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Items: 1 to 20 of 28

1.
Structural basis for the gating modulation of Kv4.3 by auxiliary subunits
Demin Ma, Cheng Zhao, Xiaochen Wang, Xiaoxiao Li, Yi Zha, Yan Zhang, Guosheng Fu, Ping Liang, Jiangtao Guo, Dongwu Lai
Cell Res. 2022 Apr; 32(4): 411–414. Published online 2022 Jan 7. doi: 10.1038/s41422-021-00608-4
PMCID:
PMC8976042
ArticlePDF–1.5M
2.
Novel KCND3 Variant Underlying Nonprogressive Congenital Ataxia or SCA19/22 Disrupt KV4.3 Protein Expression and K+ Currents with Variable Effects on Channel Properties
Ginevra Zanni, Cheng-Tsung Hsiao, Ssu-Ju Fu, Chih-Yung Tang, Alessandro Capuano, Luca Bosco, Federica Graziola, Emanuele Bellacchio, Serenella Servidei, Guido Primiano, Bing-Wen Soong, Chung-Jiuan Jeng
Int J Mol Sci. 2021 May; 22(9): 4986. Published online 2021 May 7. doi: 10.3390/ijms22094986
PMCID:
PMC8125845
AbstractArticlePDF–2.3M
3.
Inter-Regulation of Kv4.3 and Voltage-Gated Sodium Channels Underlies Predisposition to Cardiac and Neuronal Channelopathies
Jérôme Clatot, Nathalie Neyroud, Robert Cox, Charlotte Souil, Jing Huang, Pascale Guicheney, Charles Antzelevitch
Int J Mol Sci. 2020 Jul; 21(14): 5057. Published online 2020 Jul 17. doi: 10.3390/ijms21145057
PMCID:
PMC7404392
AbstractArticlePDF–2.2M
4.
KCND3 potassium channel gene variant confers susceptibility to electrocardiographic early repolarization pattern
Alexander Teumer, Teresa Trenkwalder, Thorsten Kessler, Yalda Jamshidi, Marten E. van den Berg, Bernhard Kaess, Christopher P. Nelson, Rachel Bastiaenen, Marzia De Bortoli, Alessandra Rossini, Isabel Deisenhofer, Klaus Stark, Solmaz Assa, Peter S. Braund, Claudia Cabrera, Anna F. Dominiczak, Martin Gögele, Leanne M. Hall, M. Arfan Ikram, Maryam Kavousi, Karl J. Lackner, Lifelines Cohort Study, Christian Müller, Thomas Münzel, Matthias Nauck, Sandosh Padmanabhan, Norbert Pfeiffer, Tim D. Spector, Andre G. Uitterlinden, Niek Verweij, Uwe Völker, Helen R. Warren, Mobeen Zafar, Stephan B. Felix, Jan A. Kors, Harold Snieder, Patricia B. Munroe, Cristian Pattaro, Christian Fuchsberger, Georg Schmidt, Ilja M. Nolte, Heribert Schunkert, Peter P. Pramstaller, Philipp S. Wild, Pim van der Harst, Bruno H. Stricker, Renate B. Schnabel, Nilesh J. Samani, Christian Hengstenberg, Marcus Dörr, Elijah R. Behr, Wibke Reinhard
JCI Insight. 2019 Dec 5; 4(23): e131156. Published online 2019 Dec 5. doi: 10.1172/jci.insight.131156
PMCID:
PMC6962032
AbstractArticlePDF–3.3M
5.
SCN1Bβ mutations that affect their association with Kv4.3 underlie early repolarization syndrome
Hao Yao, Jun Fan, Yun‐Jiu Cheng, Xu‐Miao Chen, Cheng‐Cheng Ji, Li‐Juan Liu, Zi‐Heng Zheng, Su‐Hua Wu
J Cell Mol Med. 2018 Nov; 22(11): 5639–5647. Published online 2018 Aug 30. doi: 10.1111/jcmm.13839
PMCID:
PMC6201368
AbstractArticlePDF–701K
6.
Histone Interaction Landscapes Visualized by Crosslinking Mass Spectrometry in Intact Cell Nuclei
Domenico Fasci, Hugo van Ingen, Richard A. Scheltema, Albert J. R. Heck
Mol Cell Proteomics. 2018 Oct; 17(10): 2018–2033. Published online 2018 Jul 18. doi: 10.1074/mcp.RA118.000924
PMCID:
PMC6166682
AbstractArticlePDF–3.8M
7.
Kv4.3 Modulates the Distribution of hERG
Xiao-Jing Zhao, Chao Zhu, Liu-Yang Tian, Yi-Cheng Fu, Yu Zhang, Xi Chen, Yun Huang, Yang Li
Sci Rep. 2017; 7: 17757. Published online 2017 Dec 19. doi: 10.1038/s41598-017-17837-6
PMCID:
PMC5736654
AbstractArticlePDF–2.6M
8.
Genome-wide CRISPR screen identifies HNRNPL as a prostate cancer dependency regulating RNA splicing
Teng Fei, Yiwen Chen, Tengfei Xiao, Wei Li, Laura Cato, Peng Zhang, Maura B. Cotter, Michaela Bowden, Rosina T. Lis, Shuang G. Zhao, Qiu Wu, Felix Y. Feng, Massimo Loda, Housheng Hansen He, X. Shirley Liu, Myles Brown
Proc Natl Acad Sci U S A. 2017 Jun 27; 114(26): E5207–E5215. Published online 2017 Jun 13. doi: 10.1073/pnas.1617467114
PMCID:
PMC5495225
AbstractArticlePDF–1.3M
9.
Characterization of SEMA3A-Encoded Semaphorin as a Naturally Occurring Kv4.3 Protein Inhibitor and its Contribution to Brugada Syndrome
Nicole J. Boczek, Dan Ye, Eric K. Johnson, Wei Wang, Lia Crotti, David J. Tester, Federica Dagradi, Yuka Mizusawa, Margherita Torchio, Marielle Alders, John R. Giudicessi, Arthur A. Wilde, Peter J. Schwartz, Jeanne M. Nerbonne, Michael J. Ackerman
Circ Res. Author manuscript; available in PMC 2016 Jun 14.
Published in final edited form as: Circ Res. 2014 Aug 1; 115(4): 460–469. Published online 2014 Jun 24. doi: 10.1161/CIRCRESAHA.115.303657
PMCID:
PMC4907370
AbstractArticlePDF–838K
10.
Spinocerebellar ataxia type 19/22 mutations alter heterocomplex Kv4.3 channel function and gating in a dominant manner
Anna Duarri, Meng-Chin A. Lin, Michiel R. Fokkens, Michel Meijer, Cleo J. L. M. Smeets, Esther A. R. Nibbeling, Erik Boddeke, Richard J. Sinke, Harm H. Kampinga, Diane M. Papazian, Dineke S. Verbeek
Cell Mol Life Sci. 2015 Sep; 72(17): 3387–3399. Published online 2015 Apr 9. doi: 10.1007/s00018-015-1894-2
PMCID:
PMC4531139
AbstractArticlePDF–2.9M
11.
Two novel Brugada syndrome-associated mutations increase KV4.3 membrane expression and function
TAO YOU, WEIKE MAO, BENZHI CAI, FAQIAN LI, HAODONG XU
Int J Mol Med. 2015 Jul; 36(1): 309–315. Published online 2015 May 26. doi: 10.3892/ijmm.2015.2223
PMCID:
PMC4494594
AbstractArticlePDF–737K
12.
The potential role of Kv4.3 K+ channel in heart hypertrophy
Rong Huo, Yue Sheng, Wen-Ting Guo, De-Li Dong
Channels (Austin) 2014 May 1; 8(3): 203–209. Published online 2014 Apr 24. doi: 10.4161/chan.28972
PMCID:
PMC4203748
AbstractArticlePDF–429K
13.
Genome-Wide Analysis of Polymorphisms Associated with Cytokine Responses in Smallpox Vaccine Recipients
Richard B. Kennedy, Inna G. Ovsyannikova, V. Shane Pankratz, Iana H. Haralambieva, Robert A. Vierkant, Gregory A. Poland
Hum Genet. Author manuscript; available in PMC 2014 Sep 22.
Published in final edited form as: Hum Genet. 2012 Sep; 131(9): 1403–1421. Published online 2012 May 19. doi: 10.1007/s00439-012-1174-2
PMCID:
PMC4170585
AbstractArticlePDF–594K
14.
Genetic Determinants of P Wave Duration and PR Segment
Niek Verweij, Irene Mateo Leach, Malou van den Boogaard, Dirk J. van Veldhuisen, Vincent M. Christoffels, LifeLines Cohort Study, Hans L. Hillege, Wiek H. van Gilst, Phil Barnett, Rudolf A. de Boer, Pim van der Harst
Circ Cardiovasc Genet. Author manuscript; available in PMC 2015 Aug 1.
Published in final edited form as: Circ Cardiovasc Genet. 2014 Aug; 7(4): 475–481. Published online 2014 May 21. doi: 10.1161/CIRCGENETICS.113.000373
PMCID:
PMC4141024
AbstractArticlePDF–410K
15.
Mutations in KCND3 cause spinocerebellar ataxia type 22
Yi-chung Lee, Alexandra Durr, Karen Majczenko, Yen-hua Huang, Yu-chao Liu, Cheng-chang Lien, Pei-chien Tsai, Yaeko Ichikawa, Jun Goto, Marie-Lorraine Monin, Jun Z. Li, Ming-yi Chung, Emeline Mundwiller, Vikram Shakkottai, Tze-tze Liu, Christelle Tesson, Yi-chun Lu, Alexis Brice, Shoji Tsuji, Margit Burmeister, Giovanni Stevanin, Bing-wen Soong
Ann Neurol. Author manuscript; available in PMC 2014 Jul 7.
Published in final edited form as: Ann Neurol. 2012 Dec; 72(6): 859–869. doi: 10.1002/ana.23701
PMCID:
PMC4085146
AbstractArticlePDF–384K
16.
Novel Mutations in the KCND3-Encoded Kv4.3 K+ Channel Associated with Autopsy-Negative Sudden Unexplained Death
John R. Giudicessi, Dan Ye, Chad J. Kritzberger, Vladislav V. Nesterenko, David J. Tester, Charles Antzelevitch, Michael J. Ackerman
Hum Mutat. Author manuscript; available in PMC 2012 Dec 11.
Published in final edited form as: Hum Mutat. 2012 Jun; 33(6): 989–997. Published online 2012 Mar 27. doi: 10.1002/humu.22058
PMCID:
PMC3518919
AbstractArticlePDF–2.9M
17.
A Meta-Analysis of Genome-Wide Association Studies of the Electrocardiographic Early Repolarization Pattern
Moritz F. Sinner, Kimmo Porthan, Peter A. Noseworthy, Aki S. Havulinna, Jani Tikkanen, Martina Müller-Nurasyid, Gina Peloso, Sheila Ulivi, Britt Maria Beckmann, A. Catharina Brockhaus, Rebecca R. Cooper, Paolo Gasparini, Christian Hengstenberg, Shih-Jen Hwang, Annamaria Iorio, M. Juhani Junttila, Norman Klopp, Mika Kähönen, Maarit A. Laaksonen, Terho Lehtimäki, Peter Lichtner, Leo-Pekka Lyytikäinen, Eimo Martens, Christa Meisinger, Thomas Meitinger, Faisal M. Merchant, Markku S. Nieminen, Annette Peters, Arto Pietilä, Siegfried Perz, Lasse Oikarinen, Olli Raitakari, Wibke Reinhard, Kaisa Silander, Barbara Thorand, H.-Erich Wichmann, Gianfranco Sinagra, Jorma Viikari, Christopher J. O’Donnell, Patrick T. Ellinor, Heikki V. Huikuri, Stefan Kääb, Christopher Newton-Cheh, Veikko Salomaa
Heart Rhythm. Author manuscript; available in PMC 2013 Oct 1.
Published in final edited form as: Heart Rhythm. 2012 Oct; 9(10): 1627–1634. Published online 2012 Jun 6. doi: 10.1016/j.hrthm.2012.06.008
PMCID:
PMC3459269
AbstractArticlePDF–826K
18.
Genome-Wide Association for Abdominal Subcutaneous and Visceral Adipose Reveals a Novel Locus for Visceral Fat in Women
Caroline S. Fox, Yongmei Liu, Charles C. White, Mary Feitosa, Albert V. Smith, Nancy Heard-Costa, Kurt Lohman, GIANT Consortium, MAGIC Consortium, GLGC Consortium, Andrew D. Johnson, Meredith C. Foster, Danielle M. Greenawalt, Paula Griffin, Jinghong Ding, Anne B. Newman, Fran Tylavsky, Iva Miljkovic, Stephen B. Kritchevsky, Lenore Launer, Melissa Garcia, Gudny Eiriksdottir, J. Jeffrey Carr, Vilmunder Gudnason, Tamara B. Harris, L. Adrienne Cupples, Ingrid B. Borecki
PLoS Genet. 2012 May; 8(5): e1002695. Published online 2012 May 10. doi: 10.1371/journal.pgen.1002695
PMCID:
PMC3349734
AbstractArticlePDF–377K
19.
The “structurally minimal” isoform KChIP2d modulates recovery of Kv4.3 N-terminal deletion mutant Δ2-39
Laura J Hovind, Donald L Campbell
Channels (Austin) 2011 May-Jun; 5(3): 225–227. Published online 2011 May 1. doi: 10.4161/chan.5.3.15313
PMCID:
PMC3225751
AbstractArticlePDF–638K
20.
Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium
Pascale Gaudet, Michael S. Livstone, Suzanna E. Lewis, Paul D. Thomas
Brief Bioinform. 2011 Sep; 12(5): 449–462. Published online 2011 Aug 27. doi: 10.1093/bib/bbr042
PMCID:
PMC3178059
AbstractArticlePDF–1.0M

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