SCO1/YBR037C Literature Guide Help

Other names published for SCO1: PET161, YBR037C

SCO1 - Disease Gene Related (6)

ReferenceOther Genes Addressed
Williams JC, et al.  (2005) Crystal structure of human SCO1: implications for redox signaling by a mitochondrial cytochrome c oxidase "assembly" protein. J Biol Chem 280(15):15202-11
Steinmetz LM, et al.  (2002) Systematic screen for human disease genes in yeast. Nat Genet 31(4):400-4
Shoubridge EA  (2001) Cytochrome c oxidase deficiency. Am J Med Genet 106(1):46-52
Dickinson EK, et al.  (2000) A human SCO2 mutation helps define the role of Sco1p in the cytochrome oxidase assembly pathway. J Biol Chem 275(35):26780-5
Paret C, et al.  (2000) The P(174)L mutation in the human hSCO1 gene affects the assembly of cytochrome c oxidase. Biochem Biophys Res Commun 279(2):341-7
Robinson BH  (2000) Human cytochrome oxidase deficiency. Pediatr Res 48(5):581-5