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期刊名:American journal of physiology-lung cellular and molecular physiology

缩写:AM J PHYSIOL-LUNG C

ISSN:1040-0605

e-ISSN:1522-1504

IF/分区:3.5/Q1

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共收录本刊相关文章索引3353
Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
Classical Article Case Reports Clinical Study Clinical Trial Clinical Trial Protocol Comment Comparative Study Editorial Guideline Letter Meta-Analysis Multicenter Study Observational Study Randomized Controlled Trial Review Systematic Review
Robin Curnow,Carl A Whitfield,Waqar Ahmed et al. Robin Curnow et al.
Biomarkers based on volatile organic compounds (VOCs) measured in human breath have been investigated in a wide range of diseases. However, the excitement surrounding such biomarkers has not yet translated to the discovery of any that are r...
Sharanya Sarkar,Roxanna Barnaby,Amanda B Nymon et al. Sharanya Sarkar et al.
Cystic Fibrosis (CF) is a multiorgan disease caused by mutations in the CFTR gene, leading to chronic pulmonary infections and hyperinflammation. Among pathogens colonizing the CF lung, Pseudomonas aeruginosa is predominant, infecting over ...
Grace Scharf,Cynthia R Davidson,Vladimir Ustiyan et al. Grace Scharf et al.
Cystic Fibrosis (CF) is characterized by impaired mucociliary clearance and pulmonary infections. Accumulating evidence suggests that fundamentally abnormal inflammatory responses also contribute to CF pathology. TGFβ, a pleiotropic cytoki...
Mrinmay Chakrabarti,Mollie Phillips,Rana Dhar et al. Mrinmay Chakrabarti et al.
Acute lung injury (ALI)/acute respiratory distress syndrome (ARDS) are inflammatory conditions with substantial rates of morbidity and mortality, but no effective treatments. The lack of effective treatments and unacceptably high mortality ...
Navneet Singh,Ceren Koçana,Eric P Schmidt et al. Navneet Singh et al.
Session V of the inaugural biennual Research Symposium on Pulmonary Injury and Repair of the Endothelium (ReSPIRE) showcased cutting-edge research on pulmonary endothelial crosstalk with end-organs and its role in vascular disease. Growing ...
Liang Fan,Rashmi S Shetty,Huy Minh Dao et al. Liang Fan et al.
Idiopathic pulmonary fibrosis (IPF) is a fatal disease characterized by progressive and irreversible loss of lung function. CSP7 exerts anti-fibrotic effects on fibrotic lung (myo)fibroblasts, which are the primary effector cells in progres...
Cathy van Horik,Joel Anne Meyboom,Anne Boerema-de Munck et al. Cathy van Horik et al.
Bronchopulmonary dysplasia (BPD) is the most common adverse outcome in preterm neonates, and a high risk for early-onset emphysema and asthma. BPD is characterized by disrupted alveolar and microvascular development, due to a variety of pat...
Thomas Carrez,Sandra Mirval,Christine Barrault et al. Thomas Carrez et al.
Trikafta (elexacaftor/tezacaftor/ivacaftor, ETI) is approved for cystic fibrosis (CF) patients with at least one F508del mutation in the CFTR gene or another responsive mutation based on in vitro data. However, the pharmacological effects o...
Reece P Stevens,Justin T Roberts,Wolfgang M Kuebler et al. Reece P Stevens et al.
Session I of the inaugural biennial Research Symposium on Pulmonary Injury and Repair of the Endothelium (ReSPIRE) highlighted recent advances in endothelial bioenergetics and metabolism and their role in pulmonary vascular diseases. Emergi...