2006
DOI: 10.1007/s00292-006-0826-1
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Morphologische Veränderungen der medikamenteninduzierten Leberschädigung

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Cited by 8 publications
(2 citation statements)
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“…33,34 The inhibitory activity of compounds 1-21 on the proliferation of activated HSC-T6 cells was evaluated (see Supporting Information, S36). These compounds consisted of oleanane type (1, 2, 5-12), ursane type (3,4,(13)(14)(15)(16)(17)(18)(19), and lupane type (20,21), according to their aglycone moieties (see Supporting Information, S1). Substitutions such as OH (1-21), carboxyl (5-9, 12-17, and 19), oxo (1, 2, 8, 9, and 17), and glucopyranoside (1, 3, 4, 10, 11, and 18) also divided them into several groups.…”
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confidence: 99%
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“…33,34 The inhibitory activity of compounds 1-21 on the proliferation of activated HSC-T6 cells was evaluated (see Supporting Information, S36). These compounds consisted of oleanane type (1, 2, 5-12), ursane type (3,4,(13)(14)(15)(16)(17)(18)(19), and lupane type (20,21), according to their aglycone moieties (see Supporting Information, S1). Substitutions such as OH (1-21), carboxyl (5-9, 12-17, and 19), oxo (1, 2, 8, 9, and 17), and glucopyranoside (1, 3, 4, 10, 11, and 18) also divided them into several groups.…”
mentioning
confidence: 99%
“…Liver fibrosis results from chronic hepatocellular damage in response to viral infection, alcoholic poisoning, drug-induced toxicity, or any other factors that cause damage to hepatocytes. The process to liver fibrosis is generally characterized by increased extracellular matrix (ECM) deposition and reduced matrix degradation . In the pathogenesis of liver fibrosis, hepatic stellate cells (HSCs) are the primary cellular source responsible for the excess production of ECM proteins .…”
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confidence: 99%