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排序方式: 共有349条查询结果,搜索用时 265 毫秒
1.
Phelps T. J. Siegrist R. L. Korte N. E. Pickering D. A. Strong-Gunderson J. M. Palumbo A. V. Walker J. F. Morrissey C. M. Mackowski R. 《Applied biochemistry and biotechnology》1994,45(1):835-845
Applied Biochemistry and Biotechnology - Soil column studies were used to evaluate petroleum hydrocarbon (PHC) remediation in soils from Kwajalein Atoll. Treatments included controls, and... 相似文献
2.
Palumbo A. V. Scarborough S. P. Pfiffner S. M. Phelps T. J. 《Applied biochemistry and biotechnology》1995,51(1):635-647
Applied Biochemistry and Biotechnology - The US Department of Energy, Office of Technology Development, has supported a field-scalein situ demonstration of trichloroethylene (TCE) bioremediation at... 相似文献
3.
Boseggia E Gatos M Lucatello L Mancin F Moro S Palumbo M Sissi C Tecilla P Tonellato U Zagotto G 《Journal of the American Chemical Society》2004,126(14):4543-4549
A series of cis-cis-triaminocyclohexane Zn(II) complex-anthraquinone intercalator conjugates, designed in such a way to allow their easy synthesis and modification, have been investigated as hydrolytic cleaving agents for plasmid DNA. The ligand structure comprises a triaminocyclohexane platform linked by means of alkyl spacers of different length (from C(4) to C(8)) to the anthraquinone group which may intercalate the DNA. At a concentration of 5 microM, the complex of the derivative with a C(8) alkyl spacer induces the hydrolytic stand scission of supercoiled DNA with a rate of 4.6 x 10(-6) s(-1) at pH 7 and 37 degrees C. The conjugation of the metal complex with the anthraquinone group leads to a 15-fold increase of the cleavage efficiency when compared with the anthraquinone lacking Zn-triaminocyclohexane complex. The straightforward synthetic procedure employed, allowing a systematic change of the spacer length, made possible to gain more insight on the role of the intercalating group in determining the reactivity of the systems. Comparison of the reactivity of the different complexes shows a remarkable increase of the DNA cleaving efficiency with the length of the spacer. In the case of too-short spacers, the advantages due to the increased DNA affinity are canceled due to the incorrect positioning of the reactive group, thus leading to cleavage inhibition. 相似文献
4.
Mild treatment of sepiomelanin and biosynthetic eumelanins with NaBH4 in 0.1 N NaOH leads to the isolation of 5,6-dihydroxyindole-2-carboxylic acid (), a component of structural interest which may account for most of the degradation products of melanins so far obtained. 相似文献
5.
6.
Palumbo Anthony V. Lee S. Y. Boerman Patrice 《Applied biochemistry and biotechnology》1994,45(1):811-822
Applied Biochemistry and Biotechnology - EDTA degradation by anAgrobacterium sp. has been examined by quantifying14C-labeled CO2 produced from iron-[2-14C] EDTA and by measured loss of nonlabeled... 相似文献
7.
Burlage Robert S. Palumbo Anthony V. Heitzer Armin Sayler Gary 《Applied biochemistry and biotechnology》1994,45(1):731-740
Applied Biochemistry and Biotechnology - Reporter strains of bacteria were tested using soil samples from several sites near a leaking fuel oil storage facility. The reporter bacteria utilized the... 相似文献
8.
Ohne Zusammenfassung 相似文献
9.
M. Palumbo F. Baccichetti C. Antonello O. Gia A. Capozzi S. Marciani Magno 《Photochemistry and photobiology》1990,52(3):533-540
The furocoumarin derivative 3,4'-dimethyl-8-methoxypsoralen (DMe-8-MOP) exhibits remarkable antiproliferative activity, but is devoid of skin phototoxicity. To gain insight into this peculiar behaviour we investigated non-covalent and covalent binding of DMe-8-MOP to calf thymus DNA, along with DNA-synthesis inhibition and mutagenic activity. The non-covalent interaction of DMe-8-MOP with the nucleic acid is quite poor as shown by equilibrium dialysis, spectroscopic, chiroptical and hydrodynamic techniques. However, it exhibits relevant photobinding ability to DNA using both isolated nucleic acid samples and cellular systems. Unlike the large majority of congeners, DMe-8-MOP undergoes predominantly photochemical monoaddition to the double helical polynucleotide. Upon examination of the products obtained by enzymatic hydrolysis of DMe-8-MOP photomodified DNA, the formation of an unusual furan side adduct is proposed, which could account for the peculiar photochemical and photobiological properties of the 3,4'-dimethyl furocoumarin derivative. 相似文献
10.
G. Zagotto O. Gia F. Baccichetti E. Uriarte M. Palumbo 《Photochemistry and photobiology》1993,58(4):486-491
The synthesis and the photobiological activity of two new hydroxymethyl derivatives of psoralen namely 4-hydroxymethyl-4'-methyl- and 4-hydroxymethyl-4'-methyl-8-rnethoxypsoralen are described. Both compounds exhibited efficient photobinding to DNA and RNA. The DNA-photobinding process was investigated using different nucleic acid structures such as double-helical DNA, ribosomal RNA, bacterial DNA and DNA organized in the nucleosomal arrangement. The test derivatives were able to induce cross-links to a similar extent as 8-methoxypsoralen (8-MOP), used as a reference photochemotherapeutic drug. In contrast to 8-MOP, they produced relatively high levels of l O2 . Most photobiological effects (DNA synthesis inhibition, T2 phage sensitization, inhibition of tumor transmitting capacity) showed a good correlation with the extent of covalent photoaddition. On the other hand, the new 4-hydroxymethylpsoralens were unable to induce skin erythema, in striking contrast with 8-MOP. Thus, neither cross-linking of the nucleic acid nor 1 O2 production were coupled with skin phototoxicity in this class of compounds. The new derivatives appear to represent an important beginning to development of new active photochemotherapeutic agents devoid of undesired phototoxic side effects. 相似文献