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11.
Mathias Sprinzl Karl-Heinz Scheit Hans Sternbach Friedrich von der Haar Friedrich Cramer 《Biochemical and biophysical research communications》1973,51(4):881-887
2′-Deoxyadenosine and 3′-deoxyadenosine (cordycepin) can be incorporated into the 3′-terminal position of tRNAPhe by tRNA nucleotidyl transferase. tRNAPhe-C-C-2′dA and tRNAPhe-C-C-3′dA, missing the cis-diol group at the 3′-terminal end are resistant to periodate oxidation and are not able to form borate complexes. In aminoacylation experiments only the tRNAPhe-C-C-3′dA proved to be chargeable. 相似文献
12.
Friedrich Leibenguth 《Biochemical genetics》1973,10(3):231-242
Esterase-2 polymorphism has been investigated quantitatively. Staining intensities of the homodimer bands mm, ff, and ss are not equally expressed but found in relative activities of 1:0.5:0.7 in fat bodies and 1:1:3 in testes and gut walls. Relative intensities of the parental bands are binomially distributed in the three-banded patterns of heterozygotes in an exactly tissue-specific manner. Organ-specific proportions of relative activity remain constant throughout postembryonic development. Among reasons which may influence genesis of allele- and organ-specific activities of homodimer bands in homozygotes and may lead to asymmetrical distribution of intensities in the patterns of heterozygotes, a hypothesis of differential allelic activity is discussed, according to which the structural alleles 2
m
, 2
f
, and 2
s
are closely linked to the alleles RG
a
, RG
b
, and RG
c
of a controlling gene.This work was supported by the Deutsche Forschungsgemeinschaft and submitted with Part I in partial fulfillment of the requirements for the degree of Dr.-habil. at the University of Tübingen. 相似文献
13.
14.
15.
Schmidt H. Friedrich S. Danert K. Wuttky 《TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik》1959,29(8):375-376
Ohne Zusammenfassung 相似文献
16.
17.
18.
Ann E. Ehrenhofer-Murray Friedrich E. Würgler Christian Sengstag 《Molecular & general genetics : MGG》1994,244(3):287-294
Several pleiotropic drug sensitivities have been described in yeast. Some involve the loss of putative drug efflux pumps analogous to mammalian P-glycoproteins, others are caused by defects in sterol synthesis resulting in higher plasma membrane permeability. We have constructed a Saccharomyces cerevisiae strain that exhibits a strong crystal violet-sensitive phenotype. By selecting cells of the supersensitive strain for normal sensitivity after transformation with a wild-type yeast genomic library, a complementing 10-kb DNA fragment was isolated, a 3.4-kb subfragment of which was sufficient for complementation. DNA sequence analysis revealed that the complementing fragment comprised the recently sequenced SGE1 gene, a partial multicopy suppressor of gal11 mutations. The supersensitive strain was found to be a sge1 null mutant. Overexpression of SGE1 on a high-copy-number plasmid increased the resistance of the supersensitive strain. Disruption of SGE1 in a wild-type strain increased the sensitivity of the strain. These features of the SGE1 phenotype, as well as sequence homologies of SGE1 at the amino acid level, confirm that the Sge1 protein is a member of the drug-resistance protein family within the major facilitator superfamily (MFS). 相似文献
19.
The gene encoding the extracellular neutral metalloprotease ShpI from Staphylococcus hyicus subsp. hyicus was cloned. DNA sequencing revealed an ORF of 1317 nucleotides encoding a 438 amino acid protein with Mr of 49698. When the cloned gene was expressed in Staphylococcus carnosus, a 42 kDa protease was found in the culture medium. The protease was purified from both S. carnosus (pCAshp1) and S. hyicus subsp. hyicus. The N-terminal amino acid sequences of the two proteases revealed that ShpI is organized as a pre-pro-enzyme with a proposed 26 amino acid signal peptide, a 75 amino acid hydrophilic pro-region, and a 337 amino acid extracellular mature form with a calculated Mr of 38394. The N-termini showed microheterogeneity in both host strains. ShpI had a maximum proteolytic activity at 55°C and pH 7.4–8.5. The protease, which had a low substrate specificity, could be inhibited by metal- and zinc-specific inhibitors, such as EDTA and 1,10-phenanthroline. Insensitivity to phosphoramidon separates ShpI from the thermolysin-like family. The conserved Zn2+ binding motif, the only homology to other proteases, and the reactivation of the apoenzyme by Zn2+, indicated that Zn2+ is the catalytic ion. Ca2+ very probably acts as a stabilizer. We also demonstrated the presence of a second extracellular protease in S. hyicus subsp. hyicus. 相似文献
20.
Molecular cloning and functional expression of bacteriophage PK1E-encoded endoneuraminidase Endo NE 总被引:10,自引:3,他引:7
Rita Gerardy-Schahn rea Bethe Thomas Brennecke † Martina Mühlenhoff Matthias Eckhardt Stefan Ziesing Friedrich Lottspeich Matthias Frosch 《Molecular microbiology》1995,16(3):441-450
Homopolymeric α-2,8-linked sialic acid (PSA) has been found as a capsular component of sepsis- and meningitis-causing bacterial pathogens, and on eukaryotic cells as a post-translational modification of the neural cell adhesion molecule (NCAM). The polysaccharide is specifically recognized and degraded by a phage-encoded enzyme, the endo-N-acetylneuraminidase E (Endo NE). Endo NE therefore has become a valuable tool in the study of bacterial pathogenesis and eukaryotic morphogenesis. In this report we describe the molecular cloning of Endo NE and the expression of a functionally active recombinant enzyme. The cloned DNA sequence (2436 bp) encodes a polypeptide of 811 amino acids, which at the 5′ end contains a totally conserved neuraminidase motif. Expressed in Escherichia coli, the enzyme migrates as a single band of approximately 74 kDa in SDS-PAGE. A central domain of 669 amino acid residues is about 90% homologous to the recently cloned Endo NF. Both phage-induced lysis of bacteria and the catalysis of PSA degradation by the recombinant enzyme are efficiently inhibited by a polyclonal antiserum raised against the intact phage particle. The C-terminal region seems to be essential to enzymatic functions, as truncation of 32 amino acids outside the homology domain completely abolishes Endo NE activity. Our data also indicate that the 38 kDa protein, previously assumed to be a subunit of the Endo NE holoenzyme, is the product of a separate gene locus and is not necessary for in vitro depolymerase activity. 相似文献