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21.
枣树具有独特的开花结果特性,为获得枣花发育基因,以金丝4号枣不同发育时期的花蕾和同时期的叶片cDNA互为试验方和驱动方,利用抑制消减杂交技术分别构建了枣花和枣叶抑制消减杂交cDNA文库(SSH文库)。枣花和枣叶SSH文库重组率分别是92.05%和90.26%,插入片段长度均介于200~2 000 bp之间,主要集中于1 000 bp左右。分别从枣花和枣叶SSH文库中随机挑选1 000个阳性克隆进行DNA测序、组装拼接,结果显示枣花SSH文库中获得96条unigene,其中contigs 43个,singletons 53个,96条unigene预测得到73个ORF,经过同源比对分析获得有注释的序列20条,按功能分为7类;枣叶SSH文库中获得86条unigene,其中contigs 45个,singletons 41个,86条unigene预测得到70个ORF,经过同源比对分析获得有23条注释的序列,按功能分为6类。  相似文献   
22.
为探索瘦肉型猪组合配套杂交方法和效果而进行试验。试验采用HN121(温氏杜洛克猪)、HN212(法系皮特兰♂×温氏杜洛克♀)为父本,以HN204(温氏大白♂×美系长白♀)为母本,对HN323(HN121×HN204)和HN424(HN212×HN204)两个组合配套进行研究。结果表明,HN424组合与HN323组合相比母猪的窝产仔数、窝产活仔数、仔猪初生窝重、21日龄仔猪成活率、21日龄窝重等繁殖性状差异不显著(P>0.05);HN424组合仔猪的体重、背膘厚降低5.63%(P<0.05),瘦肉率提高4.95%(P<0.05),眼肌面积增大33.08%(P<0.01),肉色评分降低7.19%(P<0.05),大理石纹评分降低11.30%(P<0.01),滴水损失率提高10.63%(P<0.01),其他遗传性状差异不显著;HN424组合与HN204二元母系相比,日增重提高9.26%(P<0.05),背膘厚减少16.41%(P<0.01),料肉比减少8.02%(P<0.05);HN323组合与HN204二元杂交母系相比,日增重提高7.20%(P<0.05),背膘厚减少11.43%(P<0.01),料肉比降低5.35%(P<0.05)。说明采取四元杂组合和三元杂交组合均对“大×长”(HN204)二元杂交有显著的遗传改良作用,“皮×杜×长×大”四元杂组合可显著提高猪的瘦肉率、眼肌面积,但肉色、大理石纹、滴水损失率等肉质指标变差,建议在“皮×杜×长×大”四系组合配套杂交中加入能改良肉质基因的猪种。  相似文献   
23.
喻传洲 《猪业科学》2021,38(11):26-29
文章辩证地分析了猪轮回杂交的利与弊。作者指出:畜禽经济杂交在实践中应用的各类方法都有其适用范围和局限性。只要掌握了杂种优势的基本原理以及获得杂种优势的方法,就能在生产实践中扬长避短,将轮回杂交的缺点降到最低,并将其优点发挥到极致。  相似文献   
24.
苜蓿原生质培养及体细胞杂交技术的应用   总被引:1,自引:1,他引:0  
阐述了植物原生质体培养和体细胞杂交技术以及苜蓿Medicago spp.体细胞胚胎发生特性,综述了该技术在苜蓿育种研究中的应用状况,同时介绍了我国苜蓿研究领域原生质体培养和体细胞杂交技术的研究进展.  相似文献   
25.

BACKGROUND

Cultivated bread wheat (Triticum aestivum L.) spontaneously hybridizes with wild/weedy related Aegilops populations, but little is known about the actual rates at which this hybridization occurs under field conditions. It is very important to provide reliable empirical data on this phenomenon in order to assess the potential crop–wild introgression, especially in the context of conducting risk assessments for the commercialization of genetically modified (GM) wheat, as gene flow from wheat to Aegilops species could transfer into the wild species genes coding for traits such as resistance to herbicides, insects, diseases or environmental stresses.

RESULTS

The spontaneous hybridization rates between wheat and A. geniculata and A. triuncialis, which are very abundant in the Mediterranean area, have been estimated for the first time in the northern part of the Meseta Central, the great central plateau which includes the largest area of wheat cultivation in Spain. Hybridization rates averaged 0.12% and 0.008% for A. geniculata and A. triuncialis, respectively. Hybrids were found in 26% of A. geniculata and 5% of A. triuncialis populations, at rates that can be ≤3.6% for A. geniculata and 0.24% for A. triuncialis.

CONCLUSION

The detection of Aegilops spp.–wheat hybrids in Aegilops populations indicates that gene flow can occur, although wheat is considered a crop with a low-to-medium risk for transgene escape. These data on field hybridization rates are essential for GM wheat risk assessment purposes. © 2023 Society of Chemical Industry.  相似文献   
26.
27.
Inducible responses in plants against pathogen attack play a major role in resistance to disease. The defense responses are mostly associated with the expression of various kinds of inducible genes. We employed differential hybridization to isolate elicitor-inducible genes (EIGs) of tobacco (Nicotiana tabacum cv. Samsun NN) using the tobacco-fungal elicitor system. A cDNA library was constructed from tobacco leaves treated for 12 hr with hyphal wall components (HWC) prepared from Phytophthora infestans, and six EIGs were identified. Expression of all EIGs was induced after inoculation with the soybean pathogen Pseudomonas syringae pv. glycinea (nonpathogenic on tobacco) or treatment with salicylic acid, and a variety of expression patterns of EIG mRNAs was observed. Sequence analysis of EIG cDNAs revealed similarities to genes for SAR8.2 (EIG-B39 and EIG-D14), glycine-rich protein (EIG-G7), extensin (EIG-I30), acyltransferase (EIG-I24) and unknown protein (EIG-J7). Possible roles of EIG products in disease resistance are discussed. Received 30 August 2000/ Accepted in revised form 30 November 2000  相似文献   
28.
A male specific bovine DNA fragment was used as probe to determine the sex of bovine interphase cells by in situ hybridization. This method also proved useful for determining the sex of bovine embryos.  相似文献   
29.
Abstract We examined 12 formalin-fixed paraffin-embedded feline skin tumours which had the histopathological features of fibropapillomas for the presence of papillomavirus (PV) DNA using touchdown polymerase chain recation (PCR), DNA sequencing and nonradioactive in situ hybridization. Nine of the tumours contained a 102-bp PCR product demonstrated using consensus PV primers that amplify a portion of the L1 gene. The nucleotide sequences are closely related, but not identical to that of ovine PV type 2, rabbit oral PV and reindeer PV. The deduced amino acid sequences had strong homologies with the major capsid protein L1 of deer PV, bovine papillomavirus (BPV) 1 and BPV 2, and European elk PV. Although PV antigens were not detected in any of the tumours by immunohistochemistry, PV DNA was demonstrated in individual mesenchymal cells or cell nests of 4/12 tumours by in situ hybridization. A nonproductive infection of mesenchymal fibroblast-like tumour cells with a papillomavirus would explain the lack of PV antigen expression and the absence of PV DNA in the hyperplastic epithelium. Because these tumours and their pathogenesis are similar to equine sarcoids, we suggest that they should be reclassified as 'feline sarcoids' instead of fibropapillomas.  相似文献   
30.
The use of a peroxidase labelled PCR generated probe followed by enhanced chemiluminescence hybridization assay detected infectious bursal disease virus directly from bursal imprints on a nylon membrane. Tissue imprint hybridization proved to be a simple, rapid and safe means of detecting IBD virus for screening large numbers of field samples. The PCR generated probe was highly specific for IBD virus and did not hybridize with cellular nucleic acids in control imprints. Tissue imprint hybridization was found to be a more sensitive method than conventional antigen detection assays.  相似文献   
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