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Case Report: An association of left ventricular outflow tract obstruction with 5p deletions.
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- Frontiers in Genetics, 2024, p. 1, doi. 10.3389/fgene.2024.1451746
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- Publication type:
- Article
Deposition studies of aerosol delivery by nasal cannula to infants.
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- Pediatric Pulmonology, 2019, v. 54, n. 8, p. 1319, doi. 10.1002/ppul.24326
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- Publication type:
- Article
Heterotaxy and complex structural heart defects in a mutant mouse model of primary ciliary dyskinesia.
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- 2007
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- Publication type:
- journal article
Nonoverlapping expression of Cx43 and Cx26 in the mouse placenta and decidua: A pattern of gap junction gene expression differing from that in the rat.
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- Molecular Reproduction & Development, 1995, v. 41, n. 2, p. 195, doi. 10.1002/mrd.1080410210
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- Publication type:
- Article
Profiling development of abdominal organs in the pig.
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- Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-19960-5
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- Publication type:
- Article
Impaired Neurovascular Function Underlies Poor Neurocognitive Outcomes and Is Associated with Nitric Oxide Bioavailability in Congenital Heart Disease.
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- Metabolites (2218-1989), 2022, v. 12, n. 9, p. 882, doi. 10.3390/metabo12090882
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- Publication type:
- Article
Wdpcp promotes epicardial EMT and epicardium-derived cell migration to facilitate coronary artery remodeling.
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- Science Signaling, 2018, v. 11, n. 519, p. 1, doi. 10.1126/scisignal.aah5770
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- Publication type:
- Article
Left–right patterning in congenital heart disease beyond heterotaxy.
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- American Journal of Medical Genetics. Part C: Seminars in Medical Genetics, 2020, v. 184, n. 1, p. 90, doi. 10.1002/ajmg.c.31768
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- Publication type:
- Article
Respiratory motile cilia dysfunction in a patient with cranioectodermal dysplasia.
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- American Journal of Medical Genetics. Part A, 2015, v. 167A, n. 9, p. 2188, doi. 10.1002/ajmg.a.37133
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- Publication type:
- Article
Connexin 43 expression in the mouse embryo: Localization of transcripts within developmentally significant domains.
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- Developmental Dynamics, 1992, v. 194, n. 4, p. 261, doi. 10.1002/aja.1001940403
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- Publication type:
- Article
Restrictions in gap junctional communication in the Drosophila larval epidermis.
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- Developmental Dynamics, 1992, v. 193, n. 1, p. 70, doi. 10.1002/aja.1001930110
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- Publication type:
- Article
Cytoglobin regulates NO-dependent cilia motility and organ laterality during development.
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- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-43544-0
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- Publication type:
- Article
Cerebellar and Prefrontal Structures Associated With Executive Functioning in Pediatric Patients With Congenital Heart Defects.
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- Frontiers in Neurology, 2022, v. 13, p. 1, doi. 10.3389/fneur.2022.827780
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- Publication type:
- Article
Diverse Application of MRI for Mouse Phenotyping.
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- Birth Defects Research, 2017, v. 109, n. 10, p. 758, doi. 10.1002/bdr2.1051
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- Publication type:
- Article
Phenotyping Cardiac and Structural Birth Defects in Fetal and Newborn Mice.
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- Birth Defects Research, 2017, v. 109, n. 10, p. 778, doi. 10.1002/bdr2.1048
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- Publication type:
- Article
Rapid Ex-Vivo Ciliogenesis and Dose-Dependent Effect of Notch Inhibition on Ciliogenesis of Respiratory Epithelia.
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- Biomolecules (2218-273X), 2020, v. 10, n. 8, p. 1182, doi. 10.3390/biom10081182
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- Publication type:
- Article
Cardiac Targeting Peptide, a Novel Cardiac Vector: Studies in Bio-Distribution, Imaging Application, and Mechanism of Transduction.
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- Biomolecules (2218-273X), 2018, v. 8, n. 4, p. 147, doi. 10.3390/biom8040147
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- Publication type:
- Article
High-purity enrichment of functional cardiovascular cells from human iPS cells.
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- Cardiovascular Research, 2012, v. 95, n. 3, p. 327, doi. 10.1093/cvr/cvs185
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- Publication type:
- Article
The Genetic Landscape of Hypoplastic Left Heart Syndrome.
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- Pediatric Cardiology, 2018, v. 39, n. 6, p. 1069, doi. 10.1007/s00246-018-1861-4
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- Publication type:
- Article
Mutation of LRP1 in cardiac neural crest cells causes congenital heart defects by perturbing outflow lengthening.
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- Communications Biology, 2020, v. 3, n. 1, p. 1, doi. 10.1038/s42003-020-1035-9
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- Publication type:
- Article
Correlation of GDF5 and connexin 43 mRNA expression during embryonic development.
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- Anatomical Record: Advances in Integrative Anatomy & Evolutionary Biology, 2003, v. 275A, n. 2, p. 1117, doi. 10.1002/ar.a.10125
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- Publication type:
- Article
Insights into the genetic architecture of congenital heart disease from animal modeling.
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- Zoological Research, 2023, v. 44, n. 3, p. 577, doi. 10.24272/j.issn.2095-8137.2022.463
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- Publication type:
- Article
Erratum: Genetic link between renal birth defects and congenital heart disease.
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- Nature Communications, 2016, v. 7, n. 6, p. 11910, doi. 10.1038/ncomms11910
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- Publication type:
- Article
Genetic link between renal birth defects and congenital heart disease.
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- Nature Communications, 2016, v. 7, n. 3, p. 11103, doi. 10.1038/ncomms11103
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- Publication type:
- Article
ANKS6 is the critical activator of NEK8 kinase in embryonic situs determination and organ patterning.
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- Nature Communications, 2015, v. 6, n. 1, p. 6023, doi. 10.1038/ncomms7023
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- Publication type:
- Article
Automated identification of abnormal respiratory ciliary motion in nasal biopsies.
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- Science Translational Medicine, 2015, v. 7, n. 299, p. 1, doi. 10.1126/scitranslmed.aaa1233
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- Publication type:
- Article
Clinical factors associated with microstructural connectome related brain dysmaturation in term neonates with congenital heart disease.
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- Frontiers in Neuroscience, 2022, v. 16, p. 1, doi. 10.3389/fnins.2022.952355
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- Publication type:
- Article
Autonomous and non-cell autonomous role of cilia in structural birth defects in mice.
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- PLoS Biology, 2023, v. 21, n. 12, p. 1, doi. 10.1371/journal.pbio.3002425
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- Publication type:
- Article
Perturbation in connexin 43 and connexin 26 gap-junction expression in mouse skin hyperplasia and neoplasia.
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- Molecular Carcinogenesis, 1996, v. 17, n. 2, p. 49, doi. 10.1002/(SICI)1098-2744(199610)17:2<49::AID-MC1>3.0.CO;2-O
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- Publication type:
- Article
Developmental atlas of the early first trimester human embryo.
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- Developmental Dynamics, 2010, v. 239, n. 6, p. 1585, doi. 10.1002/dvdy.22316
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- Publication type:
- Article
Patterning of coronary arteries in wildtype and connexin43 knockout miceThis article is a US Government work and, as such, is in the public domain in the United States of America.
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- Developmental Dynamics, 2006, v. 235, n. 10, p. 2786
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- Article
Developmental regulation and expression of the zebrafish connexin43 gene.
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- Developmental Dynamics, 2005, v. 233, n. 3, p. 890
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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
Cardiovascular Development and Congenital Heart Disease Modeling in the Pig.
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- 2021
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- Publication type:
- journal article
Low Nasal NO in Congenital Heart Disease With Systemic Right Ventricle and Postcardiac Transplantation.
- Published in:
- Journal of the American Heart Association, 2017, v. 6, n. 12, p. 1, doi. 10.1161/JAHA.117.007447
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- Publication type:
- Article
Differential effect of anesthetics on mucociliary clearance in vivo in mice.
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- Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-84605-y
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- Publication type:
- Article
Cilia interactome with predicted protein–protein interactions reveals connections to Alzheimer's disease, aging and other neuropsychiatric processes.
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- Scientific Reports, 2020, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41598-020-72024-4
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- Publication type:
- Article
Novel Jbts17 mutant mouse model of Joubert syndrome with cilia transition zone defects and cerebellar and other ciliopathy related anomalies.
- Published in:
- Human Molecular Genetics, 2015, v. 24, n. 14, p. 3994, doi. 10.1093/hmg/ddv137
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- Publication type:
- Article
Coronary Anomalies in Mice With Congenital Heart Defects.
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- Anatomical Record: Advances in Integrative Anatomy & Evolutionary Biology, 2015, v. 298, n. 2, p. 408, doi. 10.1002/ar.23056
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- Publication type:
- Article
Overexpression of connexin43 alters the mutant phenotype of midgestational wnt- 1 null mice resulting in recovery of the midbrain and cerebellum.
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- Anatomical Record: Advances in Integrative Anatomy & Evolutionary Biology, 2005, v. 283A, n. 1, p. 224, doi. 10.1002/ar.a.20158
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- Publication type:
- Article
Mitigation of Fetal Radiation Injury from Mid-Gestation Total-body Irradiation by Maternal Administration of Mitochondrial-Targeted GS-Nitroxide JP4-039.
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- Radiation Research, 2024, v. 202, n. 3, p. 565, doi. 10.1667/RADE-24-00095.1
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- Publication type:
- Article
Correction to: Flow blockage disrupts cilia-driven fluid transport in the epileptic brain.
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- Acta Neuropathologica, 2022, v. 144, n. 6, p. 1189, doi. 10.1007/s00401-022-02496-3
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- Publication type:
- Article
Flow blockage disrupts cilia-driven fluid transport in the epileptic brain.
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- Acta Neuropathologica, 2022, v. 144, n. 4, p. 691, doi. 10.1007/s00401-022-02463-y
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- Publication type:
- Article
Fetal Mouse Imaging Using Echocardiography: A Review of Current Technology.
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- Echocardiography, 2006, v. 23, n. 10, p. 891, doi. 10.1111/j.1540-8175.2006.00335.x
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- Publication type:
- Article
Vertebrate myosin 1d regulates left-right organizer morphogenesis and laterality.
- Published in:
- Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-018-05866-2
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- Publication type:
- Article
Evaluating the role of connexin43 in congenital heart disease: Screening for mutations in patients with outflow tract anomalies and the analysis of knock-in mouse models.
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- Journal of Cardiovascular Disease Research (Journal of Cardiovascular Disease Research), 2011, v. 2, n. 4, p. 206, doi. 10.4103/0975-3583.89804
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- Publication type:
- Article
The Golgin GMAP210/TRIP11 Anchors IFT20 to the Golgi Complex.
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- PLoS Genetics, 2008, v. 4, n. 12, p. 1, doi. 10.1371/journal.pgen.1000315
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- Publication type:
- Article
Airway Ciliary Dysfunction and Sinopulmonary Symptoms in Patients with Congenital Heart Disease.
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- Annals of the American Thoracic Society, 2014, v. 11, n. 9, p. 1426, doi. 10.1513/AnnalsATS.201405-222OC
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- Publication type:
- Article
Mechanisms of Impaired Lung Development and Ciliation in Mannosidase-1-Alpha-2 (Man1a2) Mutants.
- Published in:
- Frontiers in Physiology, 2021, v. 12, p. 1, doi. 10.3389/fphys.2021.658518
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- Publication type:
- Article
Rare and Common Variants Uncover the Role of the Atria in Coarctation of the Aorta.
- Published in:
- Genes, 2022, v. 13, n. 4, p. 636, doi. 10.3390/genes13040636
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- Publication type:
- Article