全文获取类型
收费全文 | 24892篇 |
免费 | 2323篇 |
国内免费 | 4286篇 |
出版年
2024年 | 50篇 |
2023年 | 266篇 |
2022年 | 475篇 |
2021年 | 995篇 |
2020年 | 902篇 |
2019年 | 1052篇 |
2018年 | 941篇 |
2017年 | 804篇 |
2016年 | 960篇 |
2015年 | 1471篇 |
2014年 | 1857篇 |
2013年 | 1967篇 |
2012年 | 2428篇 |
2011年 | 2256篇 |
2010年 | 1534篇 |
2009年 | 1430篇 |
2008年 | 1795篇 |
2007年 | 1535篇 |
2006年 | 1432篇 |
2005年 | 1230篇 |
2004年 | 1211篇 |
2003年 | 1077篇 |
2002年 | 994篇 |
2001年 | 562篇 |
2000年 | 441篇 |
1999年 | 322篇 |
1998年 | 277篇 |
1997年 | 162篇 |
1996年 | 159篇 |
1995年 | 165篇 |
1994年 | 118篇 |
1993年 | 89篇 |
1992年 | 78篇 |
1991年 | 57篇 |
1990年 | 47篇 |
1989年 | 53篇 |
1988年 | 40篇 |
1987年 | 32篇 |
1986年 | 34篇 |
1985年 | 37篇 |
1984年 | 18篇 |
1983年 | 15篇 |
1982年 | 24篇 |
1981年 | 9篇 |
1977年 | 5篇 |
1965年 | 5篇 |
1963年 | 4篇 |
1962年 | 4篇 |
1957年 | 5篇 |
1954年 | 4篇 |
排序方式: 共有10000条查询结果,搜索用时 46 毫秒
91.
精子介导鱼类基因转移和聚合酶链反应检测技术 总被引:18,自引:0,他引:18
金鱼精子与美洲大绵wei的抗冻蛋白基因一起保温30分钟后,再与卵子受精,共获得145尾成鱼和若干胚胎。从胚胎和成鱼中提取DNA经聚合酶链反应(PCR法)扩增和Southern blot分子杂交表明,外源的抗冻蛋白基因进入了部分受体鱼的染色体组内。测定了45尾一年龄实验鱼中,有12尾显示出明确的杂交带,阳性率为26%。 相似文献
92.
排卵,排精前后文昌鱼体内GnRH的研究 总被引:1,自引:1,他引:0
利用放射免疫分析法测定了排卵、排精前后青岛文昌鱼体内促性腺激素释放激素(GnRH)的含量变化,并通过高效液相色谱比较了雌、雄文昌鱼性腺及除性腺外体部GnRH的种类和含量的异同。结果表明:1)生殖过程中雌、雄文昌鱼体内GnRH含量的变化规律不同;雌性文昌鱼体内GnRH总含量在排卵时有所下降,排后12小时政策最为明显,以后逐渐上升到排前水平;雄性文昌鱼仅在排精时有所下降,2小时后即稳定在排水平。2)文 相似文献
93.
Jun Motoyama Keiko Taki Noriko Osumi-Yamashita Kazuhiro Eto 《Development, growth & differentiation》1994,36(3):281-288
We isolated mesenchymal cells from individual facial primordia of mouse embryos on 11 days post coitum and examined the effects of retinoic acid (RA) on chondrogenesis, induction of cell death, and the protein expression of retinoic acid receptor (RAR) β and γ in micromass culture. Under the control condition, cells of both medial and lateral nasal prominences (MNP and LNP) displayed high chondrogenic potential, while those of maxillary and mandibular prominences (Mx and Md) had constant growth activity and low chondrogenic potential. Though none of the cells expressed detectable levels of the RAR β protein, RAR γ was expressed in the cells of all the facial primordia. One μM RA inhibited the chondrogenesis, and induced cell death accompanied with the induction of the RAR β protein in LNP, MX and Md cells within 6 hr. On the contrary, both cell death and RAR β protein induction were detected in the MNP cells treated with RA for 24 hr. These results suggest that the RAR β is involved in the process of the cell death induced by the RA treatment in the mesenchymal cells of the mouse facial primordia. 相似文献
94.
Ying Cao Jun Adachi Axel Janke Svante Pääbo Masami Hasegawa 《Journal of molecular evolution》1994,39(5):519-527
The phylogenetic relationships among Primates (human), Artiodactyla (cow), Cetacea (whale), Carnivora (seal), and Rodentia (mouse and rat) were estimated from the inferred amino acid sequences of the mitochondrial genomes using Marsupialia (opossum), Aves (chicken), and Amphibia (Xenopus) as an outgroup. The overall evidence of the maximum likelihood analysis suggests that Rodentia is an outgroup to the other four eutherian orders and that Cetacea and Artiodactyla form a clade with Carnivora as a sister taxon irrespective of the assumed model for amino acid substitutions. Although there remains an uncertainty concerning the relation among Artiodactyla, Cetacea, and Carnivora, the existence of a clade formed by these three orders and the outgroup status of Rodentia to the other eutherian orders seems to be firmly established. However, analyses of individual genes do not necessarily conform to this conclusion, and some of the genes reject the putatively correct tree with nearly 5% significance. Although this discrepancy can be due to convergent or parallel evolution in the specific genes, it was pointed out that, even without a particular reason, such a discrepancy can occur in 5% of the cases if the branching among the orders in question occurred within a short period. Due to uncertainty about the assumed model underlying the phylogenetic inference, this can occur even more frequently. This demonstrates the importance of analyzing enough sequences to avoid the danger of concluding an erroneous tree. 相似文献
95.
Abstract: The effects of prostaglandin E2 (PGE2) on 86Rb efflux from rat brain synaptosomes were studied to explore its role in nerve ending potassium (K+) channel modulation. A selective dose-dependent inhibition of the calcium-activated charybdotoxin-sensitive component of efflux was found upon application of PGE2. No significant effect was seen on basal and voltage-dependent components over the concentration range of 10–8 to 10–5M. The protein kinase C (PKC) inhibitors H-7 (10 μM) and staurosporine (100 nM), as well as prolonged preincubation (90 min) with 40-phorbol 12, 13-dibutyrate, which has been reported to down-regulate PKC, abolished the PGE2-in- duced inhibition, whereas HA1004 (10 μM) and Rp-3′,5’cyclic phosphorothioate (100 nM), which are relatively more selective for protein kinase A than PKC, did not. 4β-Phorbol 12, 13-dibutyrate (100 nM), an activator of PKC, produced a similar inhibition of the Ca2+-dependent component of 86Rb efflux but also had no effect on the basal and voltage-dependent components. These data suggest that PGE2 can inhibit rat brain nerve ending calcium-activated 86Rb efflux, and this inhibition may involve PKC activation. 相似文献
96.
Effects of an antisense napin gene on seed storage compounds in transgenic Brassica napus seeds 总被引:4,自引:0,他引:4
Junko Kohno-Murase Makoto Murase Hiroaki Ichikawa Jun Imamura 《Plant molecular biology》1994,26(4):1115-1124
To manipulate the quantity and quality of storage components in Brassica napus seeds, we have constructed an antisense gene for the storage protein napin. The antisense gene was driven by the 5-flanking region of the B. napus napin gene to express antisense RNA in a seed-specific manner. Seeds of transgenic plants with antisense genes often contained reduced amounts of napin. In some transgenic plants, no accumulation of napin was observed. However, the total protein content of transgenic and wild-type seeds did not differ significantly. Seeds lacking napin accumulated 1.4 to 1.5 times more cruciferin than untransformed seeds, although the oleosin content was not affected. Fatty acid content and composition in the seeds of transgenic plants were also analyzed by gas chromatography. Though the total fatty acid content of the transformants was the same as that of non-transformants, there was a reduction in 18:1 contents and a concomitant increase of 18:2 in seeds with reduced napin levels. This observed change in fatty acid composition was inherited in the next generation. 相似文献
97.
Characteristics of Modified Leghemoglobins Isolated from Soybean (Glycine max Merr.) Root Nodules 总被引:1,自引:1,他引:0 下载免费PDF全文
Hemoprotein derivatives of an abundant soybean (Glycine max Merr.) root nodule leghemoglobin, Lba, were studied for their modified spectral characteristics and physical properties. Three modified hemoprotein derivatives of Lba (Lbam1, Lbam2, and Lbam3) were purified by preparative isoelectric focusing. The ferric forms of these pigments were green and exhibited anomalous spectra in the visible region as compared to the Lba3+ forms. These modified pigments showed a hypochromic shift of 10 nm for the charge transfer absorption maximum; however, differences were not apparent in the Soret region. Upon binding with nicotinate, the [alpha] and [beta] bands were shifted significantly into the red region as compared to the Lba3+ nicotinate complex. The three Lbam fractions were reduced by dithionite or by NADH in the presence of riboflavin. Lbam2+ also bound nicotinate and displayed absorption spectra indistinguishable from those of Lba2+ nicotinate. In contrast to Lba2+, Lbam2+ displayed aberrant spectra when bound with either O2 or CO. These complexes exhibited a prominent charge transfer band at approximately 620 nm and failed to exhibit spectra characteristic of Lba2+O2 and Lba2+CO. The protein moiety of these modified pigments was intact because their tyrosine/tryptophan ratios and their amino acid compositions were identical with those of Lba, nor were differences observed in the peptide profiles resulting from trypsin digests of purified Lba and Lbams. Automated Edman degradation of selected peaks further confirmed the intactness of the protein backbone including the absence of deamination. Pyridine hemochromogen for heme from Lbams could be formed, and the spectra displayed distinct differences compared to those of Lba. A new peak at 580 nm and a loss of a peak at 480 nm were observed for all three Lbams. 相似文献
98.
中国盲走螨属一新种和二新纪录:蜱螨亚纲:植绥螨科 总被引:1,自引:0,他引:1
本文记述我国植绥螨科盲走螨属Typhlodromus一新种和中国二新纪录:鲁盲走螨T.luensis sp.nov.,甲胄盲走螨T.lorcatus,肥厚盲走螨T.higoensis。标本保存于上海复旦大学环境和资源生物系。 相似文献
99.
A significant characteristic in a swimming pattern of a lamprey is the generation of a constant phase lag along its body in spite of the wide range of undulation frequencies. In this paper, we discuss a mathematical treatment for coupled oscillators with time-delayed interaction and propose a model for the central pattern generator (CPG) of a lamprey to account for the generation of a constant phase relation, with consideration of the signal conduction time. From this model, it is suggested that the desired phase relation can be produced by long ascending connections from the tail to the neck region of the CPG. 相似文献
100.
Two different single nucleotide transitions of hypoxanthine-guanine phosphoribosyltransferase (HPRT) were identified in a Japanese patient with Lesch-Nyhan syndrome (LNS) and a patient with hereditary gout. HPRT enzyme activities in the two patients were severely deficient, but the size and amount of mRNA were normal according to Northern analysis. Entire coding regions of HPRT cDNAs were amplified by PCR and sequenced. A G-to-A substitution at base 208 in exon 3, which predicted glycine 70 to arginine, was detected in the LNS patient (identical mutation with HPRTUtrecht). A C-to-A substitution at base 73 in exon 2, which predicted proline 25 to threonine, was detected in the gout patient (designated HPRTYonago). We transfected normal HPRT cDNA, mutant cDNA with HRPTUtrecht or mutant cDNA with HPRTYonago, respectively, to HPRT-deficient mouse cells and isolated permanent expression cell lines. The HPRT-deficient mouse cells had no detectable HPRT activity and a very low amount of HPRT mRNA. When the HPRT-deficient mouse cells were transfected with normal human cDNA, HPRT enzyme activity increased to 21.8% that of normal mouse cells. The mouse cells transfected with HPRTUtrecht showed no increase in HPRT activity; however, when the mouse cells were transfected with HPRTYonago, the activity increased to 2.4% that of normal activity. The proliferative phenotypes of these cells in HAT medium and in medium containing 6-thioguanine were similar to those of skin fibroblasts from the patients. This series of studies confirmed that each of the two point mutations was responsible for the decreases in HPRT enzyme activity, and the proliferative phenotypes in HAT medium and medium containing 6-thioguanine. 相似文献