Conditional deletion of dnaic1 in a murine model of primary ciliary dyskinesia causes chronic rhinosinusitis - Wikidata - awgldk - TriplyDB

Conditional deletion of dnaic1 in a murine model of primary ciliary dyskinesia causes chronic rhinosinusitis

Conditional deletion of dnaic1 in a murine model of primary ciliary dyskinesia causes chronic rhinosinusitis

http://www.wikidata.org/entity/Q30495744

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Whole-exome capture and sequencing identifies HEATR2 mutation as a cause of primary ciliary dyskinesia High prevalence of respiratory ciliary dysfunction in congenital heart disease patients with heterotaxy.Loss of SPEF2 function in mice results in spermatogenesis defects and primary ciliary dyskinesia Cilia in vertebrate development and disease Advantages of using the CRISPR/Cas9 system of genome editing to investigate male reproductive mechanisms using mouse models LRRC6 mutation causes primary ciliary dyskinesia with dynein arm defects Mouse models of ciliopathies: the state of the art.Tubulin polyglutamylation is essential for airway ciliary function through the regulation of beating asymmetry CRISPR/Cas9-Mediated Rapid Generation of Multiple Mouse Lines Identified Ccdc63 as Essential for Spermiogenesis Congenital heart disease and the specification of left-right asymmetry Restoring ciliary function to differentiated primary ciliary dyskinesia cells with a lentiviral vector.Continuous mucociliary transport by primary human airway epithelial cells in vitro.Ion Torrent sequencing for conducting genome-wide scans for mutation mapping analysis.Chronic rhinosinusitis as a multifactorial inflammatory disorder.Cilia and models for studying structure and function.Stages of ciliogenesis and regulation of ciliary length Overexpressing mouse model demonstrates the protective role of Muc5ac in the lungs.Reduced mucociliary clearance in old mice is associated with a decrease in Muc5b mucin Mutations in SPAG1 cause primary ciliary dyskinesia associated with defective outer and inner dynein arms.Airway Hydration, Apical K(+) Secretion, and the Large-Conductance, Ca(2+)-activated and Voltage-dependent Potassium (BK) Channel.Control of lung defence by mucins and macrophages: ancient defence mechanisms with modern functions.Adropin deficiency is associated with increased adiposity and insulin resistance.Cilia gene mutations cause atrioventricular septal defects by multiple mechanisms.Deletion of airway cilia results in noninflammatory bronchiectasis and hyperreactive airways.Contribution of mucus concentration and secreted mucins Muc5ac and Muc5b to the pathogenesis of muco-obstructive lung disease Sox2 modulates Lef-1 expression during airway submucosal gland development.Primary ciliary dyskinesia: recent advances in epidemiology, diagnosis, management and relationship with the expanding spectrum of ciliopathy.Epigenetics of idiopathic pulmonary fibrosis.Cilia and Mucociliary Clearance.A pooling-based genomewide association study identifies genetic variants associated with Staphylococcus aureus colonization in chronic rhinosinusitis patients.The establishment of rotational polarity in the airway and ependymal cilia: analysis with a novel cilium motility mutant mouse.Mast Cell Deficiency Limits the Development of Chronic Rhinosinusitis in Mice.Cytoplasmic E2f4 forms organizing centres for initiation of centriole amplification during multiciliogenesis.FoxJ1-dependent gene expression is required for differentiation of radial glia into ependymal cells and a subset of astrocytes in the postnatal brain.HMMR acts in the PLK1-dependent spindle positioning pathway and supports neural development.Revolutionizing male fertility factor research in mice by using the genome editing tool CRISPR/Cas9.Static respiratory cilia associated with mutations in Dnahc11/DNAH11: a mouse model of PCD Mucociliary Clearance in Mice Measured by Tracking Trans-tracheal Fluorescence of Nasally Aerosolized Beads

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P2860

Conditional deletion of dnaic1 in a murine model of primary ciliary dyskinesia causes chronic rhinosinusitis

http://www.wikidata.org/entity/Q30495744

description

2009 nî lūn-bûn

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2009 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

2009 թվականի օգոստոսին հրատարակված գիտական հոդված

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2009年の論文

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2009年論文

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2009年論文

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2009年論文

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2009年論文

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2009年論文

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2009年论文

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Conditional deletion of dnaic1 ...... causes chronic rhinosinusitis

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Conditional deletion of dnaic1 ...... causes chronic rhinosinusitis

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Conditional deletion of dnaic1 ...... causes chronic rhinosinusitis

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Conditional deletion of dnaic1 ...... causes chronic rhinosinusitis

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prefLabel

Conditional deletion of dnaic1 ...... causes chronic rhinosinusitis

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Conditional deletion of dnaic1 ...... causes chronic rhinosinusitis

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RCMB.2009-0118OC

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American Journal of Respiratory Cell and Molecular Biology

P1476

Conditional deletion of dnaic1 ...... causes chronic rhinosinusitis

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P2093

Barbara R Grubb

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Katie B Busalacchi

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Lawrence E Ostrowski

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Michael Chua

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Troy D Rogers

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Wanda K O'Neal

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Weining Yin

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P2860

Loss-of-function mutations in a human gene related to Chlamydomonas reinhardtii dynein IC78 result in primary ciliary dyskinesia.

Axonemal dynein intermediate-chain gene (DNAI1) mutations result in situs inversus and primary ciliary dyskinesia (Kartagener syndrome)

Mutations of DNAI1 in primary ciliary dyskinesia: evidence of founder effect in a common mutation

Increased airway epithelial Na+ absorption produces cystic fibrosis-like lung disease in mice

Mutation of the mouse hepatocyte nuclear factor/forkhead homologue 4 gene results in an absence of cilia and random left-right asymmetry

Ciliogenesis and left-right axis defects in forkhead factor HFH-4-null mice

Mutation of murine adenylate kinase 7 underlies a primary ciliary dyskinesia phenotype.

Loss of function of axonemal dynein Mdnah5 causes primary ciliary dyskinesia and hydrocephalus

Primary ciliary dyskinesia in mice lacking the novel ciliary protein Pcdp1.

Mice deficient in the axonemal protein Tektin-t exhibit male infertility and immotile-cilium syndrome due to impaired inner arm dynein function

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55-63

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10.1165/RCMB.2009-0118OC

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1

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43

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19675306

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2911571

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