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河南新县野生油茶群体表型变异特征研究 总被引:1,自引:0,他引:1
为揭示河南新县野生油茶群体的变异特征,以新县7个典型野生油茶生长区的群体为研究对象,测定了油茶叶、花、果相关的15个性状,采用变异系数、相关性分析、聚类分析和方差分析等方法,分析油茶表型性状的多样性及群体间和群体内的变异特征。结果表明,新县野生油茶叶、花、果形态在群体内及群体间的表型多样性均较为丰富,7个群体间叶、花、果形态差异均达到极显著水平。7个群体内15个性状中,鲜籽质量变异程度最高(49.79%),其次是鲜籽数、单果质量和果皮厚,变异程度最低的是叶长(10.67%);聚类分析在欧式平均距离在阈值15处,将新县野生油茶群体分为了两大类,在不同程度上反映了各群体的特征。 相似文献
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AIM: To explore whether morphine protects oxidative stress-damaged myocardial cells by inhibiting the PERK pathway to reduce endoplasmic reticulum stress and prevent mitochondrial permeability transition pore (mPTP) opening. METHODS: Rat myocardial H9c2 cells were cultured to establish an oxidative stress model, and then randomly divided into control group, H2O2 group, H2O2+morphine group, H2O2+morphine+PERK pathway inhibitor GSK2656157 group, morphine group and GSK2656157 group. Immunohistochemical method was used to detect the effects of morphine on expression of glucose-regulated protein (GRP) 78 and GRP94 induced by oxidative stress. The protein levels of PERK signaling pathway-related molecules were determined by Western blot. Confocal microscopy was used to observe the effects of morphine on mPTP opening and endoplasmic reticulum induced by oxidative stress. Cellular toxicity was detected by lactate dehydrogenase (LDH) kit and cell viability was measured by MTT assay. RESULTS: Compared with control group, GRP78 and GRP94 proteins in H2O2 group were strongly expressed, and the brown-yellow particles were significantly increased, but morphine significantly inhibited this process. Compared with control group, the phosphorylation of PERK was significantly reduced with GSK2656157 treatment at different concentrations, among which 2 μmol/L had the most significant effect (P < 0.05). Oxidative stress significantly increased the protein levels of GRP78, GRP94, p-PERK and CHOP, but significantly decreased p-GSK-3β level. These changes were inhibited by morphine, and the effects of morphine were further enhanced by GSK2656157 (P < 0.05). Compared with control group, oxidative stress significantly reduced the fluorescence intensity of mitochondrial TMRE and ER-Tracker Red. Morphine significantly inhibited this effect even when mitochondrial membrane potential was reduced, mPTP was open, and endoplasmic reticulum was damaged, while GSK2656157 further enhanced the effect of morphine (P < 0.05). Compared with control group, H2O2 significantly increased cellular toxicity and decreased the cell viability. Morphine inhibited this effect and GSK2656157 significantly enhanced the effect of morphine (P < 0.05). CONCLUSION: Morphine protects cardiac H9c2 cells under oxidative condition by inhibiting endoplasmic reticulum stress through PERK pathway and preventing the mPTP opening via GSK-3β inactivation. 相似文献
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AIM To investigate the role of fatty acid translocase (FAT/CD36) on differentiation of monocytes to macrophages. METHODS Human monocyte THP-1 cells were treated with phorbol 12-myristate 13-acetate (PMA) at 0, 100 and 200 μg /L. Small interfering RNA (siRNA) targeting CD36 (siCD36) was employed to knock down the expression of CD36 in THP-1 cells. The CD36 over-expression (CD36OE) cell line was constructed by transfection with a recombinant lentivirus containing CD36 cDNA. Optical microscopy and crystal violet staining were used to detect the monocyte morphological changes and adhesion ability. The protein expression of CD36 was measured by flow cytometry and Western blot. The mRNA levels of CD36, CD11b and CD80 were detected by real-time PCR. The protein levels of extracellular signal-regulated kinase (ERK) and Src tyrosine kinase were determined by Western blot. RESULTS The cellular adhesiveness of THP-1 cells was elevated in the process of monocytes differentiation, and the expression of CD36 was increased in this process as well (P <0.01). siCD36 was transfected into the THP-1 cells (CD36i group) and the silencing efficiency was approximately 80%. The cell surface area and cellular adhesiveness were significantly decreased in CD36i group compared with scrambled siRNA (NCi) group (P <0.01). The mRNA levels of CD11b and CD80 were decreased in CD36i group compared with NCi group (P <0.01). The cell surface area and cellular adhesiveness were increased in CD36OE group compared with empty vector (vector) group (P <0.05). The mRNA levels of CD11b and CD80 were increased in CD36OE group compared with vector group (P <0.01). The phosphorylation levels of ERK and Src were decreased in CD36i group compared with NCi group (P <0.05). CONCLUSION CD36 promotes the differentiation of human monocyte THP-1 cells to macrophages by increasing the phosphorylation of Src and further activating ERK. 相似文献
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【目的】弱筋小麦是制作饼干糕点类食品的原料,其烘烤特性很大程度上取决于蛋白质的质和量。小麦籽粒蛋白质含量(GPC,%)不仅由品种的遗传特性决定,还受到气候、土壤、栽培措施等影响。明确江苏省弱筋小麦适宜种植区域以及其地理、气候影响因素,可为江苏弱筋小麦的种植区划提供理论依据。【方法】在2年江苏省小麦品质抽样调查数据的基础上,利用随机森林算法筛选重要性指标,结合单组率Meta分析及其亚组分析,探究地理位置及气象因子对江苏省小麦籽粒蛋白质含量(GPC)达到弱筋小麦标准可能性的影响。【结果】2个年度江苏省小麦GPC平均值为13.92 %,其中2018年、2019年小麦GPC变幅分别为11.06%—18.09%、10.20%—16.50%,平均值分别为14.52%、13.33%,GPC<12.5%的样品分别占比10%、29.71%。从地理分布看,江苏的东南沿湖沿海地区小麦GPC达到弱筋小麦标准的可能性最高,达标可能性最高可达92%,其次是江苏东部沿海地区以及江苏西北部沿河一带。种植地距离一级河流和湖泊或者海岸线的最短距离为20—30 km时,达标可能性相对较高,为23.95%。从气象因子方面看,生育前期特别是出苗期和拔节期,降雨量对江苏弱筋小麦的形成影响较为重要;生育后期尤其是开花期以及灌浆期后期,积温对小麦GPC的影响更重要;且出苗和拔节期的日照时数及开花期的降雨量对江苏弱筋小麦的形成亦很重要,其中,江苏小麦GPC达标弱筋小麦标准的可能性与出苗期的降雨量呈正相关,而与出苗和拔节期的日照时数、拔节期的降雨量以及灌浆后期积温则呈负相关。【结论】江苏弱筋小麦适宜的种植范围受到水系分布与气象因素的共同制约,主要集中在东部沿海和东南沿海沿湖地区。在出苗、拔节期降雨量和开花灌浆期积温适宜的情况下,西北沿河一带的小麦GPC也可达标弱筋小麦标准。品质区划应重点考虑地理位置(水系分布等)和气候分布。 相似文献
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为了探明春季低温(倒春寒)导致小麦减产的细胞学机理,以扬麦15为材料,在小麦幼穗处于雌雄蕊分化期至药隔期之间时,设置-3 ℃低温处理,通过树脂半薄切片对颖果不同发育时期的形态结构进行观察。结果表明:(1)在颖果发育早期,低温促进了颖果的长度生长,抑制了宽度生长;与对照相比,低温处理组小麦颖果发育进程缩短;(2)低温处理组颖果果皮发育早,中果皮降解速度快;(3)低温处理增加了胚乳淀粉体的积累量,降低了蛋白体的积累量,发育后期胚乳充实度显著低于对照组;(4)与对照相比,低温处理后颖果韧皮部面积和珠心突起传递细胞面积增大。以上结果表明,春季低温处理更有利于养分运输组织的发育,使得灌浆时间缩短,最终导致淀粉积累量增加及颖果早熟。 相似文献
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为了研究不同种子处理对种子传播病毒的灭活效果,试验以番茄、辣椒、甜瓜、南瓜种子样本中被番茄花叶病毒(ToMV)、烟草花叶病毒(TMV)、黄瓜花叶瓜病毒(CMV)感染的种子为研究对象,经过酶联免疫吸附测定(ELISA)和逆转录聚合酶链反应(RT-PCR)测试选择出研究材料,采用7种病毒失活处理方法,分别为醋酸、过氧化氢、盐酸、次氯酸钠浸种,干热处理,温汤浸种和臭氧熏蒸处理。结果发现,能有效减少病毒浓度的处理为盐酸浸种、干热处理、温汤浸种(65℃)和臭氧(10 g/m3)处理,分别能将种子传播病毒的浓度平均降低51%、50%、42%和32%。其他灭活方法治疗效果较差,病毒浓度平均降低了12%~27%。盐酸浸种和干热处理是最有效的方法,对种子出芽率和活力没有影响。 相似文献
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