Rödel G - Search Results

1

Cytochrome c oxidase deficiency due to mutations in SCO2, encoding a mitochondrial copper-binding protein, is rescued by copper in human myoblasts.

Jaksch M, Paret C, Stucka R, Horn N, Müller-Höcker J, Horvath R, Trepesch N, Stecker G, Freisinger P, Thirion C, Müller J, Lunkwitz R, Rödel G, Shoubridge EA, Lochmüller H. Jaksch M, et al. Among authors: rodel g. Hum Mol Genet. 2001 Dec 15;10(26):3025-35. doi: 10.1093/hmg/10.26.3025. Hum Mol Genet. 2001. PMID: 11751685

2

The P(174)L mutation in the human hSCO1 gene affects the assembly of cytochrome c oxidase.

Paret C, Lode A, Krause-Buchholz U, Rödel G. Paret C, et al. Among authors: rodel g. Biochem Biophys Res Commun. 2000 Dec 20;279(2):341-7. doi: 10.1006/bbrc.2000.3949. Biochem Biophys Res Commun. 2000. PMID: 11118289

3

Molecular characterization of Saccharomyces cerevisiae Sco2p reveals a high degree of redundancy with Sco1p.

Lode A, Paret C, Rödel G. Lode A, et al. Among authors: rodel g. Yeast. 2002 Aug;19(11):909-22. doi: 10.1002/yea.883. Yeast. 2002. PMID: 12125048

4

Mitochondrial copper metabolism in yeast: interaction between Sco1p and Cox2p.

Lode A, Kuschel M, Paret C, Rödel G. Lode A, et al. Among authors: rodel g. FEBS Lett. 2000 Nov 17;485(1):19-24. doi: 10.1016/s0014-5793(00)02176-1. FEBS Lett. 2000. PMID: 11086158 Free article.

5

Human members of the SCO1 gene family: complementation analysis in yeast and intracellular localization.

Paret C, Ostermann K, Krause-Buchholz U, Rentzsch A, Rödel G. Paret C, et al. Among authors: rodel g. FEBS Lett. 1999 Mar 19;447(1):65-70. doi: 10.1016/s0014-5793(99)00266-5. FEBS Lett. 1999. PMID: 10218584 Free article.

6

Identification of functionally important regions of the Saccharomyces cerevisiae mitochondrial translational activator Cbs1p.

Krause-Buchholz U, Tzschoppe K, Paret C, Ostermann K, Rödel G. Krause-Buchholz U, et al. Among authors: rodel g. Yeast. 2000 Mar 15;16(4):353-63. Yeast. 2000. PMID: 10669873

7

Mitochondrial copper metabolism in yeast: mutational analysis of Sco1p involved in the biogenesis of cytochrome c oxidase.

Rentzsch A, Krummeck-Weiss G, Hofer A, Bartuschka A, Ostermann K, Rödel G. Rentzsch A, et al. Among authors: rodel g. Curr Genet. 1999 Mar;35(2):103-8. doi: 10.1007/s002940050438. Curr Genet. 1999. PMID: 10079328

8

Knockdown of human COX17 affects assembly and supramolecular organization of cytochrome c oxidase.

Oswald C, Krause-Buchholz U, Rödel G. Oswald C, et al. Among authors: rodel g. J Mol Biol. 2009 Jun 12;389(3):470-9. doi: 10.1016/j.jmb.2009.04.034. Epub 2009 Apr 22. J Mol Biol. 2009. PMID: 19393246

9

Evidence for the association of yeast mitochondrial ribosomes with Cox11p, a protein required for the Cu(B) site formation of cytochrome c oxidase.

Khalimonchuk O, Ostermann K, Rödel G. Khalimonchuk O, et al. Among authors: rodel g. Curr Genet. 2005 Apr;47(4):223-33. doi: 10.1007/s00294-005-0569-1. Epub 2005 Mar 18. Curr Genet. 2005. PMID: 15776235

10

Accumulation of the cytochrome c oxidase subunits I and II in yeast requires a mitochondrial membrane-associated protein, encoded by the nuclear SCO1 gene.

Schulze M, Rödel G. Schulze M, et al. Among authors: rodel g. Mol Gen Genet. 1989 Mar;216(1):37-43. doi: 10.1007/BF00332228. Mol Gen Genet. 1989. PMID: 2543907

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