Naïg Guéguen - Concepedia

Author

Naïg Guéguen

Also Known As

Guarch, Meritxell Espino, Gueguen, Naig, Guéguen, N., N Gueguen, N. GUEGUEN, N. Gueguen, Naig Gueguen, Naïg Gueguen, Naïg Guéguen

113

Publications

Citations

H-Index

149

Concepts

All Affiliations

Inserm Université d'Angers Centre Hospitalier Universitaire d'Angers Centre National de la Recherche Scientifique Institute for Neurosciences of Montpellier

About

Naïg Guéguen is an author at Inserm specializing in medicine, mitochondrial function, and oxidative stress.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	29	41	2.3K
2	Health Sciences	8	8	510
3	Natural Sciences	6	6	273
4	Engineering	2	2	220
5	Public Health	2	2	75

Naïg Guéguen

Publications

3.6K

Citations

H-Index

Page 1

	Year	Citations
New Insights into Muscle Fiber Types in the Pig Louis L. Lefaucheur, Patrick Ecolan, Lydia Plantard, Journal of Histochemistry & Cytochemistry HistocompatibilityMuscle FunctionEngineeringImmunologyPathology	2002	195
Mitochondrial coupling defect in Charcot–Marie–Tooth type 2A disease Dominique Loiseau, Arnaud Chevrollier, Christophe Verny, Annals of Neurology	2007	155
Resveratrol Induces a Mitochondrial Complex I-dependent Increase in NADH Oxidation Responsible for Sirtuin Activation in Liver Cells Valérie Desquiret‐Dumas, Naïg Guéguen, Géraldine Leman, Journal of Biological Chemistry Reductive StressNadh Oxidation ResponsibleBiochemistryLiver PhysiologyLipid Peroxidation	2013	132
Loss-of-Function Mutations in WDR73 Are Responsible for Microcephaly and Steroid-Resistant Nephrotic Syndrome: Galloway-Mowat Syndrome Estelle Colin, Evelyne Huynh Cong, Géraldine Mollet, The American Journal of Human Genetics Galloway-mowat SyndromeDisease MechanismGenetic DisorderMedicineGenetics	2014	132
Hereditary optic neuropathies share a common mitochondrial coupling defect Arnaud Chevrollier, Virginie Guillet, Dominique Loiseau, Annals of Neurology	2008	126
Methyl donor deficiency induces cardiomyopathy through altered methylation/acetylation of PGC‐1α by PRMT1 and SIRT1 Maira Moreno Garcia, Rosa‐Maria Guéant‐Rodriguez, Shabnam Pooya, The Journal of Pathology NutritionEpigenetic ChangeGeneticsMetabolic RemodelingEpigenetics	2011	115
Methyl donor deficiency impairs fatty acid oxidation through PGC-1α hypomethylation and decreased ER-α, ERR-α, and HNF-4α in the rat liver Shabnam Pooya, Sébastien Blaise, Maira Moreno Garcia, Journal of Hepatology Methyl Donor DeficiencyMetabolic SyndromeLipid SynthesisBiochemistryMedicine	2012	109
The human OPA1delTTAG mutation induces premature age-related systemic neurodegeneration in mouse Emmanuelle Sarzi, Claire Angebault, Marie Seveno, Brain GeneticsDominant Optic AtrophyOpa1 Mouse ModelCell DeathOptic Nerve Degeneration	2012	108
A Mitochondria-Specific Isoform of FASTK Is Present In Mitochondrial RNA Granules and Regulates Gene Expression and Function Alexis A. Jourdain, Mirko Koppen, Christopher D. Rodley, Cell Reports	2015	99
Resveratrol Directly Binds to Mitochondrial Complex I and Increases Oxidative Stress in Brain Mitochondria of Aged Mice Naïg Guéguen, Valérie Desquiret‐Dumas, Géraldine Leman, PLoS ONE Molecular BiologyResveratrol Directly BindsRedox BiologyOxidative StressMolecular Pharmacology	2015	89

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