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141.
Improved gelatinase a selectivity by novel zinc binding groups containing galardin derivatives 总被引:1,自引:0,他引:1
Augé F Hornebeck W Decarme M Laronze JY 《Bioorganic & medicinal chemistry letters》2003,13(10):1783-1786
The synthesis of several analogues of galardin, a MMP inhibitor, are presented with their in vitro inhibitory activity against MMP-1 and MMP-2. These compounds contain a distinct Zinc Binding Group (ZBG). Those having a 2-acylated-heterocycle as well as a 2-arylamide function do not exhibit a good inhibition/selectivity against the enzymes tested. On the contrary, those that are based on a hydrazide scaffold present potent selectivity for MMP-2 versus MMP-1. 相似文献
142.
Philippe Pinton Laurent Schibler Edmond Cribiu Joel Gellin Martine Yerle 《Mammalian genome》2000,11(4):306-315
In total, 113 genes that have already been located in humans and goats were cytogenetically mapped in pigs. For this purpose,
165 gene-containing bacterial artificial chromosomes (BACs) isolated in goats were used in heterologous fluorescent in situ
hybridization on porcine chromosomes. Among them, 113 (or 69%) gave clear and specific signals, and 52 did not work in heterologous
conditions. These localizations are a significant contribution to development of the porcine gene map and also to the comparative
map for humans and pigs. They allowed us to specify the information obtained by Zoo-FISH while taking the gene order into
account; the number of conserved fragments detected for human and pig chromosomes reached 84. The average size of conserved
fragments could be estimated at 33 cM. As these genes had already been mapped in goats, the comparison was extended to ruminants.
The previous results obtained in this species, suggesting a correlation between human chromosome abnormalities and evolutionary
breakpoints, were confirmed in pigs.
Received: 22 July 1999 / Accepted: 3 December 1999 相似文献
143.
144.
Martine Coué Françoise Amariglio Domenico Maiorano Stéphane Bocquet Marcel Méchali 《Experimental cell research》1998,245(2):282
MCM proteins are molecular components of the DNA replication licensing system inXenopus.These proteins comprise a conserved family made up of six distinct members which have been found to associate in large protein complexes. We have used a combination of biochemical and cytological methods to study the association of soluble and chromatin-boundXenopusMCM proteins during the cell cycle. In interphase, soluble MCM proteins are found organized in a core salt-resistant subcomplex that includes MCM subunits which are known to have high affinity for histones. The interphasic complex is modified at mitosis and the subunit composition of the resulting mitotic subcomplexes is distinct, indicating that the stability of the MCM complex is under cell cycle control. Moreover, we provide evidence that the binding of MCM proteins to chromatin may occur in sequential steps involving the loading of distinct MCM subunits. Comparative analysis of the chromatin distribution of MCM2, 3, and 4 shows that the binding of MCM4 is distinct from that of MCM2 and 3. Altogether, these data suggest that licensing of chromatin by MCMs occurs in an ordered fashion involving discrete subcomplexes. 相似文献
145.
Mark P. Foster Deborah S. Wuttke Karen R. Clemens Wolfgang Jahnke Ishwar Radhakrishnan Linda Tennant Martine Reymond John Chung Peter E. Wright 《Journal of biomolecular NMR》1998,12(1):51-71
We report the NMR resonance assignments for a macromolecular protein/DNA complex containing the three amino-terminal zinc fingers (92 amino acid residues) of Xenopus laevis TFIIIA (termed zf1-3) bound to the physiological DNA target (15 base pairs), and for the free DNA. Comparisons are made of the chemical shifts of protein backbone1 HN, 15N,13 C and13 C and DNA base and sugar protons of the free and bound species. Chemical shift changes are analyzed in the context of the structures of the zf1-3/DNA complex to assess the utility of chemical shift change as a probe of molecular interfaces. Chemical shift perturbations that occur upon binding in the zf1-3/DNA complex do not correspond directly to the structural interface, but rather arise from a number of direct and indirect structural and dynamic effects. 相似文献
146.
Martine Arpagaus Didier Combes Emmanuel Culetto Marta Grauso Yann Fedon Rita Romani Jean-Pierre Toutant 《Journal of Physiology》1998,92(5-6)
Whereas a single gene encodes acetylcholinesterase (AChE) in vertebrates and most insect species, four distinct genes have been cloned and characterized in the nematode Caenorhabditis elegans. We found that ace-1 (mapped to chromosome X) is prominently expressed in muscle cells whereas ace-2 (located on chromosome I) is mainly expressed in neurons. Ace-x and ace-y genes are located in close proximity on chromosome II where they are separated by only a few hundred base pairs. The role of these two genes is still unknown.
Résumé
À l'inverse de la situation des vertébrés et de la majorité des insectes, chez qui un gène unique code pour l'acétylcholinestérase (AChE), quatre gènes d'AChE ont été clones et caractérisés chez Caenorhabditis elegans. Le gène ace-1 (localisé sur le chromosome X) et le gène ace-2 (chromosome I) assurent respectivement l'expression de l'AChE dans les tissus musculaire (ace-1) et nerveux (ace-2). Les gènes ace-x et ace-y ne sont séparés que de quelques centaines de paires de bases sur le chromosome II et leur rôle est pour l'instant inconnu. 相似文献147.
Dominique Delforge Barbara Gillon Muriel Art Janique Dewelle Martine Raes José Remacle 《Letters in Peptide Science》1998,5(2-3):87-91
A synthetic adhesion protein was designed by chemical grafting of the RGD tailed cyclic peptide cyclo[-d-Val-Arg-Gly-Asp-Glu(-Ahx-Tyr-Cys-NH2)-] on the carrier protein bovine serum albumin (BSA). The cyclic conformation of the RGD motif grafted on the protein mimics the conformation of the motif displayed in native adhesion proteins such as fibronectin. The adhesion of the cells on polystyrene coated with the conjugate BSA–peptide was similar or even better than the one obtained when the proadhesive protein fibronectin was coated on the plates. Results also indicated that covalent coupling of the peptide on BSA is not absolutely required, since simple adsorption of the peptide on the protein coated on plates was efficient for enhancing cell adhesion. These results show that polystyrene support can be reconditioned with conformationally constrained RGD peptides to enhance cell adhesion on solid supports. The same methodology can be adapted for the development of new biomaterials based on the recognition of specific peptides. 相似文献
148.
149.
Franck-Duchenne Martine Wang Yuwen Ben Tahar Sofia Beachy Roger N. 《Plant Cell, Tissue and Organ Culture》1998,53(2):79-84
In vitro regeneration of sweet pepper (Capsicum annuum L. cvs Jupiter and Pimiento Perfection) has been performed via direct
organogenesis. The resulting shoot-buds were placed on media containing 24-epi-brassinolide (EBR) 0.1 μM, a plant steroid
lactone, in the presence or absence of zeatin 9.1 μM plus GA3 5.2 μM for further stem elongation. Different responses to these
treatments were recorded depending upon the protocols used and the genotypes tested. It appears that EBR does not always act
directly on stem elongation but may be an elicitor and/or an enhancer of elongation in concert with endogenous and other exogenously
added growth regulators. Elongated shoots were easily rooted with alpha-naphtalenacetic acid 0.5 μM (0.1 mgl-1) and transfered
to soil, and following acclimation were taken to maturity in the greenhouse.
This revised version was published online in June 2006 with corrections to the Cover Date. 相似文献
150.
Elizabeth Faris Crowell Martine GonneauSamantha Vernhettes Herman Höfte 《Comptes rendus biologies》2010,333(4):320-324
Plant growth and development depend on anisotropic cell expansion. Cell wall yielding provides the driving force for cell expansion, and is regulated in part by the oriented deposition of cellulose microfibrils around the cell. Our current understanding of anisotropic cell expansion combines hypotheses generated by more than 50 years of research. Here, we discuss the evolving views of researchers in the field of cellulose synthesis, and highlight several unresolved questions. Recent results using live-cell imaging have illustrated novel roles for cortical microtubules in cellulose synthesis, and further research using these approaches promises to reveal exciting links between the cytoskeleton, intracellular trafficking, and anisotropic growth. 相似文献