Warren ST - Search Results

1

Independent role for presynaptic FMRP revealed by an FMR1 missense mutation associated with intellectual disability and seizures.

Myrick LK, Deng PY, Hashimoto H, Oh YM, Cho Y, Poidevin MJ, Suhl JA, Visootsak J, Cavalli V, Jin P, Cheng X, Warren ST, Klyachko VA. Myrick LK, et al. Among authors: warren st. Proc Natl Acad Sci U S A. 2015 Jan 27;112(4):949-56. doi: 10.1073/pnas.1423094112. Epub 2015 Jan 5. Proc Natl Acad Sci U S A. 2015. PMID: 25561520 Free PMC article.

2

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.

3

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

4

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

5

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.

6

FMR1 in global populations.

Kunst CB, Zerylnick C, Karickhoff L, Eichler E, Bullard J, Chalifoux M, Holden JJ, Torroni A, Nelson DL, Warren ST. Kunst CB, et al. Among authors: warren st. Am J Hum Genet. 1996 Mar;58(3):513-22. Am J Hum Genet. 1996. PMID: 8644711 Free PMC article.

7

The effect of FMR1 CGG repeat interruptions on mutation frequency as measured by sperm typing.

Kunst CB, Leeflang EP, Iber JC, Arnheim N, Warren ST. Kunst CB, et al. Among authors: warren st. J Med Genet. 1997 Aug;34(8):627-31. doi: 10.1136/jmg.34.8.627. J Med Genet. 1997. PMID: 9279752 Free PMC article.

8

Purified recombinant Fmrp exhibits selective RNA binding as an intrinsic property of the fragile X mental retardation protein.

Brown V, Small K, Lakkis L, Feng Y, Gunter C, Wilkinson KD, Warren ST. Brown V, et al. Among authors: warren st. J Biol Chem. 1998 Jun 19;273(25):15521-7. doi: 10.1074/jbc.273.25.15521. J Biol Chem. 1998. PMID: 9624140 Free article.

9

FMRP associates with polyribosomes as an mRNP, and the I304N mutation of severe fragile X syndrome abolishes this association.

Feng Y, Absher D, Eberhart DE, Brown V, Malter HE, Warren ST. Feng Y, et al. Among authors: warren st. Mol Cell. 1997 Dec;1(1):109-18. doi: 10.1016/s1097-2765(00)80012-x. Mol Cell. 1997. PMID: 9659908 Free article.

10

Acetylated histones are associated with FMR1 in normal but not fragile X-syndrome cells.

Coffee B, Zhang F, Warren ST, Reines D. Coffee B, et al. Among authors: warren st. Nat Genet. 1999 May;22(1):98-101. doi: 10.1038/8807. Nat Genet. 1999. PMID: 10319871

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