Apoptosis induced in normal human hepatocytes by tumor necrosis factor-related apoptosis-inducing ligand
By Minji Jo, Tae-Hyoung Kim, D. Seol, James E. Esplen, K. Dorko, Timothy R. Billiar, S. Strom. Nature Medicine, 2000
899 citations recorded by the source corpus.
Subfields: Epidemiology, Molecular Biology
View Paper: https://www.semanticscholar.org/paper/ff9872fd370ce47804955ce0758767cf360df787
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In Epidemiology
In Molecular Biology
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Citations in the corpus
- Extrinsic versus intrinsic apoptosis pathways in anticancer chemotherapy (2006, background): “However, some concerns about potential toxic side effects on human hepatocytes or brain tissue have also been raised (Jo et al., 2000; Nitsch et al., 2000).”
- Differential hepatocyte toxicity of recombinant Apo2L/TRAIL versions (2001, methodology): “His using methods similar to those used by Jo et al.(8) and compared it with Apo2L/TRAIL.”
- Apo2L/TRAIL: apoptosis signaling, biology, and potential for cancer therapy. (2003, background): “Hepatocytes and keratinocytes are resistant to this optimized ligand version [26,27] but show significant sensitivity to apoptosis induction by non-optimized or antibody-crosslinked variants of the ligand [25].”
- Apo2L/TRAIL and its death and decoy receptors (2003, background): “evaluating results: some preparations lacking the Zn have reduced solubility and tend to aggregate, perhaps explaining the reported toxicity of certain Apo2L/TRAIL preparations to human hepatocytes.(24,25) Untagged, trimeric Apo2L/TRAIL containing stoichiometric Zn at doses up to 100 mg/ml did not i”