Nelson DL - Search Results

1

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

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

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

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

5

Advances in molecular analysis of fragile X syndrome.

Warren ST, Nelson DL. Warren ST, et al. Among authors: nelson dl. JAMA. 1994 Feb 16;271(7):536-42. JAMA. 1994. PMID: 8301769 Review.

6

Trinucleotide repeat instability: when and where?

Nelson DL, Warren ST. Nelson DL, et al. Nat Genet. 1993 Jun;4(2):107-8. doi: 10.1038/ng0693-107. Nat Genet. 1993. PMID: 8348143 No abstract available.

7

FMR1 in global populations.

Kunst CB, Zerylnick C, Karickhoff L, Eichler E, Bullard J, Chalifoux M, Holden JJ, Torroni A, Nelson DL, Warren ST. Kunst CB, et al. Among authors: nelson dl. Am J Hum Genet. 1996 Mar;58(3):513-22. Am J Hum Genet. 1996. PMID: 8644711 Free PMC article.

8

Intragenic probe used for diagnostics in fragile X families.

Verkerk AJ, deVries BB, Niermeijer MF, Fu YH, Nelson DL, Warren ST, Majoor-Krakauer DF, Halley DJ, Oostra BA. Verkerk AJ, et al. Among authors: nelson dl. Am J Med Genet. 1992 Apr 15-May 1;43(1-2):192-6. doi: 10.1002/ajmg.1320430132. Am J Med Genet. 1992. PMID: 1605192

9

Absence of expression of the FMR-1 gene in fragile X syndrome.

Pieretti M, Zhang FP, Fu YH, Warren ST, Oostra BA, Caskey CT, Nelson DL. Pieretti M, et al. Among authors: nelson dl. Cell. 1991 Aug 23;66(4):817-22. doi: 10.1016/0092-8674(91)90125-i. Cell. 1991. PMID: 1878973

10

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

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