Grzegorz J. Stępień

Author

Grzegorz J. Stępień

Centre National de la Recherche Scientifique ORCID

Also Known As

G Stepien, G. STÉPIEN, G. Stepien, Grzegorz J. Stępień, Grzegorz Jerzy Stępień

Publications

897

Citations

H-Index

Concepts

All Affiliations

Centre National de la Recherche Scientifique Emory University Hôpital Debrousse Inserm Université Claude Bernard Lyon 1

About

Grzegorz J. Stępień is an author at Centre National de la Recherche Scientifique specializing in medicine, mitochondrial function, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	8	8	777
2	Natural Sciences	4	4	659
3	Biochemistry	2	2	426
4	Health Sciences	1	1	103
5	Applied Physiology	1	1	103

Grzegorz J. Stępień

Publications

880

Citations

H-Index

Page 1

	Year	Citations
Differential expression of adenine nucleotide translocator isoforms in mammalian tissues and during muscle cell differentiation. Grzegorz J. Stępień, Antonio Torroni, A.B. Chung, Journal of Biological Chemistry Muscle FunctionNuclear GeneMuscle Cell DifferentiationRedox BiologyCellular Physiology	1992	320
Neoplastic transformation is associated with coordinate induction of nuclear and cytoplasmic oxidative phosphorylation genes Antonio Torroni, Grzegorz J. Stępień, J A Hodge, Journal of Biological Chemistry Cell RegulationMitochondrial FunctionMedicineGeneticsNatural Sciences	1990	124
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
Transcriptional control of nuclear genes for the mitochondrial muscle ADP/ATP translocator and the ATP synthase beta subunit. Multiple factors interact with the OXBOX/REBOX promoter sequences. A.B. Chung, Grzegorz J. Stępień, Y Haraguchi, Journal of Biological Chemistry GeneticsMolecular BiologyMolecular GeneticsMetabolic RemodelingNuclear Genes	1992	106
A novel gly290asp mitochondrial cytochromebmutation linked to a complex III deficiency in progressive exercise intolerance R. Dumoulin, I. Sagnol, Thérèse Ferlin, Molecular and Cellular Probes KinesiologyComplex Iii DeficiencyMitochondrial FunctionExerciseProgressive Exercise Intolerance	1996	103
Cardiac transplantation in an incomplete Kearns-Sayre syndrome with mitochondrial DNA deletion Christine Tranchant, B. Mousson, M. Mohr, Neuromuscular Disorders Mitochondrial TransplantationTransplantationMendelian DisorderMitochondrial FunctionGenetics	1993	48
Mitochondrial Activity in XTC.UC1 Cells Derived from Thyroid Oncocytoma Frédérique Savagner, Arnaud Chevrollier, Dominique Loiseau, Thyroid Xtc.uc1 CellsTumor BiologyThyroid TumorsThyroid OncocytomaMitochondrial Function	2001	36
Genetic Mapping of Human Heart-Skeletal Muscle Adenine Nucleotide Translocator and Its Relationship to the Facioscapulohumeral Muscular Dystrophy Locus Y Haraguchi, A.B. Chung, Antonio Torroni, Genomics Genetic AnalysisSkeletal MuscleGenetic DisorderGeneticsPhysiology	1993	23
Fine mapping of randomly distributed multiple deletions of mitochondrial DNA in a case of chronic progressive external ophthalmoplegia T. Ville-Ferlin, R. Dumoulin, Grzegorz J. Stępień, Molecular and Cellular Probes Ocular DiseaseOphthalmologyGeneticsMultiple DeletionsLeber Hereditary Optic Neuropathy	1995	11

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