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排序方式: 共有233条查询结果,搜索用时 531 毫秒
1.
Deborah M. Thompson Frank W. Edens Gerald A. LeBlanc R. Michael Roe 《Pesticide biochemistry and physiology》2004,80(3):131-142
Trypsin modulating oostatic factor (TMOF), a peptide hormone originally isolated from the ovaries of adult Aedes aegypti, is currently under commercial development as a new pesticide chemistry with a novel mode of action for the control of larval mosquitoes. The objective of the current research is to evaluate potential risks of the use of TMOF as an insecticide on non-target organisms. TMOF (YDPAP6) was degraded in vitro (as determined by HPLC and LC/MS) to DPAP6, PAP6, and then AP6 by leucine aminopeptidase, a pancreatic enzyme found in the digestive system of vertebrates. The rate of degradation of TMOF and PAP6 was significantly greater than that of DPAP6, while no metabolism of AP6 was found. TMOF technical insecticide was produced on a commercial scale by recombinant yeast (heat-killed before application). The technical TMOF when administered in a single dose by gavage to male and female mice at 2000 mg dry weight/kg body weight produced no negative effects as compared to controls up to 12 days after treatment. When male and female mallard ducks were treated by gavage with 1250 mg dry weight of technical TMOF/kg body weight each day for 5 days, again no toxic effects were noted through 35 days after the last treatment. TMOF technical insecticide was also applied to the shaved skin of male and female rabbits at the rate of 2000 mg/kg for 1-2 days, with no effect. The end point observations in these in vivo experiments were mortality; changes in growth rate, behavior, body structure, and color; and possible lesions observed during necropsy. Finally, Daphnia incubated with technical TMOF in rearing water at the level of 1.0 × 106 yeast cells/ml (10 mg/ml) also demonstrated no negative effects on mortality, growth, molting, time to first brood, and production of viable neonates. It appears from these studies that TMOF can be degraded by vertebrate digestive proteases and technical TMOF is not toxic to the non-target organisms examined. 相似文献
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Akihito TAKAHASHI Ajalli RAHIM Miki TAKEUCHI Emiko FUKUI Midori YOSHIZAWA Kuniaki MUKAI Makoto SUEMATSU Hidetoshi HASUWA Masaru OKABE Hiromichi MATSUMOTO 《The Journal of reproduction and development》2016,62(1):43-49
Tubulointerstitial nephritis antigen-like 1 (Tinagl1, also known as adrenocortical zonation factor 1 [AZ-1]
or lipocalin 7) is a matricellular protein. Previously, we demonstrated that Tinagl1 expression was restricted
to extraembryonic regions during the postimplantation period and detected marked expression in mouse
Reichert’s membranes. In uteri, Tinagl1 is markedly expressed in the decidual endometrium during the
postimplantation period, suggesting that it plays a physical and physiological role in embryo development
and/or decidualization of the uterine endometrium during pregnancy. In the present study, in order to
determine the role of Tinagl1 during embryonic development and pregnancy, we generated
Tinagl1-deficient mice. Although Tinagl1–/– embryos were not
lethal during development to term, homologous matings of Tinagl1–/– females and
Tinagl1–/– males showed impaired fertility during pregnancy, including failure
to carry pregnancy to term and perinatal lethality. To examine ovarian function, ovulation was induced with
equine chorionic gonadotropin (eCG) and human chorionic gonadotropin (hCG); the number of ovulated oocytes did
not differ between Tinagl1–/– and Tinagl1flox/flox.
In vitro fertilization followed by embryo culture also demonstrated the normal
developmental potential of Tinagl1-null embryos during the preimplantation period. Our
results demonstrate that Tinagl1 deficiency affects female mice and results in subfertility phenotypes, and
they suggest that although the potential of Tinagl1–/– oocytes is normal, Tinagl1
is related to fertility in adult females but is not essential for either fertilization or preimplantation
development in vitro. 相似文献
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AIM To investigate the effect of exosomes secreted by mouse melanoma cells on the expression of Ras-related C3 botulinum toxin substrate 1 (Rac1) protein in fibroblasts. METHODS Ultracentrifugation was adopted to separete exosomes secreted by mouse melanoma B16-F10 cells. The morphological structure of exosomes was observed by negative-staining electron microscopy. The size distribution of exosomes was determined by nanoparticle tracking analysis (NTA). The exosomal markers, tumor susceptibility gene 101 (Tsg101) and tyrosinase-related protein 2 (Tyrp2), were identified by Western blot. Laser confocal microscopy was used to observe the process that mouse embryonic fibroblasts (MEF) took in exosomes during co-culture. Immunocytochemical staining and Western blot were used to detect the expression of Rac1 protein in MEF. RESULTS B16-F10 cell exosomes showed a typical tea tray-like structure, with a size range of 141~255 nm, and expressed protein markers Tsg101 and Tyrp2. The results of laser confocal microscopy showed that compared with co-culture at 0 h, a small number of exosomes appeared in the MEF at 12 h, and a large number of exosomes accumulated in the MEF after co-cultured for 24 and 36 h. Western blot analysis showed that compared with co-culture at 0 h, the expression of Rac1 protein in the MEF was significantly increased at 24 h and 36 h of co-culture (P <0.01). The results of immunocytochemical staining showed that compared with co-culture at 0 h, the positive expression level of Rac1 in the MEF cells was significantly increased at 12 h, 24 h and 36 h of co-culture (P <0.05 or P <0.01). CONCLUSION Intake of exosomes secreted by mouse melanoma cells promotes the expression of Rac1 protein in fibroblasts. 相似文献
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[目的]克隆小鼠激活素受体相互作用蛋白2(ARIP2)cDNA序列,利用大肠杆菌表达ARIP2,制备兔抗小鼠ARIP2的多克隆抗血清。[方法]采用RT-PER方法,将小鼠ARIP2基因克隆到pET-32a(+)质粒,构建ARIP2原核表达载体并转化到大肠杆菌,IgrG诱导融合蛋白的表达,经亲和层析纯化获得可溶性重组蛋白,免疫家兔后制备ARIP2抗血清,分别采用ELISA,Western blot检测抗体效价和特异性。[结果]测序结果表明重组质粒pET32a(+)-ARIP2构建成功;SDS-PAGE分析表明获得的重组蛋白为可溶蛋白;经过亲和层析后得到有效分离;Elisa法测定的抗血清效价为1:50000;Westernblot鉴定结果表明抗血清能与目的蛋白特异性结合。[结论]成功将ARIP2进行了原核表达并制备了高效价、高特异性的兔抗小鼠ARIP2抗血清,为进一步研究ARIP2功能提供了有力工具。 相似文献
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一枝蒿制剂对小鼠小肠运动作用研究 总被引:1,自引:0,他引:1
用两种一枝蒿制剂对小鼠进行小肠推进实验,以甲基硫酸新斯地明、盐酸吗啡和生理盐水为对照。结果表明:一枝蒿健胃促消化机制主要是促进小肠运动。经方差分析和多重比较,其效果相似于硫酸甲基新斯地明 相似文献