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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

252 related articles for article (PubMed ID: 25109669)

  • 1. The first knockin mouse model of episodic ataxia type 2.
    Rose SJ; Kriener LH; Heinzer AK; Fan X; Raike RS; van den Maagdenberg AM; Hess EJ
    Exp Neurol; 2014 Nov; 261():553-62. PubMed ID: 25109669
    [TBL] [Abstract][Full Text] [Related]  

  • 2. RNAi silencing of P/Q-type calcium channels in Purkinje neurons of adult mouse leads to episodic ataxia type 2.
    Salvi J; Bertaso F; Mausset-Bonnefont AL; Metz A; Lemmers C; Ango F; Fagni L; Lory P; Mezghrani A
    Neurobiol Dis; 2014 Aug; 68():47-56. PubMed ID: 24768804
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Characterization of the dominant inheritance mechanism of Episodic Ataxia type 2.
    Dorgans K; Salvi J; Bertaso F; Bernard L; Lory P; Doussau F; Mezghrani A
    Neurobiol Dis; 2017 Oct; 106():110-123. PubMed ID: 28688851
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Ubiquitin Ligase RNF138 Promotes Episodic Ataxia Type 2-Associated Aberrant Degradation of Human Ca
    Fu SJ; Jeng CJ; Ma CH; Peng YJ; Lee CM; Fang YC; Lee YC; Tang SC; Hu MC; Tang CY
    J Neurosci; 2017 Mar; 37(9):2485-2503. PubMed ID: 28167673
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A CaV2.1 N-terminal fragment relieves the dominant-negative inhibition by an Episodic ataxia 2 mutant.
    Dahimene S; Page KM; Nieto-Rostro M; Pratt WS; D'Arco M; Dolphin AC
    Neurobiol Dis; 2016 Sep; 93():243-56. PubMed ID: 27260834
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Functional implications of a novel EA2 mutation in the P/Q-type calcium channel.
    Spacey SD; Hildebrand ME; Materek LA; Bird TD; Snutch TP
    Ann Neurol; 2004 Aug; 56(2):213-20. PubMed ID: 15293273
    [TBL] [Abstract][Full Text] [Related]  

  • 7. KCa channels as therapeutic targets in episodic ataxia type-2.
    Alviña K; Khodakhah K
    J Neurosci; 2010 May; 30(21):7249-57. PubMed ID: 20505091
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Aberrant cerebellar Purkinje cell activity as the cause of motor attacks in a mouse model of episodic ataxia type 2.
    Tara E; Vitenzon A; Hess E; Khodakhah K
    Dis Model Mech; 2018 Sep; 11(9):. PubMed ID: 30279196
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Epilepsy and episodic ataxia type 2: family study and review of the literature.
    Verriello L; Pauletto G; Nilo A; Lonigro I; Betto E; Valente M; Curcio F; Gigli GL
    J Neurol; 2021 Nov; 268(11):4296-4302. PubMed ID: 33983550
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Episodic ataxias 1 and 2.
    Baloh RW
    Handb Clin Neurol; 2012; 103():595-602. PubMed ID: 21827920
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Cognitive deficits in episodic ataxia type 2 mouse models.
    Bohne P; Mourabit DB; Josten M; Mark MD
    Hum Mol Genet; 2021 Sep; 30(19):1811-1832. PubMed ID: 34077522
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Abnormal excitability and episodic low-frequency oscillations in the cerebral cortex of the tottering mouse.
    Cramer SW; Popa LS; Carter RE; Chen G; Ebner TJ
    J Neurosci; 2015 Apr; 35(14):5664-79. PubMed ID: 25855180
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. In vivo impact of presynaptic calcium channel dysfunction on motor axons in episodic ataxia type 2.
    Tomlinson SE; Tan SV; Burke D; Labrum RW; Haworth A; Gibbons VS; Sweeney MG; Griggs RC; Kullmann DM; Bostock H; Hanna MG
    Brain; 2016 Feb; 139(Pt 2):380-91. PubMed ID: 26912519
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Missense CACNA1A mutation causing episodic ataxia type 2.
    Denier C; Ducros A; Durr A; Eymard B; Chassande B; Tournier-Lasserve E
    Arch Neurol; 2001 Feb; 58(2):292-5. PubMed ID: 11176968
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Missense mutations of CACNA1A are a frequent cause of autosomal dominant nonprogressive congenital ataxia.
    Travaglini L; Nardella M; Bellacchio E; D'Amico A; Capuano A; Frusciante R; Di Capua M; Cusmai R; Barresi S; Morlino S; Fernández-Fernández JM; Trivisano M; Specchio N; Valeriani M; Vigevano F; Bertini E; Zanni G
    Eur J Paediatr Neurol; 2017 May; 21(3):450-456. PubMed ID: 28007337
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Loss-of-function EA2 mutations are associated with impaired neuromuscular transmission.
    Jen J; Wan J; Graves M; Yu H; Mock AF; Coulin CJ; Kim G; Yue Q; Papazian DM; Baloh RW
    Neurology; 2001 Nov; 57(10):1843-8. PubMed ID: 11723274
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Postnatal loss of P/Q-type channels confined to rhombic-lip-derived neurons alters synaptic transmission at the parallel fiber to purkinje cell synapse and replicates genomic Cacna1a mutation phenotype of ataxia and seizures in mice.
    Maejima T; Wollenweber P; Teusner LU; Noebels JL; Herlitze S; Mark MD
    J Neurosci; 2013 Mar; 33(12):5162-74. PubMed ID: 23516282
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Cerebellar ataxia by enhanced Ca(V)2.1 currents is alleviated by Ca2+-dependent K+-channel activators in Cacna1a(S218L) mutant mice.
    Gao Z; Todorov B; Barrett CF; van Dorp S; Ferrari MD; van den Maagdenberg AM; De Zeeuw CI; Hoebeek FE
    J Neurosci; 2012 Oct; 32(44):15533-46. PubMed ID: 23115190
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.