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31.
H. Petznek M. Kleiter A. Tichy A. Fuchs-Baumgartinger C. Hohenadl 《Research in veterinary science》2014
Therapy of cats suffering from feline injection site sarcomas (FISS) is still a challenging problem, as the recurrence rate after surgery is up to 70%. Four FISS-derived primary tumour cell lines and corresponding xenograft tumour mouse models were established to evaluate the efficacy of a concomitant chemo-/radiation therapy with doxorubicin. In vitro, strongly depending upon the timing of administration, pre-treatment with 0.25 µmol doxorubicin resulted in a significant enhancement of radiation-induced (3.5 Gy) tumour cell death. This result was confirmed in vivo, where only the combined chemo-/radiation therapy resulted in a significant reduction in tumour growth compared to the respective mono-therapies with either doxorubicin or radiation. These results support the use of the concomitant chemo-/radiation therapy for adjuvant treatment of FISS, particularly in advanced or recurrent disease where surgery alone is no longer feasible. 相似文献
32.
过瘤胃保护蛋氨酸稳定性及其评定方法的研究 总被引:3,自引:0,他引:3
本研究应用双外流连续培养系统和瘤胃尼龙袋法检验动物油包被蛋氨酸在瘤胃中的稳定性。根据动物油添加比例不同(分别添加20%、30%和40%),保护性蛋氨酸分为过瘤胃保护蛋氨酸I(RPMet-I)、过瘤胃保护蛋氨酸II(RPMet-II)和过瘤胃保护蛋氨酸III(RPMet-III)。试验结果表明:与未包被蛋氨酸相比,动物油包被蛋氨酸在瘤胃中的释放率显著降低(P<0.05);动物油添加比例不同对于过瘤胃保护蛋氨酸的稳定性影响显著(P<0.05)。不同形式保护性蛋氨酸在双外流连续培养系统中的降解趋势与在瘤胃中的降解趋势相似,且应用双外流连续培养系统测定各个时间点保护性蛋氨酸的释放率简单、稳定,与瘤胃尼龙袋法相比各个时间点的释放率均存在强相关回归关系(n=5,P<0.01),因此该系统适宜于评定保护性氨基酸的稳定性。 相似文献
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Objective The physiologic mechanisms involving growth factors, including PDGF‐BB, EGF, and TGF‐β1, as potent mediators of fibroblasts and epithelial cells in corneal wound healing remain unknown. The goal of this study was to determine culture methods for equine epithelial cells and keratocytes and to investigate how exogenous growth factors influence proliferation of both cell types. Procedures Cell cultures were established from healthy corneas harvested from horses immediately following euthanasia and maintained using standard tissue culture protocols. To determine the effects of PDGF‐BB, EGF, TGF‐β1, keratocytes (1 × 105/well) and epithelial cells (2 × 105/well) were each cultured in 12 well plates and exposed separately to the growth factors. The cells were exposed to concentrations of EGF between 0 and 50 ng/mL; PDGF‐BB between 0 and 75 ng/mL; and TGF‐β1 between 0 and 10 ng/mL. Cell proliferation was measured using 3H‐thymidine assay and differences in growth determined using anova and Tukey's HSD test (P < 0.05). Results Epithelial cell and keratocyte cultures were successfully established. EGF maximally stimulated keratocyte and epithelial cells at 25 ng/mL and 5 ng/mL, respectively. PDGF‐BB maximally stimulated keratocytes and epithelial cells at 50 ng/mL and 5 ng/mL, respectively. TGF‐β1 inhibited keratocytes at 5 ng/mL and 10 ng/mL, and epithelial cells at 1 ng/mL and 2 ng/mL. Conclusions Methods were established to maintain epithelial cells and keratocytes in vitro. PDGF‐BB and EGF stimulate, while TGF‐β1 inhibits the proliferation of epithelial cells and keratocytes. These growth factors may play a role in maintenance and repair of the equine cornea. 相似文献
36.
政党文化是指政党在长期的政治实践中形成和发展起来的,为全体党员普遍认同和共同遵循的政党意识和观念。作为一个自成体系的政治组织,中国共产党有自己的政党文化系统。社会转型是当前中国共产党政党文化建设的宏观生态。社会转型往往会出现认同、信仰、整合等危机。因此,社会转型时期,中国共产党合乎逻辑的选择是大力加强自身文化建设。 相似文献
37.
影响螺旋藻生长因素的研究进展 总被引:5,自引:0,他引:5
螺旋藻具有丰富和全面的营养,同时具有重要的医疗保健价值,有着广阔的应用前景.笔者主要论述了不同的螺旋藻培养条件对其生长和产物的影响. 相似文献
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在研制猪细小病毒灭活疫苗时,应用了超滤浓缩技术,提高了合毒细胞培养液中的抗原含量。为了保证浓缩的流量,减少对滤膜的污染,对含毒细胞培养液作了预处理一离心及微滤,以便除去细胞培养液中的细胞碎片、蛋白质等大分子物质及固形微粒。超滤时选用50000Da滤膜,在20psig压力下,经过5倍浓缩的PPV细胞培养液,血凝滴度提高2个滴度以上。病毒含量测定表明,TCID50/0.2mL由107左右升至109以上,以其配制疫苗,能显著地提高疫苗的免疫原性。超滤技术具有易于操作、高效、分离精度高、没有二次污染等优点,可以根据需要选择不同的浓缩浓度,对保证疫苗的质量具有重要作用。 相似文献
40.
Yukako Tokutake Marcin Taciak Kan Sato Masaaki Toyomizu Motoi Kikusato 《Animal Science Journal》2021,92(1):e13604
Peptide transporter 1 (PepT1) is a transporter responsible for absorbing dipeptide and tripeptide in enterocytes and is upregulated by dipeptide in mammals. It has not been certain whether intestinal PepT1 expression is responsive to dipeptides in chickens because of the lack of in vitro study using the cultured enterocytes. This study established a primary culture model of chicken intestinal epithelial cells (IECs) in two-dimensional monolayer culture using collagen gel by which the response of chicken PepT1 gene expression to dipeptide stimuli was evaluated. The cultured chicken IECs showed the epithelial-like morphology attached in a patch-manner and exhibited positive expression of cytokeratin and epithelial cadherin, specific marker proteins of epithelial cells. Moreover, the chicken IECs exhibited the gene expression of intestinal cell type-specific marker, villin1, mucin 2, and chromogranin A, suggesting that the cultured IECs were composed of enterocytes as well as goblet and enteroendocrine cells. PepT1 gene expression was significantly upregulated by synthetic dipeptide, glycyl-l-glutamine, in the cultured IECs. From the results, we herein suggested that dipeptide is a factor upregulating PepT1 gene expression in chicken IECs. 相似文献