de Bruijn D - Search Results

1

LRFN5 locus structure is associated with autism and influenced by the sex of the individual and locus conversions.

Lybaek H, Robson M, de Leeuw N, Hehir-Kwa JY, Jeffries A, Haukanes BI, Berland S, de Bruijn D, Mundlos S, Spielmann M, Houge G. Lybaek H, et al. Among authors: de bruijn d. Autism Res. 2022 Mar;15(3):421-433. doi: 10.1002/aur.2677. Epub 2022 Jan 28. Autism Res. 2022. PMID: 35088940 Free PMC article.

2

Severe Progressive Autism Associated with Two de novo Changes: A 2.6-Mb 2q31.1 Deletion and a Balanced t(14;21)(q21.1;p11.2) Translocation with Long-Range Epigenetic Silencing of LRFN5 Expression.

de Bruijn DR, van Dijk AH, Pfundt R, Hoischen A, Merkx GF, Gradek GA, Lybæk H, Stray-Pedersen A, Brunner HG, Houge G. de Bruijn DR, et al. Mol Syndromol. 2010 Feb;1(1):46-57. doi: 10.1159/000280290. Epub 2010 Feb 12. Mol Syndromol. 2010. PMID: 20648246 Free PMC article.

3

RevSex duplication-induced and sex-related differences in the SOX9 regulatory region chromatin landscape in human fibroblasts.

Lybæk H, de Bruijn D, den Engelsman-van Dijk AH, Vanichkina D, Nepal C, Brendehaug A, Houge G. Lybæk H, et al. Among authors: de bruijn d. Epigenetics. 2014 Mar;9(3):416-27. doi: 10.4161/epi.27474. Epub 2013 Dec 18. Epigenetics. 2014. PMID: 24351654 Free PMC article.

4

The synovial-sarcoma-associated SS18-SSX2 fusion protein induces epigenetic gene (de)regulation.

de Bruijn DR, Allander SV, van Dijk AH, Willemse MP, Thijssen J, van Groningen JJ, Meltzer PS, van Kessel AG. de Bruijn DR, et al. Cancer Res. 2006 Oct 1;66(19):9474-82. doi: 10.1158/0008-5472.CAN-05-3726. Cancer Res. 2006. PMID: 17018603

5

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

6

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

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

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.

9

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

10

Construction of a 350-kb sequence-ready 11q13 cosmid contig encompassing the markers D11S4933 and D11S546: mapping of 11 genes and 3 tumor-associated translocation breakpoints.

van Asseldonk M, Schepens M, de Bruijn D, Janssen B, Merkx G, Geurts van Kessel A. van Asseldonk M, et al. Among authors: de bruijn d. Genomics. 2000 May 15;66(1):35-42. doi: 10.1006/geno.2000.6194. Genomics. 2000. PMID: 10843802

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