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排序方式: 共有149条查询结果,搜索用时 15 毫秒
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Yngve Hansson Mauricio Vargas-Cortes Staffan Paulie Peter Perlmann 《Cancer immunology, immunotherapy : CII》1988,27(3):205-212
Summary Lymphocytes from patients with transitional cell carcinoma (TCC) of the urinary bladder are more cytotoxic to bladder tumor cells than to a variety of control cells. This disease-related cytotoxicity has previously been shown to involve several mechanisms and different types of effector cells. To analyze further the nature of the effector cells operative in this system, peripheral blood lymphocytes from eight TCC patients were stimulated in vitro with TCC extract and cultured in the presence of interleukin 2 and allogeneic feeder cells. When tested for cytotoxicity in vitro on a target cell panel including both adherent and nonadherent cell lines, the lymphocytes killed a broad spectrum of targets in a major histocompatibility complex (MHC)-unrestricted fashion. When cloned by limiting dilution, clones were obtained which displayed a more restricted pattern of target cell killing. Some of the clones were highly but not exclusively selective for TCC-derived target cells. Phenotypically, these cells resembled mature T cells of CTL-type (CD8+/CD4–). They also expressed the CD3/5 T cell antigen receptor complex but target cell killing was not MHC-restricted. The results of various inhibition experiments suggested that the CD3/TCR complex was involved in the cytotoxicity exhibited by these effector cells. However, its precise role in target cell recognition and the identification of the tumor cell structures recognised by the effector cells require further studies. 相似文献
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A p50 surface antigen restricted to human urinary bladder carcinomas and B lymphocytes 总被引:18,自引:0,他引:18
Staffan Paulie Barbro Ehlin-Henriksson Håkan Mellstedt Hannu Koho Hedi Ben-Aissa Peter Perlmann 《Cancer immunology, immunotherapy : CII》1985,20(1):23-28
Summary We have previously described the derivation of a monoclonal antibody, S2C6, to a novel 50 Kdalton antigen associated with human urinary bladder carcinoma. No reactions were obtained with carcinomas of unrelated origin or with normal urothelial cells. However, the antibody also reacted with a similar antigen on some cell lines of B lymphocyte origin. Using large panels of target cells we have now shown that this reactivity was entirely restricted to cells of the B lineage within the haematopoietic system. As opposed to its apparent restriction to malignant cells of the urothelium, the S2C6 antigen was expressed by normal B lymphocytes as well as by many malignant B cells (chronic lymphocytic leukaemia, hairy cell leukaemia and immunocytoma). Pre-B cells derived from acute lymphocytic leukaemia and plasma cells from multiple myeloma lacked the antigen. Expression was significantly enhanced on cultured B cells from Burkitt lymphomas and on Epstein-Barr virus-transformed lymphoblastoid cell lines including those of the pre-B phenotype derived from fetal bone marrow. As judged from the molecular size and the distribution pattern displayed by the S2C6 antigen it appears to be distinct from other B cell antigens previously described. A possible relation of the S2C6 antigen to a receptor for B cell growth factors is discussed. 相似文献
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Biochemical characteristics and partial amino acid sequence of the receptor-like human B cell and carcinoma antigen CDw40 总被引:6,自引:0,他引:6
S Braesch-Andersen S Paulie H Koho H Nika P Aspenstr?m P Perlmann 《Journal of immunology (Baltimore, Md. : 1950)》1989,142(2):562-567
The Ag CDw40 (p50, Bp50) is a phosphoprotein expressed on the surface of both B lymphocytes and on certain malignant cell types of nonhemopoietic origin. Antibodies to this Ag have been shown to act as a potent co-mitogen for B cells. In order to elucidate the function of this Ag, we have now investigated some of its biochemical characteristics as well as the relationship of B cell derived CDw40 to that derived from urinary bladder carcinoma (transitional cell carcinoma, TCC) cells. CDw40 from normal B cells or from the Burkitt lymphoma line Raji showed a characteristic pattern of three bands when analyzed by SDS-PAGE and Western blotting: a main band of 47 kDa, a degradation product of 43 kDa, and a dimer of 85 kDa. The dimer was disrupted by reduction with 2-ME but was reformed spontaneously from the purified monomers under nonreducing conditions. CDw40 from two bladder cancer cell lines gave a similar pattern but formed little or no dimer. Thirty amino acids of the amino terminal end of CDw40 from Raji and 22 amino acids of that from TCC cells (HU549) were sequenced. The sequences were unusually rich in cysteines and differed only in that the cysteine in position 6 in Raji CDw40 had been replaced by glutamine in HU549. In addition there were two conservative changes in positions 15 and 19. Taken together these results show that CDw40 derived from B cells or from TCC cells are the same or closely related molecules. Comparisons of the amino acid sequence and biochemical characteristics of CDw40 with proteins having receptor functions indicated a close structural resemblance of CDw40 to the nerve growth factor-receptor. 相似文献
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Phosphorylation of Drosophila Jun by the MAP kinase rolled regulates photoreceptor differentiation. 总被引:4,自引:2,他引:2
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F A Peverali A Isaksson A G Papavassiliou P Plastina L M Staszewski M Mlodzik D Bohmann 《The EMBO journal》1996,15(15):3943-3950
Drosophila Jun (D-Jun) is a nuclear component of the receptor tyrosine kinase/Ras signal transduction pathway which triggers photoreceptor differentiation during eye development. Here we show that D-Jun is a substrate for the ERK-related Drosophila MAP kinase Rolled, which has previously been shown to be a part of this pathway. A D-Jun mutant that carries alanines in place of the Rolled phosphorylation sites acts as a dominant suppressor of photoreceptor cell fate if expressed in the eye imaginal disc. In contrast, a mutant in which the phosphorylation sites are replaced by phosphate-mimetic Asp residues, as well as a VP16-D-Jun fusion protein, can promote photoreceptor differentiation. These data implicate Jun phosphorylation in the choice between neuronal and non-neuronal fate during Drosophila eye development. 相似文献
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Hundred strains of fungi were isolated from 48 packets of Greek cigarettes. They were:Aspergillus (28 strains),Penicillium (22),Mucor (18),Alternaria (14),Cladosporium (1),Streptomyces (4),Candida (11) andGeotrichum (2). From 55 packets of cigarettes manufactured outside of Greece other 100 strains of fungi were isolated and identified asAspergillus (35),Penicillium (23),Mucor (10),Alternaria (13),Cladosporium (5),Streptomyces (4),Candida (3),Geotrichum (1),Cephalosporium (2) andScopulariopsis (4).Results of the present study are discussed in relation to the mycological flora of the air in Athens and to the coli-aerogenes bacteria of cigarettes.
Résumé Les auteurs ont isolé 100 souches de champignons à partir de 48 paquets de cigarettes préparées en Grèce. Ces souches étaient identifiées commeAspergillus (28 souches),Penicillium (22),Mucor (18),Alternaria (14),Cladosporium (1),Streptomyces (4),Candida (11) etGeotrichum (2). D'autre part on a isolé 100 souches de champignons à partir de 55 paquets de cigarettes préparées à l'étranger (surtout aux Etats-Unis et en Angleterre). Ces souches étaientAspergillus (35),Penicillium (23),Mucor (10),Alternaria (13),Cladosporium (5),Streptomyces (4),Candida (3),Geotrichum (1),Cephalosporium (2) etScopulariopsis (4).Les résultats sont discutés en relation avec la flore mycosique de l'air à Athènes et les bactéries coliformes rétrouvées dans les cigarettes préparées en Grèce.相似文献
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Sten Braesch-Andersen Staffan Paulie Christian Smedman Sohel Mia Makiko Kumagai-Braesch 《PloS one》2013,8(11)
The apoE production by tissue macrophages is crucial for the prevention of atherosclerosis and the aim of this study was to further elucidate how this apolipoprotein is regulated by cytokines present during inflammation. Here we studied apoE production in peripheral blood mononuclear cells (PBMC) and analysis was made with a newly developed apoE ELISpot assay. In PBMC, apoE secretion was restricted to monocytes with classical (CD14++CD16−) and intermediate (CD14+CD16+) monocytes being the main producers. As earlier described for macrophages, production was strongly upregulated by TGF-β and downregulated by bacterial lipopolysaccharide (LPS) and the inflammatory cytokines IFN-γ, TNF-α and IL-1β. We could here show that a similar down-regulatory effect was also observed with the type I interferon, IFN-α, while IL-6, often regarded as one of the more prominent inflammatory cytokines, did not affect TGF-β-induced apoE production. The TNF-α inhibitor Enbrel could partly block the down-regulatory effect of IFN-γ, IFN-α and IL-1β, indicating that inhibition of apoE by these cytokines may be dependent on or synergize with TNF-α. Other cytokines tested, IL-2, IL-4, IL-12, IL-13, IL-17A and IL-23, had no inhibitory effect on apoE production. In contrast to the effect on monocytes, apoE production by primary hepatocytes and the hepatoma cell line HepG2 was more or less unaffected by treatment with cytokines or LPS. 相似文献