PMC Links for Nucleotide (Select 1631890800) - PMC

Xiaojing Zhu, Rixin Li, Guojun Kang, Qi Kang, Wenwang Rao, Mingjia Yang, Bonan Cao, Mingyuan Zhang, Yaoyao Sun, Yueying Wang, Xin Chen, Yaqin Yu, Qiong Yu

Dis Markers. 2019; 2019: 8062397. Published online 2019 Apr 1. doi: 10.1155/2019/8062397

PMCID:: PMC6466926

Abstract Article PDF–691K

Select item 491365.

Molecular diversity of L-type Ca2+ channel transcripts in human fibroblasts.

N M Soldatov

Proc Natl Acad Sci U S A. 1992 May 15; 89(10): 4628–4632. doi: 10.1073/pnas.89.10.4628

PMCID:: PMC49136

Summary Page Browse PDF–1.3M

Select item 70107676.

Genetic Basis and Genotype–Phenotype Correlations in Han Chinese Patients with Idiopathic Dilated Cardiomyopathy

Xin-Lin Zhang, Jun Xie, Rong-Fang Lan, Li-Na Kang, Lian Wang, Wei Xu, Biao Xu

Sci Rep. 2020; 10: 2226. Published online 2020 Feb 10. doi: 10.1038/s41598-020-58984-7

PMCID:: PMC7010767

Abstract Article PDF–1.5M

Select item 67607317.

Capacitative calcium entry and proliferation of human osteoblast‐like MG‐63 cells

D. Labelle, C. Jumarie, R. Moreau

Cell Prolif. 2007 Dec; 40(6): 866–884. Published online 2007 Nov 15. doi: 10.1111/j.1365-2184.2007.00477.x

PMCID:: PMC6760731

Abstract Article PDF–462K

Select item 67251958.

Congenital Stationary Night Blindness Type 2 Mutations S229P, G369D, L1068P, and W1440X Alter Channel Gating or Functional Expression of Ca_v1.4 L-type Ca²⁺ Channels

Jean-Charles Hoda, Francesca Zaghetto, Alexandra Koschak, Jörg Striessnig

J Neurosci. 2005 Jan 5; 25(1): 252–259. doi: 10.1523/JNEUROSCI.3054-04.2005

PMCID:: PMC6725195

Abstract Article PDF–327K

Select item 61685489.

An African loss-of-function CACNA1C variant p.T1787M associated with a risk of ventricular fibrillation

Malorie Blancard, Amal Debbiche, Koichi Kato, Christelle Cardin, Guichard Sabrina, Estelle Gandjbakhch, Vincent Probst, Michel Haissaguerre, Fabrice Extramiana, Mélèze Hocini, Geoffroy Olivier, Antoine Leenhardt, Pascale Guicheney, Jean-Sébastien Rougier

Sci Rep. 2018; 8: 14619. Published online 2018 Oct 2. doi: 10.1038/s41598-018-32867-4

PMCID:: PMC6168548

Abstract Article PDF–1.9M

Select item 539931610.

Novel trigenic CACNA1C/DES/MYPN mutations in a family of hypertrophic cardiomyopathy with early repolarization and short QT syndrome

Yanhong Chen, Hector Barajas-Martinez, Dongxiao Zhu, Xihui Wang, Chonghao Chen, Ruijuan Zhuang, Jingjing Shi, Xueming Wu, Yijia Tao, Weidong Jin, Xiaoyan Wang, Dan Hu

J Transl Med. 2017; 15: 78. Published online 2017 Apr 20. doi: 10.1186/s12967-017-1180-1

Correction in:: J Transl Med. 2017; 15: 101.

PMCID:: PMC5399316

Abstract Article PDF–3.2M

Select item 509406011.

Identification and Functional Characterization of a Novel CACNA1C-Mediated Cardiac Disorder Characterized by Prolonged QT Intervals with Hypertrophic Cardiomyopathy, Congenital Heart Defects, and Sudden Cardiac Death

Nicole J. Boczek, Dan Ye, Fang Jin, David J. Tester, April Huseby, J. Martijn Bos, Aaron J. Johnson, Ronald Kanter, Michael J. Ackerman

Circ Arrhythm Electrophysiol. Author manuscript; available in PMC 2016 Nov 3.

Published in final edited form as: Circ Arrhythm Electrophysiol. 2015 Oct; 8(5): 1122–1132. Published online 2015 Aug 7. doi: 10.1161/CIRCEP.115.002745

PMCID:: PMC5094060

Abstract Article PDF–2.1M

Select item 465833312.

Genetic disruption of voltage-gated calcium channels in psychiatric and neurological disorders

Samuel Heyes, Wendy S. Pratt, Elliott Rees, Shehrazade Dahimene, Laurent Ferron, Michael J. Owen, Annette C. Dolphin

Prog Neurobiol. 2015 Nov; 134: 36–54. doi: 10.1016/j.pneurobio.2015.09.002

PMCID:: PMC4658333

Abstract Article PDF–1.3M

Select item 462213913.

Molecular and Cellular Characteristics of the Colonic Pseudo-obstruction in Patients With Intractable Constipation

Yoon Suh Do, Seung-Jae Myung, Sun-Young Kwak, Soohan Cho, Enoch Lee, Min Jeong Song, Chang Sik Yu, Yong Sik Yoon, Hye Kyung Lee

J Neurogastroenterol Motil. 2015 Oct; 21(4): 560–570. Published online 2015 Oct 31. doi: 10.5056/jnm15048

PMCID:: PMC4622139

Abstract Article PDF–1.2M

Select item 426225314.

Calmodulin Mutations Associated with Long QT Syndrome Prevent Inactivation of Cardiac L-type Ca²⁺ Currents and Promote Proarrhythmic Behavior in Ventricular Myocytes

Worawan B. Limpitikul, Ivy E. Dick, Rosy Joshi-Mukherjee, Michael T. Overgaard, Alfred L. George, Jr., David T. Yue

J Mol Cell Cardiol. Author manuscript; available in PMC 2015 Sep 1.

Published in final edited form as: J Mol Cell Cardiol. 2014 Sep; 74: 115–124. Published online 2014 May 8. doi: 10.1016/j.yjmcc.2014.04.022

PMCID:: PMC4262253

Abstract Article PDF–1.1M

Select item 415371315.

A CACNA1C Variant Associated with Reduced Voltage-Dependent Inactivation, Increased Ca_V1.2 Channel Window Current, and Arrhythmogenesis

Jessica A. Hennessey, Nicole J. Boczek, Yong-Hui Jiang, Joelle D. Miller, William Patrick, Ryan Pfeiffer, Brittan S. Sutphin, David J. Tester, Hector Barajas-Martinez, Michael J. Ackerman, Charles Antzelevitch, Ronald Kanter, Geoffrey S. Pitt

PLoS One. 2014; 9(9): e106982. Published online 2014 Sep 3. doi: 10.1371/journal.pone.0106982