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1 |
Material Type: Artigo
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Molecular basis for allosteric regulation of the type 2 ryanodine receptor channel gating by key modulatorsChi, Ximin ; Gong, Deshun ; Ren, Kang ; Zhou, Gewei ; Huang, Gaoxingyu ; Lei, Jianlin ; Zhou, Qiang ; Yan, NiengProceedings of the National Academy of Sciences - PNAS, 2019-12, Vol.116 (51), p.25575-25582 [Periódico revisado por pares]United States: National Academy of SciencesTexto completo disponível |
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Material Type: Artigo
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Allele Specific Silencing of Mutant mRNA Rescues Ultrastructural and Arrhythmic Phenotype in Mice Carriers of the R4496C Mutation in the Ryanodine Receptor Gene (RYR2)Bongianino, Rossana ; Denegri, Marco ; Mazzanti, Andrea ; Lodola, Francesco ; Vollero, Alessandra ; Boncompagni, Simona ; Fasciano, Silvia ; Rizzo, Giulia ; Mangione, Damiano ; Barbaro, Serena ; Di Fonso, Alessia ; Napolitano, Carlo ; Auricchio, Alberto ; Protasi, Feliciano ; Priori, Silvia GCirculation research, 2017-08, Vol.121 (5), p.525-536 [Periódico revisado por pares]United States: American Heart Association, IncTexto completo disponível |
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Material Type: Artigo
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Thyroid and Glucocorticoid Hormones Promote Functional T-Tubule Development in Human-Induced Pluripotent Stem Cell–Derived CardiomyocytesParikh, Shan S ; Blackwell, Daniel J ; Gomez-Hurtado, Nieves ; Frisk, Michael ; Wang, Lili ; Kim, Kyungsoo ; Dahl, Christen P ; Fiane, Arnt ; Tønnessen, Theis ; Kryshtal, Dmytro O ; Louch, William E ; Knollmann, Bjorn CCirculation research, 2017-12, Vol.121 (12), p.1323-1330 [Periódico revisado por pares]United States: American Heart Association, IncTexto completo disponível |
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Material Type: Artigo
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Role of cardiac ryanodine receptor calmodulin‐binding domains in mediating the action of arrhythmogenic calmodulin N‐domain mutation N54ISøndergaard, Mads T. ; Liu, Yingjie ; Guo, Wenting ; Wei, Jinhong ; Wang, Ruiwu ; Brohus, Malene ; Overgaard, Michael T. ; Chen, S. R. WayneThe FEBS journal, 2020-06, Vol.287 (11), p.2256-2280 [Periódico revisado por pares]England: Blackwell Publishing LtdTexto completo disponível |
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Material Type: Artigo
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HETEROCIGOSIDAD COMPUESTA PARA RYR1 APOYA DIAGNÓSTICO PRESUNTIVO DE MIOPATÍA CONGÉNITA AUTOSÓMICA RECESIVA EN CASO COMPLEJO DE AFECCIÓN NEUROMUSCULARValenzuela, R D Carrero ; Hurtado, M H ; Pinto, M G Vizoso ; Germain, ABAG. Journal of basic and applied genetics, 2022-12, Vol.33, p.99 [Periódico revisado por pares]Buenos Aires: Sociedad Argentina de GeneticaTexto completo disponível |
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Material Type: Artigo
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Pathological conformations of disease mutant Ryanodine Receptors revealed by cryo-EMWoll, Kellie A ; Haji-Ghassemi, Omid ; Van Petegem, FilipNature communications, 2021-02, Vol.12 (1), p.807-13, Article 807 [Periódico revisado por pares]England: Nature Publishing GroupTexto completo disponível |
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Material Type: Artigo
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Modulation of cardiac ryanodine receptor 2 by calmodulinGong, Deshun ; Chi, Ximin ; Wei, Jinhong ; Zhou, Gewei ; Huang, Gaoxingyu ; Zhang, Lin ; Wang, Ruiwu ; Lei, Jianlin ; Chen, S R Wayne ; Yan, NiengNature (London), 2019-08, Vol.572 (7769), p.347-351 [Periódico revisado por pares]England: Nature Publishing GroupTexto completo disponível |
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Material Type: Artigo
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Comparison of the structure-function of five newly members of the calcin familyHua, Xiaoyu ; Yao, Jinchi ; Liu, Xinyan ; Liu, Qing ; Deng, Yuchen ; Li, Songhua ; Valdivia, Carmen R. ; Wang, Fei ; Pozzolini, Marina ; Shou, Zhaoyong ; Valdivia, Héctor H. ; Xiao, LiangInternational journal of biological macromolecules, 2024-03, Vol.260 (Pt 1), p.129424-129424, Article 129424 [Periódico revisado por pares]Netherlands: Elsevier B.VTexto completo disponível |
9 |
Material Type: Artigo
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Molecular mechanism of the severe MH/CCD mutation Y522S in skeletal ryanodine receptor (RyR1) by cryo-EMIyer, Kavita A ; Hu, Yifan ; Klose, Thomas ; Murayama, Takashi ; Samsó, MontserratProceedings of the National Academy of Sciences - PNAS, 2022-07, Vol.119 (30), p.e2122140119-e2122140119 [Periódico revisado por pares]United States: National Academy of SciencesTexto completo disponível |
10 |
Material Type: Artigo
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Dantrolene rescues arrhythmogenic RYR2 defect in a patient‐specific stem cell model of catecholaminergic polymorphic ventricular tachycardiaJung, Christian B. ; Moretti, Alessandra ; Mederos y Schnitzler, Michael ; Iop, Laura ; Storch, Ursula ; Bellin, Milena ; Dorn, Tatjana ; Ruppenthal, Sandra ; Pfeiffer, Sarah ; Goedel, Alexander ; Dirschinger, Ralf J. ; Seyfarth, Melchior ; Lam, Jason T. ; Sinnecker, Daniel ; Gudermann, Thomas ; Lipp, Peter ; Laugwitz, Karl‐LudwigEMBO molecular medicine, 2012-03, Vol.4 (3), p.180-191 [Periódico revisado por pares]Weinheim: WILEY‐VCH VerlagTexto completo disponível |