Laetitia Pelloquin - Concepedia

Author

Laetitia Pelloquin

Université Toulouse III - Paul Sabatier ORCID

Also Known As

L Pelloquin, L. Arnauné-Pelloquin, Laeticia Arnauné-Pelloquin, Laeticia Pelloquin, Laetitia Arnauné-Pelloquin, Laetitia Arnauné-Pelloquin, Laetitia Arnauné‐Pelloquin, Laetitia Pelloquin

Publications

6.1K

Citations

H-Index

Concepts

All Affiliations

Université Toulouse III - Paul Sabatier Centre National de la Recherche Scientifique Inserm Université Fédérale de Toulouse Midi-Pyrénées Laboratoire de Biologie Cellulaire et Moléculaire du Contrôle de la Prolifération

About

Laetitia Pelloquin is an author at Université Toulouse III - Paul Sabatier specializing in medicine, mitochondrial function, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	11	11	2.1K
2	Natural Sciences	6	6	273
3	Cell Biology	5	5	311
4	Biochemistry	2	2	243
5	Biology	1	1	11

Laetitia Pelloquin

Publications

5.2K

Citations

H-Index

Page 1

	Year	Citations
Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)<sup>1</sup> Daniel J. Klionsky, Amal Kamal Abdel‐Aziz, Sara Abdelfatah, Autophagy	2021	2.5K
Nuclear gene OPA1, encoding a mitochondrial dynamin-related protein, is mutated in dominant optic atrophy Cécile Delettre, Guy Lenaers, Jean‐Michel Griffoin, Nature Genetics Neurodegenerative DiseasesMitochondrial FunctionOphthalmologyGenetic DisorderGenetics	2000	1.4K
The human dynamin‐related protein OPA1 is anchored to the mitochondrial inner membrane facing the inter‐membrane space Aurélien Olichon, Laurent J. Emorine, Eric Descoins, FEBS Letters	2002	411
The BH3‐only Bnip3 binds to the dynamin Opa1 to promote mitochondrial fragmentation and apoptosis by distinct mechanisms Thomas Landes, Laurent J. Emorine, Delphine Courilleau, EMBO Reports BiochemistryMitochondrial FunctionMedicineMitochondrial DynamicApoptosis	2010	178
Barth syndrome: Cellular compensation of mitochondrial dysfunction and apoptosis inhibition due to changes in cardiolipin remodeling linked to tafazzin (TAZ) gene mutation François Gonzalvez, Marilena D’Aurelio, Marie Boutant, Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease CardiomyopathyMitochondrial FunctionMitochondrial DysfunctionGenetic DisorderGenetics	2013	168
Effects of OPA1 mutations on mitochondrial morphology and apoptosis: Relevance to ADOA pathogenesis Aurélien Olichon, Thomas Landes, Laetitia Pelloquin, Journal of Cellular Physiology	2006	148
Identification of a Fission Yeast Dynamin-Related Protein Involved in Mitochondrial DNA Maintenance Laetitia Pelloquin, Pascale Belenguer, Yoann Menon, Biochemical and Biophysical Research Communications ChromatinMitochondrial Dna MaintenanceMitochondrial FunctionNatural SciencesGenetics	1998	80
Fission yeast msp1 is a mitochondrial dynamin-related protein Laetitia Pelloquin, Pascale Belenguer, Yoann Menon, Journal of Cell Science MitophagyMitochondrial FunctionBiochemistryMedicineNatural Sciences	1999	65
Fission yeast mfr1 activates APC and coordinates meiotic nuclear division with sporulation M. A. Blanco, Laetitia Pelloquin, Sergio Moreno Journal of Cell Science GeneticsMolecular BiologyMeiosis IiMolecular GeneticsCell Cycle	2001	63
Nuclear gene OPA1, encoding a mitochondrial dynamin-related protein, is mutated in dominant optic atrophy Cécile Delettre, Guy Lenaers, J-M Griffoin, American Journal of Ophthalmology Neurodegenerative DiseasesMitochondrial FunctionOphthalmologyGenetic DisorderGenetics	2001	60

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