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SUN Qian WANG Qi HUANG Jinxiu QI Renli YANG Feiyun WANG Ruisheng LAN Yunxian 《畜牧兽医学报》1956,51(9):2156-2164
This study was conducted to investigate the effect of Lactobacillus reuteri on the expression of miRNAs in the jejunum of piglets. Six litters of healthy 1-day-old York×Rongchang piglets were selected and randomly divided into the two group,3 litters per group(n=27). The two groups were control group (daily orally adminitrated with 0.1% sterile peptone solution per piglet),and the LR group (daily orally administrated with 1.0×1010 CFU of L. reuteri per piglet), respectively. At 10 and 20 days of age, six piglets per group were selected for slaughter, respectively, and the jejunum samples were collected. After RNA extraction, the library was constructed and the miRNA expression profile of the jejunum was detected by Solexa high-throughput sequencing technology. Bioinformatics technology was used to conduct target genes prediction and functional analysis. The results showed that: 1) A total of 8 libraries were constructed and a total of 187 103 840 clean reads were obtained, of which the 22 nt length sequence accounted for the largest proportion; 2) Three hundred and fifty-four and 352 known miRNAs were respectively identified at 10 and 20 days of age, of which 329 miRNAs were co-expressed; 3) Differentially expressed (DE) miRNAs in the jejunum were found after L. reuteri administration, 7 and 9 DE miRNAs were obtained at 10 and 20 days of age,respectively. Notably, ssc-miR-218 was expressed differentially at two ages. 4) KEGG pathway analysis and target gene prediction on the differentially expressed miRNAs revealed that 10 221 target genes were enriched in 293 biological pathways, of which 66 were significantly enriched (P<0.05), including the MAPK signaling pathway and PI3K-Akt signaling pathway, which were known to regulate intestinal development and immune. 5) Six miRNAs were selected to validate the sequencing results by qRT-PCR, the qRT-PCR expression results corresponded well with those from the sequencing. The results indicates that L. reuteri may regulate intestinal health related pathways by influencing the expression of jejunal miRNAs. 相似文献
783.
巨型艾美尔球虫感染对雏鸡肠道乳酸杆菌的影响 总被引:2,自引:2,他引:2
取200只红羽肉杂雏鸡,饲喂至8日龄,随机分为3个球虫卵囊剂量感染组(0.5×105、1.0×105和2.0×105个/羽),并设对照组;于感染后1、3、5、7 d,各组分别处死雏鸡5只,测定小肠中段乳酸杆菌的定植数量。结果表明:与对照组比较3个试验组雏鸡肠道的乳酸杆菌定植数量均有降低。其中试验Ⅰ组,在感染后1、3 d,肠道乳酸杆菌定植数对数值分别为(5.46±0.14)和(5.57±0.14),与对照组比差异不显著(P>0.05);感染5、7 d后,分别为(5.71±0.45)和(5.80±0.52),达到差异显著水平(P<0.05)。试验Ⅱ、Ⅲ组,在感染后1 d,达到差异显著水平(P<0.05)。感染后3、5、7 d,肠道乳酸杆菌定植数量对数值与对照组比较达到极显著水平(P<0.01)。试验证明大剂量球虫感染可明显降低雏鸡小肠段乳酸杆菌的定植数量。 相似文献
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786.
本文旨在分离筛选适于在猪肠道生长的嗜酸乳杆菌(Lactobacillus acidophilus)菌株。选用仔猪新鲜粪便,利用MRS培养基,以平板划线法分离纯化菌株;采用形态、生理生化和16 SrRNA基因序列分析对分离菌株进行鉴定;通过逐步提高培养基酸度、胆盐浓度和培养温度,对分离菌株进行驯化。结果表明:1)经分离纯化获得的菌株La-5,被鉴定为嗜酸乳杆菌。2)驯化后的菌株La-5c在pH=1.5~3时存活率比原始菌株La-5高出36%~44%,极低pH(1.5)条件下仍有37%的存活率。3)在0.03%~0.3%胆盐中的存活率为85%~90%,而原始菌株La-5为28%~53%。4)在50℃时的存活率为66.1%,而原始菌株La-50.01%。由此可见,与仔猪粪便分离纯化的嗜酸乳杆菌原始菌株La-5比较,驯化获得的菌株La-5c具有耐低pH、高浓度胆盐及高温的特性。 相似文献
787.
根据猪传染性胃肠炎病毒(TGEV)纤突(S)蛋白的全基因序列及表达载体质粒的基因融合特点,设计一对引物,进行PCR,获得含有TGEV S基因4个主要抗原位点的约2000 bp目的片段,将其分别与表达载体质粒pPG611.1和pPG612.1进行连接,通过电转化进入宿主菌Lacto-bacillus casei393细胞内,通过质粒提取、PCR鉴定、酶切鉴定和序列测定分析,表明TGEV S基因已成功插入到表达载体质粒中,获得了TGEV S蛋白干酪乳杆菌表达载体系统。 相似文献
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790.