Nelson DL - Search Results

1

The generation of a conditional Fmr1 knock out mouse model to study Fmrp function in vivo.

Mientjes EJ, Nieuwenhuizen I, Kirkpatrick L, Zu T, Hoogeveen-Westerveld M, Severijnen L, Rifé M, Willemsen R, Nelson DL, Oostra BA. Mientjes EJ, et al. Among authors: nelson dl. Neurobiol Dis. 2006 Mar;21(3):549-55. doi: 10.1016/j.nbd.2005.08.019. Epub 2005 Oct 26. Neurobiol Dis. 2006. PMID: 16257225

2

Rescue of behavioral phenotype and neuronal protrusion morphology in Fmr1 KO mice.

de Vrij FM, Levenga J, van der Linde HC, Koekkoek SK, De Zeeuw CI, Nelson DL, Oostra BA, Willemsen R. de Vrij FM, et al. Among authors: nelson dl. Neurobiol Dis. 2008 Jul;31(1):127-32. doi: 10.1016/j.nbd.2008.04.002. Epub 2008 Apr 25. Neurobiol Dis. 2008. PMID: 18571098 Free PMC article.

3

Ultrastructural analysis of the functional domains in FMRP using primary hippocampal mouse neurons.

Levenga J, Buijsen RA, Rifé M, Moine H, Nelson DL, Oostra BA, Willemsen R, de Vrij FM. Levenga J, et al. Among authors: nelson dl. Neurobiol Dis. 2009 Aug;35(2):241-50. doi: 10.1016/j.nbd.2009.05.004. Epub 2009 May 21. Neurobiol Dis. 2009. PMID: 19464371 Free PMC article.

4

AFQ056, a new mGluR5 antagonist for treatment of fragile X syndrome.

Levenga J, Hayashi S, de Vrij FM, Koekkoek SK, van der Linde HC, Nieuwenhuizen I, Song C, Buijsen RA, Pop AS, Gomezmancilla B, Nelson DL, Willemsen R, Gasparini F, Oostra BA. Levenga J, et al. Among authors: nelson dl. Neurobiol Dis. 2011 Jun;42(3):311-7. doi: 10.1016/j.nbd.2011.01.022. Epub 2011 Feb 21. Neurobiol Dis. 2011. PMID: 21316452

5

Fxr1 knockout mice show a striated muscle phenotype: implications for Fxr1p function in vivo.

Mientjes EJ, Willemsen R, Kirkpatrick LL, Nieuwenhuizen IM, Hoogeveen-Westerveld M, Verweij M, Reis S, Bardoni B, Hoogeveen AT, Oostra BA, Nelson DL. Mientjes EJ, et al. Among authors: nelson dl. Hum Mol Genet. 2004 Jul 1;13(13):1291-302. doi: 10.1093/hmg/ddh150. Epub 2004 May 5. Hum Mol Genet. 2004. PMID: 15128702

6

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: nelson dl. Neuron. 2005 Aug 4;47(3):339-52. doi: 10.1016/j.neuron.2005.07.005. Neuron. 2005. PMID: 16055059 Free article.

7

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: nelson dl. 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.

8

The GABAA receptor is an FMRP target with therapeutic potential in fragile X syndrome.

Braat S, D'Hulst C, Heulens I, De Rubeis S, Mientjes E, Nelson DL, Willemsen R, Bagni C, Van Dam D, De Deyn PP, Kooy RF. Braat S, et al. Among authors: nelson dl. Cell Cycle. 2015;14(18):2985-95. doi: 10.4161/15384101.2014.989114. Cell Cycle. 2015. PMID: 25790165 Free PMC article.

9

Loss of mutation at the FMR1 locus through multiple exchanges between maternal X chromosomes.

van den Ouweland AM, Deelen WH, Kunst CB, Uzielli ML, Nelson DL, Warren ST, Oostra BA, Halley DJ. van den Ouweland AM, et al. Among authors: nelson dl. Hum Mol Genet. 1994 Oct;3(10):1823-7. doi: 10.1093/hmg/3.10.1823. Hum Mol Genet. 1994. PMID: 7849707

10

Alternative splicing in the murine and human FXR1 genes.

Kirkpatrick LL, McIlwain KA, Nelson DL. Kirkpatrick LL, et al. Among authors: nelson dl. Genomics. 1999 Jul 15;59(2):193-202. doi: 10.1006/geno.1999.5868. Genomics. 1999. PMID: 10409431

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