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Richard Francis

Publications

  • Mouse model of heterotaxy with single ventricle spectrum of cardiac anomalies
  • Exploring the Genetic Basis for Congenital Heart Disease with Mouse Enu Mutagenesis
  • Quantifying cilia beat frequency using high‐speed video microscopy: Assessing frame rate requirements when imaging different ciliated tissues
  • Assessment of ciliary phenotype in primary ciliary dyskinesia by micro-optical coherence tomography
  • Distribution of raphespinal fibers in the mouse spinal cord
  • CUBIC Protocol Visualizes Protein Expression at Single Cell Resolution in Whole Mount Skin Preparations
  • DNAH6 and Its Interactions with PCD Genes in Heterotaxy and Primary Ciliary Dyskinesia
  • ANKS6 is the critical activator of NEK8 kinase in embryonic situs determination and organ patterning
  • Automated identification of abnormal respiratory ciliary motion in nasal biopsies
  • Global genetic analysis in mice unveils central role for cilia in congenital heart disease
  • Novel Jbts17 mutant mouse model of Joubert syndrome with cilia transition zone defects and cerebellar and other ciliopathy related anomalies
  • Airway ciliary dysfunction and sinopulmonary symptoms in patients with congenital heart disease
  • Decellularized Tracheal Extracellular Matrix Supports Epithelial Migration, Differentiation, and Function
  • Dexmedetomidine and fentanyl exhibit temperature dependent effects on human respiratory cilia
  • Discovery of four recessive developmental disorders using probabilistic genotype and phenotype matching among 4,125 families
  • IFT27 Links the BBSome to IFT for Maintenance of the Ciliary Signaling Compartment
  • Increased postoperative respiratory complications in heterotaxy congenital heart disease patients with respiratory ciliary dysfunction
  • Ion Torrent sequencing for conducting genome-wide scans for mutation mapping analysis
  • The effects of temperature and anesthetic agents on ciliary function in murine respiratory epithelia
  • Interrogating Congenital Heart Defects With Noninvasive Fetal Echocardiography in a Mouse Forward Genetic Screen
  • ARMC4 Mutations Cause Primary Ciliary Dyskinesia with Randomization of Left/Right Body Asymmetry
  • DYX1C1 is required for axonemal dynein assembly and ciliary motility
  • Ex vivo Method for High Resolution Imaging of Cilia Motility in Rodent Airway Epithelia
  • Imaging techniques for visualizing and phenotyping congenital heart defects in murine models
  • Microcomputed Tomography Provides High Accuracy Congenital Heart Disease Diagnosis in Neonatal and Fetal Mice
  • Wdpcp, a PCP Protein Required for Ciliogenesis, Regulates Directional Cell Migration and Cell Polarity by Direct Modulation of the Actin Cytoskeleton
  • Connexin43 Modulates Cell Polarity and Directional Cell Migration by Regulating Microtubule Dynamics
  • Disruption of Mks1 localization to the mother centriole causes cilia defects and developmental malformations in Meckel-Gruber syndrome
  • Congenital heart disease and the specification of left-right asymmetry
  • High Prevalence of Respiratory Ciliary Dysfunction in Congenital Heart Disease Patients With Heterotaxy
  • Ventricular Rotation Is Independent of Cardiac Looping: A Study in Mice With Situs Inversus Totalis Using Speckle-Tracking Echocardiography
  • Connexin 43 regulates epicardial cell polarity and migration in coronary vascular development
  • Initiation and maturation of cilia-generated flow in newborn and postnatal mouse airway
  • Massively parallel sequencing identifies the gene Megf8 with ENU-induced mutation causing heterotaxy
  • Bves directly interacts with GEFT, and controls cell shape and movement through regulation of Rac1/Cdc42 activity
  • Murine CENPF interacts with syntaxin 4 in the regulation of vesicular transport
  • Primordial germ cell deficiency in the connexin 43 knockout mouse arises from apoptosis associated with abnormal p53 activation
  • Mouse model of heterotaxy with single ventricle spectrum of cardiac anomalies
  • Heterotaxy and complex structural heart defects in a mutant mouse model of primary ciliary dyskinesia
  • Connexin 43-mediated modulation of polarized cell movement and the directional migration of cardiac neural crest cells
  • Changes in activin and activin receptor subunit expression in rat liver during the development of CCl4-induced cirrhosis
  • Connexin43 associated with an N-cadherin-containing multiprotein complex is required for gap junction formation in NIH3T3 cells
  • Endothelin receptor A blockade ameliorates hypothermic ischemia-reperfusion-related microhemodynamic disturbances during liver transplantation in the rat
  • 3D imaging of PSD-95 in the mouse brain using the advanced CUBIC method
  • Heterotaxy and complex structural heart defects in a mutant mouse model of primary ciliary dyskinesia
  • Ultra-high frequency ultrasound biomicroscopy and high throughput cardiovascular phenotyping in a large scale mouse mutagenesis screen
  • Novel use of differential image velocity invariants to categorize ciliary motion defects
  • Erratum: Microcomputed tomography provides high accuracy congenital heart disease diagnosis in neonatal and fetal mice (Circulation: Cardiovascular Imaging (2013) 6 (551-559))
  • The effects of acute hydrogen peroxide exposure on respiratory cilia motility and viability
  • Autonomous and non-cell autonomous etiology of ciliopathy associated structural birth defects

Richard Francis's public data