Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 274

1.

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.

PMID:
11487573
2.

A fragile gene.

Oostra BA, Willems PJ.

Bioessays. 1995 Nov;17(11):941-7. Review.

PMID:
8526888
3.

FMR1 premutation allele (CGG)81 is stable in mice.

Bontekoe CJ, de Graaff E, Nieuwenhuizen IM, Willemsen R, Oostra BA.

Eur J Hum Genet. 1997 Sep-Oct;5(5):293-8.

PMID:
9412786
4.

Instability of a premutation-sized CGG repeat in FMR1 YAC transgenic mice.

Peier AM, Nelson DL.

Genomics. 2002 Oct;80(4):423-32.

PMID:
12376097
5.
6.

Fragile X CGG repeat structures among African-Americans: identification of a novel factor responsible for repeat instability.

Crawford DC, Zhang F, Wilson B, Warren ST, Sherman SL.

Hum Mol Genet. 2000 Jul 22;9(12):1759-69.

PMID:
10915764
7.

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
8.

Re-examination of factors associated with expansion of CGG repeats using a single nucleotide polymorphism in FMR1.

Gunter C, Paradee W, Crawford DC, Meadows KA, Newman J, Kunst CB, Nelson DL, Schwartz C, Murray A, Macpherson JN, Sherman SL, Warren ST.

Hum Mol Genet. 1998 Nov;7(12):1935-46.

PMID:
9811938
9.

Animal model for fragile X syndrome.

Oostra BA, Hoogeveen AT.

Ann Med. 1997 Dec;29(6):563-7. Review.

PMID:
9562525
10.

Genetic variation and intergenerational FMR1 CGG-repeat stability in 100 unrelated three-generation families from the normal population.

Patsalis PC, Sismani C, Stylianou S, Ioannou P, Joseph G, Manoli P, Holden JJ, Hettinger JA.

Am J Med Genet. 1999 May 28;84(3):217-20.

PMID:
10331595
11.

Mosaicism for the fragile X syndrome full mutation and deletions within the CGG repeat of the FMR1 gene.

Milà M, Castellví-Bel S, Sánchez A, Lázaro C, Villa M, Estivill X.

J Med Genet. 1996 Apr;33(4):338-40.

12.

Nucleosome assembly on methylated CGG triplet repeats in the fragile X mental retardation gene 1 promoter.

Godde JS, Kass SU, Hirst MC, Wolffe AP.

J Biol Chem. 1996 Oct 4;271(40):24325-8.

13.

Methylation mosaicism of 5'-(CGG)(n)-3' repeats in fragile X, premutation and normal individuals.

Genç B, Müller-Hartmann H, Zeschnigk M, Deissler H, Schmitz B, Majewski F, von Gontard A, Doerfler W.

Nucleic Acids Res. 2000 May 15;28(10):2141-52.

14.

Haplotype and interspersion analysis of the FMR1 CGG repeat identifies two different mutational pathways for the origin of the fragile X syndrome.

Eichler EE, Macpherson JN, Murray A, Jacobs PA, Chakravarti A, Nelson DL.

Hum Mol Genet. 1996 Mar;5(3):319-30.

PMID:
8852655
15.

Hotspot for deletions in the CGG repeat region of FMR1 in fragile X patients.

de Graaff E, Rouillard P, Willems PJ, Smits AP, Rousseau F, Oostra BA.

Hum Mol Genet. 1995 Jan;4(1):45-9.

PMID:
7711733
16.

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.

17.

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
18.

Instability of the FMR2 trinucleotide repeat region associated with expanded FMR1 alleles.

Brown TC, Tarleton JC, Go RC, Longshore JW, Descartes M.

Am J Med Genet. 1997 Dec 31;73(4):447-55.

PMID:
9415473
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