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991.
†K. Babinski P. Haddad D. Vallerand N. McNicoll A. De Léan † H. Ong 《Journal of neurochemistry》1995,64(3):1080-1087
Abstract: There is increasing evidence that members of the natriuretic peptide family display sympathoinhibitory activity, but it remains uncertain which receptor pathway is implicated. We performed cyclic GMP production studies with chromaffin cells treated with either atrial natriuretic factor (ANF) or C-type natriuretic peptide (CNP) and found that these cells specifically express the ANF-R1C but not the ANF-R1A receptor subtype. Evidence for the existence of ANF-R2 receptors was obtained from patch-clamp experiments where C-ANF, an ANF-R2-specific agonist, inhibited nicotinic currents in single isolated chromaffin cells. Involvement of ANF-R2 receptors in the modulation of nicotinic currents was further supported by the significant loss of this inhibitory activity after the cleavage of the disulfide-bridged structure of C-ANF. This linearized form of C-ANF also displayed a lower binding affinity for ANF-R2 receptors. Like the patch-clamp studies, secretion experiments demonstrated that both CNP and C-ANF are equally effective in reducing nicotine-evoked catecholamine secretion by cultured chromaffin cells, raising the possibility that this effect of CNP is predominantly mediated by the ANF-R2 and not the ANF-R1C receptors. Finally, this response appears to be specific to nicotinic agonists because neither histamine- nor KCI-induced secretions were affected by natriuretic peptides. In the present study, we report (1) the presence of ANF-R1C and ANF-R2 receptor subtypes in bovine chromaffin cells, (2) the inhibition by natriuretic peptides of nicotinic whole-cell currents as well as nicotine-induced catecholamine secretion, (3) the possible mediation of these effects by the ANF-R2 class of receptors, and (4) the specificity of this inhibition to nicotinic agonists. Because bovine chromaffin cells release ANF, BNP, and CNP together with catecholamines, all three peptides might exert negative feedback regulation of catecholamine secretion in an autocrine manner by interacting with the nondiscriminating ANF-R2 receptor subtype. 相似文献
992.
993.
Interferon antibodies in patients with infectious diseases 总被引:2,自引:0,他引:2
G. Antonelli E. Simeoni M. Currenti F. De Pisa V. Colizzi M. Pistello F. Dianzani 《Biotherapy》1997,10(1):7-14
Interferons (IFNs) are generally recognized as the most important therapeutic agent in some infectious diseases such as chronic
hepatitis B and C. Since the early clinical trials it was documented that the therapeutic use of IFNs could be complicated
by the development of antibodies able to neutralize or to bind to the IFN molecule.
After several years of research it is now widely accepted that the presence of circulating anti-IFN antibodies may affect
the response to IFN.
Here we summarize what is currently know on the clinical significance of antibodies to IFN in IFN-treated viral diseases patients. 相似文献
994.
Xavier Isaac M. de Pádua Antônio Moraes Fernando De Miranda-Neto J. A. 《Molecular Engineering》1997,7(3-4):283-291
Starburst dendrimers are highly branched oligomers. A rigid dendritic hydrocarbon, C1134H1146, has recently been synthesized. It consists of 94 phenylacetylene units displayed in a self-similar two-dimensional skeleton
isomorphous to the three-coordinated Bethe lattice. The three-dimensional representation of phenylacetylene dendrimer shows
a globular architecture with large voids and niches in its interior, characteristic of hyperbolic surfaces. This work investigates
the geometrical scaling behavior of this starburst dendrimer using the symmetry properties of a Bethe lattice embedded in
the hyperbolic plane. The results for C1134H1146 provide its density profile and an upper bound for its macromolecular size.
This revised version was published online in June 2006 with corrections to the Cover Date. 相似文献
995.
Rodrigues C.R. Barreiro E.J. Romeiro N.C. Albuquerque M.G. De Sant'anna C.M.R. Bicca De Alencastro R. Da Motta Neto J.D. 《Molecular Engineering》1997,7(3-4):473-490
Two families of autacoids from cell membrane phospholipids have been identified. The first, the icosanoids, which are formed
from arachidonic acid, include prostaglandins and leukotrienes. The other includes modified phospholipids, as the platelet
aggregating factor (PAF). These compounds are related to inflammatory and cardiovascular diseases.
We review in this paper some of the work that has been done in our laboratories in the last few years relating to the modeling
of new potential thromboxane synthase (TXS) and 5-lipoxygenase (5-LO) and cyclooxygenase (COX) inhibitors, and TXA2 receptor antagonists derived from nitrogenated heterocycles. We include the results of the modeling of a group of proposed
PAF antagonists, and compare their structures with PAF itself and with a recently proposed PAF antagonist model.
This revised version was published online in June 2006 with corrections to the Cover Date. 相似文献
996.
Edouard Nice Bruno Catimel Martin Lackmann Steven Stacker Andrew Runting Andrew Wilks Nicos Nicola Antony Burgess 《Letters in Peptide Science》1997,4(2):107-120
The isolation of related genes with evolutionary conserved motifs by the application ofpolymerase chain reaction-based molecular biology techniques, or from database searchingstrategies, has facilitated the identification of new members of protein families. Many of theseprotein molecules will be involved in protein–protein interactions (e.g. growth factors,receptors, adhesion molecules), since such interactions are intrinsic to virtually every cellularprocess. However, the precise biological function and specific binding partners of these novelproteins are frequently unknown, hence they are known as orphan molecules.Complementary technologies are required for the identification of the specific ligands orreceptors for these and other orphan proteins (e.g., antibodies raised against crude biologicalextracts or whole cells). We describe herein several alternative strategies for the identification,purification and characterisation of orphan peptide and protein molecules, specifically thesynergistic use of micropreparative HPLC and biosensor techniques. 相似文献
997.
De Andrade Antônio V. M. Da Costa Nivan B. Longo Ricardo L. Malta Oscar L. Simas Alfredo M. De Sá Gilberto F. 《Molecular Engineering》1997,7(3-4):293-308
Theoretical techniques have been developed and/or improved to predict the molecular structure of lanthanide complexes which
were used to calculate their electronic properties, in particular, their electronic spectra and energy levels necessary to
calculate the rates of energy transfer from the ligands to the metal ion. The molecular structure has been obtained by the
SMLC/AM1 (Sparkle Model for the Calculation of Lanthanide Complexes – Austin Model 1) model where the lanthanide ion is simulated
by a sparkle implemented into the AM1 Hamiltonian used to perform a HF-SCF (Hartree-Fock Self-Consistent Field) calculation.
The previous implementation of the SMLC/AM1 model (sparkle/1) involving only two parameters has been generalized to be consistent
with the AM1 Hamiltonian and the new model (sparkle/2) significantly improved the prediction of molecular structures of Eu(III)
complexes. For the electronic spectra and energy level calculations of the lanthanide complexes the model replaces the metal
ion by a point charge with the ligands held in their positions as determined by the SMLC/AM1 model, and uses a INDO/S-CI (intermediate
neglect of differential overlap/spectroscopic-configuration interaction) model. A preliminary study of the solvent effects
on the absorption spectra of the free ligand is also presented. For the ligand-lanthanide ion energy transfer Fermi's golden
rule is used with the multipolar and exchange mechanisms being implemented and tested for several complexes. These theoretical
techniques have been applied to several complexes yielding very good results when compared to experimental data as well as
predictions for the molecular and electronic structures and the relative contributions of the mechanisms for the energy transfer
rates.
This revised version was published online in June 2006 with corrections to the Cover Date. 相似文献
998.
Timothy P. L. Smith Nestor Lopez-Corrales Michael D. Grosz Craig W. Beattie Steven M. Kappes 《Mammalian genome》1997,8(5):333-336
We report the placement of 34 new microsatellite (ms) markers, isolated from a lambda phage genomic clone library, on the
bovine genetic map by linkage to published markers. Five of these markers lie at or near the ends of linkage groups and are
used to establish chromosomal coverage and orientation. Fluorescence in situ hybridization (FISH) analysis demonstrates that
the linkage groups on the U.S. Meat Animal Research Center (MARC) map extend to the telomeric region of Chromosomes (Chrs)
7 and 10. Linkage groups on Chrs 4, 6, and 14 appear to be less inclusive.
Received: 23 September 1996 / Accepted: 28 December 1996 相似文献
999.
G. Liguori L. De Gregorio M. Tucci C. T. Lago A. Barra T. A. Dragani M. Persico 《Mammalian genome》1997,8(7):502-505
Teratocarcinoma-derived growth factor-1 (Tdgf1), a member of the ``EGF family' of growth factors, is expressed during mouse gastrulation in the forming mesoderm and later
in the truncus arteriosus of the developing heart. In humans, TDGF1 is highly expressed in germ cell tumors and in colon and
mammary carcinomas. In mouse, one gene (Tdgf1) and two pseudogenes (Tdgf1-ps1 and Tdgf1-ps2) have been isolated and characterized. Tdgf1 corresponds to the gene expressed in F9 teratocarcinoma cells. Tdgf1-ps1 and Tdgf1-ps2 are two intronless sequences with all the characteristics of retroposons. In the present paper, we assign the chromosomal
location for Tdgf1, Tdgf1-ps1, and Tdgf1-ps2 sequences to Chromosomes (Chrs) 9, 16, and 17, respectively. Two previously described mouse mutants, scant hair (sch) and fur deficient (fd), map near the Tdgf1 gene. Analysis of their DNA coding region provided no evidence that Tdgf1 could be the responsible gene for these phenotypes. Finally, analysis of the DNA from several Mus musculus strains and from Mus spretus mice revealed a highly variable restriction pattern and the absence of the Tdgf1-ps1 genomic sequence from the Mus spretus genome.
Received: 23 November 1996 / Accepted: 17 February 1997 相似文献