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51.
An acetyl-histone peptide library was used to determine the thermodynamic parameters that define acetylation-dependent bromodomain-histone interactions. Bromodomains interact with histones by binding acetylated lysines. The bromodomain used in this study, BrD3, is derived from the polybromo-1 protein, which is a subunit of the PBAF chromatin remodeling complex. Steady-state fluorescence anisotropy was used to examine the variations in specificity and affinity that drive molecular recognition. Temperature and salt concentration dependence studies demonstrate that the hydrophobic effect is the primary driving force, consistent with lysine acetylation being required for binding. An electrostatic effect was observed in only two complexes where the acetyl-lysine was adjacent to an arginine. The large change in heat capacity determined for the specific complex suggests that the dehydrated BrD3-histone interface forms a tightly bound, high-affinity complex with the target site. These explorations into the thermodynamic driving forces that confer acetylation site-dependent BrD3-histone interactions improve our understanding of how individual bromodomains work in isolation. Furthermore, this work will permit the development of hypotheses regarding how the native Pb1, and the broader class of bromodomain proteins, directs multisubunit chromatin remodeling complexes to specific acetyl-nucleosome sites in vivo. 相似文献
52.
A. Senthil Kumar V. Venkatesalu K. Kannathasan M. Chandrasekaran 《Indian journal of microbiology》2010,50(1):70-75
Bioleaching of uranium was carried out with Turamdih ore sample procured from Uranium Corporation of India Limited, Jaduguda.
The bacterial strain that was used in the leaching experiments was isolated from the Jaduguda mine water sample. Efficiency
of bioleaching was studied by varying parameters like pulp density and initial ferrous concentration as source of energy.
It is observed that the efficiency of bioleaching was 49% at 10% pulp density (w/v) and initial pH 2.0. Addition of external
has no effect on efficiency of bioleaching showing domination of direct leaching mechanism over indirect. 相似文献
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The linked-atom-least-squares (LALS) technique has been applied to generate exactly cyclized and stereochemically satisfactory conformations of the cyclic pentapeptide, malformin A, which contains an intramolecular disulfide bridge across a D-Cys—D-Cys linkage. Consistent with theoretical, ir, and x-ray evidence from studies on analogs of the LKiysteinyl—L-cysteine disulfide, it is shown that the peptide bond across the S? S bridge in malformin A can retain a cis configuration. The two all-trans structures proposed earlier by A.E. Tonelli [(1978) Biopolymers 17, 1175–1179] from solution nmr data have also been analyzed. Both P-(χs ~ 90°) and M-(χs ~ ?90°)-type helicity of the S? S bridge are found to be accessible in both the trans and the cis models in which the respective conformations of the homodetic rings are essentially preserved. The details of six different conformational states and their relative energies have been evaluated and compared. Our findings, which suggest that a variety of conformational states are accessible to malformin A, are compatible with other published results from solution studies. On the basis of hydrogen-bonding interactions, a model is proposed to explain how malformin A might be inactivated specifically by L -Hyp, and not by L -Pro or other amino acids, as has been observed from in vivo investigations [Buckhout, T.J. & Curtis, R.W. (1976) Nature 260 , 435–436] 相似文献
56.
B. V. Venkataram Prasad N. Shamala R. Nagaraj R. Chandrasekaran P. Balaram 《Biopolymers》1979,18(7):1635-1646
The crystal and molecular structure of N-benzyloxycarbonyl-α-aminoisobutyryl-L -prolyl methylamide, the amino terminal dipeptide fragment of alamethicin, has been determined using direct methods. The compound crystallizes in the orthorhombic system with the space group P212121. Cell dimensions are a = 7.705 Å, b = 11.365 Å, and c = 21.904 Å. The structure has been refined using conventional procedures to a final R factor of 0.054. The molecular structure possesses a 4 → 1 intramolecular N-H—O hydrogen bond formed between the CO group of the urethane moiety and the NH group of the methylamide function. The peptide backbone adopts the type III β-turn conformation, with ?2 = ?51.0°, ψ2 = ?39.7°, ?3 = ?65.0°, ψ3 = ?25.4°. An unusual feature is the occurrence of the proline residue at position 3 of the β-turn. The observed structure supports the view that Aib residues initiate the formation of type III β-turn conformations. The pyrrolidine ring is puckered in Cγ-exo fashion. 相似文献
57.
Transfer and Expression of a Multiple Antibiotic Resistance Plasmid in Marine Bacteria 总被引:1,自引:0,他引:1
Subramanian Chandrasekaran Balakrishnan Venkatesh Damodharan Lalithakumari 《Current microbiology》1998,37(5):347-351
Conjugal transfer of a multiresistance plasmid from Pseudomonas fluorescens to halophilic and halotolerant bacteria was studied under in vitro and in situ conditions. Mating conducted in broth as well
as on plates yielded a plasmid transfer frequency of as high as 10−3. Among these two, plate mating facilitated conjugal transfer of plasmid, because the cell-to-cell contact is more in plate
mating. When P. fluorescens was incubated in seawater, the organism progressively lost its colony forming activity within 15 days. Microscopic examination
revealed the presence of very short rods, indicating that the cells have become viable but nonculturable (VNC). Mating conducted
in natural seawater without any added nutrients revealed that the conjugal transfer is influenced by the physical state of
the donor and the recipients as well as the availability of nutrients. But a plasmid transfer frequency of 10−7 was obtained even after the donor cells have become VNC suggesting that the nonculturable state and nutrient deprived condition
may not limit plasmid transfer. The results suggest that the terrestrial bacteria entering into the seawaters with antibiotic
resistance plasmids may be responsible for the prevalence of resistance genes in the marine environment.
Received: 4 May 1998 / Accepted: 18 June 1998 相似文献
58.
Murugesan Chandrasekaran 《Biocontrol Science and Technology》2016,26(10):1366-1378
Bacterial spot disease caused by Xanthomonas campestris pv. vesicatoria is one of the most important destructive diseases of tomato in many parts of the agricultural world. Therefore, the present study aims to determine the effects of Bacillus subtilis CBR05 inoculation on bacterial spot disease severity and the induction of defence-related enzymes response in tomato. Tomato leaves were evaluated to determine the activities of antioxidant enzymes (superoxide dismutase (SOD), catalase (CAT), peroxidase (POD), and polyphenol oxidase (PPO)) and the content of malondialdehyde (MDA). A reduction in bacterial spot severity was observed in plants inoculated with B. subtilis, compared with those of uninoculated controls. A significant increase in SOD, CAT, POD, and PPO activities was observed in plants treated with B. subtilis after 24?h inoculation compared with non-inoculated pathogen control and mock-inoculated controls. Moreover, the MDA content was induced by pathogen infection, and its amount in B. subtilis inoculated plants was significantly lower than that in pathogen control. Our results suggest that early increases in antioxidant enzymes and the reduction in MDA content with B. subtilis inoculation may play a pivotal role in mitigating oxidative stress, thereby induced systemic resistance against bacterial spot disease in tomato. 相似文献
59.
Yousuf Sameena Sowrirajan Chandrasekaran 《Journal of biomolecular structure & dynamics》2016,34(7):1395-1408
This work deals with the commonly studied cyclic oligosaccharide and gains importance as it is entered on a drug delivering carbohydrate and provides insight into the oligosaccharide complex–biomolecular interaction. The binding of a flavone, baicalein, to β-cyclodextrin and calf thymus DNA is studied. The binding of baicalein to calf thymus DNA in the presence of β-cyclodextrin is analysed using the UV–vis absorption and fluorescence spectroscopy. The mode of binding and structure of the baicalein–β-cyclodextrin complex are reported. The role of the structure and the stoichiometry of the inclusion complex of baicalein–β-cyclodextrin in its influence on DNA binding are analysed.Highlights? This paper deals with the binding of a flavone, baicalein to β-cyclodextrin and/or DNA.? The inclusion complexation between baicalein and β-cyclodextrin is analysed.? The stoichiometry and the binding strength of the inclusion complex is reported.? The role of β-cyclodextrin in tuning the binding of baicalein to DNA is emphasized.? Spectroscopic and docking analysis are used to articulate the results. 相似文献
60.