Brown WT - Search Results

1

Fmr1 knockout mouse has a distinctive strain-specific learning impairment.

Dobkin C, Rabe A, Dumas R, El Idrissi A, Haubenstock H, Brown WT. Dobkin C, et al. Among authors: brown wt. Neuroscience. 2000;100(2):423-9. doi: 10.1016/s0306-4522(00)00292-x. Neuroscience. 2000. PMID: 11008180

2

Decreased GABA(A) receptor expression in the seizure-prone fragile X mouse.

El Idrissi A, Ding XH, Scalia J, Trenkner E, Brown WT, Dobkin C. El Idrissi A, et al. Among authors: brown wt. Neurosci Lett. 2005 Apr 4;377(3):141-6. doi: 10.1016/j.neulet.2004.11.087. Epub 2004 Dec 23. Neurosci Lett. 2005. PMID: 15755515

3

Neuroendocrine alterations in the fragile X mouse.

El Idrissi A, Yan X, L'Amoreaux W, Brown WT, Dobkin C. El Idrissi A, et al. Among authors: brown wt. Results Probl Cell Differ. 2012;54:201-21. doi: 10.1007/978-3-642-21649-7_11. Results Probl Cell Differ. 2012. PMID: 22009354

4

Molecular analysis of fragile X syndrome.

Nolin SL, Dobkin C, Brown WT. Nolin SL, et al. Among authors: brown wt. Curr Protoc Hum Genet. 2003 Nov;Chapter 9:Unit9.5. doi: 10.1002/0471142905.hg0905s38. Curr Protoc Hum Genet. 2003. PMID: 18428348

5

Pulsed-field gradient-gel studies around the fragile site.

Dobkin CS, Brown WT. Dobkin CS, et al. Among authors: brown wt. Am J Med Genet. 1988 May-Jun;30(1-2):593-600. doi: 10.1002/ajmg.1320300160. Am J Med Genet. 1988. PMID: 2902798

6

Mosaicism for the FMR1 gene influences adaptive skills development in fragile X-affected males.

Cohen IL, Nolin SL, Sudhalter V, Ding XH, Dobkin CS, Brown WT. Cohen IL, et al. Among authors: brown wt. Am J Med Genet. 1996 Aug 9;64(2):365-9. doi: 10.1002/(SICI)1096-8628(19960809)64:2<365::AID-AJMG26>3.0.CO;2-C. Am J Med Genet. 1996. PMID: 8844082

7

Reduced mRNA for G3BP in fragile X cells: evidence of FMR1 gene regulation.

Zhong N, Ju W, Nelson D, Dobkin C, Brown WT. Zhong N, et al. Among authors: brown wt. Am J Med Genet. 1999 May 28;84(3):268-71. doi: 10.1002/(sici)1096-8628(19990528)84:3<268::aid-ajmg20>3.0.co;2-#. Am J Med Genet. 1999. PMID: 10331605

8

Upregulation of beta-catenin expression in down syndrome model Ts65Dn mouse brain.

Ramakrishna N, Meeker HC, Li S, Brown WT, Rao R, El Idrissi A. Ramakrishna N, et al. Among authors: brown wt. Neuroscience. 2009 Jun 30;161(2):451-8. doi: 10.1016/j.neuroscience.2009.03.049. Epub 2009 Mar 26. Neuroscience. 2009. PMID: 19328224

9

Fragile X gene instability: anchoring AGGs and linked microsatellites.

Zhong N, Yang W, Dobkin C, Brown WT. Zhong N, et al. Among authors: brown wt. Am J Hum Genet. 1995 Aug;57(2):351-61. Am J Hum Genet. 1995. PMID: 7668261 Free PMC article.

10

Fragile X prenatal analyses show full mutation females at high risk for mosaic Turner syndrome: fragile X leads to chromosome loss.

Dobkin C, Radu G, Ding XH, Brown WT, Nolin SL. Dobkin C, et al. Among authors: brown wt. Am J Med Genet A. 2009 Oct;149A(10):2152-7. doi: 10.1002/ajmg.a.33011. Am J Med Genet A. 2009. PMID: 19764037

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