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81.
AIM: To investigate the differentiation from adult rat and human bone marrow mesenchymal stem cells (BMMSCs) into neuron with musk polypeptide (Mu-P).METHODS: Adult rat and human BMMSCs were induced with Mu-P.Neuron-specific enolase (NSE),neurofilament (NF),Nestin,glial fibrillary acidic protein (GFAP) were detected by immunohistochemistry.RESULTS: Simple methods with Mu-P induced adult rat and human BMMSCs exhibiting a neuronal phenotype,expressing Nestin at 3 hours to 5 hours,and expressing NE and NF at 5 hours to 7 days.But the neuron-like cells didn't express the glial astrocyte marker GFAP.CONCLUSION: Adult rat and human BMMSCs can be induced to differentiate into neurons with Mu-P.  相似文献   
82.
AIM: To investigate the effects of PD98059 on the differentiation from mesenchymal stem cells to osteoblasts.METHODS: hMSC were separated from human marrow and expanded in cuture medium. hMSC were induced with dexamethasone, β-glycerophosphate, vitamin C which acted as osteoblast differentiation inducer. PD98059 was added into the osteoblasts induction medium. The cells were assayed with cell morphology, alkaline phosphatase (AP) activity and calcium deposition. RESULTS: The isolated cultured MSC comprised a single phenotypic population and displayed a fibroblast-like morphology. After induced with osteoblasts induction medium, the cells showed changes in cell morphology from spindle-shape to cuboidal and polygonal. The AP activity increased gradually and reached the peak in 12 days, then decreased. Many scattered tangerice calcium nodes were observed. PD 98059 significantly inhibited AP activity and calcium deposition in a dose-dependent manner. A striking observation of the present study was that a few adipocytes appeared in cultures that were treated with PD 98059 and osteogenic differentiation medium. CONCLUSION: These results indicated that osteogenic diferentiation from the hMSCs was related to the activation of the ERK.  相似文献   
83.
AIM: To observe the direct effects of peripheral blood monocytes/macrophages (MO/MAC) on renal tubular epithelial cells (RTEC),and further probe into the possible mechanisms. METHODS: Conditioned medium(M-CM) of human peripheral blood MO/MAC was collected and added to HK-2,a human renal proximal tubular cell line.After incubation with M-CM for 24 hours,HK-2 cells were detected for DNA synthesis by [3H]-TdR incorporation,osteopontin (OPN) and α-smooth muscle actin (α-SMA) expression by Western blot,and fibronectin(FN) secretion by ELISA.Furthermore,anti-TGFβ1 neutralizing antibody and interlukin-10(IL-10) were used separately to antagonize the effects of M-CM on HK-2 cells. RESULTS: ①DNA synthesis,α-SMA expression and FN secretion were all increased in HK-2 cells when incubated with M-CM.②When adding with anti-TGFβ1 neutralizing antibody (5 mg/L) in the M-CM,the degree of upregulation of α-SMA and FN in HK-2 cells was much lower than that stimulated by M-CM alone.③M-CM added with IL-10 (20 μg/L) had a weaker ability to induce the increasing in α-SMA expression and FN excretion in HK-2 cells, compared with M-CM itself alone.M-CM from MO/MAC preincubated with IL-10 caused a lower upregulation of α-SMA expression in HK-2 cells than M-CM from non-preincubated MO/MAC. CONCLUSION: MO/MAC can directly induce proliferation,transdifferentiation and extracellular matrix secretion in RTEC.TGFβ1 and proinflammatory cytokines secreted by MO/MAC might be involved in the aboveeffects.  相似文献   
84.
AIM: To study the electrophysiological characteristics of ion channels of stem cell derived cardiomyocytes(SCDC) of mouse. METHODS: Embryonic stem cells of D3 line(ES-D3) were cultured on the MEF feeder layer with BRL conditioned medium, and fetal mouse heart cells(FMHC)were cultured in vitro. Then ES-D3 cells were induced to differentiate into many kinds of cells. SCDC were harvested on day 12 after differentiation initiating and identified by electro-microscope and immunocytochemistry. SCDC and FMHC were prepared for the patch-clamp research. Sodium and calcium currents together were elicited and compared between SCDC and FMHC. RESULTS: The current characteristics of sodium and calcium channels of SCDC were very similar to FMHC. CONCLUSION: The functional expression of ion channels occurred during ES-D3 cells differentiation and the electrophysiological characteristics of sodium and calcium channels of SCDC are very similar to FMHC.  相似文献   
85.
Traditional concept has been that hematopoietic stem cells (HSC) are tissue-specific stem cells, which are restricted to generate the cell types of the blood and immune system. However, recent studies have shown that there is a higher plasticity of the HSC than previous expected, it can be induced to transdifferentiated into mature cells of other nonhematopoietic organs after transplantation in vivo. In this article, the recent advances in the plasticity of HSC and its potential clinical application are reviewed.  相似文献   
86.
钙、萘乙酸对亚精胺在猕猴桃贮藏期间作用效果的影响   总被引:4,自引:0,他引:4  
以5年生中华猕猴桃品系(湘源81-2)为试材,进行了果实采收后Spd(亚精胺)、Spd+Ca2+、Spd+NAA浸果处理,研究钙、萘乙酸对多胺作用效果的影响。结果表明:不同处理均不同程度地抑制了果实的呼吸强度、果肉PG活性和细胞膜透性的增加,其中Spd+NAA浸果处理的作用效果最为显著,贮藏68d时,果肉硬度最高(0.259MPa),软果率较低(79%),好果率达100%;其次为Spd处理。  相似文献   
87.
热胁迫对辣椒花柱细胞中Ca2+ 分布的影响   总被引:5,自引:0,他引:5  
 用焦锑酸钾沉淀法研究了热胁迫对辣椒开花前后柱头和花柱细胞中Ca2+分布的影响。结果表明: 常温下Ca2+ 分布在柱头细胞表面、花柱引导组织细胞间隙等质外体系统中, 且在花粉管上呈先增加后减少的规律性变化; 热胁迫后, 除细胞间隙等质外体系统外, 细胞质和细胞核中也出现Ca2+, 花柱引导组织中通过的花粉管发生扭曲、变形, 这可能与Ca2+ 的异常分布有关。  相似文献   
88.
‘禅寺丸’甜柿2n花粉形成机制的研究   总被引:13,自引:1,他引:13  
谷晓峰  罗正荣 《园艺学报》2003,30(2):135-140
 以2n花粉发生频率较高的甜柿品种‘禅寺丸’为试材,研究影响2n花粉形成的减数分裂行为。结果表明:2n花粉形成受融合纺锤体(fused spindles),八字形纺锤体(triangle spindles)及后期Ⅱ染色单体不正常分离(abnormal disorientation of sister chromatid)3种减数分裂行为控制;融合纺锤体及八字形纺锤体形成的2n花粉占2n花粉总数的94.8%,在遗传上等同于FDR(first division restitution,第1次分裂重组)型配子;由姊妹染色单体不正常分离形成的2n花粉在遗传上等同于SDR (second division restitution,第2次分裂重组)型配子。甜柿2n花粉绝大多数为FDR型,因而在倍性育种中有重要的应用价值。  相似文献   
89.
硅对黄瓜幼苗生长及活性氧清除系统的影响   总被引:8,自引:0,他引:8  
在水培条件下,研究了营养液中硅对黄瓜幼苗生长和活性氧清除系统的影响。结果表明,施硅处理可以促进黄瓜植株的生长,叶片中叶绿素含量增加,内源抗氧化物质抗坏血酸(AsA)含量增加,超氧化物歧化酶(SOD)、过氧化物酶(POD)和过氧化氢酶(CAT)活性升高,丙二醛(MDA)含量降低。  相似文献   
90.
为探讨富铁酵母对家兔红细胞免疫功能的影响,将32只家免随机分成富铁酵母高、低剂量组,FeSO4组及空白对照组,分别灌服富铁酵母(Fe元素8 mg/kg、4 mg/kg)、FeSO4(Fe元素4 mg/kg)及空白生理盐水;连续5 d后,检测红细胞C3g受体花环率和复合物(IC)花环率.结果:富铁酵母较FeSO4及空白组能显著提高红细胞C3h受体花环和红细胞复合物(IC)花环的百分率,但高、低剂量间无显著性差异.结论:富铁酵母能显著提高红细胞免疫功能.  相似文献   
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