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7. Five siRNAs targeting three SNPs may provide therapy for three-quarters of Huntington's disease patients. Pfister EL; Kennington L; Straubhaar J; Wagh S; Liu W; DiFiglia M; Landwehrmeyer B; Vonsattel JP; Zamore PD; Aronin N Curr Biol; 2009 May; 19(9):774-8. PubMed ID: 19361997 [TBL] [Abstract][Full Text] [Related]
8. CAG repeat size in the normal HTT allele and age of onset in Huntington's disease. Aziz NA; van Roon-Mom WM; Roos RA Mov Disord; 2011 Nov; 26(13):2450-1; author reply 2451. PubMed ID: 22109852 [No Abstract] [Full Text] [Related]
9. 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]
10. 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; 86(1):47-51. PubMed ID: 36599142 [TBL] [Abstract][Full Text] [Related]
11. 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; 57(12):796-803. PubMed ID: 23051704 [TBL] [Abstract][Full Text] [Related]
12. Molecular analysis of the Huntington's disease gene in New Zealand. Whitefield JE; Williams L; Snow K; Dixon J; Winship I; Stapleton PM; Faull RM; Love DR N Z Med J; 1996 Feb; 109(1015):27-30. PubMed ID: 8606810 [TBL] [Abstract][Full Text] [Related]
13. Identification and characterization of the miniature pig Huntington's disease gene homolog: evidence for conservation and polymorphism in the CAG triplet repeat. Matsuyama N; Hadano S; Onoe K; Osuga H; Showguchi-Miyata J; Gondo Y; Ikeda JE Genomics; 2000 Oct; 69(1):72-85. PubMed ID: 11013077 [TBL] [Abstract][Full Text] [Related]
14. Analysis of triplet repeats in the huntingtin gene in Japanese families affected with Huntington's disease. Masuda N; Goto J; Murayama N; Watanabe M; Kondo I; Kanazawa I J Med Genet; 1995 Sep; 32(9):701-5. PubMed ID: 8544189 [TBL] [Abstract][Full Text] [Related]
16. Linkage disequilibrium between the expanded (CAG)n repeat and an allele of the adjacent (CCG)n repeat in Huntington's disease patients of Greek origin. Yapijakis C; Vassilopoulos D; Tzagournisakis M; Maris T; Fesdjian C; Papageorgiou C; Plaitakis A Eur J Hum Genet; 1995; 3(4):228-34. PubMed ID: 8528671 [TBL] [Abstract][Full Text] [Related]
17. MSH3 polymorphisms and protein levels affect CAG repeat instability in Huntington's disease mice. Tomé S; Manley K; Simard JP; Clark GW; Slean MM; Swami M; Shelbourne PF; Tillier ER; Monckton DG; Messer A; Pearson CE PLoS Genet; 2013; 9(2):e1003280. PubMed ID: 23468640 [TBL] [Abstract][Full Text] [Related]
18. The length of uninterrupted CAG repeats in stem regions of repeat disease associated hairpins determines the amount of short CAG oligonucleotides that are toxic to cells through RNA interference. Murmann AE; Patel M; Jeong SY; Bartom ET; Jennifer Morton A; Peter ME Cell Death Dis; 2022 Dec; 13(12):1078. PubMed ID: 36585400 [TBL] [Abstract][Full Text] [Related]
19. Expansion of a (CAG)n repeat region in a sporadic case of HD. Bozza A; Malagù S; Calzolari E; Novelletto A; Pavoni M; del Senno L Acta Neurol Scand; 1995 Aug; 92(2):132-4. PubMed ID: 7484060 [TBL] [Abstract][Full Text] [Related]
20. [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; 126(3-4):77-82. PubMed ID: 9863360 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]