Matrix metalloproteinase-13 promotes recovery from experimental liver cirrhosis in rats. (Q54353484)

28 May 2018

title

Matrix metalloproteinase-13 promotes recovery from experimental liver cirrhosis in rats. (English)

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6

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author name string

Hitoshi Endo

1

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Maki Niioka

2

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Yoshihiko Sugioka

3

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Johbu Itoh

4

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Kaori Kameyama

5

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Risto Ala-Aho

7

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Veli-Matti Kähäri

8

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Tetsu Watanabe

9

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publication date

17 August 2011

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published in

Pathobiology

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volume

78

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issue

5

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page(s)

239-252

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Gene expression and hepatitis C virus infection

cites work

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Regulation of matrix biology by matrix metalloproteinases

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Altered balance between matrix metalloproteinases and their inhibitors in experimental biliary fibrosis

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Expression of collagenase-3 (MMP-13) enhances invasion of human fibrosarcoma HT-1080 cells

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Purified human hematopoietic stem cells contribute to the generation of cardiomyocytes through cell fusion

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MMP13 mutation causes spondyloepimetaphyseal dysplasia, Missouri type (SEMD(MO)

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Hepatocyte growth factor gene therapy of liver cirrhosis in rats

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Hepatocyte growth factor in transgenic mice

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Therapeutic effect of transplanting HGF-treated bone marrow mesenchymal cells into CCl4-injured rats

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Growth inhibition and apoptosis in liver myofibroblasts promoted by hepatocyte growth factor leads to resolution from liver cirrhosis.

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Treatment with human metalloproteinase-8 gene delivery ameliorates experimental rat liver cirrhosis.

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Activation of p70S6K induces expression of matrix metalloproteinase 9 associated with hepatocyte growth factor-mediated invasion in human ovarian cancer cells

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Delivery of matrix metalloproteinase-1 attenuates established liver fibrosis in the rat.

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Biochemical characterization of human collagenase-3

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Antifibrotic effect of MMP13-encoding plasmid DNA delivered using polyethylenimine shielded with hyaluronic acid

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Selective depletion of macrophages reveals distinct, opposing roles during liver injury and repair

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Metalloproteinase inhibitor TIMP-1 affects hepatocyte cell cycle via HGF activation in murine liver regeneration

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21 January 2018

Identifiers

DOI

10.1159/000328841

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