Succinate-driven reverse electron transport in the respiratory chain of plant mitochondria. The effects of rotenone and adenylates in relation to malate and oxaloacetate metabolism...

per Rustin, P, Lance, C
Publicat 1991

Proceedings: Lymphocyte dependent cytotoxic antibody activity against human melanoma antigens.

per Vanwijck, R., Moor, M. C., Malek-Mansour, S., Rustin, P.
Publicat 1974

Mitochondrial DNA inheritance in patients with deleted mtDNA

per Quintana-Murci, L., Rotig, A., Munnich, A., Rustin, P., Bourgeron, T.
Publicat 2001

Pro-oxidant/antioxidant balance controls pancreatic β-cell differentiation through the ERK1/2 pathway

per Hoarau, E, Chandra, V, Rustin, P, Scharfmann, R, Duvillie, B
Publicat a Cell Death Dis (2014)

Deletion of mitochondrial DNA in a case of early-onset diabetes mellitus, optic atrophy, and deafness (Wolfram syndrome, MIM 222300).

per Rötig, A, Cormier, V, Chatelain, P, Francois, R, Saudubray, J M, Rustin, P, Munnich, A
Publicat 1993

Idebenone and reduced cardiac hypertrophy in Friedreich's ataxia

per Hausse, A O, Aggoun, Y, Bonnet, D, Sidi, D, Munnich, A, Rötig, A, Rustin, P
Publicat 2002

Biochemical parameters for the diagnosis of mitochondrial respiratory chain deficiency in humans, and their lack of age-related changes.

per Chretien, D, Gallego, J, Barrientos, A, Casademont, J, Cardellach, F, Munnich, A, Rötig, A, Rustin, P
Publicat 1998

Heart transplantation in children with mitochondrial cardiomyopathy

per BONNET, D, RUSTIN, P, ROTIG, A, LE BIDOIS, J, MUNNICH, A, VOUHE, P, KACHANER, J, SIDI, D
Publicat 2001

Mutation of the fumarase gene in two siblings with progressive encephalopathy and fumarase deficiency.

per Bourgeron, T, Chretien, D, Poggi-Bach, J, Doonan, S, Rabier, D, Letouzé, P, Munnich, A, Rötig, A, Landrieu, P, Rustin, P
Publicat 1994

Mutant NDUFS3 subunit of mitochondrial complex I causes Leigh syndrome

per Benit, P, Slama, A, Cartault, F, Giurgea, I, Chretien, D, Lebon, S, Marsac, C, Munnich, A, Rotig, A, Rustin, P
Publicat 2004

Maternally inherited duplication of the mitochondrial genome in a syndrome of proximal tubulopathy, diabetes mellitus, and cerebellar ataxia.

per Rötig, A, Bessis, J L, Romero, N, Cormier, V, Saudubray, J M, Narcy, P, Lenoir, G, Rustin, P, Munnich, A
Publicat 1992

Pearson's marrow-pancreas syndrome. A multisystem mitochondrial disorder in infancy.

per Rötig, A, Cormier, V, Blanche, S, Bonnefont, J P, Ledeist, F, Romero, N, Schmitz, J, Rustin, P, Fischer, A, Saudubray, J M
Publicat 1990

A high rate (20%-30%) of parental consanguinity in cytochrome-oxidase deficiency.

per von Kleist-Retzow, J C, Cormier-Daire, V, de Lonlay, P, Parfait, B, Chretien, D, Rustin, P, Feingold, J, Rötig, A, Munnich, A
Publicat 1998

Mutations in SURF1 are not specifically associated with Leigh syndrome

per VON KLEIST-RETZOW, J.-C., YAO, J., TAANMAN, J., CHANTREL, K., CHRETIEN, D., CORMIER-DAIRE, V., ROTIG, A., MUNNICH, A., RUSTIN, P., SHOUBRIDGE, E.
Publicat 2001

The molecular archaeology of a mitochondrial death effector: AIF in Drosophila

per Joza, N, Galindo, K, Pospisilik, JA, Benit, P, Rangachari, M, Kanitz, EE, Nakashima, Y, Neely, GG, Rustin, P, Abrams, JM, Kroemer, G, Penninger, JM
Publicat 2008

Recurrent de novo mitochondrial DNA mutations in respiratory chain deficiency

per Lebon, S, Chol, M, Benit, P, Mugnier, C, Chretien, D, Giurgea, I, Kern, I, Girardin, E, Hertz-Pannier, L, de Lonlay, P, Rotig, A, Rustin, P, Munnich, A
Publicat 2003

The mitochondrial DNA G13513A MELAS mutation in the NADH dehydrogenase 5 gene is a frequent cause of Leigh-like syndrome with isolated complex I deficiency

per Chol, M, Lebon, S, Benit, P, Chretien, D, de Lonlay, P, Goldenberg, A, Odent, S, Hertz-Pannier, L, Vincent-Delorme, C, Cormier-Daire, V, Rustin, P, Rotig, A, Munnich, A
Publicat 2003

Investigation of the role of SDHB inactivation in sporadic phaeochromocytoma and neuroblastoma

per Astuti, D, Morris, M, Krona, C, Abel, F, Gentle, D, Martinsson, T, Kogner, P, Neumann, H P H, Voutilainen, R, Eng, C, Rustin, P, Latif, F, Maher, E R
Publicat 2004

Wide clinical variability among 13 new Cockayne syndrome cases confirmed by biochemical assays

per Pasquier, L, Laugel, V, Lazaro, L, Dollfus, H, Journel, H, Edery, P, Goldenberg, A, Martin, D, Heron, D, Merrer, M Le, Rustin, P, Odent, S, Munnich, A, Sarasin, A, Cormier‐Daire, V
Publicat 2006

HIV-1 Tat protein directly induces mitochondrial membrane permeabilization and inactivates cytochrome c oxidase

per Lecoeur, H, Borgne-Sanchez, A, Chaloin, O, El-Khoury, R, Brabant, M, Langonné, A, Porceddu, M, Brière, J-J, Buron, N, Rebouillat, D, Péchoux, C, Deniaud, A, Brenner, C, Briand, J-P, Muller, S, Rustin, P, Jacotot, E
Publicat 2012