VIAF

Virtual International Authority File

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Leader     00000nz a2200037n 45 0
001     WKP|Q62915358  (VIAF cluster)  (Authority/Source Record)
003     WKP
005     20241120235928.0
008     241120nneanz||abbn n and d
035 ‎‡a  (WKP)Q62915358‏
024 ‎‡a  0000-0002-4401-1946‏ ‎‡2  orcid‏
024 ‎‡a  56720106700‏ ‎‡2  scopus‏
035 ‎‡a  (OCoLC)Q62915358‏
100 0 ‎‡a  Richard Francis‏ ‎‡c  researcher‏ ‎‡9  en‏
375 ‎‡a  1‏ ‎‡2  iso5218‏
400 0 ‎‡a  Richard Francis‏ ‎‡c  wetenschapper‏ ‎‡9  nl‏
670 ‎‡a  Author's Airway ciliary dysfunction and sinopulmonary symptoms in patients with congenital heart disease.‏
670 ‎‡a  Author's ANKS6 is the critical activator of NEK8 kinase in embryonic situs determination and organ patterning‏
670 ‎‡a  Author's ARMC4 mutations cause primary ciliary dyskinesia with randomization of left/right body asymmetry‏
670 ‎‡a  Author's Assessment of ciliary phenotype in primary ciliary dyskinesia by micro-optical coherence tomography.‏
670 ‎‡a  Author's Automated identification of abnormal respiratory ciliary motion in nasal biopsies.‏
670 ‎‡a  Author's Bves directly interacts with GEFT, and controls cell shape and movement through regulation of Rac1/Cdc42 activity‏
670 ‎‡a  Author's Changes in activin and activin receptor subunit expression in rat liver during the development of CCl4-induced cirrhosis‏
670 ‎‡a  Author's Congenital heart disease and the specification of left-right asymmetry‏
670 ‎‡a  Author's Connexin 43-mediated modulation of polarized cell movement and the directional migration of cardiac neural crest cells.‏
670 ‎‡a  Author's Connexin43 associated with an N-cadherin-containing multiprotein complex is required for gap junction formation in NIH3T3 cells.‏
670 ‎‡a  Author's Connexin43 modulates cell polarity and directional cell migration by regulating microtubule dynamics‏
670 ‎‡a  Author's CUBIC Protocol Visualizes Protein Expression at Single Cell Resolution in Whole Mount Skin Preparations.‏
670 ‎‡a  Author's Decellularized tracheal extracellular matrix supports epithelial migration, differentiation, and function‏
670 ‎‡a  Author's Dexmedetomidine and fentanyl exhibit temperature dependent effects on human respiratory cilia‏
670 ‎‡a  Author's Discovery of four recessive developmental disorders using probabilistic genotype and phenotype matching among 4,125 families‏
670 ‎‡a  Author's Distribution of raphespinal fibers in the mouse spinal cord‏
670 ‎‡a  Author's DNAH6 and Its Interactions with PCD Genes in Heterotaxy and Primary Ciliary Dyskinesia‏
670 ‎‡a  Author's DYX1C1 is required for axonemal dynein assembly and ciliary motility‏
670 ‎‡a  Author's Global genetic analysis in mice unveils central role for cilia in congenital heart disease‏
670 ‎‡a  Author's IFT27 links the BBSome to IFT for maintenance of the ciliary signaling compartment.‏
670 ‎‡a  Author's Increased postoperative respiratory complications in heterotaxy congenital heart disease patients with respiratory ciliary dysfunction.‏
670 ‎‡a  Author's Interrogating congenital heart defects with noninvasive fetal echocardiography in a mouse forward genetic screen‏
670 ‎‡a  Author's Ion Torrent sequencing for conducting genome-wide scans for mutation mapping analysis‏
670 ‎‡a  Author's Massively parallel sequencing identifies the gene Megf8 with ENU-induced mutation causing heterotaxy‏
670 ‎‡a  Author's Microcomputed tomography provides high accuracy congenital heart disease diagnosis in neonatal and fetal mice.‏
670 ‎‡a  Author's Novel Jbts17 mutant mouse model of Joubert syndrome with cilia transition zone defects and cerebellar and other ciliopathy related anomalies‏
670 ‎‡a  Author's The effects of temperature and anesthetic agents on ciliary function in murine respiratory epithelia‏
909 ‎‡a  (orcid) 0000000244011946‏ ‎‡9  1‏
909 ‎‡a  (scopus) 56720106700‏ ‎‡9  1‏
919 ‎‡a  effectsoftemperatureandanestheticagentsonciliaryfunctioninmurinerespiratoryepithelia‏ ‎‡A  The effects of temperature and anesthetic agents on ciliary function in murine respiratory epithelia‏ ‎‡9  1‏
919 ‎‡a  noveljbts17mutantmousemodelofjoubertsyndromewithciliatransitionzonedefectsandcerebellarandotherciliopathyrelatedanomalies‏ ‎‡A  Novel Jbts17 mutant mouse model of Joubert syndrome with cilia transition zone defects and cerebellar and other ciliopathy related anomalies‏ ‎‡9  1‏
919 ‎‡a  microcomputedtomographyprovideshighaccuracycongenitalheartdiseasediagnosisinneonatalandfetalmice‏ ‎‡A  Microcomputed tomography provides high accuracy congenital heart disease diagnosis in neonatal and fetal mice.‏ ‎‡9  1‏
919 ‎‡a  massivelyparallelsequencingidentifiesthegenemegf8withenuinducedmutationcausingheterotaxy‏ ‎‡A  Massively parallel sequencing identifies the gene Megf8 with ENU-induced mutation causing heterotaxy‏ ‎‡9  1‏
919 ‎‡a  iontorrentsequencingforconductinggenomewidescansformutationmappinganalysis‏ ‎‡A  Ion Torrent sequencing for conducting genome-wide scans for mutation mapping analysis‏ ‎‡9  1‏
919 ‎‡a  interrogatingcongenitalheartdefectswithnoninvasivefetalechocardiographyinamouseforwardgeneticscreen‏ ‎‡A  Interrogating congenital heart defects with noninvasive fetal echocardiography in a mouse forward genetic screen‏ ‎‡9  1‏
919 ‎‡a  increasedpostoperativerespiratorycomplicationsinheterotaxycongenitalheartdiseasepatientswithrespiratoryciliarydysfunction‏ ‎‡A  Increased postoperative respiratory complications in heterotaxy congenital heart disease patients with respiratory ciliary dysfunction.‏ ‎‡9  1‏
919 ‎‡a  ift27linksthebbsometoiftformaintenanceoftheciliarysignalingcompartment‏ ‎‡A  IFT27 links the BBSome to IFT for maintenance of the ciliary signaling compartment.‏ ‎‡9  1‏
919 ‎‡a  globalgeneticanalysisinmiceunveilscentralroleforciliaincongenitalheartdisease‏ ‎‡A  Global genetic analysis in mice unveils central role for cilia in congenital heart disease‏ ‎‡9  1‏
919 ‎‡a  dyx1c1isrequiredforaxonemaldyneinassemblyandciliarymotility‏ ‎‡A  DYX1C1 is required for axonemal dynein assembly and ciliary motility‏ ‎‡9  1‏
919 ‎‡a  dnah6anditsinteractionswithpcdgenesinheterotaxyandprimaryciliarydyskinesia‏ ‎‡A  DNAH6 and Its Interactions with PCD Genes in Heterotaxy and Primary Ciliary Dyskinesia‏ ‎‡9  1‏
919 ‎‡a  distributionofraphespinalfibersinthemousespinalcord‏ ‎‡A  Distribution of raphespinal fibers in the mouse spinal cord‏ ‎‡9  1‏
919 ‎‡a  discoveryof4recessivedevelopmentaldisordersusingprobabilisticgenotypeandphenotypematchingamong4125families‏ ‎‡A  Discovery of four recessive developmental disorders using probabilistic genotype and phenotype matching among 4,125 families‏ ‎‡9  1‏
919 ‎‡a  dexmedetomidineandfentanylexhibittemperaturedependenteffectsonhumanrespiratorycilia‏ ‎‡A  Dexmedetomidine and fentanyl exhibit temperature dependent effects on human respiratory cilia‏ ‎‡9  1‏
919 ‎‡a  decellularizedtrachealextracellularmatrixsupportsepithelialmigrationdifferentiationandfunction‏ ‎‡A  Decellularized tracheal extracellular matrix supports epithelial migration, differentiation, and function‏ ‎‡9  1‏
919 ‎‡a  cubicprotocolvisualizesproteinexpressionatsinglecellresolutioninwholemountskinpreparations‏ ‎‡A  CUBIC Protocol Visualizes Protein Expression at Single Cell Resolution in Whole Mount Skin Preparations.‏ ‎‡9  1‏
919 ‎‡a  connexin43modulatescellpolarityanddirectionalcellmigrationbyregulatingmicrotubuledynamics‏ ‎‡A  Connexin43 modulates cell polarity and directional cell migration by regulating microtubule dynamics‏ ‎‡9  1‏
919 ‎‡a  airwayciliarydysfunctionandsinopulmonarysymptomsinpatientswithcongenitalheartdisease‏ ‎‡A  Airway ciliary dysfunction and sinopulmonary symptoms in patients with congenital heart disease.‏ ‎‡9  1‏
919 ‎‡a  anks6isthecriticalactivatorofnek8kinaseinembryonicsitusdeterminationandorganpatterning‏ ‎‡A  ANKS6 is the critical activator of NEK8 kinase in embryonic situs determination and organ patterning‏ ‎‡9  1‏
919 ‎‡a  armc4mutationscauseprimaryciliarydyskinesiawithrandomizationofleftrightbodyasymmetry‏ ‎‡A  ARMC4 mutations cause primary ciliary dyskinesia with randomization of left/right body asymmetry‏ ‎‡9  1‏
919 ‎‡a  assessmentofciliaryphenotypeinprimaryciliarydyskinesiabymicroopticalcoherencetomography‏ ‎‡A  Assessment of ciliary phenotype in primary ciliary dyskinesia by micro-optical coherence tomography.‏ ‎‡9  1‏
919 ‎‡a  automatedidentificationofabnormalrespiratoryciliarymotioninnasalbiopsies‏ ‎‡A  Automated identification of abnormal respiratory ciliary motion in nasal biopsies.‏ ‎‡9  1‏
919 ‎‡a  bvesdirectlyinteractswithgeftandcontrolscellshapeandmovementthroughregulationofrac1cdc42activity‏ ‎‡A  Bves directly interacts with GEFT, and controls cell shape and movement through regulation of Rac1/Cdc42 activity‏ ‎‡9  1‏
919 ‎‡a  changesinactivinandactivinreceptorsubunitexpressioninratliverduringthedevelopmentofccl4inducedcirrhosis‏ ‎‡A  Changes in activin and activin receptor subunit expression in rat liver during the development of CCl4-induced cirrhosis‏ ‎‡9  1‏
919 ‎‡a  congenitalheartdiseaseandthespecificationofleftrightasymmetry‏ ‎‡A  Congenital heart disease and the specification of left-right asymmetry‏ ‎‡9  1‏
919 ‎‡a  connexin43mediatedmodulationofpolarizedcellmovementandthedirectionalmigrationofcardiacneuralcrestcells‏ ‎‡A  Connexin 43-mediated modulation of polarized cell movement and the directional migration of cardiac neural crest cells.‏ ‎‡9  1‏
919 ‎‡a  connexin43associatedwithanncadherincontainingmultiproteincomplexisrequiredforgapjunctionformationinnih3t3cells‏ ‎‡A  Connexin43 associated with an N-cadherin-containing multiprotein complex is required for gap junction formation in NIH3T3 cells.‏ ‎‡9  1‏
946 ‎‡a  b‏ ‎‡9  1‏
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