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1.
An Escherichia coli mutant unable to support site-specific recombination of bacteriophage lambda 总被引:23,自引:0,他引:23
We report the isolation of mutations in, and the characterization of, an Escherichia coli gene, hip, that is required for site-specific recombination of phage lambda. hip mutants are recessive and are located near minute 20 on the linkage map. The gene product is not vital to bacterial growth, since deletion mutants are viable. The absence of hip product reduces lambda integration to barely detectable levels and also reduces prophage excision, but less drastically. Certain mutations in the lambda int gene partially restore integration and excision in hip- hosts. Homologous recombination promoted by recA does not require hip function. In addition to their defect in site-specific recombination, hip mutants are unable to support lytic growth of phage Mu or of certain lambda mutants. Their pleiotropic phenotype closely resembles that of himA mutants, but complementation, mapping and DNA sequencing show that hip and himA are different genes. 相似文献
2.
Regulation of cardiac contractile proteins by phosphorylation 总被引:4,自引:0,他引:4
S Winegrad G McClellan R Horowits M Tucker L E Lin A Weisberg 《Federation proceedings》1983,42(1):39-44
Several of the contractile proteins of the heart can be phosphorylated, but in studies with isolated proteins only phosphorylation of the inhibitory subunit of troponin (TnI) produces a major change in the properties of the contractile system. As TnI is phosphorylated, the concentration of calcium required for activation of contraction is increased. Phosphorylation of the tropomyosin-binding subunit of troponin (TnT) or of the light chain of myosin fails to change ATPase activity of the isolated protein system. Phosphorylation of TnI is stimulated by the beta-adrenergic system and inhibited by the cholinergic system. Maximum calcium-activated force produced by the contractile system can be increased in hyperpermeable cardiac cells by cyclic AmP (cAMP) or agents that stimulate cAMP synthesis. This change in the contractile system, which appears to be part of the physiological response to beta-adrenergic stimulation, is mediated by phosphorylation of an intermediate that then modifies the contractile system. Phosphorylation of the contractile proteins is not involved. 相似文献
3.
Summary Lomasomes in the conidia ofAspergillus nidulans can be divided into at least two distinct structures. The first is a twice double membrane bound core of cytoplasmic origin. The outermost membrane of the lomasome becomes incorporated into the plasmalemma as it migrates to rest next to the cell wall. The second lomasome structure appears to be a triangle shaped series of tubules arranged in a parallel fashion. The wide end next to the cell wall connected to the plasmalemma and the opposite end to an element of the endoplasmic reticulum. The term membranosome has been coined to designate this lomasome structure with its function of plasmalemma extension. Various structures of the conidium such as wall, endoplasmic reticulum and the cytoplasmic matrix undergo changes from the conidial chain stage to the free or resting conidial stage. This suggests that after conidiation and before the resting stage, the conidium continues to mature. 相似文献
4.
The A34R glycoprotein gene is required for induction of specialized actin-containing microvilli and efficient cell-to-cell transmission of vaccinia virus. 总被引:7,自引:5,他引:2 下载免费PDF全文
The mechanisms allowing vaccinia virus to spread from cell to cell are incompletely understood. The A34R gene of vaccinia virus encodes a glycoprotein that is localized in the outer membranes of extracellular virions. The small-plaque phenotype of an A34R deletion mutant was similar to that of mutants with deletions in other envelope genes that fail to produce extracellular vaccinia virions. Transmission electron microscopy, however, revealed that the A34R mutant produced numerous extracellular particles that were labeled with antibodies to other outer-envelope proteins and with protein A-colloidal gold. Fluorescence and scanning electron microscopy indicated that expression of the A34R protein was necessary for detection of vaccinia virus-induced actin tails, which provide motility to the intracellular enveloped form of vaccinia virus, and of virus-tipped specialized microvilli that project from the cell. The ability of vaccinia virus-infected cells to form syncytia after a brief exposure to a pH below 6, known as fusion from within, failed to occur in the absence of expression of the A34R protein; nevertheless, purified A34R- virions were capable of mediating low-pH-induced fusion from without. The present study provides genetic and microscopic evidence for the involvement of a specific viral protein in the formation or stability of actin-containing microvilli and for a role of these structures in cell-to-cell spread rather than in formation of extracellular virions. 相似文献
5.
6.
On the role of the bacteriophage lambda int gene product in site specific recombination 总被引:1,自引:0,他引:1
Integrative recombination of phage λ DNA occurs in extracts made from cells synthesizing int protein. In this paper we show that extracts of cells containing temperature-sensitive int protein are inactivated more rapidly by incubation at 38 °C than are wild-type extracts. This indicates that the int protein is directly involved in the recombination reaction. 相似文献
7.
Packaging of coliphage lambda DNA. I. The role of the cohesive end site and the gene A protein 总被引:6,自引:0,他引:6
The cohesive ends of the DNA of bacteriophage λ particles are normally formed by the action of a nuclease on the cohesive end sites (cos) of concatemeric λ DNA (reviewed by Hohn et al., 1977). The nuclease also cuts the cos site of an integrated prophage, and DNA located to the right is preferentially packaged into phage particles. This process occurs with approximately the same efficiency and rate in a single lysogen as in a tandem polylysogen. Thus, the rate of cos cutting does not increase when the number of cos sites per molecule increases, an hypothesis that has been proposed to explain why cohesive ends are not formed in circular monomers of λ DNA. We propose instead that the interaction of Ter with cos is influenced by the configuration of the DNA outside of cos during packaging, and that this configuration is different for circular monomers than for other forms of λ DNA. A model that gives rise to such a difference is described.We also found that missense mutations in the λ A gene changed the efficiency of packaging of phage relative to host DNA. This was not the case for missense mutations in several phage genes required for capsid formation. Thus, the product of gene A plays a role in determining packaging specificity, as expected if it is or is part of the nuclease that cuts λ DNA at cos. 相似文献
8.
Stephen B. Weisberg 《Journal of experimental marine biology and ecology》1982,62(3):237-249
The food conversion efficiency of Fundulus heteroclitus (L.) was measured in terms of calories and nitrogen for three diets: Palaemonetes sp., Nereis sp., and Uca pugnax. Fish were allowed to feed ad libitum for 30–60 min each day. Growth, ingestion, egestion, and excretion were measured for fish fed each diet. The growth rates of Fundulus heteroclitus fed two of the single item diets of invertebrates were higher than growth rates previously estimated for mummichogs from the natural population in Canary Creek marsh. In comparison with other fish species, F. heteroclitus was found to have a higher than average assimilation efficiency ( for all three diets) and a lower than average gross growth efficiency (≈12% for two of the diets). Metabolic costs accounted for an average of 69% of ingested energy. Excretion rates were also large, with excretion accounting for more energy than egestion in two of the three diets. 相似文献
9.
Kiyoshi Mizuuchi Martin Gellert Robert A. Weisberg Howard A. Nash 《Journal of molecular biology》1980,141(4):485-494
Catenanes (interlocked circular DNA molecules) are the exclusive products of the bacteriophage λ integrative recombination reaction in vitro when the substrate is a supercoiled DNA molecule containing both the attP and attB sites. It is proposed that the catenation results from the superhelical form of the substrate DNA. We also show that both circular DNA products of a single recombination event can be recovered as superhelical molecules with a superhelical density approximately that of the substrate DNA. The recombination reaction must therefore occur as a coupled process which does not permit free rotation around single-strand breaks at any stage. 相似文献
10.
The secondary attachment site for bacteriophage lambda in the proA/B gene of Escherichia coli 总被引:5,自引:0,他引:5
We have determined the nucleotide sequence of a secondary λ attachment site in , a site that accounts for 3% of lysogens isolated from Escherichia coli strains deleted for the primary site. Direct sequence analysis of the transducing bacteriophages carrying the left and right att junctions, as well as the recombinant pro+ phage reveals that the site shares an 11-nucleotide interrupted homology with the core sequence of the primary site. We have compared the att site with other secondary attachment sites to gain insights into the structural features important for λ integration. 相似文献