These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
153 related articles for article (PubMed ID: 27013529)
1. Spontaneous shaker rat mutant - a new model for X-linked tremor/ataxia. Figueroa KP; Paul S; Calì T; Lopreiato R; Karan S; Frizzarin M; Ames D; Zanni G; Brini M; Dansithong W; Milash B; Scoles DR; Carafoli E; Pulst SM Dis Model Mech; 2016 May; 9(5):553-62. PubMed ID: 27013529 [TBL] [Abstract][Full Text] [Related]
2. X-linked transmission of the shaker mutation in rats with hereditary Purkinje cell degeneration and ataxia. Clark BR; LaRegina M; Tolbert DL Brain Res; 2000 Mar; 858(2):264-73. PubMed ID: 10708677 [TBL] [Abstract][Full Text] [Related]
3. A Novel Mutation in Isoform 3 of the Plasma Membrane Ca2+ Pump Impairs Cellular Ca2+ Homeostasis in a Patient with Cerebellar Ataxia and Laminin Subunit 1α Mutations. Calì T; Lopreiato R; Shimony J; Vineyard M; Frizzarin M; Zanni G; Zanotti G; Brini M; Shinawi M; Carafoli E J Biol Chem; 2015 Jun; 290(26):16132-41. PubMed ID: 25953895 [TBL] [Abstract][Full Text] [Related]
4. Mutation of plasma membrane Ca2+ ATPase isoform 3 in a family with X-linked congenital cerebellar ataxia impairs Ca2+ homeostasis. Zanni G; Calì T; Kalscheuer VM; Ottolini D; Barresi S; Lebrun N; Montecchi-Palazzi L; Hu H; Chelly J; Bertini E; Brini M; Carafoli E Proc Natl Acad Sci U S A; 2012 Sep; 109(36):14514-9. PubMed ID: 22912398 [TBL] [Abstract][Full Text] [Related]
5. The ataxia-linked E1081Q mutation affects the sub-plasma membrane Ca Vallese F; Maso L; Giamogante F; Poggio E; Barazzuol L; Salmaso A; Lopreiato R; Cendron L; Navazio L; Zanni G; Weber Y; Kovacevic-Preradovic T; Keren B; Torraco A; Carrozzo R; Peretto F; Peggion C; Ferro S; Marin O; Zanotti G; Calì T; Brini M; Carafoli E Cell Death Dis; 2022 Oct; 13(10):855. PubMed ID: 36207321 [TBL] [Abstract][Full Text] [Related]
6. Autophagy precedes apoptosis among at risk cerebellar Purkinje cells in the shaker mutant rat: an ultrastructural study. Erekat NS Ultrastruct Pathol; 2018; 42(2):162-169. PubMed ID: 29419349 [TBL] [Abstract][Full Text] [Related]
7. Slc9a6 mutation causes Purkinje cell loss and ataxia in the shaker rat. Figueroa KP; Anderson CJ; Paul S; Dansithong W; Gandelman M; Scoles DR; Pulst SM Hum Mol Genet; 2023 May; 32(10):1647-1659. PubMed ID: 36621975 [TBL] [Abstract][Full Text] [Related]
8. Spatial and temporal pattern of Purkinje cell degeneration in shaker mutant rats with hereditary cerebellar ataxia. Tolbert DL; Ewald M; Gutting J; La Regina MC J Comp Neurol; 1995 May; 355(4):490-507. PubMed ID: 7636028 [TBL] [Abstract][Full Text] [Related]
9. A behavioral study of the development of hereditary cerebellar ataxia in the shaker rat mutant. Wolf LW; LaRegina MC; Tolbert DL Behav Brain Res; 1996 Feb; 75(1-2):67-81. PubMed ID: 8800661 [TBL] [Abstract][Full Text] [Related]
10. FMR1 gene premutation is a frequent genetic cause of late-onset sporadic cerebellar ataxia. Brussino A; Gellera C; Saluto A; Mariotti C; Arduino C; Castellotti B; Camerlingo M; de Angelis V; Orsi L; Tosca P; Migone N; Taroni F; Brusco A Neurology; 2005 Jan; 64(1):145-7. PubMed ID: 15642922 [TBL] [Abstract][Full Text] [Related]
12. A novel PMCA3 mutation in an ataxic patient with hypomorphic phosphomannomutase 2 (PMM2) heterozygote mutations: Biochemical characterization of the pump defect. Vicario M; Calì T; Cieri D; Vallese F; Bortolotto R; Lopreiato R; Zonta F; Nardella M; Micalizzi A; Lefeber DJ; Valente EM; Bertini E; Zanotti G; Zanni G; Brini M; Carafoli E Biochim Biophys Acta Mol Basis Dis; 2017 Dec; 1863(12):3303-3312. PubMed ID: 28807751 [TBL] [Abstract][Full Text] [Related]
13. Argonaute-2-dependent rescue of a Drosophila model of FXTAS by FRAXE premutation repeat. Sofola OA; Jin P; Botas J; Nelson DL Hum Mol Genet; 2007 Oct; 16(19):2326-32. PubMed ID: 17635840 [TBL] [Abstract][Full Text] [Related]
14. A cerebellar tremor/ataxia syndrome among fragile X premutation carriers. Hagerman PJ; Greco CM; Hagerman RJ Cytogenet Genome Res; 2003; 100(1-4):206-12. PubMed ID: 14526182 [TBL] [Abstract][Full Text] [Related]
15. A V1143F mutation in the neuronal-enriched isoform 2 of the PMCA pump is linked with ataxia. Vicario M; Zanni G; Vallese F; Santorelli F; Grinzato A; Cieri D; Berto P; Frizzarin M; Lopreiato R; Zonta F; Ferro S; Sandre M; Marin O; Ruzzene M; Bertini E; Zanotti G; Brini M; Calì T; Carafoli E Neurobiol Dis; 2018 Jul; 115():157-166. PubMed ID: 29655659 [TBL] [Abstract][Full Text] [Related]
16. Presence of inclusions positive for polyglycine containing protein, FMRpolyG, indicates that repeat-associated non-AUG translation plays a role in fragile X-associated primary ovarian insufficiency. Buijsen RA; Visser JA; Kramer P; Severijnen EA; Gearing M; Charlet-Berguerand N; Sherman SL; Berman RF; Willemsen R; Hukema RK Hum Reprod; 2016 Jan; 31(1):158-68. PubMed ID: 26537920 [TBL] [Abstract][Full Text] [Related]
17. Deep cerebellar stimulation reduces ataxic motor symptoms in the shaker rat. Anderson CJ; Figueroa KP; Dorval AD; Pulst SM Ann Neurol; 2019 May; 85(5):681-690. PubMed ID: 30854718 [TBL] [Abstract][Full Text] [Related]
18. A genetic study of the FMR1 gene in a Sardinian multiple sclerosis population. Lorefice L; Tranquilli S; Fenu G; Murru MR; Frau J; Rolesu M; Coghe GC; Marrosu F; Marrosu MG; Cocco E Neurol Sci; 2015 Dec; 36(12):2213-20. PubMed ID: 26194536 [TBL] [Abstract][Full Text] [Related]
19. Active caspase-3 upregulation is augmented in at-risk cerebellar Purkinje cells following inferior olive chemoablation in the shaker mutant rat: an immunofluorescence study. Erekat NS Neurol Res; 2019 Mar; 41(3):234-241. PubMed ID: 30462592 [TBL] [Abstract][Full Text] [Related]
20. A SEL1L mutation links a canine progressive early-onset cerebellar ataxia to the endoplasmic reticulum-associated protein degradation (ERAD) machinery. Kyöstilä K; Cizinauskas S; Seppälä EH; Suhonen E; Jeserevics J; Sukura A; Syrjä P; Lohi H PLoS Genet; 2012; 8(6):e1002759. PubMed ID: 22719266 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]