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1.
Meiotic disturbances in F1 hybrids and their progenies are still major problems in wide hybridization.To investigate the genome affinity reflected in chromosome pairing and segregation,we studied chromosome behaviors during meiosis in two interspecific F1 hybrids[O.minuta×O.australiensis(Om×Oa,BCE genome)and Oa×O.ridleyi(Or,EHJ genome)]by using both traditional staining methods and genomic in situ hybridization(GISH).GISH analysis has been successfully performed on mitotic chromosomes to distinguish different Oryza genomes,but relatively fewer systematic analyses of meiotic chromosomes of interspecific hybrids have been reported.In the hybrids,highly irregular chromosome behaviors through meiosis resulted in producing microspores with unbalanced genome.At diakinesis of these two hybrids,most chromosomes present as univalent,with low frequency as bivalents and occasionally as trivalents.In a pollen mother cell,2 to 8 bivalents and 0 to 4 trivalents were observed in the hybrid Oa×Or,and 1 to 8 bivalents and 0 to 5 trivalents were observed in the hybrid Om×Oa.GISH results indicated that 51.52%bivalents in Oa×Or and 79.65%bivalents in Om×Oa involved allosyndetic association,which indicates that recombination and introgression should be possible if viable backcrosses can be recovered even from triploid hybrids.In this study,we revealed that the meiotic disturbance due to low affinities between parental genomes is the major reason for the sterility of these two triploid interspecific hybrids.The two hybrids showing vigor in reproductive growth are potential genetic resources in future breeding programs.A better understanding of genomic affinities between these distant Oryza species can facilitate planning an effective breeding program by using wide hybridization,and efficient and routine GISH analysis is helpful to monitor alien introgression in the process.  相似文献   
2.
旨在研究褪黑素(melatonin,MT)对体外培养猪精原干细胞(spermatogonial stem cells,SSCs)的作用机制。本研究采集3头7日龄健康大白公猪睾丸,利用差速贴壁法获得SSCs。后经形态学观察、碱性磷酸酶染色、标记基因检测及免疫荧光染色鉴定后以SSCs作为试验材料,设置MT浓度梯度(0、50、250、500、1 000 μmol·mL-1)组处理SSCs,每组设3个重复(n=3),空白对照组加入0.1% DMSO处理,分别检测添加MT后猪SSCs的细胞活力、活性氧(reactive oxygen species,ROS)水平、谷胱甘肽(glutathione,GSH)含量及凋亡基因表达变化。结果显示:1)分离的克隆团细胞具有SSCs的生长特性,可被碱性磷酸酶染色并表达干细胞标志基因OCT4、SOX2和SSCs标志基因NANOGPLZFUCHL1;2)50 μmol·mL-1以上的MT在处理48 h后可显著提高SSCs的细胞活力(P<0.05);3) MT可显著降低猪SSCs内ROS水平(P<0.05),极显著增加细胞内GSH含量(P<0.01);4) MT可显著抑制猪SSCs内凋亡蛋白Bax和Caspase3的表达(P<0.05)。MT具有清除猪SSCs中的ROS,提高总GSH含量,抑制凋亡基因表达进而提高细胞活力的作用,可为养殖过程中提高公猪繁殖性能提供参考。  相似文献   
3.
AIM: To investigate the effect of Linc00152 on the viability, apoptosis and radiosensitivity of cervical cancer cells. METHODS: RT-qPCR was used to detect the expression levels of Linc00152 and microRNA-376c-3p(miR-376c-3p) in human cervical cancer HeLa cells and SiHa cells, and normal cervical Ect1/E6E7 cells. The cervical cancer HeLa cells with low Linc00152 expression or miR-376c-3p over-expression were established. MTT assay, flow cytometry, colony formation assay and Western blot were used to determine the cell viability, apoptosis, radiosensitivity and related protein expression. The dual-luciferase reporter assay was used to verify the regulatory relationship between Linc00152 and miR-376c-3p in the HeLa cells. RESULTS: Compared with the Ect1/E6E7 cells, Linc00152 was up-regulated in the HeLa cells and SiHa cells, and miR-376c-3p was down-regulated (P < 0.05). Low expression of Linc00152 or over-expression of miR-376c-3p inhibited the viability of HeLa cells, induced apoptosis, enhanced the radiosensitivity, inhibited the protein expression of cyclin D and Bcl-2, and promoted the protein expression of P21 and Bax (P < 0.05). Linc00152 negatively regulated miR-376c-3p expression in the HeLa cells, and inhibition of miR-376c-3p expression reversed the effect of low expression of Linc00152 on HeLa cell viability, apoptosis and radiosensitivity. CONCLUSION: Linc00152 is highly expressed in the cervical cancer cells. Linc00152 affects the viability, apoptosis and radiosensitivity of HeLa cells by targeting miR-376c-3p, which is a potential diagnosis and treatment target for cervical cancer.  相似文献   
4.
AIM: To observe the effect of histone deacetylase inhibitor (HDACi) Belinostat on the viability of osteosarcoma cells and to study the underlying mechanism. METHODS: Osteosarcoma cell lines SAOS-2 and U2OS were incubated with Belinostat at different concentrations in vitro. The viability of the cells was measured by MTT assay. The activity of caspase-3/-7 and the DNA fragmentation were detected by fluorescence probe and ELISA, respectively. Western blot was used to detect the levels of histone acetylation, expression of PTEN, caspase-3, Bcl-xL and Akt, and phosphorylation of glycogen synthetase kinase 3β (GSK-3β) and Akt. Finally, the cells were incubated with Belinostat and doxorubicin at different concentrations, and then the combination index (CI) was calculated by MTT. RESULTS: Belinostat at 0.5, 1, 2.5 and 5 μmol/L inhibited the viability of U2OS cells and SAOS-2 cells in a dose-dependent manner, induced DNA fragmentation, enhanced caspase-3/-7 activity, and promoted the activation of caspase-3. At the same time, in the SAOS-2 cells, the expression of Bcl-xL was reduced, and the acetylation of histones H3 and H4 was increased. The results of Western blot showed that phosphorylation levels of Akt and GSK-3β in U2OS cells and SAOS-2 cells were decreased significantly after treatment with Belinostat (P<0.05). MTT results showed that combination of Belinostat and doxorubicin further reduced the viability of U2OS and SAOS-2 cells (CI<1). CONCLUSION: Belinostat inhibits the viability of osteosarcoma cells treated with doxorubicin, and the mechanism may be related to the inhibition of Akt signaling pathway.  相似文献   
5.
以采自新疆维吾尔自治区阿勒泰市阿拉哈克镇境内的罗布麻属(Apocynum)和白麻属(Poacynum)8个基因型植物的种子为材料,进行了8个基因型植物种子形态特征、千粒重和生活力测定方法探究。研究结果显示,参试罗布麻种子的长为2.75 mm,宽为0.68 mm,厚为0.49 mm。白麻属7个基因型中以紫斑中花的种子最长,为4.51 mm;青杆白花最宽,为0.90 mm;青杆白花和大叶白麻最厚,为0.61 mm。8个基因型种子的长、宽、高的变化范围分别为2.75~4.51、0.68~0.90和0.48~0.61 mm。其中,紫斑中花为最大基因型,罗布麻为最小基因型。千粒重变化范围在0.38~1.32 g,所有参试种子颜色均为褐色,其中以大叶白麻颜色最深。参试种子均表现出非休眠性种子萌发的特征,萌发时间较短,可以用来快速测定参试种子的生活力。采用四唑染色测定生活力时,参试种子均表现出不透四唑的特征,应该纵切切破种皮,预湿时间为12~14 h,染色时间为12 h,鉴定标准为种子胚80%完全染色。此次针对罗布麻属和白麻属种子形态特征与生活力测定方法的研究,能够为罗布麻种子生活力鉴定、大规模种植、种子繁育提供一定的基础。  相似文献   
6.
7.
AIM: To observe the effects and mechanisms of nitroglycerin (NTG) on cell viability and β-mercaptoethanol (β-ME) on ameliorating nitrate tolerance of peripheral blood-derived endothelial progenitor cells (EPCs) in coronary heart disease (CAD) patients.METHODS: We studied 75 patients with diagnosis of coronary artery disease who were assigned to control group and NTG group. EPCs were evaluated by flow cytometry. Vascular endothelial growth factor-A (VEGF-A) and peroxynitrite anion (ONOO-) production were measured by ELISA. EPCs were cultured in vitro with NTG and β-ME stimulation. The cell viability was determined by MTT assay. The levels of VEGF-A, ONOO- and reactive oxygen species (ROS) were measured by ELISA and DCFH-DA assay. The protein levels of Akt,p-Akt,endothelial nitric oxide synthase (eNOS) and p-eNOS were determined by Western blot. RESULTS: Compared with the control group, the circulating EPCs levels were significantly lowered, plasma ONOO- production was vitally increased, but there was a markedly decrease of VEGF-A production in the patients treated with excess NTG(P<0.05). Moderate dose of NTG increased the viability of EPCs, VEGF-A production, and phosphorylated protein levels of Akt and eNOS. Excess NTG was shown to reverse the effect of moderate dose of NTG, but β-ME improved the adverse effect of excess NTG. CONCLUSION: Moderate dose of NTG effectively promotes EPCs viability by PI3K/Akt/eNOS signaling pathway and β-ME improves NTG-induced tolerance by reducing oxidative stress and up-regulating the PI3K/Akt/eNOS signaling pathway.  相似文献   
8.
Endozoochory has been recognised as the most important dispersal mechanism in invasive Prosopis species, because their sugary, tasty pods attract animals and because some of their seeds remain intact after passing through some animals' digestive systems. In this study, we evaluated the role of the camel (Camelus dromedarius) as a potential disperser of the seeds of invasive tree Prosopis juliflora. Four camels of similar weight (ca. 400 kg) and age (ca. 2 years) were each fed with 70 fruits (1000 seeds approximately) of P. juliflora, which were retrieved from the camels' dung at 24‐h intervals for 4 days. The seeds retrieved were tested for germination and viability, along with seeds not eaten by the camels, with and without pericarp. Less than 3% of the seeds eaten were retrieved from the camels' dung. Most of the seeds (74%) were retrieved between 24 and 72 h after ingestion. The passage through the camel gut significantly accelerated and increased seed germination of P. juliflora in comparison with uneaten seeds covered with pericarp (48–75% and 15% respectively). While gut passage liberated P. juliflora seeds from the pericarp, increasing and accelerating their germination, the viability of seeds which had not germinated after germination trials were decreased (ca. ~20%) relative to uneaten seeds that had also not germinated. Our results show that, despite the low recorded seed recovery, camels can potentially disperse seeds of P. juliflora, which is in line with field observation showing P. juliflora expansion along the camels' routes in Gebel Elba National Park, south‐east Egypt.  相似文献   
9.
The incidence of fish pathogenic oomycetes, Saprolegnia, has increased significantly in aquaculture since the ban of malachite green. For the efficient characterization of anti‐Saprolegnia therapeutics, simple accurate methods are required. However, the current screening methods are limited by time, and none of them are confirming the viability of treated spores or hyphae. In this study, a modified fluorescence‐based assay for the in vitro screening of Saprolegnia inhibitors has been developed. This method involves the use of FUN‐1 viability dye combined with calcofluor white M2R, and is based on the formation of orange‐red cylindrical intravacuolar structures (CIVS) in metabolically active spores, hyphae and biofilms. Heat‐killed and bronopol‐treated Saprolegnia spores, hyphae and biofilms exhibited diffuse bright green fluorescence which confirms complete loss of viability. For boric acid‐treated spores, no germination was observed. However, tiny CIVS were observed in 50% of treated spores which indicated reduction in their viability. Our results proved that FUN‐1 dye is an efficient tool to distinguish between live and dead Saprolegnia spores, hyphae and biofilms and to monitor the change in Saprolegnia viability during qualitative evaluation of potential anti‐Saprolegnia compounds.  相似文献   
10.
花期前后高温对玉米花粉发育及结实率的影响   总被引:1,自引:0,他引:1  
为明确花期不同梯度高温对玉米开花特性和花粉活力的影响,以热敏感基因型玉米品种‘驻玉309’为试验材料,于花期(吐丝前8d~吐丝后8d)进行不同程度高温(31、34和37℃)处理,测定受精结实率、雄穗性状、开花时间、花粉活力及花粉超显微结构,分析生育期前后的高温对受精结实、开花特性及花粉活力的影响。结果表明,花期高温胁迫显著降低玉米受精结实率,对抽雄吐丝间隔期无显著影响,但盛花期提前;极端高温则导致玉米抽雄期显著提前、开花期和盛花期延后,抽雄吐丝间隔期延长;花期高温使花粉粒形态皱缩、萌发孔内陷,显著降低花粉活力,且温度越高,花粉活力降低幅度越大。因此,花期前后高温通过影响玉米影响雄穗开花特性、延长抽雄吐丝间隔期、影响花粉粒形态、降低花粉活力,从而降低玉米的小花受精率和籽粒结实率。  相似文献   
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