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62. 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]
63. Huntington's Disease and Diabetes: Chronological Sequence of its Association. Montojo MT; Aganzo M; González N J Huntingtons Dis; 2017; 6(3):179-188. PubMed ID: 28968242 [TBL] [Abstract][Full Text] [Related]
64. 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]
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69. Myricetin Reduces Toxic Level of CAG Repeats RNA in Huntington's Disease (HD) and Spino Cerebellar Ataxia (SCAs). Khan E; Tawani A; Mishra SK; Verma AK; Upadhyay A; Kumar M; Sandhir R; Mishra A; Kumar A ACS Chem Biol; 2018 Jan; 13(1):180-188. PubMed ID: 29172480 [TBL] [Abstract][Full Text] [Related]
71. Intermediate and Expanded HTT Alleles and the Risk for α-Synucleinopathies. Pérez-Oliveira S; Álvarez I; Rosas I; Menendez-González M; Blázquez-Estrada M; Aguilar M; Corte D; Buongiorno M; Molina-Porcel L; Aldecoa I; Martí MJ; Sánchez-Juan P; Infante J; González-Aramburu I; García-González P; Rosende-Roca M; Boada M; Ruiz A; Periñán MT; Macías-García D; Muñoz-Delgado L; Gómez-Garre P; Mir P; Clarimón J; Lleo A; Alcolea D; De la Casa-Fages B; Duarte I; Álvarez V; Pastor P Mov Disord; 2022 Sep; 37(9):1841-1849. PubMed ID: 35852957 [TBL] [Abstract][Full Text] [Related]
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73. Translating Antisense Technology into a Treatment for Huntington's Disease. Lane RM; Smith A; Baumann T; Gleichmann M; Norris D; Bennett CF; Kordasiewicz H Methods Mol Biol; 2018; 1780():497-523. PubMed ID: 29856033 [TBL] [Abstract][Full Text] [Related]
74. The diagnosis and natural history of Huntington disease. Pagan F; Torres-Yaghi Y; Altshuler M Handb Clin Neurol; 2017; 144():63-67. PubMed ID: 28947126 [TBL] [Abstract][Full Text] [Related]
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76. Stoichiometry of base excision repair proteins correlates with increased somatic CAG instability in striatum over cerebellum in Huntington's disease transgenic mice. Goula AV; Berquist BR; Wilson DM; Wheeler VC; Trottier Y; Merienne K PLoS Genet; 2009 Dec; 5(12):e1000749. PubMed ID: 19997493 [TBL] [Abstract][Full Text] [Related]
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79. Huntingtin HTT1a is generated in a CAG repeat-length-dependent manner in human tissues. Hoschek F; Natan J; Wagner M; Sathasivam K; Abdelmoez A; von Einem B; Bates GP; Landwehrmeyer GB; Neueder A Mol Med; 2024 Mar; 30(1):36. PubMed ID: 38459427 [TBL] [Abstract][Full Text] [Related]
80. Lack of association of somatic CAG repeat expansion with striatal neurodegeneration in HD knock-in animal models. Bai D; Yin P; Zhang Y; Sun F; Chen L; Lin L; Yan S; Li S; Li XJ Hum Mol Genet; 2021 Jul; 30(16):1497-1508. PubMed ID: 33949657 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]