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2. Knockdown of Cav2.1 calcium channels is sufficient to induce neurological disorders observed in natural occurring Cacna1a mutants in mice. Saito H; Okada M; Miki T; Wakamori M; Futatsugi A; Mori Y; Mikoshiba K; Suzuki N Biochem Biophys Res Commun; 2009 Dec; 390(3):1029-33. PubMed ID: 19854154 [TBL] [Abstract][Full Text] [Related]
3. Differential expression of T-type calcium channels in P/Q-type calcium channel mutant mice with ataxia and absence epilepsy. Nahm SS; Jung KY; Enger MK; Griffith WH; Abbott LC J Neurobiol; 2005 Feb; 62(3):352-60. PubMed ID: 15514988 [TBL] [Abstract][Full Text] [Related]
4. The ataxic groggy rat has a missense mutation in the P/Q-type voltage-gated Ca2+ channel alpha1A subunit gene and exhibits absence seizures. Tokuda S; Kuramoto T; Tanaka K; Kaneko S; Takeuchi IK; Sasa M; Serikawa T Brain Res; 2007 Feb; 1133(1):168-77. PubMed ID: 17196942 [TBL] [Abstract][Full Text] [Related]
5. Early onset, non fluctuating spinocerebellar ataxia and a novel missense mutation in CACNA1A gene. Tonelli A; D'Angelo MG; Salati R; Villa L; Germinasi C; Frattini T; Meola G; Turconi AC; Bresolin N; Bassi MT J Neurol Sci; 2006 Feb; 241(1-2):13-7. PubMed ID: 16325861 [TBL] [Abstract][Full Text] [Related]
6. Dramatically different levels of Cacna1a gene expression between pre-weaning wild type and leaner mice. Veneziano L; Albertosi S; Pesci D; Mantuano E; Frontali M; Jodice C J Neurol Sci; 2011 Jun; 305(1-2):71-4. PubMed ID: 21440913 [TBL] [Abstract][Full Text] [Related]
7. Developmental expression of neuronal nitric oxide synthase in P/Q-type voltage-gated calcium ion channel mutant mice, leaner and tottering. Frank-Cannon TC; Zeve DR; Abbott LC Brain Res; 2007 Apr; 1140():96-104. PubMed ID: 16359645 [TBL] [Abstract][Full Text] [Related]
8. Alterations in intracellular calcium ion concentrations in cerebellar granule cells of the CACNA1A mutant mouse, leaner, during postnatal development. Bawa B; Abbott LC Neurotox Res; 2011 Jan; 19(1):123-7. PubMed ID: 20043243 [TBL] [Abstract][Full Text] [Related]
9. Severely impaired neuromuscular synaptic transmission causes muscle weakness in the Cacna1a-mutant mouse rolling Nagoya. Kaja S; van de Ven RC; van Dijk JG; Verschuuren JJ; Arahata K; Frants RR; Ferrari MD; van den Maagdenberg AM; Plomp JJ Eur J Neurosci; 2007 Apr; 25(7):2009-20. PubMed ID: 17439489 [TBL] [Abstract][Full Text] [Related]
10. A novel missense mutation in CACNA1A evaluated by in silico protein modeling is associated with non-episodic spinocerebellar ataxia with slow progression. Bürk K; Kaiser FJ; Tennstedt S; Schöls L; Kreuz FR; Wieland T; Strom TM; Büttner T; Hollstein R; Braunholz D; Plaschke J; Gillessen-Kaesbach G; Zühlke C Eur J Med Genet; 2014 Apr; 57(5):207-11. PubMed ID: 24486772 [TBL] [Abstract][Full Text] [Related]
11. Rocker is a new variant of the voltage-dependent calcium channel gene Cacna1a. Zwingman TA; Neumann PE; Noebels JL; Herrup K J Neurosci; 2001 Feb; 21(4):1169-78. PubMed ID: 11160387 [TBL] [Abstract][Full Text] [Related]
12. Phenotypes of spinocerebellar ataxia type 6 and familial hemiplegic migraine caused by a unique CACNA1A missense mutation in patients from a large family. Alonso I; Barros J; Tuna A; Coelho J; Sequeiros J; Silveira I; Coutinho P Arch Neurol; 2003 Apr; 60(4):610-4. PubMed ID: 12707077 [TBL] [Abstract][Full Text] [Related]
13. New ataxic tottering-6j mouse allele containing a Cacna1a gene mutation. Li W; Zhou Y; Tian X; Kim TY; Ito N; Watanabe K; Tsuji A; Niimi K; Aoyama Y; Arai T; Takahashi E PLoS One; 2012; 7(8):e44230. PubMed ID: 22952933 [TBL] [Abstract][Full Text] [Related]
14. Congenital ataxia and hemiplegic migraine with cerebral edema associated with a novel gain of function mutation in the calcium channel CACNA1A. García Segarra N; Gautschi I; Mittaz-Crettol L; Kallay Zetchi C; Al-Qusairi L; Van Bemmelen MX; Maeder P; Bonafé L; Schild L; Roulet-Perez E J Neurol Sci; 2014 Jul; 342(1-2):69-78. PubMed ID: 24836863 [TBL] [Abstract][Full Text] [Related]
15. Differential cerebellar GABAA receptor expression in mice with mutations in CaV2.1 (P/Q-type) calcium channels. Kaja S; Payne AJ; Nielsen EØ; Thompson CL; van den Maagdenberg AM; Koulen P; Snutch TP Neuroscience; 2015 Sep; 304():198-208. PubMed ID: 26208839 [TBL] [Abstract][Full Text] [Related]
16. Neural integrator function in murine CACNA1A mutants. Stahl JS; James RA Ann N Y Acad Sci; 2005 Apr; 1039():580-2. PubMed ID: 15827027 [TBL] [Abstract][Full Text] [Related]
18. Two novel alleles of tottering with distinct Ca(v)2.1 calcium channel neuropathologies. Miki T; Zwingman TA; Wakamori M; Lutz CM; Cook SA; Hosford DA; Herrup K; Fletcher CF; Mori Y; Frankel WN; Letts VA Neuroscience; 2008 Jul; 155(1):31-44. PubMed ID: 18597946 [TBL] [Abstract][Full Text] [Related]
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20. Tottering mouse motor dysfunction is abolished on the Purkinje cell degeneration (pcd) mutant background. Campbell DB; North JB; Hess EJ Exp Neurol; 1999 Nov; 160(1):268-78. PubMed ID: 10630211 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]