Search Results - Dominique Bonneau
- Showing 1 - 20 results of 75
- Go to Next Page
-
1
Mutations of the human PTEN gene by Dominique Bonneau, Michel Longy
Published 2000Revisão -
2
A snapshot of some pLI score pitfalls by Alban Ziegler, Estelle Colin, David Goudenège, Dominique Bonneau
Published 2019Artigo -
3
-
4
-
5
-
6
-
7
Dominant optic atrophy by Guy Lenaers, Christian P. Hamel, Cécile Delettre, Patrizia Amati‐Bonneau, Vincent Procaccio, Dominique Bonneau, Pascal Reynier, Dan Miléa
Published 2012Revisão -
8
-
9
Mutation screening of the EYA1, SIX1, and SIX5 genes in a large cohort of patients harboring branchio-oto-renal syndrome calls into question the pathogenic role of SIX5 mutations by Pauline Krug, Vincent Morinière, Sandrine Marlin, Valérie Koubi, Heinz Gabriel, Estelle Colin, Dominique Bonneau, Rémi Salomon, Corinne Antignac, Laurence Heidet
Published 2010Artigo -
10
-
11
Bioinformatics Tools and Databases to Assess the Pathogenicity of Mitochondrial DNA Variants in the Field of Next Generation Sequencing by Céline Bris, David Goudenège, Valérie Desquiret‐Dumas, Majida Charif, Estelle Colin, Dominique Bonneau, Patrizia Amati‐Bonneau, Guy Lenaers, Pascal Reynier, Vincent Procaccio
Published 2018Revisão -
12
Improved Locus-Specific Database for<i>OPA1</i>Mutations Allows Inclusion of Advanced Clinical Data by Marc Ferré, Angélique Caignard, Dan Miléa, Stéphanie Leruez, Julien Cassereau, Arnaud Chevrollier, Patrizia Amati‐Bonneau, Christophe Verny, Dominique Bonneau, Vincent Procaccio, Pascal Reynier
Published 2014Artigo -
13
-
14
A Nontargeted UHPLC-HRMS Metabolomics Pipeline for Metabolite Identification: Application to Cardiac Remote Ischemic Preconditioning by Judith Kouassi Nzoughet, Cinzia Bocca, Gilles Simard, Delphine Prunier‐Mirebeau, Juan Manuel Chao de la Barca, Dominique Bonneau, Vincent Procaccio, Fabrice Prunier, Guy Lenaers, Pascal Reynier
Published 2016Artigo -
15
Enrichment of LOVD-USHbases with 152<i>USH2A</i>Genotypes Defines an Extensive Mutational Spectrum and Highlights Missense Hotspots by David Baux, Catherine Blanchet, Christian Hamel, Isabelle Meunier, Lise Larrieu, Valérie Faugère, Christel Vaché, Pierangela Castorina, Bernard Puech, Dominique Bonneau, Sue Malcolm, Mireille Claustres, Anne‐Françoise Roux
Published 2014Artigo -
16
Autophagy controls the pathogenicity of <i><scp>OPA</scp>1</i> mutations in dominant optic atrophy by 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
Published 2017Artigo -
17
Effects of OPA1 mutations on mitochondrial morphology and apoptosis: Relevance to ADOA pathogenesis by Aurélien Olichon, Thomas Landes, Laetitia Pelloquin, Laurent J. Emorine, Valérie Mils, Agnès Guichet, Cécile Delettre, Christian Hamel, Patrizia Amati‐Bonneau, Dominique Bonneau, Pascal Reynier, Guy Lenaers, Pascale Belenguer
Published 2006Artigo -
18
Resveratrol Induces a Mitochondrial Complex I-dependent Increase in NADH Oxidation Responsible for Sirtuin Activation in Liver Cells by 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
Published 2013Artigo -
19
Idebenone increases mitochondrial complex I activity in fibroblasts from LHON patients while producing contradictory effects on respiration by 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
Published 2011Artigo -
20
The addition of ketone bodies alleviates mitochondrial dysfunction by restoring complex I assembly in a MELAS cellular model by 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
Published 2016Artigo
Search Tools:
Related Subjects
Biology
Genetics
Gene
Medicine
Mutation
Phenotype
Internal medicine
Neuroscience
Missense mutation
Exome sequencing
Biochemistry
Cell biology
Mitochondrion
Atrophy
Bioinformatics
Computational biology
Intellectual disability
Mitochondrial DNA
Enzyme
Genotype
Locus (genetics)
Ophthalmology
Optic nerve
Optic neuropathy
Pathology
Psychiatry
Chemistry
Genome
Psychology
Anatomy