ATP12A: Connecting Mucus and Fibrosis in Idiopathic Pulmonary Fibrosis.
作者信息
Zabner Joseph, Birket Susan E
机构信息
Department of Internal Medicine University of Iowa Roy J. and Lucille A. Carver College of Medicine Iowa City, Iowa.
Department of Medicine University of Alabama at Birmingham Birmingham, Alabama.
出版信息
Am J Respir Cell Mol Biol. 2023 Jun;68(6):603-604. doi: 10.1165/rcmb.2023-0096ED.
Abstract
摘要
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本文引用的文献
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2
Bleomycin Induces Drug Efflux in Lungs. A Pitfall for Pharmacological Studies of Pulmonary Fibrosis.博来霉素诱导肺部药物外排。肺纤维化药物研究的一个陷阱。
Am J Respir Cell Mol Biol. 2020 Feb;62(2):178-190. doi: 10.1165/rcmb.2018-0147OC.
3
Muco-Obstructive Lung Diseases.黏液阻塞性肺部疾病
N Engl J Med. 2019 May 16;380(20):1941-1953. doi: 10.1056/NEJMra1813799.
4
XBP1S Regulates MUC5B in a Promoter Variant-Dependent Pathway in Idiopathic Pulmonary Fibrosis Airway Epithelia.XBP1S 通过启动子变异依赖性途径调控特发性肺纤维化气道上皮中的 MUC5B。
Am J Respir Crit Care Med. 2019 Jul 15;200(2):220-234. doi: 10.1164/rccm.201810-1972OC.
5
Muc5b overexpression causes mucociliary dysfunction and enhances lung fibrosis in mice.Muc5b 过表达导致小鼠黏液纤毛功能障碍和肺纤维化增强。
Nat Commun. 2018 Dec 18;9(1):5363. doi: 10.1038/s41467-018-07768-9.
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Time for a change: is idiopathic pulmonary fibrosis still idiopathic and only fibrotic?是时候改变了：特发性肺纤维化仍然是特发性的且仅纤维化吗？
Lancet Respir Med. 2018 Feb;6(2):154-160. doi: 10.1016/S2213-2600(18)30007-9.
7
Airway acidification initiates host defense abnormalities in cystic fibrosis mice.气道酸化引发囊性纤维化小鼠的宿主防御异常。
Science. 2016 Jan 29;351(6272):503-7. doi: 10.1126/science.aad5589.
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MUC5B and Idiopathic Pulmonary Fibrosis.黏蛋白5B与特发性肺纤维化
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Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis.全基因组关联研究鉴定出多个肺纤维化易感性位点。
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