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Cells lacking the fumarase tumor suppressor are protected from apoptosis through a hypoxia-inducible factor-independent, AMPK-dependent mechanism. [electronic resource] by
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Mitochondria are physiologically maintained at close to 50 °C. [electronic resource] by
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Neuroglobin involvement in respiratory chain function and retinal ganglion cell integrity. [electronic resource] by
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Expression of alternative oxidase in Drosophila ameliorates diverse phenotypes due to cytochrome oxidase deficiency. [electronic resource] by
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Evolutionarily conserved susceptibility of the mitochondrial respiratory chain to SDHI pesticides and its consequence on the impact of SDHIs on human cultured cells. [electronic resource] by
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Effect of Lon protease knockdown on mitochondrial function in HeLa cells. [electronic resource] by
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- Rustin, Pierre
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Genotyping microsatellite DNA markers at putative disease loci in inbred/multiplex families with respiratory chain complex I deficiency allows rapid identification of a novel nonsense mutation (IVS1nt -1) in the NDUFS4 gene in Leigh syndrome. [electronic resource] by
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- de Lonlay, Pascale
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- Dommergues, Marc
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Mutations in the SDHB gene are associated with extra-adrenal and/or malignant phaeochromocytomas. [electronic resource] by
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- Corvol, Pierre
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The spectrum of systemic involvement in adults presenting with renal lesion and mitochondrial tRNA(Leu) gene mutation. [electronic resource] by
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- Mougenot, Béatrice
- Grünfeld, Jean-Pierre
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CHCHD2 accumulates in distressed mitochondria and facilitates oligomerization of CHCHD10. [electronic resource] by
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- Hench, Jürgen
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CHCHD2 accumulates in distressed mitochondria and facilitates oligomerization of CHCHD10. [electronic resource] by
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- Hench, Jürgen
- Bénit, Paule
- Kozjak-Pavlovic, Vera
- Rustin, Pierre
- Frank, Stephan
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Publication details: Human molecular genetics 01 2019
In:
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Acute and chronic mitochondrial respiratory chain deficiency differentially regulate lysosomal biogenesis. [electronic resource] by
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- Rustin, Pierre
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Tubulointerstitial nephritis and Fanconi syndrome in primary biliary cirrhosis. [electronic resource] by
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- Rustin, Pierre
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- Vanhille, Philippe
- Knebelmann, Bertrand
- Grünfeld, Jean-Pierre
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In:
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Mutant NDUFV2 subunit of mitochondrial complex I causes early onset hypertrophic cardiomyopathy and encephalopathy. [electronic resource] by
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- Corral-Debrinski, Marisol
- Kerscher, Stefan
- Rustin, Pierre
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In:
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Rare presentation of familial paraganglioma without evidence of mutation in the SDH, RET and VHL genes: towards further genetic heterogeneity. [electronic resource] by
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- Sempoux, Christine
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- Horsmans, Yves
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In:
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The human cytochrome c oxidase assembly factors SCO1 and SCO2 have regulatory roles in the maintenance of cellular copper homeostasis. [electronic resource] by
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- Mattman, Andre
- Palaty, Jan
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- Winge, Dennis R
- Rustin, Pierre
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In:
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Alternative oxidase expression in the mouse enables bypassing cytochrome c oxidase blockade and limits mitochondrial ROS overproduction. [electronic resource] by
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- Dufour, Eric
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- Ramanantsoa, Nelina
- Grandchamp, Nicolas
- Csaba, Zsolt
- Duvillié, Bertrand
- Bénit, Paule
- Gallego, Jorge
- Gressens, Pierre
- Sarkis, Chamsy
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In:
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Alternative respiratory chain enzymes: Therapeutic potential and possible pitfalls. [electronic resource] by
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- Andjelković, Ana
- Debes, Paul V
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- Szibor, Marten
- Dufour, Eric
- Rustin, Pierre
- Oliveira, Marcos T
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In:
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SDHA is a tumor suppressor gene causing paraganglioma. [electronic resource] by
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- Rivière, Julie
- Tissier, Frédérique
- Jouanno, Elodie
- Jeunemaitre, Xavier
- Bénit, Paule
- Tzagoloff, Alexander
- Rustin, Pierre
- Bertherat, Jérôme
- Favier, Judith
- Gimenez-Roqueplo, Anne-Paule
Producer: 20101021
In:
Human molecular genetics vol. 19
Availability: No items available.
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