Willemsen R - Search Results

1

Nuclear organization of active and inactive chromatin domains uncovered by chromosome conformation capture-on-chip (4C).

Simonis M, Klous P, Splinter E, Moshkin Y, Willemsen R, de Wit E, van Steensel B, de Laat W. Simonis M, et al. Among authors: willemsen r. Nat Genet. 2006 Nov;38(11):1348-54. doi: 10.1038/ng1896. Epub 2006 Oct 8. Nat Genet. 2006. PMID: 17033623

2

Mutations in SMAD3 cause a syndromic form of aortic aneurysms and dissections with early-onset osteoarthritis.

van de Laar IM, Oldenburg RA, Pals G, Roos-Hesselink JW, de Graaf BM, Verhagen JM, Hoedemaekers YM, Willemsen R, Severijnen LA, Venselaar H, Vriend G, Pattynama PM, Collée M, Majoor-Krakauer D, Poldermans D, Frohn-Mulder IM, Micha D, Timmermans J, Hilhorst-Hofstee Y, Bierma-Zeinstra SM, Willems PJ, Kros JM, Oei EH, Oostra BA, Wessels MW, Bertoli-Avella AM. van de Laar IM, et al. Among authors: willemsen r. Nat Genet. 2011 Feb;43(2):121-6. doi: 10.1038/ng.744. Epub 2011 Jan 9. Nat Genet. 2011. PMID: 21217753

3

Characterization and localization of the FMR-1 gene product associated with fragile X syndrome.

Verheij C, Bakker CE, de Graaff E, Keulemans J, Willemsen R, Verkerk AJ, Galjaard H, Reuser AJ, Hoogeveen AT, Oostra BA. Verheij C, et al. Among authors: willemsen r. Nature. 1993 Jun 24;363(6431):722-4. doi: 10.1038/363722a0. Nature. 1993. PMID: 8515814

4

Variable FMR1 gene methylation of large expansions leads to variable phenotype in three males from one fragile X family.

de Vries BB, Jansen CC, Duits AA, Verheij C, Willemsen R, van Hemel JO, van den Ouweland AM, Niermeijer MF, Oostra BA, Halley DJ. de Vries BB, et al. Among authors: willemsen r. J Med Genet. 1996 Dec;33(12):1007-10. doi: 10.1136/jmg.33.12.1007. J Med Genet. 1996. PMID: 9004132 Free PMC article. Review.

5

Rapid antibody test for prenatal diagnosis of fragile X syndrome on amniotic fluid cells: a new appraisal.

Willemsen R, Los F, Mohkamsing S, van den Ouweland A, Deelen W, Galjaard H, Oostra B. Willemsen R, et al. J Med Genet. 1997 Mar;34(3):250-1. doi: 10.1136/jmg.34.3.250. J Med Genet. 1997. PMID: 9132500 Free PMC article.

6

Differential expression of FMR1, FXR1 and FXR2 proteins in human brain and testis.

Tamanini F, Willemsen R, van Unen L, Bontekoe C, Galjaard H, Oostra BA, Hoogeveen AT. Tamanini F, et al. Among authors: willemsen r. Hum Mol Genet. 1997 Aug;6(8):1315-22. doi: 10.1093/hmg/6.8.1315. Hum Mol Genet. 1997. PMID: 9259278 Free article.

7

Different targets for the fragile X-related proteins revealed by their distinct nuclear localizations.

Tamanini F, Bontekoe C, Bakker CE, van Unen L, Anar B, Willemsen R, Yoshida M, Galjaard H, Oostra BA, Hoogeveen AT. Tamanini F, et al. Among authors: willemsen r. Hum Mol Genet. 1999 May;8(5):863-9. doi: 10.1093/hmg/8.5.863. Hum Mol Genet. 1999. PMID: 10196376 Free article.

8

Knockout mouse model for Fxr2: a model for mental retardation.

Bontekoe CJ, McIlwain KL, Nieuwenhuizen IM, Yuva-Paylor LA, Nellis A, Willemsen R, Fang Z, Kirkpatrick L, Bakker CE, McAninch R, Cheng NC, Merriweather M, Hoogeveen AT, Nelson D, Paylor R, Oostra BA. Bontekoe CJ, et al. Among authors: willemsen r. Hum Mol Genet. 2002 Mar 1;11(5):487-98. doi: 10.1093/hmg/11.5.487. Hum Mol Genet. 2002. PMID: 11875043

9

Timing of the absence of FMR1 expression in full mutation chorionic villi.

Willemsen R, Bontekoe CJ, Severijnen LA, Oostra BA. Willemsen R, et al. Hum Genet. 2002 Jun;110(6):601-5. doi: 10.1007/s00439-002-0723-5. Epub 2002 Apr 16. Hum Genet. 2002. PMID: 12107447

10

The FMR1 CGG repeat mouse displays ubiquitin-positive intranuclear neuronal inclusions; implications for the cerebellar tremor/ataxia syndrome.

Willemsen R, Hoogeveen-Westerveld M, Reis S, Holstege J, Severijnen LA, Nieuwenhuizen IM, Schrier M, van Unen L, Tassone F, Hoogeveen AT, Hagerman PJ, Mientjes EJ, Oostra BA. Willemsen R, et al. Hum Mol Genet. 2003 May 1;12(9):949-59. doi: 10.1093/hmg/ddg114. Hum Mol Genet. 2003. PMID: 12700164 Free article.

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