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991.
Verena Hiebl Angela Ladurner Simone Latkolik Verena M. Dirsch 《Biotechnology advances》2018,36(6):1657-1698
Nuclear receptors (NRs) represent attractive targets for the treatment of metabolic syndrome-related diseases. In addition, natural products are an interesting pool of potential ligands since they have been refined under evolutionary pressure to interact with proteins or other biological targets.This review aims to briefly summarize current basic knowledge regarding the liver X (LXR) and farnesoid X receptors (FXR) that form permissive heterodimers with retinoid X receptors (RXR). Natural product-based ligands for these receptors are summarized and the potential of LXR, FXR and RXR as targets in precision medicine is discussed. 相似文献
992.
Development of a diagnostic system for detection of specific antibodies and antigens against Middle East respiratory syndrome coronavirus
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Kunse Lee Hae Li Ko Eun‐Young Lee Hyo‐Jung Park Young Seok Kim Yeon‐Sook Kim Nam‐Hyuk Cho Man‐Seong Park Sang‐Myeong Lee Jihye Kim Hun Kim Baik Lin Seong Jae‐Hwan Nam 《Microbiology and immunology》2018,62(9):574-584
993.
百日咳、白喉、破伤风、乙型肝炎联合疫苗的实验研究 总被引:2,自引:1,他引:1
对制备无细胞百日咳菌苗、白喉、破伤风、乙型肝炎联合疫苗的实验室条件进行了初步探索,实验结果表明,联合疫苗的配方以每毫升无细胞百日咳组分15-18μg.PN、白喉类毒素30lf、破伤风类毒素7-10lf和基因工程乙肝表面抗原20μg为宜,稀释缓冲液选用0.85%NaCl溶液吸附效果较好,动物实验证明联合疫苗中各组分均安全有效。 相似文献
994.
鸡减蛋综合征病毒(EDSV—76)末端前体蛋白的基因结构分析 总被引:1,自引:0,他引:1
从中国发病鸡群中分离的鸡减蛋综合征病毒弱毒株AA-2,经常规方法提取其病毒核酸后,组建了完整的限制性内切酶PstI及HingⅢ水解片段的基因文库,并对其中HindⅢ,-SacⅠ进行了序列测定。同源比较分析证明:其L链含编码病毒末端前体蛋白,容量为580个氨基酸残基的开放读码框架。 相似文献
995.
Three years of pollen trapping data from Barro Colorado Island, Panama, are compared with local vegetation inventories. Two hypotheses relating pollen representation to ‘messy’ pollination and flower form are tested. Dioecious taxa were found to be over‐represented in pollen spectra compared with their occurrence in local forests. Similarly, anemophilous and ‘messy’ pollination types were found to be over‐represented. While anemophilous taxa were the best dispersed pollen types, zoophilous taxa were also well‐represented in dispersal classes of 20–40 m and > 40 m. Thus pollen arriving to lake sediments is most likely to be from anemophilous species or those zoophilous species exhibiting ‘messy’ pollination syndromes. Pollination mechanisms will predictably bias the fossil record against certain flower morphologies. These data are of significance to those using the fossil pollen record to reconstruct the timing and sequence of angiosperm evolution. These data help prioritize plants to be included in modern pollen reference collections and to focus the search for ‘unknown’ types on most‐likely candidate families. 相似文献
996.
Previous work documented seasonal field response dynamics of Euschistus conspersus Uhler (Heteroptera: Pentatomidae) to Euschistus spp. pheromone [methyl (2E,4Z)‐decadienoate]‐baited traps in California processing tomatoes, Lycopersicon esculentum (Miller) (Solanaceae). A laboratory phenology model has been reported for E. conspersus egg incubation to adult emergence. In the present work, reproductive and thoracic dissections were performed on female E. conspersus collected year‐round from seasonal habitats in California's Central Valley. We used these dissection data to establish relationships between the morphology of E. conspersus and time of year, habitat, sample recovery method, and female attraction to pheromone traps in commercial tomato fields. All ovariole categories, sexually immature through postreproductive, were recorded for females collected from tomatoes by plant‐beating sample throughout the growing season. Conversely, pheromone trap captures in tomatoes over the same period revealed that females entering the traps were exclusively reproductively active with matured eggs. We conclude that early season female‐biased E. conspersus pheromone trap catch can be used to establish a ‘biofix’ from which to accumulate degree days and forecast nymphal development in the field. Focusing control efforts on the more susceptible nymph stages may improve efficacy of reduced‐risk insecticides such as the neonicotinoids. Thoracic dissection results, with no significant difference in flight muscle size or color by ovariole condition, failed to support our hypothesis of a life history trade‐off between female reproductive activity and flight capability to explain a decline in female pheromone trap response during the mid‐summer tomato‐fruiting stages. The adaptive value of the observed retention of E. conspersus flight capability over the calendar year, and across reproductive stages, is discussed. 相似文献
997.
Hepatitis C (HCV) genome is highly variable, particularly in the hypervariable region 1 (HVR1) of its E2 envelope gene. The
variability of HCV genome has been a major obstacle for developing HCV vaccines. Due to B-cell HVR1 mimotopes mimicking the
antigenicity of natural HVR1 epitopes and some T-cell epitopes from the consensus sequence of HCV genes conserving among the
different HCV genotypes, we synthesized an minigene of HCV-derived multi-epitope peptide antigen (CMEP), which contains 9
B-cell HVR1 mimotopes in E2, 2 conserved CTL epitopes in C, 1 conserved CTL epitope in NS3 and 1 conserved Th epitope in NS3.
This minigene was cloned into a GST expression vector to generate a fusion protein GST-CMEP. The immunogenic properties of
CEMP were characterized by HCV infected patients’ sera, and found that the reactivity frequency reached 75%. The cross reactivity
of anti-CEMP antibody with different natural HVR1 variants was up to 90%. Meanwhile, we constructed an HCV DNA vaccine candidate,
plasmid pVAX1.0-st-CMEP carrying the recombinant gene (st) of a secretion signal peptide and PADRE universal Th cell epitope sequence in front of the CMEP minigene. Immunization of
rabbits with pVAX1.0-st-CMEP resulted in the production of antibody, which was of the same cross reactivity as the fusion protein GST-CMEP. Our findings
indicate that the HCV-derived multi-epitope peptide antigen in some degree possessed the characteristics of neutralizing HCV
epitopes, and would be of the value as a candidate for the development of HCV vaccines. 相似文献
998.
Yuko Katayama Hitoshi Tajiri Kanae Tada Shintaro Okada Wen-yan Tong Satoshi Ishido Hak Hotta 《Microbiology and immunology》1998,42(1):75-79
An infant born prematurely and infected with hepatitis C virus (HCV) one month after birth was followed for 4.5 years. The patient did not produce detectable anti-HCV antibodies until two years after the onset of hepatitis. Before seroconversion, a single clone of HCV, as determined by quasispecies of the hypervariable region (HVR) of the HCV genome, was almost exclusively found in the serum. After seroconversion, however, another distinct lineage of HCV clones replaced it within half a year. As HCV infection persisted further in the presence of anti-HCV antibodies, many derivatives of both sequence lineages emerged to exhibit the typical quasispecies feature of HVR sequences. Neither seroconversion nor the changes in HVR sequences influenced the serum aminotransferase titers. 相似文献
999.
To study the immunological features of the hepatitis C virus (HCV) envelope protein (E2 protein), new specific monoclonal antibodies (mAbs) were generated. WKA/H rats were immunized with syngeneic cells infected with a vaccinia virus expressing the E2 protein and with soluble E2 protein obtained from Chinese hamster ovary cells with a plasmid-based expression system. By screening hybridoma cells obtained from spleen cells of the immunized rats, three specific mAbs were obtained. One mAb was reactive to a peptide corresponding to the hypervariable region 1 (HVR1) in E2 protein, while the others reacted to regions outside HVR1. The significance of these antibodies for the diagnosis of HCV infection as well as for analysis of the structure of the HCV E2 protein will be discussed. 相似文献
1000.
Georgia Vasileiou Silvia Vergarajauregui Sabine Endele Bernt Popp Christian Büttner Arif B. Ekici Marion Gerard Nuria C. Bramswig Beate Albrecht Jill Clayton-Smith Jenny Morton Susan Tomkins Karen Low Astrid Weber Maren Wenzel Janine Altmüller Yun Li Bernd Wollnik André Reis 《American journal of human genetics》2018,102(3):468-479