Willemsen R - Search Results

1

Murine hippocampal neurons expressing Fmr1 gene premutations show early developmental deficits and late degeneration.

Chen Y, Tassone F, Berman RF, Hagerman PJ, Hagerman RJ, Willemsen R, Pessah IN. Chen Y, et al. Among authors: willemsen r. Hum Mol Genet. 2010 Jan 1;19(1):196-208. doi: 10.1093/hmg/ddp479. Hum Mol Genet. 2010. PMID: 19846466 Free PMC article.

2

Characterization of FMR1 proteins isolated from different tissues.

Verheij C, de Graaff E, Bakker CE, Willemsen R, Willems PJ, Meijer N, Galjaard H, Reuser AJ, Oostra BA, Hoogeveen AT. Verheij C, et al. Among authors: willemsen r. Hum Mol Genet. 1995 May;4(5):895-901. doi: 10.1093/hmg/4.5.895. Hum Mol Genet. 1995. PMID: 7633450

3

Normal phenotype in two brothers with a full FMR1 mutation.

Smeets HJ, Smits AP, Verheij CE, Theelen JP, Willemsen R, van de Burgt I, Hoogeveen AT, Oosterwijk JC, Oostra BA. Smeets HJ, et al. Among authors: willemsen r. Hum Mol Genet. 1995 Nov;4(11):2103-8. doi: 10.1093/hmg/4.11.2103. Hum Mol Genet. 1995. PMID: 8589687

4

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.

5

In vitro reactivation of the FMR1 gene involved in fragile X syndrome.

Chiurazzi P, Pomponi MG, Willemsen R, Oostra BA, Neri G. Chiurazzi P, et al. Among authors: willemsen r. Hum Mol Genet. 1998 Jan;7(1):109-13. doi: 10.1093/hmg/7.1.109. Hum Mol Genet. 1998. PMID: 9384610

6

Screening with the FMR1 protein test among mentally retarded males.

de Vries BB, Mohkamsing S, van den Ouweland AM, Halley DJ, Niermeijer MF, Oostra BA, Willemsen R. de Vries BB, et al. Among authors: willemsen r. Hum Genet. 1998 Oct;103(4):520-2. doi: 10.1007/s004390050860. Hum Genet. 1998. PMID: 9856500

7

FMRP expression as a potential prognostic indicator in fragile X syndrome.

Tassone F, Hagerman RJ, Iklé DN, Dyer PN, Lampe M, Willemsen R, Oostra BA, Taylor AK. Tassone F, et al. Among authors: willemsen r. Am J Med Genet. 1999 May 28;84(3):250-61. Am J Med Genet. 1999. PMID: 10331602

8

A fragile X case with an amplification/deletion mosaic pattern.

García Arocena D, de Diego Y, Oostra BA, Willemsen R, Mirta Rodriguez M. García Arocena D, et al. Among authors: willemsen r. Hum Genet. 2000 Mar;106(3):366-9. doi: 10.1007/s004390051052. Hum Genet. 2000. PMID: 10798369

9

Rapid FMR1-protein analysis of fetal blood: an enhancement of prenatal diagnostics.

Lambiris N, Peters H, Bollmann R, Leschik G, Leisti J, Salonen R, Cobet G, Oostra BA, Willemsen R. Lambiris N, et al. Among authors: willemsen r. Hum Genet. 1999 Sep;105(3):258-60. doi: 10.1007/s004390051098. Hum Genet. 1999. PMID: 10987654

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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