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2.
齿龈内阿米巴形态学的观察 总被引:3,自引:0,他引:3
目的 :观察齿龈内阿米巴滋养体的形态。方法 :从口腔疾病患者牙周组织或龈隙挑取渗出物 ,生理盐水涂片后镜下观察其形态并测量大小。结果 :齿龈内阿米巴滋养体活体大小平均为 14 .93× 12 .4 2μm ,形态呈圆形、长椭圆形及不规则葫芦形等。伪足透明 ,呈指状、舌状 ,球形及草帽形等不规则形态 ,其伪足伸缩变化较大 ,运动无一定方向。与溶组织内阿米巴滋养体形态有很多相似之处。结论 :全面观察了其运动方式及其形态变化特点 ,因取材方便 ,建议在寄生虫学教学实习中代替溶组织内阿米巴滋养体 ,观察活体阿米巴运动 相似文献
3.
单克隆抗体对溶组织内阿米巴吞噬红细胞的影响 总被引:1,自引:0,他引:1
用具有抗细胞膜活性和抗细胞核、胞浆活性的单克隆抗体3F7和4G6与致病性溶组织内阿米巴HM-1∶IMSS株滋养体37℃孵育,在孵育即刻、5min、10min加入红细胞,检测滋养体吞噬红细胞的能力,并以正常小鼠血清和抗克氏锥虫抗体TCE04作为对照。结果,经单克隆抗体3F7孵育即刻的HM-1∶IMSS虫株滋养体吞噬红细胞能力明显减弱(P<0.001),而4G6抑制滋养体吞噬红细胞的作用不如前者明显。提示,抗细胞膜单克隆抗体对抑制滋养体吞噬红细胞有显著作用,但随着时间的推移,抑制作用明显减弱。 相似文献
4.
Miguel Angel Vargas Armando Isibasi Jesús Kumate Esther Orozco 《Molecular and biochemical parasitology》1990,40(2):193-201
We have cultured under monoxenic conditions and characterized an Entamoeba histolytica clone, MAV-I CINVESTAV (MAV-I), obtained from feces from an asymptomatic carrier. The clone shows the non-pathogenic E. histolytica zymodeme type I, which did not change through the process of monoxenization. Clone MAV-I was non-pathogenic in both in vivo and in vitro tests, and it did not have a functional 112-kDa adhesin. As far as we know, this is the first non-pathogenic monoxenic strain reported. Clone A (strain HM1:IMSS), a highly virulent clone with pathogenic zymodeme type II, and which has the 112-kDa adhesin, was used as a control. Protein patterns from both clones were almost identical in one-dimensional gels. In two-dimensional gels, differences in high-molecular-weight proteins were detected. Clone MAV-I adhered and phagocytosed only 12% of the red blood cells adhered and phagocytosed by clone A. MAV-I trophozoites did not destroy cell culture monolayers and did not produce hepatic abscesses in hamsters. They also showed deficiency in protease activity. The absence of virulence in clone MAV-I correlated directly with the absence of a functional 112-kDa adhesin, supporting the role that this protein plays in virulence. 相似文献
5.
齿龈内阿米巴的致病作用与致病机制的研究 总被引:1,自引:0,他引:1
在注射免疫抑制剂 1周后的大白鼠龈缘涂抹齿龈内阿米巴 (Emtamoebagingivalis ,E .g .) ,5天后 ,牙龈组织出现溃疡、牙周脓肿形成、脓液查见活E .g .、牙槽骨吸收等牙周炎病症。电镜术与生化分析发现 :E .g .伪足活跃、有丰富的溶酶体 ,所含水解酶与ACP显著较健康组高 (P <0 0 1) ,可使牙周组织溶解与受损。SOD较健康组显著性低 (P <0 0 1) ,MDA显著性增高 (P <0 0 1) ,说明E .g .感染产生较多氧自由基可使细胞膜受损 ,加上口腔共生菌的协同作用使免疫力低下的宿主发生牙周炎。 相似文献
6.
Melzer H Fortugno P Mansouri E Felici F Marinets A Wiedermann G Kollaritsch H Von Specht BU Duchêne M 《Parasite immunology》2002,24(6):321-328
Entamoeba histolytica is the protozoan parasite responsible for intestinal amoebiasis and amoebic liver abscess, which cause significant morbidity and mortality in many countries of the world. Proteophosphoglycans (PPGs, also known as lipophosphoglycans, LPGs, or lipopeptidophosphoglycans, LPPGs) represent dominant surface components of E. histolytica. Passive immunization with a monoclonal antibody (EH5) directed against these components protected SCID mice from amoebic liver abscess, so PPGs might be regarded as vaccine candidates; however, their structure is very complex and only known in part. They are glycosylphosphatidylinositol-linked polypeptides of unknown sequence carrying glycan side-chains linked to serine residues via phosphodiester bonds. In order to identify peptide mimics of the E. histolytica PPG antigens, we screened six different phage-displayed random peptide libraries with the antibody EH5. Various peptide mimics of different length were identified and, in all the peptides, a distinct consensus sequence Gly-Thr-His-Pro-X-Leu could be identified. The phages strongly bound to the antibody, and the natural antigen inhibited binding of the phages to antibody EH5. In addition, several of the phages induced a significant immunoglobulin G response against amoebic antigens in immunized mice. 相似文献
7.
Aadish Rawat Parikshit Singh Anupam Jyoti Sanket Kaushik Vijay Kumar Srivastava 《Chemical biology & drug design》2020,96(2):731-744
Amoebiasis is a parasitic infectious disease caused by the enteric protozoan Entamoeba histolytica, a leading basis of deaths accounted to parasites, succeeding malaria and schistosomiasis. Conventional treatment methodologies used to deal with amoebiasis mainly rely on the administration of anti‐amoebic compounds and vaccines but are often linked with substantial side‐effects on the patient. Besides, cases of development of drug resistance in protozoans have been recorded, contributing further to the reduction in the efficiency of the treatment. Loopholes in the efficacious management of the disease call for the development of novel methodologies to manage amoebiasis. A way to achieve this is by targeting the essential metabolic processes of ‘encystation’ and ‘excystation’, and the associated biomolecules, thus interrupting the biphasic life cycle of the parasite. Technologies like the CRISPR‐Cas9 system can efficiently be exploited to discover novel and essential molecules that regulate the protozoan's metabolism, while efficiently manipulating and managing the known drug targets, leading to an effective halt and forestall to the enteric infection. This review presents a perspective on these essential metabolic processes and the associated molecules that can be targeted efficaciously to prevent the transmission of amoebiasis, thus managing the disease and proving to be a fruitful endeavour. 相似文献
8.
Hisashi Yamaura Kunioki Araki Ken Kikuchi Ichiro Itoda Kyoichi Totsuka Takatoshi Kobayakawa 《Journal of infection and chemotherapy》2003,9(1):25-29
We improved the dot enzyme-linked immunosorbent assay (dot-ELISA) reported by Itoh and Sato, and assessed the usefulness
of this test for the diagnosis of amebiasis. The sensitivity of dot-ELISA was compared with that of plate ELISA, the indirect
hemagglutination test (IHA), and the indirect fluorescent antibody test (IFA) for the diagnosis of amebiasis. Of 37 serum
samples from patients with documented amebiasis, 36 (97.3%) were positive by dot-ELISA. There was consistency among the results
of dot-ELISA, plate ELISA, and IFA, although the positive rate of IHA was lower than that of the others (78.4%; 29 of 37 cases
were positive). The specificities of dot-ELISA and plate ELISA were assessed using a total of 68 sera, collected from 38 patients
infected with seven different parasites other than Entamoeba histolytica, 10 patients showing diarrhea or liver abscess without parasitic infection, and 20 healthy individuals. The two assays showed
no false-positive results. There were no differences in sensitivity and specificity between dot-ELISA and plate ELISA. However,
the dot-ELISA technique seems to be more feasible for clinical application than plate ELISA techniques, because the assay
does not require any specific equipment.
Received: July 8, 2002 / Accepted: December 7, 2002
RID="*"
ID="*" A summary of this paper was presented at the 74th General Meeting of the Japanese Association for Infectious Diseases
(Fukuoka, April 2000).
Acknowledgments The authors are indebted to Professor Tsutomu Takeuchi and Dr. Seiki Kobayashi, Department of Tropical Medicine and Parasitology,
Keio University School of Medicine, for supplying E. histolytica antigen, and to Dr. Hiroshi Yamasaki, Department of Parasitology, Juntendo University School of Medicine, for supplying recombinant
Toxocara canis antigen for this study. 相似文献
9.
Nozhat ZEBARDAST Ali HAGHIGHI Farshid YEGANEH Seyyed Javad SEYYED TABAEI Mohammad Javad GHARAVI Shirzad FALLAHI Zohreh LASJERDI Nima SALEHI Niloofar TAGHIPOUR Cobra KOHANSAL Farideh NADERI 《Iranian Journal of Parasitology》2014,9(4):466-473
Background
Entamoeba moshkovskii and E. dispar are impossible to differentiate microscopically from the pathogenic species E. histolytica. Multiplex polymerase chain reaction (Multiplex PCR) is a widespread molecular biology technique for amplification of multiple targets in a single PCR experiment.Methods
For detection and differentiation of the three-microscopy indistinguishable Entamoeba species in human, multiplex PCR assay using different DNA extraction methods was studied. A conserved forward primer was derived from the middle of the small-subunit rRNA gene, and reverse primers were designed from signature sequences specific to each of these three Entamoeba species.Results
A 166-bp PCR product with E. histolytica DNA, a 580-bp product with E. moshkovskii DNA and a 752-bp product with E. dispar DNA were generated in a single-round and multiplex PCR reaction.Conclusion
We recommend this PCR assay as an accurate, rapid, and effective diagnostic method for the detection and discrimination of these three Entamoeba species in both routine diagnosis of amoebiasis and epidemiological surveys. 相似文献10.
Arturo Contis Montes de Oca Andrea Cruz Baquero Rafael Campos Rodríguez Luz María Cárdenas Jaramillo José Eduardo Aguayo Flores Saúl Rojas Hernández Alfonso Olivos García Judith Pacheco Yepez 《Parasite immunology》2020,42(6):e12714
The main effector mechanisms of neutrophils are the release of neutrophil extracellular traps (NETs) and myeloperoxidase (MPO). In this work, we evaluated the role of NETs and the activity of MPO in the interactions of rodent neutrophils with amoebae and in amoebic liver abscess (ALA)-resistant and ALA-susceptible models. We showed with in vitro assays that mice produced greater amounts of NETs and MPO than did hamsters, and the elastase activity was high in both models. However, the inhibition of NETs and MPO promoted an increase in amoeba viability in the mice. The mouse ALAs showed a more profound presence of NETs and MPO than did the hamster ALAs. We concluded that both effector mechanisms were essential for the amoebic damage and could prevent the formation of ALAs in the resistant model. 相似文献