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19601por Simo, Gustave, Fogue, Pythagore Soubgwi, Melachio, Tresor Tito Tanekou, Njiokou, Flobert, Kuiate, Jules Roger, Asonganyi, Tazoacha“…DNA was extracted from midguts and specific primers were used to identify Trypanosoma congolense forest and savannah. …”
Publicado 2014
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19602por Lawson, Becki, Dastjerdi, Akbar, Shah, Sonal, Everest, David, Núñez, Alejandro, Pocknell, Ann, Hicks, Daniel, Horton, Daniel L, Cunningham, Andrew A, Irvine, Richard M“…Nucleic acid extracted from pooled liver and spleen was positive on both a pan-reovirus nested PCR targeting the RNA-dependent RNA polymerase gene and a PCR using primers specific to the ARV sigma C protein gene. …”
Publicado 2015
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19603por Gumiel, Marcia, da Mota, Fabio Faria, Rizzo, Vanessa de Sousa, Sarquis, Otília, Castro, Daniele Pereira de, Lima, Marli Maria, Garcia, Eloi de Souza, Carels, Nicolas, Azambuja, Patricia“…Additionally, we identified TcI and TcII types of T. cruzi by sequencing amplicons from the gut metagenomic DNA with primers for the mini-exon gene. RESULTS: Triatomines collected in the peridomestic ecotopes were diagnosed as T. pseudomaculata and T. brasiliensis by comparing their COI sequence with GenBank. …”
Publicado 2015
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19604por Jung-Schroers, Verena, Adamek, Mikolaj, Teitge, Felix, Hellmann, John, Bergmann, Sven Michael, Schütze, Heike, Kleingeld, Dirk Willem, Way, Keith, Stone, David, Runge, Martin, Keller, Barbara, Hesami, Shohreh, Waltzek, Thomas, Steinhagen, Dieter“…By analyzing gill tissues for CEV in seven out of eleven samples by a nested PCR, PCR products of 547 bp and 180 bp (by using nested primers) could be amplified. An outbreak of Koi Sleepy Disease was confirmed by sequencing of the PCR products. …”
Publicado 2015
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19605por Cimino, Rubén O., Jeun, Rebecca, Juarez, Marisa, Cajal, Pamela S., Vargas, Paola, Echazú, Adriana, Bryan, Patricia E., Nasser, Julio, Krolewiecki, Alejandro, Mejia, Rojelio“…RESULTS: qPCR showed higher detection rates for all parasites as compared to stool microscopy except T. trichiura. Species-specific primers and probes were able to distinguish between A. duodenale (19.1 %) and N. americanus (36.4 %) infections. …”
Publicado 2015
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19606por Latif, Ayesha, Rao, Abdul Qayyum, Khan, Muhammad Azmat Ullah, Shahid, Naila, Bajwa, Kamran Shehzad, Ashraf, Muhammad Aleem, Abbas, Malik Adil, Azam, Muhammad, Shahid, Ahmad Ali, Nasir, Idrees Ahmad, Husnain, Tayyab“…A 1.4-kb PCR product for Glyphosate and 167-bp product for Cry2A were obtained by amplification through gene specific primers. Expression level of Glyphosate and Bt proteins in two transgenic lines were recorded to be 0.362, 0.325 µg/g leaf and 0.390, 0.300 µg/g leaf respectively. …”
Publicado 2015
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19607por Nowacka-Zawisza, Maria, Forma, Ewa, Walczak, Maciej, Różański, Waldemar, Bryś, Magdalena, Krajewska, Wanda M.“…The LOH in tumors was analyzed by PCR with fluorescently labeled primers and an ABI PRISM 377 DNA Sequencer. Allele sizing was determined by GeneScan version 3.1.2 and Genotyper version 2.5 software (Applied Biosystems, USA). …”
Publicado 2015
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19608por Akter, Rumana, Vythilingam, Indra, Khaw, Loke Tim, Qvist, Rajes, Lim, Yvonne Ai-Lian, Sitam, Frankie Thomas, Venugopalan, Balan, Sekaran, Shamala Devi“…RESULTS: Thirty-five (50 %) of the 70 samples were positive for Plasmodium using genus-specific primers. These positive samples were then subjected to nested PCR targeting the 18S ribosomal RNA genes to detect all five simian malaria parasites: namely, P. knowlesi, Plasmodium inui, Plasmodium cynomolgi, Plasmodium fieldi, and Plasmodium coatneyi. …”
Publicado 2015
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19609Molecular characterization of human coronaviruses and their circulation dynamics in Kenya, 2009–2012“…A total of 417 nasopharyngeal specimens obtained between January 2009 and December 2012 from around Kenya were analyzed by a real time RT-PCR using HCoV-specific primers. HCoV-positive specimens were subsequently inoculated onto monolayers of LL-CMK2 cells. …”
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19610por Pushpanathan, Premalatha, Srikanth, Padma, Seshadri, Krishna G., Selvarajan, Sribal, Pitani, Ravi Shankar, Kumar, Thomas David, Janarthanan, R.“…DNA was extracted from fecal samples and polymerase chain reaction was done using fusion primers. Metagenomic analysis was performed using ion torrent sequencing. …”
Publicado 2016
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19611por Rehman, Saima F., Mansoor, Qaisar, Farooqi, Ammad A., Nazir, Nusrat, Kausar, Rukhsana, Jabeen, Nyla, Ismail, Muhammad“…PCR-RFLP analysis was done for C/T polymorphism at position 1595 in exon 5 of the TRAIL gene using site-specific primers and restriction enzyme. The results were statistically evaluated by SPSS14. …”
Publicado 2015
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19612por Ali, Arshad, Ullah, Farman, Ali, Irum Sabir, Faraz, Ahmad, Khan, Mumtaz, Shah, Syed Tahir Ali, Ali, Nawab, Saeed, Muhammad“…METHODS: The promoter methylation status of 50 breast tumor tissues and adjacent normal control tissues was analyzed. mRNA expression was determined using SYBR® green quantitative polymerase chain reaction (PCR), and methylation-specific PCR was performed for bisulfite-modified genomic DNA using E2F5-specific primers to assess promoter methylation. Data was statistically analyzed. …”
Publicado 2016
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19613por Damavandi, Zahra, Torkashvand, Safoora, Vasei, Mohammad, Soltani, Bahram M., Tavallaei, Mahmood, Mowla, Seyed Javad“…Formalin-fixed paraffin-embedded samples from archival collections at the pathology department of Shariati Hospital were prepared for RNA extraction using the xylene-ethanol method before total RNA was isolated with TRIzol Reagent. Specific primers were designed for cDNA synthesis and miRNA amplification. …”
Publicado 2016
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19614por Martinez-Ibeas, Ana Maria, Munita, Maria Pia, Lawlor, Kim, Sekiya, Mary, Mulcahy, Grace, Sayers, Riona“…After the DNA extraction of 54 individual eggs, the nuclear fragment ITS-2 was amplified and sequenced using the same primers. RESULTS: An apparent herd prevalence of 77.3 % was determined. …”
Publicado 2016
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19615por Mujuni, Fridolin, Mirambo, Mariam M., Rambau, Peter, Klaus, Korn, Andreas, Muller, Matovelo, Dismas, Majigo, Mtebe, Kasang, Christa, Mshana, Stephen E.“…HPV genotypes were detected using polymerase chain reaction (PCR) followed by sequencing using specific primers targeting broad range of HPV types. Cytology was done to establish squamous intraepithelial lesions. …”
Publicado 2016
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19616por Lane, Thomas, Best, Teodora, Zembower, Nicole, Davitt, Jack, Henry, Nathan, Xu, Yi, Koch, Jennifer, Liang, Haiying, McGraw, John, Schuster, Stephan, Shim, Donghwan, Coggeshall, Mark V., Carlson, John E., Staton, Margaret E.“…In addition, 1956 simple sequence repeats were identified in the PUTs, of which we identified 465 high quality DNA markers and designed flanking PCR primers. CONCLUSIONS: North American native ash trees have suffered extensive mortality due to EAB infestation, creating a need to breed or select for resistant green ash genotypes. …”
Publicado 2016
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19617por Ahmed, Mohamed E., Eldigail, Mawahib H., Elamin, Fatima M., Ali, Ibtisam A., Grobusch, Martin P., Aradaib, Imadeldin E.“…METHODS: A set of six LAMP primers, designed from the mitochondrial NADH-1 gene of EG cattle strain of genotype 5 (G5), was used as a target for LAMP assay. …”
Publicado 2016
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19618por Konongoi, Limbaso, Ofula, Victor, Nyunja, Albert, Owaka, Samuel, Koka, Hellen, Makio, Albina, Koskei, Edith, Eyase, Fredrick, Langat, Daniel, Schoepp, Randal J., Rossi, Cynthia Ann, Njeru, Ian, Coldren, Rodney, Sang, Rosemary“…Reverse transcription polymerase chain reaction (RT-PCR) utilizing flavivirus family, yellow fever, West Nile, consensus and sero type dengue primers were used to detect acute arbovirus infections and determine the infecting serotypes. …”
Publicado 2016
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19619por Ayanful-Torgby, Ruth, Oppong, Akua, Abankwa, Joana, Acquah, Festus, Williamson, Kimberly C., Amoah, Linda Eva“…In contrast, reverse transcriptase-real time PCR (RT-PCR) analysis of a subset of 35 samples estimated submicroscopic gametocyte carriage to be as high as 77% (27/35) using primers specific for Pfs25 (CT < 35) on day 0 and by day 7 this only declined to 60% (21/35). …”
Publicado 2016
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19620por Albayrak, Levent, Khanipov, Kamil, Pimenova, Maria, Golovko, George, Rojas, Mark, Pavlidis, Ioannis, Chumakov, Sergei, Aguilar, Gerardo, Chávez, Arturo, Widger, William R., Fofanov, Yuriy“…The size of the longest subsequences shared between nDNA and mtDNA in several regions of the mitochondrial genome were found to be as low as 11 bases, which not only allows using these regions to design new, very specific PCR primers, but also supports the hypothesis of the non-random introduction of mtDNA into the human nuclear DNA. …”
Publicado 2016
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