Studies on the mechanism of rapid activation of protein tyrosine phosphorylation activities, particularly c-Src kinase, by TCDD in MCF10A-Reference-Cited by-同舟云学术

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Studies on the mechanism of rapid activation of protein tyrosine phosphorylation activities, particularly c-Src kinase, by TCDD in MCF10A

Published:2005-01 Issue:6 Volume:18 Page:313-321
ISSN:1095-6670
Container-title:Journal of Biochemical and Molecular Toxicology
language:en
Short-container-title:J. Biochem. Mol. Toxicol.

Author:

Mazina Olga,Park Sujin,Sano Hiromi,Wong Patrick,Matsumura Fumio

Publisher

Wiley

Subject

Health, Toxicology and Mutagenesis,Toxicology,Molecular Biology,Molecular Medicine,Biochemistry,General Medicine

Reference28 articles.

1. Benzo[a]pyrene- and TCDD-induced alterations in tyrosine phosphorylation and insulin-like growth factor signaling pathways in the MCF-10A human mammary epithelial cell line

2. 2,3,7,8-Tetrachlorodibenzo-p-dioxin causes elevation of the levels of the protein tyrosine kinase pp60c-src

3. 2,3,7,8-Tetrachlorodibenzo-p-dioxin-Induced Activation of a Protein Tyrosine Kinase, pp60src, in Murine Hepatic Cytosol Using a Cell-Free System

4. 2,3,7,8-Tetrachlorodibenzo- p -dioxin (TCDD)-mediated membrane translocation of c-Src protein kinase in liver WB-F344 cells

5. Regulation of prostaglandin endoperoxide H synthase-2 induction by dioxin in rat hepatocytes: possible c-Src-mediated pathway

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4. Quantitative Phosphoproteomic Analysis of Early Alterations in Protein Phosphorylation by 2,3,7,8-Tetrachlorodibenzo-p-dioxin;Journal of Proteome Research;2013-01-24

5. Nongenomic Route of Action of TCDD: Identity, Characteristics, and Toxicological Significance;The AH Receptor in Biology and Toxicology;2011-11-10

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