Cecilia Lo | Academic Influence

Cecilia Lo's AcademicInfluence.com Rankings

Cecilia Lo

Biology

#2093

World Rank

#3366

Historical Rank

Genetics

#763

World Rank

#855

Historical Rank

Molecular Biology

#1024

World Rank

#1048

Historical Rank

biology Degrees

Download Badge

Biology

Cecilia Lo's Degrees

Bachelors Biology University of California, Berkeley
Masters Genetics Stanford University

Similar Degrees You Can Earn

Best Online Bachelor's in Biology 2025

Why Is Cecilia Lo Influential?

(Suggest an Edit or Addition)

According to Wikipedia, Cecilia Wen-ya Lo is a professor and the F. Sargent Cheever Chair of Developmental Biology at the University of Pittsburgh. Her research focuses on the study of congenital heart defects. Education Lo received her bachelor's degree in biology in 1974 from the Massachusetts Institute of Technology, where she worked with David Baltimore. She received her Ph.D. in 1979 from Rockefeller University.

(See a Problem?)

Cecilia Lo's Published Works

Number of citations in a given year to any of this author's works

Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author

Published Works

Identification and characterization of a fibroblast marker: FSP1 (1995) (1034)
Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probands (2017) (505)
Connexins and cell signaling in development and disease. (2004) (393)
Global genetic analysis in mice unveils central role for cilia in congenital heart disease (2015) (340)
Loss of nephrocystin-3 function can cause embryonic lethality, Meckel-Gruber-like syndrome, situs inversus, and renal-hepatic-pancreatic dysplasia. (2008) (303)
Gap junctional communication in the preimplantation mouse embryo (1979) (286)
Klf2 is an essential regulator of vascular hemodynamic forces in vivo. (2006) (265)
DYX1C1 is required for axonemal dynein assembly and ciliary motility (2013) (252)
Gap Junction–mediated Cell–Cell Communication Modulates Mouse Neural Crest Migration (1998) (246)
Modulation of mouse neural crest cell motility by N-cadherin and connexin 43 gap junctions (2001) (243)
Migration of cardiac neural crest cells in Splotch embryos. (2000) (221)
Heart and neural tube defects in transgenic mice overexpressing the Cx43 gap junction gene. (1997) (219)
Gap junctional communication in the post-implantation mouse embryo (1979) (212)
IFT27 links the BBSome to IFT for maintenance of the ciliary signaling compartment. (2014) (211)
Connexin43 Associated with an N-cadherin-containing Multiprotein Complex Is Required for Gap Junction Formation in NIH3T3 Cells* (2005) (204)
IFT25 links the signal-dependent movement of Hedgehog components to intraflagellar transport. (2012) (201)
The Golgin GMAP210/TRIP11 Anchors IFT20 to the Golgi Complex (2008) (183)
Interaction of Gata4 and Gata6 with Tbx5 is critical for normal cardiac development. (2009) (183)
Alteration in connexin 43 gap junction gene dosage impairs conotruncal heart development. (1998) (179)
Connexin 43 expression reflects neural crest patterns during cardiovascular development. (1999) (170)
Connexin 43-mediated modulation of polarized cell movement and the directional migration of cardiac neural crest cells (2006) (169)
The role of gap junction membrane channels in development (1996) (165)
High Prevalence of Respiratory Ciliary Dysfunction in Congenital Heart Disease Patients With Heterotaxy (2012) (158)
Cx43 gap junction gene expression and gap junctional communication in mouse neural crest cells. (1997) (150)
ARMC4 mutations cause primary ciliary dyskinesia with randomization of left/right body asymmetry. (2013) (148)
The complex genetics of hypoplastic left heart syndrome (2017) (143)
Null Mutation of Connexin43 Causes Slow Propagation of Ventricular Activation in the Late Stages of Mouse Embryonic Development (2001) (143)
Discovery of four recessive developmental disorders using probabilistic genotype and phenotype matching among 4,125 families (2015) (135)
Connexin 43 expression in the mouse embryo: Localization of transcripts within developmentally significant domains (1992) (134)
CCDC151 Mutations Cause Primary Ciliary Dyskinesia by Disruption of the Outer Dynein Arm Docking Complex Formation (2014) (134)
An essential role for connexin43 gap junctions in mouse coronary artery development. (2002) (134)
Role of gap junctions in cardiac conduction and development: insights from the connexin knockout mice. (2000) (125)
Localization of low abundance DNA sequences in tissue sections by in situ hybridization. (1986) (113)
ENU induced mutations causing congenital cardiovascular anomalies (2004) (105)
Identification and Characterization of a Fibroblast Marker : FSP 1 (2002) (103)
Rapid high resolution three dimensional reconstruction of embryos with episcopic fluorescence image capture. (2004) (101)
Connexin43 Modulates Cell Polarity and Directional Cell Migration by Regulating Microtubule Dynamics (2011) (101)
A Detailed Comparison of Mouse and Human Cardiac Development (2014) (99)
Heterotaxy and complex structural heart defects in a mutant mouse model of primary ciliary dyskinesia. (2007) (94)
Connexin 43 regulates epicardial cell polarity and migration in coronary vascular development (2009) (92)
Wdpcp, a PCP Protein Required for Ciliogenesis, Regulates Directional Cell Migration and Cell Polarity by Direct Modulation of the Actin Cytoskeleton (2013) (90)
MAPK phosphorylation of connexin 43 promotes binding of cyclin E and smooth muscle cell proliferation (2012) (87)
Gap junctional communication compartments in the Drosophila wing disk. (1982) (87)
Communication compartments in the gastrulating mouse embryo (1988) (87)
No turning, a mouse mutation causing left-right and axial patterning defects. (1998) (86)
High-purity enrichment of functional cardiovascular cells from human iPS cells. (2012) (85)
Gap junction communication and the modulation of cardiac neural crest cells. (1999) (82)
Heart malformations in transgenic mice exhibiting dominant negative inhibition of gap junctional communication in neural crest cells. (1998) (77)
Structure, sequence and expression of the mouse Cx43 gene encoding connexin 43. (1993) (77)
DNAH6 and Its Interactions with PCD Genes in Heterotaxy and Primary Ciliary Dyskinesia (2016) (76)
Genes, gene knockouts, and mutations in the analysis of gap junctions. (1999) (76)
Increased postoperative and respiratory complications in patients with congenital heart disease associated with heterotaxy. (2011) (75)
Connexin43 deficiency causes dysregulation of coronary vasculogenesis. (2005) (74)
Human Cardiac Development in the First Trimester: A High-Resolution Magnetic Resonance Imaging and Episcopic Fluorescence Image Capture Atlas (2009) (74)
Disruption of Mks1 localization to the mother centriole causes cilia defects and developmental malformations in Meckel-Gruber syndrome (2010) (73)
Perturbation in connexin 43 and connexin 26 gap‐junction expression in mouse skin hyperplasia and neoplasia (1996) (72)
Gap-junctional communication compartments in the Drosophila wing imaginal disk. (1984) (69)
Developmental atlas of the early first trimester human embryo (2010) (67)
A Unique Set of Centrosome Proteins Requires Pericentrin for Spindle-Pole Localization and Spindle Orientation (2014) (66)
Genetics of Congenital Heart Disease (2019) (65)
Developmental regulation and asymmetric expression of the gene encoding Cx43 gap junctions in the mouse limb bud. (1997) (65)
MMP21 is mutated in human heterotaxy and is required for normal left-right asymmetry in vertebrates (2015) (64)
Massively parallel sequencing identifies the gene Megf8 with ENU-induced mutation causing heterotaxy (2009) (63)
Bves directly interacts with GEFT, and controls cell shape and movement through regulation of Rac1/Cdc42 activity (2008) (63)
Lethal mitochondrial cardiomyopathy in a hypomorphic Med30 mouse mutant is ameliorated by ketogenic diet (2011) (62)
Developmental Biology Protocols (2000) (61)
Rump white inversion in the mouse disrupts dipeptidyl aminopeptidase-like protein 6 and causes dysregulation of Kit expression. (1998) (60)
Tracking of mouse cell lineage using microinjected DNA sequences: analyses using genomic Southern blotting and tissue-section in situ hybridizations. (1987) (59)
The complex of ciliary neurotrophic factor-ciliary neurotrophic factor receptor alpha up-regulates connexin43 and intercellular coupling in astrocytes via the Janus tyrosine kinase/signal transducer and activator of transcription pathway. (2004) (58)
Primordial germ cell deficiency in the connexin 43 knockout mouse arises from apoptosis associated with abnormal p53 activation (2006) (57)
Primary Cilia and Mammalian Hedgehog Signaling (2016) (57)
Cardiovascular phenotyping of fetal mice by noninvasive high-frequency ultrasound facilitates recovery of ENU-induced mutations causing congenital cardiac and extracardiac defects. (2005) (57)
Genetic link between renal birth defects and congenital heart disease (2016) (57)
Multimeric connexin interactions prior to the trans-Golgi network. (2001) (57)
Outflow tract cushions perform a critical valve-like function in the early embryonic heart requiring BMPRIA-mediated signaling in cardiac neural crest. (2009) (56)
Expression of a connexin 43/beta-galactosidase fusion protein inhibits gap junctional communication in NIH3T3 cells (1995) (54)
Cardiovascular assessment of fetal mice by in utero echocardiography. (2008) (52)
Increased postoperative respiratory complications in heterotaxy congenital heart disease patients with respiratory ciliary dysfunction. (2012) (52)
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 (2011) (48)
N-Cadherin and Cx43α1 Gap Junctions Modulates Mouse Neural Crest Cell Motility via Distinct Pathways (2001) (46)
Congenital heart disease and the specification of left-right asymmetry. (2012) (45)
Gap junctional communication in the extraembryonic tissues of the gastrulating mouse embryo (1989) (45)
Initiation and maturation of cilia-generated flow in newborn and postnatal mouse airway. (2009) (44)
Airway ciliary dysfunction and sinopulmonary symptoms in patients with congenital heart disease. (2014) (42)
Developmental regulation and expression of the zebrafish connexin43 gene (2005) (41)
Transformation by iontophoretic microinjection of DNA: multiple integrations without tandem insertions (1983) (41)
Interrogating Congenital Heart Defects With Noninvasive Fetal Echocardiography in a Mouse Forward Genetic Screen (2014) (40)
Cilia and Ciliopathies in Congenital Heart Disease. (2017) (40)
Patterning of coronary arteries in wildtype and connexin43 knockout mice (2006) (40)
Microcomputed Tomography Provides High Accuracy Congenital Heart Disease Diagnosis in Neonatal and Fetal Mice (2013) (40)
Prickle1 mutation causes planar cell polarity and directional cell migration defects associated with cardiac outflow tract anomalies and other structural birth defects (2016) (38)
Tbx2 Represses Expression of Connexin43 in Osteoblastic-like Cells (2004) (38)
Exome-chip meta-analysis identifies novel loci associated with cardiac conduction, including ADAMTS6 (2018) (37)
Automated identification of abnormal respiratory ciliary motion in nasal biopsies (2015) (37)
Cilia and models for studying structure and function. (2011) (37)
Fetal Mouse Imaging Using Echocardiography: A Review of Current Technology (2006) (37)
Ex vivo method for high resolution imaging of cilia motility in rodent airway epithelia. (2013) (37)
Posterior ("atypical") atrioventricular junctional reentrant tachycardia. (1994) (37)
The Genetic Landscape of Hypoplastic Left Heart Syndrome (2018) (36)
ANKS6 is the critical activator of NEK8 kinase in embryonic situs determination and organ patterning (2015) (36)
The Wheels mutation in the mouse causes vascular, hindbrain, and inner ear defects. (2001) (34)
Respiratory motile cilia dysfunction in a patient with cranioectodermal dysplasia (2015) (33)
High frequency DNA rearrangements associated with mouse centromeric satellite DNA. (1986) (33)
Imaging techniques for visualizing and phenotyping congenital heart defects in murine models. (2013) (33)
Introduction of human DNA into mouse eggs by injection of dissected chromosome fragments. (1989) (32)
Novel Jbts17 mutant mouse model of Joubert syndrome with cilia transition zone defects and cerebellar and other ciliopathy related anomalies. (2015) (31)
High-frequency ultrasound database profiling growth, development, and cardiovascular function in C57BL/6J mouse fetuses. (2004) (31)
BMP Regulation of the Mouse Connexin43 Promoter in Osteoblastic Cells and Embryos (2003) (31)
Divergent effects of two sequence variants of GJB3 (G12D and R32W) on the function of connexin 31 in vitro (2003) (30)
How insights from cardiovascular developmental biology have impacted the care of infants and children with congenital heart disease (2012) (30)
Cx43 gap junctions in cardiac development. (1998) (29)
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 (1995) (29)
Imaging modalities to assess structural birth defects in mutant mouse models. (2010) (29)
Null Mutation of Connexin 43 Causes Slow Propagation of Ventricular Activation in the Late Stages of Mouse Embryonic Development (2001) (28)
A computational framework for the detection of subcortical brain dysmaturation in neonatal MRI using 3D Convolutional Neural Networks (2018) (28)
Modulation of tk expression in mouse pericentromeric heterochromatin (1986) (26)
Mouse Model of Heterotaxy with Single Ventricle Spectrum of Cardiac Anomalies (2008) (26)
Assessment of ciliary phenotype in primary ciliary dyskinesia by micro-optical coherence tomography. (2017) (26)
The Effects of Temperature and Anesthetic Agents on Ciliary Function in Murine Respiratory Epithelia (2014) (25)
Deposition studies of aerosol delivery by nasal cannula to infants (2019) (25)
Correlation of GDF5 and connexin 43 mRNA expression during embryonic development. (2003) (25)
Cilia interactome with predicted protein–protein interactions reveals connections to Alzheimer’s disease, aging and other neuropsychiatric processes (2020) (24)
Noninvasive phenotypic analysis of cardiovascular structure and function in fetal mice using ultrasound. (2003) (24)
Cardiac Targeting Peptide, a Novel Cardiac Vector: Studies in Bio-Distribution, Imaging Application, and Mechanism of Transduction (2018) (24)
Brain Dysplasia Associated with Ciliary Dysfunction in Infants with Congenital Heart Disease. (2016) (23)
An anterior/posterior communication compartment border in engrailed wing discs: possible implications for Drosophila pattern formation. (1985) (23)
Murine CENPF interacts with syntaxin 4 in the regulation of vesicular transport (2008) (21)
A Unique Set of Centrosome Proteins Requires Pericentrin for Spindle-Pole Localization and Spindle Orientation (2014) (21)
PCC4azal teratocarcinoma stem cell differentiation in culture. I. Biochemical studies. (1980) (20)
Role of cilia in structural birth defects: insights from ciliopathy mutant mouse models. (2014) (20)
Loss of function in ROBO1 is associated with tetralogy of Fallot and septal defects (2017) (20)
Establishing normative nasal nitric oxide values in infants. (2015) (19)
Disruption of Mks1 localization to the mother centriole causes cilia defects and developmental malformations in Meckel-Gruber syndrome (2011) (19)
Organization of chromosomes in the mouse nucleus: analysis by in situ hybridization. (1988) (19)
Vertebrate myosin 1d regulates left–right organizer morphogenesis and laterality (2018) (18)
Ion Torrent sequencing for conducting genome-wide scans for mutation mapping analysis (2014) (18)
A Membrane-Tethered Ubiquitination Pathway Regulates Hedgehog Signaling and Heart Development. (2020) (17)
PCC4azal teratocarcinoma stem cell differentiation in culture. III. Cell-to-cell communication properties. (1980) (16)
Airway ciliary dysfunction and respiratory symptoms in patients with transposition of the great arteries (2018) (16)
DNAH 6 and Its Interactions with PCD Genes in Heterotaxy and Primary Ciliary Dyskinesia (2016) (15)
Airway ciliary dysfunction: Association with adverse postoperative outcomes in nonheterotaxy congenital heart disease patients. (2017) (15)
Congenital Heart Defects and Ciliopathies Associated With Renal Phenotypes (2018) (14)
Nt mutation causing laterality defects associated with deletion of rotatin (2007) (14)
PCC4azal teratocarcinoma stem cell differentiation in culture. II. Morphological characterization. (1980) (13)
Left–right patterning in congenital heart disease beyond heterotaxy (2020) (12)
Role of cilia in the pathogenesis of congenital heart disease. (2020) (12)
Engineered Human Muscle Tissue from Skeletal Muscle Derived Stem Cells and Induced Pluripotent Stem Cell Derived Cardiac Cells (2013) (11)
A novel mouse model of X-linked cardiac hypertrophy. (2008) (11)
Micro-CT imaging: Developing criteria for examining fetal skeletons in regulatory developmental toxicology studies - A workshop report. (2016) (11)
Overexpression of connexin43 alters the mutant phenotype of midgestational wnt-1 null mice resulting in recovery of the midbrain and cerebellum. (2005) (11)
Cardiovascular Development and Congenital Heart Disease Modeling in the Pig (2021) (10)
Ventricular rotation is independent of cardiac looping: a study in mice with situs inversus totalis using speckle-tracking echocardiography. (2010) (10)
Retroperitoneal actinomycosis with intraperitoneal spread. Stellate pattern on CT. (1996) (9)
Mutation of LRP1 in cardiac neural crest cells causes congenital heart defects by perturbing outflow lengthening (2020) (9)
Proteolysis of fibrillin-2 microfibrils is essential for normal skeletal development (2021) (9)
Chapter 26: Cx43 (α1) Gap Junctions in Cardiac Development and Disease (1999) (9)
Novel use of differential image velocity invariants to categorize ciliary motion defects (2011) (8)
Wdpcp promotes epicardial EMT and epicardium-derived cell migration to facilitate coronary artery remodeling (2018) (8)
Biliary-Atresia-Associated Mannosidase-1-Alpha-2 Gene Regulates Biliary and Ciliary Morphogenesis and Laterality (2020) (8)
Uncompensated mitochondrial oxidative stress underlies heart failure in an iPSC-derived model of congenital heart disease. (2022) (8)
Mitochondrial Respiration Defects in Single-Ventricle Congenital Heart Disease (2021) (8)
Phenotyping cardiac and structural birth defects in fetal and newborn mice (2017) (8)
Analysis of Cx43α1 Promoter Function in the Developing Zebrafish Embryo (2001) (8)
Chromosomal recombination and breakage associated with instability in mouse centrometric satellite DNA. (1989) (7)
Lethality of Rw/Rw mouse embryos during early postimplantation development. (1995) (7)
Molecular cloning, expression analysis, and chromosomal localization of mouse Hmg1-containing sequences (1994) (7)
High-throughput mouse genotyping using robotics automation. (2005) (7)
Analysis of Cx43alpha1 promoter function in the developing zebrafish embryo. (2001) (6)
Common deletion variants causing protocadherin-α deficiency contribute to the complex genetics of BAV and left-sided congenital heart disease (2021) (6)
Relationships Between Regional Cerebral Blood Flow and Neurocognitive Outcomes in Children and Adolescents with Congenital Heart Disease. (2021) (6)
Dexmedetomidine and Fentanyl Exhibit Temperature Dependent Effects on Human Respiratory Cilia (2015) (5)
Diverse application of MRI for mouse phenotyping (2017) (5)
Differential effect of anesthetics on mucociliary clearance in vivo in mice (2020) (5)
Disruption of Mks1 localization to the mother centriole causes cilia defects and developmental malformations in Meckel–Gruber syndrome (2011) (5)
Rapid Ex-Vivo Ciliogenesis and Dose-Dependent Effect of Notch Inhibition on Ciliogenesis of Respiratory Epithelia (2020) (4)
Gene-teratogen interactions influence the penetrance of birth defects by altering Hedgehog signaling strength (2021) (4)
Finding the Unicorn, a New Mouse Model of Midfacial Clefting (2020) (4)
Embryo transfer into pregnant mice: an alternative to pseudopregnancy. (1990) (4)
iPSC modeling shows uncompensated mitochondrial mediated oxidative stress underlies early heart failure in hypoplastic left heart syndrome (2021) (4)
Low Nasal NO in Congenital Heart Disease With Systemic Right Ventricle and Postcardiac Transplantation (2017) (4)
Role of Cilia and Left-Right Patterning in Congenital Heart Disease (2016) (4)
Gap junctions in development (2000) (3)
Sequence heterogeneity in mouse centromeric sDNA. (1988) (3)
Cx43/β-Gal Inhibits Cx43 Transport in the Golgi Apparatus (2001) (3)
Exploring the Genetic Basis for Congenital Heart Disease with Mouse ENU Mutagenesis (2010) (3)
Novel approach for restriction mapping repetitive DNA elements using DNA transformation (1985) (3)
Histochemical and Fluorochrome-Based Detection of β-Galactosidase (1997) (3)
Low Nasal Nitric Oxide and Ciliary Dysmotility in Patients with Congenital Heart Disease and Heterotaxy: The Challenge of Defining a Ciliopathy. (2009) (2)
Cx43/beta-gal inhibits Cx43 transport in the Golgi apparatus. (2001) (2)
Gap-junctional communication in a communication-defective and in a communication-competent teratocarcinoma cell line. (1985) (2)
Abstract 15746: Airway Ciliary Dysfunction in Patients with Transposition of the Great Arteries (2012) (2)
Chapter 18 – Human Cardiac Development in the First Trimester (2012) (2)
Stacked Neural Networks for end-to-end ciliary motion analysis (2018) (2)
Flow blockage disrupts cilia-driven fluid transport in the epileptic brain (2022) (2)
Increased Postoperative Respiratory Complications in Patients with Congenital Heart Disease and Heterotaxy. (2009) (2)
Erratum: Genetic link between renal birth defects and congenital heart disease (2016) (2)
A Unique Set of Centrosome Proteins Requires Pericentrin for Spindle-Pole Localization and Spindle Orientation (2014) (2)
Abstract 19570: A Multigenic Etiology 0f Hypoplastic Left Heart Syndrome: An Analysis Based on Three Novel Mutant Mouse Models of Hyoplastic Left Heart Syndrome (2012) (2)
Novel Insights into the Etiology, Genetics, and Embryology of Hypoplastic Left Heart Syndrome (2022) (2)
Reply to ‘Double-outlet right ventricle is not hypoplastic left heart syndrome’ (2019) (2)
Abstract 16375: Low Nasal Nitric Oxide as a Prognosticator of Failing Single Ventricle Physiology in Congenital Heart Disease Patients? (2014) (1)
Mechanisms of Impaired Lung Development and Ciliation in Mannosidase-1-Alpha-2 (Man1a2) Mutants (2021) (1)
Developmental Biology Protocols vol 3 (2000) (1)
Exome-chip meta-analysis identifies novel loci, including ADAMTS6 associated with cardiac conduction (2018) (1)
Ultra-high frequency ultrasound biomicroscopy and high throughput cardiovascular phenotyping in a large scale mouse mutagenesis screen (2013) (1)
Exome-chip meta-analysis identifies novel loci associated with cardiac conduction, including ADAMTS6 (2018) (1)
Rare and Common Variants Uncover the Role of the Atria in Coarctation of the Aorta (2022) (1)
Developmental biology protocols. Overview I. (2000) (1)
Role of Gap Junctions in Cardiac Conduction and Development Insights From the Connexin Knockout Mice (2000) (1)
The author line was revised to include Wendy Chung as a coauthor and now appears as follows (2013) (1)
Novel Protein–Protein Interactions Highlighting the Crosstalk between Hypoplastic Left Heart Syndrome, Ciliopathies and Neurodevelopmental Delays (2022) (1)
A ubiquitin-based mechanism for the oligogenic inheritance of heterotaxy and heart defects (2020) (1)
Biallelic pathogenic variants in roundabout guidance receptor 1 associate with syndromic congenital anomalies of the kidney and urinary tract. (2022) (1)
Abstract 16541: Abnormal Brain Connectivity and Poor Neurodevelopmental Outcome in Congenital Heart Disease Patients With Subtle Brain Dysplasia (2015) (1)
Vertebrate myosin 1d regulates left–right organizer morphogenesis and laterality (2018) (1)
Abstract 16552: Chromosomal Microarray Abnormalities in More Than 1300 Patients With Congenital Heart Disease Provide Novel Clinical and Etiological Insights (2020) (0)
Abstract 12361: Cytoglobin Regulates Cilia Length, Function and Organ System Laterality During Development (2019) (0)
Abstract 19282: NAT10 Mutaion Causes Ciliary Aplisia and Congenital Heart Disease Associated with Heterotaxy (2012) (0)
Abstract 18081: Impaired Cerebral Autoregulation is Associated With Brain Abnormalities in Neonatal Congenital Heart Disease: Initial Experience (2016) (0)
Mucociliary Clearance Scans Show Infants Undergoing Congenital Cardiac Surgery Have Poor Airway Clearance Function (2021) (0)
Abstract 15941: Identification of a Novel TPM1 Mutation in Congenital Atrial Septal Defect With Autosomal Dominant Inheritance (2017) (0)
HIGH PREVALENCE OF RESPIRATORY CILIARY DYSFUNCTION ASSOCIATED WITH TRANSPOSITION OF THE GREAT ARTERIES (2014) (0)
Nucleotide sequence of the 3' flanking region of the herpes thymidine kinase gene. (1988) (0)
Establishment of Cardiac Laterality (2016) (0)
Abstract 18007: A Novel Cell Penetrating Peptide, Cardiac Targeting Peptide, Appears to Utilize Cardiac Channels for Transduction (2016) (0)
INSIGHTS INTO VENTRICULAR MECHANICS IN THE UNLOOPED HEART: VENTRICULAR TWISTING AND UNTWISTING IN A RIGHT ATRIAL ISOMERISM SINGLE VENTRICLE FETAL MOUSE MODEL (2010) (0)
Sequence heterogeneity in mouse centromeric satellite dna (1988) (0)
Hypertrophic cardiomyopathy is a major cardiovascular disease in human adults and children (17, 22) with a prevalence of 1:500 in the young and likely higher in older (2008) (0)
Contribution of rare transmitted and de novo variants among 2 , 871 1 congenital heart disease probands (2017) (0)
PP039-SUN AST TO PLATELET INDEX IS PREDICTIVE OF CIRRHOSIS BUT NOT OF FIBROSIS IN PEDIATRIC PATIENTS WITH INTESTINAL FAILURE (2011) (0)
3D Printing for Genetic Mouse Models of Congenital Heart Disease (2019) (0)
Reply to ‘Double-outlet right ventricle is not hypoplastic left heart syndrome’ (2019) (0)
Abstract 16570: Respiratory Ciliary Motion Defect Predict Regional Brain Abnormalities and Increased Extra Axial CSF Fluid in Neonates With Complex Congenital Heart Disease (2014) (0)
Genetic resiliency associated with dominant lethal TPM1 mutation causing atrial septal defect with high heritability (2021) (0)
Cardiovascular Development in the First Trimester (2012) (0)
Abstract 19556: Hypercholesterolemia in a Pcsk5 Mouse Mutant Show P5 Proteolytic Degradation of P9 is Essential for Normal Regulation of Serum Cholesterol (2010) (0)
Coronary Anomalies in Mice With Congenital Heart Defects (2015) (0)
Abstract 17947: Large Scale Mouse Mutagenesis Screen Using Fetal Echocardiography Indicates Genetic Contribution to Hypoplastic Left Heart Syndrome and Wide Spectrum of Other Congenital Heart Defects (2011) (0)
Evaluating the role of connexin 43 in congenital heart disease : and the analysis of knockin mouse models (2014) (0)
Skeletal malformations associated with mutations causing left‐right patterning defects (2008) (0)
Novel insights into the genetic landscape of congenital heart disease with systems genetics. (2019) (0)
Abstract 17199: Airway Mucociliary Clearance is Impaired After Infant Congenital Cardiac Surgery (2018) (0)
Ion Torrent sequencing for conducting genome-wide scans for mutation mapping analysis (2013) (0)
Variations in our genome: From disease to individualized cure (2016) (0)
Histochemical and fluorochrome-based detection of beta-galactosidase. (1997) (0)
Abstract 12221: Low Nasal Nitric Oxide as a Biomarker for Increased Pulmonary Vascular Resistance in Congenital Heart Disease (2017) (0)
Molecular Pathways and Animal Models of Defects of Situs (2016) (0)
Abstract 16315: Opposing Effects of Dexmedetomidine and Fentanyl on Ciliary Beat Frequency in the Respiratory Epithelia (2011) (0)
Abstract 16615: A Rare MEGF8 Variant is Involved in the Genetic Risk for Transposition of the Great Arteries (2018) (0)
extracardiac defects ENU-induced mutations causing congenital cardiac and high-frequency ultrasound facilitates recovery of Cardiovascular phenotyping of fetal mice by noninvasive (2013) (0)
Effect Of Ciliary Dysfunction In Patients With Heterotaxy Congenital Heart Disease & Protein-Losing Enteropathy (2011) (0)
High throughput sequencing recovers the novel gene Megf8 as the ENU induced mutation causing single ventricle cardiac defect associated with randomized left-right patterning (2008) (0)
IFT74 variants cause skeletal ciliopathy and motile cilia defects in mice and humans (2023) (0)
Correction to: Flow blockage disrupts cilia-driven fluid transport in the epileptic brain (2022) (0)
8 Cardiovascular Development in the First Trimester (2018) (0)
An unconventional myosin, myosin 1d regulates Kupffer’s vesicle morphogenesis and laterality (2018) (0)
Abstract 15736: Nasal Nitric Oxide and Systemic Nitric Oxide Reserve Stratification of Surgically Palliated Congenital Heart Disease (2017) (0)
A Pipeline to Characterize Structural Heart Defects in the Fetal Mouse. (2022) (0)
Abstract 16595: Airway Ciliary Dysfunction and Increased Postoperative Respiratory Complications in Broad Spectrum of Congenital Heart Disease Patients (2014) (0)
Widespread distribution of cells containing human DNA in embryos derived from mouse eggs injected with human chromosome fragments. (1993) (0)
Abstract 485: A Mouse Model of Primary Ciliary Dyskinesia Reveals High Frequencies of Heterotaxy and Complex Congenital Heart Defects (2007) (0)
Mutation of LRP1 in cardiac neural crest cells causes congenital heart defects by perturbing outflow lengthening (2020) (0)
COMPOSITIONS AND METHODS FOR MODULATING CILIOGENESIS (2018) (0)
Profiling development of abdominal organs in the pig (2022) (0)
MO047: Biallelic pathogenic variants in ROBO1 associate with syndromic CAKUT (2022) (0)
Abstract 15276: Identification of a Novel Sarcomeric TPM1 Variant in Familial Atrial Septal Defect (2018) (0)
239: LRP1, AN ENDOCYTIC VESICLE TRAFFICKING PROTEIN ASSOCIATED WITH CHD: AN UNEXPLORED PATHWAY (2016) (0)
Abstract 17475: High Throughput Screening and Diagnosis of Structural Heart Defects in Newborn Mice Using High Resolution Micro-Computed Tomography (2011) (0)
Abstract # 1827 Cilia, an organelle central to psychoneuroimmunology – A characterization through its interactome (2016) (0)
Nasal Nitric Oxide & Ciliary Function In Patients With Non-Heterotaxy Congenital Heart Disease (2010) (0)
Abstract 16458: Cardiac Targeting Peptide Provides Efficient Transduction of Human Cardiomyocytes (2017) (0)
Mispatterned motile cilia beating causes flow blockage in the epileptic brain (2021) (0)
Abstract 19326: Microrna Regulating Protein Bicc1 Causes Dilated Cardiomyopathy Through Modulation of Polycystin-2 (2012) (0)
Abstract 18280: Mucociliary Clearance Deficit and Reduced Pulmonary Function in Congenital Heart Disease Infants Undergoing Surgery With Cardiopulmonary Bypass (2016) (0)
Abstract 16596: Dominant Mouse Mutagenesis Screen Unveils a Complex Genetic Architecture for Congenital Heart Disease (2018) (0)
F200. ELUCIDATING THE ROLE OF CILIA IN NEUROPSYCHIATRIC DISEASES THROUGH INTERACTOME ANALYSIS (2018) (0)
a large in vitro gene profile data set'' data filtering to identify new angiogenesis targets from : Focus on ''In silico Separating the wheat from the chaff (2015) (0)
Abstract 16678: Multigenic Etiology of CHD With Heterotaxy Involving PCD and Cilia Genes (2011) (0)
Abstract 16609: Characterization of Neurodevelopmental Defects Associated With a Mouse Model of Hypoplastic Left Heart Syndrome (2018) (0)

This paper list is powered by the following services:

Other Resources About Cecilia Lo

en.wikipedia.org

What Schools Are Affiliated With Cecilia Lo?

Cecilia Lo is affiliated with the following schools: