Work

Acidic Submucosal Gland pH and Elevated Protein Concentration Produce Abnormal Cystic Fibrosis Mucus

Year: 2020

Type: article

Source: Developmental Cell

DOI: 10.1016/j.devcel.2020.07.002

Authors: Yuliang Xie, Lin Lu, Xiao Xiao Tang, Thomas O. Moninger, Tony Jun Huang, David A. Stoltz, Michael J. Welsh

Institutions: University of Iowa, Howard Hughes Medical Institute, Duke University, University of Iowa Health Care

Language: English

Topic: Cystic Fibrosis Research Advances

Subfield: Pulmonary and Respiratory Medicine

Field: Medicine

Domain: Health Sciences

SDG: Good health and well-being

Open Access status: bronze

Funders: Cystic Fibrosis Foundation, National Heart, Lung, and Blood Institute, National Institute of General Medical Sciences, National Institute of Diabetes and Digestive and Kidney Diseases, National Institute of Environmental Health Sciences

Awards: Gene Therapy For Cystic Fibrosis Lung Disease, Molecular Therapies for Cystic Fibrosis Lung Disease, Airway Alkalinization and Repurposing Tromethamine as a Therapeutic Approach in Cystic Fibrosis, Origins of Cystic Fibrosis Airway Disease, Enabling Efficient, Fast, Biocompatible Exosome Separation via Acoustofluidics, Environmental Health Sciences Research Center, Precision Medicine Center for Cystic Fibrosis

OpenAlex ID: W3045693682

FWCI: 2.812

Cites: 83

Cited by: 30

Related to: 10