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There are 1494 results for: content related to: Long QT, syndactyly, joint contractures, stroke and novel CACNA1C mutation: Expanding the spectrum of Timothy syndrome

  1. Deletion of psychiatric risk gene Cacna1c impairs hippocampal neurogenesis in cell-autonomous fashion


    Volume 65, Issue 5, May 2017, Pages: 817–827, Bianca Völkening, Kai Schönig, Golo Kronenberg, Dusan Bartsch and Tillmann Weber

    Version of Record online : 23 FEB 2017, DOI: 10.1002/glia.23128

  2. Reduced levels of Cacna1c attenuate mesolimbic dopamine system function

    Genes, Brain and Behavior

    Volume 16, Issue 5, June 2017, Pages: 495–505, C. E. Terrillion, D. T. Dao, R. Cachope, M. K. Lobo, A. C. Puche, J. F. Cheer and T. D. Gould

    Version of Record online : 13 MAR 2017, DOI: 10.1111/gbb.12371

  3. You have free access to this content
    Sex-dependent modulation of age-related cognitive decline by the L-type calcium channel gene Cacna1c (Cav1.2)

    European Journal of Neuroscience

    Volume 42, Issue 8, October 2015, Pages: 2499–2507, Panos Zanos, Shambhu Bhat, Chantelle E. Terrillion, Robert J. Smith, Leonardo H. Tonelli and Todd D. Gould

    Version of Record online : 23 JUN 2015, DOI: 10.1111/ejn.12952

  4. L-type Ca2+ channels in mood, cognition and addiction: integrating human and rodent studies with a focus on behavioural endophenotypes

    The Journal of Physiology

    Volume 594, Issue 20, 15 October 2016, Pages: 5823–5837, Z. D. Kabir, A. S. Lee and A. M. Rajadhyaksha

    Version of Record online : 24 APR 2016, DOI: 10.1113/JP270673

  5. You have free access to this content
    Ca2+–calmodulin-dependent protein kinase II represses cardiac transcription of the L-type calcium channel α1C-subunit gene (Cacna1c) by DREAM translocation

    The Journal of Physiology

    Volume 589, Issue 11, June 2011, Pages: 2669–2686, Jarkko J. Ronkainen, Sandra L. Hänninen, Topi Korhonen, Jussi T. Koivumäki, Reka Skoumal, Sini Rautio, Veli-Pekka Ronkainen and Pasi Tavi

    Version of Record online : 1 JUN 2011, DOI: 10.1113/jphysiol.2010.201400

  6. You have free access to this content
    Methamphetamine acutely inhibits voltage-gated calcium channels but chronically up-regulates L-type channels

    Journal of Neurochemistry

    Volume 134, Issue 1, July 2015, Pages: 56–65, Marilou A. Andres, Ian M. Cooke, Frederick P. Bellinger, Marla J. Berry, Maribel M. Zaporteza, Rachel H. Rueli, Stephanie M. Barayuga and Linda Chang

    Version of Record online : 30 APR 2015, DOI: 10.1111/jnc.13104

  7. Comprehensive analysis of two Shank3 and the Cacna1c mouse models of autism spectrum disorder

    Genes, Brain and Behavior

    P.A. Kabitzke, D. Brunner, D. He, P.A. Fazio, K. Cox, J. Sutphen, L. Thiede, E. Sabath, T. Hanania, V. Alexandrov, R. Rasmusson, W. Spooren, A. Ghosh, P. Feliciano, B. Biemans, M. Benedetti and A.L. Clayton

    Version of Record online : 5 SEP 2017, DOI: 10.1111/gbb.12405

  8. Genetic analysis of SNPs in CACNA1C and ANK3 gene with schizophrenia: A comprehensive meta-analysis

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 168, Issue 8, December 2015, Pages: 637–648, Fayi Nie, Xiaoli Wang, Panpan Zhao, Hao Yang, Wenhua Zhu, Yaling Zhao, Bo Chen, Robert K. Valenzuela, Rui Zhang, Amelia L. Gallitano and Jie Ma

    Version of Record online : 31 JUL 2015, DOI: 10.1002/ajmg.b.32348

  9. Evaluating the association between CACNA1C rs1006737 and schizophrenia risk: A meta-analysis

    Asia-Pacific Psychiatry

    Volume 7, Issue 3, September 2015, Pages: 260–267, Hongyan Jiang, Fei Qiao, Zongfang Li, Yaping Zhang, Yuqi Cheng, Xiufeng Xu and Li Yu

    Version of Record online : 15 JAN 2015, DOI: 10.1111/appy.12173

  10. Molecular and Functional Characterization of Rare CACNA1C Variants in Sudden Unexplained Death in the Young

    Congenital Heart Disease

    Volume 11, Issue 6, November/December 2016, Pages: 683–692, Brittan S. Sutphin, Nicole J. Boczek, Héctor Barajas-Martínez, Dan Hu, Dan Ye, David J. Tester, Charles Antzelevitch and Michael J. Ackerman

    Version of Record online : 24 MAY 2016, DOI: 10.1111/chd.12371

  11. The impact of CACNA1C gene, and its epistasis with ZNF804A, on white matter microstructure in health, schizophrenia and bipolar disorder1

    Genes, Brain and Behavior

    Volume 16, Issue 4, April 2017, Pages: 479–488, E. Mallas, F. Carletti, C. A. Chaddock, S. Shergill, J. Woolley, M. M. Picchioni, C. McDonald, T. Toulopoulou, E. Kravariti, S. Kalidindi, E. Bramon, R. Murray, G. J. Barker and D. P. Prata

    Version of Record online : 29 NOV 2016, DOI: 10.1111/gbb.12355

  12. The CACNA1C risk allele selectively impacts on executive function in bipolar type I disorder

    Acta Psychiatrica Scandinavica

    Volume 128, Issue 5, November 2013, Pages: 362–369, M. G. Soeiro-de-Souza, D. S. Bio, V. V. Dias, E. Vieta, R. Machado-Vieira and R. A. Moreno

    Version of Record online : 14 FEB 2013, DOI: 10.1111/acps.12073

  13. You have full text access to this OnlineOpen article
    Analysis of ANK3 and CACNA1C variants identified in bipolar disorder whole genome sequence data

    Bipolar Disorders

    Volume 16, Issue 6, September 2014, Pages: 583–591, Alessia Fiorentino, Niamh Louise O'Brien, Devin Paul Locke, Andrew McQuillin, Alexandra Jarram, Adebayo Anjorin, Radhika Kandaswamy, David Curtis, Robert Alan Blizard and Hugh Malcolm Douglas Gurling

    Version of Record online : 10 APR 2014, DOI: 10.1111/bdi.12203

  14. Suggestive evidence for association between L-type voltage-gated calcium channel (CACNA1C) gene haplotypes and bipolar disorder in Latinos: a family-based association study

    Bipolar Disorders

    Volume 15, Issue 2, March 2013, Pages: 206–214, Suzanne Gonzalez, Chun Xu, Mercedes Ramirez, Juan Zavala, Regina Armas, Salvador A Contreras, Javier Contreras, Albana Dassori, Robin J Leach, Deborah Flores, Alvaro Jerez, Henriette Raventós, Alfonso Ontiveros, Humberto Nicolini and Michael Escamilla

    Version of Record online : 25 FEB 2013, DOI: 10.1111/bdi.12041

  15. The CACNA1C and ANK3 risk alleles impact on affective personality traits and startle reactivity but not on cognition or gating in healthy males

    Bipolar Disorders

    Volume 13, Issue 3, May 2011, Pages: 250–259, Panos Roussos, Stella G Giakoumaki, Anastasios Georgakopoulos, Nikolaos K Robakis and Panos Bitsios

    Version of Record online : 15 JUN 2011, DOI: 10.1111/j.1399-5618.2011.00924.x

  16. Timothy syndrome 1 genotype without syndactyly and major extracardiac manifestations

    American Journal of Medical Genetics Part A

    Volume 173, Issue 3, March 2017, Pages: 784–789, Róbert Sepp, Lidia Hategan, Attila Bácsi, Judit Cseklye, László Környei, János Borbás, Márta Széll, Tamás Forster, István Nagy and Zoltán Hegedűs

    Version of Record online : 17 FEB 2017, DOI: 10.1002/ajmg.a.38084

  17. Evidence for cis-acting regulation of ANK3 and CACNA1C gene expression

    Bipolar Disorders

    Volume 12, Issue 4, June 2010, Pages: 440–445, Emma M Quinn, Matthew Hill, Richard Anney, Michael Gill, Aiden P Corvin and Derek W Morris

    Version of Record online : 21 JUN 2010, DOI: 10.1111/j.1399-5618.2010.00817.x

    Corrected by:


    Vol. 14, Issue 7, 792, Version of Record online: 29 OCT 2012

  18. Common variants in CACNA1C and MDD susceptibility: A comprehensive meta-analysis

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 171, Issue 6, September 2016, Pages: 896–903, Shuquan Rao, Yao Yao, Chuan Zheng, Joanne Ryan, Canquan Mao, Fuquan Zhang, David Meyre and Qi Xu

    Version of Record online : 3 JUN 2016, DOI: 10.1002/ajmg.b.32466

  19. You have full text access to this OnlineOpen article
    Candidate gene associations with mood disorder, cognitive vulnerability, and fronto-limbic volumes

    Brain and Behavior

    Volume 4, Issue 3, May 2014, Pages: 418–430, Thomas W. Frazier, Eric A. Youngstrom, Brian A. Frankel, Giovana B. Zunta-Soares, Marsal Sanches, Michael Escamilla, David A. Nielsen and Jair C. Soares

    Version of Record online : 18 MAR 2014, DOI: 10.1002/brb3.226

  20. Expanding the phenotype of Timothy syndrome type 2: An adolescent with ventricular fibrillation but normal development

    American Journal of Medical Genetics Part A

    Volume 167, Issue 3, March 2015, Pages: 629–634, Anita Hiippala, Jonna Tallila, Samuel Myllykangas, Juha W Koskenvuo and Tero-Pekka Alastalo

    Version of Record online : 18 FEB 2015, DOI: 10.1002/ajmg.a.36924