Cecilia W. Lo

Department of Developmental Biology, University of Pittsburgh

Research Area

Developmental Biology

Biography

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JoVE Journal Publications

Article Total : 1	Year
Publication title	2022

Other Publications

Article	Year
Novel Jbts17 mutant mouse model of Joubert syndrome with cilia transition zone defects and cerebellar and other ciliopathy related anomalies. Human molecular genetics\| PubMed ID: 25877302	2015
Establishing normative nasal nitric oxide values in infants. Respiratory medicine\| PubMed ID: 26233707	2015
Automated identification of abnormal respiratory ciliary motion in nasal biopsies. Science translational medicine\| PubMed ID: 26246169	2015
Prickle1 mutation causes planar cell polarity and directional cell migration defects associated with cardiac outflow tract anomalies and other structural birth defects. Biology open\| PubMed ID: 26883626	2016
Brain Dysplasia Associated with Ciliary Dysfunction in Infants with Congenital Heart Disease. The Journal of pediatrics\| PubMed ID: 27574995	2016
Cilia and Ciliopathies in Congenital Heart Disease. Cold Spring Harbor perspectives in biology\| PubMed ID: 28159874	2017
Reply. The Journal of pediatrics\| PubMed ID: 28283257	2017
Assessment of ciliary phenotype in primary ciliary dyskinesia by micro-optical coherence tomography. JCI insight\| PubMed ID: 28289722	2017
The complex genetics of hypoplastic left heart syndrome. Nature genetics\| PubMed ID: 28530678	2017
Phenotyping cardiac and structural birth defects in fetal and newborn mice. Birth defects research\| PubMed ID: 28544620	2017
Diverse application of MRI for mouse phenotyping. Birth defects research\| PubMed ID: 28544650	2017
Loss of function in is associated with tetralogy of Fallot and septal defects. Journal of medical genetics\| PubMed ID: 28592524	2017
Airway ciliary dysfunction: Association with adverse postoperative outcomes in nonheterotaxy congenital heart disease patients. The Journal of thoracic and cardiovascular surgery\| PubMed ID: 29056267	2018
Low Nasal NO in Congenital Heart Disease With Systemic Right Ventricle and Postcardiac Transplantation. Journal of the American Heart Association\| PubMed ID: 29212650	2017
Airway ciliary dysfunction and respiratory symptoms in patients with transposition of the great arteries. PloS one\| PubMed ID: 29444099	2018
Wdpcp promotes epicardial EMT and epicardium-derived cell migration to facilitate coronary artery remodeling. Science signaling\| PubMed ID: 29487191	2018
The Genetic Landscape of Hypoplastic Left Heart Syndrome. Pediatric cardiology\| PubMed ID: 29569026	2018
A computational framework for the detection of subcortical brain dysmaturation in neonatal MRI using 3D Convolutional Neural Networks. NeuroImage\| PubMed ID: 29793060	2018
Congenital Heart Defects and Ciliopathies Associated With Renal Phenotypes. Frontiers in pediatrics\| PubMed ID: 29963541	2018
Exome-chip meta-analysis identifies novel loci associated with cardiac conduction, including ADAMTS6. Genome biology\| PubMed ID: 30012220	2018
Vertebrate myosin 1d regulates left-right organizer morphogenesis and laterality. Nature communications\| PubMed ID: 30139971	2018
Cardiac Targeting Peptide, a Novel Cardiac Vector: Studies in Bio-Distribution, Imaging Application, and Mechanism of Transduction. Biomolecules\| PubMed ID: 30441852	2018
Reply to 'Double-outlet right ventricle is not hypoplastic left heart syndrome'. Nature genetics\| PubMed ID: 30617253	2019
Deposition studies of aerosol delivery by nasal cannula to infants. Pediatric pulmonology\| PubMed ID: 30932345	2019
Left-right patterning in congenital heart disease beyond heterotaxy. American journal of medical genetics. Part C, Seminars in medical genetics\| PubMed ID: 31999049	2020
Role of cilia in the pathogenesis of congenital heart disease. Seminars in cell & developmental biology\| PubMed ID: 32418658	2021
Mutation of LRP1 in cardiac neural crest cells causes congenital heart defects by perturbing outflow lengthening. Communications biology\| PubMed ID: 32546759	2020
Rapid Ex-Vivo Ciliogenesis and Dose-Dependent Effect of Notch Inhibition on Ciliogenesis of Respiratory Epithelia. Biomolecules\| PubMed ID: 32823934	2020
A Membrane-Tethered Ubiquitination Pathway Regulates Hedgehog Signaling and Heart Development. Developmental cell\| PubMed ID: 32966817	2020
Cilia interactome with predicted protein-protein interactions reveals connections to Alzheimer's disease, aging and other neuropsychiatric processes. Scientific reports\| PubMed ID: 32973177	2020
Differential effect of anesthetics on mucociliary clearance in vivo in mice. Scientific reports\| PubMed ID: 33649513
Mucociliary Clearance Scans Show Infants Undergoing Congenital Cardiac Surgery Have Poor Airway Clearance Function. Frontiers in cardiovascular medicine\| PubMed ID: 33969015	2021
Cardiovascular Development and Congenital Heart Disease Modeling in the Pig. Journal of the American Heart Association\| PubMed ID: 34219463	2021
Mechanisms of Impaired Lung Development and Ciliation in Mannosidase-1-Alpha-2 () Mutants. Frontiers in physiology\| PubMed ID: 34366878	2021
Novel insights into the genetic landscape of congenital heart disease with systems genetics. Progress in pediatric cardiology\| PubMed ID: 34404969	2019
Gene-teratogen interactions influence the penetrance of birth defects by altering Hedgehog signaling strength. Development (Cambridge, England)\| PubMed ID: 34486668	2021
Mitochondrial Respiration Defects in Single-Ventricle Congenital Heart Disease. Frontiers in cardiovascular medicine\| PubMed ID: 34631832	2021
Relationships Between Regional Cerebral Blood Flow and Neurocognitive Outcomes in Children and Adolescents With Congenital Heart Disease. Seminars in thoracic and cardiovascular surgery\| PubMed ID: 34767938	2022
Common deletion variants causing protocadherin-α deficiency contribute to the complex genetics of BAV and left-sided congenital heart disease. HGG advances\| PubMed ID: 34888534	2021
Biallelic pathogenic variants in roundabout guidance receptor 1 associate with syndromic congenital anomalies of the kidney and urinary tract. Kidney international\| PubMed ID: 35227688	2022
Genetic resiliency associated with dominant lethal mutation causing atrial septal defect with high heritability. Cell reports. Medicine\| PubMed ID: 35243414	2022
Cerebellar and Prefrontal Structures Associated With Executive Functioning in Pediatric Patients With Congenital Heart Defects. Frontiers in neurology\| PubMed ID: 35356449	2022
Uncompensated mitochondrial oxidative stress underlies heart failure in an iPSC-derived model of congenital heart disease. Cell stem cell\| PubMed ID: 35395180	2022
Novel Protein-Protein Interactions Highlighting the Crosstalk between Hypoplastic Left Heart Syndrome, Ciliopathies and Neurodevelopmental Delays. Genes\| PubMed ID: 35456433	2022
Rare and Common Variants Uncover the Role of the Atria in Coarctation of the Aorta. Genes\| PubMed ID: 35456442	2022
Flow blockage disrupts cilia-driven fluid transport in the epileptic brain. Acta neuropathologica\| PubMed ID: 35980457	2022
Impaired Neurovascular Function Underlies Poor Neurocognitive Outcomes and Is Associated with Nitric Oxide Bioavailability in Congenital Heart Disease. Metabolites\| PubMed ID: 36144286	2022
Profiling development of abdominal organs in the pig. Scientific reports\| PubMed ID: 36171243	2022
Correction to: Flow blockage disrupts cilia-driven fluid transport in the epileptic brain. Acta neuropathologica\| PubMed ID: 36175669	2022
Clinical factors associated with microstructural connectome related brain dysmaturation in term neonates with congenital heart disease. Frontiers in neuroscience\| PubMed ID: 36466162	2022