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Case Report: An association of left ventricular outflow tract obstruction with 5p deletions.
- Published in:
- Frontiers in Genetics, 2024, p. 1, doi. 10.3389/fgene.2024.1451746
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- Publication type:
- Article
Inhibition of BK<sub>Ca</sub> channels protects neonatal hearts against myocardial ischemia and reperfusion injury.
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- Cell Death Discovery, 2022, v. 8, n. 1, p. 1, doi. 10.1038/s41420-022-00980-z
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- Publication type:
- Article
miR‐145 transgenic mice develop cardiopulmonary complications leading to postnatal death.
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- Physiological Reports, 2021, v. 9, n. 17, p. 1, doi. 10.14814/phy2.15013
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- Publication type:
- Article
Assessment of large copy number variants in patients with apparently isolated congenital left-sided cardiac lesions reveals clinically relevant genomic events.
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- American Journal of Medical Genetics. Part A, 2017, v. 173, n. 8, p. 2176, doi. 10.1002/ajmg.a.38309
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- Publication type:
- Article
A unified test of linkage analysis and rare-variant association for analysis of pedigree sequence data.
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- Nature Biotechnology, 2014, v. 32, n. 7, p. 663, doi. 10.1038/nbt.2895
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- Publication type:
- Article
Compacting the heart with Notch.
- Published in:
- Nature Medicine, 2013, v. 19, n. 2, p. 133, doi. 10.1038/nm.3071
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- Article
Impact of Mendelian inheritance in cardiovascular disease.
- Published in:
- Annals of the New York Academy of Sciences, 2010, v. 1214, n. 1, p. 122, doi. 10.1111/j.1749-6632.2010.05791.x
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- Article
Cover Image, Volume 234, Number 9, September 2019.
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- Journal of Cellular Physiology, 2019, v. 234, n. 9, p. i, doi. 10.1002/jcp.26994
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- Article
Impact of maternal hyperglycemia on cardiac development: Insights from animal models.
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- Genesis: The Journal of Genetics & Development, 2021, v. 59, n. 11, p. 1, doi. 10.1002/dvg.23449
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- Article
A Randomized Clinical Trial Demonstrating Feasibility and Preliminary Efficacy of a Videoconference-Delivered Physical Activity Lifestyle Intervention Among Adolescents With a Congenital Heart Defect.
- Published in:
- 2022
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- Publication type:
- journal article
Inhibitory Role of Notch1 in Calcific Aortic Valve Disease.
- Published in:
- PLoS ONE, 2011, v. 6, n. 11, p. 1, doi. 10.1371/journal.pone.0027743
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- Article
Calcific aortic valve disease: novel insights into nitric oxide signalling.
- Published in:
- European Heart Journal, 2022, v. 43, n. 17, p. 1665, doi. 10.1093/eurheartj/ehac050
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- Article
Correction: Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease.
- Published in:
- 2021
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- Correction Notice
Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease.
- Published in:
- PLoS Genetics, 2021, v. 17, n. 7, p. 1, doi. 10.1371/journal.pgen.1009679
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- Publication type:
- Article
Novel frameshift variant in MYL2 reveals molecular differences between dominant and recessive forms of hypertrophic cardiomyopathy.
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- PLoS Genetics, 2020, v. 16, n. 5, p. 1, doi. 10.1371/journal.pgen.1008639
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- Article
Maternal hyperglycemia and fetal cardiac development: Clinical impact and underlying mechanisms.
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- Birth Defects Research, 2018, v. 110, n. 20, p. 1504, doi. 10.1002/bdr2.1435
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- Publication type:
- Article
450 Gender Differences in the Association of Impulsive Behavior and Susceptibility to E-cigarette Use among Adolescents with Congenital Heart Defects.
- Published in:
- 2022
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- Abstract
Galectin-3 and sST2 as Prognosticators for Heart Failure Requiring Extracorporeal Life Support: Jack n' Jill.
- Published in:
- Biomolecules (2218-273X), 2021, v. 11, n. 2, p. 166, doi. 10.3390/biom11020166
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- Article
Human balanced translocation and mouse gene inactivation implicate Basonuclin 2 in distal urethral development.
- Published in:
- 2012
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- Publication type:
- Correction Notice
Subtype‐specific cardiomyocytes for precision medicine: Where are we now?
- Published in:
- Stem Cells, 2020, v. 38, n. 7, p. 822, doi. 10.1002/stem.3178
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- Publication type:
- Article
Reclassification of Variants of Uncertain Significance in Children with Inherited Arrhythmia Syndromes is Predicted by Clinical Factors.
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- Pediatric Cardiology, 2019, v. 40, n. 8, p. 1679, doi. 10.1007/s00246-019-02203-2
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- Publication type:
- Article
Abnormal Longitudinal Growth of the Aorta in Children with Familial Bicuspid Aortic Valve.
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- Pediatric Cardiology, 2017, v. 38, n. 8, p. 1709, doi. 10.1007/s00246-017-1740-4
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- Publication type:
- Article
Submicroscopic Chromosomal Copy Number Variations Identified in Children With Hypoplastic Left Heart Syndrome.
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- Pediatric Cardiology, 2012, v. 33, n. 5, p. 757, doi. 10.1007/s00246-012-0208-9
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- Publication type:
- Article
Use of a targeted, combinatorial next-generation sequencing approach for the study of bicuspid aortic valve.
- Published in:
- BMC Medical Genomics, 2014, v. 7, n. 1, p. 56, doi. 10.1186/1755-8794-7-56
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- Publication type:
- Article
Genetics of Valvular Heart Disease.
- Published in:
- Current Cardiology Reports, 2014, v. 16, n. 6, p. 1, doi. 10.1007/s11886-014-0487-2
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- Publication type:
- Article
Probing single ventricle heart defects with patient‐derived induced pluripotent stem cells and emerging technologies.
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- Birth Defects Research, 2022, v. 114, n. 16, p. 959, doi. 10.1002/bdr2.1989
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- Publication type:
- Article
Mutations in NOTCH1 cause aortic valve disease.
- Published in:
- Nature, 2005, v. 437, n. 7056, p. 270, doi. 10.1038/nature03940
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- Article
GATA4 mutations cause human congenital heart defects and reveal an interaction with TBX5.
- Published in:
- Nature, 2003, v. 424, n. 6947, p. 443, doi. 10.1038/nature01827
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- Publication type:
- Article
A Multicenter Analysis of Abnormal Chromosomal Microarray Findings in Congenital Heart Disease.
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- Journal of the American Heart Association, 2023, v. 12, n. 18, p. 1, doi. 10.1161/JAHA.123.029340
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- Publication type:
- Article
Patent Ductus Arteriosus: A Contemporary Perspective for the Pediatric and Adult Cardiac Care Provider.
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- 2022
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- Publication type:
- journal article
Endothelial Notch1 Is Required for Proper Development of the Semilunar Valves and Cardiac Outflow Tract.
- Published in:
- 2016
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- Publication type:
- journal article
Percutaneous Patent Ductus Arteriosus (PDA) Closure in Very Preterm Infants: Feasibility and Complications.
- Published in:
- 2016
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- Publication type:
- journal article
Pharmacological inhibitor of notch signaling stabilizes the progression of small abdominal aortic aneurysm in a mouse model.
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- 2014
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- Publication type:
- journal article
Disruption of myocardial Gata4 and Tbx5 results in defects in cardiomyocyte proliferation and atrioventricular septation.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 19, p. 5025, doi. 10.1093/hmg/ddu215
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- Publication type:
- Article
The Association of Global and Disease-Related Stress With Susceptibility to and Use of E-Cigarettes and Marijuana Among Adolescents With Congenital Heart Disease.
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- Journal of Pediatric Psychology, 2023, v. 48, n. 5, p. 458, doi. 10.1093/jpepsy/jsad005
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- Article
Gender Differences in Physical Activity Engagement Among Adolescents With Congenital Heart Disease.
- Published in:
- 2022
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- Publication type:
- journal article
Nestin expression is dynamically regulated in cardiomyocytes during embryogenesis.
- Published in:
- Journal of Cellular Physiology, 2018, v. 233, n. 4, p. 3218, doi. 10.1002/jcp.26165
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- Publication type:
- Article
Single-Cell RNA Sequencing Reveals Novel Genes Regulated by Hypoxia in the Lung Vasculature.
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- Journal of Vascular Research, 2022, v. 59, n. 3, p. 163, doi. 10.1159/000522340
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- Publication type:
- Article
Congenital Heart Disease--Causing Gata4 Mutation Displays Functional Deficits In Vivo.
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- PLoS Genetics, 2012, v. 8, n. 5, p. 1, doi. 10.1371/journal.pgen.1002690
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- Publication type:
- Article
Genetic Abnormalities in FOXP1 Are Associated with Congenital Heart Defects.
- Published in:
- Human Mutation, 2013, v. 34, n. 9, p. 1226, doi. 10.1002/humu.22366
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- Publication type:
- Article
Endocardial HDAC3 is required for myocardial trabeculation.
- Published in:
- Nature Communications, 2024, v. 15, n. 1, p. 1, doi. 10.1038/s41467-024-48362-6
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- Publication type:
- Article
Exome sequencing in multiplex families with left-sided cardiac defects has high yield for disease gene discovery.
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- PLoS Genetics, 2022, v. 18, n. 6, p. 1, doi. 10.1371/journal.pgen.1010236
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- Publication type:
- Article
Single-cell transcriptomic profiling unveils dysregulation of cardiac progenitor cells and cardiomyocytes in a mouse model of maternal hyperglycemia.
- Published in:
- Communications Biology, 2022, v. 5, n. 1, p. 1, doi. 10.1038/s42003-022-03779-x
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- Publication type:
- Article