Oostra BA - Search Results

1

No apparent involvement of the FMR1 gene in five patients with phenotypic manifestations of the fragile X syndrome.

Chiurazzi P, de Graaff E, Ng J, Verkerk AJ, Wolfson S, Fisch GS, Kozak L, Neri G, Oostra BA. Chiurazzi P, et al. Among authors: oostra ba. Am J Med Genet. 1994 Jul 15;51(4):309-14. doi: 10.1002/ajmg.1320510405. Am J Med Genet. 1994. PMID: 7942992

2

Fragile X founder chromosomes in Italy: a few initial events and possible explanation for their heterogeneity.

Chiurazzi P, Genuardi M, Kozak L, Giovannucci-Uzielli ML, Bussani C, Dagna-Bricarelli F, Grasso M, Perroni L, Sebastio G, Sperandeo MP, Oostra BA, Neri G. Chiurazzi P, et al. Among authors: oostra ba. Am J Med Genet. 1996 Jul 12;64(1):209-15. doi: 10.1002/(SICI)1096-8628(19960712)64:1<209::AID-AJMG38>3.0.CO;2-P. Am J Med Genet. 1996. PMID: 8826478

3

Extended gene diversity at the FMR1 locus and neighbouring CA repeats in a sub-Saharan population.

Chiurazzi P, Destro-Bisol G, Genuardi M, Oostra BA, Spedini G, Neri G. Chiurazzi P, et al. Among authors: oostra ba. Am J Med Genet. 1996 Jul 12;64(1):216-9. doi: 10.1002/(SICI)1096-8628(19960712)64:1<216::AID-AJMG39>3.0.CO;2-O. Am J Med Genet. 1996. PMID: 8826479

4

The fragile X phenotype in a mosaic male with a deletion showing expression of the FMR1 protein in 28% of the cells.

de Graaff E, de Vries BB, Willemsen R, van Hemel JO, Mohkamsing S, Oostra BA, van den Ouweland AM. de Graaff E, et al. Among authors: oostra ba. Am J Med Genet. 1996 Aug 9;64(2):302-8. doi: 10.1002/(SICI)1096-8628(19960809)64:2<302::AID-AJMG14>3.0.CO;2-J. Am J Med Genet. 1996. PMID: 8844070

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: oostra ba. Hum Mol Genet. 1998 Jan;7(1):109-13. doi: 10.1093/hmg/7.1.109. Hum Mol Genet. 1998. PMID: 9384610

6

Learning and memory in the FMR1 knockout mouse.

Fisch GS, Hao HK, Bakker C, Oostra BA. Fisch GS, et al. Among authors: oostra ba. Am J Med Genet. 1999 May 28;84(3):277-82. doi: 10.1002/(sici)1096-8628(19990528)84:3<277::aid-ajmg22>3.0.co;2-w. Am J Med Genet. 1999. PMID: 10331607

7

Synergistic effect of histone hyperacetylation and DNA demethylation in the reactivation of the FMR1 gene.

Chiurazzi P, Pomponi MG, Pietrobono R, Bakker CE, Neri G, Oostra BA. Chiurazzi P, et al. Among authors: oostra ba. Hum Mol Genet. 1999 Nov;8(12):2317-23. doi: 10.1093/hmg/8.12.2317. Hum Mol Genet. 1999. PMID: 10545613

8

The fragile X gene and its function.

Oostra BA, Chiurazzi P. Oostra BA, et al. Clin Genet. 2001 Dec;60(6):399-408. doi: 10.1034/j.1399-0004.2001.600601.x. Clin Genet. 2001. PMID: 11846731 Review.

9

Limited size of the fragile X site shown by fluorescence in situ hybridization.

Verkerk AJ, Eussen BH, Van Hemel JO, Oostra BA. Verkerk AJ, et al. Among authors: oostra ba. Am J Med Genet. 1992 Apr 15-May 1;43(1-2):187-91. doi: 10.1002/ajmg.1320430131. Am J Med Genet. 1992. PMID: 1605191

10

Intragenic probe used for diagnostics in fragile X families.

Verkerk AJ, deVries BB, Niermeijer MF, Fu YH, Nelson DL, Warren ST, Majoor-Krakauer DF, Halley DJ, Oostra BA. Verkerk AJ, et al. Among authors: oostra ba. Am J Med Genet. 1992 Apr 15-May 1;43(1-2):192-6. doi: 10.1002/ajmg.1320430132. Am J Med Genet. 1992. PMID: 1605192

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