Loss of cilia causes embryonic lung hypoplasia, liver fibrosis, and cholestasis in the talpid3 ciliopathy mutant. - Wikidata - wikimedia - TriplyDB

Loss of cilia causes embryonic lung hypoplasia, liver fibrosis, and cholestasis in the talpid3 ciliopathy mutant.

Loss of cilia causes embryonic lung hypoplasia, liver fibrosis, and cholestasis in the talpid3 ciliopathy mutant.

http://www.wikidata.org/entity/Q41819809

about

Mutations in human homologue of chicken talpid3 gene (KIAA0586) cause a hybrid ciliopathy with overlapping features of Jeune and Joubert syndromes Functional genome-wide siRNA screen identifies KIAA0586 as mutated in Joubert syndrome.Utilizing the chicken as an animal model for human craniofacial ciliopathies.Hepatotoxicity with Vismodegib: An MD Anderson Cancer Center and Research on Adverse Drug Events and Reports Project.Key Developments that Impacted the Field of Mechanobiology and Mechanotransduction.TALPID3 controls centrosome and cell polarity and the human ortholog KIAA0586 is mutated in Joubert syndrome (JBTS23)Mutations in KIAA0586 Cause Lethal Ciliopathies Ranging from a Hydrolethalus Phenotype to Short-Rib Polydactyly Syndrome.Expression analysis of Shh signaling members in early stages of chick lung development.Retinoic acid regulates avian lung branching through a molecular network.Canonical Sonic Hedgehog Signaling in Early Lung Development.Molecular Aspects of Avian Lung Development

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P2860

Loss of cilia causes embryonic lung hypoplasia, liver fibrosis, and cholestasis in the talpid3 ciliopathy mutant.

http://www.wikidata.org/entity/Q41819809

description

2014 nî lūn-bûn

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2014年の論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年论文

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2014年论文

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Andrew M Barrie

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Lucy J Freem

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Lynn McTeir

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P2860

Human and mouse mutations in WDR35 cause short-rib polydactyly syndromes due to abnormal ciliogenesis

Proteomic characterization of the human centrosome by protein correlation profiling

The Talpid3 gene (KIAA0586) encodes a centrosomal protein that is essential for primary cilia formation

Liver and kidney disease in ciliopathies

DYNC2H1 mutations cause asphyxiating thoracic dystrophy and short rib-polydactyly syndrome, type III

Jeune syndrome: description of 13 cases and a proposal for follow-up protocol

Hedgehog signaling antagonist promotes regression of both liver fibrosis and hepatocellular carcinoma in a murine model of primary liver cancer

Ciliopathies with skeletal anomalies and renal insufficiency due to mutations in the IFT-A gene WDR19

Essential function of Gli2 and Gli3 in the formation of lung, trachea and oesophagus

An Ift80 mouse model of short rib polydactyly syndromes shows defects in hedgehog signalling without loss or malformation of cilia

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