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Human Molecular Genetics|October 9, 2001
Disabled early recruitment of antioxidant defenses in Friedreich's ataxiaK Chantrel-Groussard, V Geromel, H Puccio, et al.Journal of Neuropathology and Experimental Neurology|January 1, 1997
Exercise induces myonuclear ubiquitination and apoptosis in dystrophin-deficient muscle of miceM Sandri, M Podhorska-Okolow, V Geromel, et al.Free Radical Research|November 8, 2001
Human cultured skin fibroblasts survive profound inherited ubiquinone depletionV Geromel, N Kadhom, I Ceballos-Picot, et al.Human Molecular Genetics|May 24, 2001
Superoxide-induced massive apoptosis in cultured skin fibroblasts harboring the neurogenic ataxia retinitis pigmentosa (NARP) mutation in the ATPase-6 gene of the mitochondrial DNAV Geromel, N Kadhom, I Cebalos-Picot, et al.Biochemical and Biophysical Research Communications|July 30, 1997
The consequences of a mild respiratory chain deficiency on substrate competitive oxidation in human mitochondriaV Geromel, B Parfait, J C von Kleist-Retzow, et al.Antisense & Nucleic Acid Drug Development|July 12, 2001
Mitochondria transfection by oligonucleotides containing a signal peptide and vectorized by cationic liposomesV Geromel, A Cao, D Briane, et al.Lancet (London, England)|September 6, 2000
Quinone-responsive multiple respiratory-chain dysfunction due to widespread coenzyme Q10 deficiencyA Rötig, E L Appelkvist, V Geromel, et al.Pageof 1