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排序方式: 共有266条查询结果,搜索用时 171 毫秒
1.
米氏凯伦藻(Karenia mikimotoi)近年在我国福建、浙江和广东沿海经常形成赤潮,其赤潮不仅影响到海洋生态系统的稳定,也严重威胁到水产养殖以及人类生命健康安全。本论文以米氏凯伦藻为研究对象,建立了米氏凯伦藻细胞表面膜蛋白质荧光标记技术和细胞膜蛋白质提取方法,运用荧光差异凝胶电泳技术(2-DDIGE)对膜蛋白质进行了分析,并研究了米氏凯伦藻的膜蛋白质组及其对环境温度变动的响应。实验共鉴定到44个细胞表面膜蛋白,其中有效注释27个,主要为转运蛋白、HSP70蛋白家族和捕光蛋白等。米氏凯伦藻在20°C条件下的细胞生长和光合作用要明显好于16°C和12°C,但16°C和12°C条件下的差别不大,表明低温限制了米氏凯伦藻的生长。当米氏凯伦藻从12°C快速转移至16°C和20°C时,藻细胞密度和光合作用效率短时间迅速降低,但细胞很快即适应温度变化。细胞膜上的转运蛋白和光合作用蛋白在其适应温度变化中起着重要作用。 相似文献
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以三疣梭子蟹肌肉基本营养成分、蛋白质组成、肌原纤维蛋白含量、Ca~(2+)-ATPase活性、总巯基含量、二硫键含量以及肌原纤维蛋白的SDS-PAGE分析作为指标,研究了三疣梭子蟹在不同冻藏温度下肌肉蛋白质生化特征的变化。结果表明,三疣梭子蟹是典型的高蛋白食品;随着冻藏时间的延长,水溶性蛋白含量先增加后减少,盐溶性蛋白和不溶性蛋白含量逐渐减少,碱溶性蛋白含量逐渐增加;肌原纤维蛋白含量、Ca~(2+)-ATPase活性、总巯基含量随着冻藏时间的延长,均呈现下降趋势,而二硫键含量则呈上升趋势,且–20℃和–40℃两组之间差异显著(P0.05)。SDS-PAGE分析结果表明,组成肌原纤维蛋白的各种蛋白质均有不同程度降解,且–20℃比–40℃组降解更明显。因此,–40℃冻藏对梭子蟹肌肉蛋白质生化特性的影响较小。 相似文献
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Chitosan composites and derivatives have gained wide attentions as effective biosorbents due to their low costs and high contents of amino and hydroxyl functional groups. They have showed significant potentials of removing metal ions, dyes and pro- teins from various media. Chemical modifications that lead to the formation of the chitosan derivatives and chitosan composites have been extensively studied and widely reported in literatures. The aims of this review were to summarize the important information of the bioactivities of chitosan, highlight the various preparation methods of chitosan-based active biosorbents, and outline its potential applications in the adsorption of heavy metal ions, dyes and proteins from wastewater and aqueous solutions. 相似文献
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地球三四十亿年的生命交响乐,它的主旋律是碳的化学演变。没有碳,就没有生命。碳,是生命世界的栋梁之材。我们来自何方?将去往何处?从远古的蛮荒直至今天的文明,这种疑问始终与人类相伴相随。几乎每一个人,在他有限的一生之中,或多或少都给过类似的问题以思考时间。或许因为,对于绝大多数人来说,这类思考不能解决任何实际问题,而流于一时无所事事的灵光乍现。所以迄今为止,有关生命的来源,我们仍然知之甚少。 相似文献
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Reversible protein phosphorylation, catalyzed by protein kinases and phosphatases, is an important and versatile mechanism by which eukaryotic cells regulate almost all the signaling processes. Protein phosphatase 1 (PP1) is the first and well-characterized member of the protein serine/threonine phosphatase family. In the present study, a full-length cDNA encoding the beta isoform of the catalytic subunit of protein phosphatase l(PPlcb), was for the first time isolated and sequenced from the skin tissue of flatfish turbot Scophthalmus maximus, designated SmPPlcb, by the rapid amplification of cDNA ends (RACE) technique. The cDNA sequence of SmPPlcb we obtained contains a 984 bp open reading frame (ORF), flanked by a complete 39 bp 5' untranslated region and 462 bp 3' untranslated region. The ORF encodes a putative 327 amino acid protein, and the N-terminal section of this protein is highly acidic, Met-Ala-Glu-Gly-Glu-Leu-Asp-Val-Asp, a common feature for PP1 catalytic subunit but absent in protein phosphatase 2B (PP2B). And its calculated molecular mass is 37 193 Da and pI 5.8. Sequence analysis indicated that, SmPPlcb is extremely conserved in both amino acid and nucleotide acid levels compared with the PPlcb of other vertebrates and invertebrates, and its Kozak motif contained in the 5'UTR around ATG start codon is GXXAXXGXXATGG, which is different from mammalian in two positions A6 and G3, indicating the possibility of different initiation of translation in turbot, and also the 3'UTR of SmPPlcb is highly diverse in the sequence similarity and length compared with other animals, especially zebraf'lsh. The cloning and sequencing of SmPPlcb gene lays a good foundation for the future work on the biological functions of PP1 in the flatfish turbot. 相似文献
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White spot syndrome virus (WSSV) is one of the major shrimp pathogens causing large economic losses to shrimp farming. In an attempt to identify the envelope proteins involved in the virus infection, purified WSSV virions were mixed with three antisera against WSSV envelope proteins (VP39, VP124 and VP187 ), individually. And then they were injected intramuscularly into crayfish (Procambarus clarkii) to conduct in vivo neutralization assays. The results showed that for groups injected with virions only and groups injected with the mixture of virions and antiserum against VP124, the crayfish mortalities were 100% and 60% on the 8th day postinfection, individually. The virus infection could be delayed or neutralized by antibody against the envelope protein VP124. Quantitative PCR was used to further investigate the influence of three antisera described above on the virus infection. The results showed that the antiserum against VP124 could restrain the propagation of WSSV in crayfish. All of the results suggested that the viral envelope protein VP124 played a role in WSSV infection. 相似文献