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Journal Abstract Search

154 related items for PubMed ID: 36599142

  • 1. Reduced-penetrance Huntington's disease-causing alleles with 39 CAG trinucleotide repeats could be a genetic factor of amyotrophic lateral sclerosis.
    Jih KY, Lai KL, Lin KP, Liao YC, Lee YC.
    J Chin Med Assoc; 2023 Jan 01; 86(1):47-51. PubMed ID: 36599142
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  • 2. Analysis of HTT CAG repeat expansion in Italian patients with amyotrophic lateral sclerosis.
    Manini A, Gagliardi D, Meneri M, Antognozzi S, Del Bo R, Scaglione C, Comi GP, Corti S, Ronchi D.
    Ann Clin Transl Neurol; 2022 Nov 01; 9(11):1820-1825. PubMed ID: 36285345
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  • 3. Prevalence of Huntington's disease gene CAG trinucleotide repeat alleles in patients with bipolar disorder.
    Ramos EM, Gillis T, Mysore JS, Lee JM, Alonso I, Gusella JF, Smoller JW, Sklar P, MacDonald ME, Perlis RH.
    Bipolar Disord; 2015 Jun 01; 17(4):403-8. PubMed ID: 25726852
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  • 4. Prevalence of Huntington's disease gene CAG repeat alleles in sporadic amyotrophic lateral sclerosis patients.
    Ramos EM, Keagle P, Gillis T, Lowe P, Mysore JS, Leclerc AL, Ratti A, Ticozzi N, Gellera C, Gusella JF, Silani V, Alonso I, Brown RH, MacDonald ME, Landers JE.
    Amyotroph Lateral Scler; 2012 May 01; 13(3):265-9. PubMed ID: 22409360
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  • 5. Biallelic mutations in huntington disease: A new case with just one affected parent, review of the literature and terminology.
    Uhlmann WR, Peñaherrera MS, Robinson WP, Milunsky JM, Nicholson JM, Albin RL.
    Am J Med Genet A; 2015 May 01; 167A(5):1152-60. PubMed ID: 25736541
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  • 6. Haplotype analysis of the CAG and CCG repeats in 21 Brazilian families with Huntington's disease.
    Agostinho Lde A, Rocha CF, Medina-Acosta E, Barboza HN, da Silva AF, Pereira SP, da Silva Idos S, Paradela ER, Figueiredo AL, Nogueira Ede M, Alvarenga RM, Hernan Cabello P, dos Santos SR, Paiva CL.
    J Hum Genet; 2012 Dec 01; 57(12):796-803. PubMed ID: 23051704
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  • 7. Parent-of-origin differences of mutant HTT CAG repeat instability in Huntington's disease.
    Aziz NA, van Belzen MJ, Coops ID, Belfroid RD, Roos RA.
    Eur J Med Genet; 2011 Dec 01; 54(4):e413-8. PubMed ID: 21540131
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  • 11. Amyotrophic lateral sclerosis risk for spinocerebellar ataxia type 2 ATXN2 CAG repeat alleles: a meta-analysis.
    Neuenschwander AG, Thai KK, Figueroa KP, Pulst SM.
    JAMA Neurol; 2014 Dec 01; 71(12):1529-34. PubMed ID: 25285812
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  • 12. Huntingtin gene CAG repeat size affects autism risk: Family-based and case-control association study.
    Piras IS, Picinelli C, Iennaco R, Baccarin M, Castronovo P, Tomaiuolo P, Cucinotta F, Ricciardello A, Turriziani L, Nanetti L, Mariotti C, Gellera C, Lintas C, Sacco R, Zuccato C, Cattaneo E, Persico AM.
    Am J Med Genet B Neuropsychiatr Genet; 2020 Sep 01; 183(6):341-351. PubMed ID: 32652810
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  • 13. Investigating TBP CAG/CAA trinucleotide repeat expansions in a Taiwanese cohort with ALS.
    Jih KY, Lin KP, Tsai PC, Soong BW, Liao YC, Lee YC.
    Amyotroph Lateral Scler Frontotemporal Degener; 2021 Aug 01; 22(5-6):442-447. PubMed ID: 33377399
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  • 16. Increased Steady-State Mutant Huntingtin mRNA in Huntington's Disease Brain.
    Liu W, Chaurette J, Pfister EL, Kennington LA, Chase KO, Bullock J, Vonsattel JP, Faull RL, Macdonald D, DiFiglia M, Zamore PD, Aronin N.
    J Huntingtons Dis; 2013 Aug 01; 2(4):491-500. PubMed ID: 25062733
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