全文获取类型
收费全文 | 5647篇 |
免费 | 431篇 |
国内免费 | 2篇 |
出版年
2021年 | 42篇 |
2019年 | 44篇 |
2018年 | 57篇 |
2017年 | 59篇 |
2016年 | 83篇 |
2015年 | 131篇 |
2014年 | 140篇 |
2013年 | 209篇 |
2012年 | 244篇 |
2011年 | 252篇 |
2010年 | 168篇 |
2009年 | 141篇 |
2008年 | 229篇 |
2007年 | 280篇 |
2006年 | 276篇 |
2005年 | 265篇 |
2004年 | 290篇 |
2003年 | 230篇 |
2002年 | 271篇 |
2001年 | 116篇 |
2000年 | 96篇 |
1999年 | 93篇 |
1998年 | 87篇 |
1997年 | 80篇 |
1996年 | 78篇 |
1995年 | 70篇 |
1994年 | 71篇 |
1993年 | 78篇 |
1992年 | 99篇 |
1991年 | 75篇 |
1990年 | 76篇 |
1989年 | 73篇 |
1988年 | 65篇 |
1987年 | 66篇 |
1986年 | 47篇 |
1985年 | 67篇 |
1984年 | 81篇 |
1983年 | 58篇 |
1982年 | 72篇 |
1981年 | 58篇 |
1980年 | 72篇 |
1979年 | 54篇 |
1978年 | 60篇 |
1977年 | 54篇 |
1976年 | 51篇 |
1975年 | 46篇 |
1974年 | 50篇 |
1972年 | 49篇 |
1970年 | 45篇 |
1969年 | 41篇 |
排序方式: 共有6080条查询结果,搜索用时 46 毫秒
101.
Ultrasensitive bioluminescence immunoassays for the determination of peptides and proteins (illustrated with human urinary kallikrein, bradykinin and the determination of human urinary kallikrein antibody titres) have been developed. The usable ranges of the standard curves are from 5 pg to 5000 pg per litre. The relative intra-assay coefficients of variation of the tests were between 2% and 6%, and the inter-assay coefficients of variation between 4% and 12%. 相似文献
102.
Jürgen Beckmann Armin Mehlich Werner Schröder Herbert R. Wenzel Harald Tschesche 《The protein journal》1989,8(1):101-113
The semisynthesis of homologues of aprotinin, the bovine pancreatic trypsin inhibitor, is described. The P1 lysine15 residue was replaced by two methods. The first procedure, which consisted of two enzymatic steps for the incorporation of other amino acids has previously been described. The second approach consisted of six steps of both enzymatic and chemical nature. The modified inhibitor, in which the lysine15-alanine16 peptide bond is hydrolyzed, was used as the starting material. All carboxyl groups of the modified inhibitor were esterified with methanol; the lysine15 methylester group was then selectively hydrolyzed. Afterward, lysine15 itself was split off. Arginine, glutamic acid, methionine, andl-2-aminohexanoic acid (norleucine, Nle) were incorporated using water-soluble carbodiimide combined with an acylation catalyst. The methylester group was used to prevent polymerization. The reactive-site peptide bonds were resynthesized using either chymotrypsin or trypsin. 相似文献
103.
104.
H Werner M Adamo W L Lowe C T Roberts D LeRoith 《Molecular endocrinology (Baltimore, Md.)》1989,3(2):273-279
The developmental regulation of rat brain-derived/Hep G2 glucose transporter gene expression was studied by means of Northern blot hybridization, using a rat brain glucose transporter cDNA probe, in order to directly quantify steady state glucose transporter mRNA levels. The results obtained showed different tissue-specific patterns of glucose transporter mRNA levels during ontogenesis; while in brain there was a sustained increase in the levels of the message from 20 days embryogenesis until 50 days postnatal, other organs such as heart, lung, liver, and muscle expressed maximal levels of the glucose transporter mRNA in 20-day fetuses and 1-day neonates, decreasing subsequently to very low levels. The relative expression of the glucose transporter mRNA in the different tissues, at both fetal and adult stages, was analyzed using a solution hybridization-RNase protection assay. This approach revealed that, while the heart expresses the highest levels of glucose transporter mRNA at 20 days of fetal life, the brain shows the highest levels at the adult stage. These results indicate a tissue-specific ontogenic pattern of glucose transporter gene expression, suggesting a developmental role for this glucose transporter gene product. 相似文献
105.
M. Rosa Pinol Urs Kägi Claus W. Heizmann Brigitte Vogel Jean-Marc Séquier Werner Haas Willi Hunziker 《Journal of neurochemistry》1990,54(6):1827-1833
Many processes in the CNS depend on calcium. The calcium signal is transduced into an intracellular response via Ca2(+)-binding proteins, including calbindin D-28K. In many laboratories, polyclonal antibodies against chicken intestinal calbindin D-28K have been used to study its localization in the brain (normal and degenerated) of various species, including humans, but some of these antisera cross-reacted with other proteins, including calretinin. We purified recombinant rat brain calbindin D-28K to raise antisera in rabbits and purified a recombinant rat-chicken calbindin D-28K hybrid protein to immunize mice for the generation of monoclonal antibodies. These antisera were highly specific for calbindin D-28K, as demonstrated by two-dimensional Western blotting analysis. Immunohistochemical analyses combined with in situ hybridization studies demonstrated that calbindin D-28K in the Purkinje cells of the cerebellum is independent of vitamin D. The antibodies described here will be important tools for studying the regulation of expression of calbindin D-28K and its biological function in the brain and in the PNS. 相似文献
106.
107.
Extensive changes in cytokeratin expression patterns in pathologically affected human gingiva 总被引:4,自引:0,他引:4
Franz X. Bosch Jean-Pierre Ouhayoun Bernhard L. Bader Christine Collin Christine Grund Inchul Lee Werner W. Franke 《Virchows Archiv. B, Cell pathology including molecular pathology》1989,58(1):59-77
The stratified squamous epithelium of the oral gingiva and the hard palate is characterized by a tissue architecture and a cytoskeletal composition similar to, although not identical with, that of the epidermis and fundamentally different from that of the adjacent non-masticatory oral mucosa. Using immunocytochemistry with antibodies specific for individual cytokeratins, in situ hybridization and Northern blots of RNA with riboprobes specific for individual cytokeratin mRNAs, and gel electrophoresis of cytoskeletal proteins of microdissected biopsy tissue samples, we show changes in the pattern of expression of cytokeratins and their corresponding mRNAs in pathologically altered oral gingiva. Besides a frequently, although not consistently, observed increase in the number of cells producing cytokeratins 4 and 13 (which are normally found as abundant components in the sulcular epithelium and the alveolar mucosa but not in the oral gingiva) and a reduction in the number of cells producing cytokeratins 1, 10 and 11, the most extensive change was noted for cytokeratin 19, a frequent cytokeratin in diverse one-layered and complex epithelia. While in normal oral gingiva cytokeratin 19 is restricted to certain, sparsely scattered cells of --or near--the basal cell layer, probably neuroendocrine (Merkel) cells, in altered tissue of inflamed samples it can appear in larger regions of the basal cell layer(s) and, in apparently more advanced stages, also in a variable number of suprabasal cells. Specifically, our in situ hybridization experiments show that this altered suprabasal cytokeratin 19 expression is more extended at the mRNA than at the protein level, indicating that cytokeratin 19 mRNA synthesis may be a relatively early event during the alteration. These changes in cytokeratin expression under an external pathological influence are discussed in relation to other factors known to contribute to the expression of certain cytokeratins and with respect to changes occurring during dysplasia and malignant transformation of oral epithelia. 相似文献
108.
Surjit Singh Gernot Fritze Bingliang Fang Shoji Harada Yong K. Paik Rolf Eckey Dharam P. Agarwal H. Werner Goedde 《Human genetics》1989,83(2):119-121
Summary Genotyping of mitochondrial aldehyde dehydrogenase (ALDH I) was performed in enzymatically amplified DNA of 20 Chinese, Japanese and South Korean families (85 individuals) and in 113 unrelated persons by employing allele-specific oligonucleotide probes and dot blot hybridization. Genotyping individuals with phenotypic deficiency of ALDH I activity always showed the presence of at least one mutant allele. The data are compatible with a model assuming dominant inheritance of the mutant allele, which we have previously suggested on the basis of a population study. 相似文献
109.
Duplication of an Xp segment that includes the ZFX locus causes sex inversion in man 总被引:6,自引:6,他引:0
Gerd Scherer Werner Schempp Carlo Baccichetti Elisabetta Lenzini Franca Dagna Bricarelli Laura Doria Lamba Carbone Ulrich Wolf 《Human genetics》1989,81(3):291-294
Summary Two 46,XY females with tandem duplications of an X short arm segment were studied by cytogenetic and Southern blot analysis. The results show that the duplicated segment in each case included the Xp21.2–Xp22.2 interval, resulting in a double dose of ZFX on the single active X chromosome. The results from our two cases, in conjunction with those reported by other workers, lead us to conclude that the duplication is the reason for the sex inversion. If ZFY and ZFX are indeed sex-determining gene loci, these findings favour a model of sex determination characterized by antagonistic interaction between these genes. 相似文献