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2. Ectopic expression of the striatal-enriched GTPase Rhes elicits cerebellar degeneration and an ataxia phenotype in Huntington's disease. Swarnkar S; Chen Y; Pryor WM; Shahani N; Page DT; Subramaniam S Neurobiol Dis; 2015 Oct; 82():66-77. PubMed ID: 26048156 [TBL] [Abstract][Full Text] [Related]
3. The role of Rhes, Ras homolog enriched in striatum, in neurodegenerative processes. Harrison LM; Lahoste GJ Exp Cell Res; 2013 Sep; 319(15):2310-5. PubMed ID: 23583659 [TBL] [Abstract][Full Text] [Related]
4. Bioinformatics analysis of Ras homologue enriched in the striatum, a potential target for Huntington's disease therapy. Carbo M; Brandi V; Pascarella G; Staid DS; Colotti G; Polticelli F; Ilari A; Morea V Int J Mol Med; 2019 Dec; 44(6):2223-2233. PubMed ID: 31638189 [TBL] [Abstract][Full Text] [Related]
6. Striatal Induction and Spread of the Huntington's Disease Protein: A Novel Rhes Route. Subramaniam S J Huntingtons Dis; 2022; 11(3):281-290. PubMed ID: 35871361 [TBL] [Abstract][Full Text] [Related]
7. Huntington's disease is a disorder of the corpus striatum: focus on Rhes (Ras homologue enriched in the striatum). Subramaniam S; Snyder SH Neuropharmacology; 2011 Jun; 60(7-8):1187-92. PubMed ID: 21044641 [TBL] [Abstract][Full Text] [Related]
8. Rhes, a striatal specific protein, mediates mutant-huntingtin cytotoxicity. Subramaniam S; Sixt KM; Barrow R; Snyder SH Science; 2009 Jun; 324(5932):1327-30. PubMed ID: 19498170 [TBL] [Abstract][Full Text] [Related]
9. Attenuation of Rhes activity significantly delays the appearance of behavioral symptoms in a mouse model of Huntington's disease. Baiamonte BA; Lee FA; Brewer ST; Spano D; LaHoste GJ PLoS One; 2013; 8(1):e53606. PubMed ID: 23349722 [TBL] [Abstract][Full Text] [Related]
10. Msh2 acts in medium-spiny striatal neurons as an enhancer of CAG instability and mutant huntingtin phenotypes in Huntington's disease knock-in mice. Kovalenko M; Dragileva E; St Claire J; Gillis T; Guide JR; New J; Dong H; Kucherlapati R; Kucherlapati MH; Ehrlich ME; Lee JM; Wheeler VC PLoS One; 2012; 7(9):e44273. PubMed ID: 22970194 [TBL] [Abstract][Full Text] [Related]
11. Wild-type huntingtin ameliorates striatal neuronal atrophy but does not prevent other abnormalities in the YAC128 mouse model of Huntington disease. Van Raamsdonk JM; Pearson J; Murphy Z; Hayden MR; Leavitt BR BMC Neurosci; 2006 Dec; 7():80. PubMed ID: 17147801 [TBL] [Abstract][Full Text] [Related]
12. Silencing mutant huntingtin by adeno-associated virus-mediated RNA interference ameliorates disease manifestations in the YAC128 mouse model of Huntington's disease. Stanek LM; Sardi SP; Mastis B; Richards AR; Treleaven CM; Taksir T; Misra K; Cheng SH; Shihabuddin LS Hum Gene Ther; 2014 May; 25(5):461-74. PubMed ID: 24484067 [TBL] [Abstract][Full Text] [Related]
13. Global Rhes knockout in the Q175 Huntington's disease mouse model. Heikkinen T; Bragge T; Kuosmanen J; Parkkari T; Gustafsson S; Kwan M; Beltran J; Ghavami A; Subramaniam S; Shahani N; Ramírez-Jarquín UN; Park L; Muñoz-Sanjuán I; Marchionini DM PLoS One; 2021; 16(10):e0258486. PubMed ID: 34648564 [TBL] [Abstract][Full Text] [Related]
14. Full length mutant huntingtin is required for altered Ca2+ signaling and apoptosis of striatal neurons in the YAC mouse model of Huntington's disease. Zhang H; Li Q; Graham RK; Slow E; Hayden MR; Bezprozvanny I Neurobiol Dis; 2008 Jul; 31(1):80-8. PubMed ID: 18502655 [TBL] [Abstract][Full Text] [Related]
15. Olesoxime suppresses calpain activation and mutant huntingtin fragmentation in the BACHD rat. Clemens LE; Weber JJ; Wlodkowski TT; Yu-Taeger L; Michaud M; Calaminus C; Eckert SH; Gaca J; Weiss A; Magg JC; Jansson EK; Eckert GP; Pichler BJ; Bordet T; Pruss RM; Riess O; Nguyen HP Brain; 2015 Dec; 138(Pt 12):3632-53. PubMed ID: 26490331 [TBL] [Abstract][Full Text] [Related]
16. Antisense oligonucleotide-mediated correction of transcriptional dysregulation is correlated with behavioral benefits in the YAC128 mouse model of Huntington's disease. Stanek LM; Yang W; Angus S; Sardi PS; Hayden MR; Hung GH; Bennett CF; Cheng SH; Shihabuddin LS J Huntingtons Dis; 2013; 2(2):217-28. PubMed ID: 25063516 [TBL] [Abstract][Full Text] [Related]
17. Suppressing aberrant GluN3A expression rescues synaptic and behavioral impairments in Huntington's disease models. Marco S; Giralt A; Petrovic MM; Pouladi MA; Martínez-Turrillas R; Martínez-Hernández J; Kaltenbach LS; Torres-Peraza J; Graham RK; Watanabe M; Luján R; Nakanishi N; Lipton SA; Lo DC; Hayden MR; Alberch J; Wesseling JF; Pérez-Otaño I Nat Med; 2013 Aug; 19(8):1030-8. PubMed ID: 23852340 [TBL] [Abstract][Full Text] [Related]
18. Therapeutic silencing of mutant huntingtin with siRNA attenuates striatal and cortical neuropathology and behavioral deficits. DiFiglia M; Sena-Esteves M; Chase K; Sapp E; Pfister E; Sass M; Yoder J; Reeves P; Pandey RK; Rajeev KG; Manoharan M; Sah DW; Zamore PD; Aronin N Proc Natl Acad Sci U S A; 2007 Oct; 104(43):17204-9. PubMed ID: 17940007 [TBL] [Abstract][Full Text] [Related]
19. Rhes deletion is neuroprotective in the 3-nitropropionic acid model of Huntington's disease. Mealer RG; Subramaniam S; Snyder SH J Neurosci; 2013 Feb; 33(9):4206-10. PubMed ID: 23447628 [TBL] [Abstract][Full Text] [Related]
20. Golgi protein ACBD3 mediates neurotoxicity associated with Huntington's disease. Sbodio JI; Paul BD; Machamer CE; Snyder SH Cell Rep; 2013 Sep; 4(5):890-7. PubMed ID: 24012756 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]