Nelson DL - Search Results

1

RNA-binding proteins hnRNP A2/B1 and CUGBP1 suppress fragile X CGG premutation repeat-induced neurodegeneration in a Drosophila model of FXTAS.

Sofola OA, Jin P, Qin Y, Duan R, Liu H, de Haro M, Nelson DL, Botas J. Sofola OA, et al. Among authors: nelson dl. Neuron. 2007 Aug 16;55(4):565-71. doi: 10.1016/j.neuron.2007.07.021. Neuron. 2007. PMID: 17698010 Free PMC article.

2

Evolution of the cryptic FMR1 CGG repeat.

Eichler EE, Kunst CB, Lugenbeel KA, Ryder OA, Davison D, Warren ST, Nelson DL. Eichler EE, et al. Among authors: nelson dl. Nat Genet. 1995 Nov;11(3):301-8. doi: 10.1038/ng1195-301. Nat Genet. 1995. PMID: 7581454

3

The fragile X syndromes.

Nelson DL. Nelson DL. Semin Cell Biol. 1995 Feb;6(1):5-11. doi: 10.1016/1043-4682(95)90009-8. Semin Cell Biol. 1995. PMID: 7620122 Review.

4

Intragenic loss of function mutations demonstrate the primary role of FMR1 in fragile X syndrome.

Lugenbeel KA, Peier AM, Carson NL, Chudley AE, Nelson DL. Lugenbeel KA, et al. Among authors: nelson dl. Nat Genet. 1995 Aug;10(4):483-5. doi: 10.1038/ng0895-483. Nat Genet. 1995. PMID: 7670500

5

Length of uninterrupted CGG repeats determines instability in the FMR1 gene.

Eichler EE, Holden JJ, Popovich BW, Reiss AL, Snow K, Thibodeau SN, Richards CS, Ward PA, Nelson DL. Eichler EE, et al. Among authors: nelson dl. Nat Genet. 1994 Sep;8(1):88-94. doi: 10.1038/ng0994-88. Nat Genet. 1994. PMID: 7987398

6

Population survey of the human FMR1 CGG repeat substructure suggests biased polarity for the loss of AGG interruptions.

Eichler EE, Hammond HA, Macpherson JN, Ward PA, Nelson DL. Eichler EE, et al. Among authors: nelson dl. Hum Mol Genet. 1995 Dec;4(12):2199-208. doi: 10.1093/hmg/4.12.2199. Hum Mol Genet. 1995. PMID: 8634688

7

Large domains of apparent delayed replication timing associated with triplet repeat expansion at FRAXA and FRAXE.

Subramanian PS, Nelson DL, Chinault AC. Subramanian PS, et al. Among authors: nelson dl. Am J Hum Genet. 1996 Aug;59(2):407-16. Am J Hum Genet. 1996. PMID: 8755928 Free PMC article.

8

Genetic variation and evolutionary stability of the FMR1 CGG repeat in six closed human populations.

Eichler EE, Nelson DL. Eichler EE, et al. Among authors: nelson dl. Am J Med Genet. 1996 Jul 12;64(1):220-5. doi: 10.1002/(SICI)1096-8628(19960712)64:1<220::AID-AJMG40>3.0.CO;2-M. Am J Med Genet. 1996. PMID: 8826480

9

Haplotype and interspersion analysis of the FMR1 CGG repeat identifies two different mutational pathways for the origin of the fragile X syndrome.

Eichler EE, Macpherson JN, Murray A, Jacobs PA, Chakravarti A, Nelson DL. Eichler EE, et al. Among authors: nelson dl. Hum Mol Genet. 1996 Mar;5(3):319-30. doi: 10.1093/hmg/5.3.319. Hum Mol Genet. 1996. PMID: 8852655

10

Drosophila fragile X protein, DFXR, regulates neuronal morphology and function in the brain.

Morales J, Hiesinger PR, Schroeder AJ, Kume K, Verstreken P, Jackson FR, Nelson DL, Hassan BA. Morales J, et al. Among authors: nelson dl. Neuron. 2002 Jun 13;34(6):961-72. doi: 10.1016/s0896-6273(02)00731-6. Neuron. 2002. PMID: 12086643 Free article.

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