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The pathophysiology of fragile x syndrome.
Penagarikano O, Mulle JG, Warren ST. Penagarikano O, et al. Among authors: warren st. Annu Rev Genomics Hum Genet. 2007;8:109-29. doi: 10.1146/annurev.genom.8.080706.092249. Annu Rev Genomics Hum Genet. 2007. PMID: 17477822 Review.
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
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.
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
Isolation and characterization of a highly polymorphic human locus (DXS455) in proximal Xq28.
Consalez GG, Stayton CL, Freimer NB, Goonewardena P, Brown WT, Gilliam TC, Warren ST. Consalez GG, et al. Among authors: warren st. Genomics. 1992 Apr;12(4):710-4. doi: 10.1016/0888-7543(92)90299-8. Genomics. 1992. PMID: 1572645
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
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.
Molecular evidence for true isochromosome 21q.
Priest JH, Blackston RD, Pearse LA, Warren ST. Priest JH, et al. Among authors: warren st. Hum Genet. 1988 Dec;81(1):1-3. doi: 10.1007/BF00283718. Hum Genet. 1988. PMID: 2974012
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
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
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