Matrix biomechanics and dynamics in pulmonary fibrosis.

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Idiopathic pulmonary fibrosis: Epithelial-mesenchymal interactions and emerging therapeutic targets.

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Matrix biomechanics and dynamics in pulmonary fibrosis.

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年學術文章

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2017年學術文章

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Matrix biomechanics and dynamics in pulmonary fibrosis.

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Matrix biomechanics and dynamics in pulmonary fibrosis.

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Matrix biomechanics and dynamics in pulmonary fibrosis.

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Matrix biomechanics and dynamics in pulmonary fibrosis.

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Matrix biomechanics and dynamics in pulmonary fibrosis.

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Matrix biomechanics and dynamics in pulmonary fibrosis.

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Matrix biomechanics and dynamics in pulmonary fibrosis.

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Andrew J Haak

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Daniel J Tschumperlin

http://www.w3.org/2001/XMLSchema#string

Qi Tan

http://www.w3.org/2001/XMLSchema#string

P2860

Analysis of the myosin-II-responsive focal adhesion proteome reveals a role for β-Pix in negative regulation of focal adhesion maturation

TAZ promotes cell proliferation and epithelial-mesenchymal transition and is inhibited by the hippo pathway

Fibulin1C peptide induces cell attachment and extracellular matrix deposition in lung fibroblasts

Feedback amplification of fibrosis through matrix stiffening and COX-2 suppression

Fragments of extracellular matrix as mediators of inflammation

Myofibroblast contraction activates latent TGF-beta1 from the extracellular matrix

Up-regulation and profibrotic role of osteopontin in human idiopathic pulmonary fibrosis

Diverse functions of matrix metalloproteinases during fibrosis

Always cleave up your mess: targeting collagen degradation to treat tissue fibrosis

Matrix biology of idiopathic pulmonary fibrosis: a workshop report of the national heart, lung, and blood institute

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scholarly article

review article

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10.1016/J.MATBIO.2017.12.004

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2017-12-21T00:00:00Z

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29274939

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biomechanics

pulmonary fibrosis

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6013326

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Matrix biomechanics and dynamics in pulmonary fibrosis.

about

P2860

P2860

Matrix biomechanics and dynamics in pulmonary fibrosis.

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