Tuyển tập báo cáo các nghiên cứu khoa học quốc tế ngành y học dành cho các bạn tham khảo đề tài: Silver nanoparticles inhibit VEGF-and IL-1 -induced vascular permeability via Src dependent pathway in porcine retinal endothelial cells | Journal of Nanobiotechnology BioMed Central Research Silver nanoparticles inhibit VEGF-and IL-1 -induced vascular permeability via Src dependent pathway in porcine retinal endothelial cells Sardarpasha Sheikpranbabuf1 Kalimuthu Kalishwaralab1 Deepak Venkataraman1 Soo Hyun Eom2 Jongsun Park3 and Sangiliyandi Gurunathan 1 Open Access Address Department of Biotechnology Division of Molecular and Cellular Biology Kalasalingam University Kalasalingam Academy of Research and Education Anand Nagar Krishnankoil-626190 Tamilnadu India 2Department of Life Science Cell Dynamics Research Center Systems Biology Research Center Gwangju Institute of Science and Technology Gwangju 500-712 South Korea and 3Cell Signaling Laboratory Cancer Research Institute Department of Pharmacology College of Medicine Chungnam National University 6 Munhwa-dong Jung-gu Taejon 301131 South Korea Email Sardarpasha Sheikpranbabu - apbsheik@ Kalimuthu Kalishwaralal - kalishbio@ Deepak Venkataraman - deepssodeep@ Soo Hyun Eom - eom@ Jongsun Park - insulin@ Sangiliyandi Gurunathan - lvsangs@ Corresponding author tEqual contributors Published 30 October 2009 Received 26 June 2009 Accepted 30 October 2009 Journal of Nanobiotechnology 2009 7 8 doi 1477-3155-7-8 This article is available from http content 7 1 8 2009 Sheikpranbabu et al licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License http licenses by which permits unrestricted use distribution and reproduction in any medium provided the original work is properly cited. Abstract The aim of this study is to determine the effects of silver nanoparticles Ag-NP on vascular endothelial growth factor VEGF -and interleukin-l beta IL-1 P -induced vascular permeability and to detect the underlying signaling mechanisms involved in endothelial cells. Porcine retinal .
