Nelson DL - Search Results

1

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

2

DNA methylation represses FMR-1 transcription in fragile X syndrome.

Sutcliffe JS, Nelson DL, Zhang F, Pieretti M, Caskey CT, Saxe D, Warren ST. Sutcliffe JS, et al. Among authors: nelson dl. Hum Mol Genet. 1992 Sep;1(6):397-400. doi: 10.1093/hmg/1.6.397. Hum Mol Genet. 1992. PMID: 1301913

3

Frequent small amplifications in the FMR-1 gene in fra(X) families: limits to the diagnosis of 'premutations'.

Macpherson JN, Nelson DL, Jacobs PA. Macpherson JN, et al. Among authors: nelson dl. J Med Genet. 1992 Nov;29(11):802-6. doi: 10.1136/jmg.29.11.802. J Med Genet. 1992. PMID: 1453431 Free PMC article.

4

Triplet repeat mutations in human disease.

Caskey CT, Pizzuti A, Fu YH, Fenwick RG Jr, Nelson DL. Caskey CT, et al. Among authors: nelson dl. Science. 1992 May 8;256(5058):784-9. doi: 10.1126/science.1589758. Science. 1992. PMID: 1589758 Review.

5

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.

6

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

7

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.

8

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

9

An n-allele model for progressive amplification in the FMR1 locus.

Morris A, Morton NE, Collins A, Macpherson J, Nelson D, Sherman S. Morris A, et al. Proc Natl Acad Sci U S A. 1995 May 23;92(11):4833-7. doi: 10.1073/pnas.92.11.4833. Proc Natl Acad Sci U S A. 1995. PMID: 7761409 Free PMC article.

10

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

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