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101.
本试验利用禽用开放式呼吸测热装置进行能量代谢试验,通过间接测热法结合替代法测定不同类型玉米在产蛋期蛋鸡饲粮中的表观代谢能和净能。选用34周龄产蛋期海兰褐蛋鸡180只,随机分为6组,每组30只。试验选用1种玉米-豆粕型基础饲粮和5种待测饲粮。待测饲粮由5种待测玉米(3种2018年10月收获的正常玉米和2种2016年收获储存3年的陈化玉米),分别以50%比例替代基础饲粮构成。试验鸡在舍内笼养,预试期7 d,正试期27 d,其中正试期分为3期,每期9 d(适应3 d、呼吸测热3 d、绝食测热3 d)。每期试验中,从每组中选择4只试验鸡,称重后分别放入呼吸测热装置的12个代谢室(每个代谢室2只),每2个代谢室对应1种饲粮,测定气体交换和排泄物总量,呼吸测热的同时进行消化代谢试验。结果表明:与基础饲粮相比,5种玉米待测饲粮的表观代谢能显著提高(P<0.05),3种正常玉米待测饲粮的净能显著高于基础饲粮和2种陈化玉米待测饲粮(P<0.05);2种陈化玉米的表观代谢能和净能显著低于3种正常玉米(P<0.05)。本试验中,3种正常玉米的表观代谢能分别为16.19、15.85、16.17 MJ/kg,2种陈化玉米的表观代谢能分别为15.12和15.06 MJ/kg;3种正常玉米的净能分别为12.39、12.57、12.25 MJ/kg,2种陈化玉米的净能分别为11.29和12.05 MJ/kg。 相似文献
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AIM To explore the expression and mechanisms of circular RNA hsa_circ_087631 in the patients with primary biliary cholangitis (PBC). METHODS RT-qPCR was used to detect the expression of hsa_circ_087631 in PBC patients and healthy controls. Hsa-miR-346-overexpressing lentiviral vector pLenti-EF1a-EGFP-F2A-Puro-CMV-MCS was constructed and transfected into human acute T cell leukemia Jurkat cells, and then the expression levels of hsa_circ_087631, Bcl-6 mRNA and interleukin-21 (IL-21) mRNA were detected by RT-qPCR. Dual-luciferase reporter assay was performed to identify the interactions between hsa_circ_087631 and hsa-miR-346. RESULTS The expression of hsa_circ_087631 in the PBC patients was significantly increased compared with the healthy subjects. Hsa-miR-346-overexpressing lentiviral vector pLenti-EF1a-EGFP-F2A-Puro-CMV-MCS was successfully constructed. The expression of hsa-miR-346 was significantly increased after the hsa-miR-346-overexpressing lentiviral vector was transfected into the Jurkat cells, while the expression levels of hsa_circ_0087631, Bcl-6 mRNA and IL-21 mRNA were significantly decreased. After wild-type or mutant hsa_circ_087631 vector and hsa-miR-346 mimics were transfected into 293T cells, the results of dual-luciferase reporter assay showed that hsa-miR-346 significantly decreased the luciferase activity of wild-type hsa_circ_087631 (P <0.01), but the regulation did not change significantly after mutation of the predicted binding site. CONCLUSION Peripheral blood hsa_circ_087631 level is elevated in the PBC patients. The hsa_circ_087631/hsa-miR-346/Bcl-6 signaling may take effect in human T cells. Hsa-miR-346 significantly reduces the expression of hsa_circ_087631, but it may not be regulated by predicted binding sites. 相似文献
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Xiang-dong LUO Jian LIU Jun ZHAO Liang-fang DAI Ya-ling CHEN Ling ZHANG Fantao ZHANG Biao-lin HU Jian-kun XIE 《农业科学学报》2018,17(2):265-275
Cold stress is a major problem in rice production. To rapidly identify genes for cold tolerance in Dongxiang wild rice(DWR, Oryza rufipogon Griff.), sequencing-based bulked segregant analysis of QTL-seq method was used to resequence the extremely resistant(R) and susceptible(S) bulks of a backcross inbred lines(BILs) population(derived from Oryza sativa×O. rufipogon) and their parents. Single nucleotide polymorphisms(SNP)-index graphs and corresponding Δ(SNPindex) graphs(at 99 and 95% confidence levels) for R-and S-bulks detected a total of 2 609 candidate SNPs, including 58 candidate cold-tolerance genes. Quantitative real-time PCR analysis revealed that 5 out of the 58 candidate genes had significant differences in expression between O. sativa and O. rufipogon. Structural variation and functional annotations of the 5 candidate genes were also analyzed, and allowed us to identify 2 insertion-deletion(InDel) markers(12-7 and 12-16) that were linked with candidate genes on chromosome 12 in DWR. These results are helpful for cloning and using cold tolerance genes from common wild rice in cultivated rice. 相似文献
107.
XU Ya-fang CHEN Chuang-fu WANG Hao FU Qiang SHI Hui-jun SUN Zhi-hua ZHANG Hui GUO Fei 《中国畜牧兽医》2016,43(6):1437-1445
In order to investigate the effect of AIR on inflammatory reaction infected by Brucellamelitensis (16M), the AIR domain of Tecpr1 gene of murine macrophages RAW264.7 were knocked down (I-A), overexpressed (O-A) and reversed (OA-IA). Using the chlorine fluorescein (DCFH-DA) as a probe, we detected the variation of ROS production and mitochondria distribution by confocal laser scanning microscopy. We observed the expression changes of NLRP3, ASC and Caspase-1 by qRT-PCR and the expression changes of IL-18,IL-1β and Caspase-1 in host cells by ELISA. The results showed that 16M could stimulate RAW264.7 cells to produce ROS by time-dependent pathway, and I-A group and O-A group showed more abnormal accumulation of mitochondrial. The results of qRT-PCR and ELISA suggested that it had effect on the expression levels of NLRP3, ASC,Caspase-1 and IL-18, IL-1β and Caspase-1 in cells of different groups. Those results indicated that with AIR gene deletion, the release amount of ROS changed, mitochondrial clustered abnormally, and AIR was closely related to the activation of inflammasomes and induction of inflammatory reactions. 相似文献
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本试验旨在研究添加复合酶对临武鸭瓜尔豆胚芽养分、氨基酸和能量利用率的影响。试验选用24只体重2.0 kg左右的健康成年临武鸭公鸭,随机分为3组,每组8个重复,每个重复1只鸭。采用绝食强饲-全收粪法进行代谢试验。1、2组试验鸭每只强饲60 g/d饲粮,2组饲粮中添加250 mg/kg的复合酶,3组强饲60 g/d无氮饲粮。测定添加复合酶对临武鸭瓜尔豆胚芽中干物质(DM)、粗蛋白质(CP)、粗脂肪(EE)、粗纤维(CF)和17种氨基酸的表观利用率、真可利用率、表观代谢能(AME)和真代谢能(TME)。结果表明,临武鸭对瓜尔豆胚芽DM、CP、EE、CF和能量的真可利用率分别为67.07%、67.57%、65.52%、82.88%和77.39%,AME和TME分别为11.34和13.31 MJ/kg,17种氨基酸的真可利用率为67.72%~93.70%;添加复合酶使临武鸭的DM、CP、EE、CF和能量的真可利用率分别提高了5.23%、8.02%、5.80%、3.66%和3.31%(P0.05),AME和TME分别提高了3.97%和3.27%(P0.05),17种氨基酸的真可利用率提高了1.73%~11.62%,其中丝氨酸、甘氨酸、亮氨酸、酪氨酸和苯丙氨酸的真可利用率显著提高(P0.05)。由此可知,添加含有蛋白酶和非淀粉多糖酶的复合酶能够提高临武鸭对瓜尔豆胚芽中养分、氨基酸和能量的利用率。 相似文献