van Oost B - Search Results

1

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. Among authors: van oost b. Genomics. 1995 Apr 10;26(3):461-6. doi: 10.1016/0888-7543(95)80163-g. Genomics. 1995. PMID: 7607668 Free article.

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. Among authors: van oost ba. Genomics. 1997 Oct 15;45(2):434-7. doi: 10.1006/geno.1997.4930. Genomics. 1997. PMID: 9344673

3

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. Among authors: van oost ba. Mamm Genome. 1999 Jan;10(1):49-53. doi: 10.1007/s003359900941. Mamm Genome. 1999. PMID: 9892733

4

A multipoint linkage map around the locus for myotonic dystrophy on chromosome 19.

Brunner HG, Smeets H, Lambermon HM, Coerwinkel-Driessen M, van Oost BA, Wieringa B, Ropers HH. Brunner HG, et al. Among authors: van oost ba. Genomics. 1989 Oct;5(3):589-95. doi: 10.1016/0888-7543(89)90027-x. Genomics. 1989. PMID: 2575588

5

Human ApoCI HpaI restriction site polymorphism revealed by the polymerase chain reaction.

Nillesen WM, Smeets HJ, van Oost BA. Nillesen WM, et al. Among authors: van oost ba. Nucleic Acids Res. 1990 Jun 11;18(11):3428. doi: 10.1093/nar/18.11.3428-a. Nucleic Acids Res. 1990. PMID: 1972565 Free PMC article.

6

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: van oost ba. Neurology. 1998 Jun;50(6):1749-54. doi: 10.1212/wnl.50.6.1749. Neurology. 1998. PMID: 9633722

7

A 4-base pair deletion in the mitochondrial cytochrome b gene associated with parkinsonism/MELAS overlap syndrome.

De Coo IF, Renier WO, Ruitenbeek W, Ter Laak HJ, Bakker M, Schägger H, Van Oost BA, Smeets HJ. De Coo IF, et al. Among authors: van oost ba. Ann Neurol. 1999 Jan;45(1):130-3. doi: 10.1002/1531-8249(199901)45:1<130::aid-art21>3.3.co;2-q. Ann Neurol. 1999. PMID: 9894888

8

Prader-Willi syndrome and Angelman syndrome in cousins from a family with a translocation between chromosomes 6 and 15.

Smeets DF, Hamel BC, Nelen MR, Smeets HJ, Bollen JH, Smits AP, Ropers HH, van Oost BA. Smeets DF, et al. Among authors: van oost ba. N Engl J Med. 1992 Mar 19;326(12):807-11. doi: 10.1056/NEJM199203193261206. N Engl J Med. 1992. PMID: 1538725 Free article. No abstract available.

9

Aberrant splicing of the COL4A5 gene in patients with Alport syndrome.

Lemmink HH, Kluijtmans LA, Brunner HG, Schröder CH, Knebelmann B, Jelínková E, van Oost BA, Monnens LA, Smeets HJ. Lemmink HH, et al. Among authors: van oost ba. Hum Mol Genet. 1994 Feb;3(2):317-22. doi: 10.1093/hmg/3.2.317. Hum Mol Genet. 1994. PMID: 8004101

10

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: van oost ba. Hum Genet. 1996 Mar;97(3):337-9. doi: 10.1007/BF02185767. Hum Genet. 1996. PMID: 8786077 Free article.

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