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991.
目的:通过克隆LC3.I基因,体外原核表达LC3-I蛋白后制备抗LC3单克隆抗体,作为自噬研究中的标记分子检测自噬的发生和发展过程。方法:RT.PCR方法从RAW264.7细胞基因组中克隆LC3基因,亚克隆至pQE80L原核表达载体后转化E.cobDH5a进行诱导表达,SDS—PAGE电泳及Westemblot鉴定表达蛋白。蛋白纯化后免疫BALB/c小鼠。采用淋巴细胞杂交瘤技术,制备分泌抗LC3.I杂交瘤细胞株,体内诱生腹水制备mAb,间接ELISA法测定其效价,辛酸一硫酸铵沉淀法及亲和层析法纯化mAb。结果:成功克隆了LC3一I基因,并对其在E.coilDH5a进行诱导表达,SDS-PAGE分析表明在相对分子量Mr为20×10^3有特异条带,Westernblot验证表达产物具有一定的生物学活性。建立了3株稳定分泌特异性抗LC3-ImAb的杂交瘤细胞株,诱导产生的腹水获得的抗体效价在10^5-10^7之间,结论:在E.coli中对LC3-I进行表达,并制备特异性较强抗LC3-I蛋白的单克隆抗体。为自噬研究提供了良好的标记分子,可对自噬形成和发展进行有效的检测。 相似文献
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994.
This paper presents a general, process-based mass balance model (CoastMab) for total phosphorus (TP) in defined coastal areas
(at the ecosystem scale). The model is based on ordinary differential equations and calculates inflow, outflow and internal
fluxes on a monthly basis. It consists of four compartments: surface water, deep water, erosion/transportation areas for fine
sediments and accumulation areas for fine sediments. The separation between surface water and deep water is not done based
on water temperature, but on sedimentological criteria instead (from the theoretical wave base). There are algorithms for
all major internal TP fluxes (sedimentation, resuspension, diffusion, mixing and burial). Validations were performed using
data from 21 different Baltic coastal areas. The results show that the model predicts monthly TP in water and chlorophyll a very well (generally within the uncertainty bands of the empirical data). The model has also been put through sensitivity
tests, which show that the most important factor regulating the predictions of the model is generally the TP concentration
in the sea beyond the coast. The model is simple to apply, since all driving variables may be accessed from maps or monitoring
programs. The driving variables include coastal area, section area (between the defined coastal area and the adjacent sea),
mean and maximum depths, latitude (used to predict water temperatures, stratification and mixing), salinity and TP concentration
in the sea. Many of the model structures are general and could be used for areas other than those included in this study,
e.g., for open coasts, estuaries or tidal coasts, as well as for other substances than phosphorus. 相似文献
995.
van Leeuwen BN van der Wulp AM Duijnstee I van Maris AJ Straathof AJ 《Applied microbiology and biotechnology》2012,93(4):1377-1387
Isobutene (2-methylpropene) is one of those chemicals for which bio-based production might replace the petrochemical production
in the future. Currently, more than 10 million metric tons of isobutene are produced on a yearly basis. Even though bio-based
production might also be achieved through chemocatalytic or thermochemical methods, this review focuses on fermentative routes
from sugars. Although biological isobutene formation is known since the 1970s, extensive metabolic engineering is required
to achieve economically viable yields and productivities. Two recent metabolic engineering developments may enable anaerobic
production close to the theoretical stoichiometry of 1isobutene + 2CO2 + 2H2O per mol of glucose. One relies on the conversion of 3-hydroxyisovalerate to isobutene as a side activity of mevalonate diphosphate
decarboxylase and the other on isobutanol dehydration as a side activity of engineered oleate hydratase. The latter resembles
the fermentative production of isobutanol followed by isobutanol recovery and chemocatalytic dehydration. The advantage of
a completely biological route is that not isobutanol, but instead gaseous isobutene is recovered from the fermenter together
with CO2. The low aqueous solubility of isobutene might also minimize product toxicity to the microorganisms. Although developments
are at their infancy, the potential of a large scale fermentative isobutene production process is assessed. The production
costs estimate is 0.9 € kg−1, which is reasonably competitive. About 70% of the production costs will be due to the costs of lignocellulose hydrolysate,
which seems to be a preferred feedstock. 相似文献
996.
Mi Li Lianqing Liu Xiubin Xiao Ning Xi Yuechao Wang 《Journal of biological physics》2016,42(4):551-569
Methotrexate is a commonly used anti-cancer chemotherapy drug. Cellular mechanical properties are fundamental parameters that reflect the physiological state of a cell. However, so far the role of cellular mechanical properties in the actions of methotrexate is still unclear. In recent years, probing the behaviors of single cells with the use of atomic force microscopy (AFM) has contributed much to the field of cell biomechanics. In this work, with the use of AFM, the effects of methotrexate on the viscoelastic properties of four types of cells were quantitatively investigated. The inhibitory and cytotoxic effects of methotrexate on the proliferation of cells were observed by optical and fluorescence microscopy. AFM indenting was used to measure the changes of cellular viscoelastic properties (Young’s modulus and relaxation time) by using both conical tip and spherical tip, quantitatively showing that the stimulation of methotrexate resulted in a significant decrease of both cellular Young’s modulus and relaxation times. The morphological changes of cells induced by methotrexate were visualized by AFM imaging. The study improves our understanding of methotrexate action and offers a novel way to quantify drug actions at the single-cell level by measuring cellular viscoelastic properties, which may have potential impacts on developing label-free methods for drug evaluation. 相似文献
997.
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The Ugi four-component reaction (U-4CR) was utilized to prepare divalent and trivalent cluster mannosides with different scaffolds. The glycoclusters obtained were tested for their relative inhibitory potency against the binding of yeast mannan to concanavalin A by solid-phase enzyme-linked lectin assays (ELLA) using methyl alpha-D-mannopyranoside as a standard. Among them, a divalent mannoside containing aromatic groups showed the strongest binding affinity to concanavalin A. 相似文献
1000.
从土壤中富集筛选获得一株产β-葡萄糖苷酶的菌株,经菌落的形态和18S rDNA鉴定确定为黑曲霉。将筛选出的黑曲霉菌株接种于发酵培养基,利用含有京尼平苷的栀子粉作为底物发酵,通过对发酵条件优化,得到在装液量50/250 mL,栀子粉浓度为10%,转速为180 r/min,发酵时间为96 h时,京尼平的微生物转化率达到最大22%。这种微生物转化法简化了京尼平的生产工艺,大大降低了生产成本。利用微生物转化获得的京尼平交联胶原蛋白材料,研究表明其具有较好的交联特性,是一种在食品、医药等领域都具有应用前景的生物交联剂。 相似文献