Arachidonic acid promotes skin wound healing through induction of human MSC migration by MT3-MMP-mediated fibronectin degradation.

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2015 nî lūn-bûn

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2015年の論文

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2015年学术文章

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2015年学术文章

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2015年学术文章

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2015年学术文章

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2015年學術文章

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Arachidonic acid promotes skin ...... iated fibronectin degradation.

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Arachidonic acid promotes skin ...... iated fibronectin degradation.

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Arachidonic acid promotes skin ...... iated fibronectin degradation.

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Arachidonic acid promotes skin ...... iated fibronectin degradation.

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Arachidonic acid promotes skin ...... iated fibronectin degradation.

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Arachidonic acid promotes skin ...... iated fibronectin degradation.

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Arachidonic acid promotes skin ...... iated fibronectin degradation.

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H J Lee

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S Y Oh

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S-J Lee

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Y H Jung

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Selective activation of Akt1 by mammalian target of rapamycin complex 2 regulates cancer cell migration, invasion, and metastasis

PRR5L degradation promotes mTORC2-mediated PKC-δ phosphorylation and cell migration downstream of Gα12

A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding

Galectin-1 stimulates motility of human umbilical cord blood-derived mesenchymal stem cells by downregulation of smad2/3-dependent collagen 3/5 and upregulation of NF-κB-dependent fibronectin/laminin 5 expression

Identification of soluble type of membrane-type matrix metalloproteinase-3 formed by alternatively spliced mRNA

Prolonged rapamycin treatment inhibits mTORC2 assembly and Akt/PKB

Rac1 is required for epithelial stem cell function during dermal and oral mucosal wound healing but not for tissue homeostasis in mice.

Reactive oxygen species induce MMP12-dependent degradation of collagen 5 and fibronectin to promote the motility of human umbilical cord-derived mesenchymal stem cells.

Cell therapy with human MSCs isolated from the umbilical cord Wharton jelly associated to a PVA membrane in the treatment of chronic skin wounds.

Mesenchymal stem cells: paracrine signaling and differentiation during cutaneous wound repair

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10.1038/CDDIS.2015.114

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Ho Jae Han

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