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Items: 1 to 20 of 96

1.

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.

Nat Genet. 1993 Jul;4(3):244-51.

PMID:
8358432
2.

Characterization and localization of the FMR-1 gene product associated with fragile X syndrome.

Verheij C, Bakker CE, de Graaff E, Keulemans J, Willemsen R, Verkerk AJ, Galjaard H, Reuser AJ, Hoogeveen AT, Oostra BA.

Nature. 1993 Jun 24;363(6431):722-4.

PMID:
8515814
3.

Sequence of the murine Huntington disease gene: evidence for conservation, alternate splicing and polymorphism in a triplet (CCG) repeat [corrected].

Lin B, Nasir J, MacDonald H, Hutchinson G, Graham RK, Rommens JM, Hayden MR.

Hum Mol Genet. 1994 Jan;3(1):85-92. Erratum in: Hum Mol Genet 1994 Mar;3(3):530.

PMID:
8162057
4.

Hypermethylation of telomere-like foldbacks at codon 12 of the human c-Ha-ras gene and the trinucleotide repeat of the FMR-1 gene of fragile X.

Smith SS, Laayoun A, Lingeman RG, Baker DJ, Riley J.

J Mol Biol. 1994 Oct 21;243(2):143-51. Review.

PMID:
7932745
5.

Novel point mutation within intron 10 of FMR-1 gene causing fragile X syndrome.

Wang YC, Lin ML, Lin SJ, Li YC, Li SY.

Hum Mutat. 1997;10(5):393-9.

PMID:
9375856
6.

Alternative splicing in the fragile X gene FMR1.

Verkerk AJ, de Graaff E, De Boulle K, Eichler EE, Konecki DS, Reyniers E, Manca A, Poustka A, Willems PJ, Nelson DL, et al.

Hum Mol Genet. 1993 Apr;2(4):399-404. Erratum in: Hum Mol Genet. 1993 Aug;2(8):1348.

PMID:
8504300
7.

The FMR-1 protein is cytoplasmic, most abundant in neurons and appears normal in carriers of a fragile X premutation.

Devys D, Lutz Y, Rouyer N, Bellocq JP, Mandel JL.

Nat Genet. 1993 Aug;4(4):335-40.

PMID:
8401578
8.

[Detection of FMR-1 gene expression by RT-PCR].

Zheng L, Fan Y, Huang T, Zhu N, Shen Y, Wu G.

Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 1995 Dec;17(6):407-11. Chinese.

PMID:
9208564
10.

[Unstable DNA sequence and methylation in fragile X syndrome].

Fu SD, Shen Y, Fan Y.

Zhonghua Yi Xue Za Zhi. 1994 Oct;74(10):611-4, 646-7. Chinese.

PMID:
7842338
11.

The chicken FMR1 gene is highly conserved with a CCT 5'-untranslated repeat and encodes an RNA-binding protein.

Price DK, Zhang F, Ashley CT Jr, Warren ST.

Genomics. 1996 Jan 1;31(1):3-12.

PMID:
8808273
12.

Identification of FMR2, a novel gene associated with the FRAXE CCG repeat and CpG island.

Gu Y, Shen Y, Gibbs RA, Nelson DL.

Nat Genet. 1996 May;13(1):109-13.

PMID:
8673086
13.

A point mutation in the FMR-1 gene associated with fragile X mental retardation.

De Boulle K, Verkerk AJ, Reyniers E, Vits L, Hendrickx J, Van Roy B, Van den Bos F, de Graaff E, Oostra BA, Willems PJ.

Nat Genet. 1993 Jan;3(1):31-5.

PMID:
8490650
14.

Alternative splicing in the murine and human FXR1 genes.

Kirkpatrick LL, McIlwain KA, Nelson DL.

Genomics. 1999 Jul 15;59(2):193-202.

PMID:
10409431
15.

Variation of the CGG repeat in FMR-1 gene in normal and fragile X Chinese subjects.

Chen TA, Lu XF, Che PK, Ho WK.

Ann Clin Biochem. 1997 Sep;34 ( Pt 5):517-20.

PMID:
9293305
17.

Effect of in vitro promoter methylation and CGG repeat expansion on FMR-1 expression.

Sandberg G, Schalling M.

Nucleic Acids Res. 1997 Jul 15;25(14):2883-7.

18.
19.

Fragile x mental retardation (Fmr-1) gene expression is down regulated in brain of mice during aging.

Singh K, Gaur P, Prasad S.

Mol Biol Rep. 2007 Sep;34(3):173-81.

PMID:
17136426
20.

Instability of a (CGG)98 repeat in the Fmr1 promoter.

Bontekoe CJ, Bakker CE, Nieuwenhuizen IM, van der Linde H, Lans H, de Lange D, Hirst MC, Oostra BA.

Hum Mol Genet. 2001 Aug 1;10(16):1693-9.

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