Warren ST - Search Results

1

Nuclease sensitivity of permeabilized cells confirms altered chromatin formation at the fragile X locus.

Eberhart DE, Warren ST. Eberhart DE, et al. Among authors: warren st. Somat Cell Mol Genet. 1996 Nov;22(6):435-41. doi: 10.1007/BF02369435. Somat Cell Mol Genet. 1996. PMID: 9131013

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

CGG repeat polymorphism at the c-Ha-ras oncogene locus.

Riggins GJ, Lokey LK, Warren ST. Riggins GJ, et al. Among authors: warren st. Hum Mol Genet. 1992 Dec;1(9):775. doi: 10.1093/hmg/1.9.775. Hum Mol Genet. 1992. PMID: 1302617 No abstract available.

4

Human genes containing polymorphic trinucleotide repeats.

Riggins GJ, Lokey LK, Chastain JL, Leiner HA, Sherman SL, Wilkinson KD, Warren ST. Riggins GJ, et al. Among authors: warren st. Nat Genet. 1992 Nov;2(3):186-91. doi: 10.1038/ng1192-186. Nat Genet. 1992. PMID: 1345166

5

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

6

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

7

Strategy for molecular cloning of the fragile X site DNA.

Warren ST, Zhang FP, Sutcliffe JS, Peters JF. Warren ST, et al. Am J Med Genet. 1988 May-Jun;30(1-2):613-23. doi: 10.1002/ajmg.1320300162. Am J Med Genet. 1988. PMID: 3177473

8

Fragile X syndrome: a hypothesis regarding the molecular mechanism of the phenotype.

Warren ST. Warren ST. Am J Med Genet. 1988 May-Jun;30(1-2):681-8. doi: 10.1002/ajmg.1320300169. Am J Med Genet. 1988. PMID: 3177478

9

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.

10

FMR1 protein: conserved RNP family domains and selective RNA binding.

Ashley CT Jr, Wilkinson KD, Reines D, Warren ST. Ashley CT Jr, et al. Among authors: warren st. Science. 1993 Oct 22;262(5133):563-6. doi: 10.1126/science.7692601. Science. 1993. PMID: 7692601

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