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...

door Rustin, P, Lance, C
Gepubliceerd in 1991

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

door Vanwijck, R., Moor, M. C., Malek-Mansour, S., Rustin, P.
Gepubliceerd in 1974

Mitochondrial DNA inheritance in patients with deleted mtDNA

door Quintana-Murci, L., Rotig, A., Munnich, A., Rustin, P., Bourgeron, T.
Gepubliceerd in 2001

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

door Hoarau, E, Chandra, V, Rustin, P, Scharfmann, R, Duvillie, B
Gepubliceerd in Cell Death Dis (2014)

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

door Rötig, A, Cormier, V, Chatelain, P, Francois, R, Saudubray, J M, Rustin, P, Munnich, A
Gepubliceerd in 1993

Idebenone and reduced cardiac hypertrophy in Friedreich's ataxia

door Hausse, A O, Aggoun, Y, Bonnet, D, Sidi, D, Munnich, A, Rötig, A, Rustin, P
Gepubliceerd in 2002

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

door Chretien, D, Gallego, J, Barrientos, A, Casademont, J, Cardellach, F, Munnich, A, Rötig, A, Rustin, P
Gepubliceerd in 1998

Heart transplantation in children with mitochondrial cardiomyopathy

door BONNET, D, RUSTIN, P, ROTIG, A, LE BIDOIS, J, MUNNICH, A, VOUHE, P, KACHANER, J, SIDI, D
Gepubliceerd in 2001

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

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

Mutant NDUFS3 subunit of mitochondrial complex I causes Leigh syndrome

door Benit, P, Slama, A, Cartault, F, Giurgea, I, Chretien, D, Lebon, S, Marsac, C, Munnich, A, Rotig, A, Rustin, P
Gepubliceerd in 2004

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

door Rötig, A, Bessis, J L, Romero, N, Cormier, V, Saudubray, J M, Narcy, P, Lenoir, G, Rustin, P, Munnich, A
Gepubliceerd in 1992

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

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

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

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

Mutations in SURF1 are not specifically associated with Leigh syndrome

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

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

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

Recurrent de novo mitochondrial DNA mutations in respiratory chain deficiency

door 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
Gepubliceerd in 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

door 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
Gepubliceerd in 2003

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

door 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
Gepubliceerd in 2004

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

door 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
Gepubliceerd in 2006

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

door 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
Gepubliceerd in 2012