Dinjens WNM - Search Results

1

RET Fluorescence In Situ Hybridization Analysis Is a Sensitive but Highly Unspecific Screening Method for RET Fusions in Lung Cancer.

Radonic T, Geurts-Giele WRR, Samsom KG, Roemen GMJM, von der Thüsen JH, Thunnissen E, Meijssen IC, Sleddens HFBM, Dinjens WNM, Boelens MC, Weijers K, Speel EJM, Finn SP, O'Brien C, van Wezel T, Cohen D, Monkhorst K, Roepman P, Dubbink HJ. Radonic T, et al. Among authors: dinjens wnm. J Thorac Oncol. 2021 May;16(5):798-806. doi: 10.1016/j.jtho.2021.01.1619. Epub 2021 Feb 12. J Thorac Oncol. 2021. PMID: 33588111 Free article.

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. Cancer Res. 1994 Dec 1;54(23):6061-4. Cancer Res. 1994. PMID: 7954446

3

Molecular assessment of clonality leads to the identification of a new germ line TP53 mutation associated with malignant cystosarcoma phyllodes and soft tissue sarcoma.

Bot FJ, Sleddens HF, Dinjens WN. Bot FJ, et al. Diagn Mol Pathol. 1998 Dec;7(6):295-301. doi: 10.1097/00019606-199812000-00002. Diagn Mol Pathol. 1998. PMID: 10207667

4

Losses of chromosomes 1p and 3q are early genetic events in the development of sporadic pheochromocytomas.

Dannenberg H, Speel EJ, Zhao J, Saremaslani P, van Der Harst E, Roth J, Heitz PU, Bonjer HJ, Dinjens WN, Mooi WJ, Komminoth P, de Krijger RR. Dannenberg H, et al. Am J Pathol. 2000 Aug;157(2):353-9. doi: 10.1016/S0002-9440(10)64547-6. Am J Pathol. 2000. PMID: 10934139 Free PMC article.

5

Establishment of cell lines from adenocarcinomas of the esophagus and gastric cardia growing in vivo and in vitro.

de Both NJ, Wijnhoven BP, Sleddens HF, Tilanus HW, Dinjens WN. de Both NJ, et al. Virchows Arch. 2001 May;438(5):451-6. doi: 10.1007/s004280000358. Virchows Arch. 2001. PMID: 11407472

6

Determination of the molecular relationship between multiple tumors within one patient is of clinical importance.

van der Sijp JR, van Meerbeeck JP, Maat AP, Zondervan PE, Sleddens HF, van Geel AN, Eggermont AM, Dinjens WN. van der Sijp JR, et al. J Clin Oncol. 2002 Feb 15;20(4):1105-14. doi: 10.1200/JCO.2002.20.4.1105. J Clin Oncol. 2002. PMID: 11844836

7

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.

8

p53 alterations and their relationship to SDHD mutations in parasympathetic paragangliomas.

van Nederveen FH, Dannenberg H, Sleddens HF, de Krijger RR, Dinjens WN. van Nederveen FH, et al. Mod Pathol. 2003 Sep;16(9):849-56. doi: 10.1097/01.MP.0000084111.03922.4D. Mod Pathol. 2003. PMID: 13679447

9

Molecular genetic alterations in adrenal and extra-adrenal pheochromocytomas and paragangliomas.

Dannenberg H, Komminoth P, Dinjens WN, Speel EJ, de Krijger RR. Dannenberg H, et al. Endocr Pathol. 2003 Winter;14(4):329-50. doi: 10.1385/ep:14:4:329. Endocr Pathol. 2003. PMID: 14739490 Review.

10

Microarray-based CGH of sporadic and syndrome-related pheochromocytomas using a 0.1-0.2 Mb bacterial artificial chromosome array spanning chromosome arm 1p.

Aarts M, Dannenberg H, deLeeuw RJ, van Nederveen FH, Verhofstad AA, Lenders JW, Dinjens WN, Speel EJ, Lam WL, de Krijger RR. Aarts M, et al. Genes Chromosomes Cancer. 2006 Jan;45(1):83-93. doi: 10.1002/gcc.20268. Genes Chromosomes Cancer. 2006. PMID: 16215979

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