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19801por Taft, Diana H, Ambalavanan, Namasivayam, Schibler, Kurt R, Yu, Zhuoteng, Newburg, David S, Ward, Doyle V, Morrow, Ardythe L“…DNA extracted from stool was used to sequence the 16S rRNA gene by Illumina MiSeq using universal primers. Resulting operational taxonomic unit tables were analyzed for differences between years and hospitals using linear discriminant analysis effect size algorithm (LEfSe; significance, p < 0.05). …”
Publicado 2014
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19802por Ceccarelli, Marcello, Galluzzi, Luca, Sisti, Davide, Bianchi, Barbara, Magnani, Mauro“…RESULTS: The qPCR performed on CS samples showed better sensitivity (87%) and specificity (96%) than assays carried out using BC samples, regardless of the primers used. The haematochemical parameters haemoglobin and globulins were found to be significantly associated with qPCR positivity. …”
Publicado 2014
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19803por Dhawan, Benu, Rawre, Jyoti, Ghosh, Arnab, Malhotra, Neena, Ahmed, Mir Muneer, Sreenivas, Vishnubhatla, Chaudhry, Rama“…METHOD: Endocervical swabs, collected from 200 infertile women were tested for C. trachomatis by three different PCR assays viz. in-house real time-PCR targeting the cryptic plasmid using published primers, along with omp1 gene and cryptic plasmid based conventional PCR assays. …”
Publicado 2014
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19804por Durmaz, Riza, Kalaycioglu, Atila Taner, Acar, Sumeyra, Bakkaloglu, Zekiye, Karagoz, Alper, Korukluoglu, Gulay, Ertek, Mustafa, Torunoglu, Mehmet Ali“…Rotavirus G and P genotypes were determined by reverse transcription polymerase chain reaction (RT-PCR) using consensus primers detecting the VP7 and VP4 genes, followed by semi-nested type-specific multiplex PCR. …”
Publicado 2014
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19805por Garcia-Seco, Daniel, Zhang, Yang, Gutierrez-Mañero, Francisco J, Martin, Cathie, Ramos-Solano, Beatriz“…Since blackberries are tetraploids, the possibility of artefactual gene chimeras resulting from mis-assembly was tested with one of the genes sequenced by RNAseq, Chalcone Synthase (CHS). cDNAs encoding this protein were cloned and sequenced. Primers designed to the assembled sequences accurately distinguished different contigs, at least for chalcone synthase genes. …”
Publicado 2015
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19806por Thapa Shrestha, Upendra, Adhikari, Nabaraj, Maharjan, Rojina, Banjara, Megha R, Rijal, Komal R, Basnyat, Shital R, Agrawal, Vishwanath P“…The screening of the ctx genes (ctxA2-B gene) were performed by PCR method using a pair of primers; C2F (5′-AGGTGTAAAATTCCTTGACGA-3′) and C2R (5′-TCCTCAGGGTATCCTTCATC-3′) to identify the toxigenic strains of V. cholerae. …”
Publicado 2015
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19807por Sales, Kamila Gaudêncio da Silva, Costa, Pietra Lemos, de Morais, Rayana Carla Silva, Otranto, Domenico, Brandão-Filho, Sinval Pinto, Cavalcanti, Milena de Paiva, Dantas-Torres, Filipe“…METHODS: Six pairs of primers were designed based on cytochrome b gene sequences available in GenBank of the following potential hosts: dog, cat, horse, chicken, black rat, and human. …”
Publicado 2015
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19808“…To demonstrate transfection efficiency of the constructed carrier, reverse transcription polymerase chain reaction (RT-PCR) was carried out using human insulin specific primers on total RNA extracted from upper part of small intestine of 48-hour post-transfected rats (sampled by simple random selection, n = 3). …”
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19809“…A total of 15 SCoT and 17 CBDP primers detected genetic polymorphism among 39 Jojoba genotypes (22 females and 17 males). …”
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19810por Cretoiu, Mariana Silvia, Berini, Francesca, Kielak, Anna Maria, Marinelli, Flavia, van Elsas, Jan Dirk“…Using the chiA-targeted PCR, which is based on degenerate primers, the five fosmids all produced amplicons, of which the sequences were related to predicted chitinolytic enzyme-encoding genes of four different host organisms, including Stenotrophomonas maltophilia. …”
Publicado 2015
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19811por Aliotta, Jason M., Pereira, Mandy, Sears, Edmund H., Dooner, Mark S., Wen, Sicheng, Goldberg, Laura R., Quesenberry, Peter J.“…In addition, murine Lin-/Sca-1+ cells were cultured with CFSE-labelled LDEV isolated from rats, and RT-PCR analysis was performed on LDEV+ and – cells using species-specific primers for surfactant (rat/mouse hybrid co-cultures). …”
Publicado 2015
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19812por Brisotto, Giulia, di Gennaro, Alessandra, Damiano, Valentina, Armellin, Michela, Perin, Tiziana, Maestro, Roberta, Santarosa, Manuela“…METHODS: Our strategy, named normalized-BSP (NBSP), takes advantage of tailed C-balanced primers and a normalization procedure based on C/T ratio to overcome BSP-associated noise problems and nucleotide signal unbalance. …”
Publicado 2015
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19813por Huang, Yuan, He, Lan, Hu, Jinfang, He, Pei, He, Junwei, Yu, Long, Malobi, Ngabu, Zhou, Yanqin, Shen, Bang, Zhao, JunLong“…METHODS: 30 pairs of primers were designed based on the full genome sequence of B. orientalis (unpublished data) and by aligning reported apicoplast genomes of Babesia bovis and Theileria parva. …”
Publicado 2015
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19814“…The results will supply valuable information about genetic variation, which can be used in the process of designing primers for population studies and conservation genetics research. …”
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19815por Jilani, Md. Shariful Alam, Robayet, Jamshedul Alam Mohammad, Mohiuddin, Md., Hasan, Md. Rokib, Ahsan, Chowdhury Rafiqul, Haq, Jalaluddin Ashraful“…Suspected colonies of B. pseudomallei were identified by biochemical and serological test, and by polymerase chain reaction (PCR) using 16s rRNA specific primers. Blood samples were collected from 940 healthy individuals of four districts to determine anti- B. pseudomallei IgG antibody levels by indirect enzyme linked immunosorbent assay (ELISA) using sonicated crude antigen. …”
Publicado 2016
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19816por Bolch, Susan N., Dugger, Donald R., Chong, Timothy, McDowell, J. Hugh, Smith, W. Clay“…RESULTS: PCR from mouse retinal cDNA using Bbs5-specific primers amplified a unique cDNA that was shown to be a splice variant of BBS5 resulting from the use of cryptic splicing sites in Intron 7. …”
Publicado 2016
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19817por Nagaraja, H., Chennappa, G., Poorna Chandra Rao, K., Mahadev Prasad, G., Sreenivasa, M. Y.“…The manually identified Fusarium spp. were further confirmed by PCR-based detection using ITS1 and ITS4 primers followed by sequencing of the PCR amplicons. …”
Publicado 2016
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19818“…Killer cell immunoglobulin-like receptor low resolution genotyping was performed by the polymerase chain reaction (PCR)-sequence-specific primers (SSP)/sequence-specific oligonucleotide (SSO) method and haplotype assignment was done by gene content analysis. …”
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19819“…Does this parasite develop with equal efficiency in both snail species, and does this have implications for transmission in different habitat types? METHODS: Primers for PCR amplification of the S. mansoni ND5 gene were designed and tested for sensitivity and specificity. …”
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19820por Arunrut, Narong, Kampeera, Jantana, Sirithammajak, Sarawut, Sanguanrut, Piyachat, Proespraiwong, Porranee, Suebsing, Rungkarn, Kiatpathomchai, Wansika“…The target for the special set of six LAMP primers used was the VP(AHPND) Pir(vp)A gene. The LAMP reaction was carried out at 65°C for 45 min followed by addition of the red AuNP solution and further incubation at 65°C for 5 min, allowing any Pir(vp)A gene amplicons present to hybridize with the probe. …”
Publicado 2016
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