These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

171 related articles for article (PubMed ID: 15574425)

  • 1. 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; 280(6):4498-503. PubMed ID: 15574425
    [TBL] [Abstract][Full Text] [Related]  

  • 2. AGG/CCT interruptions affect nucleosome formation and positioning of healthy-length CGG/CCG triplet repeats.
    Volle CB; Delaney S
    BMC Biochem; 2013 Nov; 14():33. PubMed ID: 24261641
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Interruptions in the triplet repeats of SCA1 and FRAXA reduce the propensity and complexity of slipped strand DNA (S-DNA) formation.
    Pearson CE; Eichler EE; Lorenzetti D; Kramer SF; Zoghbi HY; Nelson DL; Sinden RR
    Biochemistry; 1998 Feb; 37(8):2701-8. PubMed ID: 9485421
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The ATTCT repeats of spinocerebellar ataxia type 10 display strong nucleosome assembly which is enhanced by repeat interruptions.
    Hagerman KA; Ruan H; Edamura KN; Matsuura T; Pearson CE; Wang YH
    Gene; 2009 Apr; 434(1-2):29-34. PubMed ID: 19171184
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Structural Dynamics Role of AGG Interruptions in Inhibition CGG Repeat Expansion Associated with Fragile X Syndrome.
    Shen YI; Cheng KC; Wei YJ; Lee IR
    ACS Chem Neurosci; 2024 Jan; 15(2):230-235. PubMed ID: 38133821
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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; 271(40):24325-8. PubMed ID: 8798682
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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. PubMed ID: 8634688
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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. PubMed ID: 22498846
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Methylation of expanded CCG triplet repeat DNA from fragile X syndrome patients enhances nucleosome exclusion.
    Wang YH; Griffith J
    J Biol Chem; 1996 Sep; 271(38):22937-40. PubMed ID: 8798475
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Role of replication and CpG methylation in fragile X syndrome CGG deletions in primate cells.
    Nichol Edamura K; Leonard MR; Pearson CE
    Am J Hum Genet; 2005 Feb; 76(2):302-11. PubMed ID: 15625623
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Detecting AGG Interruptions in Male and Female FMR1 Premutation Carriers by Single-Molecule Sequencing.
    Ardui S; Race V; Zablotskaya A; Hestand MS; Van Esch H; Devriendt K; Matthijs G; Vermeesch JR
    Hum Mutat; 2017 Mar; 38(3):324-331. PubMed ID: 27883256
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Sequence analysis of the fragile X trinucleotide repeat: implications for the origin of the fragile X mutation.
    Snow K; Tester DJ; Kruckeberg KE; Schaid DJ; Thibodeau SN
    Hum Mol Genet; 1994 Sep; 3(9):1543-51. PubMed ID: 7833909
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Interruption of the fragile X syndrome expanded sequence d(CGG)(n) by interspersed d(AGG) trinucleotides diminishes the formation and stability of d(CGG)(n) tetrahelical structures.
    Weisman-Shomer P; Cohen E; Fry M
    Nucleic Acids Res; 2000 Apr; 28(7):1535-41. PubMed ID: 10710419
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Assays for Determining Repeat Number, Methylation Status, and AGG Interruptions in the Fragile X-Related Disorders.
    Hayward BE; Usdin K
    Methods Mol Biol; 2019; 1942():49-59. PubMed ID: 30900174
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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. PubMed ID: 21499798
    [TBL] [Abstract][Full Text] [Related]  

  • 16. CGG repeat length and AGG interruptions as indicators of fragile X-associated diminished ovarian reserve.
    Lekovich J; Man L; Xu K; Canon C; Lilienthal D; Stewart JD; Pereira N; Rosenwaks Z; Gerhardt J
    Genet Med; 2018 Sep; 20(9):957-964. PubMed ID: 29267266
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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; 49(32):6826-37. PubMed ID: 20695523
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Chromatin structure of repeating CTG/CAG and CGG/CCG sequences in human disease.
    Wang YH
    Front Biosci; 2007 May; 12():4731-41. PubMed ID: 17485409
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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; 51(49):9814-25. PubMed ID: 23157165
    [TBL] [Abstract][Full Text] [Related]  

  • 20. DNA methylation and replication: implications for the "deletion hotspot" region of FMR1.
    Nichol Edamura K; Pearson CE
    Hum Genet; 2005 Nov; 118(2):301-4. PubMed ID: 16133176
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.