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991.
Tissue-specific expression of the platelet GPIIb gene 总被引:6,自引:0,他引:6
G Uzan M Prenant M H Prandini F Martin G Marguerie 《The Journal of biological chemistry》1991,266(14):8932-8939
992.
The Spanish ``Asturiana' cattle breed is characterized by the segregation of a genetically determined muscular hypertrophy
referred to as double-muscling or ``culones'. We demonstrate by linkage analysis that this muscular hypertrophy involves
the mh locus previously shown to cause double-muscling in the Belgian Blue cattle breed, pointing towards locus homogeneity of this
trait across both breeds. Moreover, using a twopoint and multipoint maximum likelihood approach, we show that flanking microsatellite
markers are in linkage disequilibrium with the mh locus in both breeds albeit with different alleles. Finally, we discuss how allelic homogeneity across breeds might be exploited
to achieve efficient genetic fine-mapping of the mh locus.
Received: 13 September 1996 / Accepted: 20 January 1997 相似文献
993.
994.
Repression of the Escherichia coli modABCD (molybdate transport) operon by ModE. 总被引:5,自引:1,他引:4 下载免费PDF全文
A M Grunden R M Ray J K Rosentel F G Healy K T Shanmugam 《Journal of bacteriology》1996,178(3):735-744
995.
996.
Clinicians rely heavily on expert based systems-consultation with colleagues, journal reviews and textbooks, and continuing education activities-to obtain new information. The usefulness of sources such as these depends on the relevance and validity of the information and the work it takes to obtain it. Useful information can be distinguished from the useless by asking three questions: Does the information focus on an outcome that my patients care about? Is the issue common to my practice, and is the intervention feasible? If the information is true, will it require me to change my practice? If the answer to all three questions is yes, then the information is a common POEM (patient oriented evidence that matters), capable of improving the lives of your patients and must be evaluated for validity. Conclusions based on results of well designed clinical trials are more likely to be valid than those drawn from observations based on experience in clinical practice. Both members of the team, clinicians and experts, must take responsibility for their respective roles. 相似文献
997.
The synthesis, translocation, and decarboxylation of phosphatidylserine can occur in a cell-free system (Voelker, D. R. (1989) J. Biol. Chem. 264, 8019-8025). We made use of the spatial separation of the site of biosynthesis and the site of decarboxylation of phosphatidylserine to demonstrate that mitochondrial contact sites are intimately involved in the translocation of phosphatidylserine prior to decarboxylation. In that sense, the inhibition of phosphatidylserine decarboxylase leads to an accumulation of this phospholipid in the contact site-enriched fractions without mixing the inner membrane phospholipid pool. On the other hand, newly synthesized phosphatidylethanolamine can be exported very rapidly to the mitochondrial surface in the same way, i.e. via contact sites. These data provide further evidence for the existence of a structural and functional microcompartmentation at the inner mitochondrial membrane surface. 相似文献
998.
The rate of proteolysis is an important determinant of the intracellular protein content. Part of the degradation of intracellular
proteins occurs in the lysosomes and is mediated by macroautophagy. In liver, macroautophagy is very active and almost completely
accounts for starvation-induced proteolysis. Factors inhibiting this process include amino acids, cell swelling and insulin.
In the mechanisms controlling macroautophagy, protein phosphorylation plays an important role. Activation of a signal transduction
pathway, ultimately leading to phosphorylation of ribosomal protein S6, accompanies inhibition of macroautophagy. Components
of this pathway may include a heterotrimeric Gi3-protein, phosphatidylinositol 3- kinase and p70S6 kinase. Recent evidence
indicates that lysosomal protein degradation can be selective and occurs via ubiquitin- dependent and -independent pathways.
This revised version was published online in November 2006 with corrections to the Cover Date. 相似文献
999.
1000.
Colicin import and pore formation: a system for studying protein transport across membranes? 总被引:5,自引:2,他引:3
Claude J. Lazdunski 《Molecular microbiology》1995,16(6):1059-1066
Pore-forming colicins are a family of protein toxins (Mr40–70kDa) produced by Escherichia coli and related bacteria. They are bactericidal by virtue of their ability to form ion channels in the inner membrane of target cells. They provide a useful means of studying questions such as toxin action, polypeptide translocation across and into membranes, voltage-gated channels and receptor function. These colicins bind to a receptor in the outer membrane before being translocated across the cell envelope with the aid of helper proteins that belong to nutrient-uptake systems and the so-called‘Tol’proteins, the function of which has not yet been properly defined. A distinct domain appears to be associated with each of three steps (receptor binding, translocation and formation of voltage-gated channels). The Tol-dependent uptake pathway is described here. The structures and interactions of TolA, B, Q and R have by now been quite clearly defined. Transmembrane α-helix interactions are required for the functional assembly of the E. coli Tol complex, which is preferentially located at contact sites between the inner and outer membranes. The number of colicin translocation sites is about 1000 per cell. The role and the involvement of the OmpF porin (with colicins A and N) have been described in a recent study on the structural and functional interactions of a colicin-resistant mutant of OmpF. The X-ray crystal structure of the channel-forming fragment of colicin A and that of the entire colicin la have provided the basis for biophysical and site-directed muta-genesis studies. Thanks to this powerful combination, it has been established that the interaction with the receptor in the outer membrane leads to a very substantial conformational change, as a result of which the N-terminal domains of colicins interact with the lumen of the OmpF pore and then with the C-terminal domain of TolA. A molten globular conformation of colicins probably constitutes the intermediate translocation/insertion competent state. Once the pore has formed, the polypeptide chain spans the whole cell envelope. Three distinct steps occur in the last stage of the process: (i) fast binding of the C-terminal domain to the outer face of the cytoplasmic membrane; (ii) a slow insertion of the polypeptide chain into the outer face of the inner membrane in the absence of Δψ and (iii) a profound reorganization of the helix association, triggered by the transmembrane potential and resulting in the formation of the colicin channel. 相似文献