全文获取类型
收费全文 | 14623篇 |
免费 | 1041篇 |
国内免费 | 1611篇 |
专业分类
林业 | 1018篇 |
农学 | 814篇 |
基础科学 | 773篇 |
1460篇 | |
综合类 | 7345篇 |
农作物 | 1047篇 |
水产渔业 | 608篇 |
畜牧兽医 | 2253篇 |
园艺 | 1130篇 |
植物保护 | 827篇 |
出版年
2024年 | 129篇 |
2023年 | 363篇 |
2022年 | 789篇 |
2021年 | 685篇 |
2020年 | 622篇 |
2019年 | 633篇 |
2018年 | 451篇 |
2017年 | 762篇 |
2016年 | 517篇 |
2015年 | 681篇 |
2014年 | 805篇 |
2013年 | 881篇 |
2012年 | 1216篇 |
2011年 | 1335篇 |
2010年 | 1234篇 |
2009年 | 1152篇 |
2008年 | 1125篇 |
2007年 | 1023篇 |
2006年 | 788篇 |
2005年 | 589篇 |
2004年 | 412篇 |
2003年 | 243篇 |
2002年 | 221篇 |
2001年 | 258篇 |
2000年 | 221篇 |
1999年 | 74篇 |
1998年 | 9篇 |
1997年 | 5篇 |
1996年 | 4篇 |
1995年 | 6篇 |
1994年 | 2篇 |
1993年 | 2篇 |
1992年 | 7篇 |
1991年 | 3篇 |
1990年 | 3篇 |
1989年 | 1篇 |
1988年 | 2篇 |
1987年 | 4篇 |
1986年 | 3篇 |
1981年 | 2篇 |
1964年 | 1篇 |
1962年 | 4篇 |
1958年 | 1篇 |
1956年 | 3篇 |
1955年 | 4篇 |
排序方式: 共有10000条查询结果,搜索用时 218 毫秒
991.
生长因子EGF、bFGF对猪孤雌胚体外发育的影响 总被引:1,自引:0,他引:1
在胚胎发育的不同阶段,分别在培养基中添加EGF和bFGF,研究EGF和bFGF对猪孤雌胚体外发育的作用。结果表明:在1细胞阶段添加EGF或bFGF,添加EGF能够显著提高孤雌胚的卵裂率(P〈0.05);2~4细胞阶段添加EGF和bFGF,添加EGF组和添加bFGF组的囊胚率都显著高于对照组(P〈0.05),而添加bFGF组的囊胚率和囊胚细胞数都略高于对照组和添加EGF组。说明EGF和bFGF有利于猪孤雌胚的体外发育,而且,bF-GF能够通过提高囊胚细胞数而提高猪孤雌胚的质量。 相似文献
992.
肉鸡肠道PepT1 mRNA表达的肠段差异性与发育性变化 总被引:1,自引:0,他引:1
选用遗传背景相同的1日龄父母代雄性Arbor Acre(AA)鸡和父母代雄性岭南黄肉雏鸡各120羽,采用相对定量RT-PCR方法,以30 d时岭南黄鸡肠道样品为模板,研究肉鸡肠道寡肽转运载体1(Peptide transporter 1,PepT1)mRNA表达的肠段差异性;以AA肉鸡和岭南黄鸡十二指肠和空肠样品为模板,研究不同品种肉鸡肠道PepT1 mRNA表达的发育性变化。结果显示:(1)岭南黄肉鸡肠道PepT1 mRNA的表达丰度从十二指肠、空肠、回肠到结直肠依次降低,其中十二指肠显著高于结直肠(P<0.05);(2)AA鸡和岭南黄肉鸡PepT1 mRNA在十二指肠及空肠中的表达具有相同的发育模式,16 d表达丰度最高,16~44 d逐渐下降,58 d略微回升;不同基因型之间PepT1 mRNA丰度比较,AA鸡和岭南黄肉鸡两品种间PepT1 mRNA的表达没有显著差异(P>0.05)。以上结果说明:(1)随着肠道空间位置的后移,岭南黄肉鸡肠道PepT1 mRNA的表达丰度逐渐降低,其中十二指肠的表达丰度显著高于结直肠(P<0.05);(2)不同品种肉鸡十二指肠及空肠PepT1 mRNA的表达具有相同的发育模式,且同日龄两品种间的表达丰度未见明显差异,表明PepT1 mRNA表达受到发育阶段的调控,但品种间具有稳定性。 相似文献
993.
994.
A群猪轮状病毒JS株vp7基因序列分析 总被引:1,自引:0,他引:1
根据已发表的猪轮状病毒OSU毒株vp7基因核苷酸序列ORF两端保守区序列,设计一对特异引物,以猪轮状病毒JS毒株反转录cDNA为模板,通过PCR方法扩增出长约1000 bp目的片段。将其进行T-A克隆、序列测定和分析。结果表明,vp7基因全长1062 bp,含有一个981 bp的开放阅读框,编码326个氨基酸。与已知的15个毒株vp7全长基因的核苷酸及推导的氨基酸序列比较,同源性分别为74.5%~78.5%和75.2%~83.1%,核苷酸系统发育进化树结果表明,JS毒株与轮状病毒G9型参考毒株ICB2185、O-1亲缘关系较近,分为一个群,表明JS毒株血清型为G9型。目前,我国尚未见猪及其它动物轮状病毒G9型流行株的报道。 相似文献
995.
996.
Advances in research on Agaricus bitorquis mating and breeding systems,and the breeding of new strains of this mushroom both in China and overseas,have been reviewed.Progress in our understanding of the genetic basis of homokaryotic fruiting,nuclear migration and mitochondrial inheritance,has been presented.The three main groups of A.bitorquis strains (temperate,bridging and tropical) categorized on the basis of mating behavior,and the distribution of homogenic and heterogenic incompatibility within the groups,have been discussed.Existing problems have been identified,and proposals made for future research. 相似文献
997.
998.
999.
YIN Zhi-hua JIANG Wei-hong LI Feng YANG Xu-yu FENG Xiang-ling YAO Kai-tai 《园艺学报》2007,23(12):2374-2378
AIM: To examine the latent membrane protein 1(LMP1)-DNA sequence in nasopharyngeal carcinoma(NPC) and detect mRNA expression of LMP1,EBNA1,EBNA2,and to explore the relationship between EBV infectious status,expression products and NPC carcinogenesis.METHODS: LMP1 DNA was detected in NPC by PCR.Direct sequence was applied to analyze the difference between NPC-LMP1-DNA and B95-8- LMP1-DNA.mRNA expressions of LMP1,EBNA1,EBNA2 in NPC were detected by nested RT-PCR.RESULTS: LMP1 DNA existed in all 47 NPC tissues.Several single nucleotide variations were found between NPC-LMP1-DNA and B95-8- LMP1-DNA.The notable variation was the lost of XhoⅠrestriction site in NPC.Direct sequence showed 30 bp deletion in NPC.The mRNA expressions of LMP1,EBNA1 and EBNA2 in NPC were 76.6%,80.0% and 74.5% respectively by nested RT-PCR.The expression of EBNA1 in NPC was promoted by Q promoter while the expression of EBNA1 in B95-8 was promoted by C promoter.CONCLUSION: The way of EBV involved in NPC is complex.Latent genes such as LMP1,EBNA1 and EBNA2 as well as early lytic gene BARF1 may all play certain roles in NPC carcinogenesis. 相似文献
1000.
ZHANG Shui-jun ZHU Sheng-xing LI Jie MA Xiu-xian FENG Liu-shun FAN Zheng-jun 《园艺学报》2007,23(8):1480-1483
AIM:To investigate how brain-dead state affects the heart structure and function and the effect of PKC-α in BA-Ma mini pigs.METHODS:Ten Ba-Ma mini pigs were randomized into 2 groups: brain-dead group (n=5),and control group (n=5). The brain-dead model was made by increasing intracranial pressure,while the control group was maintained anesthesia for 24 h. The concentrations of cTnT,TNF-α,IL-1β and IL-6 in serum were determined at 6,12 and 24 h after brain death. At 24 h,heart tissues were observed by HE staining and electron microscope. The expression of PKC-α was detected by immunohistochemistry and RT-PCR.RESULTS:(1) Histological changes of myocardium: flaky bleeding under endocardium and dissolution of myocardium were found in optical microscope. In electron microscope dropsical mitochondria and confluent muscle fiber were found. (2) Changes of serum cTnT: serum cTnT for brain-dead group began to increase gradually since 6 h,and were significantly higher at each time point than those in control group (P<0.05). (3) Changes of inflammatory factors: IL-1β,IL-6,and TNF-α in brain-dead group began to increase gradually since 6 h,and were significantly higher at each time point than those in control group (P<0.05). (4) Changes of PKC-α expression: PKC-α mRNA and protein expressions in brain-dead group increased significantly at 24 h (P<0.05).CONCLUSION:Brain death may evoke heart structure and functional injury,and increase the levels of inflammatory factors and PKC-α. The activation of PKC-α may participate in the process of heart injury. 相似文献