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262 related items for PubMed ID: 24191263

  • 21. Intergenerational and striatal CAG repeat instability in Huntington's disease knock-in mice involve different DNA repair genes.
    Dragileva E, Hendricks A, Teed A, Gillis T, Lopez ET, Friedberg EC, Kucherlapati R, Edelmann W, Lunetta KL, MacDonald ME, Wheeler VC.
    Neurobiol Dis; 2009 Jan; 33(1):37-47. PubMed ID: 18930147
    [Abstract] [Full Text] [Related]

  • 22. Dramatic mutation instability in HD mouse striatum: does polyglutamine load contribute to cell-specific vulnerability in Huntington's disease?
    Kennedy L, Shelbourne PF.
    Hum Mol Genet; 2000 Oct 12; 9(17):2539-44. PubMed ID: 11030759
    [Abstract] [Full Text] [Related]

  • 23. Modifiers of Somatic Repeat Instability in Mouse Models of Friedreich Ataxia and the Fragile X-Related Disorders: Implications for the Mechanism of Somatic Expansion in Huntington's Disease.
    Zhao X, Kumari D, Miller CJ, Kim GY, Hayward B, Vitalo AG, Pinto RM, Usdin K.
    J Huntingtons Dis; 2021 Oct 12; 10(1):149-163. PubMed ID: 33579860
    [Abstract] [Full Text] [Related]

  • 24. A slipped-CAG DNA-binding small molecule induces trinucleotide-repeat contractions in vivo.
    Nakamori M, Panigrahi GB, Lanni S, Gall-Duncan T, Hayakawa H, Tanaka H, Luo J, Otabe T, Li J, Sakata A, Caron MC, Joshi N, Prasolava T, Chiang K, Masson JY, Wold MS, Wang X, Lee MYWT, Huddleston J, Munson KM, Davidson S, Layeghifard M, Edward LM, Gallon R, Santibanez-Koref M, Murata A, Takahashi MP, Eichler EE, Shlien A, Nakatani K, Mochizuki H, Pearson CE.
    Nat Genet; 2020 Feb 12; 52(2):146-159. PubMed ID: 32060489
    [Abstract] [Full Text] [Related]

  • 25. Disease-associated repeat instability and mismatch repair.
    Schmidt MHM, Pearson CE.
    DNA Repair (Amst); 2016 Feb 12; 38():117-126. PubMed ID: 26774442
    [Abstract] [Full Text] [Related]

  • 26. Length-dependent CTG·CAG triplet-repeat expansion in myotonic dystrophy patient-derived induced pluripotent stem cells.
    Du J, Campau E, Soragni E, Jespersen C, Gottesfeld JM.
    Hum Mol Genet; 2013 Dec 20; 22(25):5276-87. PubMed ID: 23933738
    [Abstract] [Full Text] [Related]

  • 27. Mismatch repair genes Mlh1 and Mlh3 modify CAG instability in Huntington's disease mice: genome-wide and candidate approaches.
    Pinto RM, Dragileva E, Kirby A, Lloret A, Lopez E, St Claire J, Panigrahi GB, Hou C, Holloway K, Gillis T, Guide JR, Cohen PE, Li GM, Pearson CE, Daly MJ, Wheeler VC.
    PLoS Genet; 2013 Oct 20; 9(10):e1003930. PubMed ID: 24204323
    [Abstract] [Full Text] [Related]

  • 28. 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]

  • 29. Partial resistance to malonate-induced striatal cell death in transgenic mouse models of Huntington's disease is dependent on age and CAG repeat length.
    Hansson O, Castilho RF, Korhonen L, Lindholm D, Bates GP, Brundin P.
    J Neurochem; 2001 Aug 01; 78(4):694-703. PubMed ID: 11520890
    [Abstract] [Full Text] [Related]

  • 30. Antagonistic roles of canonical and Alternative-RPA in disease-associated tandem CAG repeat instability.
    Gall-Duncan T, Luo J, Jurkovic CM, Fischer LA, Fujita K, Deshmukh AL, Harding RJ, Tran S, Mehkary M, Li V, Leib DE, Chen R, Tanaka H, Mason AG, Lévesque D, Khan M, Razzaghi M, Prasolava T, Lanni S, Sato N, Caron MC, Panigrahi GB, Wang P, Lau R, Castel AL, Masson JY, Tippett L, Turner C, Spies M, La Spada AR, Campos EI, Curtis MA, Boisvert FM, Faull RLM, Davidson BL, Nakamori M, Okazawa H, Wold MS, Pearson CE.
    Cell; 2023 Oct 26; 186(22):4898-4919.e25. PubMed ID: 37827155
    [Abstract] [Full Text] [Related]

  • 31. Modelling and inference reveal nonlinear length-dependent suppression of somatic instability for small disease associated alleles in myotonic dystrophy type 1 and Huntington disease.
    Higham CF, Monckton DG.
    J R Soc Interface; 2013 Nov 06; 10(88):20130605. PubMed ID: 24047873
    [Abstract] [Full Text] [Related]

  • 32. Tissue-dependent regulation of RNAP II dynamics: the missing link between transcription and trinucleotide repeat instability in diseases?
    Goula AV, Festenstein R, Merienne K.
    Transcription; 2013 Nov 06; 4(4):172-6. PubMed ID: 23989661
    [Abstract] [Full Text] [Related]

  • 33. Gene expression profiling of R6/2 transgenic mice with different CAG repeat lengths reveals genes associated with disease onset and progression in Huntington's disease.
    Tang B, Seredenina T, Coppola G, Kuhn A, Geschwind DH, Luthi-Carter R, Thomas EA.
    Neurobiol Dis; 2011 Jun 06; 42(3):459-67. PubMed ID: 21334439
    [Abstract] [Full Text] [Related]

  • 34. DNA instability in replicating Huntington's disease lymphoblasts.
    Cannella M, Maglione V, Martino T, Ragona G, Frati L, Li GM, Squitieri F.
    BMC Med Genet; 2009 Feb 11; 10():11. PubMed ID: 19210789
    [Abstract] [Full Text] [Related]

  • 35. 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 11; 40():57-66. PubMed ID: 26994442
    [Abstract] [Full Text] [Related]

  • 36. Pms2 is a genetic enhancer of trinucleotide CAG.CTG repeat somatic mosaicism: implications for the mechanism of triplet repeat expansion.
    Gomes-Pereira M, Fortune MT, Ingram L, McAbney JP, Monckton DG.
    Hum Mol Genet; 2004 Aug 15; 13(16):1815-25. PubMed ID: 15198993
    [Abstract] [Full Text] [Related]

  • 37. Di-valent siRNA-mediated silencing of MSH3 blocks somatic repeat expansion in mouse models of Huntington's disease.
    O'Reilly D, Belgrad J, Ferguson C, Summers A, Sapp E, McHugh C, Mathews E, Boudi A, Buchwald J, Ly S, Moreno D, Furgal R, Luu E, Kennedy Z, Hariharan V, Monopoli K, Yang XW, Carroll J, DiFiglia M, Aronin N, Khvorova A.
    Mol Ther; 2023 Jun 07; 31(6):1661-1674. PubMed ID: 37177784
    [Abstract] [Full Text] [Related]

  • 38. Striatal phosphodiesterase mRNA and protein levels are reduced in Huntington's disease transgenic mice prior to the onset of motor symptoms.
    Hebb AL, Robertson HA, Denovan-Wright EM.
    Neuroscience; 2004 Jun 07; 123(4):967-81. PubMed ID: 14751289
    [Abstract] [Full Text] [Related]

  • 39. MSH2 ATPase domain mutation affects CTG*CAG repeat instability in transgenic mice.
    Tomé S, Holt I, Edelmann W, Morris GE, Munnich A, Pearson CE, Gourdon G.
    PLoS Genet; 2009 May 07; 5(5):e1000482. PubMed ID: 19436705
    [Abstract] [Full Text] [Related]

  • 40. Somatic expansion behaviour of the (CTG)n repeat in myotonic dystrophy knock-in mice is differentially affected by Msh3 and Msh6 mismatch-repair proteins.
    van den Broek WJ, Nelen MR, Wansink DG, Coerwinkel MM, te Riele H, Groenen PJ, Wieringa B.
    Hum Mol Genet; 2002 Jan 15; 11(2):191-8. PubMed ID: 11809728
    [Abstract] [Full Text] [Related]

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