Patrick Lestienne - Concepedia

Author

Patrick Lestienne

Also Known As

P LESTIENNE, P Lestienne, P. Lestienne, PATRICK P. LESTIENNE, Patrick LESTIENNE, Patrick Lestienne, Patrick P. Lestienne

Publications

2.6K

Citations

H-Index

102

Concepts

All Affiliations

Inserm Université d'Angers Université de Bordeaux Centre National de la Recherche Scientifique École Polytechnique

About

Patrick Lestienne is an author at Inserm specializing in medicine, natural sciences, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	20	31	1.2K
2	Natural Sciences	14	19	638
3	Public Health	2	2	121
4	Engineering	1	1	10
5	Health Sciences	1	1	32

Patrick Lestienne

Publications

1.6K

Citations

H-Index

Page 1

	Year	Citations
Normal Mitochondrial Genome in Brain from Patients with Parkinson's Disease and Complex I Defect Patrick Lestienne, Julien Nelson, Peter Riederer, Journal of Neurochemistry Mitochondrial MyopathyNeurodegenerative DiseasesRespiratory ChainMendelian DisorderMitochondrial Biogenesis	1990	131
Mitochondrial DNA expression in mitochondrial myopathies and coordinated expression of nuclear genes involved in ATP production Abdelaziz Heddi, Patrick Lestienne, D.C. Wallace, Journal of Biological Chemistry Muscle FunctionGeneticsMolecular BiologyMolecular GeneticsMitochondrial Biology	1993	109
Oligoasthenospermia associated with multiple mitochondrial DNA rearrangements Patrick Lestienne Molecular Human Reproduction InfertilityAndrologyDnaDevelopmental BiologyMitochondrial Function	1997	108
Autogenous control of Escherichia coli threonyl-tRNA synthetase expression in Vivo Mathias Springer, Jacqueline Plumbridge, J. Scott Butler, Journal of Molecular Biology BiosynthesisProtein ExpressionNatural SciencesProtein BiosynthesisAutogenous Control	1985	102
Different mechanisms inferred from sequences of human mitochondrial DNA deletions in ocular myopathies Françoise Degoul, Isabelle Nelson, Serge Amselem, Nucleic Acids Research GeneticsMolecular BiologyMolecular GeneticsDeletion BoundariesMitochondrial Myopathy	1991	71
Mapping of heteroplasmic mitochondrial DNA deletions in Kearns-Sayre syndrome Isabelle Nelson, Françoise Degoul, B. Obermaier–Kusser, Nucleic Acids Research	1989	66
Activation of human leukocyte elastase activity by excess substrate, hydrophobic solvents, and ionic strength. Patrick Lestienne, Joseph G. Bieth Journal of Biological Chemistry Proteinlipid InteractionBiochemistryHydrophobic SolventsMembrane TransportBioanalysis	1980	62
Adenosine triphosphatase pontin is overexpressed in hepatocellular carcinoma and coregulated with reptin through a new posttranslational mechanism† Valérie Haurie, Ludovic Ménard, Alexandra Nicou, Hepatology	2009	61
RuvbL1 and RuvbL2 enhance aggresome formation and disaggregate amyloid fibrils Nava Zaarur, Xiaobin Xu, Patrick Lestienne, The EMBO Journal Alzheimer's DiseaseBiochemistryDisaggregate Amyloid FibrilsDegenerative PathologyProtein Misfolding	2015	61
Mitochondrial myopathies: divergences of genetic deletions, biochemical defects and the clinical syndromes Klaus-Dieter Gerbitz, B. Obermaier–Kusser, S. Zierz, Journal of Neurology Mitochondrial MyopathyMendelian DisorderMitochondrial FunctionGeneticsPathology	1990	58

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