Warren ST - Search Results

1

Identification of PSMB5 as a genetic modifier of fragile X-associated tremor/ataxia syndrome.

Kong HE, Lim J, Linsalata A, Kang Y, Malik I, Allen EG, Cao Y, Shubeck L, Johnston R, Huang Y, Gu Y, Guo X, Zwick ME, Qin Z, Wingo TS, Juncos J, Nelson DL, Epstein MP, Cutler DJ, Todd PK, Sherman SL, Warren ST, Jin P. Kong HE, et al. Among authors: warren st. Proc Natl Acad Sci U S A. 2022 May 31;119(22):e2118124119. doi: 10.1073/pnas.2118124119. Epub 2022 May 26. Proc Natl Acad Sci U S A. 2022. PMID: 35617426 Free PMC article.

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

PCR amplification and analysis of yeast artificial chromosomes.

Sutcliffe JS, Zhang F, Caskey CT, Nelson DL, Warren ST. Sutcliffe JS, et al. Among authors: warren st. Genomics. 1992 Aug;13(4):1303-6. doi: 10.1016/0888-7543(92)90051-s. Genomics. 1992. PMID: 1380485

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

6

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: warren st. Genomics. 1990 Mar;6(3):475-81. doi: 10.1016/0888-7543(90)90477-c. Genomics. 1990. PMID: 2328990

7

Isolation of the human chromosomal band Xq28 within somatic cell hybrids by fragile X site breakage.

Warren ST, Knight SJ, Peters JF, Stayton CL, Consalez GG, Zhang FP. Warren ST, et al. Proc Natl Acad Sci U S A. 1990 May;87(10):3856-60. doi: 10.1073/pnas.87.10.3856. Proc Natl Acad Sci U S A. 1990. PMID: 2339126 Free PMC article.

8

CGG-repeat polymorphism of the BCR gene rules out predisposing alleles leading to the Philadelphia chromosome.

Riggins GJ, Sherman SL, Phillips CN, Stock W, Westbrook CA, Warren ST. Riggins GJ, et al. Among authors: warren st. Genes Chromosomes Cancer. 1994 Feb;9(2):141-4. doi: 10.1002/gcc.2870090211. Genes Chromosomes Cancer. 1994. PMID: 7513545

9

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: warren st. Nat Genet. 1995 Nov;11(3):301-8. doi: 10.1038/ng1195-301. Nat Genet. 1995. PMID: 7581454

10

Normal variation at the myotonic dystrophy locus in global human populations.

Zerylnick C, Torroni A, Sherman SL, Warren ST. Zerylnick C, et al. Among authors: warren st. Am J Hum Genet. 1995 Jan;56(1):123-30. Am J Hum Genet. 1995. PMID: 7825567 Free PMC article.

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