Small airways in idiopathic pulmonary fibrosis. Comparison of morphologic and physiologic observations
about
The influence of cigarette smoking on lung function in patients with idiopathic pulmonary fibrosisRedox mechanisms in age-related lung fibrosisMorphologic-physiologic correlates of the severity of fibrosis and degree of cellularity in idiopathic pulmonary fibrosisAssociation of bronchiolitis with connective tissue disorders.Bronchiolar disorders.Protein kinase D is increased and activated in lung epithelial cells and macrophages in idiopathic pulmonary fibrosis.Upregulation of platelet-derived growth factor-A and -B gene expression in alveolar macrophages of individuals with idiopathic pulmonary fibrosis.Enhanced alveolar macrophage-mediated antigen-induced T-lymphocyte proliferation in sarcoidosis.Spontaneous expression of the interleukin 2 receptor gene and presence of functional interleukin 2 receptors on T lymphocytes in the blood of individuals with active pulmonary sarcoidosisAlpha 1-antitrypsin deficiency caused by the alpha 1-antitrypsin Nullmattawa gene. An insertion mutation rendering the alpha 1-antitrypsin gene incapable of producing alpha 1-antitrypsinOxidant-mediated epithelial cell injury in idiopathic pulmonary fibrosis.A sigmoidal fit for pressure-volume curves of idiopathic pulmonary fibrosis patients on mechanical ventilation: clinical implications.Acute tropical pulmonary eosinophilia. Characterization of the lower respiratory tract inflammation and its response to therapy.Oxidants spontaneously released by alveolar macrophages of cigarette smokers can inactivate the active site of alpha 1-antitrypsin, rendering it ineffective as an inhibitor of neutrophil elastaseZ-type alpha 1-antitrypsin is less competent than M1-type alpha 1-antitrypsin as an inhibitor of neutrophil elastase.Neutrophil elastase in respiratory epithelial lining fluid of individuals with cystic fibrosis induces interleukin-8 gene expression in a human bronchial epithelial cell line.Modulation of airway inflammation in cystic fibrosis. In vivo suppression of interleukin-8 levels on the respiratory epithelial surface by aerosolization of recombinant secretory leukoprotease inhibitor.Recombinant DNA-produced alpha 1-antitrypsin administered by aerosol augments lower respiratory tract antineutrophil elastase defenses in individuals with alpha 1-antitrypsin deficiency.Evaluation of fibronectin gene expression by in situ hybridization. Differential expression of the fibronectin gene among populations of human alveolar macrophages.Extensive posttranscriptional deletion of the coding sequences for part of nucleotide-binding fold 1 in respiratory epithelial mRNA transcripts of the cystic fibrosis transmembrane conductance regulator gene is not associated with the clinical manifAnchoring fibrils. A new connective tissue structure in fibrotic lung disease.Lung inflammation in sarcoidosis: comparison of serum angiotensin-converting enzyme levels with bronchoalveolar lavage and gallium-67 scanning assessment of the T lymphocyte alveolitis.The larger bronchi in cryptogenic fibrosing alveolitis: a morphometric study.Vertical gradients of lung density in supine subjects with fibrosing alveolitis or pulmonary emphysemaEnhancing Autophagy with Drugs or Lung-directed Gene Therapy Reverses the Pathological Effects of Respiratory Epithelial Cell Proteinopathy.Cryptogenic obliterative bronchiolitis in adultsInterrelationship between lung volume, expiratory flow, and lung transfer factor in fibrosing alveolitis.Mechanisms of pulmonary fibrosis. Spontaneous release of the alveolar macrophage-derived growth factor in the interstitial lung disorders.Expression of the alpha-1-antitrypsin gene in mononuclear phagocytes of normal and alpha-1-antitrypsin-deficient individualsFibronectin in human bronchopulmonary lavage fluid. Elevation in patients with interstitial lung diseaseDanazol-induced augmentation of serum alpha 1-antitrypsin levels in individuals with marked deficiency of this antiprotease.Expression of HLA class II genes in alveolar macrophages of patients with sarcoidosis.Accumulation of Langerhans' cells on the epithelial surface of the lower respiratory tract in normal subjects in association with cigarette smoking.Functional significance of anti-T-lymphocyte antibodies in sarcoidosis.A novel segmental challenge model for bleomycin-induced pulmonary fibrosis in sheep.Clinical features and history of the destructive lung disease associated with alpha-1-antitrypsin deficiency of adults with pulmonary symptoms.Preferential usage of the T-cell antigen receptor beta-chain constant region C beta 1 element by lung T-lymphocytes of patients with pulmonary sarcoidosis.Fatores prognósticos em fibrose pulmonar idiopática
P2860
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P2860
Small airways in idiopathic pulmonary fibrosis. Comparison of morphologic and physiologic observations
description
1977 nî lūn-bûn
@nan
1977 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
1977 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
1977年の論文
@ja
1977年論文
@yue
1977年論文
@zh-hant
1977年論文
@zh-hk
1977年論文
@zh-mo
1977年論文
@zh-tw
1977年论文
@wuu
name
Small airways in idiopathic pu ...... c and physiologic observations
@ast
Small airways in idiopathic pu ...... c and physiologic observations
@en
Small airways in idiopathic pu ...... c and physiologic observations
@nl
type
label
Small airways in idiopathic pu ...... c and physiologic observations
@ast
Small airways in idiopathic pu ...... c and physiologic observations
@en
Small airways in idiopathic pu ...... c and physiologic observations
@nl
prefLabel
Small airways in idiopathic pu ...... c and physiologic observations
@ast
Small airways in idiopathic pu ...... c and physiologic observations
@en
Small airways in idiopathic pu ...... c and physiologic observations
@nl
P2093
P2860
P3181
P356
P1476
Small airways in idiopathic pu ...... c and physiologic observations
@en
P2093
E R von Gal
J D Fulmer
R G Grystal
W C Roberts
P2860
P304
P3181
P356
10.1172/JCI108811
P407
P577
1977-09-01T00:00:00Z