Oostra BA - Search Results

1

Differential epigenetic modifications in the FMR1 gene of the fragile X syndrome after reactivating pharmacological treatments.

Tabolacci E, Pietrobono R, Moscato U, Oostra BA, Chiurazzi P, Neri G. Tabolacci E, et al. Among authors: oostra ba. Eur J Hum Genet. 2005 May;13(5):641-8. doi: 10.1038/sj.ejhg.5201393. Eur J Hum Genet. 2005. PMID: 15741991

2

Quantitative analysis of DNA demethylation and transcriptional reactivation of the FMR1 gene in fragile X cells treated with 5-azadeoxycytidine.

Pietrobono R, Pomponi MG, Tabolacci E, Oostra B, Chiurazzi P, Neri G. Pietrobono R, et al. Nucleic Acids Res. 2002 Jul 15;30(14):3278-85. doi: 10.1093/nar/gkf434. Nucleic Acids Res. 2002. PMID: 12136110 Free PMC article.

3

Molecular dissection of the events leading to inactivation of the FMR1 gene.

Pietrobono R, Tabolacci E, Zalfa F, Zito I, Terracciano A, Moscato U, Bagni C, Oostra B, Chiurazzi P, Neri G. Pietrobono R, et al. Hum Mol Genet. 2005 Jan 15;14(2):267-77. doi: 10.1093/hmg/ddi024. Epub 2004 Nov 24. Hum Mol Genet. 2005. PMID: 15563507

4

Understanding the biological underpinnings of fragile X syndrome.

Chiurazzi P, Neri G, Oostra BA. Chiurazzi P, et al. Among authors: oostra ba. Curr Opin Pediatr. 2003 Dec;15(6):559-66. doi: 10.1097/00008480-200312000-00003. Curr Opin Pediatr. 2003. PMID: 14631199 Review.

5

A fragile balance: FMR1 expression levels.

Oostra BA, Willemsen R. Oostra BA, et al. Hum Mol Genet. 2003 Oct 15;12 Spec No 2:R249-57. doi: 10.1093/hmg/ddg298. Epub 2003 Sep 2. Hum Mol Genet. 2003. PMID: 12952862 Review.

6

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

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

7

Instability of the CGG repeat and expression of the FMR1 protein in a male fragile X patient with a lung tumor.

de Graaff E, Willemsen R, Zhong N, de Die-Smulders CE, Brown WT, Freling G, Oostra B. de Graaff E, et al. Am J Hum Genet. 1995 Sep;57(3):609-18. Am J Hum Genet. 1995. PMID: 7668289 Free PMC article.

8

Apparent regression of the CGG repeat in FMR1 to an allele of normal size.

Vits L, De Boulle K, Reyniers E, Handig I, Darby JK, Oostra B, Willems PJ. Vits L, et al. Hum Genet. 1994 Nov;94(5):523-6. doi: 10.1007/BF00211019. Hum Genet. 1994. PMID: 7959688

9

Fragile X syndrome: From protein function to therapy.

Bagni C, Oostra BA. Bagni C, et al. Among authors: oostra ba. Am J Med Genet A. 2013 Nov;161A(11):2809-21. doi: 10.1002/ajmg.a.36241. Epub 2013 Sep 24. Am J Med Genet A. 2013. PMID: 24115651 Review.

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. Among authors: oostra ba. 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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