Bakker CE - Search Results

1

Deletion of FMR1 in Purkinje cells enhances parallel fiber LTD, enlarges spines, and attenuates cerebellar eyelid conditioning in Fragile X syndrome.

Koekkoek SK, Yamaguchi K, Milojkovic BA, Dortland BR, Ruigrok TJ, Maex R, De Graaf W, Smit AE, VanderWerf F, Bakker CE, Willemsen R, Ikeda T, Kakizawa S, Onodera K, Nelson DL, Mientjes E, Joosten M, De Schutter E, Oostra BA, Ito M, De Zeeuw CI. Koekkoek SK, et al. Among authors: bakker ce. Neuron. 2005 Aug 4;47(3):339-52. doi: 10.1016/j.neuron.2005.07.005. Neuron. 2005. PMID: 16055059 Free article.

2

Understanding fragile X syndrome: insights from animal models.

Bakker CE, Oostra BA. Bakker CE, et al. Cytogenet Genome Res. 2003;100(1-4):111-23. doi: 10.1159/000072845. Cytogenet Genome Res. 2003. PMID: 14526171 Review.

3

Elevated Fmr1 mRNA levels and reduced protein expression in a mouse model with an unmethylated Fragile X full mutation.

Brouwer JR, Mientjes EJ, Bakker CE, Nieuwenhuizen IM, Severijnen LA, Van der Linde HC, Nelson DL, Oostra BA, Willemsen R. Brouwer JR, et al. Among authors: bakker ce. Exp Cell Res. 2007 Jan 15;313(2):244-53. doi: 10.1016/j.yexcr.2006.10.002. Epub 2006 Oct 13. Exp Cell Res. 2007. PMID: 17150213 Free PMC article.

4

Exceptional good cognitive and phenotypic profile in a male carrying a mosaic mutation in the FMR1 gene.

Govaerts LC, Smit AE, Saris JJ, VanderWerf F, Willemsen R, Bakker CE, De Zeeuw CI, Oostra BA. Govaerts LC, et al. Among authors: bakker ce. Clin Genet. 2007 Aug;72(2):138-44. doi: 10.1111/j.1399-0004.2007.00829.x. Clin Genet. 2007. PMID: 17661818

5

Altered differentiation of neural stem cells in fragile X syndrome.

Castrén M, Tervonen T, Kärkkäinen V, Heinonen S, Castrén E, Larsson K, Bakker CE, Oostra BA, Akerman K. Castrén M, et al. Among authors: bakker ce. Proc Natl Acad Sci U S A. 2005 Dec 6;102(49):17834-9. doi: 10.1073/pnas.0508995102. Epub 2005 Nov 28. Proc Natl Acad Sci U S A. 2005. PMID: 16314562 Free PMC article.

6

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: bakker ce. Hum Mol Genet. 1995 May;4(5):895-901. doi: 10.1093/hmg/4.5.895. Hum Mol Genet. 1995. PMID: 7633450

7

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: bakker ce. Nature. 1993 Jun 24;363(6431):722-4. doi: 10.1038/363722a0. Nature. 1993. PMID: 8515814

8

Macroorchidism in FMR1 knockout mice is caused by increased Sertoli cell proliferation during testicular development.

Slegtenhorst-Eegdeman KE, de Rooij DG, Verhoef-Post M, van de Kant HJ, Bakker CE, Oostra BA, Grootegoed JA, Themmen AP. Slegtenhorst-Eegdeman KE, et al. Among authors: bakker ce. Endocrinology. 1998 Jan;139(1):156-62. doi: 10.1210/endo.139.1.5706. Endocrinology. 1998. PMID: 9421410 Free article.

9

No evidence for disruption of normal patterns of mRNA localization in dendrites or dendritic transport of recently synthesized mRNA in FMR1 knockout mice, a model for human fragile-X mental retardation syndrome.

Steward O, Bakker CE, Willems PJ, Oostra BA. Steward O, et al. Among authors: bakker ce. Neuroreport. 1998 Feb 16;9(3):477-81. doi: 10.1097/00001756-199802160-00022. Neuroreport. 1998. PMID: 9512393

10

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: bakker ce. Hum Mol Genet. 1999 May;8(5):863-9. doi: 10.1093/hmg/8.5.863. Hum Mol Genet. 1999. PMID: 10196376 Free article.

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