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Results: 1 to 20 of 332

Similar articles for PubMed (Select 10631132)

1.

Elevated levels of FMR1 mRNA in carrier males: a new mechanism of involvement in the fragile-X syndrome.

Tassone F, Hagerman RJ, Taylor AK, Gane LW, Godfrey TE, Hagerman PJ.

Am J Hum Genet. 2000 Jan;66(1):6-15.

2.

Transcription of the FMR1 gene in individuals with fragile X syndrome.

Tassone F, Hagerman RJ, Chamberlain WD, Hagerman PJ.

Am J Med Genet. 2000 Fall;97(3):195-203.

PMID:
11449488
4.

Fragile X males with unmethylated, full mutation trinucleotide repeat expansions have elevated levels of FMR1 messenger RNA.

Tassone F, Hagerman RJ, Loesch DZ, Lachiewicz A, Taylor AK, Hagerman PJ.

Am J Med Genet. 2000 Sep 18;94(3):232-6.

PMID:
10995510
5.

Reduced FMR1 mRNA translation efficiency in fragile X patients with premutations.

Primerano B, Tassone F, Hagerman RJ, Hagerman P, Amaldi F, Bagni C.

RNA. 2002 Dec;8(12):1482-8.

6.
7.

Expression of the FMR1 gene.

Tassone F, Hagerman PJ.

Cytogenet Genome Res. 2003;100(1-4):124-8. Review.

PMID:
14526172
8.
9.

A neuropsychological investigation of male premutation carriers of fragile X syndrome.

Moore CJ, Daly EM, Schmitz N, Tassone F, Tysoe C, Hagerman RJ, Hagerman PJ, Morris RG, Murphy KC, Murphy DG.

Neuropsychologia. 2004;42(14):1934-47.

PMID:
15381024
10.

Elevated FMR1 mRNA in premutation carriers is due to increased transcription.

Tassone F, Beilina A, Carosi C, Albertosi S, Bagni C, Li L, Glover K, Bentley D, Hagerman PJ.

RNA. 2007 Apr;13(4):555-62. Epub 2007 Feb 5.

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13.

A study of the distributional characteristics of FMR1 transcript levels in 238 individuals.

Allen EG, He W, Yadav-Shah M, Sherman SL.

Hum Genet. 2004 Apr;114(5):439-47. Epub 2004 Feb 3.

PMID:
14758538
14.

Clinical involvement and protein expression in individuals with the FMR1 premutation.

Tassone F, Hagerman RJ, Taylor AK, Mills JB, Harris SW, Gane LW, Hagerman PJ.

Am J Med Genet. 2000 Mar 13;91(2):144-52.

PMID:
10748416
15.

The effect of pre-mutation of X chromosome CGG trinucleotide repeats on brain anatomy.

Moore CJ, Daly EM, Tassone F, Tysoe C, Schmitz N, Ng V, Chitnis X, McGuire P, Suckling J, Davies KE, Hagerman RJ, Hagerman PJ, Murphy KC, Murphy DG.

Brain. 2004 Dec;127(Pt 12):2672-81. Epub 2004 Oct 13.

16.

Instability of the CGG repeat and expression of the FMR1 protein in a male fragile X patient with a lung tumor.

de Graaff E, Willemsen R, Zhong N, de Die-Smulders CE, Brown WT, Freling G, Oostra B.

Am J Hum Genet. 1995 Sep;57(3):609-18.

17.

A deletion of 1.6 kb proximal to the CGG repeat of the FMR1 gene causes the clinical phenotype of the fragile X syndrome.

Meijer H, de Graaff E, Merckx DM, Jongbloed RJ, de Die-Smulders CE, Engelen JJ, Fryns JP, Curfs PM, Oostra BA.

Hum Mol Genet. 1994 Apr;3(4):615-20.

PMID:
8069307
18.

Apparent regression of the CGG repeat in FMR1 to an allele of normal size.

Vits L, De Boulle K, Reyniers E, Handig I, Darby JK, Oostra B, Willems PJ.

Hum Genet. 1994 Nov;94(5):523-6.

PMID:
7959688
19.

A fragile balance: FMR1 expression levels.

Oostra BA, Willemsen R.

Hum Mol Genet. 2003 Oct 15;12 Spec No 2:R249-57. Epub 2003 Sep 2. Review.

20.

Deletion of all CGG repeats plus flanking sequences in FMR1 does not abolish gene expression.

Grønskov K, Hjalgrim H, Bjerager MO, Brøndum-Nielsen K.

Am J Hum Genet. 1997 Oct;61(4):961-7.

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