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991.
992.
Spicer Michelle Elise Radhamoni Harikrishnan Venugopalan Nair Duguid Marlyse C. Queenborough Simon A. Comita Liza S. 《Plant Ecology》2022,223(2):117-129
Plant Ecology - Studies conducted in forests have resulted in much of the ecological theory we build upon today. However, our basic understanding of forest ecology comes almost exclusively from the... 相似文献
993.
994.
In Dysdercus cingulatus, extirpation of the median neurosecretory cells inhibits flight-muscle breakdown. However, implantation of median neurosecretory cells or corpus allatum into females lacking these neurosecretory cells induces muscle histolysis. Median neurosecretory cells stimulate the corpus allatum to produce juvenile hormone which in turn induces muscle degeneration. Topical application of kinoprene induces muscle breakdown, even in males and starved virgin females. The direct participation of juvenile hormone in muscle degeneration is further confirmed by observations on the effect of precocene II which inhibits muscle histolysis in many individuals. The endocrine basis of vitellogenesis and flight-muscle degeneration could be identical; vitellogenesis however appears to require a higher threshold concentration of juvenile hormone. 相似文献
995.
Panda Debashish Mohanty Subham Allen Maximilian L. Dheer Arjun Sharma Ajay Pandey Puneet Lee Hang Singh Randeep 《Acta theriologica》2023,68(2):129-141
Mammal Research - Scavenging of carrion is an important ecological process that influences ecological communities and food webs. The competitive inter- and intra-specific interactions in... 相似文献
996.
Distribution of the zot (zonula occludens toxin) gene among strains of Vibrio cholerae 01 and non-01 总被引:4,自引:0,他引:4
Tadahiro Karasawa Tatsuya Mihara Hisao Kurazono G. Balakrish Nair Surabhi Garg T. Ramamurthy Yoshifumi Takeda 《FEMS microbiology letters》1993,106(2):143-145
Abstract The distribution of the zot gene that encodes the zonula occludens toxin, a newly described toxin of Vibrio cholerae , among clinical, environmental and food isolates of V. cholerae 01 and non-01 was investigated. Both the zot gene and the ctx gene that encode cholera toxin were found in 247 of 257 clinical strains and 62 of 415 environmental or food isolates of V. cholerae 01. The zot gene, but not the ctx gene was found in 37 strains (one clinical strain and 36 environmental or food isolates). In addition, two of 31 clinical strains and six of 98 environmental or food isolates of V. cholerae non-01 possessed both the zot gene and the ctx gene. These results demonstrated the predominantly concurrent occurrence of the zot gene and ctx genes among strains of V. cholerae 01 which suggests a possible synergistic role of ZOT in the causation of acute dehydrating diarrhea produced by V. cholerae 01. 相似文献
997.
Using a mouse monoclonal antibody (MAb) 2F raised against Vibrio cholerae non-O1 heat-stable enterotoxin (NAG-ST) which also recognizes a shared epitope of Yersinia enterocolitica heat-stable enterotoxin (Y-ST), a competitive enzyme-linked immunosorbent assay (ELISA) was developed for independent detection of NAG-ST and Y-ST. There was good concordance between the Y-ST ELISA and the suckling mouse assay (SMA) for detection of Y-ST from test strains of Y. enterocolitica, and the Y-ST ELISA can effectively replace the SMA for routine detection of Y-ST. On the contrary, evaluation of the NAG-ST ELISA and the SMA using 139 strains of V. cholerae non-O1 showed discordant results and this was attributed to the presence of the suckling mice active factor(s) such as El Tor hemolysin and to the production of low amounts of NAG-ST. Concentration of culture supernatants of V. cholerae non-O1 followed by heating at 100 C was essential to obtain reproducible results by both the NAG-ST ELISA and the SMA. The ELISA developed in this study can be used for the identification of biologically active strains. While recently genetic methods such as polymerase chain reaction became available and were very reliable and simple techniques, the ELISA in this study has an advantage in detecting biologically toxic gene products of the strains. The genetic methods cannot differentiate silent STa genes which we often encounter in the case of Y. enterocolitica. 相似文献
998.
999.
Progesterone receptor structure and function altered by geldanamycin, an hsp90-binding agent. 总被引:21,自引:7,他引:14 下载免费PDF全文
D F Smith L Whitesell S C Nair S Chen V Prapapanich R A Rimerman 《Molecular and cellular biology》1995,15(12):6804-6812
The assembly of progesterone receptor (PR) heterocomplexes in vitro involves at least eight components of the molecular chaperone machinery, and as earlier reports have shown, these proteins exhibit complex, dynamic, but ordered, interactions with one another and PR. Using the selective hsp90 binding agent geldanamycin (GA), we have found that PR assembly in vitro can be arrested at a previously observed intermediate assembly step. Like mature PR complexes, the intermediate complexes contain hsp90, but they differ from mature complexes by the presence of hsp70, p60, and p48 and the absence of immunophilins and p23. Arrest of PR assembly is likely due to GA's ability to directly block binding of p23 to hsp90. An important functional consequence of GA-mediated assembly arrest in vitro is the inability of the resulting PR complexes to bind progesterone, despite the presence of hsp90 in the receptor complexes. The biological significance of the in vitro observations is demonstrated by GA's ability to (i) rapidly block PR's hormone binding capacity in intact cells and (ii) alter the composition of COS cell PR complexes in a manner similar to that observed during in vitro reconstitutions. An updated model for the cyclic assembly pathway of PR complexes that incorporates the present findings with earlier results is presented. 相似文献
1000.
The in vitro effect of histamine and its antagonists, cimetidine and clemastine fumarate, on natural killer (NK) and antibody-dependent cellular Cytotoxicity (ADCC) activities of human lymphocytes was investigated. The histamine 1 (H1) antagonist, clemastine fumarate, and the histamine 2 (H2) antagonist, cimetidine, but not histamine alone, inhibited the NK and ADCC activities of lymphocytes when added directly to the mixture of effector and target cells in a 51Cr-release assay. This inhibition was proportional to the concentration of drugs added and was observed at various effector to target ratios against several targets. H1 and H2 antagonists also inhibited NK activities of T cells as well as Percoll-separated, NK-enriched effector cells. The inhibition was significantly reversed by histamine. In target binding assays, clemastine fumarate and cimetidine also decreased the target binding capacity of effector lymphocytes. Further, PBL precultured with histamine (10?3–10?4M) for 24 hr showed a significant decrease in their NK and ADCC activities. In coculture experiments, PBL precultured with histamine suppressed the NK activity of normal autologous effector lymphocytes. PBL precultured with histamine showed an increased number of OKT8+ cells, as estimated using monoclonal antibodies. The suppression of Cytotoxicity was not due to either direct toxicity, steric hindrance, crowding, or cell death, but by functionally viable suppressor cells. An immunoregulatory role for histamine in NK and ADCC reactions is proposed. 相似文献