State of the Art in Idiopathic Pulmonary Fibrosis-Reference-Cited by-同舟云学术

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State of the Art in Idiopathic Pulmonary Fibrosis

Published:2022-08-11 Issue:16 Volume:11 Page:2487
ISSN:2073-4409
Container-title:Cells
language:en
Short-container-title:Cells

Author:

El Agha Elie^ORCID,Wygrecka Malgorzata^ORCID

Abstract

Idiopathic pulmonary fibrosis (IPF) is a form of usual interstitial pneumonia (UIP), though its origin is unknown [...]

Funder

Deutsche Forschungsgemeinschaft

German Center for Lung Research

Else Kröner-Fresenius-Stiftung

Publisher

MDPI AG

Subject

General Medicine

Link

https://www.mdpi.com/2073-4409/11/16/2487/pdf

Reference28 articles.

1. Unravelling the progressive pathophysiology of idiopathic pulmonary fibrosis

2. Differential LysoTracker Uptake Defines Two Populations of Distal Epithelial Cells in Idiopathic Pulmonary Fibrosis

3. Alveolar regeneration through a Krt8+ transitional stem cell state that persists in human lung fibrosis

4. Single-cell RNA-seq reveals ectopic and aberrant lung-resident cell populations in idiopathic pulmonary fibrosis

5. Single-cell RNA sequencing reveals profibrotic roles of distinct epithelial and mesenchymal lineages in pulmonary fibrosis

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Human Lung Organoids—A Novel Experimental and Precision Medicine Approach;Cells;2023-08-15

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