Topical dihydroartemisinin inhibits suture-induced neovascularization in rat corneas through ERK1/2 and p38 pathways.

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MK2 inhibitor reduces alkali burn-induced inflammation in rat cornea.Dihydroartemisinin targets VEGFR2 via the NF-κB pathway in endothelial cells to inhibit angiogenesis.

P2860

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P2860

Topical dihydroartemisinin inhibits suture-induced neovascularization in rat corneas through ERK1/2 and p38 pathways.

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http://www.wikidata.org/entity/Q41769139

description

2011 nî lūn-bûn

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2011年の論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年论文

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2011年论文

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2011年论文

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name

Topical dihydroartemisinin inh ...... rough ERK1/2 and p38 pathways.

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type

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label

Topical dihydroartemisinin inh ...... rough ERK1/2 and p38 pathways.

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prefLabel

Topical dihydroartemisinin inh ...... rough ERK1/2 and p38 pathways.

@en

P1476

Topical dihydroartemisinin inh ...... rough ERK1/2 and p38 pathways.

@en

P2093

Hai-Feng Zhang

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

Jia-Xi Zhong

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

Lang Bai

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

Xiao-He Lu

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

Yan-Yan Zhong

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

P2860

Antimalarial Drug Toxicity

Thalidomide is an inhibitor of angiogenesis

Signaling transduction mechanisms mediating biological actions of the vascular endothelial growth factor family

Prevention of corneal neovascularization: evaluation of various commercially available compounds in an experimental rat model

Vascular endothelial growth factor (VEGF) receptor-2 signaling mediates VEGF-C(deltaNdeltaC)- and VEGF-A-induced angiogenesis in vitro

Vascular endothelial growth factor (VEGF)-driven actin-based motility is mediated by VEGFR2 and requires concerted activation of stress-activated protein kinase 2 (SAPK2/p38) and geldanamycin-sensitive phosphorylation of focal adhesion kinase

Mitogen-activated protein kinase pathways mediated by ERK, JNK, and p38 protein kinases

Corneal neovascularization.

Molecular biology of the VEGF and the VEGF receptor family.

Qinghaosu (artemisinin): an antimalarial drug from China.

P304

150-155

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P31

scholarly article

P356

10.3980/J.ISSN.2222-3959.2011.02.08

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P433

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

P478

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2011-04-18T00:00:00Z

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P5875

224889354

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P698

22553631

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P921

neovascularization

P932

3340693

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

Topical dihydroartemisinin inhibits suture-induced neovascularization in rat corneas through ERK1/2 and p38 pathways.

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P2860

P2860

Topical dihydroartemisinin inhibits suture-induced neovascularization in rat corneas through ERK1/2 and p38 pathways.

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