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41.
42.
Biological activity of the antitumor protein neocarzinostatin coupled to a monoclonal antibody by N-succinimidyl 3-(2-pyridyldithio)-propionate 总被引:6,自引:0,他引:6
Gundram Jung Wolfgang Köhnlein Gerd Lüders 《Biochemical and biophysical research communications》1981,101(2):599-606
The chromophore free apoprotein of neocarzinostatin was coupled to monoclonal IgG1 antibody using N-Succinimidyl 3-(2-pyridyldithio)-propionate as heterobifunctional reagent. After coupling active chromophore was reassociated with the apoprotein. We present here experimental evidence that the hybrid protein retains biological activity as measured by the degradation of T2-DNA and bacteriostatic action. 相似文献
43.
The DNA content of spermatids of mice carrying Cattanach's translocation has been measured with high precision by flow cytometry. The observation that the two peaks of DNA content in the haploid region of the DNA histograms represent X-and Y-bearing spermatids was tested and confirmed. Using flow cytometry, the difference in DNA content between the X and Y chromosomes in these mice was measured to be 5.2±0.1% of the total haploid genome as compared to 3.4±0.1% in normal mice. These results demonstrated the precision of flow cytometry for cytogenetic studies. Additional information on spermatogenesis in mice bearing Cattanach's translocation was obtained and showed a gradual loss of cells during spermatogenesis in those bearing the balanced form of the translocation. 相似文献
44.
Lucy A. Barrett Wolfgang J. Mergner Benjamin F. Trump 《In vitro cellular & developmental biology. Plant》1979,15(12):957-966
Summary Segments of human thoracic aorta were maintained in long-term explant culture for 18 weeks in serum-supplemented medium. The
aortas were grossly normal in appearance, and random samples fixed for light microscopy prior to culture revealed a normal
morphology. The intima contained no more than five layers of smooth muscle cells. After 7 days in culture, the intima was
noticeably thicker than the uncultured segments. The increased thickness was due to proliferating smooth muscle cells and
production of extracellular material. After several months in culture, extracellular material consisting of collagen and flocculent
material was present in areas resembling atherosclerotic fibrous plaques. A peripheral growth, which formed around the explant,
was composed of fibroblastlike cells and added to the overall thickness of the intima. However, aortic segment maintained
for up to 2 months in serum-free culture medium showed no cellular proliferation. This study demonstrates that changes resembling
early stages of atherosclerosis occur in human aortas maintained in explant culture using routine culture procedures.
Supported in part by the Pangborn Fund and the Graduate School of the University of Maryland.
This is publication 443 from the Cellular Pathobiology Laboratory. 相似文献
45.
46.
The enzyme catalyzing the reduction of sulfite by reduced benzyl viologen (BVH) was partially purified and characterized from two strains of wine yeasts, a sulfite-producing strain and a non-producing strain.Both enzymes showed corresponding features in pH-optima, optima of buffer and benzyl viologen concentrations.The enzymes did not catalyze the reduction of nitrite by reduced viologen dyes, but the reduction of sulfite was uncompetitively inhibited by nitrite. Compounds of sulfur metabolism such as sulfate, thiosulfate, cysteine, serine and methionine did not influence the activity of either of the enzymes. The main differences between the two enzymes exist in the specific activities in crude extracts, the K
m
-values for sulfite, substrate inhibition rates, and localization in different fractions during (NH4)2SO4 precipitation. The specific activity in crude extracts of the sulfite-producing strain (0.052 moles S2- x min-1 x mg-1) was about three fold higher than that of the non-producing strain (0.0179 moles S2- x min-1 x mg-1). On the other hand the sulfite-producing strain had a higher K
m
-value for sulfite (2×10-3 M) and was more strongly inhibited by the substrate than the non-producing strain (6×10-3 M). 相似文献
47.
48.
49.
Differential expression analysis for sequence count data 总被引:22,自引:0,他引:22
High-throughput sequencing assays such as RNA-Seq, ChIP-Seq or barcode counting provide quantitative readouts in the form
of count data. To infer differential signal in such data correctly and with good statistical power, estimation of data variability
throughout the dynamic range and a suitable error model are required. We propose a method based on the negative binomial distribution,
with variance and mean linked by local regression and present an implementation, DESeq, as an R/Bioconductor package. 相似文献
50.
Bulwin GC Wälter S Schlawinsky M Heinemann T Schulze A Höhne W Krause G Kalka-Moll W Fraser P Volk HD Löhler J Milford EL Utku N 《PloS one》2008,3(2):e1576
Classically, HLA-DR expressed on antigen presenting cells (APC) initiates lymphocyte activation via presentation of peptides to TCR bearing CD4+ T-Cells. Here we demonstrate that HLA-DR alpha 2 domain (sHLA-DRalpha2) also induces negative signals by engaging TIRC7 on lymphocytes. This interaction inhibits proliferation and induces apoptosis in CD4+ and CD8+ T-cells via activation of the intrinsic pathway. Proliferation inhibition is associated with SHP-1 recruitment by TIRC7, decreased phosphorylation of STAT4, TCR-zeta chain & ZAP70, and inhibition of IFN-gamma and FasL expression. HLA-DRalpha2 and TIRC7 co-localize at the APC-T cell interaction site. Triggering HLA-DR - TIRC7 pathway demonstrates that sHLA-DRalpha2 treatment inhibits proinflammatory-inflammatory cytokine expression in APC & T cells after lipopolysaccaride (LPS) stimulation in vitro and induces apoptosis in vivo. These results suggest a novel antiproliferative role for HLA-DR mediated via TIRC7, revise the notion of an exclusive stimulatory interaction of HLA-DR with CD4+ T cells and highlights a novel physiologically relevant regulatory pathway. 相似文献