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Select item 77038101.

Plasma Growth Differentiation Factors 8 and 11 levels in cats with congestive heart failure secondary to hypertrophic cardiomyopathy

Vicky K. Yang, John E. Rush, Shalender Bhasin, Amy J. Wagers, Richard T. Lee

J Vet Cardiol. Author manuscript; available in PMC 2020 Nov 30.

Published in final edited form as: J Vet Cardiol. 2019 Oct; 25: 41–51. Published online 2019 Sep 1. doi: 10.1016/j.jvc.2019.08.002

PMCID:: PMC7703810

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Select item 70464932.

Positron emission tomography (¹⁵O-water, ¹¹C-acetate, ¹¹C-HED) risk markers and nonsustained ventricular tachycardia in hypertrophic cardiomyopathy

Peter Magnusson, Jonny Nordström, Hendrik J. Harms, Mark Lubberink, Fredrik Gadler, Jens Sörensen, Stellan Mörner

Int J Cardiol Heart Vasc. 2020 Feb; 26: 100452. Published online 2019 Dec 20. doi: 10.1016/j.ijcha.2019.100452

PMCID:: PMC7046493

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Select item 62049763.

Newly designed 11-gene panel reveals first case of hereditary amyloidosis captured by massive parallel sequencing

Zuzana Chyra Kufova, Tereza Sevcikova, Jaroslav Januska, Petr Vojta, Arpad Boday, Pavla Vanickova, Jana Filipova, Katerina Growkova, Tomas Jelinek, Marian Hajduch, Roman Hajek

J Clin Pathol. 2018 Aug; 71(8): 687–694. Published online 2018 Feb 17. doi: 10.1136/jclinpath-2017-204978

PMCID:: PMC6204976

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Select item 55794514.

Septal alcoholization in hypertrophic cardiomyopathy: about 11 cases

Yibar Kambiré, Georges Rosario Christian Millogo, Claire Dauphin, Jean-René Lusson

Pan Afr Med J. 2017; 27: 196. Published online 2017 Jul 13. doi: 10.11604/pamj.2017.27.196.9639

PMCID:: PMC5579451

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Select item 100307815.

Late-onset and classic phenotypes of Fabry disease in males with the GLA-Thr410Ala mutation

Kati Valtola, Marja Hedman, Ilkka Kantola, Susanne Walls, Seppo Helisalmi, Maleeha Maria, Joose Raivo, Christiane Auray-Blais, Johanna Kuusisto

Open Heart. 2023; 10(1): e002251. Published online 2023 Mar 16. doi: 10.1136/openhrt-2023-002251

PMCID:: PMC10030781

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Select item 99269326.

Constitutive Protein Kinase G Activation Exacerbates Stress-induced Cardiomyopathy

Gerburg K. Schwaerzer, Darren E. Casteel, Federico Cividini, Hema Kalyanaraman, Shunhui Zhuang, Yusu Gu, Kirk L. Peterson, Wolfgang Dillmann, Gerry R. Boss, Renate B. Pilz

Br J Pharmacol. Author manuscript; available in PMC 2023 Jun 1.

Published in final edited form as: Br J Pharmacol. 2022 Jun; 179(11): 2413–2429. Published online 2021 Jun 21. doi: 10.1111/bph.15530

PMCID:: PMC9926932

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Select item 98573427.

Abnormal Cellular Phenotypes Induced by Three TMPO/LAP2 Variants Identified in Men with Cardiomyopathies

Nathalie Vadrot, Flavie Ader, Maryline Moulin, Marie Merlant, Françoise Chapon, Estelle Gandjbakhch, Fabien Labombarda, Pascale Maragnes, Patricia Réant, Caroline Rooryck, Vincent Probst, Erwan Donal, Pascale Richard, Ana Ferreiro, Brigitte Buendia

Cells. 2023 Jan; 12(2): 337. Published online 2023 Jan 16. doi: 10.3390/cells12020337

PMCID:: PMC9857342

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Select item 97737518.

Nationwide screening of Fabry disease in patients with hypertrophic cardiomyopathy in Czech Republic

David Zemánek, Jaroslav Januška, Tomáš Honěk, Karol Čurila, Miloš Kubánek, Štěpánka Šindelářová, Lucie Zahálková, Petr Klofáč, Eliška Laštůvková, Eva Lichnerová, Renata Aiglová, Jan Lhotský, Jiří Vondrák, Gabriela Dostálová, Miloš Táborský, David Kasper, Aleš Linhart

ESC Heart Fail. 2022 Dec; 9(6): 4160–4166. Published online 2022 Sep 10. doi: 10.1002/ehf2.14135

PMCID:: PMC9773751

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Select item 90698029.

Echocardiographic characteristics of PRKAG2 syndrome: a research using three-dimensional speckle tracking echocardiography compared with sarcomeric hypertrophic cardiomyopathy

Lu Tang, Xuejie Li, Nianwei Zhou, Yingying Jiang, Cuizhen Pan, Xianhong Shu

Cardiovasc Ultrasound. 2022; 20: 14. Published online 2022 May 5. doi: 10.1186/s12947-022-00284-3

PMCID:: PMC9069802

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Select item 906737910.

Human cardiac myosin-binding protein C phosphorylation- and mutation-dependent structural dynamics monitored by time-resolved FRET

Rhye-Samuel Kanassatega, Thomas A. Bunch, Victoria C. Lepak, Christopher Wang, Brett A. Colson

J Mol Cell Cardiol. Author manuscript; available in PMC 2023 May 1.

Published in final edited form as: J Mol Cell Cardiol. 2022 May; 166: 116–126. Published online 2022 Feb 25. doi: 10.1016/j.yjmcc.2022.02.005

PMCID:: PMC9067379

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Select item 889104411.

Differential Expression of Members of SOX Family of Transcription Factors in Failing Human Hearts

Chia-Feng Liu, Ying Ni, Varun Thachil, Michael Morley, Christine S. Moravec, W. H. Wilson Tang

Transl Res. Author manuscript; available in PMC 2023 Apr 1.

Published in final edited form as: Transl Res. 2022 Apr; 242: 66–78. Published online 2021 Oct 22. doi: 10.1016/j.trsl.2021.10.002

PMCID:: PMC8891044

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Select item 887278512.

Molecular basis of force-pCa relation in MYL2 cardiomyopathy mice: Role of the super-relaxed state of myosin

Chen-Ching Yuan, Katarzyna Kazmierczak, Jingsheng Liang, Weikang Ma, Thomas C. Irving, Danuta Szczesna-Cordary

Proc Natl Acad Sci U S A. 2022 Feb 22; 119(8): e2110328119. Published online 2022 Feb 17. doi: 10.1073/pnas.2110328119

PMCID:: PMC8872785

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Select item 871129813.

Congenital polyvalvular disease expands the cardiac phenotype of the RASopathies

Dena R. Matalon, David A. Stevenson, Elizabeth J. Bhoj, Avni B. Santani, Beth Keena, Meryl S. Cohen, Angela E. Lin, Sarah E. Sheppard, Elaine H. Zackai

Am J Med Genet A. Author manuscript; available in PMC 2022 May 1.

Published in final edited form as: Am J Med Genet A. 2021 May; 185(5): 1486–1493. Published online 2021 Mar 8. doi: 10.1002/ajmg.a.62146

PMCID:: PMC8711298

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Select item 847565914.

Myocardial Perfusion Defects in Hypertrophic Cardiomyopathy Mutation Carriers

Rebecca K. Hughes, Claudia Camaioni, João B. Augusto, Kristopher Knott, Ellie Quinn, Gabriella Captur, Andreas Seraphim, George Joy, Petros Syrris, Perry M. Elliott, Saidi Mohiddin, Peter Kellman, Hui Xue, Luis R. Lopes, James C. Moon

J Am Heart Assoc. 2021 Aug 3; 10(15): e020227. Published online 2021 Jul 26. doi: 10.1161/JAHA.120.020227

PMCID:: PMC8475659

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Select item 838005915.

Alpha-protein kinase 3 (ALPK3) truncating variants are a cause of autosomal dominant hypertrophic cardiomyopathy

Luis R Lopes, Soledad Garcia-Hernández, Massimiliano Lorenzini, Marta Futema, Olga Chumakova, Dmitry Zateyshchikov, Maria Isidoro-Garcia, Eduardo Villacorta, Luis Escobar-Lopez, Pablo Garcia-Pavia, Raquel Bilbao, David Dobarro, Maria Sandin-Fuentes, Claudio Catalli, Blanca Gener Querol, Ainhoa Mezcua, Jose Garcia Pinilla, Torsten Bloch Rasmussen, Ana Ferreira-Aguar, Pablo Revilla-Martí, Maria Teresa Basurte Elorz, Alicia Bautista Paves, Juan Ramon Gimeno, Ana Virginia Figueroa, Raul Franco-Gutierrez, Maria Eugenia Fuentes-Cañamero, Marina Martinez Moreno, Martin Ortiz-Genga, Jesus Piqueras-Flores, Karina Analia Ramos, Ainars Rudzitis, Luis Ruiz-Guerrero, Ricardo Stein, Mayte Triguero-Bocharán, Luis de la Higuera, Juan Pablo Ochoa, Dad Abu-Bonsrah, Cecilia Y T Kwok, Jacob B Smith, Enzo R Porrello, Mohammed M Akhtar, Joanna Jager, Michael Ashworth, Petros Syrris, David A Elliott, Lorenzo Monserrat, Perry M Elliott

Eur Heart J. 2021 Aug 21; 42(32): 3063–3073. Published online 2021 Jul 15. doi: 10.1093/eurheartj/ehab424

PMCID:: PMC8380059

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Select item 826087316.

Protein haploinsufficiency drivers identify MYBPC3 variants that cause hypertrophic cardiomyopathy

Carmen Suay-Corredera, Maria Rosaria Pricolo, Elías Herrero-Galán, Diana Velázquez-Carreras, David Sánchez-Ortiz, Diego García-Giustiniani, Javier Delgado, Juan José Galano-Frutos, Helena García-Cebollada, Silvia Vilches, Fernando Domínguez, María Sabater Molina, Roberto Barriales-Villa, Giulia Frisso, Javier Sancho, Luis Serrano, Pablo García-Pavía, Lorenzo Monserrat, Jorge Alegre-Cebollada

J Biol Chem. 2021 Jul; 297(1): 100854. Published online 2021 Jun 5. doi: 10.1016/j.jbc.2021.100854

PMCID:: PMC8260873

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Select item 825526317.

Regional myocardial function at preclinical disease stage of hypertrophic cardiomyopathy in female gene variant carriers

Rahana Y. Parbhudayal, Celine Seegers, Pierre Croisille, Patrick Clarysse, Albert C. van Rossum, Tjeerd Germans, Jolanda van der Velden

Int J Cardiovasc Imaging. 2021; 37(6): 2001–2010. Published online 2021 Feb 9. doi: 10.1007/s10554-020-02156-1

PMCID:: PMC8255263

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Select item 819145218.

NGS testing for cardiomyopathy: Utility of adding RASopathy-associated genes

Ozge Ceyhan-Birsoy, Maya M Miatkowski, Elizabeth Hynes, Birgit H Funke, Heather Mason-Suares

Hum Mutat. Author manuscript; available in PMC 2021 Jun 10.

Published in final edited form as: Hum Mutat. 2018 Jul; 39(7): 954–958. Published online 2018 May 16. doi: 10.1002/humu.23535

PMCID:: PMC8191452

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Select item 798921019.

Multi-omics integration identifies key upstream regulators of pathomechanisms in hypertrophic cardiomyopathy due to truncating MYBPC3 mutations

J. Pei, M. Schuldt, E. Nagyova, Z. Gu, S. el Bouhaddani, L. Yiangou, M. Jansen, J. J. A. Calis, L. M. Dorsch, C. Snijders Blok, N. A. M. van den Dungen, N. Lansu, B. J. Boukens, I. R. Efimov, M. Michels, M. C. Verhaar, R. de Weger, A. Vink, F. G. van Steenbeek, A. F. Baas, R. P. Davis, H. W. Uh, D. W. D. Kuster, C. Cheng, M. Mokry, J. van der Velden, F. W. Asselbergs, M. Harakalova

Clin Epigenetics. 2021; 13: 61. Published online 2021 Mar 23. doi: 10.1186/s13148-021-01043-3

PMCID:: PMC7989210

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Select item 797184220.

Paternal genetic variants and risk of obstructive heart defects: A parent-of-origin approach

Jenil Patel, Emine Bircan, Xinyu Tang, Mohammed Orloff, Charlotte A. Hobbs, Marilyn L. Browne, Lorenzo D. Botto, Richard H. Finnell, Mary M. Jenkins, Andrew Olshan, Paul A. Romitti, Gary M. Shaw, Martha M. Werler, Jingyun Li, Wendy N. Nembhard, the National Birth Defects Prevention Study

PLoS Genet. 2021 Mar; 17(3): e1009413. Published online 2021 Mar 8. doi: 10.1371/journal.pgen.1009413

PMCID:: PMC7971842

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