Heterotaxy and complex structural heart defects in a mutant mouse model of primary ciliary dyskinesia - Wikidata - awgldk - TriplyDB

Heterotaxy and complex structural heart defects in a mutant mouse model of primary ciliary dyskinesia

Heterotaxy and complex structural heart defects in a mutant mouse model of primary ciliary dyskinesia

http://www.wikidata.org/entity/Q36151690

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CCDC151 mutations cause primary ciliary dyskinesia by disruption of the outer dynein arm docking complex formation Mutations in axonemal dynein assembly factor DNAAF3 cause primary ciliary dyskinesia.ARMC4 mutations cause primary ciliary dyskinesia with randomization of left/right body asymmetry DYX1C1 is required for axonemal dynein assembly and ciliary motility High prevalence of respiratory ciliary dysfunction in congenital heart disease patients with heterotaxy.DNAH6 and Its Interactions with PCD Genes in Heterotaxy and Primary Ciliary Dyskinesia Global genetic analysis in mice unveils central role for cilia in congenital heart disease Targeted inactivation of Cerberus like-2 leads to left ventricular cardiac hyperplasia and systolic dysfunction in the mouse Mouse models of ciliopathies: the state of the art.Monocilia in the embryonic mouse heart suggest a direct role for cilia in cardiac morphogenesis IFT25 links the signal-dependent movement of Hedgehog components to intraflagellar transport Cauli: a mouse strain with an Ift140 mutation that results in a skeletal ciliopathy modelling Jeune syndrome Initiation and maturation of cilia-generated flow in newborn and postnatal mouse airway.Conditional deletion of dnaic1 in a murine model of primary ciliary dyskinesia causes chronic rhinosinusitis Congenital heart disease and the specification of left-right asymmetry Restoring ciliary function to differentiated primary ciliary dyskinesia cells with a lentiviral vector.Assessment of ciliary phenotype in primary ciliary dyskinesia by micro-optical coherence tomography.Laterality defects other than situs inversus totalis in primary ciliary dyskinesia: insights into situs ambiguus and heterotaxy.Increased postoperative and respiratory complications in patients with congenital heart disease associated with heterotaxy.Clinical and genetic aspects of primary ciliary dyskinesia/Kartagener syndrome.The ciliary protein Ftm is required for ventricular wall and septal development.Molecular basis of the obesity associated with Bardet-Biedl syndrome.The prevalence of clinical features associated with primary ciliary dyskinesia in a heterotaxy population: results of a web-based survey.Cilia and models for studying structure and function.How insights from cardiovascular developmental biology have impacted the care of infants and children with congenital heart disease.Loss of the ciliary kinase Nek8 causes left-right asymmetry defects.Primary ciliary dyskinesia: improving the diagnostic approach.PIERCE1 is critical for specification of left-right asymmetry in mice.Mutations in Dnaaf1 and Lrrc48 Cause Hydrocephalus, Laterality Defects, and Sinusitis in Mice.Ex vivo method for high resolution imaging of cilia motility in rodent airway epithelia.Cilia gene mutations cause atrioventricular septal defects by multiple mechanisms.Imaging techniques for visualizing and phenotyping congenital heart defects in murine models.Cilia and coordination of signaling networks during heart development.Laterality defects are influenced by timing of treatments and animal model.Brain Dysplasia Associated with Ciliary Dysfunction in Infants with Congenital Heart Disease.Airway ciliary dysfunction and respiratory symptoms in patients with transposition of the great arteries.Cilia and Ciliopathies in Congenital Heart Disease.

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P2860

Heterotaxy and complex structural heart defects in a mutant mouse model of primary ciliary dyskinesia

http://www.wikidata.org/entity/Q36151690

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Heterotaxy and complex structu ...... of primary ciliary dyskinesia

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Heterotaxy and complex structu ...... of primary ciliary dyskinesia

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Heterotaxy and complex structu ...... of primary ciliary dyskinesia

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Bishwanath Chatterjee

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Cecilia W Lo

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Julie Rosenthal

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Kaari L Linask

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Linda Leatherbury

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Luciann Bracero

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Mathew P Daniels

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Patricia S Connelly

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Qing Yu

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Richard J Francis

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P2860

Randomization of left-right asymmetry due to loss of nodal cilia generating leftward flow of extraembryonic fluid in mice lacking KIF3B motor protein

Mutations in DNAH5 cause primary ciliary dyskinesia and randomization of left-right asymmetry

Congenital heart disease and other heterotaxic defects in a large cohort of patients with primary ciliary dyskinesia

DNAH5 mutations are a common cause of primary ciliary dyskinesia with outer dynein arm defects.

The role of Pitx2 during cardiac development. Linking left-right signaling and congenital heart diseases

lefty-1 is required for left-right determination as a regulator of lefty-2 and nodal

Inversin, a novel gene in the vertebrate left-right axis pathway, is partially deleted in the inv mouse

Targeted deletion of the ATP binding domain of left-right dynein confirms its role in specifying development of left-right asymmetries

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

Left-right asymmetry and kinesin superfamily protein KIF3A: new insights in determination of laterality and mesoderm induction by kif3A-/- mice analysis

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