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Journal Abstract Search

1192 related items for PubMed ID: 26742514

  • 1.
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  • 2. FAN1 modifies Huntington's disease progression by stabilizing the expanded HTT CAG repeat.
    Goold R, Flower M, Moss DH, Medway C, Wood-Kaczmar A, Andre R, Farshim P, Bates GP, Holmans P, Jones L, Tabrizi SJ.
    Hum Mol Genet; 2019 Feb 15; 28(4):650-661. PubMed ID: 30358836
    [Abstract] [Full Text] [Related]

  • 3. Promotion of somatic CAG repeat expansion by Fan1 knock-out in Huntington's disease knock-in mice is blocked by Mlh1 knock-out.
    Loupe JM, Pinto RM, Kim KH, Gillis T, Mysore JS, Andrew MA, Kovalenko M, Murtha R, Seong I, Gusella JF, Kwak S, Howland D, Lee R, Lee JM, Wheeler VC, MacDonald ME.
    Hum Mol Genet; 2020 Nov 04; 29(18):3044-3053. PubMed ID: 32876667
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  • 4. Expanding the Spectrum of Genes Involved in Huntington Disease Using a Combined Clinical and Genetic Approach.
    Mariani LL, Tesson C, Charles P, Cazeneuve C, Hahn V, Youssov K, Freeman L, Grabli D, Roze E, Noël S, Peuvion JN, Bachoud-Levi AC, Brice A, Stevanin G, Durr A.
    JAMA Neurol; 2016 Sep 01; 73(9):1105-14. PubMed ID: 27400454
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  • 6. Clinical phenotype in carriers of intermediate alleles in the huntingtin gene.
    Savitt D, Jankovic J.
    J Neurol Sci; 2019 Jul 15; 402():57-61. PubMed ID: 31103960
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  • 8. A Study of Triplet-Primed PCR for Identification of CAG Repeat Expansion in the HTT Gene in a Cohort of 503 Indian Cases with Huntington's Disease Symptoms.
    Chheda P, Chanekar M, Salunkhe Y, Dama T, Pais A, Pande S, Bendre R, Shah N.
    Mol Diagn Ther; 2018 Jun 15; 22(3):353-359. PubMed ID: 29619771
    [Abstract] [Full Text] [Related]

  • 9. A disorder similar to Huntington's disease is associated with a novel CAG repeat expansion.
    Margolis RL, O'Hearn E, Rosenblatt A, Willour V, Holmes SE, Franz ML, Callahan C, Hwang HS, Troncoso JC, Ross CA.
    Ann Neurol; 2001 Dec 15; 50(6):373-80. PubMed ID: 11761463
    [Abstract] [Full Text] [Related]

  • 10. Investigations of Huntington's Disease and Huntington's Disease-Like Syndromes in Indian Choreatic Patients.
    Kaur J, Parveen S, Shamim U, Sharma P, Suroliya V, Sonkar AK, Ahmad I, Garg J, Anand KS, Laskar S, Chowdhury D, Kushwaha S, Goyal V, Srivastava AK, Singh G, Faruq M.
    J Huntingtons Dis; 2020 Dec 15; 9(3):283-289. PubMed ID: 32675418
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  • 11. 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]

  • 12. Novel BAC Mouse Model of Huntington's Disease with 225 CAG Repeats Exhibits an Early Widespread and Stable Degenerative Phenotype.
    Wegrzynowicz M, Bichell TJ, Soares BD, Loth MK, McGlothan JS, Mori S, Alikhan FS, Hua K, Coughlin JM, Holt HK, Jetter CS, Pomper MG, Osmand AP, Guilarte TR, Bowman AB.
    J Huntingtons Dis; 2015 May 03; 4(1):17-36. PubMed ID: 26333255
    [Abstract] [Full Text] [Related]

  • 13. Huntington's disease: how intermediate are intermediate repeat lengths?
    Squitieri F, Jankovic J.
    Mov Disord; 2012 Dec 03; 27(14):1714-7. PubMed ID: 23008174
    [Abstract] [Full Text] [Related]

  • 14. Genetic Contributors to Intergenerational CAG Repeat Instability in Huntington's Disease Knock-In Mice.
    Neto JL, Lee JM, Afridi A, Gillis T, Guide JR, Dempsey S, Lager B, Alonso I, Wheeler VC, Pinto RM.
    Genetics; 2017 Feb 03; 205(2):503-516. PubMed ID: 27913616
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  • 15. [Study of the association of genotype and phenotype features of the pathogenesis of Huntington's chorea].
    Hryshchenko NV, Kucherenko AM, Patskun EI, Livshyts' LA.
    Tsitol Genet; 2009 Feb 03; 43(3):42-7. PubMed ID: 19938636
    [Abstract] [Full Text] [Related]

  • 16. High resolution time-course mapping of early transcriptomic, molecular and cellular phenotypes in Huntington's disease CAG knock-in mice across multiple genetic backgrounds.
    Ament SA, Pearl JR, Grindeland A, St Claire J, Earls JC, Kovalenko M, Gillis T, Mysore J, Gusella JF, Lee JM, Kwak S, Howland D, Lee MY, Baxter D, Scherler K, Wang K, Geman D, Carroll JB, MacDonald ME, Carlson G, Wheeler VC, Price ND, Hood LE.
    Hum Mol Genet; 2017 Mar 01; 26(5):913-922. PubMed ID: 28334820
    [Abstract] [Full Text] [Related]

  • 17. Clinical Features of Huntington's Disease.
    Ghosh R, Tabrizi SJ.
    Adv Exp Med Biol; 2018 Mar 01; 1049():1-28. PubMed ID: 29427096
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  • 18. Huntington's disease: clinical presentation and treatment.
    Novak MJ, Tabrizi SJ.
    Int Rev Neurobiol; 2011 Mar 01; 98():297-323. PubMed ID: 21907093
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  • 19. Biological and clinical manifestations of juvenile Huntington's disease: a retrospective analysis.
    Fusilli C, Migliore S, Mazza T, Consoli F, De Luca A, Barbagallo G, Ciammola A, Gatto EM, Cesarini M, Etcheverry JL, Parisi V, Al-Oraimi M, Al-Harrasi S, Al-Salmi Q, Marano M, Vonsattel JG, Sabatini U, Landwehrmeyer GB, Squitieri F.
    Lancet Neurol; 2018 Nov 01; 17(11):986-993. PubMed ID: 30243861
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  • 20. Clinical and genetic characteristics in patients with Huntington's disease from China.
    Yang J, Chen K, Wei Q, Chen Y, Cao B, Burgunder JM, Shang HF.
    Neurol Res; 2016 Oct 01; 38(10):916-20. PubMed ID: 27483361
    [Abstract] [Full Text] [Related]

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