Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 163

1.
2.

FISH-detected delay in replication timing of mutated FMR1 alleles on both active and inactive X-chromosomes.

Yeshaya J, Shalgi R, Shohat M, Avivi L.

Hum Genet. 1999 Jul-Aug;105(1-2):86-97.

PMID:
10480360
3.

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
4.

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
5.
6.
7.

Expansion mutation frequency and CGG/GCC repeat polymorphism in FMR1 and FMR2 genes in an Indian population.

Sharma D, Gupta M, Thelma BK.

Genet Epidemiol. 2001 Jan;20(1):129-144.

PMID:
11119302
8.

Timing of the absence of FMR1 expression in full mutation chorionic villi.

Willemsen R, Bontekoe CJ, Severijnen LA, Oostra BA.

Hum Genet. 2002 Jun;110(6):601-5. Epub 2002 Apr 16.

PMID:
12107447
9.

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.

10.

Deletions in Xq26.3-q27.3 including FMR1 result in a severe phenotype in a male and variable phenotypes in females depending upon the X inactivation pattern.

Wolff DJ, Gustashaw KM, Zurcher V, Ko L, White W, Weiss L, Van Dyke DL, Schwartz S, Willard HF.

Hum Genet. 1997 Aug;100(2):256-61.

PMID:
9254860
11.

Reverse mutations in the fragile X syndrome.

Brown WT, Houck GE Jr, Ding X, Zhong N, Nolin S, Glicksman A, Dobkin C, Jenkins EC.

Am J Med Genet. 1996 Aug 9;64(2):287-92.

PMID:
8844067
12.

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.

13.

Structural and functional characterization of the human FMR1 promoter reveals similarities with the hnRNP-A2 promoter region.

Drouin R, Angers M, Dallaire N, Rose TM, Khandjian EW, Rousseau F.

Hum Mol Genet. 1997 Nov;6(12):2051-60.

PMID:
9328468
14.

An assay for X inactivation based on differential methylation at the fragile X locus, FMR1.

Carrel L, Willard HF.

Am J Med Genet. 1996 Jul 12;64(1):27-30.

PMID:
8826444
15.

Association of fragile X syndrome with delayed replication of the FMR1 gene.

Hansen RS, Canfield TK, Lamb MM, Gartler SM, Laird CD.

Cell. 1993 Jul 2;73(7):1403-9.

PMID:
8324827
16.
17.

Loss of mutation at the FMR1 locus through multiple exchanges between maternal X chromosomes.

van den Ouweland AM, Deelen WH, Kunst CB, Uzielli ML, Nelson DL, Warren ST, Oostra BA, Halley DJ.

Hum Mol Genet. 1994 Oct;3(10):1823-7.

PMID:
7849707
18.

Epigenetic variation illustrated by DNA methylation patterns of the fragile-X gene FMR1.

Stöger R, Kajimura TM, Brown WT, Laird CD.

Hum Mol Genet. 1997 Oct;6(11):1791-801.

PMID:
9302255
19.
20.

Mosaicism for the full mutation and a microdeletion involving the CGG repeat and flanking sequences in the FMR1 gene in eight fragile X patients.

Grasso M, Faravelli F, Lo Nigro C, Chiurazzi P, Sperandeo MP, Argusti A, Pomponi MG, Lecora M, Sebastio GF, Perroni L, Andria G, Neri G, Bricarelli FD.

Am J Med Genet. 1999 Jul 30;85(3):311-6.

PMID:
10398249

Supplemental Content

Support Center