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19061por Savino, Francesco, Cordisco, Lisa, Tarasco, Valentina, Locatelli, Emanuela, Di Gioia, Diana, Oggero, Roberto, Matteuzzi, Diego“…RESULTS: Strains of coliforms were isolated from stools of 45 colicky and 42 control breastfed infants in McConkey Agar and identified using PCR with species-specific primers, and the BBL™ Enterotube™ II system for Enterobacteriaceae. …”
Publicado 2011
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19062por Ke, Tao, Liang, Su, Huang, Jin, Mao, Han, Chen, Jibao, Dong, Caihua, Huang, Junyan, Liu, Shengyi, Kang, Jianxiong, Liu, Dongqi, Ma, Xiangdong“…RESULTS: Two or four primers were used to synthesize each AMP gene in a single step PCR. …”
Publicado 2012
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19063por Sahin, Ziver, Bıcakcıgil, Muge, Aksu, Kenan, Kamali, Sevil, Akar, Servet, Onen, Fatos, Karadag, Omer, Ozbalkan, Zeynep, Ates, Askin, Ozer, Huseyin TE, Yilmaz, Vuslat, Seyahi, Emire, Ozturk, Mehmet A, Cefle, Ayse, Cobankara, Veli, Onat, A Mesut, Tunc, Ercan, Düzgün, Nursen, Aydin, Sibel Z, Yilmaz, Neslihan, Fresko, İzzet, Karaaslan, Yasar, Kiraz, Sedat, Akkoc, Nurullah, Inanc, Murat, Keser, Gokhan, Uyar, F Aytul, Direskeneli, Haner, Saruhan-Direskeneli, Güher“…DNA samples from the patients and healthy controls (HC; n = 210) were isolated, and the presence of HLA-B*51 or HLA-B*52 was screened for by using PCR with sequence-specific primers. RESULTS: We found a significant association of HLA-B*52 with TAK (20.9% vs HC = 6.7%, P = 0.000, OR = 3.7, 95% CI = 2.02 to 6.77). …”
Publicado 2012
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19064por Botkin, Douglas J., Galli, Lucía, Sankarapani, Vinoth, Soler, Michael, Rivas, Marta, Torres, Alfredo G.“…In the current study, we investigated whether enterohemorrhagic E. coli (EHEC), Shiga toxin-producing E. coli (STEC), and enteropathogenic E. coli (EPEC) strains can be rapidly and specifically differentiated with multiplex PCR (mPCR) utilizing selected biomarkers associated with each strain’s respective virulence genotype. Primers were designed to amplify multiple intimin (eae) and long polar fimbriae (lpfA) variants, the bundle-forming pilus gene bfpA, and the Shiga toxin-encoding genes stx1 and stx2. …”
Publicado 2012
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19065por Pollak, Dana Walters, Bostick, Michael W., Yoon, Hyeryoung, Wang, Jamie, Hollerbach, Dieter H., He, Hongxian, Damude, Howard G., Zhang, Hongxiang, Yadav, Narendra S., Hong, Seung-Pyo, Sharpe, Pamela, Xue, Zhixiong, Zhu, Quinn“…A full length Δ5 desaturase gene from Euglena gracilis (EgΔ5D) was isolated by cloning the products of polymerase chain reaction with degenerate oligonucleotides as primers, followed by 5′ and 3′ rapid amplification of cDNA ends. …”
Publicado 2012
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19066por Yang, Ruifang, Sun, Chunlong, Bai, Jianjiang, Luo, Zhixiang, Shi, Biao, Zhang, Jianming, Yan, Wengui, Piao, Zhongze“…SBE3 which codes for starch branching enzyme was identified as a candidate gene within the putative region. Nine pairs of primers covering 22 exons were designed to sequence genomic DNA of the wild type for SBE3 and the mutant for sbe3-rs comparatively. …”
Publicado 2012
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19067por Zhu, Jiang, O’Dell, Sijy, Ofek, Gilad, Pancera, Marie, Wu, Xueling, Zhang, Baoshan, Zhang, Zhenhai, Mullikin, James C., Simek, Melissa, Burton, Dennis R., Koff, Wayne C., Shapiro, Lawrence, Mascola, John R., Kwong, Peter D.“…PGT135–137-gene family specific primers were used to amplify heavy-chain and light-chain variable-domain sequences. …”
Publicado 2012
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19068por Li, Gang, Liu, Ka, Jiao, Shasha, Liu, Haibo, Blair, Hugh T, Zhang, Peng, Cui, Xiaoran, Tan, Pingping, Gao, Jianfeng, Ma, Runlin Z“…RESULTS: A total of 119 pairs of comparative bovine oligo primers were utilized to screen an ovine BAC library for positive clones and the orders and overlapping relationships of the identified clones were determined by DNA fingerprinting, BAC-end sequencing, and sequence-specific PCR. …”
Publicado 2012
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19069por Patnaik, Bharat Bhusan, Kim, Dong Hyun, Oh, Seung Han, Song, Yong-Su, Chanh, Nguyen Dang Minh, Kim, Jong Sun, Jung, Woo-jin, Saha, Atul Kumar, Bindroo, Bharat Bhushan, Han, Yeon Soo“…In order to characterize the full-length gene sequence in detail, the partial cDNA was cloned and sequenced using degenerate primers, followed by 5′- and 3′-rapid amplification of cDNA ends (RACE-PCR). …”
Publicado 2012
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19070por Zhao, Hongxia, Guo, Mei, Sun, Xuedong, Sun, Wanjun, Hu, Hailan, Wei, Li, Ai, Huisheng“…Recent thymic emigrants (RTEs) were assessed by real-time polymerase chain reaction (PCR) using primers specific to the 257-bp T cell receptor rearrangement excision circles (sjTRECs). …”
Publicado 2013
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19071por Ma, Dongzhu, Jasinska, Anna, Kristoff, Jan, Grobler, J. Paul, Turner, Trudy, Jung, Yoon, Schmitt, Christopher, Raehtz, Kevin, Feyertag, Felix, Martinez Sosa, Natalie, Wijewardana, Viskam, Burke, Donald S., Robertson, David L., Tracy, Russell, Pandrea, Ivona, Freimer, Nelson, Apetrei, Cristian“…Viruses infecting AGMs in the Free State, which are separated from those on the coastal side by the Drakensberg Mountains, formed a separate cluster in the phylogenetic trees; this observation supports a long standing presence of SIV in AGMs, at least from the time of their speciation to their Plio-Pleistocene migration. Specific primers/probes were synthesized based on the pol sequence data and viral loads (VLs) were quantified. …”
Publicado 2013
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19072“…Recently published as well as self-designed primers were used for amplification. RESULTS: Blood from eight patients was finally used for analysis. …”
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19073por Oshikata, Chiyako, Tsurikisawa, Naomi, Saito, Akemi, Watanabe, Maiko, Kamata, Yoichi, Tanaka, Maki, Tsuburai, Takahiro, Mitomi, Hiroyuki, Takatori, Kosuke, Yasueda, Hiroshi, Akiyama, Kazuo“…Partial sequences of the beta-tubulin gene were determined by using the primers Bt2a and Bt2b for PCR amplification and sequencing and underwent a BLAST search at the National Centre for Biotechnology Information, these results confirmed that the isolated fungus was P. digitatum. …”
Publicado 2013
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19074por Santos, Helena Lúcia Carneiro, Bandyopadhyay, Kakali, Bandea, Rebecca, Peralta, Regina Helena Saramago, Peralta, José Mauro, Da Silva, Alexandre Januário“…METHODS: PCR amplification was performed with biotinylated Entamoeba sp 18S rRNA gene primers, designed to amplify a fragment ranging from 382 to 429 bp of the Entamoeba spp studied. …”
Publicado 2013
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19075por Muniz, Cláudia P., Troncoso, Lian L., Moreira, Miguel A., Soares, Esmeralda A., Pissinatti, Alcides, Bonvicino, Cibele R., Seuánez, Héctor N., Sharma, Bechan, Jia, Hongwei, Shankar, Anupama, Switzer, William M., Santos, André F., Soares, Marcelo A.“…We tested a large collection of genomic DNA (n = 332) comprising 14 genera of NWP species for the presence of SFV polymerase (pol) sequences using generic PCR primers. Further molecular characterization of positive samples was carried out by LTR-gag and larger pol sequence analysis. …”
Publicado 2013
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19076por Tangprasittipap, Amornrat, Srisala, Jiraporn, Chouwdee, Saisunee, Somboon, Montagan, Chuchird, Niti, Limsuwan, Chalor, Srisuvan, Thinnarat, Flegel, Timothy W, Sritunyalucksana, Kallaya“…Our objective was to compare the newly found pathogen with E. hepatopenaei and to determine its causal relationship with WFS. RESULTS: Generic primers used to amplify a fragment of the small subunit ribosomal RNA (ssu rRNA) gene for cloning and sequencing revealed that the new parasite from WFS ponds had 99% sequence identity to that of E. hepatopenaei, suggesting it was conspecific. …”
Publicado 2013
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19077por Robinson, Max, Suh, Yae-eun, Paleri, Vinidh, Devlin, Debbie, Ayaz, Bushra, Pertl, Laura, Thavaraj, Selvam“…The detection of high-risk HPV was carried out by screening all cases for p16 using immunohistochemistry and HPV DNA by polymerase chain reaction (PCR) using GP5+/6+ primers. All cases with p16 over-expression or positive for HPV by PCR were then examined by high-risk HPV DNA in-situ hybridisation and genotype analysis by PCR. …”
Publicado 2013
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19078“…RESULTS: In total, 157 PCR fragments that were amplified using the degenerate primers for the reverse transcriptase (RT) domain of copia-type retroelements were sequenced and aligned to construct the neighbor-joining tree. …”
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19079por Lata, Sneh, Ronsard, Larance, Sood, Vikas, Dar, Sajad A., Ramachandran, Vishnampettai G., Das, Shukla, Banerjea, Akhil C.“…METHODS: HIV-1 tat exon 1 and vpr were amplified from the genomic DNA isolated from the blood of HIV-1 infected individuals using specific primers by Polymerase Chain reaction (PCR) and subjected to extensive genetic analysis (CLUSTAL W, Simplot etc). …”
Publicado 2013
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19080por Abou Shousha, Mohamed, Santos, Andrea Rachelle C., Oechsler, Rafael A., Iovieno, Alfonso, Maestre-Mesa, Jorge, Ruggeri, Marco, Echegaray, Jose J., Dubovy, Sander R., Perez, Victor L., Miller, Darlene, Alfonso, Eduardo C., Bajenaru, M. Livia“…The fungal infection was monitored with periodic slit-lamp examination and in vivo SD-OCT imaging of the rat eye, and confirmed by histology, counting of viable fungi in the infected rat cornea, and PCR with specific primers for Fusarium sp. RESULTS: We imaged and measured the rat cornea with SD-OCT. …”
Publicado 2013
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