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31.
Crisan M Yap S Casteilla L Chen CW Corselli M Park TS Andriolo G Sun B Zheng B Zhang L Norotte C Teng PN Traas J Schugar R Deasy BM Badylak S Buhring HJ Giacobino JP Lazzari L Huard J Péault B 《Cell Stem Cell》2008,3(3):301-313
Mesenchymal stem cells (MSCs), the archetypal multipotent progenitor cells derived in cultures of developed organs, are of unknown identity and native distribution. We have prospectively identified perivascular cells, principally pericytes, in multiple human organs including skeletal muscle, pancreas, adipose tissue, and placenta, on CD146, NG2, and PDGF-Rbeta expression and absence of hematopoietic, endothelial, and myogenic cell markers. Perivascular cells purified from skeletal muscle or nonmuscle tissues were myogenic in culture and in vivo. Irrespective of their tissue origin, long-term cultured perivascular cells retained myogenicity; exhibited at the clonal level osteogenic, chondrogenic, and adipogenic potentials; expressed MSC markers; and migrated in a culture model of chemotaxis. Expression of MSC markers was also detected at the surface of native, noncultured perivascular cells. Thus, blood vessel walls harbor a reserve of progenitor cells that may be integral to the origin of the elusive MSCs and other related adult stem cells. 相似文献
32.
Three major low-pI zones of aldehyde dehydrogenase (aldehyde:NAD+ oxidoreductase, EC 1.2.1.3) may be visualized with specific histochemical staining after starch gel electrophoresis at pH 7.4 of Caucasian human liver extracts, whereas about 50% of Chinese human liver extracts show only two such zones. The three zones of activity were purified to apparent homogeneity from Caucasian liver. The substrate specificity of each form was investigated by double reciprocal plots using 13 aldehydes of various chemistries. The acetaldehyde-preferring isozyme I lacking in 50% of Chinese livers had a slightly lower native and subunit molecular weight than the "universal' isozymes IIa and IIb. All forms were highly sensitive to disulfiram inhibition. This inhibition could be protected against, or reversed, by dithiothreitol. 2,2'-Dithiodipyridine was a slower inhibitor of isoenzyme I. All three purified forms of the enzyme, as well as crude extracts of normal and isozyme I-deficient Chinese livers, showed positive immunoreactivity to antibodies prepared in rabbits against type I enzyme. Tryptic peptide maps of forms IIa and IIb were almost identical, whereas that of form I, although showing some similarities, was clearly different. These results provide a consistent explanation for the acetaldehyde-mediated extreme sensitivity to moderate alcohol ingestion shown normally by about 50% of oriental subjects and during disulfiram (Antabuse) therapy by all subjects. 相似文献
33.
荧光假单胞菌抗噬菌体菌株的选育 总被引:4,自引:2,他引:4
本实验从荧光假单胞菌(Pseudomonasfluorescens)AS—3菌株的不正常发酵液中分离到一种噬菌体,将其命名为PFAS。AS—3菌株能利用葡萄糖发酵产生D-异维生素C的前体物质2-酮基-D-葡萄糖酸。电镜观察表明PFAS噬菌体呈蝌蚪形,具有直径为66nm的六角形头部及长117nm的尾部。通过紫外线诱变及自然选育两种途径,配合简便有效的初筛方法,经多次分离、纯化、复筛最终在摇并发酵试验中获得6株产量稳定地高于对照敏感菌的抗噬菌体菌株,可望用于生产。 相似文献
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Successful immune-mediated regression of solid tumors is difficult because of the small number of cytotoxic T lymphocytes (CTLs) that were traffic to the tumor site. Here, the targeting of tumor-specific infiltrating CTLs was dependent on a fusion protein consisting of human epidermal growth factor (EGF) and staphylococcal enterotoxin A (SEA) with the D227A mutation. EGF-SEA strongly restrained the growth of murine solid sarcoma 180 (S180) tumors (control versus EGF-SEA, mean tumor weight: 1.013 versus 0.197 g, difference = 0.816 g). In mice treated with EGF-SEA, CD4+, CD8+ and SEA-reactive T lymphocytes were enriched around the EGFR expressing tumor cells. The EGF receptors were potentially phosphorylated by EGF-SEA stimulation and the fusion protein promoted T cells to release the tumoricidal cytokines interferon-γ (IFN-γ) and tumor necrosis factor-α (TNF-α). Intratumoral CTLs secreted cytolytic pore-forming perforins and granzyme B proteins near the surface of carcinomas, causing the death of many tumor cells. We additionally show that labeled EGF-SEA was directly targeted to the tumor tissue after intravenous (i.v.) injection. The findings demonstrate that antibody-like EGF-SEA plays an important role in arresting CTLs in the solid tumor site and has therapeutic potential as a tumor-targeting agent. 相似文献
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38.
Meng F Han Y Teng W Li Y Li W 《TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik》2011,123(8):1459-1465
Soybean aphid (Aphis glycines Matsumura) results in severe yield loss of soybean in many soybean-growing countries of the world. A few loci have been previously
identified to be associated with the aphid resistance in soybean. However, none of them was via isoflavone-mediated antibiosis
process. The aim of the present study was to conduct genetic analysis of aphid resistance and to identify quantitative trait
loci (QTL) underlying aphid resistance in a Chinese soybean cultivar with high isoflavone content. One hundred and thirty
F5:6 derived recombinant inbred lines from the ‘Zhongdou 27’ × ‘Jiunong 20’ cross were used. Two QTL were directly associated
with resistance to aphid as measured by aphid damage index. qRa_1, close to Satt470 on soybean linkage group (LG) A2 (chromosome
8), was consistently detected for 3- and 4-week ratings and explained a large portion of phenotypic variations ranging from
25 to 35%. qRa_2, close to Satt144 of LG F (chromosome 13), was detected for 3- and 4-week ratings and could explain 7 and
11% of the phenotypic variation, respectively. These two QTL were highly associated with high isoflavone content and both
positive alleles were derived from ‘Zhongdou 27’, a cultivar with higher isoflavone content. The results revealed that higher
individual or total isoflavones contents in soybean lines could protect soybean against aphid attack. These two QTL detected
jointly provide potential for marker-assisted selection to improve the resistance of soybean cultivars to aphid along with
the increase of isoflavone content. 相似文献
39.
Dondra Bailey Mohammed Abul Basar Sanjay Nag Nivedita Bondhu Shaloei Teng Atanu Duttaroy 《BMC developmental biology》2017,17(1):1