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951.
M. Murai    H. B. KC  N. Gima  C. Jung 《Plant Breeding》2003,122(5):410-415
Norin‐PL8 (‘PL8’) is an extremely cool‐tolerant line of rice in Japan that contains genes for cool tolerance originating from a javanica landrace. It was investigated to see whether the dwarfing gene d18‐k (kotaketamanishiki dwarf) exerts its pleiotropic effect on enhancing the cool tolerance at the booting stage in the genetic background of PL8. The d18‐k isogenic line of the recurrent parent PL8 (D8), PL8, and two commercial cultivars ‘Hayayuki’ and ‘Kirara 397’ were used. For each line/cultivar, the 12°C‐5‐day treatment was conducted at various times during the booting stage. In addition to spikelet fertility, the ratio (%) of the fertilized‐spikelet number of each treated panicle to the varietal mean of fertilized‐spikelet number per panicle in the control (FS‐T/C) was adopted to estimate cool temperature damage. For FS‐T/C, the lines‐cultivars ranked in the order of D8 > PL8 > ‘Hayayuki’ > ‘Kirara 397’, reflecting their cool tolerances. D8 exceeded PL8 in both pollen grain number per anther in the control and as an indicator of pollen fertility after the treatment, as a result of the effects of d18‐k. Consequently, d18‐k can be used to develop super‐highly cool‐tolerant cultivars for cool‐weather areas.  相似文献   
952.
本课题组在前期的研究中利用Al Cl3胁迫筛选碱茅全长c DNAs酵母表达文库获得到一个与铝毒害相关的未知基因(基因编号为018,用put018表示),该基因与拟南芥中未知基因(基因号为At5g57345,本研究中用At018表示)有较高的同源性。为了获得At018的纯化蛋白,本研究将拟南芥At018基因克隆后构建原核表达载体p GEX-6p-3-At018,再将其转入大肠杆菌BL21(DE3)菌株,利用异丙基-β-D-硫代半乳糖苷(IPTG)进行诱导表达。同时运用传统方法优化诱导条件,以提高重组融合蛋白的表达效率。SDS-PAGE分析结果表明,30℃下0.1 mmol/L IPTG的条件下诱导3 h后,GST-At018融合蛋白的表达量最大,蛋白分子质量与预测值相符,该蛋白主要以可溶性形式存在;接着利用Glutathione Sepharose4 Fast Flow亲核层析树脂纯化最终获得GST-At018融合蛋白。本研究可为进一步进行At018的功能解析提供基础。  相似文献   
953.
云南3种野生稻中抗白叶枯病基因的鉴定   总被引:1,自引:0,他引:1  
白叶枯病是水稻生产上最重要的细菌性病害之一,培育抗病新品种是防治白叶枯病最经济有效的途径。然而,栽培稻来源的抗病基因数量有限,并且部分抗病基因的抗病谱窄。因此,从野生稻中发掘抗病基因,将有利于培育抗病谱广且抗病能力强的水稻新品种。本研究通过抗性鉴定和PCR分析,检测云南野生稻中的抗白叶枯病基因。结果表明,云南野生稻对2个代表性白叶枯病菌Y8和PXO99具有不同程度的抗性,疣粒野生稻甚至达到免疫的程度。功能标记检测结果显示,3种野生稻中均不含xa5、xa13和Xa21抗病基因,元江普通野生稻含Xa23和Xa3/Xa26基因或其同源基因,景洪普通野生稻中含Xa1、Xa3/Xa26和Xa27基因或同源基因,药用野生稻含Xa3/Xa26基因或同源基因,而疣粒野生稻含有Xa27抗性基因。本研究结果为进一步发掘和克隆云南野生稻中的抗白叶枯病新基因提供了理论参考。  相似文献   
954.
利用华北地区流行的白粉菌菌株E09和E20,分别对河南省小麦新品种(系)区域和预备试验参试材料908份(2009—2013年度)和412份(2009—2012年度)进行苗期白粉病抗性鉴定,同时利用与Pm2、Pm4a、Pm8和Pm21基因连锁的分子标记检测相关抗病基因的分布。结果显示,抗E09的材料占21.9%(199/908),抗E20的材料占9.5%(39/412),同时抗E09和E20的材料仅占3.6%(15/412)。在908份供试材料中,580份含有1BL/1RS,占63.9%,含Pm8或新的1RS来源抗白粉病基因;另有2份材料含6AL/6VS来源广谱抗白粉病基因Pm21,8份可能携带Pm2,2份可能含有Pm4a;有6份材料可能含有多个抗白粉病基因。表明河南省近年育成的小麦新品种(系)依然含有对我国白粉菌菌系有效的抗白粉病基因,但抗源遗传基础较窄,部分已经或正在丧失抗性,应加快引进和利用新的多样化抗病基因资源。  相似文献   
955.
曹征  李曼菲  孙伟  张丹  张祖新 《作物学报》2015,41(11):1632-1639
BEL1-like(BELL)家族蛋白是植物中普遍存在的一类具有同源异型结构域的转录因子。拟南芥中BELL家族蛋白能与KNOTTED1-like蛋白互作形成异源二聚体,并结合到特异顺式作用元件来调控基因的表达,从而影响植物生长发育进程。本文采用隐马可夫(HMM)模型,在玉米基因组中鉴定到15个BELL家族基因(Zm BELL),分布于7条玉米染色体。通过与拟南芥BELL基因的序列比较将这些基因分为两大类。在玉米8种组织中Zm BELL有不同的表达模式,具有明显的组织表达特异性。基于基因共表达分析及BELL-like蛋白特异结合的顺式元件分析,预测到86个可能受Zm BELL调控的下游靶标基因。这86个基因和12个Zm BELL表达模式相同,并且在基因启动子区存在与BEL1-like蛋白结合的顺式元件。这些结果为进一步解析玉米BELL家族基因的功能和作用机制积累了有价值的资料。  相似文献   
956.
A random amplified polymorphic DNA marker OPG17450 linked to the Ns gene that confers resistance of potato to potato virus S (PVS), was used to develop sequence‐characterized amplified region (SCAR) markers. After cloning and sequencing of OPG17450 new polymerase chain reaction (PCR) primers were designed to generate dominant (SCG17321) and codominant (SCG17448) markers. For SCG17448, polymorphism between susceptible and resistant genotypes was recovered after digestion of the marker with the restriction enzyme Muni. In addition to the band corresponding to ‘susceptible’ allele that does not contain the Muni cleavage site, two bands of approximately 251 bp and 197 bp were observed in the resistant genotypes. The usefulness of these SCAR markers was verified in diploid potatoes possessing the Ns locus from clone G‐LKS 678147/60, and in tetraploid potatoes derived from G‐LKS 678147/60 and from clone MPI 65118/3.  相似文献   
957.
Wheat microsatellite XGWM261, due to its closely linked to the dwarfing gene Rht8, has been adopted as the diagnostic molecular marker of Rht8. Screening 408 Chinese and 98 exotic varieties showed 13 allele variants in locus of XGWM261, with 6 alleles only to be found in Chinese varieties and 2 only in exotic varieties, respectively. Sequencing results of the 13 alleles revealed their absolute fragment sizes with 216, 212, 210, 206, 204, 202, 200, 196, 194, 192, 190, 174, and 164 bp, respectively. Allelic distribution analysis showed that the 204, 192, 174, and 164 bp alleles were prevailing in Chinese varieties, and the diagnostic 192 bp allele to Rht8 had a very high percentage in the Yellow and Huai River Valleys Facultative Wheat Zone than in the Northern Winter Wheat Zone in China. The GT → AC substitution at position 35 was found in 216, 200, and 174 bp alleles. Moreover, the AG insertion immediately at the end of CT-repeat region was also found in 216, 200, 174, and 164 bp alleles.  相似文献   
958.
J. Zhang    X. Li    G. Jiang    Y. Xu    Y. He 《Plant Breeding》2006,125(6):600-605
‘Minghui 63’ is a restorer line widely used in hybrid rice production in China for the last two decades. This line and its derived hybrids, including ‘Shanyou 63’, are susceptible to bacterial blight (BB), caused by Xanthomonas oryzae pv. oryzae (Xoo). To improve the bacterial blight resistance of hybrid rice, two resistance genes Xa21 and Xa7, have been introgressed into ‘Minghui 63’ by marker‐assisted selection and conventional backcrossing, respectively. The single resistance gene‐introgressed lines, Minghui 63 (Xa21) and Minghui 63 (Xa7) had higher levels of resistance to bacterial blight than their derived hybrids, Shanyou 63 (Xa21) or Shanyou 63 (Xa7). Both Xa21 and Xa7 showed incomplete dominance in the heterozygous background of rice hybrids by infection with GX325 and KS‐1‐21. The improved restorer lines, with the homozygous genotypes, Xa21Xa21 or Xa7Xa7, were more resistant than their hybrids with the heterozygous genotypes Xa21xa21 or Xa7xa7. To further enhance the bacterial blight resistance of ‘Minghui 63’ and its hybrids, Xa21 and Xa7 were pyramided into the same background using molecular marker‐aided selection. The restorer lines developed with the resistance genes Xa21 and Xa7, and their derived hybrids were evaluated for resistance after inoculation with 10 isolates of pathogens from China, Japan and the Philippines, and showed a higher level of resistance to BB than the restorer lines and derived hybrids having only one of the resistance genes. The pyramided double resistance lines and their derived hybrids have the same high level of resistance to BB. These results clearly indicate that pyramiding of dominant genes is a useful approach for improving BB resistance in hybrid rice.  相似文献   
959.
Genetic mapping of loci determining long glumes in the genus Triticum   总被引:1,自引:0,他引:1  
Elongated glumes are present in thetetraploid wheat species T.polonicum, T. turanicum, T.durum convar. falcatum and in thehexaploid species T. petropavlovskyi.Inheritance of glume length was studiedwith the aim to map the respective lociusing wheat microsatellite markers. In T. polonicum and T. petropavlovskyiloci conferring long glume were mapped nearthe centromere on chromosome 7A. These twoloci are designated P-A pol 1 andP-A pet 1, respectively. It isshown that both are probably homoeoallelicto each other and to the P gene ofT. ispahanicum on chromosome 7B. The loci determining elongated glumes in T. turanicum and T. durum conv. falcatum are not homoeologous to the P loci in the centromeric region of thegroup 7 chromosomes.  相似文献   
960.
A trisomic series was produced from a triploid plant of barley (Hordeum vulgare L. cv. ‘Golden Promise’) derived from tissue culture. Its characteristics are briefly described and compared with two trisomic series reported previously. Trisomic number 1 performed poorly under glasshouse conditions. Number 2 failed to set any seed after selfing and must be maintained by pollinating with ‘Golden Promise’. The series was subsequently used to locate a recessive chlorina gene on barley chromosome 3.  相似文献   
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