全文获取类型
收费全文 | 197篇 |
免费 | 6篇 |
国内免费 | 1篇 |
出版年
2023年 | 2篇 |
2022年 | 1篇 |
2021年 | 2篇 |
2020年 | 1篇 |
2019年 | 2篇 |
2018年 | 5篇 |
2017年 | 1篇 |
2016年 | 5篇 |
2015年 | 7篇 |
2014年 | 6篇 |
2013年 | 12篇 |
2012年 | 20篇 |
2011年 | 13篇 |
2010年 | 8篇 |
2009年 | 15篇 |
2008年 | 9篇 |
2007年 | 7篇 |
2006年 | 13篇 |
2005年 | 6篇 |
2004年 | 11篇 |
2003年 | 3篇 |
2002年 | 3篇 |
2001年 | 5篇 |
2000年 | 5篇 |
1999年 | 7篇 |
1998年 | 3篇 |
1997年 | 2篇 |
1996年 | 3篇 |
1995年 | 3篇 |
1994年 | 2篇 |
1993年 | 1篇 |
1992年 | 2篇 |
1991年 | 2篇 |
1988年 | 6篇 |
1987年 | 1篇 |
1986年 | 2篇 |
1984年 | 1篇 |
1983年 | 3篇 |
1982年 | 1篇 |
1981年 | 1篇 |
1977年 | 1篇 |
1972年 | 1篇 |
排序方式: 共有204条查询结果,搜索用时 0 毫秒
201.
202.
Marcin Okroj Leticia Corrales Anna Stokowska Ruben Pio Anna M. Blom 《Cancer immunology, immunotherapy : CII》2009,58(11):1771-1780
The complement system can be specifically targeted to tumor cells due to molecular changes on their surfaces that are recognized
by complement directly or via naturally occurring antibodies. However, tumor cells often overexpress membrane-bound complement
inhibitors protecting them from complement attack. We have previously shown that non-small cell lung cancer (NSCLC) cells,
additionally to membrane-bound inhibitors, produce substantial amounts of soluble regulators such as factor I (FI) and factor
H (FH). Since low oxygen concentration is associated with rapidly growing solid tumors, we studied how NSCLC cells protect
themselves from complement attack under hypoxic conditions. Unexpectedly, mRNA levels and secretion of both FI and FH were
significantly decreased already after 24 h exposure to hypoxia while cell viability measured by XTT assay and annexin V/7-AAD
staining was affected only marginally. Furthermore, we observed decrease of mRNA level and loss of membrane-bound complement
inhibitor CD46 and increased deposition of early (C3b) and terminal (C9) complement components on hypoxic NSCLC cells. All
three complement pathways (classical, lectin and alternative) were employed to deposit C3b on cell surface. Taken together,
our results imply that under hypoxic conditions NSCLC give up some of their available defense mechanisms and become more prone
to complement attack. 相似文献
203.
204.
J. Bujn G. Pascual R. Lpez C. Corrales M. Rodríguez F. Turgano J. M. Belln 《Cryobiology》2001,42(4):256-265
This study was designed to test a slow, controlled, automated process for the thawing of cryopreserved arteries, whereby specimen warming is synchronized with the warming of its environment. Segments of minipig iliac artery, 4-5 cm in length, were subjected to controlled, automated cryopreservation in a biological freezer at a cooling rate of 1 degrees C/min to -120 degrees C, followed by storage in liquid nitrogen at -196 degrees C for 30 days. Following storage, the arterial segments were subjected to rapid (warming rate of approximately 100 degrees C/min) or gradual (1 degrees C/min) thawing. Thawed specimens were processed for light microscopy and for scanning and transmission electron microscopy, Cell death was determined by the TUNEL method. Metalloproteinase (MMP) expression was estimated by immunohistochemical analysis. Most of the cryopreserved vessels subjected to rapid thawing showed spontaneous fractures, mainly microfractures, whereas these were absent in slowly thawed specimens. In rapidly thawed vessels, the proportion of damaged cells was double that observed in those thawed more gradually. Increased intensity and extent of MMP-2 expression was shown by rapidly thawed specimens. The slow-thawing protocol tested avoids the formation of spontaneous fractures and microfractures and the accumulation of fluid within the arterial wall tissue. This results in improved tissue preservation. 相似文献