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221.
Characterization of the expression products of recombinant human choriogonadotropin and subunits 总被引:3,自引:0,他引:3
J Lustbader S Birken S Pollak L Levinson E Bernstine N Hsiung R Canfield 《The Journal of biological chemistry》1987,262(29):14204-14212
Human choriogonadotropin (hCG) is a placental glycoprotein hormone composed of a 92-amino acid alpha subunit noncovalently linked to a 145-amino acid beta subunit. We report here the expression of biologically active hCG in mouse C127 cells transfected with expression vectors containing the DNA coding for both subunits. In addition, the same cell line was used to express the alpha subunit alone. The expression products were purified by affinity chromatography using specific monoclonal antibodies to hCG or its subunits. The system secreting biologically active hCG also produced a 10-fold or greater molar excess of free beta subunit. The dimeric hormone, as well as the excess beta subunit, resembles the standard urinary hCG and beta subunit by chemical and biological criteria. In contrast, when the vector encoding for the alpha subunit was expressed alone, the alpha subunit had a higher molecular weight than both standard alpha and the alpha found in the expressed dimeric hormone. The molecular weight difference between expressed alpha subunit and standard alpha was found to reside in the alpha peptide consisting of residues 52-91 which contained all of the carbohydrate of the alpha subunit. The N-asparagine-linked carbohydrate moieties in the recombinant alpha were found to be triantennary in contrast to biantennary in urinary alpha, and this hyperglycosylation was responsible for the higher molecular weight of the alpha subunit when it was expressed alone. We found no evidence of O-threonine glycosylation at position alpha 39 reported to be present in free forms of the alpha subunit; however, the companion paper (Corless, C.L., Bielinska, M., Ramabhadran, T. V., Daniels-McQueen, S. Otani, T., Reitz, B. A., Tiemeier, D. C., and Boime, I. (1987) J. Biol Chem. 262, 14197-14203) finds a small quantity of O-glycosylation. Since the excess beta subunit appears to be of normal size and contains the expected complement of sugars, only free alpha subunit seems to be a potential substrate for addition of extra sugar moieties. No large beta subunit forms have been found by others, while large alpha subunits have been described both clinically and in tissue culture systems. These observations imply that the conformation of the free alpha subunit, in the regions of the glycosylation recognition sites, allows easier access for glycosyltransferases than those same sites in the beta subunit. When alpha is combined with beta, the local structures around the alpha glycosylation sites are apparently altered so as to make the synthesis of triantennary chains less favorable. 相似文献
222.
Prophylactic and therapeutic treatment with acyclovir of genital herpes in the guinea pig 总被引:5,自引:0,他引:5
D Myerson G D Hsiung 《Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine (New York, N.Y.)》1983,174(2):147-152
The antiviral drug, acyclovir, was tested on experimentally infected guinea pigs with either of two herpes simplex virus type 1 (HSV-1) isolates following intravaginal inoculation. The drug was continuously infused subcutaneously utilizing an osmotic pump. Infusion was begun either prior to virus inoculation (prophylactic) or after virus inoculation at the time of first appearance of lesions (therapeutic). Prophylactic treatment markedly reduced the severity of the genital lesions, the appearance of acute neurologic sequellae, and the virus excretion in the genital tract of guinea pigs infected with either of the two strains tested. Therapeutic acyclovir treatment, however, did not decrease the incidence of acute neurologic sequellae with one of the two HSV-1 strains tested, nor did it reduce the severity of the genital lesions of either strain. These neurologic sequellae may be due to insufficient levels of ACV in the central nervous system as the concentration of ACV in the dorsal root ganglia was found to exceed that of the plasma, but only trace amounts of acyclovir were present in the brain and spinal cord. Continuous perfusion of ACV gave far higher tissue levels than intermittent injections. These findings suggest that prophylactic ACV is far more effective than therapeutic treatment for genital herpes in the guinea pig model. 相似文献
223.
224.
The synthesis of the n-hydroxysuccinimide ester of N-(2-nitro-4-azidophenyl)glycine (NAG) is described. This reacts with E. coli phe-tRNA(Phe) to yield the photoaffinity label NAG-Phe-tRNA(Phe). This peptidyl tRNA analogue binds correctly to the peptidyl site of the E. coli ribosome. The only significant covalent products found after irradiation of a peptidyl site bound NAG-Phe-tRNA(Phe)-70S-poly(U) complex are 50S proteins L11 and L18. After irradiation the complex can still bind [(3)H]Phe-tRNA to the amino acyl site and participate in peptide bond formation with the covalently attached NAG-Phe moiety. Alternatively, one can allow peptide bond formation to occur first, prior to photolysis. The reaction products are still L11 and L18. Hence, both of these two proteins appear to be centrally located at the peptidyl transferase center. 相似文献
225.
Norman S. Swack Dr. G. D. Hsiung 《In vitro cellular & developmental biology. Plant》1974,10(5-6):260-267
Summary A survey study of primary cell cultures prepared from primate and nonprimate tissues has shown that viruses are commonly found
as endogenous agents in these cultures. Cultures prepared from monkey tissues yielded the greatest variety of virus isolates.
Almost all strain 2 guinea pig cultures contained a Herpes-like virus, and both strain 2 and Hartley animals contained C-type
virus. Bovine embryo and rabbit kidney cell cultures were rarely infected with viruses. Toxoplasmas and microfilariae were
also detected. Most of the endogenous viral agents were obtained by holding the cultures for long-term incubation while testing
for cytopathic effect, hemadsorption, and staining with hematoxylin and eosin for virus-induced cellular inclusions. Fluorescent
antibody staining and electron microscopy were found to be efficient for detection of certain types of viruses. The screening
of animals by testing for the presence of neutralizing antibody was not an effective procedure in selecting virus-free animals
for cell culture purposes.
This study was supported in part by the Food and Drug Administration, Department of Health, Education and Welfare, Contract
NIH-DBS-72-2105, and Research Grant AI 08648 from the Institute of Allergy and Infectious Diseases, National Institutes of
Health.
Presented at the Session in Depth on Endogenous Viruses in Cell Culture at the Twenty-fifth Annual Meeting of the Tissue Culture
Association, June 1974. 相似文献
226.
227.
The extent of alkylation of DNA by dimethyl sulfate, nitrogen mustard, and the antibiotic mitomycin C is related to the resulting decrease in the fluorescence of intercalated ethidium. The fluorescence losses due to the first two types of reagents show a marked pH dependence, with greater losses of fluorescence being observed at alkaline pH values. At pH 11.6 the fluorescence shows a slow recovery, so that with low levels of methylation (4% deoxyguanosine residues modified) one observes complete return of fluorescence. We postulate that these phenomena are due to conversion of 7-methyldeoxyguanosine to the zwitterionic form, and partial denaturation of the DNA duplex with loss of ethidium binding sites. Hydroxide-ion-catalyzed imidazole ring opening, and the removal of the positive charge permits reannealing with concomitant return of the ethidium intercalation sites. This conclusion is substantiated by enzymatic hydrolysis of 14C-labelled methylated DNA and identifiions of the ethidium assay. The distinctly different behavior of mitomycin C confirms previous conclusions that its alkylation, preferentially on guanine, does not take part at the N-7 position. 相似文献
228.
Synthesis of the human insulin gene. Part III. Chemical synthesis of 5'-phosphomonoester group containing deoxyribooligonucleotides by the modified phosphotriester method. Its application in the synthesis of seventeen fragments constituting human insulin C-chain DNA. 总被引:4,自引:3,他引:1
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A method for phosphorylating a protected deoxyribooligonucleotide containing phosphotriester linkages is described. The modified phosphotriester method of chemical synthesis is further refined in terms of (i) better final deblocking conditions and (ii) new chromatography solvent systems containing acetone-water-ethyl acetate to yield pure oligomers. The effectiveness of these improvements has been demonstrated in the rapid and efficient synthesis of seventeen fragments constituting the sequence of human insulin C-chain DNA. 相似文献
229.
230.
Simian cytomegalovirus infections were studied in captive, naturally infected primates and in experimentally infected rhesus monkeys. Neutralizing antibody to simian cytomegalovirus was prevalent in selected species of Old World Monkeys. Naturally infected, rhesus monkeys shed virus in their urine during the entire two-year period of study. Similarly, experimentally infected rhesus monkeys showed neutralizing antibody and viruria for more than two years. The indirect fluorescent antibody procedure was found more sensitive than the neutralization antibody technique but appeared less specific for antibody to cytomegalovirus strains. 相似文献