Nelson DL - Search Results

1

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

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

Positional cloning reaches maturity.

Nelson DL. Nelson DL. Curr Opin Genet Dev. 1995 Jun;5(3):298-303. doi: 10.1016/0959-437x(95)80042-5. Curr Opin Genet Dev. 1995. PMID: 7549422 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

The gene encoding the VP16-accessory protein HCF (HCFC1) resides in human Xq28 and is highly expressed in fetal tissues and the adult kidney.

Wilson AC, Parrish JE, Massa HF, Nelson DL, Trask BJ, Herr W. Wilson AC, et al. Among authors: nelson dl. Genomics. 1995 Jan 20;25(2):462-8. doi: 10.1016/0888-7543(95)80046-o. Genomics. 1995. PMID: 7789979

6

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

7

Isolation of a GCC repeat showing expansion in FRAXF, a fragile site distal to FRAXA and FRAXE.

Parrish JE, Oostra BA, Verkerk AJ, Richards CS, Reynolds J, Spikes AS, Shaffer LG, Nelson DL. Parrish JE, et al. Among authors: nelson dl. Nat Genet. 1994 Nov;8(3):229-35. doi: 10.1038/ng1194-229. Nat Genet. 1994. PMID: 7874164

8

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

9

Methods for finding genes. A major rate-limiting step in positional cloning.

Parrish JE, Nelson DL. Parrish JE, et al. Among authors: nelson dl. Genet Anal Tech Appl. 1993 Apr;10(2):29-41. doi: 10.1016/1050-3862(93)90043-i. Genet Anal Tech Appl. 1993. PMID: 8217302 Review.

10

High resolution methylation analysis of the FMR1 gene trinucleotide repeat region in fragile X syndrome.

Hornstra IK, Nelson DL, Warren ST, Yang TP. Hornstra IK, et al. Among authors: nelson dl. Hum Mol Genet. 1993 Oct;2(10):1659-65. doi: 10.1093/hmg/2.10.1659. Hum Mol Genet. 1993. PMID: 8268919

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