๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Tumor Angiogenesis Inhibitors

โœ Scribed by S. M. Kiselev; S. V. Lutsenko; S. E. Severin; E. S. Severin


Book ID
111538037
Publisher
Springer
Year
2003
Tongue
English
Weight
449 KB
Volume
68
Category
Article
ISSN
0006-2979

No coin nor oath required. For personal study only.


๐Ÿ“œ SIMILAR VOLUMES


Metalloproteinases and their inhibitors
โœ Madeleine M. Handsley; Dylan R. Edwards ๐Ÿ“‚ Article ๐Ÿ“… 2005 ๐Ÿ› John Wiley and Sons ๐ŸŒ French โš– 298 KB ๐Ÿ‘ 1 views

## Abstract Angiogenesis is the process by which new blood vessels are formed from preexisting vasculature. It is an essential feature of the female reproductive cycle, embryonic development and wound repair. Angiogenesis has also been identified as a causal or contributing factor in several pathol

Angiogenesis inhibitors overcome tumor i
โœ Arjan W. Griffioen; Cora A. Damen; Kevin H. Mayo; Annemarie F. Barendsz-Janson; ๐Ÿ“‚ Article ๐Ÿ“… 1999 ๐Ÿ› John Wiley and Sons ๐ŸŒ French โš– 154 KB

We report here that tumor angiogenesis-mediated endothelial cell (EC) anergy can be overcome by inhibitors of angiogenesis. We found previously that tumor growth, known to be dependent on angiogenesis, results in down-regulation of endothelial adhesion molecules and tumor EC anergy to inflammatory s

Histone deacetylase inhibitor FK228 inhi
โœ Ho Jeong Kwon; Myoung Sook Kim; Min Jung Kim; Hidenori Nakajima; Kyu-Won Kim ๐Ÿ“‚ Article ๐Ÿ“… 2001 ๐Ÿ› John Wiley and Sons ๐ŸŒ French โš– 796 KB

## Abstract FK228 (formerly FR901228) was recently isolated from __Chromobacterium violaceum__ as a potent antitumor agent and its biologic target protein was identified as histone deacetylase (HDAC). Because of its unique chemical structure (__i.e.__, bicyclic depsipeptide) and activity profile in