Warren ST - Search Results

1

The mGluR theory of fragile X mental retardation.

Bear MF, Huber KM, Warren ST. Bear MF, et al. Among authors: warren st. Trends Neurosci. 2004 Jul;27(7):370-7. doi: 10.1016/j.tins.2004.04.009. Trends Neurosci. 2004. PMID: 15219735 Review.

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: warren st. Hum Mol Genet. 1992 Sep;1(6):397-400. doi: 10.1093/hmg/1.6.397. Hum Mol Genet. 1992. PMID: 1301913

3

Variation of the CGG repeat at the fragile X site results in genetic instability: resolution of the Sherman paradox.

Fu YH, Kuhl DP, Pizzuti A, Pieretti M, Sutcliffe JS, Richards S, Verkerk AJ, Holden JJ, Fenwick RG Jr, Warren ST, et al. Fu YH, et al. Among authors: warren st. Cell. 1991 Dec 20;67(6):1047-58. doi: 10.1016/0092-8674(91)90283-5. Cell. 1991. PMID: 1760838

4

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: warren st. Cell. 1991 Aug 23;66(4):817-22. doi: 10.1016/0092-8674(91)90125-i. Cell. 1991. PMID: 1878973

5

Triplet repeat expansion mutations: the example of fragile X syndrome.

Warren ST, Ashley CT Jr. Warren ST, et al. Annu Rev Neurosci. 1995;18:77-99. doi: 10.1146/annurev.ne.18.030195.000453. Annu Rev Neurosci. 1995. PMID: 7605075 Review. No abstract available.

6

Translational suppression by trinucleotide repeat expansion at FMR1.

Feng Y, Zhang F, Lokey LK, Chastain JL, Lakkis L, Eberhart D, Warren ST. Feng Y, et al. Among authors: warren st. Science. 1995 May 5;268(5211):731-4. doi: 10.1126/science.7732383. Science. 1995. PMID: 7732383

7

Quantitative comparison of FMR1 gene expression in normal and premutation alleles.

Feng Y, Lakkis L, Devys D, Warren ST. Feng Y, et al. Among authors: warren st. Am J Hum Genet. 1995 Jan;56(1):106-13. Am J Hum Genet. 1995. PMID: 7825564 Free PMC article.

8

Cryptic and polar variation of the fragile X repeat could result in predisposing normal alleles.

Kunst CB, Warren ST. Kunst CB, et al. Among authors: warren st. Cell. 1994 Jun 17;77(6):853-61. doi: 10.1016/0092-8674(94)90134-1. Cell. 1994. PMID: 7911740

9

Advances in molecular analysis of fragile X syndrome.

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

10

Human and murine FMR-1: alternative splicing and translational initiation downstream of the CGG-repeat.

Ashley CT, Sutcliffe JS, Kunst CB, Leiner HA, Eichler EE, Nelson DL, Warren ST. Ashley CT, et al. Among authors: warren st. Nat Genet. 1993 Jul;4(3):244-51. doi: 10.1038/ng0793-244. Nat Genet. 1993. PMID: 8358432

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