Zobrazeno 1 - 10
of 1 013
pro vyhledávání: '"Idiopathic pulmonary fibrosis (IPF)"'
Autor:
Reyhaneh Niayesh-Mehr, Mojtaba Kalantar, Giulio Bontempi, Claudia Montaldo, Saeedeh Ebrahimi, Abdolamir Allameh, Ghader Babaei, Faezeh Seif, Raffaele Strippoli
Publikováno v:
Cell Communication and Signaling, Vol 22, Iss 1, Pp 1-16 (2024)
Abstract Despite the tremendous advancements in the knowledge of the pathophysiology and clinical aspects of SARS-CoV-2 infection, still many issues remain unanswered, especially in the long-term effects. Mounting evidence suggests that pulmonary fib
Externí odkaz:
https://doaj.org/article/eb2fbefc3d8f4831a55341f22cd70047
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-17 (2024)
Abstract The role and detailed mechanisms of lncRNAs in idiopathic pulmonary fibrosis (IPF) are not fully understood. qPCR was conducted to verify lncRNA FEZF1-AS1 expression in the transforming growth factor-beta 1 (TGF-β1)-stimulated human lung fi
Externí odkaz:
https://doaj.org/article/c129fc45804843d087d1c687c930c70f
Publikováno v:
BMC Pulmonary Medicine, Vol 24, Iss 1, Pp 1-12 (2024)
Abstract Background Idiopathic pulmonary fibrosis (IPF), an interstitial lung disease, is characterized by the exacerbation of progressive pulmonary fibrosis (PF). IPF primarily affects older individuals and can lead to respiratory failure. This stud
Externí odkaz:
https://doaj.org/article/6511ab07fe734c668e461999f7fdfa9d
Publikováno v:
Pulmonary Therapy, Vol 10, Iss 3, Pp 331-346 (2024)
Abstract Introduction Clinical practice guidelines recommend autoimmune serological testing in patients newly diagnosed with interstitial lung disease of apparently unknown cause who may have idiopathic pulmonary fibrosis (IPF), in order to exclude c
Externí odkaz:
https://doaj.org/article/61e00689d1d841d5bcbfc129184fdb88
Autor:
Ziheng Yuan, Wanyang Lei, Xiqian Xing, Xiaohua He, Xiaoxian Huang, Li Wei, Yuanyuan Lv, Shuyi Qiu, Ziyu Yuan, Jiyang Wang, Mei Yang
Publikováno v:
BMC Pulmonary Medicine, Vol 24, Iss 1, Pp 1-7 (2024)
Abstract Background Observational studies have shown that smoking is related to the diffusing capacity of the lungs for carbon monoxide (DLCO) in individuals with idiopathic pulmonary fibrosis (IPF). Nevertheless, further investigation is needed to d
Externí odkaz:
https://doaj.org/article/e011ed930080413892b8ddcd28a77cfa
Autor:
Tatsuru Ishikawa, Hirotaka Nishikiori, Yuki Mori, Keiko Fujino, Atsushi Saito, Mamoru Takahashi, Koji Kuronuma, Shiro Hinotsu, Hirofumi Chiba
Publikováno v:
BMC Pulmonary Medicine, Vol 24, Iss 1, Pp 1-11 (2024)
Abstract Background Idiopathic pulmonary fibrosis (IPF) is a progressive disease with a poor prognosis. Pulmonary function tests (PFTs) aid in evaluating the disease status of IPF. The clinical significance of oscillometry measurements in interstitia
Externí odkaz:
https://doaj.org/article/02a9b6267fda44a782cee53fcbb5f3fc
Autor:
Vera Ciornolutchii, Victoria Maria Ruta, Adina Milena Man, Nicoleta Stefania Motoc, Stefan-Lucian Popa, Dan L. Dumitrascu, Abdulrahman Ismaiel, Daniel-Corneliu Leucuta
Publikováno v:
Medicina, Vol 60, Iss 10, p 1702 (2024)
Background and Objectives: Pulmonary fibrosis, including idiopathic pulmonary fibrosis (IPF) and secondary pulmonary fibrosis (SPF), is a progressive lung disease that significantly impairs respiratory function. Accurate differentiation between IPF a
Externí odkaz:
https://doaj.org/article/aa1af8d9720945839c6dd15cdf8d8379
Autor:
Ying-Wei Lan, Ying-Cheng Chen, Chih-Ching Yen, Hsiao-Ling Chen, Min-Che Tung, Hueng-Chuen Fan, Chuan-Mu Chen
Publikováno v:
Biomedicine & Pharmacotherapy, Vol 174, Iss , Pp 116431- (2024)
Background: Idiopathic pulmonary fibrosis (IPF) is a progressive and life-threatening lung disease with high mortality rates. The limited availability of effective drugs for IPF treatment, coupled with concerns regarding adverse effects and restricte
Externí odkaz:
https://doaj.org/article/02ad12454b9f4cb48a602df5058f4789
Publikováno v:
Biomolecules & Biomedicine (2024)
Idiopathic pulmonary fibrosis (IPF) is a progressive and chronic disease that significantly impacts patient quality of life, and its incidence is on the rise. The pathogenesis of IPF remains poorly understood. Alveolar type 2 (AT2) cells are crucial
Externí odkaz:
https://doaj.org/article/9800a6fc4d6b4827abfcdc137db55e63
Autor:
Wanyang Lei, Mei Yang, Ziyu Yuan, Runlin Feng, Xiao Kuang, Zhiqiang Liu, Zongqi Deng, Xianglin Hu, Wenlin Tai
Publikováno v:
Respiratory Research, Vol 24, Iss 1, Pp 1-8 (2023)
Abstract Background Several observational studies have found that physical inactivity and sedentary time are associated with idiopathic pulmonary fibrosis (IPF) risk. However, the causality between them still requires further investigation. Therefore
Externí odkaz:
https://doaj.org/article/cd1115c4d893406998816bae0c3048d4