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Alveolar macrophages in pulmonary alveolar proteinosis: origin, function, and therapeutic strategies

Frontiers in immunology, 2023-06, Vol.14, p.1195988-1195988

2023

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Development of a scoring system with multidimensional markers for fibrosing interstitial lung disease

Scientific reports, 2022-08, Vol.12 (1), p.14217-14217, Article 14217

2022

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Dodecaphenyltetracene

Angewandte Chemie International Edition, 2019-02, Vol.58 (9), p.2831-2833

International ed. in English, 2019

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Incidence and impact of extra-pulmonary organ failures on hospital mortality in acute exacerbation of idiopathic pulmonary fibrosis

Scientific reports, 2020-07, Vol.10 (1), p.10742-10742, Article 10742

2020

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Acute exacerbations of fibrosing interstitial lung disease associated with connective tissue diseases: a population-based study

BMC pulmonary medicine, 2019-11, Vol.19 (1), p.215-215, Article 215

2019

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Investigation of the impact of fiber incorporation on the properties of high belite cement

Journal of materials research and technology, 2024-05, Vol.30, p.930-944

2024

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Synthesis and Structures of Polyphenylphenanthrenes

Chemistry : a European journal, 2020-07, Vol.26 (38), p.8458-8464

2020

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α1-antitrypsin promotes lung adenocarcinoma metastasis through upregulating fibronectin expression

International journal of oncology, 2017-06, Vol.50 (6), p.1955-1964

2017

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Associations of Serological Biomarkers of sICAM-1, IL-1β, MIF, and su-PAR with 3-Month Mortality in Acute Exacerbation of Idiopathic Pulmonary Fibrosis

Mediators of inflammation, 2020, Vol.2020, p.4534272-9

2020

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Tumor-intrinsic RGS1 potentiates checkpoint blockade response via ATF3-IFNGR1 axis

Oncoimmunology, 2023-12, Vol.12 (1), p.2279800-2279800

2023

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Elevated Expression of Growth Differentiation Factor-15 Is Associated With Acute Exacerbation of Idiopathic Pulmonary Fibrosis

Frontiers in immunology, 2022-06, Vol.13, p.891448-891448

2022

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Inhaled granulocyte-macrophage colony stimulating factor for mild-to-moderate autoimmune pulmonary alveolar proteinosis - a six month phase II randomized study with 24 months of follow-up

Orphanet journal of rare diseases, 2020-07, Vol.15 (1), p.1-174, Article 174

2020

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Long-term follow-up and successful treatment of pulmonary alveolar proteinosis without hypercholesterolemia with statin therapy: a case report

Journal of international medical research, 2021-04, Vol.49 (4), p.3000605211010046-3000605211010046

2021

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A long-term retrospective study of patients with biopsy-proven cryptogenic organizing pneumonia

Chronic respiratory disease, 2019-01, Vol.16, p.1479973119853829-1479973119853829

2019

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Lung carcinoma with diffuse cystic lesions misdiagnosed as pulmonary langerhans cell histocytosis: a case report

BMC pulmonary medicine, 2020-02, Vol.20 (1), p.30-30, Article 30

2020

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Plasma Leptin Is Elevated in Acute Exacerbation of Idiopathic Pulmonary Fibrosis

Mediators of inflammation, 2016-01, Vol.2016, p.6940480-7

2016

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Correlation between serum bilirubin levels and the severity as well as the prognosis of idiopathic pulmonary fibrosis

Chronic respiratory disease, 2020, Vol.17, p.147997312095767-1479973120957676

2020

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Prediction model for the pretreatment evaluation of mortality risk in anti-melanoma differentiation-associated gene 5 antibody-positive dermatomyositis with interstitial lung disease

Frontiers in immunology, 2022-09, Vol.13, p.978708-978708

2022

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Protective function of interleukin‐22 in pulmonary fibrosis

Clinical and translational medicine, 2021-08, Vol.11 (8), p.e509-n/a

2021

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Novel 3D-based deep learning for classification of acute exacerbation of idiopathic pulmonary fibrosis using high-resolution CT

BMJ open respiratory research, 2024-03, Vol.11 (1), p.e002226

2024

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Pretreatment mortality risk prediction model in patients with polymyositis/dermatomyositis-associated interstitial lung disease

Rheumatic & musculoskeletal diseases open, 2024-04, Vol.10 (2), p.e003850

2024

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Giant cell interstitial pneumonia： unusual lung disorder and an update

Chinese medical journal, 2014, Vol.127 (15), p.2819-2823

2014

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Dodecaphenyltetracene

Angewandte Chemie, 2019-02, Vol.131 (9), p.2857-2859

2019

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Effectiveness and safety of inhaled granulocyte-macrophage colony-stimulating factor therapy in idiopathic pulmonary alveolar proteinosis

Zhong hua yi xue za zhi, 2015-09, Vol.95 (34), p.2766-2770

2015

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The clinical significance of the levels of serum KL-6 mucin and interleukin-13 in pulmonary alveolar proteinosis

Zhonghua jiehe he huxi zazhi, 2015-02, Vol.38 (2), p.110

2015

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Alveolar macrophages in pulmonary alveolar proteinosis: origin, function, and therapeutic strategies

Development of a scoring system with multidimensional markers for fibrosing interstitial lung disease

Dodecaphenyltetracene

Incidence and impact of extra-pulmonary organ failures on hospital mortality in acute exacerbation of idiopathic pulmonary fibrosis

Acute exacerbations of fibrosing interstitial lung disease associated with connective tissue diseases: a population-based study

Investigation of the impact of fiber incorporation on the properties of high belite cement

Synthesis and Structures of Polyphenylphenanthrenes

α1-antitrypsin promotes lung adenocarcinoma metastasis through upregulating fibronectin expression

Associations of Serological Biomarkers of sICAM-1, IL-1β, MIF, and su-PAR with 3-Month Mortality in Acute Exacerbation of Idiopathic Pulmonary Fibrosis

Tumor-intrinsic RGS1 potentiates checkpoint blockade response via ATF3-IFNGR1 axis

Elevated Expression of Growth Differentiation Factor-15 Is Associated With Acute Exacerbation of Idiopathic Pulmonary Fibrosis

Inhaled granulocyte-macrophage colony stimulating factor for mild-to-moderate autoimmune pulmonary alveolar proteinosis - a six month phase II randomized study with 24 months of follow-up

Long-term follow-up and successful treatment of pulmonary alveolar proteinosis without hypercholesterolemia with statin therapy: a case report

A long-term retrospective study of patients with biopsy-proven cryptogenic organizing pneumonia

Lung carcinoma with diffuse cystic lesions misdiagnosed as pulmonary langerhans cell histocytosis: a case report

Plasma Leptin Is Elevated in Acute Exacerbation of Idiopathic Pulmonary Fibrosis

Correlation between serum bilirubin levels and the severity as well as the prognosis of idiopathic pulmonary fibrosis

Prediction model for the pretreatment evaluation of mortality risk in anti-melanoma differentiation-associated gene 5 antibody-positive dermatomyositis with interstitial lung disease

Protective function of interleukin‐22 in pulmonary fibrosis

Novel 3D-based deep learning for classification of acute exacerbation of idiopathic pulmonary fibrosis using high-resolution CT

Pretreatment mortality risk prediction model in patients with polymyositis/dermatomyositis-associated interstitial lung disease

Giant cell interstitial pneumonia： unusual lung disorder and an update

Dodecaphenyltetracene

Effectiveness and safety of inhaled granulocyte-macrophage colony-stimulating factor therapy in idiopathic pulmonary alveolar proteinosis

The clinical significance of the levels of serum KL-6 mucin and interleukin-13 in pulmonary alveolar proteinosis

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