全文获取类型
收费全文 | 167695篇 |
免费 | 6778篇 |
国内免费 | 935篇 |
专业分类
175408篇 |
出版年
2022年 | 486篇 |
2021年 | 942篇 |
2020年 | 567篇 |
2019年 | 721篇 |
2018年 | 12558篇 |
2017年 | 11345篇 |
2016年 | 8757篇 |
2015年 | 2961篇 |
2014年 | 2997篇 |
2013年 | 4024篇 |
2012年 | 8716篇 |
2011年 | 17270篇 |
2010年 | 14841篇 |
2009年 | 10876篇 |
2008年 | 13696篇 |
2007年 | 15322篇 |
2006年 | 4359篇 |
2005年 | 4570篇 |
2004年 | 5107篇 |
2003年 | 4753篇 |
2002年 | 4533篇 |
2001年 | 1116篇 |
2000年 | 761篇 |
1999年 | 912篇 |
1998年 | 1194篇 |
1997年 | 875篇 |
1996年 | 794篇 |
1995年 | 759篇 |
1994年 | 744篇 |
1993年 | 713篇 |
1992年 | 642篇 |
1991年 | 637篇 |
1990年 | 585篇 |
1989年 | 621篇 |
1988年 | 545篇 |
1987年 | 522篇 |
1986年 | 458篇 |
1985年 | 592篇 |
1984年 | 750篇 |
1983年 | 655篇 |
1982年 | 761篇 |
1981年 | 795篇 |
1980年 | 721篇 |
1979年 | 499篇 |
1978年 | 557篇 |
1977年 | 527篇 |
1976年 | 525篇 |
1974年 | 498篇 |
1972年 | 516篇 |
1971年 | 537篇 |
排序方式: 共有10000条查询结果,搜索用时 0 毫秒
111.
John S Schutzbach 《Glycoconjugate journal》1997,14(2):175-182
The enzymes in the dolichol pathway are membrane-proteins that utilize a combination of hydrophilic and extremely hydrophobic
substrates. The enzymes in this pathway that have been purified and characterized to any extent have either been shown to
be stabilized by mixed phospholipid/detergent micelles, or else require a lipid matrix for catalytic activity. Further understanding
of the mechanisms of these essential enzymes may require developing methods for the reconstitution of the glycosyltransferases
and their hydrophobic substrates in appropriate lipid matrices. Abbreviations: CHO, Chinese hamster ovary; Dol, dolichol;
DAG, diacylglycerol; DOPC, dioleolylphosphatidylcholine; DOPE, dioleolyphosphatidylethanolamine; ER, endoplasmic reticulum;
PC, phosphatidylcholine; PE, phosphatidylethanolamine; PG, phosphatidylglycerol; PI, phosphatidylinositol
This revised version was published online in November 2006 with corrections to the Cover Date. 相似文献
112.
David A. Smith John L. Glover Laurace E. Townsend Diane E. Maupin 《In vitro cellular & developmental biology. Animal》1991,27(12):914-920
Summary Myocardial cell culture methods are now well established for animal and fetal human tissue. We present here a method for harvesting
and culturing adult human atrial myocardiocytes. Cells are obtained from fresh atrial tissue normally discarded after being
removed to cannulate the right atrium during open heart surgery. The atrial tissue is minced and then digested using collagenase.
The single cell suspension is initially cultured in serum-containing growth medium, then transferred to defined medium, selective
for myocardial cell growth. The cells are characterized by immunoperoxidase stains and transmission electron microscopy. The
cultured cells stain positive for myoglobin, whereas control cultured fibroblasts and endothelial cells do not. Electron microscopy
shows the presence of numerous myofibrils, Z-bodies, pleomorphic mitochondria, and secretory granules. The chronological age
of the donor was an important factor in culturing the adult tissue, the younger tissue correlated with a higher success rate.
This method provides a means for in vitro study of human adult myocardial cells and provides guidelines for appropriate atrial
tissue to use. 相似文献
113.
114.
Huw A. John 《Biochemical and biophysical research communications》1980,92(4):1223-1230
The technique of isoelectric focusing in polyacrylamide gels was used to determine whether differences could be distinguished between the heavy chains of myosin prepared from physiologically different muscles of chicken. The results of focusing a mixture of fast, slow, embryonic skeletal and cardiac myosin indicated that two different heavy chains only were resolved. In fast, slow and embryonic myosin these were present in approximately equal amounts but the chain with the more acidic isoelectric point was present in greater quantity in cardiac myosin. 相似文献
115.
116.
John A. Ryle 《BMJ (Clinical research ed.)》1936,2(3960):1067-1072
117.
The development of aspartate aminotransferase subforms in vitro was followed by densitometry after thin-film isoelectric focusing. At the same time ammonia production was measured. Each reaction can be expressed in terms of a first-order process in which 2 mol of glutamine or asparagine/mol of dimer are deamidated with a half time of 22 days. The more negatively charged subforms developed in vitro were almost fully active. Another process occurred leading to inactivation by coenzyme modification, and this was independent of deamidation. Although the enzyme formed absorbed maximally at 340nm, it was different from the naturally occurring inactive enzyme that absorbs at this wavelength. 相似文献
118.
119.
John T. Penniston 《生物化学与生物物理学报:生物膜》1982,688(3):735-739
In the absence of Mg2+, the observed activity of the erythrocyte plasma membrane Ca2+-ATPase is due to the hydrolysis of CaATP at a low rate. In the presence of Mg2+, the activity of the enzyme is much higher, but it is inhibited by high levels of free Mg2+. This inhibition appears to be due to competition of Mg2+ and Ca2+ for a site on the enzyme, rather than for ATP. 相似文献
120.
From crosses within a 2n = 43 line of Syrian hamsters (Mesocricetus auratus) lacking one derivative (der 11) of an 11;20 reciprocal translocation we have obtained homozygotes with only 42 chromosomes These animals are homozygous deficient (nullisomic) for the centromere and short arm of chromosome 11 and for the bulk of the long arm of chromosome 20. — During cytogenetic studies, we investigated the frequency patterns of early-replicating bands in the surviving derivative (der 20) at two cytologically defined sub-phases of S using short-term fibroblast cultures. These patterns were compared with those observed in the component, untranslocated arms in normal 2n = 44 cells at the same two sub-phases. — Very close agreement was found, indicating that neither the nullisomy, nor the new arm combination has interfered detectably with the pattern or programme of early band replication. 相似文献