全文获取类型
收费全文 | 2938篇 |
免费 | 156篇 |
专业分类
3094篇 |
出版年
2021年 | 17篇 |
2020年 | 17篇 |
2019年 | 32篇 |
2018年 | 33篇 |
2017年 | 29篇 |
2016年 | 50篇 |
2015年 | 68篇 |
2014年 | 70篇 |
2013年 | 261篇 |
2012年 | 182篇 |
2011年 | 183篇 |
2010年 | 101篇 |
2009年 | 123篇 |
2008年 | 161篇 |
2007年 | 170篇 |
2006年 | 163篇 |
2005年 | 163篇 |
2004年 | 172篇 |
2003年 | 165篇 |
2002年 | 160篇 |
2001年 | 46篇 |
2000年 | 42篇 |
1999年 | 40篇 |
1998年 | 36篇 |
1997年 | 39篇 |
1996年 | 31篇 |
1995年 | 35篇 |
1994年 | 38篇 |
1993年 | 29篇 |
1992年 | 39篇 |
1991年 | 24篇 |
1990年 | 28篇 |
1989年 | 23篇 |
1988年 | 27篇 |
1987年 | 23篇 |
1986年 | 11篇 |
1985年 | 20篇 |
1984年 | 28篇 |
1983年 | 9篇 |
1982年 | 13篇 |
1981年 | 27篇 |
1980年 | 12篇 |
1979年 | 14篇 |
1977年 | 16篇 |
1976年 | 13篇 |
1974年 | 10篇 |
1973年 | 16篇 |
1972年 | 9篇 |
1970年 | 11篇 |
1966年 | 8篇 |
排序方式: 共有3094条查询结果,搜索用时 0 毫秒
11.
Immunohistochemical localization of Na+-dependent glucose transporter in rat jejunum 总被引:2,自引:0,他引:2
Kuniaki Takata Toshiko Kasahara Michihiro Kasahara Osamu Ezaki Hiroshi Hirano 《Cell and tissue research》1992,267(1):3-9
Summary Glucose is actively absorbed via a Na+-dependent active glucose transporter (Na-GT) in the small intestine. We raised a polyclonal antibody against the peptide corresponding to amino acids 564–575 of rabbit intestinal Na-GT, and localized it immunohistochemically in the rat jejunum. By means of immunofluorescence staining, Na-GT was located at the brush border of the absorptive epithelial cells of the intestinal villi. Electron-microscopic examination showed that Na-GT was localized at the plasma membrane of the apical microvilli of these cells. Little Na-GT was found at the basolateral plasma membrane. Along the crypt-villus axis, all of the absorptive epithelial cells in the villus were positive for Na-GT. In addition to the brush border staining, the supranuclear positive staining, which was shown to be the Golgi apparatus by use of electron microscopy, was seen in cells located between the base to the middle of the villus. Cells in crypts exhibited little or no staining for Na-GT. Goblet cells scattered in the intestinal epithelium were negative for Na-GT staining. These observations show that Na-GT is specific to the apical plasma membrane of the absorptive epithelial cells, and that the onset of Na-GT synthesis may occur near the crypt-villus junction. 相似文献
12.
A leptomycin B resistance gene of Schizosaccharomyces pombe encodes a protein similar to the mammalian P-glycoproteins 总被引:4,自引:0,他引:4
Kazunori Nishi Minoru Yoshida Marie Nishimura Mitsuo Nishikawa Makoto Nishiyama Sueharu Horinouchi Teruhiko Beppu 《Molecular microbiology》1992,6(6):761-769
Screening for leptomycin B (LMB)-resistant transformants in a gene library constructed in Schizosaccharomyces pombe with the chromosomal DNA of an LMB-resistant mutant of S. pombe and with multicopy plasmid pDB248' as the vector led to the isolation of a gene, named pmd1+, encoding a 1362-amino-acid protein. This protein showed great similarity in amino acid sequence to the mammalian P-glycoprotein encoded by the multidrug resistance gene, mdr, and the Saccharomyces cerevisiae a-factor transporter encoded by STE6. In addition, computer analyses predicted that the protein encoded by pmd1+ formed an intramolecular duplicated structure and each of the halves contained six transmembrane regions as well as two ATP-binding domains, as observed with the P-glycoproteins and the STE6 product. Consistent with this was that S. pombe cells containing the pmd1+ gene on a multicopy plasmid showed resistance not only to LMB but also to several cytotoxic agents. The pmd1 null mutants derived by gene disruption were viable and hypersensitive to these agents. All these data suggest that the pmd1+ gene encodes a protein that is a structural and functional counterpart of mammalian mdr proteins. 相似文献
13.
Specific binding sites for atrial natriuretic peptide (ANP) in cultured mesenchymal nonmyocardial cells from rat heart 总被引:3,自引:0,他引:3
Y Hirata M Tomita S Takata I Inoue 《Biochemical and biophysical research communications》1985,131(1):222-229
Specific binding sites for atrial natriuretic peptide (ANP) were studied in cultured mesenchymal nonmyocardial cells (NMC) from rat heart. Binding study using 125I-labeled synthetic rat (r) ANP revealed the presence of a single class of high-affinity binding sites for rANP in cultured NMCs derived from both atria and ventricles; the apparent dissociation constant (Kd) was approximately 0.2 - 0.3 nM and the number of maximal binding sites was approximately 190,000 - 300,000 sites/cell. rANP significantly stimulated intracellular cGMP formation of cardiac NMCs in a dose-dependent manner (1.6 X 10(-8) M - 3.2 X 10(-7) M). rANP had no effect on synthesis of prostaglandin I2 by cultured cardiac NMCs. The physiological significance of ANP action on cardiac tissue remains to be determined. 相似文献
14.
A membrane-associated receptor involved in a specific uptake of formaldehyde-treated serum albumin (f-Alb) was purified from rat livers by Triton X-100 solubilization of a 105,000 X g membrane preparation and affinity chromatography on an f-Alb-Sepharose column. The purified receptor exhibited Mr = 125,000, consisting of two noncovalently linked glycoprotein components with Mr = 53,000 and Mr = 30,000, respectively. Incubation of 125I-receptor with f-Alb, but not with native albumin, resulted in a marked shift of pI value from 5.9 to 5.1, reflecting the presence of a specific ligand-receptor interaction. The receptor incorporated into liposomes displayed a saturable binding to 125I-f-Alb and the binding was effectively replaced by the presence of unlabeled f-Alb, with binding parameters being similar to those obtained from 125I-f-Alb binding to the sinusoidal liver cell membrane (Horiuchi, S., Takata, K., and Morino, Y. (1985) J. Biol. Chem. 260, 475-481). Reaction of anti-f-Alb receptor antibody with extracts of sinusoidal cells resulted in a specific precipitation of two proteins whose molecular weights were identical to those for the purified receptor. The anti-receptor IgG fraction effectively blocked 125I-f-Alb binding to the sinusoidal cell membranes. These results indicate that the purified protein represents the membrane-associated receptor which is presumably involved in a specific uptake of this ligand from the circulation. 相似文献
15.
Molecular Genetic Analysis of Myelin-Deficient Mice: Shiverer Mutant Mice Show Deletion in Gene(s) Coding for Myelin Basic Protein 总被引:17,自引:6,他引:11
16.
17.
18.
19.
Summary Spectinomycin resistant (spc
r) mutants were obtained by treating the cells of E. coli K12, W3637 with nitrosoguanidine. The compositions of ribosomal proteins were analyzed for six out of eleven such spc
r-mutants with chromatography on a carboxymethyl cellulose (CMC) column. The 30s ribosomal subunit from all of the spc
r-mutants was found to contain the altered 30-4 protein component, while no difference was detected in 50s ribosomal proteins between spc
r and spc
s bacteria.Abbreviations used CMC
carboxymethyl cellulose
-
str
streptomycin
-
spc
spectinomycin 相似文献
20.
Effect of Ethanol on the Sodium and Potassium Conductances of the Squid Axon Membrane 总被引:8,自引:6,他引:2 下载免费PDF全文
The effects of ethanol on squid giant axons were studied by means of the sucrose-gap technique. The membrane action potential height is moderately reduced and the duration sometimes shortened by ethanol in sea water. Voltage clamp experiments showed that ethanol in sea water reduced the maximum membrane conductances for sodium (g'Na) and potassium (g'K). In experiments with multiple application of ethyl alcohol to the same spot of membrane, a reduction of g'Na to 82 per cent and of g'K to 80 per cent of their value in sea water was brought about by 3 per cent ethanol (by volume) while 6 per cent caused a decrease of g'Na to 59 per cent and of g'K to 69 per cent. Ethanol has no significant effect on the steady-state inactivation of gNa (as a function of conditioning membrane potential) or on such kinetic parameters as τh or the time course of turning on gi gNa and gK. It is concluded that ethanol mainly reduces gNa and gK in the Hodgkin-Huxley terminology. 相似文献