias, Marta Momtchilova, Diana Rodriguez, Abdelhamid Slama, Guy Lenaers, Vincent Procaccio, Patrizia Amati‐Bonneau, Pascal Reynier

    Foilsithe / Cruthaithe 2014
    Faigh an téacs iomlán Faigh an téacs iomlán
    Carta
    Cuir le mo chuid Ceanán
    Sábháilte in:
  14. 14
    CLUH couples mitochondrial distribution to the energetic and metabolic status

    CLUH couples mitochondrial distribution to the energetic and metabolic status de réir Jamal Wakim, David Goudenège, Rodolphe Perrot, Naïg Guéguen, Valérie Desquiret‐Dumas, Juan Manuel Chao de la Barca, Ilaria Dalla Rosa, Florence Manero, Morgane Le Mao, Stéphanie Chupin, Arnaud Chevrollier, Vincent Procaccio, Dominique Bonneau, David C. Logan, Pascal Reynier, Guy Lenaers, Salim Khiati

    Foilsithe / Cruthaithe 2017
    Faigh an téacs iomlán
    Artigo
    Cuir le mo chuid Ceanán
    Sábháilte in:
  15. 15
    Loss-of-Function Mutations in WDR73 Are Responsible for Microcephaly and Steroid-Resistant Nephrotic Syndrome: Galloway-Mowat Syndrome

    Loss-of-Function Mutations in WDR73 Are Responsible for Microcephaly and Steroid-Resistant Nephrotic Syndrome: Galloway-Mowat Syndrome de réir Estelle Colin, Evelyne Huynh Cong, Géraldine Mollet, Agnès Guichet, Olivier Gribouval, Christelle Arrondel, Olivia Boyer, Laurent Daniel, Marie‐Claire Gubler, Zelal Ekinci, Michel Tsimaratos, B. Chabrol, Nathalie Boddaert, Alain Verloès, Arnaud Chevrollier, Naïg Guéguen, Valérie Desquiret‐Dumas, Marc Ferré, Vincent Procaccio, Laurence Richard, Benoît Funalot, Anne Moncla, Dominique Bonneau, Corinne Antignac

    Foilsithe / Cruthaithe 2014
    Faigh an téacs iomlán
    Artigo
    Cuir le mo chuid Ceanán
    Sábháilte in:
  16. 16
    The metabolomic signature of Leber’s hereditary optic neuropathy reveals endoplasmic reticulum stress

    The metabolomic signature of Leber’s hereditary optic neuropathy reveals endoplasmic reticulum stress de réir Juan Manuel Chao de la Barca, Gilles Simard, Patrizia Amati‐Bonneau, Zainab Safiedeen, Delphine Prunier‐Mirebeau, Stéphanie Chupin, Cédric Gadras, Lydie Tessier, Naïg Guéguen, Arnaud Chevrollier, Valérie Desquiret‐Dumas, Marc Ferré, Céline Bris, Judith Kouassi Nzoughet, Cinzia Bocca, Stéphanie Leruez, Christophe Verny, Dan Miléa, Dominique Bonneau, Guy Lenaers, María Carmen Martínez, Vincent Procaccio, Pascal Reynier

    Foilsithe / Cruthaithe 2016
    Faigh an téacs iomlán Faigh an téacs iomlán
    Artigo
    Cuir le mo chuid Ceanán
    Sábháilte in:
  17. 17
    Mutations in DNM1L, as in OPA1, result in dominant optic atrophy despite opposite effects on mitochondrial fusion and fission

    Mutations in DNM1L, as in OPA1, result in dominant optic atrophy despite opposite effects on mitochondrial fusion and fission de réir S. Gerber, Majida Charif, Arnaud Chevrollier, Tanguy Chaumette, Claire Angebault, Mariame Selma Kane, Aurélien Paris, Jennifer Alban, Mélanie Quilès, Cécile Delettre, Dominique Bonneau, Vincent Procaccio, Patrizia Amati‐Bonneau, Pascal Reynier, Stéphanie Leruez, Raphaël Calmon, Nathalie Boddaert, Benoît Funalot, Marlène Rio, D. Bouccara, Isabelle Meunier, Hiromi Sesaki, Josseline Kaplan, Christian P. Hamel, Jean‐Michel Rozet, Guy Lenaers

    Foilsithe / Cruthaithe 2017
    Faigh an téacs iomlán Faigh an téacs iomlán
    Artigo
    Cuir le mo chuid Ceanán
    Sábháilte in:
  18. 18
    Mutations in the m-AAA proteases AFG3L2 and SPG7 are causing isolated dominant optic atrophy

    Mutations in the m-AAA proteases AFG3L2 and SPG7 are causing isolated dominant optic atrophy de réir Majida Charif, Arnaud Chevrollier, Naïg Guéguen, Céline Bris, David Goudenège, Valérie Desquiret‐Dumas, Stéphanie Leruez, Estelle Colin, Audrey Meunier, Catherine Vignal, Vasily Smirnov, Sabine Defoort‐Dhellemmes, Isabelle Drumare Bouvet, Cyril Goizet, Marcela Votruba, Neringa Jurkutė, Patrick Yu‐Wai‐Man, Fabrizio Tagliavini, Leonardo Caporali, Chiara La Morgia, Valério Carelli, Vincent Procaccio, Xavier Zanlonghi, Isabelle Meunier, Pascal Reynier, Dominique Bonneau, Patrizia Amati‐Bonneau, Guy Lenaers

    Foilsithe / Cruthaithe 2020
    Faigh an téacs iomlán Faigh an téacs iomlán
    Artigo
    Cuir le mo chuid Ceanán
    Sábháilte in:

Uirlisí cuardaigh: