全文获取类型
收费全文 | 21059篇 |
免费 | 1700篇 |
国内免费 | 1704篇 |
出版年
2024年 | 55篇 |
2023年 | 315篇 |
2022年 | 711篇 |
2021年 | 1152篇 |
2020年 | 765篇 |
2019年 | 977篇 |
2018年 | 912篇 |
2017年 | 618篇 |
2016年 | 914篇 |
2015年 | 1340篇 |
2014年 | 1518篇 |
2013年 | 1584篇 |
2012年 | 1935篇 |
2011年 | 1706篇 |
2010年 | 1001篇 |
2009年 | 927篇 |
2008年 | 1090篇 |
2007年 | 907篇 |
2006年 | 829篇 |
2005年 | 650篇 |
2004年 | 510篇 |
2003年 | 450篇 |
2002年 | 373篇 |
2001年 | 323篇 |
2000年 | 323篇 |
1999年 | 324篇 |
1998年 | 208篇 |
1997年 | 242篇 |
1996年 | 191篇 |
1995年 | 189篇 |
1994年 | 162篇 |
1993年 | 129篇 |
1992年 | 181篇 |
1991年 | 143篇 |
1990年 | 146篇 |
1989年 | 98篇 |
1988年 | 90篇 |
1987年 | 87篇 |
1986年 | 63篇 |
1985年 | 65篇 |
1984年 | 43篇 |
1983年 | 47篇 |
1982年 | 21篇 |
1981年 | 16篇 |
1980年 | 14篇 |
1979年 | 12篇 |
1978年 | 10篇 |
1969年 | 9篇 |
1968年 | 8篇 |
1965年 | 16篇 |
排序方式: 共有10000条查询结果,搜索用时 15 毫秒
201.
202.
辽河三角洲湿地的景观破碎化分析 总被引:111,自引:13,他引:98
利用遥感、GIS手段对辽河三角洲的湿地景观进行研究,并选用6种不同的方法对研究区的景观破碎化程度进行分析.结果表明,研究区的景观破碎化程度较低,总体斑块密度为0.286个·km-2,廊道密度为1.098km·km-2,聚集度指数为0.955.景观破碎化与人类活动密切相关,随着人类活动的增加,景观破碎化程度加深.廊道景观的发展是景观破碎化的前提与动因. 相似文献
203.
大鼠正中神经一级传入纤维在脊髓胶状质定位投射的定量分析——FRAP法 总被引:1,自引:0,他引:1
本文用抗氟化物酸性磷酸酶(FRAP)法和显微测量,对大鼠正中神经一级传入纤维在脊髓胶状质(SG)的定位投射进行了定量分析.大鼠正中神经向SG的纵向投射主要为C_5~T_1.C_5~T_1各节段SG水平向眉毛状反应带所测均值(mm)分别为0.888、0.935、0.957、0.905和 0.776,而正中神经向C_5~T_1各节段SG水平向投射所测均值(mm)分别在0~0.204、0~0.303、0~0.409、0~0.432和0~0.336的范围,这显示了正中神经投射区均位于SG的内侧带和部分中间带. 相似文献
204.
本文以L-苹果酸生产为例,采用新型的分段内循环气升式反应器分批培养产延胡索酸酶的产氨短杆菌MA-2,并与同等规模机械搅拌反应器中接着的结果相比较。数据表明,采用气升式发酵设备进行培养,该菌体的收率能提高近3%,且发酵周期能缩短一半左右,显著降低培养成本,该类型的反应器具有广阔的应用前景。 相似文献
205.
报道了一种修饰SOD的方法。所得硬脂酸修饰SOD比活力为每毫克蛋白10000单位,经鉴定已达均一程度。测得其分子量为35000.修饰SOD和天然SOD在紫外光区的最大吸收均在265nm。修饰SOD对温度、pH、蛋白酶水解的稳定性比天然SOD增强,且免疫原性消除。在低浓度的某些有机介质中活性比在水中高。 相似文献
206.
胡启明 《热带亚热带植物学报》1996,4(3):15-17
本文对过去一直认为是日本特有的两种珍珠菜属植物作了归并和组合:将Lysimachia,tashiroiMakino归并作L.patungensisHand.-Mazz.的异名,将L.tanakaeMaxim.降级作L.christinaeHance的亚种处理.对此间植物在中国和日本的地理替代现象作了讨论. 相似文献
207.
208.
Summary Based on the organelle differences between egg and sperm cells inPelargonium hortorum, the zygote, proembryo, and endosperm were examined under the transmission electron microscope. Plastids and mitochondria in the egg cell are significantly different from those of the sperm cell. Egg plastids are starch-containing and less electron dense. They appear circular, elliptical irregular elongate in sections. Sperm cell plastids are relatively electrondense, mostly cup-shaped or dumbbell and devoid of starch granules. Mitochondria of the egg cell are giant and mostly cup-shaped while sperm mitochondria are smaller and usually circular in section. Double fertilization is completed by 24 h after pollination and the pollen tube can be seen in the degenerated synergid. In the zygote, plastids and mitochondria from male and female gametes can be distinguished by their characteristic differences. Moreover, paternal and maternal organelles appear to be distributed at random in the zygote. Aside from the pollen tube and its released starch granules, there is no enucleated cytoplasmic body in the degenerated synergid. Two days after pollination, the zygote undergoes one transverse division to form a 2-celled proembryo which consists of one larger vacuolated basal cell and one smaller densely cytoplasmic apical cell. Paternal and maternal organelles can be detected in both cells of the proembryo and also in the endosperm at this stage. From these results, it can be concluded that plastids and mitochondria from both male and female gametes have been transmitted into the apical cell of the proembryo and most probably to the following generation.Abbreviations TEM
transmission electron microscope
- DAPI
4,6-diamidino-2-phenylindole
- RFLP
restriction fragment length polymorphism 相似文献
209.
稀有鮈鲫──一种新的鱼类毒性试验材料 总被引:7,自引:0,他引:7
本文研究了稀有鲫(Gobiocyprisrarus)作为毒性试验材料的可行性。采用换水式试验,在硬度为200mg/L(以CaCO3计)、pH7.8±0.2、温度24-25℃条件下研究了铬、铜、锌和五氯酚(PCP)对稀有鲫的急性毒性。重铬酸钾对2日龄稀有鲫的24h和96h和LC50控制范围分别263.6-334.7和1153-178.5mg/L(n=8)。铬、铜、锌和五氯酚对2日龄稀有鲫的急性毒性值(96hLC50)范围,从铜的52.2μg/L到铬的52000μg/L,毒性大小的顺序是铜>五氯酚>锌>铬。研究结果表明,稀有鲫有可能发展成为一种较为理想的毒性试验材料。 相似文献
210.
Mutational analysis of Saccharomyces cerevisiae U4 small nuclear RNA identifies functionally important domains. 总被引:1,自引:0,他引:1
下载免费PDF全文
![点击此处可从《Molecular and cellular biology》网站下载免费的PDF全文](/ch/ext_images/free.gif)
U4 small nuclear RNA (snRNA) is essential for pre-mRNA splicing, although its role is not yet clear. On the basis of a model structure (C. Guthrie and B. Patterson, Annu. Rev. Genet. 22:387-419, 1988), the molecule can be thought of as having six domains: stem II, 5' stem-loop, stem I, central region, 3' stem-loop, and 3'-terminal region. We have carried out extensive mutagenesis of the yeast U4 snRNA gene (SNR14) and have obtained information on the effect of mutations at 105 of its 160 nucleotides. Fifteen critical residues in the U4 snRNA have been identified in four domains: stem II, the 5' stem-loop, stem I, and the 3'-terminal region. These domains have been shown previously to be insensitive to oligonucleotide-directed RNase H cleavage (Y. Xu, S. Petersen-Bjørn, and J. D. Friesen, Mol. Cell. Biol. 10:1217-1225, 1990), suggesting that they are involved in intra- or intermolecular interactions. Stem II, a region that base pairs with U6 snRNA, is the most sensitive to mutation of all U4 snRNA domains. In contrast, stem I is surprisingly insensitive to mutational change, which brings into question its role in base pairing with U6 snRNA. All mutations in the putative Sm site of U4 snRNA yield a lethal or conditional-lethal phenotype, indicating that this region is important functionally. Only two nucleotides in the 5' stem-loop are sensitive to mutation; most of this domain can tolerate point mutations or small deletions. The 3' stem-loop, while essential, is very tolerant of change. A large portion of the central domain can be removed or expanded with only minor effects on phenotype, suggesting that it has little function of its own. Analysis of conditional mutations in stem II and stem I indicates that although these single-base changes do not have a dramatic effect on U4 snRNA stability, they are defective in RNA splicing in vivo and in vitro, as well as in spliceosome assembly. These results are discussed in the context of current knowledge of the interactions involving U4 snRNA. 相似文献