首页 | 本学科首页   官方微博 | 高级检索  
文章检索
  按 检索   检索词:      
出版年份:   被引次数:   他引次数: 提示:输入*表示无穷大
  收费全文   7747篇
  免费   555篇
  国内免费   6篇
  2023年   41篇
  2022年   57篇
  2021年   188篇
  2020年   107篇
  2019年   128篇
  2018年   200篇
  2017年   146篇
  2016年   244篇
  2015年   336篇
  2014年   357篇
  2013年   527篇
  2012年   593篇
  2011年   594篇
  2010年   355篇
  2009年   349篇
  2008年   444篇
  2007年   473篇
  2006年   417篇
  2005年   412篇
  2004年   355篇
  2003年   327篇
  2002年   313篇
  2001年   128篇
  2000年   99篇
  1999年   105篇
  1998年   67篇
  1997年   71篇
  1996年   41篇
  1995年   55篇
  1994年   47篇
  1993年   53篇
  1992年   59篇
  1991年   63篇
  1990年   53篇
  1989年   54篇
  1988年   55篇
  1987年   40篇
  1986年   30篇
  1985年   35篇
  1984年   42篇
  1983年   28篇
  1982年   17篇
  1981年   24篇
  1980年   23篇
  1979年   16篇
  1978年   16篇
  1977年   20篇
  1976年   16篇
  1975年   16篇
  1974年   13篇
排序方式: 共有8308条查询结果,搜索用时 0 毫秒
61.
Krafft points of diacylglycerophosphocholines (PC) were measured in alkanes-cyclohexane solutions by differential scanning calorimetry, and it was found that they were regularly increased following the increase in alkane content in the solutions and the chain length of the alkanes. From these results it was deduced that the mixing of PC with alkanes occurred in the gel state of the PC, but not in micelles at higher temperatures above the Krafft points. where micellar solutions are provided. The penetration of alkanes into gel state PC was found to be dominated by Langmuir type interaction, and the affinity of alkanes increases with increasing in chain lengths. Above the Krafft points, the micelle formation was confirmed by using the fluorescence probe technique.  相似文献   
62.
Presence of mast cell precursors in the yolk sac of mice   总被引:3,自引:0,他引:3  
Concentration of mast-cell precursors in hematopoietic tissues of mouse embryos was evaluated by a limiting dilution method. Cells from yolk sacs, livers, and bodies of (WB x C57BL/6)F1 (hereafter called WBB6F1)- +/+ embryos were injected directly into the skin of adult WBB6F1-W/Wv mice which were genetically depleted of tissue mast cells. Concentration of mast-cell precursors was calculated from the proportion of injection sites at which mast cells did not appear. Since the concentration of mast-cell precursors in the yolk sac was about 30 times as great as that of embryonic body at Day 9.5 of the pregnancy, the mast-cell precursors seemed to be generated within the yolk sac. The concentration in the yolk sac reached the maximum level at Day 11, and then dropped markedly at Day 13. In contrast, mast-cell precursors increased from Day 11 to Day 15 in the fetal liver. As a result, the concentration of 11-day yolk sacs was comparable to that of 15-day fetal liver. Although intravenous injection of 15-day fetal liver cells (2 x 10(6)) rescued the general mast-cell depletion of WBB6F1-W/Wv mice, the intravenous injection of the same number of 11-day yolk sac cells did not rescue it. In contrast with fetal livers, yolk sacs scarcely contained hematopoietic stem cells which were measured by spleen colony formation. Therefore, the mast-cell precursors of the yolk sac may not originate from such stem cells.  相似文献   
63.
64.
65.
66.
The pattern of breakage and exchange induced by X-irradiation of human lymphocytes at G1 has been analysed in PHA transformed cultures at X1 metaphase in cells treated with trypsin. All the events observed occurred in interband segments. Moreover, as far as the autosomes were concerned, these events appear to be at random in relation to trypsin interband length but give some indication of non-randomness when total chromosome length is considered. The X and Y chromosomes, on the other hand, show far fewer breaks than would be expected whichever criterion is adopted, and in particular appear to be isolated from the autosomes with respect to the occurrence of exchange events. — The analysis of specific break points in relation to trypsin banding sequences, makes it clear that conclusions regarding chromosome rearrangements based solely on conventional preparations may be misleading.  相似文献   
67.
In the negative EOG-generating process a cation which can substitute for Na+ was sought among the monovalent ions, Li+, Rb+, Cs+, NH4+, and TEA+, the divalent ions, Mg++, Ca++, Sr++, Ba++, Zn++, Cd++, Mn++, Co++, and Ni++, and the trivalent ions, Al+++ and Fe+++. In Ringer solutions in which Na+ was replaced by one of these cations the negative EOG's decreased in amplitude and could not maintain the original amplitudes. In K+-Ringer solution in which Na+ was replaced by K+, the negative EOG's reversed their polarity. Recovery of these reversed potentials was examined in modified Ringer solutions in which Na+ was replaced by one of the above cations. Complete recovery was found only in the normal Ringer solution. Thus, it was clarified that Na+ plays an irreplaceable role in the generation of the negative EOG's. The sieve hypothesis which was valid for the positive EOG-generating membrane or IPSP was not found applicable in any form to the negative EOG-generating membrane. The reversal of the negative EOG's found in K+- , Rb+- , and Ba++-Ringer solutions was attributed to the exit of the internal K+. It is, however, not known whether or not Cl- permeability increases in these Na+-free solutions and contributes to the generation of the reversed EOG's.  相似文献   
68.
Significance of 12S Toxin of Clostridium botulinum Type E   总被引:16,自引:0,他引:16       下载免费PDF全文
The pathogenesis of type E botulism is discussed as an aspect of the physicochemical and biological properties of 12S toxins (prototoxin and trypsin-activated 12S toxin) and the Ealpha and Ebeta components of each 12S toxin. A molecular weight of 350,000 was determined for each 12S toxin and 150,000 for Ealpha and Ebeta. Owing to the structure comprising the subunits Ealpha and Ebeta, 12S toxins are much more stable than Ealpha at low pH values and high temperatures. Such was also the case with type A 19S toxin and its alpha component. The Ealpha component alone accounts for the total toxicity of type E toxin. The toxic substance detected in the blood of the animals administered 12S toxins orally or parenterally was identified as Ealpha from the molecular size and the chromatographic pattern. Prototoxin escaping from detoxification in the stomach owing to the subunit structure may undergo dissociation in the intestine to release the Ealpha component. After absorption, the activated Ealpha appeared in the circulating blood without any further signs of dissociation or enzymatic digestion.  相似文献   
69.
70.
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号