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51.
Krásná E Kolesár L Slavcev A Valhová S Kronosová B Jaresová M Stríz I 《Inflammation》2005,29(1):33-37
IL-18 is a multifunctional cytokine that augments both innate and acquired immunity and potentiates Th1 and Th2 reactions.
We studied the expression of IL-18 receptor (IL-18R) on renal and respiratory epithelial cell lines. Both cell lines upregulated
IL-18R mRNA and IL-18R membrane expression in response to TNF alpha and other proinflammatory cytokines. The function of IL-18R
was confirmed by induction of IL-8 release from epithelial cells in response to recombinant IL-18. Epithelial cells may represent
an important target for IL-18, mainly under inflammatory conditions associated with TNF alpha release. 相似文献
52.
Functional topography of discrete domains of human CD38 总被引:6,自引:0,他引:6
Ausiello CM Urbani F Lande R la Sala A Di Carlo B Baj G Surico N Hilgers J Deaglio S Funaro A Malavasi F 《Tissue antigens》2000,56(6):539-547
53.
Shirai Y Hashimoto M Kato R Kawamura YI Kirikae T Yano H Takashima J Kirihara Y Saito Y Fujino MA Dohi T 《Journal of clinical immunology》2004,24(1):42-52
Despite the huge number of colonized Gram-negative bacteria in the colon, the normal colon maintains its homeostasis without any excessive immune response. To investigate the potential mechanisms involved, human colonic lamina propria mononuclear cells (LPMCs) obtained from uninflamed mucosa were cultured with lipopolysaccharide (LPS) prepared from Bacteroides vulgatus (BV-LPS) or Bacteroides fragilis (BF-LPS), as representatives of indigenous flora, or pathogenic Salmonella minnesota (SM-LPS). Colonic LPMCs failed to produce inflammatory cytokines in response to any type of LPS. Colonic macrophages barely expressed mRNA for MD-2, an essential association molecule for LPS signaling via Toll-like receptor 4. Further, BV-LPS induced CD25 and Foxp3 expression in lymphocytes and CD4(+)CD25(+) cells expressed IL-10 mRNA. Thus, the low expression of functioning LPS receptor molecules and induction of IL-10-producing CD4(+)CD25(+) lymphocytes by indigenous LPS may play a central role in the maintenance of colonic immunological homeostasis. 相似文献
54.
Resino S Rivero L Ruiz-Mateos E Galán I Franco JM Munoz-Fernández MA Leal M 《Journal of clinical immunology》2004,24(4):379-388
We evaluated phenotypic and functional parameters of immune restoration of 27 HIV-infected patients on highly active antiretroviral therapy (HAART) (HIV-cases) with HIV-RNA levels below detectable limits at least during 18 months, and CD4+ cell per microliter higher than 500 at the moment of the study and lower than 300 anytime before. These patients were compared with 11 HIV-controls that never had less than 500 CD4+ cell per microliter and 20 healthy-controls (HIV seronegative subjects) in a cross-sectional study. HIV-cases had lower counts of naïve CD4+ than HIV-controls and healthy-controls. HIV-patients (both HIV-cases and HIV-controls) showed higher values of naïve and memory CD8+ counts than healthy-controls. TREC-bearing cell levels were significantly lower in HIV-cases than in healthy-controls. Peripheral blood mononuclear cells (PBMC) cultures, HIV-cases had lower values in proliferation to streptokinase (SK) and tetanus toxin (TT) than in healthy-controls. HIV-cases had lower IFN-γ and higher IL-5 production with pokeweed than healthy-controls (P < 0.01). However, IL-5 production of HIV-cases after TT stimulation was lower than in HIV-controls and healthy-controls. Total IgG and IgG1 levels were significantly higher in HIV-cases than in HIV-controls and healthy-controls. Also, IgM levels were significantly higher in HIV-cases than in healthy-controls. Nevertheless, IgG2 levels were significantly lower in HIV-cases and HIV-controls than in healthy-controls. The levels of specific Igs antipneumococcal capsular polysaccharide and TT were significantly lower in HIV-cases than in healthy-controls. HIV-patients with a previous state of severe-moderate immunosuppression normalizing their CD4+ counts have a incomplete immune reconstitution after HAART. Long-term consequences of this subclinical immune deficiency remain to be determined. 相似文献
55.
Miodrag ?oli? Nada Pejnovi? Milena Kataranovski Ljiljana Popovi? Sonja Ga?I? Aleksandar Duji? 《Clinical & developmental immunology》1992,2(2):151-160
Rat thymic epithelial cells (TEC) in long-term culture were characterized by
anticytokeratin monoclonal antibodies (mAbs) and electron microscopy. Phenotypic
analysis performed by a large panel of mAbs showed that the highest percentage of
these cells was of the subcapsular/medullary type.
Recombinant rat interferon (IFN)-gamma up-regulated class-I and class-II MHC
expression by TEC in culture as confirmed by immunohistochemistry and flow
cytometry, but did not significantly alter other cell markers. TEC supernatants of IFN-gamma-
treated cultures showed higher interleukin-6 (IL-6) activity, compared to the
control, as determined by proliferation of the IL-6-sensitive B9-cell line. Increased IL-6
activity was probably not a consequence of increased TEC number in IFN-gammatreated
cultures because IFN did not significantly stimulate TEC proliferation in vitro. In
contrast, IL-6 significantly stimulated TEC proliferation, indicating that this cytokine is
not only a regulatory molecule for T-cell proliferation, but could also be an autocrine
growth factor for thymic epithelium. 相似文献
56.
Experimental arthritis induced by continuous infusion of IL-8 into rabbit knee joints. 总被引:1,自引:1,他引:1
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H Endo T Akahoshi A Nishimura M Tonegawa K Takagishi S Kashiwazaki K Matsushima H Kondo 《Clinical and experimental immunology》1994,96(1):31-35
To determine the roles of IL-8 in inflammatory synovitis, examination was made of the results of continuously injecting human recombinant IL-8 into the knee joints of New Zealand while rabbits. Recombinant human IL-8 was infused continuously into the joint cavity at 75 ng/h for 14 days by a polypropylene catheter connected to a mini-osmotic pump implanted in each rabbit. Infiltration of inflammatory cells into joint cavity and histopathological changes in synovial tissue were examined at 7 and 14 days following the start of infusion. The continuous infusion of IL-8 for 14 days led to severe arthritis characterized by apparent erythema and joint pain, the accumulation of leucocytes, infiltration of mononuclear cells in synovial tissue, and marked hypervascularization in the synovial lining layer. IL-8 may be a factor which can contribute to the inflammatory process of chronic arthritis by mediating leucocyte recruitment and hypervascularization in inflamed joints. 相似文献
57.
Malyak Mark Smith Michael F. Abel Ashley A. Arend William P. 《Journal of clinical immunology》1994,14(1):20-30
Journal of Clinical Immunology - The objective of this study was to characterize interleukin-1 receptor antagonist (IL-1ra) and interleukin-1β (IL-1β) production by human peripheral blood... 相似文献
58.
O. O. Obukhova A. P. Shvayuk O. M. Gorbenko A. N. Trunov L. A. Trunova 《Bulletin of experimental biology and medicine》2008,146(6):803-805
The concentrations of cytokines (interleukin-1β, interleukin-6, and interferon-γ) in blood plasma from patients with remission
of chronic herpes infection were measured during immunocorrective therapy. Our results indicate that immunocorrection is pathogenetically
substantiated and immunologically effective. It was manifested in reduction of inflammation and activation of antiviral protection
Translated from Byulleten’ Eksperimental’noi Biologii i Meditsiny, Suppl. 1, pp. 63–66, 2008 相似文献
59.
Carl F. Ware 《Immunological reviews》2008,223(1):186-201
Summary: Cytokines mediate key communication pathways essential for regulation of immune responses. Full activation of antigen-responding lymphocytes requires cooperating signals from the tumor necrosis factor (TNF)-related cytokines and their specific receptors. LIGHT, a lymphotoxin-β (LTβ)-related TNF family member, modulates T-cell activation through two receptors, the herpesvirus entry mediator (HVEM) and indirectly through the LT-β receptor. An unexpected finding revealed a non-canonical binding site on HVEM for the immunoglobulin superfamily member, B and T lymphocyte attenuator (BTLA), and an inhibitory signaling protein suppressing T-cell activation. Thus, HVEM can act as a molecular switch between proinflammatory and inhibitory signaling. The non-canonical HVEM–BTLA pathway also acts to counter LTβR signaling that promotes the proliferation of antigen-presenting dendritic cells (DCs) within lymphoid tissue microenvironments. These results indicate LTβ receptor and HVEM–BTLA pathways form an integrated signaling circuit. Targeting these cytokine pathways with specific antagonists (antibody or decoy receptor) can alter lymphocyte differentiation and activation. Alternately, agonists directed at their cell surface receptors can restore homeostasis and potentially reset immune and inflammatory processes, which may be useful in treating autoimmune and infectious diseases and cancer. 相似文献
60.
Effects of prostaglandin E2 on Th0-type human T cell clones: modulation of functions of nuclear proteins involved in cytokine production 总被引:3,自引:0,他引:3
Watanabe Sumiko; Yssel Hans; Harada Yoshio; Arai Ken-ichi 《International immunology》1994,6(4):523-532
The effects of prostaglandin E2 (PGE2) on cytokine productionand proliferation of the CD4+ human helper T cell clone SP-B21were investigated. In cells stimulated with antl-CD3 mAb, PGE2inhibited cell proliferation and the production of all the cytokinesexamined. Addition of rlL-2 fully restored the prollferatlveresponse and partially restored the production of IL-4 and IL-5,but not that of other cytokines. In contrast, In cells stimulatedwith phorbol myrlstate acetate (PMA)/A23187, PGE2 enhanced theproduction of IL-4 and IL-5, and only partially inhibited theproduction of other cytokines. Therefore, the effects of PGE2vary depending on the mode of T cell activation, and the IL-4and IL-5 are regulated differently from other cytokines. Ina mobility shift assay, only the NF-B (p50/p5O) homodlmer wasobserved in a complex formed with the B sequence in unstlmulatedSP-B21 cells. When cells were stimulated with antl-CD3 mAb orPMA/A23187, a complex formation of NF-B (p50/p65) heterodlmerwith the B sequence was induced. Interestingly, PGE2 or di-butyryl(Bt2cAMP abolished the binding of NF-B (p50/p65) heterodlmerto the B sequence in cells stimulated with antl-CD3 mAb butnot with PMA/A23187. Our results suggest that the target ofPGE2 action is a component in the signal transductlon pathwayleading to the activation of protein klnase C. However, theinhibition of the T cell activation signals by PGE2 is selective.PGE2 enhanced the complex formation with NF-AT, AP-1 and CLEOsequences when the cells were activated by either anti-CD3 mAbor PMA/A23187 stimulation. It seems therefore that PGE2, byelevating cAMP levels, interferes with the activation pathwayfor NF-B but not for NF-AT, AP-1 or CLEO binding protein. 相似文献