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Items: 1 to 20 of 194

1.

A pathogenic cytochrome b mutation reveals new interactions between subunits of the mitochondrial bc1 complex.

Saint-Georges Y, Bonnefoy N, di Rago JP, Chiron S, Dujardin G.

J Biol Chem. 2002 Dec 20;277(51):49397-402. Epub 2002 Oct 15.

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Analysis of exon and intron mutants in the cytochrome b mitochondrial gene of Saccharomyces cerevisiae.

Bonjardim CA, Pereira LS, Nobrega FG.

Curr Genet. 1996 Aug;30(3):200-5.

PMID:
8753647
11.

Cytochrome b mutations that modify the ubiquinol-binding pocket of the cytochrome bc1 complex and confer anti-malarial drug resistance in Saccharomyces cerevisiae.

Kessl JJ, Ha KH, Merritt AK, Lange BB, Hill P, Meunier B, Meshnick SR, Trumpower BL.

J Biol Chem. 2005 Apr 29;280(17):17142-8. Epub 2005 Feb 17.

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A mitochondrial cytochrome b mutation but no mutations of nuclearly encoded subunits in ubiquinol cytochrome c reductase (complex III) deficiency.

Valnot I, Kassis J, Chretien D, de Lonlay P, Parfait B, Munnich A, Kachaner J, Rustin P, Rötig A.

Hum Genet. 1999 Jun;104(6):460-6.

PMID:
10453733
16.

QO site deficiency can be compensated by extragenic mutations in the hinge region of the iron-sulfur protein in the bc1 complex of Saccharomyces cerevisiae.

Brasseur G, Lemesle-Meunier D, Reinaud F, Meunier B.

J Biol Chem. 2004 Jun 4;279(23):24203-11. Epub 2004 Mar 23.

17.

A structural analysis of the transient interaction between the cytochrome bc1 complex and its substrate cytochrome c.

Nyola A, Hunte C.

Biochem Soc Trans. 2008 Oct;36(Pt 5):981-5. doi: 10.1042/BST0360981.

PMID:
18793174

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