Works matching DE "HEART disease genetics"
Results: 210
Myocardial Fibrosis in the Pathogenesis, Diagnosis, and Treatment of Hypertrophic Cardiomyopathy.
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- Cardiovascular Innovations & Applications (CVIA), 2021, v. 5, n. 4, p. 267, doi. 10.15212/CVIA.2021.0008
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- Article
Sex differences in response to miRNA-34a therapy in mouse models of cardiac disease: identification of sex-, disease- and treatment-regulated miRNAs.
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- Journal of Physiology, 2016, v. 594, n. 20, p. 5959, doi. 10.1113/JP272512
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- Article
The genetics of hypertrophic cardiomyopathy.
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- Global Cardiology Science & Practice, 2018, v. 2018, n. 3, p. 1, doi. 10.21542/gcsp.2018.36
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- Publication type:
- Article
Genetics of channelopathies associated with sudden cardiac death.
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- Global Cardiology Science & Practice, 2015, v. 2015, n. 3, p. 1, doi. 10.5339/gcsp.2015.39
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- Publication type:
- Article
Prenatal ultrasound diagnosis of MYH7 non-compaction cardiomyopathy.
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- Ultrasound in Obstetrics & Gynecology, 2013, v. 41, n. 3, p. 336, doi. 10.1002/uog.12279
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- Publication type:
- Article
Assessment of arterial stiffness in women with gestational diabetes.
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- Diabetic Medicine, 2012, v. 29, n. 2, p. 227, doi. 10.1111/j.1464-5491.2011.03471.x
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- Publication type:
- Article
Genetic Testing in Cardiovascular Medicine.
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- Texas Heart Institute Journal, 2018, v. 45, n. 04, p. 231, doi. 10.14503/THIJ-18-6674
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- Publication type:
- Article
Attacking Heart Disease at Its Genetic Base.
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- Agricultural Research, 1999, v. 47, n. 7, p. 20
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- Publication type:
- Article
Polymorphisms of selected genes related to increased cardiovascular risk in patients with acute coronary syndromes and their relation to the severity of coronary artery disease.
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- Advances in Interventional Cardiology / Postępy w Kardiologii Interwencyjnej, 2012, v. 8, n. 1, p. 25, doi. 10.5114/pwki.2012.27922
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- Publication type:
- Article
The heart of the matter--new insights into the genetics of cardiomyopathy.
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- 2000
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- Publication type:
- journal article
Association study of genetic variants at newly identified lipid gene TRIB1 with coronary heart disease in Chinese Han population.
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- Lipids in Health & Disease, 2015, v. 14, n. 1, p. 1, doi. 10.1186/s12944-015-0043-0
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- Publication type:
- Article
Intermittent hypoxia causes NOX2-dependent remodeling of atrial connexins.
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- BMC Cell Biology, 2017, v. 18, p. 1, doi. 10.1186/s12860-016-0117-5
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- Publication type:
- Article
An application of conditional logistic regression and multifactor dimensionality reduction for detecting gene-gene Interactions on risk of myocardial infarction: The importance of model validation.
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- BMC Bioinformatics, 2004, v. 5, p. 49, doi. 10.1186/1471-2105-5-49
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- Publication type:
- Article
SNPing Away at Genome-Wide Disease Association Studies.
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- Bio-IT World, 2007, v. 6, n. 6, p. 28
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- Publication type:
- Article
NitroMed Ties Gene Biomarkers to BiDil Benefit.
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- Bio-IT World, 2006, v. 5, n. 3, p. 21
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- Publication type:
- Article
A novel variant in plakophilin-2 gene detected in a family with arrhythmogenic right ventricular cardiomyopathy.
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- Journal of Interventional Cardiac Electrophysiology, 2012, v. 34, n. 1, p. 11, doi. 10.1007/s10840-011-9643-4
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- Publication type:
- Article
MicroRNA-21 contributes to myocardial disease by stimulating MAP kinase signalling in fibroblasts.
- Published in:
- 2008
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- Publication type:
- Letter
A genetic framework for improving arrhythmia therapy.
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- Nature, 2008, v. 451, n. 7181, p. 929, doi. 10.1038/nature06799
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- Publication type:
- Article
Genetic Architecture of Susceptibility to PCB126-Induced Developmental Cardiotoxicity in Zebrafish.
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- Toxicological Sciences, 2011, v. 122, n. 2, p. 466, doi. 10.1093/toxsci/kfr136
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- Publication type:
- Article
Validated context-dependent associations of coronary heart disease risk with genotype variation in the chromosome 9p21 region: the Atherosclerosis Risk in Communities study.
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- Human Genetics, 2014, v. 133, n. 9, p. 1105, doi. 10.1007/s00439-014-1451-3
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- Publication type:
- Article
Low mutation rate in the TTN gene in paediatric patients with dilated cardiomyopathy – a pilot study.
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- Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-52911-1
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- Publication type:
- Article
Association of Increased Levels of lncRNA H19 in PBMCs with Risk of Coronary Artery Disease.
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- Cell Journal (Yakhteh), 2019, v. 20, n. 4, p. 564, doi. 10.22074/cellj.2019.5544
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- Publication type:
- Article
Major congenital coronary artery anomalies in a paediatric and adult population: a prospective echocardiographic study.
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- European Heart Journal - Cardiovascular Imaging, 2014, v. 15, n. 7, p. 761, doi. 10.1093/ehjci/jet287
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- Publication type:
- Article
Assessment of myocardial adrenergic innervation with a solid-state dedicated cardiac cadmium–zinc–telluride camera: first clinical experience.
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- European Heart Journal - Cardiovascular Imaging, 2014, v. 15, n. 5, p. 575, doi. 10.1093/ehjci/jet258
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- Publication type:
- Article
The World in Medicine.
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- JAMA: Journal of the American Medical Association, 1999, v. 282, n. 18, p. 1713
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- Publication type:
- Article
Congenital Aortic Stenosis.
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- Annals of Internal Medicine, 1963, v. 58, n. 3, p. 486, doi. 10.7326/0003-4819-58-3-486
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- Publication type:
- Article
P270Cardiac specific microRNA-125b deficiency impairs mitochondrial function in mouse neonatal and adult heart.
- Published in:
- 2018
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- Publication type:
- Abstract
Arrhythmogenic cardiomyopathy: pathology, genetics, and concepts in pathogenesis.
- Published in:
- Cardiovascular Research, 2017, v. 113, n. 12, p. 1521, doi. 10.1093/cvr/cvx150
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- Publication type:
- Article
SH2B1 is critical for the regulation of cardiac remodelling in response to pressure overload.
- Published in:
- Cardiovascular Research, 2015, v. 107, n. 2, p. 203, doi. 10.1093/cvr/cvv170
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- Publication type:
- Article
Arrhythmogenic right ventricular cardiomyopathy mutations alter shear response without changes in cell–cell adhesion.
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- Cardiovascular Research, 2014, v. 104, n. 2, p. 280, doi. 10.1093/cvr/cvu212
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- Publication type:
- Article
17β-Estradiol treatment reversed left ventricular dysfunction in castrated male rats: an echocardiographic study.
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- Canadian Journal of Physiology & Pharmacology, 2018, v. 96, n. 8, p. 850, doi. 10.1139/cjpp-2017-0596
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- Publication type:
- Article
Analyzing gene expression profiles with preliminary validations in cardiac hypertrophy induced by pressure overload.
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- Canadian Journal of Physiology & Pharmacology, 2018, v. 96, n. 8, p. 701, doi. 10.1139/cjpp-2017-0585
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- Publication type:
- Article
microRNA-29a inhibits cardiac fibrosis in Sprague-Dawley rats by downregulating the expression of DNMT3A.
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- Anatolian Journal of Cardiology / Anadolu Kardiyoloji Dergisi, 2018, v. 20, n. 4, p. 198, doi. 10.14744/AnatolJCardiol.2018.98511
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- Publication type:
- Article
Beta myosin heavy chain mutations R403QLW, V606M, K615N and R663H in patients with hypertrophic cardiomyopathy.
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- Anatolian Journal of Cardiology / Anadolu Kardiyoloji Dergisi, 2014, v. 14, n. 3, p. 244, doi. 10.5152/akd.2014.4730
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- Publication type:
- Article
Dissecting the genetics of cardiomyopathy in India: A tale of ten steps.
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- Journal of Biosciences, 2009, v. 34, n. 1, p. 1, doi. 10.1007/s12038-009-0002-x
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- Publication type:
- Article
Tetra primer ARMS-PCR relates folate/homocysteine pathway genes and ACE gene polymorphism with coronary artery disease.
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- Molecular & Cellular Biochemistry, 2011, v. 355, n. 1/2, p. 289, doi. 10.1007/s11010-011-0866-6
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- Publication type:
- Article
Cell type-specific expression of endogenous cardiac Troponin I antisense RNA in the neonatal rat heart.
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- Molecular & Cellular Biochemistry, 2009, v. 324, n. 1/2, p. 1
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- Publication type:
- Article
Engineered Human Cardiac Tissue.
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- Pediatric Cardiology, 2011, v. 32, n. 3, p. 334, doi. 10.1007/s00246-011-9888-9
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- Publication type:
- Article
Genetic and Genomic Dissection of Cardiogenesis in the Drosophila Model.
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- Pediatric Cardiology, 2010, v. 31, n. 3, p. 325, doi. 10.1007/s00246-009-9612-1
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- Publication type:
- Article
Familial Hypertrophic Cardiomyopathy Associated with Cardiac β-Myosin Heavy Chain and Troponin I Mutations.
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- Pediatric Cardiology, 2008, v. 29, n. 4, p. 846, doi. 10.1007/s00246-007-9177-9
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- Publication type:
- Article
The Classification Concept of the ESC Working Group on Myocardial and Pericardial Diseases for Dilated Cardiomyopathy.
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- Herz, 2007, v. 32, n. 6, p. 446, doi. 10.1007/s00059-007-3045-5
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- Publication type:
- Article
Phenotypic Variation of Familial Hypertrophic Cardiomyopathy Caused by the Phe[sup 110] →Ile Mutation in Cardiac Troponin T.
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- Cardiology, 2000, v. 93, n. 3, p. 155, doi. 10.1159/000007020
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- Publication type:
- Article
Early identification of hERG liability in drug discovery programs by automated patch clamp.
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- Frontiers in Pharmacology, 2014, v. 5, p. 1, doi. 10.3389/fphar.2014.00203
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- Publication type:
- Article
Cardiovascular disease risk factor knowledge assessment among medical students.
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- National Journal of Physiology, Pharmacy & Pharmacology, 2016, v. 6, n. 3, p. 251, doi. 10.5455/njppp.2016.6.20022016129
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- Publication type:
- Article
Muscle-Specific Mis-Splicing and Heart Disease Exemplified by RBM20.
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- Genes, 2018, v. 9, n. 1, p. 18, doi. 10.3390/genes9010018
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- Publication type:
- Article
Reclassification of genetic-based risk predictions as GWAS data accumulate.
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- Genome Medicine, 2016, v. 8, p. 1, doi. 10.1186/s13073-016-0272-5
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- Publication type:
- Article
Mutations in the cardiac Troponin C gene are a cause of idiopathic dilated cardiomyopathy in childhood.
- Published in:
- 2007
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- Publication type:
- Case Study
Clinical investigations over 13 years to establish the nature of the cardiac defects in patients having abnormalities of lateralization.
- Published in:
- 2007
- By:
- Publication type:
- journal article
Variants of the CFC1 gene in patients with laterality defects associated with congenital cardiac disease.
- Published in:
- Cardiology in the Young, 2007, v. 17, n. 3, p. 268, doi. 10.1017/S1047951107000455
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- Publication type:
- Article
Searching for order among disorders of laterality.
- Published in:
- 2007
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- Publication type:
- commentary