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A Functional Aryl Hydrocarbon Receptor Genetic Variant, Alone and in Combination with Parental Exposure, is a Risk Factor for Congenital Heart Disease.
- Published in:
- Cardiovascular Toxicology, 2018, v. 18, n. 3, p. 261, doi. 10.1007/s12012-017-9436-9
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- Publication type:
- Article
Functional characterization and circulating expression profile of dysregulated microRNAs in BAV-associated aortopathy.
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- Heart & Vessels, 2020, v. 35, n. 3, p. 432, doi. 10.1007/s00380-019-01509-8
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- Publication type:
- Article
Marine Collagen-Based Bioink for 3D Bioprinting of a Bilayered Skin Model.
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- Pharmaceutics, 2023, v. 15, n. 5, p. 1331, doi. 10.3390/pharmaceutics15051331
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- Publication type:
- Article
Independent and Combined Effects of Telomere Shortening and mtDNA4977 Deletion on Long-term Outcomes of Patients with Coronary Artery Disease.
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- International Journal of Molecular Sciences, 2019, v. 20, n. 21, p. 5508, doi. 10.3390/ijms20215508
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- Article
miRNome Profiling in Bicuspid Aortic Valve-Associated Aortopathy by Next-Generation Sequencing.
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- International Journal of Molecular Sciences, 2017, v. 18, n. 11, p. 2498, doi. 10.3390/ijms18112498
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- Article
Effects of Highly Polluted Environment on Sperm Telomere Length: A Pilot Study.
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- International Journal of Molecular Sciences, 2017, v. 18, n. 8, p. 1703, doi. 10.3390/ijms18081703
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- Publication type:
- Article
Dysregulated insulin secretion is associated with pancreatic β‐cell hyperplasia and direct acinar‐β‐cell trans‐differentiation in partially eNOS‐deficient mice.
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- Physiological Reports, 2022, v. 10, n. 16, p. 1, doi. 10.14814/phy2.15425
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- Article
Cobalt-protoporphyrin improves heart function by blunting oxidative stress and restoring NO synthase equilibrium in an animal model of experimental diabetas.
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- Frontiers in Physiology, 2012, v. 3, p. 1, doi. 10.3389/fphys.2012.00160
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- Publication type:
- Article
Individual and joint effects of genetic polymorphisms in microRNA-machinery genes on congenital heart disease susceptibility.
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- Cardiology in the Young, 2021, v. 31, n. 6, p. 965, doi. 10.1017/S1047951120004874
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- Article
Partial Deletion of eNOS Gene Causes Hyperinsulinemic State, Unbalance of Cardiac Insulin Signaling Pathways and Coronary Dysfunction Independently of High Fat Diet.
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- PLoS ONE, 2014, v. 9, n. 8, p. 1, doi. 10.1371/journal.pone.0104156
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- Publication type:
- Article
Reproductive outcomes and Y chromosome instability in radiation‐exposed male workers in cardiac catheterization laboratory.
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- Environmental & Molecular Mutagenesis, 2020, v. 61, n. 3, p. 361, doi. 10.1002/em.22341
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- Publication type:
- Article
A Novel Frailty Score Based on Laboratory Parameters (FIMS Score) for the Management of Older Patients with Severe Aortic Stenosis.
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- Journal of Clinical Medicine, 2023, v. 12, n. 18, p. 5927, doi. 10.3390/jcm12185927
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- Article
When the heart sleeps… Is the vagus resetting the myocardial ‘redox clock’?
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- 2008
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- Publication type:
- Editorial
Targeted Next-Generation Sequencing in Patients with Non-syndromic Congenital Heart Disease.
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- Pediatric Cardiology, 2018, v. 39, n. 4, p. 682, doi. 10.1007/s00246-018-1806-y
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- Publication type:
- Article
Lack of Association of the 3′-UTR Polymorphism (rs1017) in the ISL1 Gene and Risk of Congenital Heart Disease in the White Population.
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- Pediatric Cardiology, 2013, v. 34, n. 4, p. 938, doi. 10.1007/s00246-012-0578-z
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- Publication type:
- Article
Environmental pollutants: genetic damage and epigenetic changes in male germ cells.
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- Environmental Science & Pollution Research, 2016, v. 23, n. 23, p. 23339, doi. 10.1007/s11356-016-7728-4
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- Publication type:
- Article
Insulin resistance is a major determinant of myocardial blood flow impairment in anginal patients.
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- European Journal of Nuclear Medicine & Molecular Imaging, 2013, v. 40, n. 12, p. 1905, doi. 10.1007/s00259-013-2523-7
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- Publication type:
- Article
Increased mitochondrial DNA4977-bp deletion in catheterization laboratory workers with long-term low-dose exposure to ionizing radiation.
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- European Journal of Preventive Cardiology, 2019, v. 26, n. 9, p. 976, doi. 10.1177/2047487319831495
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- Publication type:
- Article
The Ultimate Method for Determination of S-Nitrosoglutathione (GSNO): Enzymatic/Copper Mediated Decomposition plus DAF-NO Reaction®.
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- FASEB Journal, 2008, v. 22, p. 65, doi. 10.1096/fasebj.22.2_supplement.65
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- Publication type:
- Article
Radiobiological Effectiveness of Ultrashort Laser-Driven Electron Bunches: Micronucleus Frequency, Telomere Shortening and Cell Viability.
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- Radiation Research, 2016, v. 186, n. 3, p. 245, doi. 10.1667/RR14266.1
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- Publication type:
- Article
A Comprehensive Review of COVID-19-Related Olfactory Deficiency: Unraveling Associations with Neurocognitive Disorders and Magnetic Resonance Imaging Findings.
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- Diagnostics (2075-4418), 2024, v. 14, n. 4, p. 359, doi. 10.3390/diagnostics14040359
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- Publication type:
- Article
Low HDL cholesterol and the eNOS Glu298Asp polymorphism are associated with inducible myocardial ischemia in patients with suspected stable coronary artery disease.
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- BMC Cardiovascular Disorders, 2024, v. 24, n. 1, p. 1, doi. 10.1186/s12872-024-03846-7
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- Publication type:
- Article
The Impact of Acute Heart Failure on Frailty Degree and Outcomes in Elderly Patients with Severe Aortic Stenosis and Chronic Heart Failure with Preserved Ejection Fraction.
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- Journal of Cardiovascular Development & Disease (JCDD), 2024, v. 11, n. 5, p. 150, doi. 10.3390/jcdd11050150
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- Publication type:
- Article
Psychological Impact of a Prenatal Diagnosis of Congenital Heart Disease on Parents: Is It Time for Tailored Psychological Support?
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- Journal of Cardiovascular Development & Disease (JCDD), 2024, v. 11, n. 1, p. 31, doi. 10.3390/jcdd11010031
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- Publication type:
- Article
Sequencing of NOTCH1, GATA5, TGFBR1 and TGFBR2 genes in familial cases of bicuspid aortic valve.
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- BMC Medical Genetics, 2013, v. 14, n. 1, p. 1, doi. 10.1186/1471-2350-14-44
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- Publication type:
- Article
T<sup>-786</sup>→C polymorphism of the endothelial nitric oxide synthase gene is associated with insulin resistance in patients with ischemic or non ischemic cardiomyopathy.
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- BMC Medical Genetics, 2012, v. 13, n. 1, p. 92, doi. 10.1186/1471-2350-13-92
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- Publication type:
- Article