Vogel R - Search Results

1

Vogel R, Nijtmans L, Ugalde C, van den Heuvel L, Smeitink J. Vogel R, et al. Curr Opin Neurol. 2004 Apr;17(2):179-86. doi: 10.1097/00019052-200404000-00016. Curr Opin Neurol. 2004. PMID: 15021246

2

Human mitochondrial complex I assembly is mediated by NDUFAF1.

Vogel RO, Janssen RJ, Ugalde C, Grovenstein M, Huijbens RJ, Visch HJ, van den Heuvel LP, Willems PH, Zeviani M, Smeitink JA, Nijtmans LG. Vogel RO, et al. FEBS J. 2005 Oct;272(20):5317-26. doi: 10.1111/j.1742-4658.2005.04928.x. FEBS J. 2005. PMID: 16218961 Free article.

3

Identification of mitochondrial complex I assembly intermediates by tracing tagged NDUFS3 demonstrates the entry point of mitochondrial subunits.

Vogel RO, Dieteren CE, van den Heuvel LP, Willems PH, Smeitink JA, Koopman WJ, Nijtmans LG. Vogel RO, et al. J Biol Chem. 2007 Mar 9;282(10):7582-90. doi: 10.1074/jbc.M609410200. Epub 2007 Jan 5. J Biol Chem. 2007. PMID: 17209039 Free article.

4

Cytosolic signaling protein Ecsit also localizes to mitochondria where it interacts with chaperone NDUFAF1 and functions in complex I assembly.

Vogel RO, Janssen RJ, van den Brand MA, Dieteren CE, Verkaart S, Koopman WJ, Willems PH, Pluk W, van den Heuvel LP, Smeitink JA, Nijtmans LG. Vogel RO, et al. Genes Dev. 2007 Mar 1;21(5):615-24. doi: 10.1101/gad.408407. Genes Dev. 2007. PMID: 17344420 Free PMC article.

5

Investigation of the complex I assembly chaperones B17.2L and NDUFAF1 in a cohort of CI deficient patients.

Vogel RO, van den Brand MA, Rodenburg RJ, van den Heuvel LP, Tsuneoka M, Smeitink JA, Nijtmans LG. Vogel RO, et al. Mol Genet Metab. 2007 Jun;91(2):176-82. doi: 10.1016/j.ymgme.2007.02.007. Epub 2007 Mar 26. Mol Genet Metab. 2007. PMID: 17383918

6

Human mitochondrial complex I assembly: a dynamic and versatile process.

Vogel RO, Smeitink JA, Nijtmans LG. Vogel RO, et al. Biochim Biophys Acta. 2007 Oct;1767(10):1215-27. doi: 10.1016/j.bbabio.2007.07.008. Epub 2007 Aug 9. Biochim Biophys Acta. 2007. PMID: 17854760 Free article. Review.

7

Assembly factors as a new class of disease genes for mitochondrial complex I deficiency: cause, pathology and treatment options.

Nouws J, Nijtmans LG, Smeitink JA, Vogel RO. Nouws J, et al. Brain. 2012 Jan;135(Pt 1):12-22. doi: 10.1093/brain/awr261. Epub 2011 Oct 27. Brain. 2012. PMID: 22036961 Review.

8

Human mitochondrial complex I assembles through the combination of evolutionary conserved modules: a framework to interpret complex I deficiencies.

Ugalde C, Vogel R, Huijbens R, Van Den Heuvel B, Smeitink J, Nijtmans L. Ugalde C, et al. Among authors: vogel r. Hum Mol Genet. 2004 Oct 15;13(20):2461-72. doi: 10.1093/hmg/ddh262. Epub 2004 Aug 18. Hum Mol Genet. 2004. PMID: 15317750

9

Transcriptome analysis of complex I-deficient patients reveals distinct expression programs for subunits and assembly factors of the oxidative phosphorylation system.

van der Lee R, Szklarczyk R, Smeitink J, Smeets HJ, Huynen MA, Vogel R. van der Lee R, et al. Among authors: vogel r. BMC Genomics. 2015 Sep 15;16:691. doi: 10.1186/s12864-015-1883-8. BMC Genomics. 2015. PMID: 26369791 Free PMC article.

10

Subunits of mitochondrial complex I exist as part of matrix- and membrane-associated subcomplexes in living cells.

Dieteren CE, Willems PH, Vogel RO, Swarts HG, Fransen J, Roepman R, Crienen G, Smeitink JA, Nijtmans LG, Koopman WJ. Dieteren CE, et al. Among authors: vogel ro. J Biol Chem. 2008 Dec 12;283(50):34753-61. doi: 10.1074/jbc.M807323200. Epub 2008 Sep 30. J Biol Chem. 2008. PMID: 18826940 Free PMC article.

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