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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

533 related items for PubMed ID: 25662336

  • 21. Maternal germline-specific effect of DNA ligase I on CTG/CAG instability.
    Tomé S, Panigrahi GB, López Castel A, Foiry L, Melton DW, Gourdon G, Pearson CE.
    Hum Mol Genet; 2011 Jun 01; 20(11):2131-43. PubMed ID: 21378394
    [Abstract] [Full Text] [Related]

  • 22. CAG size-specific risk estimates for intermediate allele repeat instability in Huntington disease.
    Semaka A, Kay C, Doty C, Collins JA, Bijlsma EK, Richards F, Goldberg YP, Hayden MR.
    J Med Genet; 2013 Oct 01; 50(10):696-703. PubMed ID: 23896435
    [Abstract] [Full Text] [Related]

  • 23. A CAG repeat threshold for therapeutics targeting somatic instability in Huntington's disease.
    Aldous SG, Smith EJ, Landles C, Osborne GF, Cañibano-Pico M, Nita IM, Phillips J, Zhang Y, Jin B, Hirst MB, Benn CL, Bond BC, Edelmann W, Greene JR, Bates GP.
    Brain; 2024 May 03; 147(5):1784-1798. PubMed ID: 38387080
    [Abstract] [Full Text] [Related]

  • 24. A genetic association study of glutamine-encoding DNA sequence structures, somatic CAG expansion, and DNA repair gene variants, with Huntington disease clinical outcomes.
    Ciosi M, Maxwell A, Cumming SA, Hensman Moss DJ, Alshammari AM, Flower MD, Durr A, Leavitt BR, Roos RAC, TRACK-HD team, Enroll-HD team, Holmans P, Jones L, Langbehn DR, Kwak S, Tabrizi SJ, Monckton DG.
    EBioMedicine; 2019 Oct 03; 48():568-580. PubMed ID: 31607598
    [Abstract] [Full Text] [Related]

  • 25. Continuous and periodic expansion of CAG repeats in Huntington's disease R6/1 mice.
    Møllersen L, Rowe AD, Larsen E, Rognes T, Klungland A.
    PLoS Genet; 2010 Dec 09; 6(12):e1001242. PubMed ID: 21170307
    [Abstract] [Full Text] [Related]

  • 26. Instability of highly expanded CAG repeats in mice transgenic for the Huntington's disease mutation.
    Mangiarini L, Sathasivam K, Mahal A, Mott R, Seller M, Bates GP.
    Nat Genet; 1997 Feb 09; 15(2):197-200. PubMed ID: 9020849
    [Abstract] [Full Text] [Related]

  • 27. Unstable familial transmissions of Huntington disease alleles with 27-35 CAG repeats (intermediate alleles).
    Semaka A, Collins JA, Hayden MR.
    Am J Med Genet B Neuropsychiatr Genet; 2010 Jan 05; 153B(1):314-20. PubMed ID: 19455596
    [Abstract] [Full Text] [Related]

  • 28. Msh2 deficiency prevents in vivo somatic instability of the CAG repeat in Huntington disease transgenic mice.
    Manley K, Shirley TL, Flaherty L, Messer A.
    Nat Genet; 1999 Dec 05; 23(4):471-3. PubMed ID: 10581038
    [Abstract] [Full Text] [Related]

  • 29. Neil1 is a genetic modifier of somatic and germline CAG trinucleotide repeat instability in R6/1 mice.
    Møllersen L, Rowe AD, Illuzzi JL, Hildrestrand GA, Gerhold KJ, Tveterås L, Bjølgerud A, Wilson DM, Bjørås M, Klungland A.
    Hum Mol Genet; 2012 Nov 15; 21(22):4939-47. PubMed ID: 22914735
    [Abstract] [Full Text] [Related]

  • 30. Dramatic tissue-specific mutation length increases are an early molecular event in Huntington disease pathogenesis.
    Kennedy L, Evans E, Chen CM, Craven L, Detloff PJ, Ennis M, Shelbourne PF.
    Hum Mol Genet; 2003 Dec 15; 12(24):3359-67. PubMed ID: 14570710
    [Abstract] [Full Text] [Related]

  • 31. The nucleotide sequence, DNA damage location, and protein stoichiometry influence the base excision repair outcome at CAG/CTG repeats.
    Goula AV, Pearson CE, Della Maria J, Trottier Y, Tomkinson AE, Wilson DM, Merienne K.
    Biochemistry; 2012 May 08; 51(18):3919-32. PubMed ID: 22497302
    [Abstract] [Full Text] [Related]

  • 32. Length of Uninterrupted CAG, Independent of Polyglutamine Size, Results in Increased Somatic Instability, Hastening Onset of Huntington Disease.
    Wright GEB, Collins JA, Kay C, McDonald C, Dolzhenko E, Xia Q, Bečanović K, Drögemöller BI, Semaka A, Nguyen CM, Trost B, Richards F, Bijlsma EK, Squitieri F, Ross CJD, Scherer SW, Eberle MA, Yuen RKC, Hayden MR.
    Am J Hum Genet; 2019 Jun 06; 104(6):1116-1126. PubMed ID: 31104771
    [Abstract] [Full Text] [Related]

  • 33. The Contribution of Somatic Expansion of the CAG Repeat to Symptomatic Development in Huntington's Disease: A Historical Perspective.
    Monckton DG.
    J Huntingtons Dis; 2021 Jun 06; 10(1):7-33. PubMed ID: 33579863
    [Abstract] [Full Text] [Related]

  • 34. Bidirectional transcription stimulates expansion and contraction of expanded (CTG)*(CAG) repeats.
    Nakamori M, Pearson CE, Thornton CA.
    Hum Mol Genet; 2011 Feb 01; 20(3):580-8. PubMed ID: 21088112
    [Abstract] [Full Text] [Related]

  • 35. Similar Progression of Morphological and Metabolic Phenotype in R6/2 Mice with Different CAG Repeats Revealed by In Vivo Magnetic Resonance Imaging and Spectroscopy.
    Sawiak SJ, Wood NI, Morton AJ.
    J Huntingtons Dis; 2016 Oct 01; 5(3):271-283. PubMed ID: 27662335
    [Abstract] [Full Text] [Related]

  • 36. Trinucleotide repeats in the human genome: size distributions for all possible triplets and detection of expanded disease alleles in a group of Huntington disease individuals by the repeat expansion detection method.
    Hofferbert S, Schanen NC, Chehab F, Francke U.
    Hum Mol Genet; 1997 Jan 01; 6(1):77-83. PubMed ID: 9002673
    [Abstract] [Full Text] [Related]

  • 37. CTG trinucleotide repeat "big jumps": large expansions, small mice.
    Gomes-Pereira M, Foiry L, Nicole A, Huguet A, Junien C, Munnich A, Gourdon G.
    PLoS Genet; 2007 Apr 06; 3(4):e52. PubMed ID: 17411343
    [Abstract] [Full Text] [Related]

  • 38. Triplet repeat mutation length gains correlate with cell-type specific vulnerability in Huntington disease brain.
    Shelbourne PF, Keller-McGandy C, Bi WL, Yoon SR, Dubeau L, Veitch NJ, Vonsattel JP, Wexler NS, US-Venezuela Collaborative Research Group, Arnheim N, Augood SJ.
    Hum Mol Genet; 2007 May 15; 16(10):1133-42. PubMed ID: 17409200
    [Abstract] [Full Text] [Related]

  • 39. A polymorphism in the MSH3 mismatch repair gene is associated with the levels of somatic instability of the expanded CTG repeat in the blood DNA of myotonic dystrophy type 1 patients.
    Morales F, Vásquez M, Santamaría C, Cuenca P, Corrales E, Monckton DG.
    DNA Repair (Amst); 2016 Apr 15; 40():57-66. PubMed ID: 26994442
    [Abstract] [Full Text] [Related]

  • 40. Mutagenic stress modulates the dynamics of CTG repeat instability associated with myotonic dystrophy type 1.
    Piñeiro E, Fernàndez-López L, Gamez J, Marcos R, Surrallés J, Velázquez A.
    Nucleic Acids Res; 2003 Dec 01; 31(23):6733-40. PubMed ID: 14627806
    [Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 27.