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31.
Patrick Diep Heping Leo Shen Julian A. Wiesner Nadia Mykytczuk Vladimiros Papangelakis Alexander F. Yakunin Radhakrishnan Mahadevan 《Engineering in Life Science》2023,23(7):2200133
Mine wastewater often contains dissolved metals at concentrations too low to be economically extracted by existing technologies, yet too high for environmental discharge. The most common treatment is chemical precipitation of the dissolved metals using limestone and subsequent disposal of the sludge in tailing impoundments. While it is a cost-effective solution to meet regulatory standards, it represents a lost opportunity. In this study, we engineered Escherichia coli to overexpress its native NikABCDE transporter and a heterologous metallothionein to capture nickel at concentrations in local effluent streams. We found the engineered strain had a 7-fold improvement in the bioaccumulation performance for nickel compared to controls, but also observed a drastic decrease in cell viability due to metabolic burden or inducer (IPTG) toxicity. Growth kinetic analysis revealed the IPTG concentrations used based on past studies lead to growth inhibition, thus delineating future avenues for optimization of the engineered strain and its growth conditions to perform in more complex environments. 相似文献
32.
A brachiopod fauna including 19 species of 17 genera from an exotic block in the Indus–Tsangpo suture zone in southern Tibet is described and illustrated. The brachiopod fauna is dominated by Martinia elegans and two new taxa: Jinomarginifera lhazeensis gen. et sp. nov. and Zhejiangospirifer giganteus sp. nov. The fauna is closely comparable with those from the middle and upper parts of the Wargal Formation and the Chhidru Formation in the Salt Range of Pakistan, the Chitichun Limestone in southern Tibet, and the Basleo area of West Timor, and these correlations suggest a Wuchiapingian age. The fauna exhibits substantial links with both peri–Gondwanan and Cathaysian faunas, which may imply that it is a seamount biota originally located in the southern margin of the Neotethys during the Late Permian, and was later (in the early Cenozoic) displaced and became sandwiched into younger marine deposits in the collision process between India and Eurasia. 相似文献
33.
34.
应用二维电泳技术,分析了经水分胁迫(PEG)、盐分胁迫(NaCl)和热激(40℃)处理后林生山黧豆(LathyrussylvestrisL.)体内蛋白质多肽及其含量的变化。有些蛋白质经PEG、NaCl和热激处理后可以产生相同的变化。两种不同的胁迫因子对某些蛋白质的影响有一定的共同性。特定的胁迫条件可以造成特定的影响。不同胁迫因子对同一蛋白质多肽可以造成不同的影响。胁迫下蛋白质的变化可能与林生山黧豆抵抗和适应胁迫条件的能力以及体内非蛋白质氨基酸的代谢有关 相似文献
35.
萌发花生种子子叶肽链内切酶的纯化和性质 总被引:1,自引:0,他引:1
萌发花生种子子叶的肽链内切酶经硫酸铵沉淀,SephadexG-100凝胶层析,DEAE-纤维素23阴离子交换层析和DEAE-SephadexA50层析,得到纯化的酶,该酶有两条同工酶,分子量分别为58和55KD,Km为9.9μmol/L,是半胱氨型肽链内切酶(EC3.4.22),对未萌发花生种子的贮藏蛋白没有明显降解作用. 相似文献
36.
Isoform-specific complementation of the yeast sac6 null mutation by human fimbrin. 总被引:4,自引:1,他引:3 下载免费PDF全文
The actin cytoskeleton is a fundamental component of eukaryotic cells, with both structural and motile roles. Actin and many of the actin-binding proteins found in different cell types are highly conserved, showing considerable similarity in both primary structure and biochemical properties. To make detailed comparisons between homologous proteins, it is necessary to know whether the various proteins are functionally, as well as structurally, conserved. Fimbrin is an example of a cytoskeletal component that, as shown by sequence determinations and biochemical characterizations, is conserved between organisms as diverse as Saccharomyces cerevisiae and humans. In this study, we examined whether the human homolog can substitute for the yeast protein in vivo. We report here that two isoforms of human fimbrin, also referred to as T- and L-plastin, can both substitute in vivo for yeast fimbrin, also known as Sac6p, whereas a third isoform, I-fimbrin (or I-plastin), cannot. We demonstrate that the human T- and L-fimbrins, in addition to complementing the temperature-sensitive growth defect of the sac6 null mutant, restore both normal cytoskeletal organization and cell shape to the mutant cells. In addition, we show that human T- and L-fimbrins can complement a sporulation defect caused by the sac6 null mutation. These findings indicate that there is a high degree of functional conservation in the cytoskeleton, even between organisms as diverse as S. cerevisiae and humans. 相似文献
37.
Thermotolerance in cultures of Chlorella zofingiensis was induced by heat shock treatment at supraoptimal temperatures (40and
45 °C for 30 min). Thermotolerance was assayed by two methods: the survival of the cells at 70 °C and the growth of diluted
cultures at 35 and 45 °C. A culture without heat shock treatment was unable to grow at 45 °C. According to eletrophoretic
analyses, the synthesis of proteins of 95, 73, 60, 43 and 27 kDa was induced by heat shock treatment. The large molecular
weight proteins (95, 73, 60 and43 kDa) were present in non-heat treated cells, but the heat shock treatment increased their
quantity in cells. The synthesis of a low molecular weight protein (27 kDa) was induced by heat shock treatment. The induced
thermotolerance could be inhibited by the presence of an 80S ribosomal translation inhibitor, cycloheximide(CHI). The first
12 amino acid residues from the N-terminus of the27 kDa heat shock induced protein are Val-Glu-Trp-Try-Gly-Pro-Asn-Arg-Ala-Lys-Phe-Leu.
This revised version was published online in August 2006 with corrections to the Cover Date. 相似文献
38.
HhaI and HpaII DNA methyltransferases bind DNA mismatches, methylate uracil and block DNA repair. 总被引:10,自引:7,他引:3 下载免费PDF全文
The hydrolytic deamination of 5-methylcytosine (5-mC) to thymine (T) is believed to be responsible for the high mutability of the CpG dinucleotide in DNA. We have shown a possible alternate mechanism for mutagenesis at CpG in which HpaII DNA-(cytosine-5) methyltransferase (M.HpaII) can enzymatically deaminate cytosine (C) to uracil (U) in DNA [Shen, J.-C., Rideout, W.M., III and Jones, P.A., Cell, 71, 1073-1080, (1992)]. Both the hydrolytic deamination of 5-mC and enzymatic deamination of C create premutagenic DNA mismatches (G:U and G:T) with the guanine (G) originally paired to the normal C. Surprisingly, we found that DNA-(cytosine-5) methyltransferases have higher affinities for these DNA mismatches than for their normal G:C targets and are capable of transferring a methyl group to the 5-position of U, creating T at low efficiencies. This binding by methyltransferase to mismatches at the recognition site prevented repair of G:U mismatches by uracil DNA glycosylase in vitro. 相似文献
40.