Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Surabhi Vashistha"'
Epidermal growth factor receptor (EGFR) plays a critical role in oncogenesis, which makes it an attractive target for pharmacologic inhibition. Yet, EGFR inhibition with tyrosine kinase inhibitors (TKI) does not result in a measurable and sustainable
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0315c87c5776af4cb7df505da99cced8
https://doi.org/10.1158/1541-7786.c.6542269
https://doi.org/10.1158/1541-7786.c.6542269
Supplementary Figures 1-5 from Cancer-Associated Fibroblasts Derived from EGFR-TKI–Resistant Tumors Reverse EGFR Pathway Inhibition by EGFR-TKIs
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::333d48bfd1a489acce041fbf2725251d
https://doi.org/10.1158/1541-7786.22519051
https://doi.org/10.1158/1541-7786.22519051
Publikováno v:
Molecular Cancer Research. 8:809-820
Epidermal growth factor receptor (EGFR) plays a critical role in oncogenesis, which makes it an attractive target for pharmacologic inhibition. Yet, EGFR inhibition with tyrosine kinase inhibitors (TKI) does not result in a measurable and sustainable
Publikováno v:
Journal of Cancer Science & Therapy.
Interferon ? (IFN?), a potent inhibitor of proliferation,inducer of apoptosis and an immune modulator of mammalian cells, has been used as an anticancer agent in cancer therapy. Several molecular mechanisms, depending upon the differences in the line
Publikováno v:
The Cancer Handbook
Translational research examining the progression and treatment of prostate cancer (PCa) is benefited significantly from the availability of models that faithfully mimic the in vivo disease. It is advantageous if the model system maximally recapitulat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::56f99f833e47383a9544516d1a09e523
https://doi.org/10.1002/9780470025079.chap382
https://doi.org/10.1002/9780470025079.chap382
Publikováno v:
Cytokine. 37(2)
We had earlier shown that human foetal epithelial cells (WISH), growth-inhibited by interferon gamma (IFNgamma), were reversibly detained at a point prior to DNA synthesis. In the present study, we determined the window of action of IFNgamma in the G
Autor:
Surabhi Vashistha, Parthasarathi Ajitkumar, Kumaravel Somasundaram, Jeena Joseph, Giridhar Mudduluru, Sini Antony
Histone deacetylase (HDAC) inhibitors induce growth arrest and apoptosis in a variety of human cancer cells. Sodium butyrate (NaB), a short chain fatty acid, is a HDAC inhibitor and is produced in the colonic lumen as a consequence of microbial degra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d714ba6438902aaa2f74f384ec97e0f9
http://eprints.iisc.ernet.in/2122/
http://eprints.iisc.ernet.in/2122/
Publikováno v:
BioEssays; Apr2013, Vol. 35 Issue 4, p366-376, 11p