de Coo RF - Search Results

1

The structure of the human NDUFV1 gene encoding the 51-kDa subunit of mitochondrial complex I.

de Coo RF, Buddiger PA, Smeets HJ, van Oost BA. de Coo RF, et al. Mamm Genome. 1999 Jan;10(1):49-53. doi: 10.1007/s003359900941. Mamm Genome. 1999. PMID: 9892733

2

Molecular cloning and characterization of the human mitochondrial NADH:oxidoreductase 10-kDa gene (NDUFV3).

de Coo RF, Buddiger P, Smeets HJ, van Oost BA. de Coo RF, et al. Genomics. 1997 Oct 15;45(2):434-7. doi: 10.1006/geno.1997.4930. Genomics. 1997. PMID: 9344673

3

Molecular cloning and characterization of the active human mitochondrial NADH:ubiquinone oxidoreductase 24-kDa gene (NDUFV2) and its pseudogene.

de Coo R, Buddiger P, Smeets H, Geurts van Kessel A, Morgan-Hughes J, Weghuis DO, Overhauser J, van Oost B. de Coo R, et al. Genomics. 1995 Apr 10;26(3):461-6. doi: 10.1016/0888-7543(95)80163-g. Genomics. 1995. PMID: 7607668 Free article.

4

Duplication of the proteolipid protein gene is the major cause of Pelizaeus-Merzbacher disease.

Sistermans EA, de Coo RF, De Wijs IJ, Van Oost BA. Sistermans EA, et al. Among authors: de wijs ij, de coo rf. Neurology. 1998 Jun;50(6):1749-54. doi: 10.1212/wnl.50.6.1749. Neurology. 1998. PMID: 9633722

5

Human NDUFS3 gene coding for the 30-kDa subunit of mitochondrial complex I: genomic organization and expression.

Procaccio V, Lescuyer P, Bourges I, Beugnot R, Duborjal H, Depetris D, Mousson B, Montfort MF, Smeets H, De Coo R, Issartel JP. Procaccio V, et al. Mamm Genome. 2000 Sep;11(9):808-10. doi: 10.1007/s003350010160. Mamm Genome. 2000. PMID: 10967146 No abstract available.

6

A (G-to-A) mutation in the initiation codon of the proteolipid protein gene causing a relatively mild form of Pelizaeus-Merzbacher disease in a Dutch family.

Sistermans EA, de Wijs IJ, de Coo RF, Smit LM, Menko FH, van Oost BA. Sistermans EA, et al. Among authors: de wijs ij, de coo rf. Hum Genet. 1996 Mar;97(3):337-9. doi: 10.1007/BF02185767. Hum Genet. 1996. PMID: 8786077 Free article.

7

Mutation detection in the aspartoacylase gene in 17 patients with Canavan disease: four new mutations in the non-Jewish population.

Sistermans EA, de Coo RF, van Beerendonk HM, Poll-The BT, Kleijer WJ, van Oost BA. Sistermans EA, et al. Among authors: de coo rf. Eur J Hum Genet. 2000 Jul;8(7):557-60. doi: 10.1038/sj.ejhg.5200477. Eur J Hum Genet. 2000. PMID: 10909858

8

Mutation analysis of the entire mitochondrial genome using denaturing high performance liquid chromatography.

van Den Bosch BJ, de Coo RF, Scholte HR, Nijland JG, van Den Bogaard R, de Visser M, de Die-Smulders CE, Smeets HJ. van Den Bosch BJ, et al. Among authors: de coo rf, de visser m, de die smulders ce. Nucleic Acids Res. 2000 Oct 15;28(20):E89. doi: 10.1093/nar/28.20.e89. Nucleic Acids Res. 2000. PMID: 11024191 Free PMC article.

9

Regional absence of mitochondria causing energy depletion in the myocardium of muscle LIM protein knockout mice.

van den Bosch BJ, van den Burg CM, Schoonderwoerd K, Lindsey PJ, Scholte HR, de Coo RF, van Rooij E, Rockman HA, Doevendans PA, Smeets HJ. van den Bosch BJ, et al. Among authors: de coo rf. Cardiovasc Res. 2005 Feb 1;65(2):411-8. doi: 10.1016/j.cardiores.2004.10.025. Cardiovasc Res. 2005. PMID: 15639480

10

Influence of mutation type on clinical expression of Leber hereditary optic neuropathy.

Spruijt L, Kolbach DN, de Coo RF, Plomp AS, Bauer NJ, Smeets HJ, de Die-Smulders CE. Spruijt L, et al. Among authors: de coo rf. Am J Ophthalmol. 2006 Apr;141(4):676-82. doi: 10.1016/j.ajo.2005.11.007. Am J Ophthalmol. 2006. PMID: 16564802

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