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Cell Metabolism|December 26, 2006
The human cytochrome c oxidase assembly factors SCO1 and SCO2 have regulatory roles in the maintenance of cellular copper homeostasisScot C Leary, Paul A Cobine, Brett A Kaufman, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|October 21, 2018
Alternative respiratory chain enzymes: Therapeutic potential and possible pitfallsSina Saari, Geovana S Garcia, Katharina Bremer, et al.
Orphanet Journal of Rare Diseases|October 31, 2019
Arabidopsis thaliana alternative dehydrogenases: a potential therapy for mitochondrial complex I deficiency? Perspectives and pitfallsAlessia Catania, Arcangela Iuso, Juliette Bouchereau, et al.
Human Molecular Genetics|May 21, 2010
SDHA is a tumor suppressor gene causing paragangliomaNelly Burnichon, Jean-Jacques Brière, Rossella Libé, et al.
Molecular and Cellular Endocrinology|July 1, 2015
From Nf1 to Sdhb knockout: Successes and failures in the quest for animal models of pheochromocytomaCharlotte Lepoutre-Lussey, Constance Thibault, Alexandre Buffet, et al.
Human Molecular Genetics|November 11, 2008
The gene responsible for Dyggve-Melchior-Clausen syndrome encodes a novel peripheral membrane protein dynamically associated with the Golgi apparatusAriane Dimitrov, Vincent Paupe, Charles Gueudry, et al.
American Journal of Human Genetics|December 14, 2004
Impaired mitochondrial glutamate transport in autosomal recessive neonatal myoclonic epilepsyFlorence Molinari, Annick Raas-Rothschild, Marlene Rio, et al.
Human Molecular Genetics|December 10, 2002
Cell complementation using Genebridge 4 human:rodent hybrids for physical mapping of novel mitochondrial respiratory chain deficiency genesPascale De Lonlay, Claude Mugnier, Damien Sanlaville, et al.
Human Molecular Genetics|February 22, 2013
KBP-cytoskeleton interactions underlie developmental anomalies in Goldberg-Shprintzen syndromeLoïc Drévillon, André Megarbane, Bénédicte Demeer, et al.
Cell Reports|May 28, 2013
Disconnecting mitochondrial content from respiratory chain capacity in PGC-1-deficient skeletal muscleGlenn C Rowe, Ian S Patten, Zsuzsanna K Zsengeller, et al.
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