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8. Dominant effects of the Huntington's disease HTT CAG repeat length are captured in gene-expression data sets by a continuous analysis mathematical modeling strategy. Lee JM; Galkina EI; Levantovsky RM; Fossale E; Anne Anderson M; Gillis T; Srinidhi Mysore J; Coser KR; Shioda T; Zhang B; Furia MD; Derry J; Kohane IS; Seong IS; Wheeler VC; Gusella JF; MacDonald ME Hum Mol Genet; 2013 Aug; 22(16):3227-38. PubMed ID: 23595883 [TBL] [Abstract][Full Text] [Related]
9. RNA toxicity induced by expanded CAG repeats in Huntington's disease. Martí E Brain Pathol; 2016 Nov; 26(6):779-786. PubMed ID: 27529325 [TBL] [Abstract][Full Text] [Related]
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11. 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; 54(4):e413-8. PubMed ID: 21540131 [TBL] [Abstract][Full Text] [Related]
12. Patterns of CAG repeat instability in the central nervous system and periphery in Huntington's disease and in spinocerebellar ataxia type 1. Mouro Pinto R; Arning L; Giordano JV; Razghandi P; Andrew MA; Gillis T; Correia K; Mysore JS; Grote Urtubey DM; Parwez CR; von Hein SM; Clark HB; Nguyen HP; Förster E; Beller A; Jayadaev S; Keene CD; Bird TD; Lucente D; Vonsattel JP; Orr H; Saft C; Petrasch-Parwez E; Wheeler VC Hum Mol Genet; 2020 Aug; 29(15):2551-2567. PubMed ID: 32761094 [TBL] [Abstract][Full Text] [Related]
13. Missing the pathological expansion in Huntington disease: de novo c.51C>G variant on the expanded allele causing intrafamilial allele dropout. Magri S; Nanetti L; Mongelli A; Rizzo E; Taroni F; Mariotti C; Gellera C Am J Med Genet A; 2021 Feb; 185(2):397-400. PubMed ID: 33247537 [TBL] [Abstract][Full Text] [Related]
14. Base editing strategies to convert CAG to CAA diminish the disease-causing mutation in Huntington's disease. Choi DE; Shin JW; Zeng S; Hong EP; Jang JH; Loupe JM; Wheeler VC; Stutzman HE; Kleinstiver B; Lee JM Elife; 2024 Jun; 12():. PubMed ID: 38869243 [TBL] [Abstract][Full Text] [Related]
15. HD CAGnome: a search tool for huntingtin CAG repeat length-correlated genes. Galkina EI; Shin A; Coser KR; Shioda T; Kohane IS; Seong IS; Wheeler VC; Gusella JF; Macdonald ME; Lee JM PLoS One; 2014; 9(4):e95556. PubMed ID: 24751919 [TBL] [Abstract][Full Text] [Related]
16. Evidence for a predisposing background for CAG expansion leading to HTT mutation in a Chinese population. Ma M; Yang Y; Shang H; Su D; Zhang H; Ma Y; Liu Y; Tao D; Zhang S J Neurol Sci; 2010 Nov; 298(1-2):57-60. PubMed ID: 20864123 [TBL] [Abstract][Full Text] [Related]
17. A pathogenic mechanism in Huntington's disease involves small CAG-repeated RNAs with neurotoxic activity. Bañez-Coronel M; Porta S; Kagerbauer B; Mateu-Huertas E; Pantano L; Ferrer I; Guzmán M; Estivill X; Martí E PLoS Genet; 2012; 8(2):e1002481. PubMed ID: 22383888 [TBL] [Abstract][Full Text] [Related]
18. 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; 4(1):17-36. PubMed ID: 26333255 [TBL] [Abstract][Full Text] [Related]
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20. Uncovering the Genetic and Molecular Features of Huntington's Disease in Northern Colombia. Ahmad M; Ríos-Anillo MR; Acosta-López JE; Cervantes-Henríquez ML; Martínez-Banfi M; Pineda-Alhucema W; Puentes-Rozo P; Sánchez-Barros C; Pinzón A; Patel HR; Vélez JI; Villarreal-Camacho JL; Pineda DA; Arcos-Burgos M; Sánchez-Rojas M Int J Mol Sci; 2023 Nov; 24(22):. PubMed ID: 38003344 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]