全文获取类型
收费全文 | 2342篇 |
免费 | 226篇 |
国内免费 | 5篇 |
出版年
2023年 | 9篇 |
2021年 | 31篇 |
2020年 | 15篇 |
2019年 | 31篇 |
2018年 | 41篇 |
2017年 | 24篇 |
2016年 | 53篇 |
2015年 | 79篇 |
2014年 | 92篇 |
2013年 | 139篇 |
2012年 | 145篇 |
2011年 | 167篇 |
2010年 | 104篇 |
2009年 | 80篇 |
2008年 | 127篇 |
2007年 | 109篇 |
2006年 | 119篇 |
2005年 | 114篇 |
2004年 | 115篇 |
2003年 | 120篇 |
2002年 | 120篇 |
2001年 | 36篇 |
2000年 | 20篇 |
1999年 | 30篇 |
1998年 | 31篇 |
1997年 | 28篇 |
1996年 | 21篇 |
1995年 | 23篇 |
1994年 | 18篇 |
1993年 | 21篇 |
1992年 | 21篇 |
1991年 | 21篇 |
1990年 | 14篇 |
1989年 | 24篇 |
1988年 | 32篇 |
1987年 | 23篇 |
1986年 | 24篇 |
1985年 | 15篇 |
1984年 | 16篇 |
1983年 | 16篇 |
1982年 | 29篇 |
1981年 | 30篇 |
1980年 | 30篇 |
1979年 | 9篇 |
1978年 | 25篇 |
1977年 | 13篇 |
1976年 | 19篇 |
1975年 | 9篇 |
1974年 | 11篇 |
1973年 | 14篇 |
排序方式: 共有2573条查询结果,搜索用时 15 毫秒
11.
Don G. Lin Naomichi Nishio Tapan Kumar Mazumder Shiro Nagai 《Applied microbiology and biotechnology》1989,30(2):196-200
Summary The selective formation of three tetrapyrroles, Co-containing corrinoids, Ni-containing factor F430 and Fe-containing cytochromes (haems) by Methanosarcina barkeri Fusaro (DSM 804) was achieved as a function of the concentrations of Co2+, Ni2+ and Fe2+ in a methanol minimmum medium. It was found that about 70% of the total tetrapyrroles synthesized was excreted into the culture supernatant. Hence, the continuous production of tetrapyrroles in a fixed-bed reactor (supporter: porous diatomaceous clay) was carried out at a dilution rate of 10 day-1 (850 ml medium/85 ml column/day). The effluent discharged from the reactor contained the excreted tetrapyrroles, the concentrations of which were dependent upon the Co2+, Ni2+ and Fe2+ concentrations in the feed medium. The maximum productivities from the reactor (1 l basis) were 52 M corrinoids/day, 24 M F430/day and 8 M haems/day, respectively. 相似文献
12.
The mechanism of secretory granule formation and exocytosis in the endocrine cells of normal and transplanted rat pancreas was studied using electron microscopy. On the one hand, formation of secretory granules starts with the dilatation of the 2 ends or the vesicularization of the middle parts of rough endoplasmatic reticulum (RER). On the other hand, prohormone ribosomes condense into the vesicles of the GOLGI apparatus. This probably indicates that the GOLGI complex is not the only source of formation of secretory granules. Exocytosis occurs with the formation of an electron dense streak between the perigranular membrane and the apical cell membrane. This is followed by the rupture of the streak at this midpoint allowing the granule to extrude into the space between the cell membrane and the parenchymal basal membrane. This fusion-rupture-extrusion mechanism repeats itself at the parenchymal and capillary basal membranes and also at the endothelium until it gets into the capillary lumen, showing that hormones of pancreatic endocrine cells may be actively transported into circulation as intact secretory granules. There is no significant morphological difference between the mechanism of secretory granule formation in normal and transplanted pancreatic tissue. 相似文献
13.
P A Husain J E Colbert S R Sirimanne D G VanDerveer H H Herman S W May 《Analytical biochemistry》1989,178(1):177-183
A chiral derivatizing reagent, N-succinimidyl-2-(S)-methoxy-2-phenylacetic acid ester (SMPA), directed toward reaction with primary amine-containing compounds has been synthesized and characterized. This reagent is suitable for HPLC resolution from enzymatic-scale reactions where only microgram quantities of chiral products may be obtainable. SMPA derivatization was shown to be effective in the resolution of the enantiomers of a number of different racemic compounds. SMPA was used to resolve the diastereoisomeric derivatives of a previously unknown enzymatically oxygenated product, allowing determination of the stereochemical course of the enzymatic reaction. SMPA is easily prepared from an inexpensive, commercially available, and enantiomerically pure precursor with the formation of a shelf-stable crystalline product which is utilizable in water-containing solutions. In addition to its usefulness for micro-determinations, SMPA is useful for preparative-scale resolutions of enantiomers since the reagent is cleaved from the diastereoisomeric derivative by acid hydrolysis. 相似文献
14.
15.
Summary To extend the available information on the significance of the interactions between glycolytic enzymes and the actin component of the cellular ultrastructure, investigations into the compositional characteristics of the actin binding site on one of the major glycolytic enzymes, aldolase, have been undertaken. As the electrostatic nature of the association has been previously reported indicative of a cationic region on the enzyme involved in the binding, these studies have investigated the possibility of the involvement of histidine residues in this binding region. By the use of the histidine specific reagent, diethylpyrocarbonate, we have been able to establish a difference in nature of an actin binding domain and the active site domain which does contain an essential histidine. The results have been discussed in relation to the significance of this finding with respect to the binding of aldolase to subcellular structure. 相似文献
16.
The periplasmic location of enzymes A and B of the thiosulphate-oxidizing multienzyme system of Thiobacillus versutus has been further confirmed by differential radiolabelling of periplasmic and cytoplasmic proteins. The stoichiometries of respiration-driven proton translocation in T. versutus were determined using the oxygen pulse and the initial rate methods. A value for the H+/O quotient (number of protons translocated per oxygen atom reduced) of about 2.8 was found for the oxidation of thiosulphate, and of about 2.5 for sulphite. The H+/O quotient for endogenous respiration was about 5.7. The data are shown to be in good agreement with the scheme proposed previously for thiosulphate oxidation by this organism. Proton generation during the oxidation of thiosulphate or sulphite is indicated to occur in the periplasm rather than by pumping across the cytoplasmic membrane. The results also suggest that a H+/O quotient of six occurs during NADH oxidation (from endogenous metabolism measurements) and that the terminal cytochrome oxidase, aa3, does not function as a proton pump.Abbreviations DCCD
dicyclohexyl carbodiimide
- FCCP
carbonyl cyanide p-trifluoromethoxyphenylhydrazone
- HQNO
2-n-heptyl-4-hydroxyquinoline N-oxide
- TMPD
N,N,N,N-tetramethyl-p-phenylenediamine
- IEF
isoelectric focusing
- HIC
hydrophobic interaction chromatography
- EAI
ethyl acetimidate hydrochloride
- IAI
isethionyl acetimidate 相似文献
17.
Don J. Melnick 《International journal of primatology》1988,9(3):195-231
Among rhesus macaques (Macaca mulatta)and other cercopithecine monkeys, social groups occupying adjacent home ranges (i.e., members of the same local population)
exchange individuals and genes and thus exhibit marked genetic similarities. To assess the degree to which this pattern extends
beyond the local population, the genetic structure of M. mulattaand six other primate species was determined using Nei’s (1973) gene-diversity analysis. The genetic similarities seen among
social groups in the Dunga Gali population of M. mulatta (Melnick et al.,1984a) can be seen over the entire species range. Comparison of these results with the structures of other similarly organized
primate species indicates that (1) the average social group contains most of its local population’s genetic diversity, (2)
the average local population contains the majority of the genetic diversity found in the region to which it belongs, and (3)
the proportion of species gene diversity found in the average regional population varies substantially between species. Genetic
homogeneity within local and regional populations is probably the product of gene flow. The application of a number of analytical
models of selection and gene flow strongly suggests that gene flow, genetic drift, and zoogeography offer a more parsimonious
and plausible explanation for interspecific variation in regional differentiation than does stabilizing selection. 相似文献
18.
Age structure of nematode populations around maize growing in sandy soils in Iowa was studied at soil depths of 0-15and 15-30 cm for 2 years. Numbers of Longidorus breviannulatus were generally greater at 0-15 cm than at 15-30 cm deep until mid to late season. The decline in numbers of females as the season progressed indicates that fecundity slowed and is evidence of only one generation per year. Peak populations of Pratylenchus scribneri and Xiphinema americanum occurred in late August or early September. Adults of Hoplolaimus galeatus were few in the roots but common in the soil, indicating that fertilization occurred mostly in the soil. Numbers of P. scribneri were generally greater at the lower depth, especially late in the season. Community diversity (H'') was less when nematode biomass was used instead of numbers. Numbers of H. galeatus did not decline over the winter. Numbers of L. breviannulatus, P. scribneri, and X. americanum declined significantly over the winter, but not between spring cultivation and planting. 相似文献
19.
Salas-Prato Milagros Tanguay Jean-Francois Lefebvre Yves Wojciechowicz Don Liem H. Heng Barnes David W. Ouellette Ginette Muller-Eberhard Ursula 《In vitro cellular & developmental biology. Plant》1988,24(5):470-470
In Vitro Cellular &; Developmental Biology - Plant - 相似文献
20.
Summary Most of the inducible mutagenesis observed in Escherichia coli after treatment with many DNA damaging agents is dependent upon the products of the umuD,C operon. RecA-mediated proteolytic processing of UmuD yields a carboxyl-terminal fragment (UmuD) that is active for mutagenesis. Processing of UmuD is therefore a critical step in the fixation of mutations. In this paper we have analyzed the requirements for UmuD processing in vivo. Standard immuno-detection assays, coupled with a sensitive chemiluminescence detection assay, have been utilized to probe levels of chromosomally encoded Umu proteins from whole-cell E. coli extracts. We found that the derepression of additional SOS gene products, other than RecA, was not required for UmuD processing. Moreover, efficient cleavage of UmuD was observed only in the presence of elevated levels of activated RecA, suggesting that efficient processing would occur only under conditions of severe DNA damage. Detection of chromosomally encoded Umu proteins has allowed us, for the first time, to measure directly the cellular steady-state levels of these proteins under various SOS inducing conditions. UmuD was present at 180 copies per uninduced cell and was measured at 2400 copies per cell in strains that lacked a functional repressor. Induced levels of UmuC were approximately 12-fold lower than UmuD with 200 molecules per cell. These levels of cellular UmuC protein suggest that it functions through specific protein-DNA or protein-protein interactions, possibly as a lesion recognition protein or by interacting with DNA polymerase III. 相似文献