全文获取类型
收费全文 | 25507篇 |
免费 | 2110篇 |
国内免费 | 2099篇 |
专业分类
29716篇 |
出版年
2024年 | 66篇 |
2023年 | 352篇 |
2022年 | 807篇 |
2021年 | 1331篇 |
2020年 | 866篇 |
2019年 | 1056篇 |
2018年 | 1001篇 |
2017年 | 746篇 |
2016年 | 1054篇 |
2015年 | 1554篇 |
2014年 | 1831篇 |
2013年 | 1934篇 |
2012年 | 2364篇 |
2011年 | 2022篇 |
2010年 | 1283篇 |
2009年 | 1024篇 |
2008年 | 1392篇 |
2007年 | 1166篇 |
2006年 | 1054篇 |
2005年 | 898篇 |
2004年 | 745篇 |
2003年 | 636篇 |
2002年 | 580篇 |
2001年 | 490篇 |
2000年 | 378篇 |
1999年 | 430篇 |
1998年 | 255篇 |
1997年 | 218篇 |
1996年 | 255篇 |
1995年 | 205篇 |
1994年 | 252篇 |
1993年 | 152篇 |
1992年 | 220篇 |
1991年 | 183篇 |
1990年 | 174篇 |
1989年 | 113篇 |
1988年 | 83篇 |
1987年 | 75篇 |
1986年 | 49篇 |
1985年 | 63篇 |
1984年 | 48篇 |
1983年 | 39篇 |
1982年 | 37篇 |
1981年 | 24篇 |
1980年 | 16篇 |
1979年 | 25篇 |
1977年 | 15篇 |
1976年 | 16篇 |
1975年 | 15篇 |
1973年 | 17篇 |
排序方式: 共有10000条查询结果,搜索用时 0 毫秒
21.
22.
The effects of phosphorylation on the interaction between spectrin and ankyrin were investigated. Spectrin and ankyrin were phosphorylated using purified human erythrocyte membrane and cytosolic (casein kinase A) kinases. These two kinases have similar properties as well as activities toward spectrin and ankyrin. Both kinases catalyzed the incorporation of about 2 mol of phosphate/mol of spectrin and about 7 mol of phosphate/mol of ankyrin. These phosphates were incorporated primarily into seryl and threonyl residues of the proteins. The phosphopeptide maps of ankyrin phosphorylated by the membrane kinase and casein kinase A were identical. Binding studies indicate that ankyrin exhibits different affinities for spectrin dimers (KD = 2.5 +/- 0.9 X 10(-6) M) and tetramers (KD = 2.7 +/- 0.8 X 10(-7) M). These dissociation constants were not appreciably affected by the phosphorylation of spectrin. On the other hand, phosphorylation of ankyrin was found to significantly reduce its affinity for either phosphorylated or unphosphorylated spectrin tetramers (KD = 1.2 +/- 0.1 X 10(-6) M) but not spectrin dimers (KD = 2.5 +/- 0.4 X 10(-6) M). The same results were obtained using either the membrane kinase or casein kinase A as the phosphorylating enzyme. The above observation suggests that ankyrin phosphorylation may provide an important mechanism for the regulation of the erythrocyte membrane cytoskeletal network. 相似文献
23.
24.
When an exponentially growing culture of Escherichia coli is cooled to below 8 °C, initiation of protein synthesis appears to be blocked, while the elongation of initiated proteins continues until they are completed. This is demonstrated here by showing that nascent polypeptide chains increase in size during a 5 °C incubation and that f2 viral coat protein is completed, but not initiated. Upon rewarming, the cells initiate protein synthesis synchronously. This is demonstrated by a transient rise in the incorporation of methionine which is used to initiate protein synthesis. 相似文献
25.
26.
Successful replacement of avulsed scalp. Case report 总被引:2,自引:0,他引:2
M M Lu 《Plastic and reconstructive surgery》1969,43(3):231-234
27.
28.
Role of recurrent hydrophobic residues in catalysis of helix formation by T cell-presented peptides in the presence of lipid vesicles 总被引:2,自引:0,他引:2
S Lu V E Reyes R A Lew J Anderson J Mole R E Humphreys T Ciardelli 《Journal of immunology (Baltimore, Md. : 1950)》1990,145(3):899-904
We tested the hypothesis that the recurrence of hydrophobic amino acids in a polypeptide at positions falling in an axial, hydrophobic strip if the sequence were coiled as an alpha helix, can lead to helical nucleation on a hydrophobic surface. The hydrophobic surface could anchor such residues, whereas the peptide sequence grows in a helical configuration that is stabilized by hydrogen bonds among carbonyl and amido NH groups along the peptidyl backbone of the helix, and by other intercycle interactions among amino acid side chains. Such bound, helical structures might protect peptides from proteases and/or facilitate transport to a MHC-containing compartment and thus be reflected in the selection of T cell-presented segments. Helical structure in a series of HPLC-purified peptides was estimated from circular dichroism measurements in: 1) 0.01 M phosphate buffer, pH 7.0, 2) that buffer with 45% trifluoroethanol (TFE), and 3) that buffer with di-O-hexadecyl phosphatidylcholine vesicles. By decreasing the dielectric constant of the buffer, TFE enhances intrapeptide interactions generally, whereas the lipid vesicles only provide a surface for hydrophobic interactions. The peptides varied in their strip-of-helix hydrophobicity indices (SOHHI; the mean Kyte-Doolittle hydrophobicities of residues in an axial strip of an alpha helix) and in proline content. Structural order for peptides with helical circular dichroism spectra was estimated as percentage helicity from circular dichroism theta 222 nm values and peptide concentration. A prototypic alpha helical peptide with three cycles plus two amino acids and an axial hydrophobic strip of four leucyl residues (SOHHI = 3.8) was disordered in phosphate buffer, 58% helical in that buffer with 48% TFE, and 36% helical in that buffer with vesicles. Percentage helicity in the presence of vesicles of the subset of peptides without proline followed their SOHHI values. Peptides with multiple prolyl residues had circular dichroism spectra with strong signals, but since they did not have altered spectra in the presence of vesicles relative to phosphate buffer alone, the hydrophobic surface of the vesicle did not appear to stabilize those structures. 相似文献
29.
30.
Retrovirus-mediated transgenic keratin expression in cultured fibroblasts: specific domain functions in keratin stabilization and filament formation. 总被引:37,自引:0,他引:37
With retrovirus-mediated gene transfer, we used intact and deleted keratin proteins to investigate the molecular basis of intermediate filament function. Three levels of assembly show a different stringency for the involvement of individual keratin domains: protein accumulation requires the alpha helix domains; stable filament formation additionally requires both N- and C-terminal domains of either one of the two interacting keratins, suggesting that head to tail homotypic interaction is important for effective elongation; and higher order organization of the cytoplasmic network depends on correct type I-type II pairing of keratins. The presence of two distinct interaction sites along potentially different axes may explain the characteristic morphology of keratin intermediate filament networks. 相似文献