HuGE Literature Finder
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| Cardiomyocyte apoptosis contributes to contractile dysfunction in stem cell model of MYH7 E848G hypertrophic cardiomyopathy. bioRxiv : the preprint server for biology 2023 2 . Loiben Alexander M, Chien Wei-Ming, Friedman Clayton E, Chao Leslie S-L, Weber Gerhard, Goldstein Alex, Sniadecki Nathan, Murry Charles E, Yang Kai-Ch |
| Cardiomyocyte Apoptosis Is Associated with Contractile Dysfunction in Stem Cell Model of MYH7 E848G Hypertrophic Cardiomyopathy. International journal of molecular sciences 2023 3 24 (5): . Loiben Alexander M, Chien Wei-Ming, Friedman Clayton E, Chao Leslie S-L, Weber Gerhard, Goldstein Alex, Sniadecki Nathan J, Murry Charles E, Yang Kai-Ch |
| Genotype-Phenotype Correlation in Hypertrophic Cardiomyopathy: New Variant p.Arg652Lys in MYH7. Genes 2022 Feb 13 (2): . Antoniutti Guido, Caimi-Martinez Fiama Giuliana, Álvarez-Rubio Jorge, Morlanes-Gracia Paula, Pons-Llinares Jaume, Rodríguez-Picón Blanca, Fortuny-Frau Elena, Torres-Juan Laura, Heine-Suner Damian, Ripoll-Vera Tom |
| Association of variants in MYH7, MYBPC3 and TNNT2 with sudden cardiac death-related risk factors in Brazilian patients with hypertrophic cardiomyopathy. Forensic science international. Genetics 2021 2 52 102478. Mori Augusto Akira, Castro Lara Reinel de, Bortolin Raul Hernandes, Bastos Gisele Medeiros, Oliveira Victor Fernandes de, Ferreira Glaucio Monteiro, Hirata Thiago Dominguez Crespo, Fajardo Cristina Moreno, Sampaio Marcelo Ferraz, Moreira Dalmo Antonio Ribeiro, Pachón-Mateos José Carlos, Correia Edileide de Barros, Sousa Amanda Guerra de Moraes Rego, Brión Maria, Carracedo Angel, Hirata Rosario Dominguez Crespo, Hirata Mario Hiroyu |
| The Influence of Genotype on the Phenotype, Clinical Course, and Risk of Adverse Events in Children with Hypertrophic Cardiomyopathy. Heart failure clinics 2021 11 18 (1): 1-8. Girolami Francesca, Passantino Silvia, Verrillo Federica, Palinkas Eszter Dalma, Limongelli Giuseppe, Favilli Silvia, Olivotto Iaco |
| An Important Role for DNMT3A-Mediated DNA Methylation in Cardiomyocyte Metabolism and Contractility. Circulation 2020 9 142 (16): 1562-1578. Madsen Alexandra, Höppner Grit, Krause Julia, Hirt Marc N, Laufer Sandra D, Schweizer Michaela, Tan Wilson Lek Wen, Mosqueira Diogo, Anene-Nzelu Chukwuemeka George, Lim Ives, Foo Roger S Y, Hansen Arne, Eschenhagen Thomas, Stenzig Just |
| Identification of a novel titin-cap/telethonin mutation in a Portuguese family with hypertrophic cardiomyopathy. Revista portuguesa de cardiologia 2020 6 39 (6): 317-327. Toste Alexandra, Perrot Andreas, Özcelik Cemil, Cardim Nu |
| Wolff-Parkinson-White syndrome: De novo variants and evidence for mutational burden in genes associated with atrial fibrillation. American journal of medical genetics. Part A 2020 4 182 (6): 1387-1399. Coban-Akdemir Zeynep H, Charng Wu-Lin, Azamian Mahshid, Paine Ingrid S, Punetha Jaya, Grochowski Christopher M, Gambin Tomasz, Valdes Santiago O, Cannon Bryan, Zapata Gladys, Hernandez Patricia P, Jhangiani Shalini, Doddapaneni Harsha, Hu Jianhong, Boricha Fatima, Muzny Donna M, Boerwinkle Eric, Yang Yaping, Gibbs Richard A, Posey Jennifer E, Wehrens Xander H T, Belmont John W, Kim Jeffrey J, Miyake Christina Y, Lupski James R, Lalani Seema |
| Baseline Characteristics of the VANISH Cohort. Circulation. Heart failure 2019 12 12 (12): e006231. Axelsson Raja Anna, Shi Ling, Day Sharlene M, Russell Mark, Zahka Kenneth, Lever Harry, Colan Steven D, Margossian Renee, Hall E Kevin, Becker Jason, Jefferies John Lynn, Patel Amit R, Choudhury Lubna, Murphy Anne M, Canter Charles, Bach Richard, Taylor Matthew, Mestroni Luisa, Wheeler Matthew T, Benson Lee, Owens Anjali T, Rossano Joseph, Lin Kimberly Y, Pahl Elfriede, Pereira Alexandre C, Bundgaard Henning, Lewis Gregory D, Vargas Jose D, Cirino Allison L, McMurray John J V, MacRae Calum A, Solomon Scott D, Orav E John, Braunwald Eugene, Ho Carolyn |
| Cardiac Phenotypes, Genetics, and Risks in Familial Noncompaction Cardiomyopathy. Journal of the American College of Cardiology 2019 4 73 (13): 1601-1611. van Waning Jaap I, Caliskan Kadir, Michels Michelle, Schinkel Arend F L, Hirsch Alexander, Dalinghaus Michiel, Hoedemaekers Yvonne M, Wessels Marja W, IJpma Arne S, Hofstra Robert M W, van Slegtenhorst Marjon A, Majoor-Krakauer Daniel |
| Clinical and ECG variables to predict the outcome of genetic testing in hypertrophic cardiomyopathy. European journal of medical genetics 2019 9 63 (3): 103754. Robyns Tomas, Breckpot Jeroen, Nuyens Dieter, Vandenberk Bert, Corveleyn Anniek, Kuiperi Cuno, Van Aelst Lucas, Van Cleemput Johan, Willems R |
| Genetic characterization and genotype-phenotype associations in a large cohort of patients with hypertrophic cardiomyopathy - An ancillary study of the Portuguese registry of hypertrophic cardiomyopathy. International journal of cardiology 2018 Dec . Lopes Luis Rocha, Brito Dulce, Belo Adriana, Cardim Nuno, |
| A novel mutation of the MYH7 gene in a patient with hypertrophic cardiomyopathy. The Turkish journal of pediatrics 2018 12 60 (3): 315-318. Goel Nicholas, Huddleston Charles B, Fiore Andrew |
| Evidence for troponin C (TNNC1) as a gene for autosomal recessive restrictive cardiomyopathy with fatal outcome in infancy. American journal of medical genetics. Part A 2016 Sep . Ploski Rafal, Rydzanicz Malgorzata, Ksiazczyk Tomasz M, Franaszczyk Maria, Pollak Agnieszka, Kosinska Joanna, Michalak Ewa, Stawinski Piotr, Ziolkowska Lidia, Bilinska Zofia T, Werner Boze |
| A Long Term Follow-up Study of Carriers of Hypertrophic Cardiomyopathy Mutations. Heart, lung & circulation 2016 May . McTaggart Don R, Ogden Kathryn J, Marathe Jessica |
| MYBPH acts as modifier of cardiac hypertrophy in hypertrophic cardiomyopathy (HCM) patients. Human genetics 2016 Mar . Mouton J M, van der Merwe L, Goosen A, Revera M, Brink P A, Moolman-Smook J C, Kinnear |
| [Mutation and clinical relevance in a large cohort of unrelated Chinese patients with hypertrophic cardiomyopathy]. Zhonghua xin xue guan bing za zhi 2015 Aug 43 (8): 682-9. Jie Liu, Wenling Liu, Dayi Hu, Tiangang Zhu, Wen Liu, Zhanfeng Ma, Jie Yang, Wenli Xie, Cuilan Li, Lei Li, Guozhong P |
| Coexistence of Digenic Mutations in Both Thin (TPM1) and Thick (MYH7) Filaments of Sarcomeric Genes Leads to Severe Hypertrophic Cardiomyopathy in a South Indian FHCM. DNA and cell biology 2015 May 34 (5): 350-9. Selvi Rani Deepa, Nallari Pratibha, Dhandapany Perundurai S, Rani Jhansi, Meraj Khunza, Ganesan Mala, Narasimhan Calambur, Thangaraj Kumarasa |
| Genetic variations of beta-MYH7 in Venezuelan patients with hypertrophic cardiomyopathy. Investigación clínica 2014 Mar 55 (1): 23-31. Rodríguez Rosalva, Guerrero David, Rivas Yoyna, Lacruz Andrea, Flores Yr |
| Screening of MYH7, MYBPC3, and TNNT2 genes in Brazilian patients with hypertrophic cardiomyopathy. American heart journal 2013 Oct 166 (4): 775-82. Marsiglia Julia Daher Carneiro, Credidio Flávia Laghi, de Oliveira Théo Gremen Mimary, Reis Rafael Ferreira, Antunes Murillo de Oliveira, de Araujo Aloir Queiroz, Pedrosa Rodrigo Pinto, Barbosa-Ferreira João Marcos Bemfica, Mady Charles, Krieger José Eduardo, Arteaga-Fernandez Edmundo, Pereira Alexandre da Cos |
| Mutation spectrum in a large cohort of unrelated Chinese patients with hypertrophic cardiomyopathy. The American journal of cardiology 2013 Aug 112 (4): 585-9. Liu Wen, Liu Wenling, Hu Dayi, Zhu Tiangang, Ma Zhanfeng, Yang Jie, Xie Wenli, Li Cuilan, Li Lei, Yang Jingang, Li Tianchang, Bian Hong, Tong Qigua |
| Somatic MYH7, MYBPC3, TPM1, TNNT2 and TNNI3 mutations in sporadic hypertrophic cardiomyopathy. Circulation journal : official journal of the Japanese Circulation Society 2013 77 (9): 2358-65. Núñez Lucía, Gimeno-Blanes Juan Ramón, Rodríguez-García María Isabel, Monserrat Lorenzo, Zorio Esther, Coats Caroline, McGregor Christopher G, Hernandez del Rincón Juan Pedro, Castro-Beiras Alfonso, Hermida-Prieto Manu |
| A novel genetic variant in the transcription factor Islet-1 exerts gain of function on myocyte enhancer factor 2C promoter activity. European journal of heart failure 2012 Nov . Friedrich FW, Dilanian G, Khattar P, Juhr D, Gueneau L, Charron P, Fressart V, Vilquin JT, Isnard R, Gouya L, Richard P, Hammoudi N, Komajda M, Bonne G, Eschenhagen T, Dubourg O, Villard E, Carrier L |
| Resequencing the whole MYH7 gene (including the intronic, promoter, and 3' UTR sequences) in hypertrophic cardiomyopathy. The Journal of molecular diagnostics : JMD 2012 Sep 14 (5): 518-24. Coto Eliecer, Reguero Julián R, Palacín María, Gómez Juan, Alonso Belén, Iglesias Sara, Martín María, Tavira Beatriz, Díaz-Molina Beatriz, Morales Carlos, Morís César, Rodríguez-Lambert José L, Corao Ana I, Díaz Marta, Alvarez Victor |
| Novel correlations between the genotype and the phenotype of hypertrophic and dilated cardiomyopathy: results from the German Competence Network Heart Failure. European journal of heart failure 2011 Nov 13 (11): 1185-92. Waldmüller Stephan, Erdmann Jeanette, Binner Priska, Gelbrich Götz, Pankuweit Sabine, Geier Christian, Timmermann Bernd, Haremza Janine, Perrot Andreas, Scheer Steffen, Wachter Rolf, Schulze-Waltrup Norbert, Dermintzoglou Anastassia, Schönberger Jost, Zeh Wolfgang, Jurmann Beate, Brodherr Turgut, Börgel Jan, Farr Martin, Milting Hendrik, Blankenfeldt Wulf, Reinhardt Richard, Özcelik Cemil, Osterziel Karl-Josef, Loeffler Markus, Maisch Bernhard, Regitz-Zagrosek Vera, Schunkert Heribert, Scheffold Thomas, |
| Sarcomere protein gene mutations in patients with apical hypertrophic cardiomyopathy. Circulation. Cardiovascular genetics 2011 Jun 4 (3): 288-95. Gruner Christiane, Care Melanie, Siminovitch Katherine, Moravsky Gil, Wigle E Douglas, Woo Anna, Rakowski Har |
| [Study of mutations causing hypertrophic cardiomyopathy in a group of patients from Espirito Santo, Brazil]. Arquivos brasileiros de cardiologia 2010 Jan 94 (1): 10-7. Marsiglia Júlia Daher Carneiro, Batitucci Maria do Carmo Pimentel, Paula Flávia de, Barbirato Clara, Arteaga Edmundo, Araújo Aloir Queiroz |
| Screening mutations in myosin binding protein C3 gene in a cohort of patients with Hypertrophic Cardiomyopathy. BMC medical genetics 2010 11 (1): 67. Rodríguez-García María Isabel, Monserrat Lorenzo, Ortiz Martín, Fernández Xusto, Cazón Laura, Núñez Lucía, Barriales-Villa Roberto, Maneiro Emilia, Veira Elena, Castro-Beiras Alfonso, Hermida-Prieto Manu |
| Genetic and clinical profile of Indian patients of idiopathic restrictive cardiomyopathy with and without hypertrophy. Molecular and cellular biochemistry 2009 Nov 331 (1-2): 187-92. Rai Taranjit Singh, Ahmad Shamim, Ahluwalia Tarunveer Singh, Ahuja Monica, Bahl Ajay, Saikia Uma Nahar, Singh Balvinder, Talwar Kewal K, Khullar Mad |
| Prevalence and spectrum of mutations in a cohort of 192 unrelated patients with hypertrophic cardiomyopathy. European journal of medical genetics 0 53 (5): 261-7. Millat Gilles, Bouvagnet Patrice, Chevalier Philippe, Dauphin Claire, Jouk Pierre Simon, Da Costa Antoine, Prieur Fabienne, Bresson Jean-Luc, Faivre Laurence, Eicher Jean-Christophe, Chassaing Nicolas, Crehalet Hervé, Porcher Raphael, Rodriguez-Lafrasse Claire, Rousson Robe |
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- Page last updated:Mar 22, 2023
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