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| 1 | Comparison of the RE and B1 gene for detection of Toxoplasma gondii infection in children with cancer显示文摘 | Sh. Fallahi B. Kazemi S.J. Seyyed tabaei M. Bandehpour Z. Lasjerdi N. Taghipour N. Zebardast B. Nikmanesh V. Fallah Omrani F. Ebrahimzadeh | 2014 | Parasitology International2014，，1： | 2 |
| 2 | Cloning and expression of soluble vascular endothelial growth factors receptor-1 (sFlt-1) fragments in CHO-K1 显示文摘 | Farnia P Bandehpour M Ghanavi J | 2013 | Int J Clin Exp Med2013，6，9： | 1 |
| 3 | Expres- sion of recombinant human coagulation factor VII by the lizard Leishmania expression system 显示文摘 | Mirzaahmadi S Asaadi-Tehrani G Bandehpour M | 2011 | J Biomed Bix technol 20 l 12011，2011，： | 1 |
| 4 | Gene Cloning of 30kDa Toxoplasma gondii Tachyzoites Surface Antigen(SAG1)显示文摘 | Kazemi B Bandehpour M Maghen L | 2007 | Iranian J Parasitol2007，2，2： | 1 |
| 5 | Application of recombinant Echinococcus granulosus antigen B to ELISA kits for diagnosing hydatidosis显示文摘 | KALANTARI E BANDEHPOUR M PAZOKI R | 2010 | Parasitol Res2010，106，4： | 1 |
| 6 | First molecular identification of Leishmania species in a new endemic area of cutaneous leishmaniasis in Lorestan,Iran显示文摘Objective:To identify Leishman{u using PCR.Methods:This studs was conducted from April2009 to March 2011 in order to identify Leishmania species in a new endemic area of CL in Lorestan.Iran.Samples were taken from 62 patients that referred to the health centers in different cities of Lorestan province,the presence of Leishmcania was confirmed using direct smear and then grown in NNN media and mass cultured in RPM!1640 medium supplemented with 10%heat-inactivated fetal bovine serum.DNA was extracted from cultured promastigotes and used in P15-PCR.Results:45(72.6%)samples out of 62 showed a hand in the range of 485 hp and 17(27.4%)with a hand in the range of 626 hp which were similar to standard strains of Leichmania tropica(L.tropical and Leishnrania major(L.major),respectively.50(65.80%)of samples were collected from people with no history of travel in at least a year prior to the onset which shows that indigenous source of infection.Conclusions:Since the vector and reservoir of the two species are different.so precise and extensive control and prevention methods should be designed and earned out. | Farnaz Kheirandish Ali Chegeni Sharafi Bahram Kazemi Mojgan Bandehpour Mohamad javad Tarahi Ali Khamesipour | 2013 | Asian Pacific Journal of Tropical Medicine2013，6，9： | 0 |
| 7 | Cytokine changes and embryo attachment in mouse endometrial cells following treated with peripheral blood mononuclear cells(PBMCs)expressing ectopic hCG,and hCG-activated PBMCs显示文摘Objective:To compare the effect of human chorionic gonadotropin(hCG)-producing peripheral blood mononuclear cells(PBMCs)and PBMCs activated by hCG in vitro and expressions of related immune genes in mouse implantation.Methods:hCG-producing PBMCs(transfected PBMC)and PBMCs activated by hCG in vitro were introduced into isolated mouse endometrial cells,while cell cultures were divided into four groups:the control,PBMC,transfected,and activated PBMC groups.The expression of studied genes(IL-1β,IL-6,Lif,and Vegf)was evaluated and blastocyst attachment on the cocultured cells(isolated endometrial cells and PBMC cells)was monitored in all four groups.Results:Data showed that expression decreased in the PBMC group compared to the treated PBMC(transfected and activated PBMCs)and increased in transfected PBMC compared to the activated PBMC.Attachment and migration of blastocysts were dramatically enhanced in the transfected PBMC group compared to the activated PBMC group(P<0.05).Conclusions:Use of hCG-producing PBMCs(transfected PBMC)has more influence on endometrial receptivity. | Delsuz Rezaee Mojgan Bandehpour Bahram Kazemi Saiyad Bastaminejad Sajad Najafi Mohammad Salehi | 2023 | Asian pacific Journal of Reproduction2023，12，2： | 0 |
| 8 | Cloning and expression of Neisseria meningitides luxS gene显示文摘Neisseria meningitides is a Gram-negative bacterium which is an important causative agent of septicemia and meningitis.Numerous pathogenic bacteria contain luxS,which is required for autoinducer-2 production.Neisseria meningitides contains a functional copy of luxS that is necessary for full meningococcal virulence.Neisseria meningitides DNA was extracted and its luxS gene was amplified by nested PCR.PCR product was purified and cloned in to pQE-30 expression vector.Recombinant plasmid was transformed and mass cultured.luxS was expressed in E.coli and confirmed by western blot analysis.In this study,N.meningitides luxS was amplified, cloned and expressed successfully.The sequencing of PCR product confirmed that amplified gene was luxS. Gene was expressed and observed in SDS-PAGE.Protein was reacted by his tag monoclonal antibody through western blot analysis. | Bahram Kazemi Nazila Baghalzadeh-Mohammadi Reza Hadavi Mojgan Bandehpour Elham Ghayour Majid Moghbeli Kazem Parivar | 2008 | Asian Pacific Journal of Tropical Medicine2008，1，2： | 0 |
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