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ArticlesPeer ReviewedFull Text
Inherited calcium channelopathies in the pathophysiology of arrhythmias
Author / Creator:Venetucci, Luigi ; Denegri, Marco ; Napolitano, Carlo ; Priori, Silvia G.
Publisher:London: Nature Publishing Group UK
Journal title:Nature reviews cardiology, 2012-10, Vol.9 (10), p.561-575
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Adeno-associated virus-mediated CASQ2 delivery rescues phenotypic alterations in a patient-specific model of recessive catecholaminergic polymorphic ventricular tachycardia
Author / Creator:Lodola, Francesco ; Morone, Diego ; Denegri, Marco ; Bongianino, Rossana ; Nakahama, Hiroko ; Rutigliano, Lucia ; Gosetti, Rosanna ; Rizzo, Giulia ; Vollero, Alessandra ; Buonocore, Michelangelo ; Napolitano, Carlo ; Condorelli, Gianluigi ; Priori, Silvia G ; Di Pasquale, Elisa
Publisher:London: Nature Publishing Group UK
Journal title:Cell death & disease, 2016-10, Vol.7 (10), p.e2393-e2393
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Deep-time gene expression shift reveals an ancient change in avian muscle phenotypes
Author / Creator:Harvey, Christina M. ; Fuxjager, Matthew J. ; Pease, James B.
Publisher:United States: Public Library of Science
Journal title:PLoS genetics, 2025-04, Vol.21 (4), p.e1011663
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Calsequestrin, a key protein in striated muscle health and disease
Author / Creator:Rossi, Daniela ; Gamberucci, Alessandra ; Pierantozzi, Enrico ; Amato, Caterina ; Migliore, Loredana ; Sorrentino, Vincenzo
Publisher:Cham: Springer International Publishing
Journal title:Journal of muscle research and cell motility, 2021-06, Vol.42 (2), p.267-279
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Casq2 deletion causes sarcoplasmic reticulum volume increase, premature Ca2+ release, and catecholaminergic polymorphic ventricular tachycardia
Author / Creator:Knollmann, Björn C ; Chopra, Nagesh ; Hlaing, Thinn ; Akin, Brandy ; Yang, Tao ; Ettensohn, Kristen ; Knollmann, Barbara E C ; Horton, Kenneth D ; Weissman, Neil J ; Holinstat, Izabela ; Zhang, Wei ; Roden, Dan M ; Jones, Larry R ; Franzini-Armstrong, Clara ; Pfeifer, Karl
Publisher:United States: American Society for Clinical Investigation
Journal title:The Journal of clinical investigation, 2006-09, Vol.116 (9), p.2510-2520
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Patient-Specific Human Induced Pluripotent Stem Cell Model Assessed with Electrical Pacing Validates S107 as a Potential Therapeutic Agent for Catecholaminergic Polymorphic Ventricular Tachycardia
Author / Creator:Sasaki, Kenichi ; Makiyama, Takeru ; Yoshida, Yoshinori ; Wuriyanghai, Yimin ; Kamakura, Tsukasa ; Nishiuchi, Suguru ; Hayano, Mamoru ; Harita, Takeshi ; Yamamoto, Yuta ; Kohjitani, Hirohiko ; Hirose, Sayako ; Chen, Jiarong ; Kawamura, Mihoko ; Ohno, Seiko ; Itoh, Hideki ; Takeuchi, Ayako ; Matsuoka, Satoshi ; Miura, Masaru ; Sumitomo, Naokata ; Horie, Minoru ; Yamanaka, Shinya ; Kimura, Takeshi
Publisher:United States: Public Library of Science
Journal title:PloS one, 2016-10, Vol.11 (10), p.e0164795-e0164795
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Calsequestrin 2 overexpression in breast cancer increases tumorigenesis and metastasis by modulating the tumor microenvironment
Author / Creator:Kim, Ju Hee ; Lee, Eun‐Shin ; Yun, Jihui ; Ryu, Han Suk ; Kim, Hong Kyu ; Ju, Young Wook ; Kim, Kwangsoo ; Kim, Jong‐Il ; Moon, Hyeong‐Gon
Publisher:United States: John Wiley & Sons, Inc
Journal title:Molecular oncology, 2022-01, Vol.16 (2), p.466-484
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The structure of a calsequestrin filament reveals mechanisms of familial arrhythmia
Author / Creator:Titus, Erron W. ; Deiter, Frederick H. ; Shi, Chenxu ; Wojciak, Julianne ; Scheinman, Melvin ; Jura, Natalia ; Deo, Rahul C.
Publisher:New York: Nature Publishing Group US
Journal title:Nature structural & molecular biology, 2020-12, Vol.27 (12), p.1142-1151
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Cardiomyocytes generated from CPVTD307H patients are arrhythmogenic in response to β‐adrenergic stimulation
Author / Creator:Novak, Atara ; Barad, Lili ; Zeevi‐Levin, Naama ; Shick, Revital ; Shtrichman, Ronit ; Lorber, Avraham ; Itskovitz‐Eldor, Joseph ; Binah, Ofer
Publisher:Oxford, UK: Blackwell Publishing Ltd
Journal title:Journal of cellular and molecular medicine, 2012-03, Vol.16 (3), p.468-482
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Functional abnormalities in iPSC‐derived cardiomyocytes generated from CPVT1 and CPVT2 patients carrying ryanodine or calsequestrin mutations
Author / Creator:Novak, Atara ; Barad, Lili ; Lorber, Avraham ; Gherghiceanu, Mihaela ; Reiter, Irina ; Eisen, Binyamin ; Eldor, Liron ; Itskovitz‐Eldor, Joseph ; Eldar, Michael ; Arad, Michael ; Binah, Ofer
Publisher:England: John Wiley & Sons, Inc
Journal title:Journal of cellular and molecular medicine, 2015-08, Vol.19 (8), p.2006-2018
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Pacing Dynamics Determines the Arrhythmogenic Mechanism of the CPVT2-Causing CASQ2 G112+5X Mutation in a Guinea Pig Ventricular Myocyte Computational Model
Author / Creator:Paudel, Roshan ; Jafri, Mohsin Saleet ; Ullah, Aman
Publisher:Switzerland
Journal title:Genes, 2022-12, Vol.14 (1)
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ERG1A K + channel increases intracellular calcium concentration through modulation of calsequestrin1 in C 2 C 12 myotubes
Author / Creator:Hockerman, Gregory H ; Pratt, Evan ; Guha, Shalini ; LaVigne, Emily ; Whitmore, Clayton ; Khader, Omar ; McClure, Natalie ; Zampieri, Sandra ; Koran, Jennifer ; Wang, W-H ; Pond, Amber L
Publisher:England
Journal title:Scientific reports, 2025-03, Vol.15 (1), p.9480
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Effects of acute ischemia and hypoxia in young and adult calsequestrin (CSQ2) knock-out and wild-type mice
Author / Creator:Neumann, Joachim ; Bödicker, Konrad ; Buchwalow, Igor B. ; Schmidbaur, Constanze ; Ramos, Gustavo ; Frantz, Stefan ; Hofmann, Ulrich ; Gergs, Ulrich
Publisher:New York: Springer US
Journal title:Molecular and cellular biochemistry, 2022-06, Vol.477 (6), p.1789-1801
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Phylogenetic and biochemical analysis of calsequestrin structure and association of its variants with cardiac disorders
Author / Creator:Wang, Qian ; Tautvydas, Paskevicius ; Filbert, Alexander ; Qin Wenying ; Kim Hyeong Jin ; Xing-Zhen, Chen ; Tang, Jingfeng ; Dacks, Joel B ; Agellon, Luis B ; Michalak Marek
Publisher:London: Nature Publishing Group
Journal title:Scientific reports, 2020-10, Vol.10 (1)
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SK4 K+ channels are therapeutic targets for the treatment of cardiac arrhythmias
Author / Creator:Haron‐Khun, Shiraz ; Weisbrod, David ; Bueno, Hanna ; Yadin, Dor ; Behar, Joachim ; Peretz, Asher ; Binah, Ofer ; Hochhauser, Edith ; Eldar, Michael ; Yaniv, Yael ; Arad, Michael ; Attali, Bernard
Publisher:London: Nature Publishing Group UK
Journal title:EMBO molecular medicine, 2017-04, Vol.9 (4), p.415-429
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Genetic Analysis of Arrhythmogenic Diseases in the Era of NGS: The Complexity of Clinical Decision-Making in Brugada Syndrome
Author / Creator:Allegue, Catarina ; Coll, Mònica ; Mates, Jesus ; Campuzano, Oscar ; Iglesias, Anna ; Sobrino, Beatriz ; Brion, Maria ; Amigo, Jorge ; Carracedo, Angel ; Brugada, Pedro ; Brugada, Josep ; Brugada, Ramon
Publisher:United States: Public Library of Science
Journal title:PloS one, 2015-07, Vol.10 (7), p.e0133037-e0133037
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Investigation of a Large Kindred Reveals Cardiac Calsequestrin (CASQ2) as a Cause of Brugada Syndrome
Author / Creator:d’Apolito, Maria ; Santoro, Francesco ; Ranaldi, Alessandra ; Ragnatela, Ilaria ; Colia, Anna Laura ; Cannito, Sara ; Margaglione, Alessandra ; D’Arienzo, Girolamo ; D’Andrea, Giovanna ; Pellegrino, PierLuigi ; Santacroce, Rosa ; Brunetti, Natale Daniele ; Margaglione, Maurizio
Publisher:Switzerland: MDPI AG
Journal title:Genes, 2024-07, Vol.15 (7), p.822
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Calsequestrin: a well-known but curious protein in skeletal muscle
Author / Creator:Woo, Jin Seok ; Jeong, Seung Yeon ; Park, Ji Hee ; Choi, Jun Hee ; Lee Eun Hui
Publisher:Seoul: Springer Nature B.V
Journal title:Experimental & molecular medicine, 2020-12, Vol.52 (12), p.1908-1925
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Molecular characterization and functional properties of cardiomyocytes derived from human inducible pluripotent stem cells
Author / Creator:Germanguz, Igal ; Sedan, Oshra ; Zeevi‐Levin, Naama ; Shtrichman, Ronit ; Barak, Efrat ; Ziskind, Anna ; Eliyahu, Sivan ; Meiry, Gideon ; Amit, Michal ; Itskovitz‐Eldor, Joseph ; Binah, Ofer
Publisher:Oxford, UK: Blackwell Publishing Ltd
Journal title:Journal of cellular and molecular medicine, 2011-01, Vol.15 (1), p.38-51
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Calsequestrin 2 (CASQ2) mutations increase expression of calreticulin and ryanodine receptors, causing catecholaminergic polymorphic ventricular tachycardia
Author / Creator:Song, Lei ; Alcalai, Ronny ; Arad, Michael ; Wolf, Cordula M. ; Toka, Okan ; Conner, David A. ; Berul, Charles I. ; Eldar, Michael ; Seidman, Christine E. ; Seidman, J.G.
Publisher:United States: American Society for Clinical Investigation
Journal title:The Journal of clinical investigation, 2007-07, Vol.117 (7), p.1814-1823
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Inherited calcium channelopathies in the pathophysiology of arrhythmias

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Adeno-associated virus-mediated CASQ2 delivery rescues phenotypic alterations in a patient-specific model of recessive catecholaminergic polymorphic ventricular tachycardia

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Deep-time gene expression shift reveals an ancient change in avian muscle phenotypes

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Calsequestrin, a key protein in striated muscle health and disease

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Casq2 deletion causes sarcoplasmic reticulum volume increase, premature Ca2+ release, and catecholaminergic polymorphic ventricular tachycardia

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Patient-Specific Human Induced Pluripotent Stem Cell Model Assessed with Electrical Pacing Validates S107 as a Potential Therapeutic Agent for Catecholaminergic Polymorphic Ventricular Tachycardia

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Calsequestrin 2 overexpression in breast cancer increases tumorigenesis and metastasis by modulating the tumor microenvironment

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The structure of a calsequestrin filament reveals mechanisms of familial arrhythmia

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Cardiomyocytes generated from CPVTD307H patients are arrhythmogenic in response to β‐adrenergic stimulation

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Functional abnormalities in iPSC‐derived cardiomyocytes generated from CPVT1 and CPVT2 patients carrying ryanodine or calsequestrin mutations

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Pacing Dynamics Determines the Arrhythmogenic Mechanism of the CPVT2-Causing CASQ2 G112+5X Mutation in a Guinea Pig Ventricular Myocyte Computational Model

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ERG1A K + channel increases intracellular calcium concentration through modulation of calsequestrin1 in C 2 C 12 myotubes

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Effects of acute ischemia and hypoxia in young and adult calsequestrin (CSQ2) knock-out and wild-type mice

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Phylogenetic and biochemical analysis of calsequestrin structure and association of its variants with cardiac disorders

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SK4 K+ channels are therapeutic targets for the treatment of cardiac arrhythmias

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Genetic Analysis of Arrhythmogenic Diseases in the Era of NGS: The Complexity of Clinical Decision-Making in Brugada Syndrome

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Investigation of a Large Kindred Reveals Cardiac Calsequestrin (CASQ2) as a Cause of Brugada Syndrome

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Calsequestrin: a well-known but curious protein in skeletal muscle

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Molecular characterization and functional properties of cardiomyocytes derived from human inducible pluripotent stem cells

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Calsequestrin 2 (CASQ2) mutations increase expression of calreticulin and ryanodine receptors, causing catecholaminergic polymorphic ventricular tachycardia

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