Van den Bogert C - Search Results

1

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, van den bogert c. Am J Hum Genet. 1995 Oct;57(4):954-7. Am J Hum Genet. 1995. PMID: 7573056 Free PMC article. No abstract available.

2

Rapid shift in genotype of human mitochondrial DNA in a family with Leber's hereditary optic neuropathy.

Bolhuis PA, Bleeker-Wagemakers EM, Ponne NJ, Van Schooneveld MJ, Westerveld A, Van den Bogert C, Tabak HF. Bolhuis PA, et al. Among authors: van schooneveld mj, van den bogert c. Biochem Biophys Res Commun. 1990 Aug 16;170(3):994-7. doi: 10.1016/0006-291x(90)90490-e. Biochem Biophys Res Commun. 1990. PMID: 2390098

3

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, van den bogert c. Biochem Biophys Res Commun. 1995 Oct 24;215(3):1001-5. doi: 10.1006/bbrc.1995.2563. Biochem Biophys Res Commun. 1995. PMID: 7488023

4

[Diseases caused by mitochondrial DNA mutations].

Wijburg FA, van den Bogert C, de Visser M, Oostra RJ, Bakker PA, Bolhuis PA. Wijburg FA, et al. Among authors: van den bogert c. Ned Tijdschr Geneeskd. 1995 Jul 1;139(26):1322-6. Ned Tijdschr Geneeskd. 1995. PMID: 7617049 Review. Dutch. No abstract available.

5

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, van den bogert c. Hum Genet. 1998 Mar;102(3):327-31. doi: 10.1007/s004390050700. Hum Genet. 1998. PMID: 9544847

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, van den bogert c. Curr Genet. 1997 Aug;32(2):115-24. doi: 10.1007/s002940050255. Curr Genet. 1997. PMID: 9294259

7

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, van den bogert c. 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.

8

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

9

Differentiation and proliferation of respiration-deficient human myoblasts.

Herzberg NH, Zwart R, Wolterman RA, Ruiter JP, Wanders RJ, Bolhuis PA, van den Bogert C. Herzberg NH, et al. Among authors: van den bogert c. Biochim Biophys Acta. 1993 Mar 24;1181(1):63-7. doi: 10.1016/0925-4439(93)90091-e. Biochim Biophys Acta. 1993. PMID: 7681329

10

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 den berg m, van galen mj, van den bogert c. Eur J Cell Biol. 1993 Aug;61(2):400-8. Eur J Cell Biol. 1993. PMID: 8223726

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