Inhibition of apoptosis of activated hepatic stellate calls by TIMP-1 is mediated via effects on MMP inhibition: Implications for revesibility of liver fibrosis

Inhibition of apoptosis of activated hepatic stellate calls by TIMP-1 is mediated via effects on MMP inhibition: Implications for revesibility of liver fibrosis

Manylion Llyfryddiaeth
Prif Awduron:	Murphy, F, Issa, R, Zhou, X, Ratnarajah, S, Nagase, H, Soloway, P, Arthur, M, Benyon, C, Iredale, J
Fformat:	Journal article
Cyhoeddwyd:	2002

Eitemau Tebyg

Inhibition of apoptosis of activated hepatic stellate cells by TIMP-1 is mediated via effects on MMP inhibition: Implications for reversibility of liver fibrosis
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Inhibition of apoptosis of activated hepatic stellate cells by tissue inhibitor of metalloproteinase-1 is mediated via effects on matrix metalloproteinase inhibition: implications for reversibility of liver fibrosis.
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Individual Timp deficiencies differentially impact pro-MMP-2 activation.
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TIMP-2 inhibits metastasis and predicts prognosis of colorectal cancer via regulating MMP-9
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NDRG2 ameliorates hepatic fibrosis by inhibiting the TGF-β1/Smad pathway and altering the MMP2/TIMP2 ratio in rats.
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TIMP-3 inhibits the procollagen N-proteinase ADAMTS-2.
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p85α Inactivates MMP-2 and Suppresses Bladder Cancer Invasion by Inhibiting MMP-14 Transcription and TIMP-2 Degradation
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MMP-2 and MMP-9 Activities and TIMP-1 and TIMP-2 Expression in the Prostatic Tissue of Two Ethanol-Preferring Rat Models
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RANKL inhibits activation of hepatic stellate cells during hepatic fibrosis in mice
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Structure and function of matrix metalloproteinases and TIMPs.
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