全文获取类型
收费全文 | 4406篇 |
免费 | 610篇 |
专业分类
5016篇 |
出版年
2021年 | 75篇 |
2018年 | 43篇 |
2017年 | 50篇 |
2016年 | 62篇 |
2015年 | 123篇 |
2014年 | 166篇 |
2013年 | 155篇 |
2012年 | 265篇 |
2011年 | 245篇 |
2010年 | 143篇 |
2009年 | 132篇 |
2008年 | 188篇 |
2007年 | 206篇 |
2006年 | 173篇 |
2005年 | 170篇 |
2004年 | 173篇 |
2003年 | 184篇 |
2002年 | 174篇 |
2001年 | 161篇 |
2000年 | 126篇 |
1999年 | 104篇 |
1998年 | 65篇 |
1997年 | 58篇 |
1996年 | 39篇 |
1995年 | 37篇 |
1994年 | 38篇 |
1993年 | 42篇 |
1992年 | 81篇 |
1991年 | 104篇 |
1990年 | 82篇 |
1989年 | 83篇 |
1988年 | 75篇 |
1987年 | 62篇 |
1986年 | 84篇 |
1985年 | 63篇 |
1984年 | 56篇 |
1983年 | 60篇 |
1982年 | 42篇 |
1981年 | 41篇 |
1980年 | 42篇 |
1979年 | 56篇 |
1978年 | 51篇 |
1977年 | 36篇 |
1976年 | 47篇 |
1975年 | 47篇 |
1974年 | 45篇 |
1973年 | 49篇 |
1972年 | 59篇 |
1969年 | 35篇 |
1968年 | 34篇 |
排序方式: 共有5016条查询结果,搜索用时 15 毫秒
61.
Most of the hybrid clones derived from a cross of Chinese hamster fibroblasts (DON) with rat hepatoma cells (Faza 967) showed preferential loss of rat chromosomes. Two of the hybrid clones retained the rat chromosomes, and both showed extinction of 4 liver-specific enzymes: aldolase B, liver alcohol dehydrogenase, and the inducible enzymes tyrosine aminotransferase and alanine aminotransferase. Subcloning of 1 of these hybrids, which contained 2 sets of hepatoma chromosomes and 1 set of hamster chromosomes, permitted the isolation of some clones which reexpressed 1 or more of the liver-specific enzymes. Liver alcohol dehydrogenase was the most frequently reexpressed enzyme and aldolase B the least. Tyrosine aminotransferase inducibility was reexpressed independently of basal activity, and the enzyme produced by the reexpressing hybrid cells was precipitated by a specific antiserum. No correlation was detected between the presence or absence of the marker chromosomes (large metacentrics) of the hamster parent and the extinction and reexpression of the hepatic enzymes. The results reported confirm and extend to interspecific hybrids the observation of the stable and independent reexpression of tissue-specific enzymes. 相似文献
62.
After constricting the aorta ascendens of rabbits, the influence of chronic administration of dipyridamole (8 mg/kg i.m. on 6 out of 7 days of the week for 3 months) upon heart hypertrophy, hemodynamics and the hydroxyproline content in the right and left ventricles, the incorporation rate of 2-[14C]-glycine into the actomyosin and soluble protein of the left ventricle was studied. The dipyridamole treatment had no effect on the increase in systolic pressure, the contractility index of the aorta-stenosed animals and heart rate. In contrast, the hypertrophic development, and consequently the increase in hydroxyproline concentration and the increased incorporation rate of 2-[14C]-glycine into the soluble protein were inhibited. The possible mechanism of action of dipyridamole on the development of heart hypertrophy in the rabbit is discussed. 相似文献
63.
Jan Klein Christophe Benoist Chella S. David Peter Demant Kirsten Fischer Lindahl Lorraine Flaherty Richard A. Flavell Ulrich Hämmerling Leroy E. Hood Stephen W. Hunt III Patricia P. Jones Philippe Kourilsky Hugh O. McDevitt Daniel Meruelo Donal B. Murphy Stanley G. Nathenson David H. Sachs Michael Steinmetz Susumu Tonegawa Edward K. Wakeland Elizabeth H. Weiss 《Immunogenetics》1990,32(3):147-149
64.
Critical requirement for the membrane-proximal cytosolic tyrosine residue for CD28-mediated costimulation in vivo 总被引:2,自引:0,他引:2
Harada Y Tokushima M Matsumoto Y Ogawa S Otsuka M Hayashi K Weiss BD June CH Abe R 《Journal of immunology (Baltimore, Md. : 1950)》2001,166(6):3797-3803
The YMNM motif that exists in the CD28 cytoplasmic domain is known as a binding site for phosphatidylinositol 3-kinase and Grb-2 and is considered to be important for CD28-mediated costimulation. To address the role of the YMNM motif in CD28 cosignaling in primary T cells, we generated transgenic mice on a CD28 null background that express a CD28 mutant lacking binding ability to phosphatidylinositol 3-kinase and Grb-2. After anti-CD3 and anti-CD28 Ab stimulation in vitro, the initial proliferative response and IL-2 secretion in CD28 Y189F transgenic T cells were severely compromised, while later responses were intact. In contrast to anti-CD3 and anti-CD28 Ab stimulation, PMA and anti-CD28 Ab stimulation failed to induce IL-2 production from CD28 Y189F transgenic T cells at any time point. Using the graft-vs-host reaction system, we assessed the role of the YMNM motif for CD28-mediated costimulation in vivo and found that CD28 Y189F transgenic spleen cells failed to engraft and could not induce acute graft-vs-host reaction. Together, these results suggest that the membrane-proximal tyrosine of CD28 is required for costimulation in vivo. Furthermore, these results indicate that the results from in vitro assays of CD28-mediated costimulation may not always correlate with T cell activation in vivo. 相似文献
65.
66.
67.
Superoxide radicals have been shown to play a role in the cellular injury of reperfused ischemic tissues. We examined the protective effect of superoxide dismutase (SOD), a superoxide radical scavenger, on the reperfusion injury of replanted vascularized bone grafts after 4- and 8-hour periods of ischemia in a rat model. Histologic, fluorochrome, and histomorphometric analyses showed no difference between 4-hour superoxide dismutase-treated and control grafts, with both groups appearing viable. Similar analyses of the 8-hour ischemic grafts revealed both a qualitative and statistically significant quantitative difference (p less than 0.001) between the superoxide dismutase-treated and control grafts in parameters related to viability. Our results indicated that the administration of superoxide dismutase to free vascularized grafts by means of intraarterial perfusion after prolonged periods of warm ischemia significantly enhances the survival of these grafts. 相似文献
68.
Rosane Ness-Abramof Dan Nabriski Caroline M. Apovian Mark Niven Eliahu Weiss Menachem S. Shapiro Louis Shenkman 《Obesity (Silver Spring, Md.)》2002,10(12):1217-1221
Objective: Reevaluation of the validity of the 1-mg overnight dexamethasone suppression test (ODST) as a screening test for Cushing's syndrome in obese patients. Research Methods and Procedures: Eighty-six obese patients (body mass index, 30 to 53 kg/m2) that were referred to a general endocrine outpatient clinic for evaluation of simple obesity, diabetes mellitus, hypertension, polycystic ovary disease, or pituitary tumor. One milligram dexamethasone was administered orally at 11:00 pm , and serum cortisol levels were measured the following morning between 8:00 am and 9:00 am . Suppression of serum cortisol to <80 nM (3 μg/dL) was chosen as the cut-off point for normal suppression. Patients with serum cortisol levels ≥80 nM were evaluated for Cushing's syndrome. Results: Suppression of morning cortisol levels to <80 nM occurred in 79 of the 86 obese patients. Seven patients had serum cortisol levels higher than 80 nM; five were eventually diagnosed with Cushing's syndrome and two were considered false positive results in view of normal 24-hour free urinary cortisol and normal suppression on a low dose dexamethasone suppression test (0.5 mg of dexamethasone every 6 hours for 2 days). We found a false positive rate of 2.3% for the ODST using a cut-off serum cortisol of 80 nM. Discussion: The ODST is a valid screening test for Cushing's syndrome in the obese population. The false positive rate was 2.3%, even when using a strict cut-off serum cortisol of 80 nM. Abnormal cortisol suppression in obese patients should be investigated and not be considered false positive results. 相似文献
69.
Luo Q Upadhya R Zhang H Madrid-Aliste C Nieves E Kim K Angeletti RH Weiss LM 《Microbes and infection / Institut Pasteur》2011,13(14-15):1199-1210
Glycoproteins are involved in many important molecular recognition processes including invasion, adhesion, differentiation, and development. To identify the glycoproteins of Toxoplasma gondii, a proteomic analysis was undertaken. T. gondii proteins were prepared and fractioned using lectin affinity chromatography. The proteins in each fraction were then separated using SDS-PAGE and identified by tryptic in gel digestion followed by tandem mass spectrometry. Utilizing these methods 132 proteins were identified. Among the identified proteins were 17 surface proteins, 9 microneme proteins, 15 rhoptry proteins, 11 heat shock proteins (HSP), and 32 hypothetical proteins. Several proteins had 1–5 transmembrane domains (TMD) with some being as large as 608.3 kDa. Both lectin-fluorescence labeling and lectin blotting were employed to confirm the presence of carbohydrates on the surface or cytoplasm of T. gondii parasites. PCR demonstrated that selected hypothetical proteins were expressed in T. gondii tachyzoites. This data provides a large-scale analysis of the T. gondii glycoproteome. Studies of the function of glycosylation of these proteins may help elucidate mechanism(s) involved in invasion improving drug therapy as well as identify glycoproteins that may prove to be useful as vaccine candidates. 相似文献