Results 1 - 20 of 2,395 for All Library Resources
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| Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
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| 1 |
Material Type: Article
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Transthyretin Amyloid Cardiomyopathy: JACC State-of-the-Art ReviewJournal of the American College of Cardiology, 2019-06, Vol.73 (22), p.2872-2891 [Peer Reviewed Journal]Copyright © 2019 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved. ;2019. American College of Cardiology Foundation ;ISSN: 0735-1097 ;EISSN: 1558-3597 ;DOI: 10.1016/j.jacc.2019.04.003 ;PMID: 31171094Full text available |
| 2 |
Material Type: Article
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Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samplesGenetics in medicine, 2017-02, Vol.19 (2), p.192-203 [Peer Reviewed Journal]2017 The Author(s) ;Copyright Nature Publishing Group Feb 2017 ;Copyright © 2017 Official journal of the American College of Medical Genetics and Genomics 2017 Official journal of the American College of Medical Genetics and Genomics ;ISSN: 1098-3600 ;EISSN: 1530-0366 ;DOI: 10.1038/gim.2016.90 ;PMID: 27532257Full text available |
| 3 |
Material Type: Article
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Mitophagy Is Essential for Maintaining Cardiac Function During High Fat Diet-Induced Diabetic CardiomyopathyCirculation research, 2019-04, Vol.124 (9), p.1360-1371 [Peer Reviewed Journal]2019 American Heart Association, Inc. ;ISSN: 0009-7330 ;EISSN: 1524-4571 ;DOI: 10.1161/CIRCRESAHA.118.314607 ;PMID: 30786833Full text available |
| 4 |
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PRMT4 promotes ferroptosis to aggravate doxorubicin-induced cardiomyopathy via inhibition of the Nrf2/GPX4 pathwayCell death and differentiation, 2022-10, Vol.29 (10), p.1982-1995 [Peer Reviewed Journal]2022. The Author(s), under exclusive licence to ADMC Associazione Differenziamento e Morte Cellulare. ;The Author(s), under exclusive licence to ADMC Associazione Differenziamento e Morte Cellulare 2022. ;The Author(s), under exclusive licence to ADMC Associazione Differenziamento e Morte Cellulare 2022 ;ISSN: 1350-9047 ;EISSN: 1476-5403 ;DOI: 10.1038/s41418-022-00990-5 ;PMID: 35383293Full text available |
| 5 |
Material Type: Article
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Inherited cardiomyopathies: molecular genetics and clinical genetic testing in the postgenomic eraThe Journal of molecular diagnostics : JMD, 2013-03, Vol.15 (2), p.158-170 [Peer Reviewed Journal]Copyright © 2013 American Society for Investigative Pathology and the Association for Molecular Pathology. Published by Elsevier Inc. All rights reserved. ;EISSN: 1943-7811 ;DOI: 10.1016/j.jmoldx.2012.09.002 ;PMID: 23274168Full text available |
| 6 |
Material Type: Article
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Cardiomyopathy in Children: Classification and Diagnosis: A Scientific Statement From the American Heart AssociationCirculation (New York, N.Y.), 2019-07, Vol.140 (1), p.e9-e68 [Peer Reviewed Journal]2019 by the American College of Cardiology Foundation and the American Heart Association, Inc. ;ISSN: 0009-7322 ;EISSN: 1524-4539 ;DOI: 10.1161/CIR.0000000000000682 ;PMID: 31132865Full text available |
| 7 |
Material Type: Article
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Using high-resolution variant frequencies to empower clinical genome interpretationGenetics in medicine, 2017-10, Vol.19 (10), p.1151-1158 [Peer Reviewed Journal]Copyright Nature Publishing Group Oct 2017 ;Copyright © 2017 The Author(s) 2017 The Author(s) ;ISSN: 1098-3600 ;EISSN: 1530-0366 ;DOI: 10.1038/gim.2017.26 ;PMID: 28518168Full text available |
| 8 |
Material Type: Article
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Adaptation and validation of the ACMG/AMP variant classification framework for MYH7-associated inherited cardiomyopathies: recommendations by ClinGen's Inherited Cardiomyopathy Expert PanelGenetics in medicine, 2018-03, Vol.20 (3), p.351-359 [Peer Reviewed Journal]Copyright Nature Publishing Group Mar 2018 ;Copyright © 2018 The Author(s) 2018 The Author(s) ;ISSN: 1098-3600 ;EISSN: 1530-0366 ;DOI: 10.1038/gim.2017.218 ;PMID: 29300372Full text available |
| 9 |
Material Type: Article
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Genetic Variants Associated With Cancer Therapy–Induced CardiomyopathyCirculation (New York, N.Y.), 2019-07, Vol.140 (1), p.31-41 [Peer Reviewed Journal]2019 by the American College of Cardiology Foundation and the American Heart Association, Inc. ;2019 The Authors. 2019 ;ISSN: 0009-7322 ;EISSN: 1524-4539 ;DOI: 10.1161/CIRCULATIONAHA.118.037934 ;PMID: 30987448Full text available |
| 10 |
Material Type: Article
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FGF21-Sirtuin 3 Axis Confers the Protective Effects of Exercise Against Diabetic Cardiomyopathy by Governing Mitochondrial IntegrityCirculation (New York, N.Y.), 2022-11, Vol.146 (20), p.1537-1557 [Peer Reviewed Journal]ISSN: 0009-7322 ;EISSN: 1524-4539 ;DOI: 10.1161/CIRCULATIONAHA.122.059631 ;PMID: 36134579Full text available |
| 11 |
Material Type: Article
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Systematic large-scale assessment of the genetic architecture of left ventricular noncompaction reveals diverse etiologiesGenetics in medicine, 2021-05, Vol.23 (5), p.856-864 [Peer Reviewed Journal]The Author(s) 2020. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2020 ;ISSN: 1098-3600 ;EISSN: 1530-0366 ;DOI: 10.1038/s41436-020-01049-x ;PMID: 33500567Full text available |
| 12 |
Material Type: Article
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Classification, Epidemiology, and Global Burden of CardiomyopathiesCirculation research, 2017-09, Vol.121 (7), p.722-730 [Peer Reviewed Journal]2017 American Heart Association, Inc. ;Copyright Lippincott Williams & Wilkins Ovid Technologies Sep 15, 2017 ;ISSN: 0009-7330 ;EISSN: 1524-4571 ;DOI: 10.1161/CIRCRESAHA.117.309711 ;PMID: 28912179Full text available |
| 13 |
Material Type: Article
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Truncating FLNC Mutations Are Associated With High-Risk Dilated and Arrhythmogenic CardiomyopathiesJournal of the American College of Cardiology, 2016-12, Vol.68 (22), p.2440-2451 [Peer Reviewed Journal]American College of Cardiology Foundation ;2016 American College of Cardiology Foundation ;Copyright © 2016 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved. ;Copyright Elsevier Limited Dec 6, 2016 ;ISSN: 0735-1097 ;EISSN: 1558-3597 ;DOI: 10.1016/j.jacc.2016.09.927 ;PMID: 27908349Full text available |
| 14 |
Material Type: Article
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Clinical and Mechanistic Insights Into the Genetics of CardiomyopathyJournal of the American College of Cardiology, 2016-12, Vol.68 (25), p.2871-2886 [Peer Reviewed Journal]The Authors ;2016 The Authors ;Copyright © 2016 The Authors. Published by Elsevier Inc. All rights reserved. ;Copyright Elsevier Limited Dec 27, 2016 ;ISSN: 0735-1097 ;EISSN: 1558-3597 ;DOI: 10.1016/j.jacc.2016.08.079 ;PMID: 28007147Full text available |
| 15 |
Material Type: Article
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Shared Genetic Predisposition in Peripartum and Dilated CardiomyopathiesThe New England journal of medicine, 2016-01, Vol.374 (3), p.233-241 [Peer Reviewed Journal]Copyright © 2016 Massachusetts Medical Society. All rights reserved. ;ISSN: 0028-4793 ;EISSN: 1533-4406 ;DOI: 10.1056/NEJMoa1505517 ;PMID: 26735901Full text available |
| 16 |
Material Type: Article
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Genotype and Phenotype of Transthyretin Cardiac Amyloidosis: THAOS (Transthyretin Amyloid Outcome Survey)Journal of the American College of Cardiology, 2016-07, Vol.68 (2), p.161-172 [Peer Reviewed Journal]Copyright © 2016 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved. ;Copyright Elsevier Limited Jul 12, 2016 ;ISSN: 0735-1097 ;ISSN: 1558-3597 ;EISSN: 1558-3597 ;DOI: 10.1016/j.jacc.2016.03.596 ;PMID: 27386769Full text available |
| 17 |
Material Type: Article
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Echocardiographic phenotype and prognosis in transthyretin cardiac amyloidosisEuropean heart journal, 2020-04, Vol.41 (14), p.1439-1447 [Peer Reviewed Journal]Published on behalf of the European Society of Cardiology. All rights reserved. © The Author(s) 2020. For permissions, please email: journals.permissions@oup.com. 2020 ;Published on behalf of the European Society of Cardiology. All rights reserved. © The Author(s) 2020. For permissions, please email: journals.permissions@oup.com. ;ISSN: 0195-668X ;EISSN: 1522-9645 ;DOI: 10.1093/eurheartj/ehz905 ;PMID: 31950987Full text available |
| 18 |
Material Type: Article
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Genetic evaluation of cardiomyopathy: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG)Genetics in medicine, 2018-09, Vol.20 (9), p.899-909 [Peer Reviewed Journal]Copyright Nature Publishing Group Sep 2018 ;ISSN: 1098-3600 ;EISSN: 1530-0366 ;DOI: 10.1038/s41436-018-0039-z ;PMID: 29904160Full text available |
| 19 |
Material Type: Article
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WWP2 regulates pathological cardiac fibrosis by modulating SMAD2 signalingNature communications, 2019-08, Vol.10 (1), p.3616-19, Article 3616 [Peer Reviewed Journal]2019. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;Attribution ;The Author(s) 2019 ;ISSN: 2041-1723 ;EISSN: 2041-1723 ;DOI: 10.1038/s41467-019-11551-9 ;PMID: 31399586Full text available |
| 20 |
Material Type: Article
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Circular RNA CircMAP3K5 Acts as a MicroRNA-22-3p Sponge to Promote Resolution of Intimal Hyperplasia Via TET2-Mediated Smooth Muscle Cell DifferentiationCirculation (New York, N.Y.), 2021-01, Vol.143 (4), p.354-371 [Peer Reviewed Journal]ISSN: 0009-7322 ;EISSN: 1524-4539 ;DOI: 10.1161/CIRCULATIONAHA.120.049715 ;PMID: 33207953Full text available |
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