Van Galen MJ - Search Results

1

Altered kinetics of cytochrome c oxidase in a patient with severe mitochondrial encephalomyopathy.

Nijtmans LG, Barth PG, Lincke CR, Van Galen MJ, Zwart R, Klement P, Bolhuis PA, Ruitenbeek W, Wanders RJ, Van den Bogert C. Nijtmans LG, et al. Among authors: van galen mj. Biochim Biophys Acta. 1995 Apr 24;1270(2-3):193-201. doi: 10.1016/0925-4439(95)00044-5. Biochim Biophys Acta. 1995. PMID: 7727543 Free article.

2

Expression and fate of the nuclearly encoded subunits of cytochrome-c oxidase in cultured human cells depleted of mitochondrial gene products.

Nijtmans LG, Spelbrink JN, Van Galen MJ, Zwaan M, Klement P, Van den Bogert C. Nijtmans LG, et al. Among authors: van galen mj. Biochim Biophys Acta. 1995 Mar 16;1265(2-3):117-26. doi: 10.1016/0167-4889(94)00203-q. Biochim Biophys Acta. 1995. PMID: 7696340 Free article.

3

Regulation of the expression of mitochondrial proteins: relationship between mtDNA copy number and cytochrome-c oxidase activity in human cells and tissues.

Van den Bogert C, De Vries H, Holtrop M, Muus P, Dekker HL, Van Galen MJ, Bolhuis PA, Taanman JW. Van den Bogert C, et al. Among authors: van galen mj. Biochim Biophys Acta. 1993 Sep 13;1144(2):177-83. doi: 10.1016/0005-2728(93)90170-k. Biochim Biophys Acta. 1993. PMID: 8396443

4

The mitochondrial DNA mutation ND6*14,484C associated with leber hereditary optic neuropathy, leads to deficiency of complex I of the respiratory chain.

Oostra RJ, Van Galen MJ, Bolhuis PA, Bleeker-Wagemakers EM, Van den Bogert C. Oostra RJ, et al. Among authors: van galen mj. Biochem Biophys Res Commun. 1995 Oct 24;215(3):1001-5. doi: 10.1006/bbrc.1995.2563. Biochem Biophys Res Commun. 1995. PMID: 7488023

5

Mitochondria in cultured human muscle cells depleted of mitochondrial DNA.

Herzberg NH, Middelkoop E, Adorf M, Dekker HL, Van Galen MJ, Van den Berg M, Bolhuis PA, Van den Bogert C. Herzberg NH, et al. Among authors: van galen mj. Eur J Cell Biol. 1993 Aug;61(2):400-8. Eur J Cell Biol. 1993. PMID: 8223726

6

Preferential amplification and phenotypic selection in a population of deleted and wild-type mitochondrial DNA in cultured cells.

Spelbrink JN, Zwart R, Van Galen MJ, Van den Bogert C. Spelbrink JN, et al. Among authors: van galen mj. Curr Genet. 1997 Aug;32(2):115-24. doi: 10.1007/s002940050255. Curr Genet. 1997. PMID: 9294259

7

Familial mitochondrial DNA depletion in liver: haplotype analysis of candidate genes.

Spelbrink JN, Van Galen MJ, Zwart R, Bakker HD, Rovio A, Jacobs HT, Van den Bogert C. Spelbrink JN, et al. Among authors: van galen mj. Hum Genet. 1998 Mar;102(3):327-31. doi: 10.1007/s004390050700. Hum Genet. 1998. PMID: 9544847

8

Simultaneous occurrence of the 11778 (ND4) and the 9438 (COX III) mtDNA mutations in Leber hereditary optic neuropathy: molecular, biochemical, and clinical findings.

Oostra RJ, Van den Bogert C, Nijtmans LG, van Galen MJ, Zwart R, Bolhuis PA, Bleeker-Wagemakers EM. Oostra RJ, et al. Among authors: van galen mj. Am J Hum Genet. 1995 Oct;57(4):954-7. Am J Hum Genet. 1995. PMID: 7573056 Free PMC article. No abstract available.

9

In-vitro stability and cytostatic activity of liposomal formulations of 5-fluoro-2'-deoxyuridine and its diacylated derivatives.

van Borssum Waalkes M, van Galen M, Morselt H, Sternberg B, Scherphof GL. van Borssum Waalkes M, et al. Biochim Biophys Acta. 1993 May 14;1148(1):161-72. doi: 10.1016/0005-2736(93)90174-x. Biochim Biophys Acta. 1993. PMID: 8499464

10

Gadolinium chloride-induced shifts in intrahepatic distributions of liposomes.

Lázár G, van Galen M, Scherphof GL. Lázár G, et al. Biochim Biophys Acta. 1989 May 10;1011(2-3):97-101. doi: 10.1016/0167-4889(89)90194-8. Biochim Biophys Acta. 1989. PMID: 2713404

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