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Journal Abstract Search

344 related items for PubMed ID: 9217976

  • 21. Repeat expansion diseases.
    Paulson H.
    Handb Clin Neurol; 2018; 147():105-123. PubMed ID: 29325606
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  • 22. Trinucleotide repeat expansions in neurological disease.
    Warren ST, Nelson DL.
    Curr Opin Neurobiol; 1993 Oct; 3(5):752-9. PubMed ID: 8260825
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  • 23. [Triplet repeat disease, with particular emphasis of spinal and bulbar muscular atrophy (SBMA)].
    Sobue G.
    Rinsho Shinkeigaku; 2000 Dec; 40(12):1193-5. PubMed ID: 11464455
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  • 24. Molecular genetics of triplet repeats: unstable expansion of triplet repeats as a new mechanism for neurodegenerative diseases.
    Tsuji S.
    Intern Med; 1997 Jan; 36(1):3-8. PubMed ID: 9058092
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  • 25. [Importance of the number of trinucleotide repeat expansions in the clinical manifestations of Huntington's chorea].
    Vojvodić N, Culjković B, Romac S, Stojković O, Sternić N, Sokić D, Kostić VS.
    Srp Arh Celok Lek; 1998 Jan; 126(3-4):77-82. PubMed ID: 9863360
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  • 29. 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; 15(2):197-200. PubMed ID: 9020849
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  • 31. Genetic anticipation. Expanding tandem repeats.
    Carpenter NJ.
    Neurol Clin; 1994 Nov; 12(4):683-97. PubMed ID: 7845337
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  • 32. 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
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  • 33. Spinal and bulbar muscular atrophy: a trinucleotide-repeat expansion neurodegenerative disease.
    Brooks BP, Fischbeck KH.
    Trends Neurosci; 1995 Oct 06; 18(10):459-61. PubMed ID: 8545913
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  • 34. DNA repair in the trinucleotide repeat disorders.
    Jones L, Houlden H, Tabrizi SJ.
    Lancet Neurol; 2017 Jan 06; 16(1):88-96. PubMed ID: 27979358
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  • 35. Molecular genetics of hereditary spinocerebellar ataxia: mutation analysis of spinocerebellar ataxia genes and CAG/CTG repeat expansion detection in 225 Italian families.
    Brusco A, Gellera C, Cagnoli C, Saluto A, Castucci A, Michielotto C, Fetoni V, Mariotti C, Migone N, Di Donato S, Taroni F.
    Arch Neurol; 2004 May 06; 61(5):727-33. PubMed ID: 15148151
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  • 40. Is the 31 CAG repeat allele of the spinocerebellar ataxia 1 (SCA1) gene locus non-specifically associated with trinucleotide expansion diseases?
    Savić D, Topisirović I, Keckarević M, Keckarević D, Major T, Culjković B, Stojković O, Rakocević-Stojanović V, Mladenović J, Todorović S, Apostolski S, Romac S.
    Psychiatr Genet; 2001 Dec 06; 11(4):201-5. PubMed ID: 11807410
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