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ZHANG Zhi CHENG Xiao-na FAN Ya-ting DONG Ya-qin LIU Shuang WU Fa-xing SHAO Wei-xing LI Xiao-cheng 《中国畜牧兽医》2015,42(7):1654-1660
To ascertain a diarrhea case in a pig farm in Shandong province,the pathological changes of dead piglets were observed and nested RT-PCR test was carried out on 7 diarrhea samples for porcine epidemic diarrhea virus (PEDV).Pathological examination revealed that intestine was detected as enlargement,hyperemia and edema.After histological examination,the typical microscopic lesions of intestine were disappearance of epithelial cells,villus shrinkage and shortening.The result of nested RT-PCR showed that all of the 7 samples could amplify a specific target band of PEDV.Molecular characteristics of two field strains showed that they had an amino acid homology of 92.3% to 92.4% with vaccine CV777 and 96.6% to 98.6% with other previous field strains which sequences were downloaded from GenBank.Phylogenetic tree analysis further revealed that all of PEDV strains could be mainly divided into two clusters of G1 and G2. G2 consisted of the field strains of our study and other field strains from USA,China and so on,which had the same sequence characteristics of two insertions and one deletion,while G1 consisted of all vaccines of CV777 and several older field strains from China and Korea.These results indicated that our field strains were the dominant strains in recent epidemic diarrhea occurrence.Moreover,its molecular characteristics might be a characterization of differentiating the field and vaccine strains. 相似文献
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Jaime Aguayo Cline Fourrier‐Jeandel Xavier Capdevielle Fabrice Vtillard Dominique Piou Eugenia Iturritxa Ccile Robin 《Forest Pathology》2020,50(1)
Fusarium circinatum is the causal agent of pitch canker, a destructive disease that threatens natural and planted pine forests around the world. Although pitch canker has caused problems in Spain and Portugal, concerning Europe as a whole, the fungus is not established across the pine distribution area. Its dispersion by wind and/or insect vectors could nevertheless play a role in the colonization of currently uninfected stands. It is therefore crucial to develop monitoring tools for its detection. To this end, we assessed the molecular detection of the pathogen in environmental samples of bark beetles and passive spore traps, collected in two infected Pinus radiata plantations in Basque country, Spain. The spread pattern of F. circinatum was assessed by an experimental design that included insect and spore traps installed at the centre, at the edge and outside the plots. Our results showed that F. circinatum was detected in both types of samples, at almost all collection dates. In both type of samples, positive detections were mainly found at the centre of the plots, a lower proportion at the edge, and very few outside. This suggests that long‐distance dispersion of Fusarium circinatum does not rely on wind spore dispersal neither on insect flight. Our study also shows that molecular methods are a powerful tool to monitor the pathogen in environmental samples. 相似文献
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[目的]进一步了解茶树小分子量热激蛋白基因CsHSP17.2在逆境胁迫条件下的分子生物学功能.[方法]利用RT-PCR技术从茶树‘迎霜’中克隆得到CsHSP1 7.2基因,运用生物信息学软件分析其核苷酸和编码蛋白,通过Real-timePCR分析其表达模式.[结果]该基因开放阅读框长度为453 bp,编码150个氨基酸,蛋白质相对分子质量为17.2×10a,理论等电点5.56;无信号肽位点,属于非分泌型蛋白;被定位于细胞质中.系统发育树分析表明,茶树CsHSP1 7.2与水稻(GenBank登录号:P27777)和花生(ABC41131)的进化关系较近,属于小分子量热激蛋白基因家族第Ⅰ亚族.qRT-PCR分析发现,茶树CsHSP17.2属于组成型基因;高温(38℃)处理1h能显著提高CsHSP17.2 mRNA的相对表达量(P<0.05);干旱(100 g·L-1 PEG 6000)、高盐(200 mmol· L-1 NaCl)和外源脱落酸(200 mg· L-1 ABA)处理条件下,该基因的转录水平均出现不同程度的上调.[结论]克隆得到茶树‘迎霜’小分子量热激蛋白基因CsHSP17.2,其在花中表达量最高,且响应高温、干旱、高盐和外源脱落酸胁迫. 相似文献
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Nazgol Emrani Mario Hasler Dilan S. R. Patiranage Maldonado-Taipe Nathaly Elodie Rey Christian Jung 《Plant Breeding》2020,139(6):1190-1200
Quinoa offers a promising alternative for staple food, considering its outstanding nutritional value and tolerance to abiotic stresses. To develop breeding programmes in quinoa, a reliable crossing method for increasing the genetic variation is required. In the following study, we aimed to develop segregating populations in quinoa. We tested the efficiency of three different crossing methods (hand emasculation, warm water emasculation and no emasculation). Moreover we developed a two-stage selection strategy based on morphological traits and molecular markers for the selection of hybrid plants. We reported hand emasculation to be the most efficient crossing method, followed by warm water emasculation and no emasculation. Our results demonstrated that crosses in quinoa can be successfully performed, despite its complicated flower structure and high self-pollination rate. Additionally, we developed 30 segregating populations from crosses between accessions of different origins with varying phylogenetic relationship, which offers a promising perspective for quinoa breeding programmes in the future. 相似文献
48.
动物的尾巴具有改变方向、控制升降、调整速度、支撑身体、防御、攻击、保温、示警、逃生和捕食等作用。鸟类的尾巴在飞行过程中起到平衡身体的关键作用,但在进化过程中尾部却出现了缩短和融合现象,如中国的瓢鸡及智利的Araucana鸡。作者简述了近年来关于鸡无尾性状的解剖学研究成果,发现无尾鸡在胚胎发育HH19期(Hamburger和Humilton标准分期)就已经出现无尾现象,而在结构上无尾鸡缺乏尾脂腺、尾羽、镰羽、尾椎骨和尾综骨。同时作者分析了导致尾部体节停止发育的分子遗传机制,包括周期性表达基因的转录调控影响尾部延伸过程、后端化因子梯度诱导尾部形成、Hox基因影响体节特化过程及基因突变有可能导致的无尾现象等,从而提出了可能导致家禽无尾性状的胚胎发育时期的关键分子及信号通路,包括Irx1和Irx2基因、Notch信号通路、Wnt信号通路、Fgf信号通路、RA信号通路等。研究鸡无尾性状的分子机制不仅可深入了解脊椎动物胚胎发育中尾部发育机制,更有利于揭示鸟类在进化过程中发生的尾部缩短及融合的机理。 相似文献
49.
最近,笔者实验室在青藏高原地区发现两种新亚型藏猪源猪流行性腹泻病毒(PEDV),为进一步调查新型PEDV是否在四川腹泻猪群中存在或流行,对实验室2018-2019年保存的116份猪腹泻粪便或肠组织样本进行PEDV的检测及其纤突蛋白基因(spike)分子特征研究。结果表明:腹泻样本的PEDV检出率为42.2%(49/116,95% CI=33.1%~51.8%),并获得了13条完整的S基因序列,全长为4 149~4 170 bp,序列相似性为94.2%~99.9%,其中SWUN-H3-CH-SCYA-2019的S基因与藏猪源新G1亚群PEDV的序列相似性高达97.0%~98.6%。遗传演化研究结果表明13株PEDV S基因划分为G1和G2大群,其中SWUN-H3-CH-SCYA-2019位于藏猪源新G1亚群;SWUN-19-CH-SCZY-2018、SWUN-4-CH-SCXC-2018、SWUN-1-CH-SCNJ-2019和SWUN-3CH-CH-SCZG-2019位于G2亚群中一个独立的分支,且与藏猪源新G2亚群毒株有着较近的亲缘关系。为了进一步研究13株PEDV的演化过程,以贝叶斯进化分析软件包(BEAST)进行分歧时间估算,结果表明SWUN-H3-CH-SCYA-2019的分歧时间约为2012.3年,早于藏猪源新G1亚群其余毒株的最早分歧时间(2015.7年);SWUN-4-CH-SCXC-2018、SWUN-19-CH-SCZY-2018和SWUN-3CH-CH-SCZG-2019的分歧时间约为2014.2年,早于G2亚群的藏猪源毒株2014.7年,所有藏猪源PEDV的分歧时间均晚于四川毒株。本研究在四川地区首次发现了藏猪源PEDV,并且从毒株的分歧时间推断青藏高原的藏猪源PEDV来源于四川,为新型PEDV分子遗传进化的监测提供了依据。 相似文献
50.
以鹰嘴豆蛋白为原料,建立复合酶分步酶解法制备鹰嘴豆短肽的工艺。在鹰嘴豆蛋白碱性蛋白酶Alcalase水解的基础上,进一步采用中性蛋白酶和风味蛋白酶Flavourzyme继续水解鹰嘴豆蛋白碱性蛋白酶Alcalase酶解物,并对各影响因素进行研究,建立短肽得率与各影响因素的回归模型,利用高效液相色谱法和氨基酸自动分析仪等测定鹰嘴豆短肽的相对分子质量、氨基酸组成、一般营养成分,评价鹰嘴豆短肽的营养价值。结果表明,中性蛋白酶和风味蛋白酶Flavourzyme制备鹰嘴豆短肽的最佳工艺参数为:复合酶添加量5 678 U/g,pH 7.0,水解时间216 min,水解温度55℃,在此条件下,短肽得率为63.79%,与碱性蛋白酶Alcalase单独酶解相比明显提高,水解度为26.74%;大部分水解产物的相对分子质量低于1 000、脂肪含量低,蛋白质、必需氨基酸等含量丰富,与FAO/WHO推荐的成人需求量模式相比,其第一限制氨基酸是蛋氨酸和半胱氨酸,与学龄儿童需求量模式相比,其第一限制氨基酸是苏氨酸,氨基酸分分别高达138.18和103.25;必需氨基酸与非必需氨基酸比值(EAA/NEAA)为0.73,接近FAO/WHO参考标准值0.6。该研究为进一步开发利用和工业化生产鹰嘴豆短肽奠定了基础。 相似文献