Nelson DL - Search Results

1

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

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

The Lowe's oculocerebrorenal syndrome gene encodes a protein highly homologous to inositol polyphosphate-5-phosphatase.

Attree O, Olivos IM, Okabe I, Bailey LC, Nelson DL, Lewis RA, McInnes RR, Nussbaum RL. Attree O, et al. Among authors: nelson dl. Nature. 1992 Jul 16;358(6383):239-42. doi: 10.1038/358239a0. Nature. 1992. PMID: 1321346

4

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

5

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

6

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.

7

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

8

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.

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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