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19521por Fernandes, Jason D., Hinrichs, Angie S., Clawson, Hiram, Gonzalez, Jairo Navarro, Lee, Brian T., Nassar, Luis R., Raney, Brian J., Rosenbloom, Kate R., Nerli, Santrupti, Rao, Arjun, Schmelter, Daniel, Zweig, Ann S., Lowe, Todd M., Ares, Manuel, Corbet-Detig, Russ, Kent, W. James, Haussler, David, Haeussler, Maximilian“…Annotated data include predicted and validated immune epitopes, promising antibodies, RT-PCR and sequencing primers, CRISPR guides (from research, diagnostics, vaccines, and therapies), and points of interaction between human and viral genes. …”
Publicado 2020
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19522por Hardiati, Aprilia, Safika, Safika, Wibawan, I Wayan Teguh, Indrawati, Agustin, Pasaribu, Fachriyan Hasmi“…Detection of antibiotic resistance coding genes was carried out by PCR using specific oligonucleotide primers. Statistical analysis was carried out with one-way analysis of variance. …”
Publicado 2021
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19523por Baltrušis, Paulius, Charvet, Claude L., Halvarsson, Peter, Mikko, Sofia, Höglund, Johan“…Based on the sequencing data, new primers and probes were designed and validated with a novel droplet digital PCR assay for the quantification of the deletion containing “resistant” allele in genomic DNA samples. …”
Publicado 2021
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19524“…Furthermore, we cloned the conserved sequences of parthenogenetic RWW REC8 and Tws, and designed primers based on the parthenogenetic RWW sequence to detect expression patterns by quantitative PCR (Q-PCR). …”
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19525por Marín, Sabrina, Cortés, Mayra, Acosta, Mauricio, Delgado, Karla, Escuti, Camila, Ayma, Diego, Demergasso, Cecilia“…Oxygen reduction, CO(2) and N(2) fixation/uptake, iron and sulfur oxidation, and response to osmotic stress were the metabolisms selected regarding research results previously reported in the system. After that, qPCR primers for each candidate gene were designed and validated. …”
Publicado 2021
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19526por Tarroum, Mohamed, Ben Romdhane, Walid, Ali, Ahmed Abdelrahim Mohamed, Al-Qurainy, Fahad, Al-Doss, Abdullah, Fki, Lotfi, Hassairi, Afif“…Phylogenetic analyses of DNA sequences amplified by ITS1 and ITS4 primers identified the isolated fungi as: Byssochlamys spectabilis, Chaetomium globosum, Cephalotheca foveolata, Penicillium melinii, Alternaria tenuissima, and Nigrospora chinensis. …”
Publicado 2021
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19527“…Multiplex PCR was performed on individual cells with Pyrodinium-specific primers targeting the 18S rRNA gene and sxtA4. The results reveal that within discrete natural populations of P. bahamense, both sxtA4+ and sxtA4- genotypes occur, and the sxtA4+ genotype dominates. …”
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19528“…As a member of the integrins family, ITGβ5 can bind to the extracellular matrix and mediate various cellular processes. In our study, primers spanning six potential insertion/deletion (indel) polymorphisms within the ITGβ5 gene were designed and 696 ovary samples from different individuals, the vast majority not in oestrum were collected for genetic variation detection. …”
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19529por Ayobola, EHWARIEME Daniel, Oscar, WHILIKI Onoriadjeren, Ejovwokoghene, EJUKONEMU Francis“…Investigation with specific primers indicated 11, 15, 7, 1 and 0 for qnrA, qnrB, qnrS, qepA and Aac(6′)-Ib-cr genes respectively, out of 1018 Q-r and 29 PMQR isolates. …”
Publicado 2021
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19530“…These genes were isolated by amplification by PCR method with specific primers, gel purified and cloned in the pLATE31 (Thermo) expression vector. …”
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19531por de Souza, Gleyce Hellen de Almeida, Rossato, Luana, Brito, Gabriel Teixeira, Bet, Graciela Mendonça dos Santos, Simionatto, Simone“…A PCR assay using oprD-specific primers failed to show the presence of mutations in this gene. …”
Publicado 2021
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19532“…We performed RT-PCR with divergent primers, mRNA stability assay, and RNase R digestion assay to characterize circCOL1A1 in gastric cancer cell lines. qRT-PCR was applied to detect the level of circCOL1A1 in both gastric cancer cell lines and tissues. …”
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19533por Lefoulon, Emilie, Truchon, Alex, Clark, Travis, Long, Courtney, Frey, Daniel, Slatko, Barton E.“…Using next-generation sequencing, we also surveyed the insect gut microbiomes of a subset of flies, using Illumina and PacBio 16S rRNA gene sequencing with barcoded primers. The composition of Proteobacteria also varied from fly to fly, with components belonging to Gammaproteobacteria making up the largest percentage of organisms (30 to 70%) among the microbiome samples. …”
Publicado 2021
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19534por Orina, Aleksandra S., Gavrilova, Olga P., Gogina, Nadezhda N., Gannibal, Philipp B., Gagkaeva, Tatiana Yu.“…Grain contamination with Alternaria fungi belonging to sections Alternaria and Infectoriae was analysed using qPCR with specific primers. The occurrence of four mycotoxins produced by Alternaria, AOH, AME, TEN, and TeA, was defined by HPLC-MS/MS. …”
Publicado 2021
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19535por Kuba, Gabrielle M., Spalding, Heather L., Hill-Spanik, Kristina M., Fullerton, Heather“…A portion of the V3-V4 variable region of the small-subunit rRNA gene was amplified for high-throughput sequencing using universal bacterial primers to elucidate the core and variable algal microbiome. …”
Publicado 2021
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19536“…Methods: Genomic DNA extracted from lung tissues of patients with IPF (n = 20; 10 non-survivors) and age- and sex-matched controls (n = 20) was amplified using fusion primers targeting the V3 and V4 regions of the 16S RNA genes with indexing barcodes. …”
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19537por Holman, Devin B., Klima, Cassidy L., Gzyl, Katherine E., Zaheer, Rahat, Service, Cara, Jones, Tineke H., McAllister, Tim A.“…All samples/swabs were enriched for Enterococcus spp., and suspected enterococci isolates were identified using species-specific PCR primers. Enterococcus faecalis was the most frequently isolated species, followed by Enterococcus hirae, which was found mostly on post-hide removal carcasses and in ground beef. …”
Publicado 2021
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19538por Medo, Juraj, Žiarovská, Jana, Ďuračka, Michal, Tvrdá, Eva, Baňas, Štefan, Gábor, Michal, Kyseľ, Matúš, Kačániová, Miroslava“…To amplify the V4 region of the 16S rRNA bacterial gene, universal primers 515F and 806R enhanced by a 6 bp barcode identification sequence were used. …”
Publicado 2021
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19539“…Capsular serotypes, rmpA, magA, allS, mrkD, entB, kfu, and iutA were identified using specific primers by polymerase chain reaction. The biofilm mass was determined using the microtiter plate assay measured by optical density (OD, 570nm). …”
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19540“…Chromosome 6Agi2 was identif ied by PCR with chromosome-specif ic primers and by genomic in situ hybridization (GISH). …”
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