Format
Items per page
Sort by

Send to:

Choose Destination

Results: 1 to 20 of 117

1.

AGG/CCT interruptions affect nucleosome formation and positioning of healthy-length CGG/CCG triplet repeats.

Volle CB, Delaney S.

BMC Biochem. 2013 Nov 22;14:33. doi: 10.1186/1471-2091-14-33.

PMID:
24261641
[PubMed - indexed for MEDLINE]
Free PMC Article
2.

Effect of CAT or AGG interruptions and CpG methylation on nucleosome assembly upon trinucleotide repeats on spinocerebellar ataxia, type 1 and fragile X syndrome.

Mulvihill DJ, Nichol Edamura K, Hagerman KA, Pearson CE, Wang YH.

J Biol Chem. 2005 Feb 11;280(6):4498-503. Epub 2004 Dec 1.

PMID:
15574425
[PubMed - indexed for MEDLINE]
Free Article
3.

Nucleosomal occupancy and CGG repeat expansion: a comparative analysis of triplet repeat region from mouse and human fragile X mental retardation gene 1.

Datta S, Alam MP, Majumdar SS, Mehta AK, Maiti S, Wadhwa N, Brahmachari V.

Chromosome Res. 2011 May;19(4):445-55. doi: 10.1007/s10577-011-9206-7. Epub 2011 Apr 16.

PMID:
21499798
[PubMed - indexed for MEDLINE]
4.

Population survey of the human FMR1 CGG repeat substructure suggests biased polarity for the loss of AGG interruptions.

Eichler EE, Hammond HA, Macpherson JN, Ward PA, Nelson DL.

Hum Mol Genet. 1995 Dec;4(12):2199-208.

PMID:
8634688
[PubMed - indexed for MEDLINE]
5.

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.

PMID:
8798682
[PubMed - indexed for MEDLINE]
Free Article
6.

AGG interruptions in (CGG)(n) DNA repeat tracts modulate the structure and thermodynamics of non-B conformations in vitro.

Jarem DA, Huckaby LV, Delaney S.

Biochemistry. 2010 Aug 17;49(32):6826-37. doi: 10.1021/bi1007782.

PMID:
20695523
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

CAG/CTG repeats alter the affinity for the histone core and the positioning of DNA in the nucleosome.

Volle CB, Delaney S.

Biochemistry. 2012 Dec 11;51(49):9814-25. doi: 10.1021/bi301416v. Epub 2012 Nov 27.

PMID:
23157165
[PubMed - indexed for MEDLINE]
Free PMC Article
8.
9.

AGG interruptions within the maternal FMR1 gene reduce the risk of offspring with fragile X syndrome.

Yrigollen CM, Durbin-Johnson B, Gane L, Nelson DL, Hagerman R, Hagerman PJ, Tassone F.

Genet Med. 2012 Aug;14(8):729-36. doi: 10.1038/gim.2012.34. Epub 2012 Apr 12.

PMID:
22498846
[PubMed - indexed for MEDLINE]
Free PMC Article
10.

The role of AGG interruptions in the transcription of FMR1 premutation alleles.

Yrigollen CM, Tassone F, Durbin-Johnson B, Tassone F.

PLoS One. 2011;6(7):e21728. doi: 10.1371/journal.pone.0021728. Epub 2011 Jul 19.

PMID:
21818263
[PubMed - indexed for MEDLINE]
Free PMC Article
11.

FMR1 in global populations.

Kunst CB, Zerylnick C, Karickhoff L, Eichler E, Bullard J, Chalifoux M, Holden JJ, Torroni A, Nelson DL, Warren ST.

Am J Hum Genet. 1996 Mar;58(3):513-22.

PMID:
8644711
[PubMed - indexed for MEDLINE]
Free PMC Article
12.

Translation of the FMR1 mRNA is not influenced by AGG interruptions.

Ludwig AL, Raske C, Tassone F, Garcia-Arocena D, Hershey JW, Hagerman PJ.

Nucleic Acids Res. 2009 Nov;37(20):6896-904. doi: 10.1093/nar/gkp713. Epub 2009 Sep 14.

PMID:
19752155
[PubMed - indexed for MEDLINE]
Free PMC Article
13.

CGG repeat interruptions in the FMR1 gene in patients with infantile autism.

Poon PM, Chen QL, Lai KY, Wong CK, Pang CP.

Clin Chem Lab Med. 1998 Aug;36(8):649-53.

PMID:
9806479
[PubMed - indexed for MEDLINE]
14.

Fragile X AGG analysis provides new risk predictions for 45-69 repeat alleles.

Nolin SL, Sah S, Glicksman A, Sherman SL, Allen E, Berry-Kravis E, Tassone F, Yrigollen C, Cronister A, Jodah M, Ersalesi N, Dobkin C, Brown WT, Shroff R, Latham GJ, Hadd AG.

Am J Med Genet A. 2013 Apr;161A(4):771-8. doi: 10.1002/ajmg.a.35833. Epub 2013 Feb 26.

PMID:
23444167
[PubMed - indexed for MEDLINE]
15.

FMR1 CGG repeat lengths mediate different regulation of reporter gene expression in comparative transient and locus specific integration assays.

SĂžlvsten C, Nielsen AL.

Gene. 2011 Oct 15;486(1-2):15-22. doi: 10.1016/j.gene.2011.06.034. Epub 2011 Jul 13.

PMID:
21767618
[PubMed - indexed for MEDLINE]
16.

Sequence analysis of long FMR1 arrays in the Japanese population: insights into the generation of long (CGG)n tracts.

Hirst MC, Arinami T, Laird CD.

Hum Genet. 1997 Dec;101(2):214-8.

PMID:
9402973
[PubMed - indexed for MEDLINE]
17.

Histone deacetylases suppress CGG repeat-induced neurodegeneration via transcriptional silencing in models of fragile X tremor ataxia syndrome.

Todd PK, Oh SY, Krans A, Pandey UB, Di Prospero NA, Min KT, Taylor JP, Paulson HL.

PLoS Genet. 2010 Dec 9;6(12):e1001240. doi: 10.1371/journal.pgen.1001240.

PMID:
21170301
[PubMed - indexed for MEDLINE]
Free PMC Article
18.

Secondary structure and dynamics of the r(CGG) repeat in the mRNA of the fragile X mental retardation 1 (FMR1) gene.

Zumwalt M, Ludwig A, Hagerman PJ, Dieckmann T.

RNA Biol. 2007 Sep;4(2):93-100. Epub 2007 Sep 12.

PMID:
17962727
[PubMed - indexed for MEDLINE]
Free Article
19.

Length of uninterrupted CGG repeats determines instability in the FMR1 gene.

Eichler EE, Holden JJ, Popovich BW, Reiss AL, Snow K, Thibodeau SN, Richards CS, Ward PA, Nelson DL.

Nat Genet. 1994 Sep;8(1):88-94.

PMID:
7987398
[PubMed - indexed for MEDLINE]
20.

Distribution of CGG repeat sizes within the fragile X mental retardation 1 (FMR1) homologue in a non-human primate population.

Garcia Arocena D, Breece KE, Hagerman PJ.

Hum Genet. 2003 Oct;113(5):371-6. Epub 2003 Aug 7.

PMID:
12905066
[PubMed - indexed for MEDLINE]
Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk