全文获取类型
收费全文 | 3579篇 |
免费 | 277篇 |
出版年
2023年 | 12篇 |
2022年 | 30篇 |
2021年 | 44篇 |
2020年 | 30篇 |
2019年 | 43篇 |
2018年 | 54篇 |
2017年 | 53篇 |
2016年 | 97篇 |
2015年 | 134篇 |
2014年 | 124篇 |
2013年 | 214篇 |
2012年 | 230篇 |
2011年 | 223篇 |
2010年 | 148篇 |
2009年 | 126篇 |
2008年 | 188篇 |
2007年 | 204篇 |
2006年 | 216篇 |
2005年 | 173篇 |
2004年 | 179篇 |
2003年 | 168篇 |
2002年 | 173篇 |
2001年 | 92篇 |
2000年 | 96篇 |
1999年 | 78篇 |
1998年 | 45篇 |
1997年 | 46篇 |
1996年 | 38篇 |
1995年 | 26篇 |
1994年 | 22篇 |
1993年 | 34篇 |
1992年 | 63篇 |
1991年 | 53篇 |
1990年 | 52篇 |
1989年 | 37篇 |
1988年 | 32篇 |
1987年 | 40篇 |
1986年 | 34篇 |
1985年 | 22篇 |
1984年 | 16篇 |
1983年 | 14篇 |
1982年 | 14篇 |
1981年 | 16篇 |
1980年 | 11篇 |
1979年 | 16篇 |
1978年 | 8篇 |
1977年 | 9篇 |
1976年 | 8篇 |
1969年 | 13篇 |
1967年 | 9篇 |
排序方式: 共有3856条查询结果,搜索用时 31 毫秒
21.
Summary High yields of protoplasts were obtained from leaves of aseptically grown plants and calli originated from different explants, in several cultivars of Cajanus cajan L. The protoplasts divided to form cell clusters in modified KM 8p medium and developed to protocolonies after dilution with liquid Caboche's medium within three to four weeks of culture. The protocolonies proliferated to form green calli on solid Caboche's medium. No shoots or plants were obtained.Abbreviations BAP
6-benzylaminopurine
- NAA
-napthaleneacetic acid
- 2,4-D
2,4-dichlorophenoxyacetic acid
- Kin
kinetin
- Zea
zeatin
- Adn S
adenine sulphate
- GA 3
gibberellic acid 相似文献
22.
Xenopus M phase MAP kinase: isolation of its cDNA and activation by MPF. 总被引:53,自引:15,他引:38
下载免费PDF全文
![点击此处可从《The EMBO journal》网站下载免费的PDF全文](/ch/ext_images/free.gif)
Y Gotoh K Moriyama S Matsuda E Okumura T Kishimoto H Kawasaki K Suzuki I Yahara H Sakai E Nishida 《The EMBO journal》1991,10(9):2661-2668
MAP kinase is activated and phosphorylated during M phase of the Xenopus oocyte cell cycle, and induces the interphase-M phase transition of microtubule dynamics in vitro. We have carried out molecular cloning of Xenopus M phase MAP kinase and report its entire amino acid sequence. There is no marked change in the MAP kinase mRNA level during the cell cycle. Moreover, studies with an anti-MAP kinase antiserum indicate that MAP kinase activity may be regulated posttranslationally, most likely by phosphorylation. We show that MAP kinase can be activated by microinjection of MPF into immature oocytes or by adding MPF to cell-free extracts of interphase eggs. These results suggest that MAP kinase functions as an intermediate between MPF and the interphase-M phase transition of microtubule organization. 相似文献
23.
H Kitagawa H Nakada Y Numata A Kurosaka S Fukui I Funakoshi T Kawasaki I Yamashina 《Journal of biochemistry》1988,104(5):817-821
A murine monoclonal antibody, designated as MSW 113, was generated using a human colonic cancer cell line, SW 1116, as the immunogen. MSW 113 was shown to be directed mainly to mucin-type oligosaccharide with sialyl-Lea antigens. The reactivity of MSW 113 to sialyl-Lea was stronger than that of NS 19-9, which is believed to be raised against the same determinant group. MSW 113 binds to sialyl-Lea-ol, LS-tetrasaccharide a, and disialyllacto-N-tetraose with higher affinities, compared to NS 19-9. These two antibodies could clearly be distinguished in that MSW 113 bound to sialic acid but not to fucose, whereas NS 19-9 bound to fucose but not to sialic acid. Thus, MSW 113 is directed more toward sialic acid-containing terminal structures while NS 19-9 is directed toward fucose-containing internal structures. MSW 113 was found to be useful for detecting antigens in the bloodstream of patients, especially those with pancreas cancer. Even NS 19-9 negative patient sera were positive for MSW 113. 相似文献
24.
Site-directed mutagenesis of the alpha subunit of tryptophan synthase from Salmonella typhimurium 总被引:1,自引:0,他引:1
S A Ahmed H Kawasaki R Bauerle H Morita E W Miles 《Biochemical and biophysical research communications》1988,151(2):672-678
Site-specific mutagenesis has been used to prepare two mutant forms of the alpha subunit of tryptophan synthase from Salmonella typhimurium in which either cysteine-81 or cysteine-118 is replaced by a serine residue. These mutant proteins are potentially useful for x-ray crystallographic studies since a heavy metal binding site is specifically eliminated in each mutant. The purified mutant proteins are fully active in four reactions catalyzed by the wild type alpha 2 beta 2 complex of tryptophan synthase. However, the mutant alpha 2 beta 2 complexes dissociate more readily and are less heat-stable than the wild type alpha 2 beta 2 complex. Thus, cysteine-81 and cysteine-118 of the alpha subunit serve structural but not functional roles. 相似文献
25.
In order to investigate whether endogenous GHRH and somatostatin were involved in the mechanism of the paradoxical GH rise after TRH injection, changes in serum GH and plasma GHRH were examined before and after TRH injection in 12 cancer patients and changes in serum TSH and GH were similarly studied in 76 cancer patients including 31 GH-responders and 45 GH-nonresponders to TRH. TRH stimulated GH secretions without altering the circulating GHRH concentration in 4 of the 12 cancer patients. There was neither a significant correlation between the increase from the basal to maximum GH and GHRH after TRH injection in the 12 cancer patients nor a reciprocal relationship between the increase in GH and TSH after TRH injection in the 76 cancer patients. These findings suggested that the paradoxical GH rise after TRH injection in cancer patients was exerted by its direct action at the pituitary level, and not mediated through the hypothalamus. 相似文献
26.
Microtubule-binding domain of tau proteins 总被引:12,自引:0,他引:12
H Aizawa H Kawasaki H Murofushi S Kotani K Suzuki H Sakai 《The Journal of biological chemistry》1988,263(16):7703-7707
Limited chymotryptic digestion of whole tau proteins produced a fragment of Mr 14,000 (CT14), which was able to bind to microtubules reconstituted from tubulin alone in the presence of taxol. This fragment was also found to persist in microtubules when microtubules consisting of tau proteins and tubulin were digested by chymotrypsin. Analysis of amino acid composition revealed that CT14 was rich in lysine and proline residues, suggesting unique structure of microtubule-binding domain of tau proteins. Amino-terminal sequence of CT14 was determined to be Ser-Ser-Pro-Gly-Ser-Pro-Gly-Thr-Pro-Gly-Ser-Arg-Ser-Arg-X-Pro-Ser-Leu-Pr o. No heterogeneity was detected in this amino-terminal sequence of 19 residues. Five species of polypeptides consisting of tau proteins were separated from each other by gel electrophoresis and subjected to chymotryptic digestion. CT14 was produced from each of the tau polypeptides by chymotryptic digestion, indicating that all tau polypeptides have a common microtubule-binding domain. 相似文献
27.
Detection and characterization of a novel factor that stimulates DNA polymerase alpha 总被引:2,自引:0,他引:2
A novel factor that stimulates DNA polymerase alpha activity on poly(dA) X oligo(dT) has been identified and partially purified from mouse FM3A cells. The assay system for the factor contained poly(ethylene glycol) 6000. The activities of DNA polymerase alpha on poly(dA) X oligo(dT) in the presence and absence of the stimulating factor were increased greatly by the addition of poly(ethylene glycol). Stimulation by the factor was observed at all the primer to template ratios tested from 0.01 to 0.3. The highest activity was observed at the ratio of 0.05, corresponding to about 3.3 primers on one template in the presence of the factor. The concentration of DNA polymerase alpha used in the assay affected the stimulation by the factor, and the stimulation became more prominent at concentrations of the enzyme lower than 0.04 unit per assay. The stimulating factor lowered the Km value of DNA polymerase alpha for the template-primer, though they had no effect on the Km value for dTTP substrate. The results of product analysis suggested that the stimulation by the factor is mainly due to the increase in the initiation frequency of DNA synthesis from the primers. The stimulating factor specifically stimulated DNA polymerase alpha but not DNA polymerases beta and gamma. Furthermore, the factor formed a complex with DNA polymerase alpha under a certain condition. 相似文献
28.
P B Hausman H Kawasaki R M O'Hara M Minami D H Sherr M E Dorf 《Journal of immunology (Baltimore, Md. : 1950)》1986,137(12):3717-3725
The role of accessory cell populations in the generation of effector suppressor (Ts3) cells was studied. By using an in vitro culture system, it was previously determined that the induction of NP-specific effector suppressor activity requires T cells, antigen, and an anti-idiotypic B cell population. We now demonstrate that the generation of Ts3 cells in this system also requires accessory cells. The accessory population appears to play a role in the processing and presentation of antigen. These antigen-presenting accessory cells are required early in the induction phase of Ts3 generation. These accessory cells can present NP coupled to immunogenic or non-immunogenic polypeptide carriers, including polymers of L-amino acids. However, NP coupled to polymers of poorly metabolized D-amino acids fail to induce suppressor T cell generation. Furthermore, the data demonstrate that an H-2 homology must exist between the Ts3 precursors and the antigen-presenting cell population if suppressor activity is to be generated. We also characterize the differential genetic restrictions that govern the induction of Ts3 cells that control suppression of either T cell or B cell responses. The data suggest that although I-J region encoded gene products control the induction and effector phases of suppressor cell activity as measured on T cell responses, the suppression of B cell responses appear to be controlled by I-A gene products. Possible cellular mechanisms that might explain these findings are discussed. 相似文献
29.
Kaijiro Anzai Shunsuke Kobayashi Narumi Kitamura Yuri Kanai Hiromichi Nakajima Yoshioki Suehiro Sataro Goto 《Journal of neurochemistry》1986,47(3):673-677
We isolated a mouse genomic clone that hybridized with small RNA present in the cytoplasm of the brain. The RNA was about 150 nucleotides long. This RNA seemed to be specific to the brain, since it was not found in the liver or kidney. The clone DNA contained a sequence homologous to 82-nucleotide "identifier" core sequence of cDNA clones of rat. The sequence contained a split promoter for RNA polymerase III and was flanked by a 12-nucleotide direct repeat (ATAAATAATTTA). 相似文献
30.
H Sakurai H Uchikubo T Yoshimura M Maeda K Kawasaki 《Biochemical and biophysical research communications》1985,130(3):1254-1260
Thiol-containing penta (Leu-Ala-Cys-Ser-Leu) and nona (Leu-Ala-Cys-Ser-Leu-Ile-Glu-Ser-Leu) peptides corresponding to residues 132-136 and 132-140, respectively, of apo-P450 from Psuedomonas putida were synthesized to examine heme-binding by the enzymes in the oxidized (ferric) form. The peptide-hemin complexes prepared in solution were characterized by their optical and ESR spectra. In these complexes without nitrogenous ligands, no ferric complexes in the low-spin state were observed, suggesting that simultaneous axial coordination of Cys-134 (thiolate) and Ser-139 (hydroxyl) of apo-P450cam to the heme is unlikely to occur. In the presence of nitrogenous ligands, such as py, Im and MeIm, the resulting complexes were good models of apo-P450cam-nitrogenous ligand adducts in the low-spin ferric state retaining a thiolate-Fe(III)-nitrogen axial coordination mode, as judged by their spectral pattern as well as by crystal field analysis of ESR g-values. 相似文献