• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利：CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法，用中文像聊天一样搜索，搜遍4000万医学文献。AI智能推荐，让科研检索更轻松。

立即免费搜索

文件翻译

保留排版，准确专业，支持PDF/Word/PPT等文件格式，支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述，25分钟生成高质量综述，智能提取关键信息，辅助科研写作。

立即免费体验

Human airway ion transport. Part two.

作者信息

Boucher R C

机构信息

Division of Pulmonary Diseases, University of North Carolina at Chapel Hill 27599-7020.

出版信息

Am J Respir Crit Care Med. 1994 Aug;150(2):581-93. doi: 10.1164/ajrccm.150.2.8049852.

DOI:10.1164/ajrccm.150.2.8049852
PMID:8049852
Abstract
摘要

相似文献

1
Human airway ion transport. Part two.人类气道离子转运。第二部分。
Am J Respir Crit Care Med. 1994 Aug;150(2):581-93. doi: 10.1164/ajrccm.150.2.8049852.
2
Ion transport in normal and CF airway epithelia.正常和囊性纤维化气道上皮中的离子转运。
Adv Exp Med Biol. 1991;290:105-15; discussion 115-8. doi: 10.1007/978-1-4684-5934-0_13.
3
Electrolyte transport by airway epithelia.气道上皮细胞的电解质转运
Physiol Rev. 1987 Oct;67(4):1143-84. doi: 10.1152/physrev.1987.67.4.1143.
4
Cystic fibrosis from bench to bedside.从实验室到临床的囊性纤维化
N Engl J Med. 1991 Aug 22;325(8):575-7. doi: 10.1056/NEJM199108223250809.
5
[Ion transports across the respiratory epithelium].[离子跨呼吸上皮的转运]
Rev Pneumol Clin. 1997;53(2):71-8.
6
Is cystic fibrosis respiratory epithelium characterized by a single defect (Cl-) or multiple ion transport defects?囊性纤维化呼吸道上皮的特征是单一缺陷（氯离子）还是多种离子转运缺陷？
Prog Clin Biol Res. 1987;254:89-100.
7
Trends in therapy of abnormal airway epithelial ion and liquid transport.气道上皮离子和液体转运异常的治疗趋势
Monaldi Arch Chest Dis. 1993;48(2):140-3.
8
Comparison of vectorial ion transport in primary murine airway and human sinonasal air-liquid interface cultures, models for studies of cystic fibrosis, and other airway diseases.原发性小鼠气道和人鼻旁窦气液界面培养物中向量离子转运的比较，囊性纤维化及其他气道疾病研究模型。
Am J Rhinol Allergy. 2009 Mar-Apr;23(2):149-52. doi: 10.2500/ajra.2009.23.3285.
9
Protocols for in vivo measurement of the ion transport defects in cystic fibrosis nasal epithelium.囊性纤维化鼻上皮离子转运缺陷的体内测量方案。
Eur Respir J. 1994 Nov;7(11):2050-6.
10
Expression of cystic fibrosis transmembrane conductance regulator corrects defective chloride channel regulation in cystic fibrosis airway epithelial cells.囊性纤维化跨膜传导调节因子的表达可纠正囊性纤维化气道上皮细胞中缺陷性氯离子通道调节。
Nature. 1990 Sep 27;347(6291):358-63. doi: 10.1038/347358a0.

引用本文的文献

1
Water Sorption and Structural Properties of Human Airway Mucus in Health and Muco-Obstructive Diseases.健康及黏液阻塞性疾病中人体气道黏液的水吸附与结构特性
Biomacromolecules. 2024 Mar 11;25(3):1578-1591. doi: 10.1021/acs.biomac.3c01170. Epub 2024 Feb 9.
2
Impact of high- and low-flow nebulised saline on airway hydration and mucociliary transport.高流量和低流量雾化盐水对气道水化和黏液纤毛运输的影响。
ERJ Open Res. 2023 Jun 12;9(3). doi: 10.1183/23120541.00724-2022. eCollection 2023 May.
3
Physiology and pathophysiology of human airway mucus.
人类气道黏液的生理学和病理生理学。
Physiol Rev. 2022 Oct 1;102(4):1757-1836. doi: 10.1152/physrev.00004.2021. Epub 2022 Jan 10.
4
Molecular mechanisms of activation and regulation of ANO1-Encoded Ca-Activated Cl channels.ANO1 编码钙激活氯离子通道的激活和调节的分子机制。
Channels (Austin). 2021 Dec;15(1):569-603. doi: 10.1080/19336950.2021.1975411.
5
New Therapeutic Approaches in Cystic Fibrosis.囊性纤维化的新治疗方法
Turk J Pharm Sci. 2020 Dec 23;17(6):686-697. doi: 10.4274/tjps.galenos.2020.76401.
6
ENaC inhibition in cystic fibrosis: potential role in the new era of CFTR modulator therapies.囊性纤维化中的上皮钠通道抑制：在囊性纤维化跨膜传导调节因子调节剂疗法新时代的潜在作用。
Eur Respir J. 2020 Dec 24;56(6). doi: 10.1183/13993003.00946-2020. Print 2020 Dec.
7
Measurement of Multi Ion Transport through Human Bronchial Epithelial Cell Line Provides an Insight into the Mechanism of Defective Water Transport in Cystic Fibrosis.通过人支气管上皮细胞系测量多离子转运有助于深入了解囊性纤维化中水分转运缺陷的机制。
Membranes (Basel). 2020 Mar 12;10(3):43. doi: 10.3390/membranes10030043.
8
Concurrent absorption and secretion of airway surface liquids and bicarbonate secretion in human bronchioles.人细支气管中气道表面液体的同时吸收和分泌以及碳酸氢盐分泌。
Am J Physiol Lung Cell Mol Physiol. 2019 May 1;316(5):L953-L960. doi: 10.1152/ajplung.00545.2018. Epub 2019 Mar 6.
9
A Comparison between Two Pathophysiologically Different yet Microbiologically Similar Lung Diseases: Cystic Fibrosis and Chronic Obstructive Pulmonary Disease.两种病理生理不同但微生物学相似的肺部疾病的比较：囊性纤维化和慢性阻塞性肺疾病
Int J Respir Pulm Med. 2018;5(2). doi: 10.23937/2378-3516/1410098. Epub 2018 Nov 29.
10
Technological strategies to estimate and control diffusive passage times through the mucus barrier in mucosal drug delivery.通过黏膜给药技术估计和控制扩散通过黏液屏障的传递时间。
Adv Drug Deliv Rev. 2018 Jan 15;124:64-81. doi: 10.1016/j.addr.2017.12.002. Epub 2017 Dec 12.