Dinjens WN - Search Results

1

Distinct gene mutation profiles among luminal-type and basal-type breast cancer cell lines.

Hollestelle A, Nagel JH, Smid M, Lam S, Elstrodt F, Wasielewski M, Ng SS, French PJ, Peeters JK, Rozendaal MJ, Riaz M, Koopman DG, Ten Hagen TL, de Leeuw BH, Zwarthoff EC, Teunisse A, van der Spek PJ, Klijn JG, Dinjens WN, Ethier SP, Clevers H, Jochemsen AG, den Bakker MA, Foekens JA, Martens JW, Schutte M. Hollestelle A, et al. Among authors: dinjens wn. Breast Cancer Res Treat. 2010 May;121(1):53-64. doi: 10.1007/s10549-009-0460-8. Epub 2009 Jul 11. Breast Cancer Res Treat. 2010. PMID: 19593635

2

Loss of heterozygosity of chromosome 8 microsatellite loci implicates a candidate tumor suppressor gene between the loci D8S87 and D8S133 in human prostate cancer.

Trapman J, Sleddens HF, van der Weiden MM, Dinjens WN, Konig JJ, Schroder FH, Faber PW, Bosman FT. Trapman J, et al. Among authors: dinjens wn. Cancer Res. 1994 Dec 1;54(23):6061-4. Cancer Res. 1994. PMID: 7954446

3

Human oesophageal adenocarcinoma cell lines JROECL 47 and JROECL 50 are admixtures of the human colon carcinoma cell line HCT 116.

Wijnhoven BP, Tilanus MG, Morris AG, Darnton SJ, Tilanus HW, Dinjens WN. Wijnhoven BP, et al. Among authors: dinjens wn. Br J Cancer. 2000 May;82(9):1510-2. doi: 10.1054/bjoc.1999.1170. Br J Cancer. 2000. PMID: 10789716 Free PMC article.

4

Malignant mesenchymoma of the uterus, arising in a leiomyoma.

den Bakker MA, Hegt VN, Sleddens HB, Nuijten AS, Dinjens WN. den Bakker MA, et al. Among authors: dinjens wn. Histopathology. 2002 Jan;40(1):65-70. doi: 10.1046/j.1365-2559.2002.01290.x. Histopathology. 2002. PMID: 11903599

5

Frequent germ-line succinate dehydrogenase subunit D gene mutations in patients with apparently sporadic parasympathetic paraganglioma.

Dannenberg H, Dinjens WN, Abbou M, Van Urk H, Pauw BK, Mouwen D, Mooi WJ, de Krijger RR. Dannenberg H, et al. Among authors: dinjens wn. Clin Cancer Res. 2002 Jul;8(7):2061-6. Clin Cancer Res. 2002. PMID: 12114404

6

Clinical importance of molecular determinations in gynecologic patients with multiple tumors.

Dinjens WN, van der Burg ME, Chadha S, Sleddens HF, Burger CW, Ewing PC. Dinjens WN, et al. Cancer. 2003 Apr 1;97(7):1766-74. doi: 10.1002/cncr.11249. Cancer. 2003. PMID: 12655534 Free article.

7

Von Hippel-Lindau gene alterations in sporadic benign and malignant pheochromocytomas.

Dannenberg H, De Krijger RR, van der Harst E, Abbou M, IJzendoorn Y, Komminoth P, Dinjens WN. Dannenberg H, et al. Among authors: dinjens wn. Int J Cancer. 2003 Jun 10;105(2):190-5. doi: 10.1002/ijc.11060. Int J Cancer. 2003. PMID: 12673678 Free article.

8

Microsatellite instability in a pleomorphic rhabdomyosarcoma in a patient with hereditary non-polyposis colorectal cancer.

den Bakker MA, Seynaeve C, Kliffen M, Dinjens WN. den Bakker MA, et al. Among authors: dinjens wn. Histopathology. 2003 Sep;43(3):297-9. doi: 10.1046/j.1365-2559.2003.01681.x. Histopathology. 2003. PMID: 12940783

9

Allelotype of 28 human breast cancer cell lines and xenografts.

Harkes IC, Elstrodt F, Dinjens WN, Molier M, Klijn JG, Berns EM, Schutte M. Harkes IC, et al. Among authors: dinjens wn. Br J Cancer. 2003 Dec 15;89(12):2289-92. doi: 10.1038/sj.bjc.6601448. Br J Cancer. 2003. PMID: 14676808 Free PMC article.

10

The CHEK2(*)1100delC mutation has no major contribution in oesophageal carcinogenesis.

Koppert LB, Schutte M, Abbou M, Tilanus HW, Dinjens WN. Koppert LB, et al. Among authors: dinjens wn. Br J Cancer. 2004 Feb 23;90(4):888-91. doi: 10.1038/sj.bjc.6601551. Br J Cancer. 2004. PMID: 14970869 Free PMC article.

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