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111.
112.
HLA-B27 misfolding in transgenic rats is associated with activation of the unfolded protein response 总被引:7,自引:0,他引:7
Turner MJ Sowders DP DeLay ML Mohapatra R Bai S Smith JA Brandewie JR Taurog JD Colbert RA 《Journal of immunology (Baltimore, Md. : 1950)》2005,175(4):2438-2448
The mechanism by which the MHC class I allele, HLA-B27, contributes to spondyloarthritis pathogenesis is unknown. In contrast to other alleles that have been examined, HLA-B27 has a tendency to form high m.w. disulfide-linked H chain complexes in the endoplasmic reticulum (ER), bind the ER chaperone BiP/Grp78, and undergo ER-associated degradation. These aberrant characteristics have provided biochemical evidence that HLA-B27 is prone to misfold. Recently, similar biochemical characteristics of HLA-B27 were reported in cells from HLA-B27/human beta2-microglobulin transgenic (HLA-B27 transgenic) rats, an animal model of spondyloarthritis, and correlated with disease susceptibility. In this study, we demonstrate that the unfolded protein response (UPR) is activated in macrophages derived from the bone marrow of HLA-B27 transgenic rats with inflammatory disease. Microarray analysis of these cells also reveals an IFN response signature. In contrast, macrophages derived from premorbid rats do not exhibit a strong UPR or evidence of IFN exposure. Activation of macrophages from premorbid HLA-B27 transgenic rats with IFN-gamma increases HLA-B27 expression and leads to UPR induction, while no UPR is seen in cells from nondisease-prone HLA-B7 transgenic or wild-type (nontransgenic) animals. This is the first demonstration, to our knowledge, that HLA-B27 misfolding is associated with ER stress that results in activation of the UPR. These observations link HLA-B27 expression with biological effects that are independent of immunological recognition, but nevertheless may play an important role in the pathogenesis of inflammatory diseases associated with this MHC class I allele. 相似文献
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Toxicity studies of two commercial carbamate insecticides, carbaryl and carbofuran with the nitrogen-fixing filamentous cyanobacterium Anabaena PCC 7120, are described. Under nitrogen-fixing conditions and with calcium nitrate supplementation, 100 and 120 ppm carbaryl were the respective lethal concentrations (LC100), while 20 to 80 ppm (nitrogen-fixing conditions) and 20 to 100 ppm (with nitrate supplementation) were the partial lethal doses (相似文献
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Summary Five strains ofTrichophyton mentagrophytes were isolated, four from guinea pigs and one from rabbit. The symptoms of the disease were studied. The morphological characters and the pathogenicity of the isolates were studied in detail. The significance of the findings is discussed. 相似文献
117.
Kalpesh R. Patil Purusottam Mohapatra Harun M. Patel Sameer N. Goyal Shreesh Ojha Chanakya N. Kundu Chandragouda R. Patil 《PloS one》2015,10(5)
Pentacyclic Triterpenoids (PTs) and their analogues as well as derivatives are emerging as important drug leads for various diseases. They act through a variety of mechanisms and a majority of them inhibit the nuclear factor kappa-beta (NF-κB) signaling pathway. In this study, we examined the effects of the naturally occurring PTs on IκB kinase-β (IKKβ), which has great scientific relevance in the NF-κB signaling pathway. On virtual screening, 109 PTs were screened through the PASS (prediction of activity spectra of substances) software for prediction of NF-κB inhibitory activity followed by docking on the NEMO/IKKβ association complex (PDB: 3BRV) and testing for compliance with the softened Lipinski’s Rule of Five using Schrodinger (LLC, New York, USA). Out of the projected 45 druggable PTs, Corosolic Acid (CA), Asiatic Acid (AA) and Ursolic Acid (UA) were assayed for IKKβ kinase activity in the cell free medium. The UA exhibited a potent IKKβ inhibitory effect on the hotspot kinase assay with IC50 of 69 μM. Whereas, CA at 50 μM concentration markedly reduced the NF-κB luciferase activity and phospho-IKKβ protein expressions. The PTs tested, attenuated the expression of the NF-κB cascade proteins in the LPS-stimulated RAW 264.7 cells, prevented the phosphorylation of the IKKα/β and blocked the activation of the Interferon-gamma (IFN-γ). The results suggest that the IKKβ inhibition is the major mechanism of the PTs-induced NF-κB inhibition. PASS predictions along with in-silico docking against the NEMO/IKKβ can be successfully applied in the selection of the prospective NF-κB inhibitory downregulators of IKKβ phosphorylation. 相似文献
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Jhillu S Yadav Pragna P Das T Lakshminarayan Reddy Indira Bag Priyadarshini M Lavanya Bulusu Jagannadh Debendra K Mohapatra Manika Pal Bhadra Utpal Bhadra 《Journal of nanobiotechnology》2011,9(1):10
Background
Organic nanomaterials having specific biological properties play important roles in in vivo delivery and clearance from the live cells. To develop orally deliverable nanomaterials for different biological applications, we have synthesized several fluorescently labelled, self-assembled PABA nanoparticles using possible acid side chain combinations and tested against insect and human cell lines and in vivo animal model. Flurophores attached to nanostructures help in rapid in vivo screening and tracking through complex tissues. The sub-cellular internalization mechanism of the conjugates was determined. A set of physio-chemical parameters of engineered nanoskeletons were also defined that is critical for preferred uptake in multiple organs of live Drosophila. 相似文献120.
Mohapatra B Warrell DA Suraweera W Bhatia P Dhingra N Jotkar RM Rodriguez PS Mishra K Whitaker R Jha P;Million Death Study Collaborators 《PLoS neglected tropical diseases》2011,5(4):e1018