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81.
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
82.
多年生黑麦草高频再生体系的建立及优化 总被引:2,自引:2,他引:2
从外植体预处理方式、基本培养基、激素浓度等方面着手,对多年生黑麦草愈伤组织诱导、继代、不定芽分化及再生过程中的影响因素进行了研究,提高了再生频率。结果如下:切取胚端半粒种子,经75%乙醇处理1min,0.1%HgCl处理15min,在经无菌水清洗4~6次后接种方式较好;愈伤组织诱导培养基以MS+2,4—D 8.0 mg/L(或另添加甘露醇25 g/L)为佳;愈伤组织接种于MS+2,4—D 8.0mg/L+甘露醇25 g/L上进行1~2次继代后于NB+6—BA2.0 mg/L上进行分化;不定芽转接至MS+6—BA2.0 mg/L上进行扩繁或于1/2MS+NAA0.5mg/L+IAA0.5mg/L上进行生根。 相似文献
83.
贵德黑裘皮羊耳成纤维细胞系的建立和生物学特性的研究 总被引:4,自引:1,他引:4
以贵德黑裘皮羊耳缘组织为材料,采用组织块贴壁培养法和细胞冷冻技术成功构建了成纤维细胞系,并对培养细胞进行了形态学、生长动力学观察、细胞活力测定、核型分析和微生物检测。结果表明:细胞群体倍增时间(PDT)约为36h,冻存前细胞活力为96.2%,以DMEM/F-12+20%FBS中添加10%DMSO冻存成纤维细胞,解冻后细胞活力为93.6%,24h后的贴壁率为85%。在传代10次之前,细胞染色体中二倍体(2n=54)占主体,约为82%~90%,细菌、真菌、病毒、支原体检测为阴性。该细胞系的建立,使贵德黑裘皮羊这一国家重要种质资源在细胞水平上保存下来,也为体细胞克隆等研究提供了理想的生物材料。 相似文献
84.
PB McKenna 《New Zealand veterinary journal》2013,61(6):312-314
Abstract AIM: To determine what, if any, changes have taken place in the optimum time, for undertaking faecal egg count reduction tests (FECRT) in sheep in New Zealand. METHODS: A comparison was made between the numbers and types of nematode genera adequately represented for testing purposes (faecal nematode egg count (FEC) of >50 epg) in initial FECRT case submissions to a veterinary laboratory in New Zealand, during two 4-year periods, in 1992–1995 and 2006–2009. RESULTS: Although there were some minor differences between them, the seasonal patterns of occurrence remained basically the same for all parasite genera in both datasets, with their individual peak periods of representation occurring during February to May in all instances. Not surprisingly, this period of maximum seasonal occurrence for each parasite genus also coincided with those months of the year when the greatest numbers of worm genera were adequately represented for faecal nematode egg count reduction (FECR) testing. CONCLUSIONS: The results of this study indicate that the optimum time for conducting FECRT in sheep in New Zealand continues to be during the late summer-autumn months of February to May. However, they also reaffirmed that even during this optimal period there are still likely to be many occasions when relatively few nematode genera may be sufficiently well represented for satisfactory FECR testing. Accordingly, veterinary practitioners ought to be aware that, in order to obtain a complete picture of the resistance status of all worm genera on a particular property, such testing may need to be carried out on more than one occasion. 相似文献
85.
86.
为研究云南半细毛羊毛囊干细胞(hair follicle stem cells,HFSCs)的生物学特性,采用组织块法分离培养云南半细毛羊HFSCs,并对其细胞形态、生长动力学、冷冻与复苏、染色体核型等生物学特性进行分析.结果表明:HFSCs为贴壁生长,体积小,核质比高,呈典型的铺路石状,在显微镜下折光性强、胞体透亮.细胞生长曲线为“S”型.冻存前细胞活率98.2%,复苏后细胞活率96.4%.染色体中正常二倍体数目2n=54,其中,长染色体中有3对为中着丝点染色体,23对为端着丝点染色体,X染色体为最大的近端着丝点染色体,Y染色体为最小的亚中着丝点染色体.所得细胞呈现典型的HFSCs特征,细胞活性好,细胞系为稳定的二倍体细胞系. 相似文献
87.
88.
Goo Jang So Gun Hong Byeong Chun Lee 《Journal of veterinary science (Suw?n-si, Korea)》2011,12(1):83-89
Somatic cell nuclear transfer (SCNT) is considered to be a critical tool for propagating valuable animals. To determine the productivity calves resulting from embryos derived with different culture media, enucleated oocytes matured in vitro were reconstructed with fetal fibroblasts, fused, and activated. The cloned embryos were cultured in modified synthetic oviduct fluid (mSOF) or a chemically defined medium (CDM) and developmental competence was monitored. After 7 days of culturing, the blastocysts were transferred into the uterine horn of estrus-synchronized recipients. SCNT embryos that were cultured in mSOF or CDM developed to the blastocysts stages at similar rates (26.6% vs. 22.5%, respectively). A total of 67 preimplantational stage embryos were transferred into 34 recipients and six cloned calves were born by caesarean section, or assisted or natural delivery. Survival of transferred blastocysts to live cloned calves in the mSOF and the CDM was 18.5% (to recipients), 9.6% (to blastocysts) and 42.9% (to recipients), 20.0% (to blastocysts), respectively. DNA analysis showed that all cloned calves were genetically identical to the donor cells. These results demonstrate that SCNT embryos cultured in CDM showed higher viability as judged by survival of the calves that came to term compared to blastocysts derived from mSOF cultures. 相似文献
89.
90.