Mast cells are critical for the limitation of thrombin-induced skin inflammation.

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Mast cells are critical for the limitation of thrombin-induced skin inflammation.

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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年學術文章

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2017年學術文章

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2017年學術文章

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Mast cells are critical for the limitation of thrombin-induced skin inflammation.

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Mast cells are critical for the limitation of thrombin-induced skin inflammation.

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Mast cells are critical for the limitation of thrombin-induced skin inflammation.

@en

Mast cells are critical for the limitation of thrombin-induced skin inflammation.

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Mast cells are critical for the limitation of thrombin-induced skin inflammation.

@en

Mast cells are critical for the limitation of thrombin-induced skin inflammation.

@nl

P1476

Mast cells are critical for the limitation of thrombin-induced skin inflammation.

@en

P2093

Astrid Geldmacher

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Cathleen A Suender

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Magnus Åbrink

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Mandy Leist

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Martin Steinhoff

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Patricia Valentin

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P2860

CD40 ligand on activated platelets triggers an inflammatory reaction of endothelial cells

PAR3 is a cofactor for PAR4 activation by thrombin

The chymase, mouse mast cell protease 4, constitutes the major chymotrypsin-like activity in peritoneum and ear tissue. A role for mouse mast cell protease 4 in thrombin regulation and fibronectin turnover

Regulation of neutrophilic inflammation by proteinase-activated receptor 1 during bacterial pulmonary infection.

Mast cells can enhance resistance to snake and honeybee venoms.

Expression of protease-activated receptor-1, -2, -3, and -4 in control and experimentally inflamed mouse bladder.

The chymase mouse mast cell protease 4 degrades TNF, limits inflammation, and promotes survival in a model of sepsis.

Agonists and antagonists of protease activated receptors (PARs).

Thrombin-induced expression of endothelial P-selectin and intercellular adhesion molecule-1: a mechanism for stabilizing neutrophil adhesion.

Mast cell chymase degrades the alarmins heat shock protein 70, biglycan, HMGB1, and interleukin-33 (IL-33) and limits danger-induced inflammation

P31

scholarly article

P356

10.1111/EXD.13407

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Martin Metz

Marcus Maurer

P577

2017-08-08T00:00:00Z

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P698

28787094

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P921

mast cells