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61.
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以淀粉珠为载体的亲和层析法分离纯化高温α淀粉酶张学忠,宋伦,王群,吴晓霞,唐锌进(吉林大学酶工程国家重点实验室,长春130023;南京师范大学生物系,南京210024)金凤燮等人从酒曲中筛选出高产热稳定α淀粉酶的菌株,命名为Bacillussp-JF... 相似文献
63.
Bi(Ⅲ)与金属硫蛋白作用性质研究张保林,黄辉,朱凌燕,岳晟,唐雯霞(南京大学配位化学研究所,配位化学国家重点实验室,南京210093)如何降低顺铂或其它抗癌铂的毒性,一直是癌症化疗中的重要课题之一,最近研究发现预先给大鼠或肺癌病人服用铋盐,可以极大... 相似文献
64.
Escherichia coli protein StpA stimulates self-splicing by promoting RNA assembly in vitro. 总被引:5,自引:1,他引:4 下载免费PDF全文
An Escherichia coli gene, stpA, has been identified and cloned based on its ability to suppress the Td- phenotype of a resident, splicing-defective phage T4 td (thymidylate synthase) gene. The stpA gene, which was localized to 60.24 min on the E. coli chromosome, encodes a 15.3-kDa protein. Overproduction of StpA in vivo led to an increase in td pre-mRNA levels and modest enhancement of td mRNA:pre-mRNA ratios. Consistent with its in vivo effect, purified StpA promoted RNA splicing in vitro, and facilitated RNA annealing and strand exchange with model substrates. These results suggest that StpA promotes splicing of the intron by binding RNA nonspecifically, resolving misfolded precursor molecules and facilitating association of critical base pair elements. Furthermore, proteinase K treatment of StpA-assembled precursors prior to the initiation of the splicing reaction still resulted in splicing enhancement, indicating that StpA is not required for the catalytic step, unlike the Neurospora splicing effector CYT-18, whose presence was necessary for catalysis to proceed. Together these results suggest that StpA has chaperone activity in vitro, with the property of promoting assembly of the precursors into an active conformation, in contrast to splicing effectors that stabilize the catalytically active intron structure. 相似文献
65.
Seeds of seven dune species were collected from sand dunes of Lakes Erie and Huron and buried to various depths in a natural sand dune habitat along Lake Huron. The seed samples were then retrieved after varying lengths of time and examined for their germinability and dormancy. Results showed that buried seeds remained viable for at least 2.5 years and had the potential to form a persistent seed bank. Seed banks were larger and longer lasting at greater depths of burial than those at shallow burial depths. The results suggested that failure to verify the existence of effective seed banks in previous studies may be due to insufficient number of samples, shallow sample depth, local population variations, and fruiting events. Several species also possessed a temporary, aboveground seed reserve formed by retention of a small proportion of viable seeds on the previous year's inflorescences. In some species, seeds retained aboveground were dormant and thus capable of forming a persistent seed bank when they entered the soil. 相似文献
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Cloning of the nupC gene of Escherichia coli encoding a nucleoside transport system, and identification of an adjacent Insertion element, IS 186 总被引:1,自引:0,他引:1
Escherichia coli is known to contain more than one active transport system for nucleoside uptake. In the present study we report the sequence of a gene encoding a second nucleoside transport system, nupC (in addition to nupG.) An open reading frame (ORF) of 1200bp was identified that codes for a hydrophobic polypeptide of 43 560 Da and an NupC fusion protein was shown to be membrane associated. The native NupC protein is also identified, following over-expression. NupC exhibits short regions of homology to several membrane-associated proteins, including LacY and Cyd. Analysis of the nupC promoter region revealed the presence of at least two putative CRP-binding sites, centred at–40bp and–89bp, which probably flank a CytR-binding site. In addition, an adjacent IS186 element was identified and found to reside within a putative terminator structure, downstream from the nupC ORF. This arrangement is shown to reflect the previously established gene order on the E. coli chromosome. 相似文献
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Yoshihito Suzuki Noboru Murofushi Yun-Hui Zhang Yasutomo Takeuchi 《Journal of Plant Growth Regulation》1994,13(2):63-67
Endogenous gibberellins were analyzed from a parasitic plant, clover broomrape (Orobanche minor Smith), and its host, clover (Trifolium repens L.). Members of both the early-13- and the early-non-hydroxylation pathways were identified from both the parasite and the host (GA12, GA24, GA9 GA4, GA44, GA19, GA20, and GA1 from clover broomrape; GA9, GA4, GA44, GA19, GA20, and GA1 from clover). Quantitative analyses showed that GA44 was present at high levels in both host and parasite. The similarity in the gibberellins suggests the possibility that the major gibberellins in clover broomrape are transported from clover. However gibberellins such as GA58, GA38, and notably GA47 which was identified from a plant for the first time were detected only from clover broomrape, suggesting that the parasite may have the ability to produce at least those gibberellins 相似文献