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Connexin43 modulates cell polarity and directional cell migration by regulating microtubule dynamicsARMC4 mutations cause primary ciliary dyskinesia with randomization of left/right body asymmetryDYX1C1 is required for axonemal dynein assembly and ciliary motilityNovel Jbts17 mutant mouse model of Joubert syndrome with cilia transition zone defects and cerebellar and other ciliopathy related anomaliesMassively 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 activityDecellularized tracheal extracellular matrix supports epithelial migration, differentiation, and functionDNAH6 and Its Interactions with PCD Genes in Heterotaxy and Primary Ciliary DyskinesiaIFT27 links the BBSome to IFT for maintenance of the ciliary signaling compartment.Global genetic analysis in mice unveils central role for cilia in congenital heart diseaseAutomated identification of abnormal respiratory ciliary motion in nasal biopsies.Interrogating congenital heart defects with noninvasive fetal echocardiography in a mouse forward genetic screen.Congenital heart disease and the specification of left-right asymmetryThe effects of temperature and anesthetic agents on ciliary function in murine respiratory epitheliaDexmedetomidine and fentanyl exhibit temperature dependent effects on human respiratory cilia.Distribution of raphespinal fibers in the mouse spinal cordAssessment of ciliary phenotype in primary ciliary dyskinesia by micro-optical coherence tomography.Connexin43 associated with an N-cadherin-containing multiprotein complex is required for gap junction formation in NIH3T3 cells.Ion Torrent sequencing for conducting genome-wide scans for mutation mapping analysis.ANKS6 is the critical activator of NEK8 kinase in embryonic situs determination and organ patterning.Microcomputed tomography provides high accuracy congenital heart disease diagnosis in neonatal and fetal mice.Increased postoperative respiratory complications in heterotaxy congenital heart disease patients with respiratory ciliary dysfunction.CUBIC Protocol Visualizes Protein Expression at Single Cell Resolution in Whole Mount Skin Preparations.Discovery of four recessive developmental disorders using probabilistic genotype and phenotype matching among 4,125 families.Airway ciliary dysfunction and sinopulmonary symptoms in patients with congenital heart disease.Connexin 43-mediated modulation of polarized cell movement and the directional migration of cardiac neural crest cells.
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description
researcher
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wetenschapper
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հետազոտող
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name
Richard Francis
@ast
Richard Francis
@en
Richard Francis
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Richard Francis
@nl
type
label
Richard Francis
@ast
Richard Francis
@en
Richard Francis
@es
Richard Francis
@nl
prefLabel
Richard Francis
@ast
Richard Francis
@en
Richard Francis
@es
Richard Francis
@nl
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0000-0002-4401-1946