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4. Partial resistance to malonate-induced striatal cell death in transgenic mouse models of Huntington's disease is dependent on age and CAG repeat length. Hansson O; Castilho RF; Korhonen L; Lindholm D; Bates GP; Brundin P J Neurochem; 2001 Aug; 78(4):694-703. PubMed ID: 11520890 [TBL] [Abstract][Full Text] [Related]
5. Tauroursodeoxycholic acid, a bile acid, is neuroprotective in a transgenic animal model of Huntington's disease. Keene CD; Rodrigues CM; Eich T; Chhabra MS; Steer CJ; Low WC Proc Natl Acad Sci U S A; 2002 Aug; 99(16):10671-6. PubMed ID: 12149470 [TBL] [Abstract][Full Text] [Related]
6. Riluzole prolongs survival time and alters nuclear inclusion formation in a transgenic mouse model of Huntington's disease. Schiefer J; Landwehrmeyer GB; Lüesse HG; Sprünken A; Puls C; Milkereit A; Milkereit E; Kosinski CM Mov Disord; 2002 Jul; 17(4):748-57. PubMed ID: 12210870 [TBL] [Abstract][Full Text] [Related]
7. N-Acetylaspartate and DARPP-32 levels decrease in the corpus striatum of Huntington's disease mice. van Dellen A; Welch J; Dixon RM; Cordery P; York D; Styles P; Blakemore C; Hannan AJ Neuroreport; 2000 Nov; 11(17):3751-7. PubMed ID: 11117485 [TBL] [Abstract][Full Text] [Related]
9. Metabotropic glutamate receptor 5 positive allosteric modulators are neuroprotective in a mouse model of Huntington's disease. Doria JG; Silva FR; de Souza JM; Vieira LB; Carvalho TG; Reis HJ; Pereira GS; Dobransky T; Ribeiro FM Br J Pharmacol; 2013 Jun; 169(4):909-21. PubMed ID: 23489026 [TBL] [Abstract][Full Text] [Related]
10. Creatine-supplemented diet extends Purkinje cell survival in spinocerebellar ataxia type 1 transgenic mice but does not prevent the ataxic phenotype. Kaemmerer WF; Rodrigues CM; Steer CJ; Low WC Neuroscience; 2001; 103(3):713-24. PubMed ID: 11274790 [TBL] [Abstract][Full Text] [Related]
11. Treatment with a herbal formula B401 enhances neuroprotection and angiogenesis in the R6/2 mouse model of Huntington's disease. Wang SE; Lin CL; Hsu CH; Sheu SJ; Chien CT; Wu CH Drug Des Devel Ther; 2015; 9():887-900. PubMed ID: 25733809 [TBL] [Abstract][Full Text] [Related]
12. Transgenic mice expressing mutated full-length HD cDNA: a paradigm for locomotor changes and selective neuronal loss in Huntington's disease. Reddy PH; Charles V; Williams M; Miller G; Whetsell WO; Tagle DA Philos Trans R Soc Lond B Biol Sci; 1999 Jun; 354(1386):1035-45. PubMed ID: 10434303 [TBL] [Abstract][Full Text] [Related]
13. Dendritic spine pathology and deficits in experience-dependent dendritic plasticity in R6/1 Huntington's disease transgenic mice. Spires TL; Grote HE; Garry S; Cordery PM; Van Dellen A; Blakemore C; Hannan AJ Eur J Neurosci; 2004 May; 19(10):2799-807. PubMed ID: 15147313 [TBL] [Abstract][Full Text] [Related]
14. Neuroprotective Effects of Doxycycline in the R6/2 Mouse Model of Huntington's Disease. Paldino E; Balducci C; La Vitola P; Artioli L; D'Angelo V; Giampà C; Artuso V; Forloni G; Fusco FR Mol Neurobiol; 2020 Apr; 57(4):1889-1903. PubMed ID: 31879858 [TBL] [Abstract][Full Text] [Related]
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17. Striatal atrophy and dendritic alterations in a knock-in mouse model of Huntington's disease. Lerner RP; Trejo Martinez Ldel C; Zhu C; Chesselet MF; Hickey MA Brain Res Bull; 2012 Apr; 87(6):571-8. PubMed ID: 22326483 [TBL] [Abstract][Full Text] [Related]
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19. LBH589, A Hydroxamic Acid-Derived HDAC Inhibitor, is Neuroprotective in Mouse Models of Huntington's Disease. Chopra V; Quinti L; Khanna P; Paganetti P; Kuhn R; Young AB; Kazantsev AG; Hersch S J Huntingtons Dis; 2016 Dec; 5(4):347-355. PubMed ID: 27983565 [TBL] [Abstract][Full Text] [Related]
20. Combination therapy with coenzyme Q10 and creatine produces additive neuroprotective effects in models of Parkinson's and Huntington's diseases. Yang L; Calingasan NY; Wille EJ; Cormier K; Smith K; Ferrante RJ; Beal MF J Neurochem; 2009 Jun; 109(5):1427-39. PubMed ID: 19476553 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]