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AIM To investigate the effects of astragaloside on the levels of sex hormone and oxidative stress in rats with polycystic ovary syndrome (PCOS). METHODS Female SD rats (n =60) were randomly divided into normal control group, model group, Diane-35 (0.339 2 mg/kg) group, low dose astragaloside (12.5 mg/kg) group and high dose astragaloside (50 mg/kg) group, with 12 rats in each group. The PCOS model was induced by letrozole (1 mg/kg), which was administered by gavage once a day for 3 weeks. After administration, the estrus cycle of the rats was observed by vaginal smear, and the ovarian index was calculated. HE staining was used to observe the histopathological changes of the ovaries. Serum levels of the sex hormones testosterone (T), estradiol (E2), luteinizing hormone (LH) and follicle-stimulating hormone (FSH) were measured by ELISA. The levels of superoxide dismutase (SOD), malondialdehyde (MDA) and glutathione peroxidase (GSH-Px) in serum and ovarian tissue were detected by colorimetry, and the protein levels of steroidogenetic acute regulatory protein (StAR) and apoptosis-related proteins cleaved caspase-3, Bax and Bcl-2 in ovarian tissue were detected by Western blot. RESULT Compared with control group, the oestrous cycle of the rats in model group was disorder, and the ovarian index was increased, ovary was polycystic. The serum levels of T, LH and MDAwere significantly increased (P <0.05), while the contents of E2, FSH and the activities of GSH-Px and SOD were significantly decreased (P <0.05). The levels of MDA, StAR, cleaved caspase-3 and Bax proteins in ovarian tissue were significantly up-regulated (P <0.05). GSH-Px and SOD activities and Bcl-2 protein levels were significantly down-regulated (P <0.05). CONCLUSION Astragalosideeffectively balances the levels of sex hormone in PCOS rats and relieves the oxidative stress injury, the mechanism may be related to the inhibition of StAR expression. 相似文献
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为了探究低氧胁迫对中华绒螯蟹血淋巴细胞影响的分子机制,实验通过使用Nova Seq 6000测序技术,检测了低氧组 (1.5±0.5) mg/L和对照组 (6.0±0.5) mg/L分别处理24 h后的中华绒螯蟹血淋巴细胞的转录组数据变化。首先,对测序得到的原始数据进行拼接、注释以及筛选,分析获得的128 614个转录本和128 614条基因,平均长度为2 634 bp (N50),Q30 > 92%。其次,以1.2倍为阈值,共筛选出1 687个差异表达基因,其中上调基因899个,下调基因788个。GO和KEGG分析发现,低氧胁迫对中华绒螯蟹血细胞的三羧酸循环、糖酵解途径、ECM-受体相互作用、间隙连接、细胞凋亡、酚氧化酶系统以及其他免疫相关基因等产生了显著影响。最后,随机挑选转录组数据中的10个基因进行实时荧光定量 PCR(qRT-PCR)验证,结果显示与转录组数据分析相一致,其中包括6个上调的基因:整合素1、铜/锌超氧化物歧化酶、磷酸肌醇3激酶、磷酸甘油酸突变酶2、PDGF/VEGF相关因子1和relish;4个下调的基因:无脊椎连接蛋白7、热休克蛋白90、线粒体ATP合成酶α和天冬氨酸转氨酶。本研究初步阐明了中华绒螯蟹血淋巴细胞短时间内应对低氧胁迫的分子机制,同时该结果也可为今后研究其他甲壳动物在应对低氧胁迫时的生理机制和分子机制提供参考。 相似文献
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AIM:To explore the inhibitory mechanism of isorhapontigenin (ISO) on the proliferation, migration and invasion of UMUC3 bladder cancer cells. METHODS:Human UMUC3 bladder cancer cells were pretreated with ISO, and the proliferation of the cells was observed under phase-contrast microscope and by ATPase assay. The expression of cyclin D1 was determined by RT-PCR and Western blotting. The cell cycle alteration was detected by flow cytometry, and the cell migration was examined by wound-healing assay. RESULTS:Over 20 μmol/L of ISO significantly inhibited the proliferation of UMUC3 cells with the IC50 of (22.5±2.8) μmol/L. The mRNA and protein levels of cyclin D1 in UMUC3 cells were markedly decreased after treatment with ISO. Exposure of UMUC3 cells to low dose (5 μmol/L) of ISO led to significant induction of G0/G1 growth arrest at both 12 h (58.82%) and 24 h (63.94%), compared with the negative control cells (47.33%) without inducing obvious apoptosis. ISO at dose of 5 μmol/L also markedly inhibited the cell migration. CONCLUSION:ISO significantly exhibits inhibitory effects on the proliferation and migration of human bladder cancer cells by down-regulation of cyclin D1 expression accompanying with G0/G1 cell cycle arrest. 相似文献
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围绕事务所内部较为典型的5种利益现象,建立了事务所和执业人员收益的数学模型,从建立的数学模型出发,对上述5种利益现象进行了经济学解释并提出了一些初步的对策及建议. 相似文献
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单生育期水分胁迫对温室葡萄根际土壤酶活性及微生物群落的影响 总被引:1,自引:0,他引:1
为明确单生育期水分胁迫对土壤酶活性和微生物群落结构的影响,选取5a生'红地球'鲜食葡萄为试验材料,采用单因素完全随机试验设计,以全生育期充分供水为对照(CK),依次在葡萄5个生育期分别设置轻度(M)和重度(S)两个水分胁迫水平进行大田试验,利用Illumina高通量测序技术分析土壤微生物的群落构成和多样性.结果表明:葡... 相似文献