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131.
Oleg Kurtenkov Kersti Klaamas Ljudmila Miljukhina Ljudmila Shljapnikova Malle Ellamaa Nikolai Bovin Torkel Wadström 《FEMS immunology and medical microbiology》1999,24(2):227-232
Individuals of the Le(b+)/secretor phenotype revealed a stronger natural immune response to Le(x) and Le(y) epitopes irrespective of Helicobacter pylori serologic status. In contrast, H. pylori-infected Le(b-) type individuals showed a significantly higher proportion of strong responders to Le(x) antigen compared with the H. pylori-uninfected subgroup. The data suggest that the immune response to Lewis type 2 determinants is related to both the H. pylori serologic status and the Le(a,b) phenotype of the host. 相似文献
132.
Fluorescent probe analysis of purified elastin using 1-anilinonaphthalene-8-sulfonate has been used to investigate reversible structural changes that accompany stretching of this rubberlike protein. There is a specific binding of 1-anilinonaphthalene-8-sulfonate to elastin with a single dye molecule attached per 74,000 molecular-weight protein subunit. When labeled elastin is stretched, the intensity of the 1-anilinonaphthalene-8-sulfonate fluorescence decreases reversibly, and this decrease appears to be linked to an increase in the environmental polarity in the immediate vicinity of the bound dye molecule. The results of experiments carried out in H2O and D2O indicate that this polarity change is due to an increase in the exposure of the 1-anilinonaphthalene-8-sulfonate to water as the hydrophobic interior of the protein subunit is unfolded during stretching. The data are consistent with the proposal that the elastin network is a two-phase system of hydrophobic protein globules surrounded by free solvent spaces. 相似文献
133.
Production of Bacterial Substrate by Marine Copepods: Effect of Phytoplankton Biomass and Cell Size 总被引:1,自引:0,他引:1
Laboratory experiments were performed to evaluate the importanceof grazing activity of the marine copepod Acartia tonsa forproduction of substrate for bacteria. Acartia tonsa were feda range of concentrations of the nanoflagellate Rhodomonas baltica,the diatom Ditylum brightwelli and the dinoflagellate Ceratiumlineatum. Regardless of the concentration of R. baltica, nodetectable response in bacterial biomass was observed due tograzing. However, when A. tonsa grazed the larger phytoplanktoncells of D. brightwelli and C. lineatum, responses in bacterioplanktonwere observed. It was estimated that approximately 5469%of the grazed carbon was lost to the surroundings when A. tonsawas feeding on these large phytoplankton species. The laboratoryresults were applied to a dataset from a coastal temperate ecosystem.This analysis showed that the copepod contribution to the DOCpool was as important as the leakage from the primary producers.It is concluded, that the DOM contribution from copepods willbe largest when grazing plankton communities are composed oflarge species. 相似文献
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Kanthi Kiran Kondepudi Padma Ambalam Ingrid Nilsson Torkel Wadström Åsa Ljungh 《Anaerobe》2012,18(5):489-497
Bifidobacterium breve 46, Bifidobacterium lactis 8:8 and Bifidobacterium longum 6:18 and three reference strains B. breve CCUG 24611, B. lactis JCM 10602, and Bifidobacterium pseudocatenulatum JCM 1200 were examined for acid and bile tolerance, prebiotic utilization and antimicrobial activity against four Clostridium difficile (CD) strains including the hypervirulent strain, PCR ribotype NAP1/027. B. lactis 8:8 and B. lactis JCM 10602 exhibited a high tolerance in MRSC broth with pH 2.5 for 30 min. B. breve 46 and B. lactis 8:8 remained 100% viable in MRSC broth with 5% porcine bile after 4 h. All six strains showed a high prebiotic degrading ability (prebiotic score) with galactooligosaccharides (GOS), isomaltooligosaccharides (IMOS) and lactulose as carbon sources and moderate degradation of fructooligosaccharides (FOS). Xylooligosaccharides (XOS) was metabolized to a greater extent by B. lactis 8:8, B. lactis JCM 10602, B. pseudocatenulatum JCM 1200 and B. longum 6:18 (prebiotic score >50%). All strains exhibited extracellular antimicrobial activity (AMA) against four CD strains including the CD NAP1/027. AMA of B. breve 46, B. lactis 8:8 and B. lactis JCM 10602 strains was mainly ascribed to a combined action of organic acids and heat stable, protease sensitive antimicrobial peptides when cells were grown in MRSC broth with glucose and by acids when grown with five different prebiotic-non-digestible oligosaccharides (NDOs). None of C. difficile strains degraded five prebiotic-NDOs. Whole cells of B. breve 46 and B. lactis 8:8 and their supernatants inhibited the growth and toxin production of the CD NAP1/027 strain. 相似文献
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Staphylococcus aureus, which mediated binding to heparan sulfate, and also strains of coagulase-negative staphylococci (CNS) adhered in high numbers
to polymers with end-point attached heparin. A characteristic feature of several cell growth factors is strong affinity for
heparin. In the present study, binding of the 125I-labeled heparin-binding growth factors (HBGF), acidic and basic fibroblast growth factor (aFGF, bFGF), and platelet-derived
growth factor (PDGF) by S. aureus and CNS strains was examined. Staphylococcal strains used in this study bind bFGF and PDGF, but not aFGF. The binding of
bFGF and PDGF was time dependent, influenced by pH and ionic strength for S. aureus Cowan 1. Preincubation of staphylococcal cells with unlabeled bFGF enhanced bFGF binding, but heparin, protamine sulfate,
poly-L-lysine, and suramin were potent inhibitors of 125I-bFGF binding to cells of S. aureus Cowan 1. Glycosaminoglycans of comparable size (chondroitin sulfate), other polysulfated polymers (λ-carrageenan, fucoidan),
and some polysulfated polysaccharides (dextran sulfate, pentosan polysulfate) inhibited binding of both GFs to various extents.
The partial inhibition of binding of both GFs after protease and periodate treatments indicates that both proteinaceous and
other carbohydrate moieties participate in the binding. A lysozyme cell surface extract and bacterial lysates of S. aureus Cowan 1 competitively inhibited binding of 125I-bFGF and 125I-PDGF. These results suggest that staphylococci have the ability to bind two of the HBGFs, bFGF and PDGF, but not aFGF, via
more than one cell structure. These binding structures seem to be exposed on the cell surface and deeply anchored in the cytoplasmic
membrane as well. 相似文献
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