Ottenheim C - Search Results

1

[From gene to disease; ataxia telangiectasia].

Broeks A, van 't Veer LJ, Ottenheim C, Hiel JA, Kleijer WJ, Weemaes C. Broeks A, et al. Among authors: ottenheim c. Ned Tijdschr Geneeskd. 2003 Mar 1;147(9):386-9. Ned Tijdschr Geneeskd. 2003. PMID: 12661456 Review. Dutch.

2

Use of fluorescence in situ hybridization to measure chromosome aberrations as a predictor of radiosensitivity in human tumour cells.

Coco-Martin JM, Smeets MF, Poggensee M, Mooren E, Hofland I, van den Brug M, Ottenheim C, Bartelink H, Begg AC. Coco-Martin JM, et al. Among authors: ottenheim c. Int J Radiat Biol. 1994 Sep;66(3):297-307. doi: 10.1080/09553009414551231. Int J Radiat Biol. 1994. PMID: 7930832

3

Potential of radiation-induced chromosome aberrations to predict radiosensitivity in human tumour cells.

Coco Martin JM, Mooren E, Ottenheim C, Burrill W, Nunez MI, Sprong D, Bartelink H, Begg AC. Coco Martin JM, et al. Among authors: ottenheim c. Int J Radiat Biol. 1999 Sep;75(9):1161-8. doi: 10.1080/095530099139638. Int J Radiat Biol. 1999. PMID: 10528924

4

Lethality of radiation-induced chromosome aberrations in human tumour cell lines with different radiosensitivities.

Coco-Martin JM, Ottenheim CP, Bartelink H, Begg AC. Coco-Martin JM, et al. Among authors: ottenheim cp. Int J Radiat Biol. 1996 Mar;69(3):337-44. doi: 10.1080/095530096145896. Int J Radiat Biol. 1996. PMID: 8613683

5

Automatic detection of stable and unstable chromosome aberrations visualized by three-color imaging after fluorescence in situ hybridization with a painting and a pancentromeric DNA probe.

Coco-Martin JM, Lolkus M, Ottenheim CP, Oomen LC, Blommestijn GJ, Begg AC. Coco-Martin JM, et al. Among authors: ottenheim cp. Cytometry. 1998 Aug 1;32(4):327-36. Cytometry. 1998. PMID: 9701402

6

Mechanisms of MRP over-expression in four human lung-cancer cell lines and analysis of the MRP amplicon.

Eijdems EW, De Haas M, Coco-Martin JM, Ottenheim CP, Zaman GJ, Dauwerse HG, Breuning MH, Twentyman PR, Borst P, Baas F. Eijdems EW, et al. Among authors: ottenheim cp. Int J Cancer. 1995 Mar 3;60(5):676-84. doi: 10.1002/ijc.2910600518. Int J Cancer. 1995. PMID: 7860142

7

VAMP5 and VAMP8 are most likely not involved in primary open-angle glaucoma.

Brinkman JF, Ottenheim CP, de Jong LA, Zegers RH, de Smet MD, de Jong PT, Bergen AA. Brinkman JF, et al. Among authors: ottenheim cp. Mol Vis. 2005 Aug 4;11:582-6. Mol Vis. 2005. PMID: 16110299 Free article.

8

Gene symbol: CYP1B1. Disease: glaucoma, primary congenital. Accession #Hm0541.

Brinkmann JF, Ottenheim CP, Zegers RH, de Jong PT, Bergen AA. Brinkmann JF, et al. Among authors: ottenheim cp. Hum Genet. 2006 Feb;118(6):779. Hum Genet. 2006. PMID: 17297696 No abstract available.

9

Gene symbol: CYP1B1. Disease: Glaucoma, primary congenital. Accession #Hd0513.

Brinkmann JF, Ottenheim CP, Zegers RH, de Jong PT, Bergen AA. Brinkmann JF, et al. Among authors: ottenheim cp. Hum Genet. 2006 Feb;118(6):775. Hum Genet. 2006. PMID: 17297682 No abstract available.

10

Targeted carrier screening for four recessive disorders: high detection rate within a founder population.

Mathijssen IB, Henneman L, van Eeten-Nijman JM, Lakeman P, Ottenheim CP, Redeker EJ, Ottenhof W, Meijers-Heijboer H, van Maarle MC. Mathijssen IB, et al. Among authors: ottenheim cp. Eur J Med Genet. 2015 Mar;58(3):123-8. doi: 10.1016/j.ejmg.2015.01.004. Epub 2015 Jan 30. Eur J Med Genet. 2015. PMID: 25641760

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