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19121por Britton, Sumudu, Cheng, Qin, Grigg, Matthew J., Poole, Catherine B., Pasay, Cielo, William, Timothy, Fornace, Kimberley, Anstey, Nicholas M., Sutherland, Colin J., Drakeley, Chris, McCarthy, James S.“…RESULTS: The high throughput LAMP-P. vivax assay (HtLAMP-Pv) performed with an estimated limit of detection of 1.4 parasites/ μL. Assay primers demonstrated cross-reactivity with P. knowlesi but not with other Plasmodium spp. …”
Publicado 2016
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19122por Yan, Dong, Zhang, Tao, Su, Jing, Zhao, Li-Li, Wang, Hao, Fang, Xiao-Mei, Zhang, Yu-Qin, Liu, Hong-Yu, Yu, Li-Yan“…The airborne fungal community in these samples was analyzed using the Illumina Miseq platform with fungi-specific primers targeting the internal transcribed spacer 1 region of the large subunit rRNA gene. …”
Publicado 2016
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19123por Fan, Hongying, Zhao, Fuping, Zhu, Caiye, Li, Fadi, Liu, Jidong, Zhang, Li, Wei, Caihong, Du, Lixin“…In order to characterize the mitogenomes of 3 Chinese sheep breeds (Altay sheep [AL], Shandong large-tailed sheep [SD], and small-tailed Hulun Buir sheep [sHL]), 19 sets of primers were employed to amplify contiguous, overlapping segments of the complete mitochondrial DNA (mtDNA) sequence of each breed. …”
Publicado 2016
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19124por Lin, Yung-Feng, Li, Ling-Hui, Lin, Chih-Hung, Tsou, Mei-Hua, Chuang, Ming-Tai Kiffer, Wu, Keh-Ming, Liao, Tsai-Lien, Li, Jian-Chiuan, Wang, Wei-Jie, Tomita, Angela, Tomita, Beverly, Huang, Shiu-Feng, Tsai, Shih-Feng“…A total of 2,293 pairs of primers were designed for 1,449 exonic and upstream promoter regions to amplify and sequence 76.8–114 Mb on human chromosome 4. …”
Publicado 2016
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19125por Nie, Gang, Huang, Linkai, Zhang, Xinquan, Taylor, Megan, Jiang, Yiwei, Yu, Xiaoqing, Liu, Xinchun, Wang, Xinyu, Zhang, Yajie“…A collection of 138 individuals was selected for conducting a 3-year trial of biomass production and analyzed by using 104 pairs of SRAP, ISAP, and SSR primers for genetic diversity as well as marker-trait association. …”
Publicado 2016
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19126por Loh, Siew-May, Gofton, Alexander W., Lo, Nathan, Gillett, Amber, Ryan, Una M., Irwin, Peter J., Oskam, Charlotte L.“…The present study investigated the presence of Borrelia in 97 Bothriocroton concolor ticks parasitizing echidnas in Queensland, New South Wales, and Victoria, Australia, using nested PCR with Borrelia-specific primers targeting the 16S rRNA (16S) and flaB genes. …”
Publicado 2016
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19127por Hora, Bhavna, Keating, Sheila M., Chen, Yue, Sanchez, Ana M., Sabino, Ester, Hunt, Gillian, Ledwaba, Johanna, Hackett, John, Swanson, Priscilla, Hewlett, Indira, Ragupathy, Viswanath, Vikram Vemula, Sai, Zeng, Peibin, Tee, Kok-Keng, Chow, Wei Zhen, Ji, Hezhao, Sandstrom, Paul, Denny, Thomas N., Busch, Michael P., Gao, Feng“…Three group O viruses were only characterized with additional group O-specific RT-PCR primers employed by one site. These results indicate that PCR protocols and subtyping tools should be standardized to efficiently amplify diverse viruses and more consistently assign virus genotypes, which is critical for accurate global subtype and drug resistance surveillance. …”
Publicado 2016
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19128por Tabibnejad, Mahsa, Alikhani, Mohammad Yousef, Arjomandzadegan, Mohammad, Hashemi, Seyed Hamid, Naseri, Zahra“…The specificity of the primers was evaluated by DNA from pure and approved Brucella colonies found in the blood samples, by DNA from other bacteria, and by ordinary PCR. …”
Publicado 2016
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19129por Masumura, Kenichi, Sakamoto, Yasuteru, Kumita, Wakako, Honma, Masamitsu, Nishikawa, Akiyoshi, Nohmi, Takehiko“…The copy number and arrangement of the transgene were analyzed. PCR primers for quick genotyping of gpt delta mice and rats have been designed. …”
Publicado 2015
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19130por Kho, Alvin T., Sharma, Sunita, Davis, Joshua S., Spina, Joseph, Howard, Dagnie, McEnroy, Kevin, Moore, Kip, Sylvia, Jody, Qiu, Weiliang, Weiss, Scott T., Tantisira, Kelan G.“…Using a TaqMan microRNA array containing 754 microRNA primers, we tested for the presence of known asthma microRNAs, and assessed the association of the individual microRNAs with lung function as measured by FEV(1)/FVC, FEV(1)% and FVC%. …”
Publicado 2016
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19131“…PCR was used to detect the expression of HPV genome employing specific primers for HPV 16 and 18 types. The results showed that there was 47.2 and 63.9% positive HIF-1α and P-gp expression in the study group. …”
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19132por Coşkun, Salih, Varol, Sefer, Özdemir, Hasan H, Çelik, Sercan Bulut, Balduz, Metin, Camkurt, Mehmet Akif, Çim, Abdullah, Arslan, Demet, Çevik, Mehmet Uğur“…Eight common missense mutations of the MEFV gene, known as M694V, M694I, M680I, V726A, R761H, K695R, P369S, and E148Q, were genotyped using real-time polymerase chain reaction with 5′ nuclease assays, which include sequence specific primers, and probes with a reporter dye. When mutations were evaluated separately among the patient and control groups, only the heterozygote E148Q carrier was found to be significantly higher in the control group than in the patient group (P=0.029, odds ratio [95% confidence interval] =0.45 [0.21–0.94]). …”
Publicado 2016
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19133Evaluation and Comparison of Vitamin D Responsive Gene Expression in Ovine, Canine and Equine Kidneypor Azarpeykan, Sara, Dittmer, Keren E., Marshall, Jonathan C., Perera, Kalyani C., Gee, Erica K., Acke, Els, Thompson, Keith G.“…Renal tissue samples were harvested post-mortem from 10 horses, 10 sheep, and five dogs. Primers were designed for each gene. For each sample total RNA was extracted, cDNA synthesised, and RT-qPCR was performed. …”
Publicado 2016
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19134por Damanka, Susan, Lartey, Belinda, Agbemabiese, Chantal, Dennis, Francis E., Adiku, Theophilus, Nyarko, Kofi, Ofori, Michael, Armah, George E.“…METHODS: Viral RNA was extracted and rotavirus VP7 and VP4 genes amplified by one step RT-PCR using gene-specific primers. The DNA was purified, sequenced and genotypes determined using BLAST and RotaC v2.0. …”
Publicado 2016
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19135por Qi, Yuexiao, Wei, Yuehua, Wang, Qiaoli, Xu, Hui, Wang, You, Yao, Anqi, Yang, Hui, Gao, Yan, Zhou, Fuxiang“…Wild-type and mutant sequences were separately amplified using allele-specific primers and, subsequently, the PCR products containing the mtDNA 10398 site were ligated into vectors to construct a standard plasmid DNA construct. …”
Publicado 2016
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19136por Tang, Min, Hardman, Chloe J., Ji, Yinqiu, Meng, Guanliang, Liu, Shanlin, Tan, Meihua, Yang, Shenzhou, Moss, Ellen D., Wang, Jiaxin, Yang, Chenxue, Bruce, Catharine, Nevard, Tim, Potts, Simon G., Zhou, Xin, Yu, Douglas W.“…Direct inspection and an analysis with species‐specific primers suggested that these putative false positives were most likely due to incorrect morphological IDs. …”
Publicado 2015
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19137por Wang, Haiyan, Dai, Keli, Xiao, Jin, Yuan, Chunxia, Zhao, Renhui, Doležel, Jaroslav, Wu, Yufeng, Cao, Aizhong, Chen, Peidu, Zhang, Shouzhong, Wang, Xiue“…The intron length polymorphisms suitable for designing H. villosa primers were evaluated with criteria. Consequently, we designed a total of 359 intron targeting (IT) markers, among which 232 (64.62%) markers were specific for tracing the 4VS chromatin in the wheat background. …”
Publicado 2017
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19138por Gao, Caixia, Quan, Jinqiang, Jiang, Xinjie, Li, Changwen, Lu, Xiaoye, Chen, Hongyan“…In this study, we identified 61 alleles at five polymorphic SLA loci (SLA-1, SLA-2, SLA-3, DRB1, and DQB1) representing 17 class I haplotypes and 11 class II haplotypes using reverse transcription-polymerase chain reaction (RT-PCR) sequence-based typing and PCR-sequence specific primers methods in 367 Canadian SPF Yorkshire and Landrace pigs. …”
Publicado 2017
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19139por Bustamante-Rengifo, Javier Andres, Matta, Andres Jenuer, Pazos, Alvaro Jairo, Bravo, Luis Eduardo“…DNA from H. pylori isolates was amplified using primers specific for cagA and vacA genes. The phylogenetic relationships among isolates obtained before and after treatment were established by conglomerate analysis based on random amplified polymorphic DNA (RAPD) fingerprinting. …”
Publicado 2017
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19140por Zanga, Josue, Mbanzulu, Makola Kennedy, Kabasele, Arnold-Freddy, Ngatu, Nlandu Roger, Wumba, Dimosi Roger“…METHODS: This was a prospective cross-sectional study that consisted of a laboratory analysis of blood samples from 78 pregnant women to check for the presence of RUBV IgG antibodies, and also determine RUBV genotypes in seropositive samples (using primers targeting RUBV nucleoprotein), with the use of serological and molecular methods, respectively. …”
Publicado 2017
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