Nelson DL - Search Results

1

Impaired conditioned fear and enhanced long-term potentiation in Fmr2 knock-out mice.

Gu Y, McIlwain KL, Weeber EJ, Yamagata T, Xu B, Antalffy BA, Reyes C, Yuva-Paylor L, Armstrong D, Zoghbi H, Sweatt JD, Paylor R, Nelson DL. Gu Y, et al. Among authors: nelson dl. J Neurosci. 2002 Apr 1;22(7):2753-63. doi: 10.1523/JNEUROSCI.22-07-02753.2002. J Neurosci. 2002. PMID: 11923441 Free PMC article.

2

A de novo deletion in FMR1 in a patient with developmental delay.

Gu Y, Lugenbeel KA, Vockley JG, Grody WW, Nelson DL. Gu Y, et al. Among authors: nelson dl. Hum Mol Genet. 1994 Sep;3(9):1705-6. doi: 10.1093/hmg/3.9.1705. Hum Mol Genet. 1994. PMID: 7530551 No abstract available.

3

An integrated physical and genetic map of a 35 Mb region on chromosome Xp22.3-Xp21.3.

Ferrero GB, Franco B, Roth EJ, Firulli BA, Borsani G, Delmas-Mata J, Weissenbach J, Halley G, Schlessinger D, Chinault AC, Zoghbi HY, Nelson DL, Ballabio A. Ferrero GB, et al. Among authors: nelson dl. Hum Mol Genet. 1995 Oct;4(10):1821-7. doi: 10.1093/hmg/4.10.1821. Hum Mol Genet. 1995. PMID: 8595402

4

Identification of FMR2, a novel gene associated with the FRAXE CCG repeat and CpG island.

Gu Y, Shen Y, Gibbs RA, Nelson DL. Gu Y, et al. Among authors: nelson dl. Nat Genet. 1996 May;13(1):109-13. doi: 10.1038/ng0596-109. Nat Genet. 1996. PMID: 8673086

5

130 kb of DNA sequence reveals two new genes and a regional duplication distal to the human iduronate-2-sulfate sulfatase locus.

Timms KM, Lu F, Shen Y, Pierson CA, Muzny DM, Gu Y, Nelson DL, Gibbs RA. Timms KM, et al. Among authors: nelson dl. Genome Res. 1995 Aug;5(1):71-8. doi: 10.1101/gr.5.1.71. Genome Res. 1995. PMID: 8717057 Free article.

6

Interruptions in the triplet repeats of SCA1 and FRAXA reduce the propensity and complexity of slipped strand DNA (S-DNA) formation.

Pearson CE, Eichler EE, Lorenzetti D, Kramer SF, Zoghbi HY, Nelson DL, Sinden RR. Pearson CE, et al. Among authors: nelson dl. Biochemistry. 1998 Feb 24;37(8):2701-8. doi: 10.1021/bi972546c. Biochemistry. 1998. PMID: 9485421

7

(Over)correction of FMR1 deficiency with YAC transgenics: behavioral and physical features.

Peier AM, McIlwain KL, Kenneson A, Warren ST, Paylor R, Nelson DL. Peier AM, et al. Among authors: nelson dl. Hum Mol Genet. 2000 May 1;9(8):1145-59. doi: 10.1093/hmg/9.8.1145. Hum Mol Genet. 2000. PMID: 10767339

8

Large expansion of the ATTCT pentanucleotide repeat in spinocerebellar ataxia type 10.

Matsuura T, Yamagata T, Burgess DL, Rasmussen A, Grewal RP, Watase K, Khajavi M, McCall AE, Davis CF, Zu L, Achari M, Pulst SM, Alonso E, Noebels JL, Nelson DL, Zoghbi HY, Ashizawa T. Matsuura T, et al. Among authors: nelson dl. Nat Genet. 2000 Oct;26(2):191-4. doi: 10.1038/79911. Nat Genet. 2000. PMID: 11017075

9

Multiple pathogenic and benign genomic rearrangements occur at a 35 kb duplication involving the NEMO and LAGE2 genes.

Aradhya S, Bardaro T, Galgóczy P, Yamagata T, Esposito T, Patlan H, Ciccodicola A, Munnich A, Kenwrick S, Platzer M, D'Urso M, Nelson DL. Aradhya S, et al. Among authors: nelson dl. Hum Mol Genet. 2001 Oct 15;10(22):2557-67. doi: 10.1093/hmg/10.22.2557. Hum Mol Genet. 2001. PMID: 11709543

10

Physical and genetic characterization reveals a pseudogene, an evolutionary junction, and unstable loci in distal Xq28.

Aradhya S, Woffendin H, Bonnen P, Heiss NS, Yamagata T, Esposito T, Bardaro T, Poustka A, D'Urso M, Kenwrick S, Nelson DL. Aradhya S, et al. Among authors: nelson dl. Genomics. 2002 Jan;79(1):31-40. doi: 10.1006/geno.2001.6680. Genomics. 2002. PMID: 11827455

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