de Bruijn D - Search Results

1

Demonstration of a new pathogenic mutation in human complex I deficiency: a 5-bp duplication in the nuclear gene encoding the 18-kD (AQDQ) subunit.

van den Heuvel L, Ruitenbeek W, Smeets R, Gelman-Kohan Z, Elpeleg O, Loeffen J, Trijbels F, Mariman E, de Bruijn D, Smeitink J. van den Heuvel L, et al. Among authors: de bruijn d. Am J Hum Genet. 1998 Feb;62(2):262-8. doi: 10.1086/301716. Am J Hum Genet. 1998. PMID: 9463323 Free PMC article.

2

Nuclear localization of SYT, SSX and the synovial sarcoma-associated SYT-SSX fusion proteins.

dos Santos NR, de Bruijn DR, Balemans M, Janssen B, Gärtner F, Lopes JM, de Leeuw B, Geurts van Kessel A. dos Santos NR, et al. Among authors: de bruijn dr, de leeuw b. Hum Mol Genet. 1997 Sep;6(9):1549-58. doi: 10.1093/hmg/6.9.1549. Hum Mol Genet. 1997. PMID: 9285793

3

Mapping and characterization of the mouse and human SS18 genes, two human SS18-like genes and a mouse Ss18 pseudogene.

de Bruijn DR, Kater-Baats E, Eleveld M, Merkx G, Geurts Van Kessel A. de Bruijn DR, et al. Cytogenet Cell Genet. 2001;92(3-4):310-9. doi: 10.1159/000056920. Cytogenet Cell Genet. 2001. PMID: 11435705

4

Targeted disruption of the synovial sarcoma-associated SS18 gene causes early embryonic lethality and affects PPARBP expression.

de Bruijn DR, Peters WJ, Chuva de Sousa Lopes SM, van Dijk AH, Willemse MP, Pfundt R, de Boer P, Geurts van Kessel A. de Bruijn DR, et al. Among authors: de boer p. Hum Mol Genet. 2006 Oct 1;15(19):2936-44. doi: 10.1093/hmg/ddl235. Epub 2006 Aug 22. Hum Mol Genet. 2006. PMID: 16926188

5

Molecular cytogenetics of bone and soft tissue tumors.

Geurts van Kessel A, dos Santos NR, Simons A, de Bruijn D, Forus A, Fodstad O, Myklebost O, Balemans M, Baats E, Olde Weghuis D, Suijkerbuijk RF, van den Berg E, Molenaar WM, de Leeuw B. Geurts van Kessel A, et al. Among authors: de leeuw b, de bruijn d. Cancer Genet Cytogenet. 1997 May;95(1):67-73. doi: 10.1016/s0165-4608(96)00241-5. Cancer Genet Cytogenet. 1997. PMID: 9140455 Free article. Review. No abstract available.

6

Disruption of the gene Euchromatin Histone Methyl Transferase1 (Eu-HMTase1) is associated with the 9q34 subtelomeric deletion syndrome.

Kleefstra T, Smidt M, Banning MJ, Oudakker AR, Van Esch H, de Brouwer AP, Nillesen W, Sistermans EA, Hamel BC, de Bruijn D, Fryns JP, Yntema HG, Brunner HG, de Vries BB, van Bokhoven H. Kleefstra T, et al. Among authors: de brouwer ap, de vries bb, de bruijn d. J Med Genet. 2005 Apr;42(4):299-306. doi: 10.1136/jmg.2004.028464. J Med Genet. 2005. PMID: 15805155 Free PMC article.

7

Assignment of the human adipocyte fatty acid-binding protein gene (FABP4) to chromosome 8q21 using somatic cell hybrid and fluorescence in situ hybridization techniques.

Prinsen CF, de Bruijn DR, Merkx GF, Veerkamp JH. Prinsen CF, et al. Among authors: de bruijn dr. Genomics. 1997 Feb 15;40(1):207-9. doi: 10.1006/geno.1996.4534. Genomics. 1997. PMID: 9070949 Free article. No abstract available.

8

The human TRIDENT/HFH-11/FKHL16 gene: structure, localization, and promoter characterization.

Korver W, Roose J, Heinen K, Weghuis DO, de Bruijn D, van Kessel AG, Clevers H. Korver W, et al. Among authors: de bruijn d. Genomics. 1997 Dec 15;46(3):435-42. doi: 10.1006/geno.1997.5065. Genomics. 1997. PMID: 9441747

9

de Bruijn DR, dos Santos NR, Kater-Baats E, Thijssen J, van den Berk L, Stap J, Balemans M, Schepens M, Merkx G, van Kessel AG. de Bruijn DR, et al. Genes Chromosomes Cancer. 2002 Jul;34(3):285-98. doi: 10.1002/gcc.10073. Genes Chromosomes Cancer. 2002. PMID: 12007189

10

Towards the isolation of a human malignant extragonadal germ cell tumour-associated breakpoint in chromosome 11q13.

Sinke RJ, van Asseldonk M, de Bruijn D, Strijk JA, Merkx G, Olde Weghuis D, de Jong B, Oosterhuis JW, Geurts van Kessel A. Sinke RJ, et al. Among authors: de jong b, de bruijn d. APMIS. 1998 Jan;106(1):73-8; discussion 78-9. doi: 10.1111/j.1699-0463.1998.tb01321.x. APMIS. 1998. PMID: 9524564

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