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...

od Rustin, P, Lance, C
Izdano 1991

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

od Vanwijck, R., Moor, M. C., Malek-Mansour, S., Rustin, P.
Izdano 1974

Mitochondrial DNA inheritance in patients with deleted mtDNA

od Quintana-Murci, L., Rotig, A., Munnich, A., Rustin, P., Bourgeron, T.
Izdano 2001

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

od Hoarau, E, Chandra, V, Rustin, P, Scharfmann, R, Duvillie, B
Izdano u Cell Death Dis (2014)

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

od Rötig, A, Cormier, V, Chatelain, P, Francois, R, Saudubray, J M, Rustin, P, Munnich, A
Izdano 1993

Idebenone and reduced cardiac hypertrophy in Friedreich's ataxia

od Hausse, A O, Aggoun, Y, Bonnet, D, Sidi, D, Munnich, A, Rötig, A, Rustin, P
Izdano 2002

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

od Chretien, D, Gallego, J, Barrientos, A, Casademont, J, Cardellach, F, Munnich, A, Rötig, A, Rustin, P
Izdano 1998

Heart transplantation in children with mitochondrial cardiomyopathy

od BONNET, D, RUSTIN, P, ROTIG, A, LE BIDOIS, J, MUNNICH, A, VOUHE, P, KACHANER, J, SIDI, D
Izdano 2001

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

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

Mutant NDUFS3 subunit of mitochondrial complex I causes Leigh syndrome

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

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

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

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

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

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

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

Mutations in SURF1 are not specifically associated with Leigh syndrome

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

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

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

Recurrent de novo mitochondrial DNA mutations in respiratory chain deficiency

od 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
Izdano 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

od 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
Izdano 2003

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

od 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
Izdano 2004

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

od 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
Izdano 2006

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

od 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
Izdano 2012