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71.
NaCl胁迫对白蜡种子生理特性的影响   总被引:1,自引:0,他引:1  
为了给盐碱地造林树种选择提供依据,以采自秦皇岛和保定的白蜡种子为试材,采用不同浓度的NaCl胁迫处理,研究了其萌发过程中发芽率、细胞膜透性、保护酶活性、丙二醛MDA的变化,结果表明:(1)随着NaCl胁迫浓度的增加,两地白蜡种子发芽率均呈现逐渐降低的变化趋势,秦皇岛各处理的白蜡种子发芽率分别比对照降低了8.9%、52.6%、56.3%、61.6%、87.9%、91.1%,而保定的白蜡种子分别比对照降低20.2%、56.2%、68.7%、86.5%、89.9%、100.0%;(2)随着浓度的升高,种子的相对电导值、K+、Na+渗透率升高,种子的SOD酶活性降低,MDA含量增加,NaCl胁迫浓度越高,种子所受到的伤害越深;(3)0.20%浓度的NaCl胁迫对白蜡种子萌发影响不大。对于不同种源的白蜡种子,秦皇岛的白蜡种子抗盐性要优于保定的白蜡种子。  相似文献   
72.
本试验旨在探究围产期奶牛血钙浓度影响因素及其与生产性能的关系。于2018年7月20日—8月15日对北京地区36头围产期健康荷斯坦牛的血钙浓度进行测定,收集该牛场奶牛生产性能测定(DHI)报告,利用固定效应模型分析不同胎次、体况评分(BCS)、健康状况及血钙浓度变异度对血钙浓度的影响。结果表明:血钙浓度与产后天数存在显著的正向相关关系;经产牛的血钙浓度(1.40 mmol/L)极显著高于初产牛(1.31 mmol/L);不同BCS分组奶牛血钙浓度差异不显著;健康组的血钙浓度(1.41 mmol/L)显著高于患病组(1.30 mmol/L);血钙浓度变异度的大小影响奶牛的产奶量,初产奶牛低变异度组的产奶量(16.70 kg/d)显著高于中变异度组(9.75 kg/d)和高变异度组(5.63 kg/d)。本研究进一步揭示了围产期荷斯坦牛血钙浓度的变化规律以及其影响因素,为预防奶牛产后低血钙症的发生以及制定提高奶牛生产性能的饲养管理策略提供参考。  相似文献   
73.
AIM: To explore the effects and mechanism of eleutheroside (ETS) B or E on the proliferation of HBZY-1 cells treated with high glucose. METHODS: The HBZY-1 cells were cultured under high glucose condition. The 4th generation of HBZY-1 cells was used for determining the optimal cell density, which was consistent with the growth regulation curve of the cells. The cells were divided into 6 groups: low glucose (LG) group, high glucose (HG) group, high glucose plus ETS-B/E (low dose, medium dose and high dose) groups, and high glucose plus losartan (LTG) group. After all cells were treated with the corresponding drugs at 24 h, 48 h and 72 h, the inhibitory rate of the proliferation was measured, and the expression of TGF-β1 and PPARγ was detected by immunocytochemistry and Western blotting. RESULTS: The best cell density was 2 000 cells/well, which was complied with the basic rules of the cell growth, and high glucose significantly promoted the HBZY-1 cell proliferation. At each time point, the inhibitory effects of ETS-B/E were significantly different between HG group and LTG group on the proliferation of the HBZY-1 cells (P<0.05). The expression of TGF-β1 was significantly inhibited, and the expression of PPARγ was significantly promoted by ETS-B/E (P<0.05). ETS-E showed stronger effect than ETS-B (P<0.05) in a concentration- and time-dependent manner. CONCLUSION: ETS-B/E significantly inhibits the proliferation of HBZY-1 cells under high glucose condition by decreasing TGF-β1 expression and promoting PPARγ expression.  相似文献   
74.
miR-let-7a在动物细胞的分化、增殖与凋亡等方面发挥越来越重要的作用。甲状腺激素(TH)作用非常广泛,机体的每个细胞几乎都是TH作用的靶细胞,其可以促进组织分化、生长和成熟。本实验用甲状腺素(T4)浓度分别为(0、0.02、0.03、0.05、0.075、0.1、0.2μmol/L)在体外培养猪的小肠上皮细胞。结果表明:T4处理组的细胞体积形态相对于空白对照组没有明显变化;当T4添加浓度为0.03μmol/L时,细胞的增殖率显著低于其他组(P0.05);当T4浓度为0~0.03μmol/L时,let-7a的表达随着添加剂量的增加而升高,浓度从0.03~0.2μmol/L变化时,let-7a的表达呈现降低趋势,浓度为0.03μmol/L时表达量极显著高于其他组(P0.01)。let-7a的表达量与细胞增殖呈负相关。  相似文献   
75.
试验旨在探究在H2O2诱导的氧化应激状态下,超氧化物歧化酶模拟物(SODm)对仔猪空肠上皮细胞系(IPEC-J2)的保护作用。利用MTT法筛选出构建氧化应激模型H2O2的适宜浓度;将IPEC-J2细胞分别用0、0.05、0.5、5、50、500、2 000 U/mL SODm进行培养,利用MTT法分别在2、4、8、12 h时测定各组细胞存活率,筛选出SODm作用的适宜浓度和时间;根据构建的氧化应激模型和SODm适宜浓度和时间,将IPEC-J2细胞随机分为空白组、模型组、SODm处理组(SODm0.5、SODm5、SODm50)和超氧化物歧化酶(SOD)处理组(SOD0.5、SOD5、SOD50),分别测定各组细胞存活率、活性氧(ROS)含量及细胞内SOD、谷胱甘肽过氧化物酶(GSH-Px)活性及丙二醛(MDA)含量和总抗氧化能力(T-AOC)。结果表明:①H2O2构建细胞氧化应激模型的适宜浓度是1.0 mmol/mL。②当不同浓度SODm分别作用4、8、12 h时,0.5~50 U/mL SODm组细胞存活率显著高于空白组(P<0.05);且8 h时存活率最高,在12 h时处于下降趋势。③除空白组外,SODm5和SOD5预处理的IPEC-J2存活率显著高于其他组(P<0.05);且SODm和SOD组中细胞ROS含量显著低于模型组(P<0.05);模型组与空白组相比,均显著降低了SOD、GSH-Px活性和T-AOC水平,提高了MDA含量(P<0.05);与模型组相比,所有SODm和SOD处理组均显著提高了SOD、GSH-Px活性和T-AOC水平,降低了MDA含量(P<0.05),同时SODm50组T-AOC水平显著低于SOD50组(P<0.05)。综上,SODm对H2O2诱导氧化损伤状态下IPEC-J2具有保护作用。  相似文献   
76.
【目的】探究苦参碱对体外培养的奶牛乳腺上皮细胞(BMECs)增殖、凋亡及抗氧化能力的影响。【方法】利用含0(A组),25(B组),50(C组),75(D组)和100μg/mL(E组)苦参碱的培养基培养奶牛乳腺上皮细胞。通过四甲基偶氮唑盐(MTT)法检测BMECs活性,采用流式细胞仪(AnnexinV/PI双染法)检测苦参碱对BMECs凋亡的影响,并检测苦参碱对BMECs抗氧化酶活性及丙二醛(MDA)含量的影响,采用real-time PCR对BMECs中Caspase-3、p53、STAT1和SOCS3基因的相对表达量进行检测。【结果】用药5d时,低质量浓度(25和50μg/mL)苦参碱对BMECs增殖具有促进作用,高质量浓度(75和100μg/mL)苦参碱对细胞增殖具有抑制作用;B~E组BMECs的凋亡率均极显著高于A组(P0.01);B~E组BMECs培养上清液中NO和乳酸脱氢酶(LDH)水平明显高于A组。B~E组BMECs的过氧化氢酶(CAT)活性均比A组高,其中C组极显著高于A组(P0.01);B~E组的谷胱甘肽过氧化物酶(GSH-Px)活性均极显著高于A组(P0.01),E组的超氧化物歧化酶(SOD)水平极显著高于A组(P0.01),各组MDA含量无显著性差异。与A组相比,苦参碱上调了B~E组BMECs中Caspase-3、p53、STAT1和SOCS3基因的相对表达量。【结论】低质量浓度苦参碱能够促进BMECs增殖,高质量浓度苦参碱则会抑制BMECs增殖;不同质量浓度苦参碱均可提高BMECs的抗氧化能力,其中50μg/mL苦参碱提高BMECs抗氧化能力的效果最明显。  相似文献   
77.
AIM: To investigate the ultrastructural changes of islet microvascular endothelial cells in STZ-induced type 1 diabetic mice. METHODS: BALB/c mice were randomly divided into diabetic group and control group. The expression of insulin and platelet-endothelial cell adhesion molecule-1 (CD31) in islet microvessels was detected by immunohistochemical staining. The ultrastructural changes of islet β cells and islet microvessels were observed under transmission electron microscope. RESULTS: Compared with control group, the number of islet β cells, ratio of β cells/α cells, average number of secretory granules in β cells and insulin expression area per islet in diabetic group were significantly decreased (P<0.01). Besides, diabetic group had fewer microvessels with lower expression of CD31 (P<0.01). Mitochondria in islet microvascular endothelial cells and pericytes in diabetic group were swelling. The basement membrane of islet microvessels became thicker in diabetic group (P<0.01). CONCLUSION: Islet microvascular endothelial cells were impaired in type 1 diabetic mice.  相似文献   
78.
AIM: In order to observe the myocardial differentiation capacity of the dedifferentiated fat (DFAT) cells treated with vitamin C in vitro. METHODS: DFAT cells were dedifferentiated from the mature rat adipocytes with ceiling adherent culture. The DFAT cells of passage 3 were used in the study. Vitamin C and/or neonatal rat heart tissue lysate were added into the culture medium to induce myocardial differentiation for 3 weeks. The cell morphology was observed under microscope. The myocardial-specific markers, such as cTnT, GATA-4 and NKx2.5, were examined by the methods of immunofluorescence, PCR and Western blot. RESULTS: Mature rat adipocytes dedifferentiated into fibroblast-like DFAT cells after ceiling adherent culture. The DFAT cells spontaneously differentiated into cardiomyocyte-like cells under normal culture condition with a low incidence. After treated with neonatal rat heart cell lysate, the DFAT cells became cardiomyocyte-like cells that had bigger size, longer shape and myotubule-structure. The expression of cTnT, GATA-4 and NKx2.5 was remarkably increased at both mRNA and protein levels as compared with the normal cultured DFAT cells. The expression of cTnT, GATA-4 and NKx2.5 was further increased in DFAT cells after treating with vitamin C. No spontaneous beating cell was observed. CONCLUSION: Vitamin C enhances the differentiation of DFAT cells into cardiomyocyte-like cells.  相似文献   
79.
80.
Oxidative stress can induce apoptosis of granulosa cells and lead to follicular atresia, thereby reducing the number of pigs giving birth. The aim of this study was to investigate the protective effect of Periplaneta americana peptide (PAP) on the apoptosis of the granulosa cells of pig ovaries (PGCs) induced by hydrogen peroxide (H2O2) via FoxO1. PGCs were treated with H2O2 to establish a cell apoptosis model. Cell viability was measured using the cell counting kit-8 (CCK-8) assay, and cell apoptosis was detected using flow cytometry. The malondialdehyde (MDA) level and nitric oxide (NO) content were detected to reflect the oxidative stress. Western blotting, qRT-PCR and overexpression were undertaken to determine the expression of FoxO1 and caspase-3, and immunofluorescence was used to detect FoxO1 in the nucleus and cytoplasm. PGCs were treated with 100 μM H2O2 for 6 hr, which resulted in oxidative damage and apoptosis and an apoptosis rate for PGCs of 32.95%. Next, PGCs were treated with 400 μg/ml PAP for 24 hr to repair the apoptosis induced by H2O2. PAP improved cell viability in H2O2-stimulated PGCs, the increased MDA level and NO content caused by H2O2 stimulation were reversed and the apoptotic rate of PGCs was reduced. The qRT-PCR and Western blotting results indicated that PAP decreased the H2O2-induced apoptosis and the expression of FoxO1 and caspase-3 in PGCs. The effect of PAP was the same following FoxO1 overexpression. FoxO1 was expressed in the nucleus when stimulated by H2O2 or overexpression; however, it migrated to the cytoplasm following PAP treatment. PAP decreased the apoptosis of PGCs induced by H2O2 by regulating FoxO1 expression and nuclear translocation.  相似文献   
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