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71.
AVRAM HERSHKO PIERRE MAMONT ROBERT SHIELDS GORDON M. TOMKINS 《Nature: New biology》1971,232(33):206-211
A hypothesis has been developed to relate stringent control in bacteria to a set of interactions involved in the regulation of growth of transformed and untransformed mammalian cells. 相似文献
72.
Kimball and Wilson1 reported that the arabinose analogue of cytidine (ara-C) inhibited DNA polymerase in a crude extract prepared from Ehrlich ascites cells. Furth and Cohen2 observed cytosine arabinoside triphosphate (ara-CTP) inhibited DNA polymerase in extracts from either calf thymus or bovine lymphosarcoma tissue, although these investigators3 had already found no effect of ara-CTP on DNA polymerase from Escherichia coli. The inhibition in both of these cases could be substantially reversed by dCTP; but incorporation of the arabinose nucleotide (ara-CMP) into DNA could not be unequivocally demonstrated. Graham and Whitmore4 reported the incorporation of ara-C into DNA in vivo and the inhibition of a DNA polymerase from L cells by ara-CTP. They found that ara-CMP was initially incorporated into small DNA strands but subsequently appeared in long strands. Momparler5 has presented evidence that, in vitro, ara-C incorporation was limited to the 3′-hydroxyl end of DNA chains. Such incorporation might be expected to block further chain elongation but this expectation was not supported by the evidence presented by Graham and Whitmore. 相似文献
73.
ALINA TAYLOR 《Nature: New biology》1971,234(48):144-145
JACOB and Fuerst1,2 demonstrated the presence of a bacteriolytic enzyme (λ-endolysin) in the induced cultures of lysogenic Escherichia coli K12 (λ). The enzyme was later identified as the product of gene R; of phage λ3 which is involved in bacterial lysis at the end of a latent period. The enzyme is apt to form spheroplast-like structures in E. coli2 and one would therefore expect its substrate to be murein. 相似文献
74.
75.
76.
Intron-dependent transient expression of the maize GapA1 gene 总被引:2,自引:0,他引:2
77.
Summary To study the influence of phosphorylation and oxidation on the repeat domains of human Tau protein, we faced the challenge to selectively dimerize two cysteine-containing peptides in the presence of a nearby phosphate group. To this end, we were able to demonstrate the utility of a selective dimerization approach by forming disulfide bonds in unprotected phosphopeptides and extended the methodology to unprotected glycopeptides. Activation of one cysteine of a peptide chain with 2,2-dithiodipyridine and coupling this thiopyridyl-peptide to another peptide chain, containing an unprotected cysteine residue, yielded the mixed dimers in high purities and reasonable yields. Phosphate or sugar side chains on either peptide component remained unaffected during the activation and dimerization processes. While for mixed dimers the activated peptides were isolated by chromatography, homodimers were obtained by a simple one-pot reaction after 1 h. We demonstrate that cysteines can be dimerized in unprotected phosphopeptides and glycopeptides, without any side reactions affecting these posttranslational modifications.Abbreviations DCM
dichloromethane
- DMF
N,N-dimethylformamide
- DTP
2,2-dithiodipyridine
- Fmoc
9-fluorenylmethyloxycarbonyl
- HPLC
high-performance liquid chromatography
- MALDI
matrix-assisted laser desorption/ionization
- MS
mass spectrometry
- NFT
neurofibrillary tangles
- PHF
paired helical filaments
- PKC
protein kinase C
- RP
reversed phase
-
human Tau protein
- TFA
trifluoroacetic acid
Parts of this paper were presented at the 24th European Peptide Symposium in Edinburgh, Scotland, U.K., September 8–13, 1996. 相似文献
78.
79.
Summary The CCs are the site of Cl– transport in teleosts in sea water. The gills of freshwater teleosts contain at least two types of mitochondria-rich cell, the type and the type (Pisam and Rambourg, 1991). During seawater acclimation, the cells vanish and the cells are transformed and proliferate, and accessory cells appear in addition. This gives rise to the question of the function of cells in fish living in fresh water.According to the studies reviewed here, although they deal only with extrabranchial epithelia, the majority of evidence indicates that CCs (or MRCs) function as sites of active Ca2+ transport in freshwater teleosts. Moreover, some experimental results suggest that CCs are the Cl– uptake site in freshwater teleosts. The main problem in characterizing the CC function is that they have not yet been adequately described from the biochemical standpoint. This applies particularly to their metabolic pattern and the composition of their apical and basolateral membranes, including their integrated proteins and cell-cell junctions.Experiments with organ tissue cultures such as gill organ cultures from Oncorhynchus mykiss (McCormick and Bern, 1989) and opercular membrane cultures from Oreochromis mossambicus (McCormick, 1990) will almost certainly yield important results. Primary cell cultures of CCs would be even better for characterizing CCs. Such a cell culture of rainbow trout respiratory cells has already been established (Pärt et al., 1993). 相似文献
80.
A topological model for the haemolysin translocator protein HlyD 总被引:8,自引:0,他引:8
Ralf Schülein Ivaylo Gentschev Hans-Joachim Mollenkopf Werner Goebel 《Molecular & general genetics : MGG》1992,234(1):155-163
Summary A topological model for HlyD is proposed that is based on results obtained with gene fusions of lacZ and phoA to hlyD. Active H1yD-LacZ fusion proteins were only generated when lacZ was fused to hlyD. within the first 180 by (60 amino acids). H1yD-PhoA proteins exhibiting alkaline phosphatase (AP) activity were obtained when phoA was inserted into hlyD. between nucleotides 262 (behind amino acid position 87) and 1405 (behind amino acid position 468, only 10 amino acids away from the C-terminus of HlyD Active insertions of phoA into the middle region of hlyD. were not observed on in vivo transposition but such fusions exhibiting AP activity could be constructed by in vitro techniques. A fusion protein that carried the PhoA part close to the C-terminal end of HlyD proved to be the most stable HlyD-PhoA fusion protein. In contrast to the other, rather unstable, HlyD-PhoA+ fusions, no proteolytic degradation product of this HlyD-PhoA protein was observed and nearly all the alkaline phosphatase activity was membrane bound. Protease accessibility and cell fractionation experiments indicated that the alkaline phosphatase moiety of this fusion protein was located in the periplasm as for all other HlyD-PhoA+ proteins. These data and computer-assisted predictions suggest a topological model for HlyD with the N-terminal 60 amino acids located in the cytoplasm, a single transmembrane segment from amino acids 60 to 80 and a large periplasmic region extending from amino acid 80 to the C-terminus. Neither the HlyD fusion proteins obtained nor a mutant HlyD protein that had lost the last 10 amino acids from the C-terminus of HlyD exhibited translocator activity for HlyA or other reporter proteins carrying the HlyA signal sequence. The C-terminal 10 amino acids of HlyD showed significant similarity with the corresponding sequences of other HlyD-related proteins involved in protein secretion. 相似文献