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Aberrant innate immune sensing leads to the rapid progression of idiopathic pulmonary fibrosis.
- Published in:
- Fibrogenesis & Tissue Repair, 2012, v. 5, n. Suppl 1, p. 1, doi. 10.1186/1755-1536-5-S1-S3
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- Article
T regulatory cells and attenuated bleomycininduced fibrosis in lungs of CCR7<sup>-/-</sup> mice.
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- Fibrogenesis & Tissue Repair, 2010, v. 3, p. 18, doi. 10.1186/1755-1536-3-18
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- Article
Chronic Expression of a Clinical SFTPC Mutation Causes Murine Lung Fibrosis with Idiopathic Pulmonary Fibrosis Features.
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- American Journal of Respiratory Cell & Molecular Biology, 2023, v. 68, n. 4, p. 358, doi. 10.1165/rcmb.2022-0203MA
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- Article
CCR4-deficient Mice are Susceptible to CpG Challenge in an Acute Exacerbation Model of Bleomycin-induced Fibrosis as a Result of Phenotypic Changes in Macrophage Polarization.
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- FASEB Journal, 2008, v. 22, p. 425, doi. 10.1096/fasebj.22.2_supplement.425
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- Article
TLR9 Differentiates Rapidly from Slowly Progressing Forms of Idiopathic Pulmonary Fibrosis.
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- Science Translational Medicine, 2010, v. 2, n. 57, p. 1, doi. 10.1126/scitranslmed.3001510
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- Article