Nelson DL - Search Results

1

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

2

Rapid isolation of DNA probes within specific chromosome regions by interspersed repetitive sequence polymerase chain reaction.

Ledbetter SA, Nelson DL, Warren ST, Ledbetter DH. Ledbetter SA, et al. Among authors: nelson dl. Genomics. 1990 Mar;6(3):475-81. doi: 10.1016/0888-7543(90)90477-c. Genomics. 1990. PMID: 2328990

3

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

4

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.

5

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

6

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

7

Fine structure of the human FMR1 gene.

Eichler EE, Richards S, Gibbs RA, Nelson DL. Eichler EE, et al. Among authors: nelson dl. Hum Mol Genet. 1993 Aug;2(8):1147-53. doi: 10.1093/hmg/2.8.1147. Hum Mol Genet. 1993. PMID: 8401496

8

Alternative splicing in the fragile X gene FMR1.

Verkerk AJ, de Graaff E, De Boulle K, Eichler EE, Konecki DS, Reyniers E, Manca A, Poustka A, Willems PJ, Nelson DL, et al. Verkerk AJ, et al. Among authors: nelson dl. Hum Mol Genet. 1993 Apr;2(4):399-404. doi: 10.1093/hmg/2.4.399. Hum Mol Genet. 1993. PMID: 8504300

9

Anomalous rapid electrophoretic mobility of DNA containing triplet repeats associated with human disease genes.

Chastain PD 2nd, Eichler EE, Kang S, Nelson DL, Levene SD, Sinden RR. Chastain PD 2nd, et al. Among authors: nelson dl. Biochemistry. 1995 Dec 12;34(49):16125-31. doi: 10.1021/bi00049a027. Biochemistry. 1995. PMID: 8519769

10

A muscle-specific DNase I-like gene in human Xq28.

Parrish JE, Ciccodicola A, Wehhert M, Cox GF, Chen E, Nelson DL. Parrish JE, et al. Among authors: nelson dl. Hum Mol Genet. 1995 Sep;4(9):1557-64. doi: 10.1093/hmg/4.9.1557. Hum Mol Genet. 1995. PMID: 8541839

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