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  1. 8361
    “…Second, the presence of 29 of the 33 characteristic single nucleotide polymorphisms (SNPs) in the Omicron variant S-gene was identified by Sanger sequencing of nine amplicons. The final two strategies involved identification of 47 of the 50 non-synonymous and indel mutations attributed to Omicron by rapid nanopore whole genome sequencing (WGS) and by Illumina WGS technology. …”
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    Alternative molecular and genomic strategies to provide a rapid response to alerts concerning the introduction of new emerging SARS-CoV-2 variants: the Omicron alert
  2. 8362
    “…Two foetuses were diagnosed with Down syndrome by chromosomal microarray analysis via umbilical vein puncture and had significantly elevated cord blood leucocyte counts with large numbers of blasts. The GATA1 Sanger sequencing results suggested the presence of a [NM_002049.4(GATA1):c.220G > A (p. …”
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    Prenatal diagnosis of Down syndrome combined with transient abnormal myelopoiesis in foetuses with a GATA1 gene variant: two case reports
  3. 8363
    “…We also conducted BRAF and TERT mutations analyses through Sanger sequencing. Disease-free survival (DFS) was assessed using Kaplan–Meier curves. …”
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    Loss of CDH16 expression is a strong independent predictor for lymph node metastasis in Middle Eastern papillary thyroid cancer
  4. 8364
    “…METHODS: CircRNAs were screened and characterized using transcriptome sequencing, Sanger sequencing, actinomycin D treatment, and Ribonuclease R assay. …”
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    Hsa_circ_0041150 serves as a novel biomarker for monitoring chemotherapy resistance in small cell lung cancer patients treated with a first-line chemotherapy regimen
  5. 8365
    “…Methods: Germline sequencing was carried out with NGS technology using a 52-gene panel, and cascade testing was performed by Sanger sequencing or MLPA. Results: In a cohort of 1785 breast cancer patients (families), 20.3% were found to have PVs/LPVs. …”
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    Only 32.3% of Breast Cancer Families with Pathogenic Variants in Cancer Genes Utilized Cascade Genetic Testing
  6. 8366
    “…Whole-exome sequencing was performed on probands to screen the causative variants, and all suspected pathogenic variants were determined via Sanger sequencing. Furthermore, co-segregation analysis was performed on available family members. …”
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    Four different gene-related cone–rod dystrophy: clinical and genetic findings in six Chinese families with diverse modes of inheritance
  7. 8367
    “…Whole-exome sequencing and Sanger sequencing were performed to identify mutations in candidate genes. …”
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    Splicing mutations in AMELX and ENAM cause amelogenesis imperfecta
  8. 8368
    “…The expression of circRNAs from the tyrosylprotein sulfotransferase 2 (TPST2) gene and miRNAs was evaluated through qPCR, while the circular structure of circTPST2 was verified using Sanger sequencing and RNase R. Through Western blotting, biotin-labeled RNA pulldown, RNA immunoprecipitation, mass spectrometry, and rescue experiments, we discovered miR-770-5p and nucleolin as downstream targets of circTPST2. …”
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    Circular RNA from Tyrosylprotein Sulfotransferase 2 Gene Inhibits Cisplatin Sensitivity in Head and Neck Squamous Cell Carcinoma by Sponging miR-770-5p and Interacting with Nucleolin
  9. 8369
    “…Two previously validated PCR tests for Theileria followed by DNA sequencing were performed to test blood samples collected from 219 cattle in Alabama, USA, during the period of 2022–2023. Bidirectional Sanger sequencing revealed that the MPSP gene sequences (639–660 bp) from two cattle in Lee and Mobile Counties of Alabama exhibited a 100% match with those of recognized T. orientalis Ikeda strains, and showed similarities ranging from 76% to 88% with ten other T. orientalis genotypes. …”
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    Theileria orientalis Ikeda in Cattle, Alabama, USA
  10. 8370
    “…BACKGROUND: Sanger-based sequencing (SBS) remains the gold standard for HIV-1 drug resistance testing (DRT). …”
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    633. Nanopore Sequencing and In-house Bioinformatic Pipeline for Rapid and Accurate Detection of NRTI, NNRTI, PI, and INSTI Drug Resistance Mutations
  11. 8371
    “…A subgroup of 40 isolates with RS underwent Sanger sequencing to detect rpoB single nucleotide polymorphisms (SNPs). …”
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    682. Novel rpoB mutations and trends in clinical Clostridioides difficile isolates with reduced fidaxomicin susceptibility
  12. 8372
    “…Organisms with meropenem MIC >1 mg/L and Escherichia coli, Klebsiella pneumoniae, Klebsiella oxytoca, and Proteus mirabilis with aztreonam or ceftazidime MIC >1 mg/L were screened for β-lactamase genes by PCR and Sanger sequencing. RESULTS: In total, 5,473 isolates were identified as CRE based on resistance to meropenem. …”
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    2149. In vitro Activity of Aztreonam-avibactam and Comparator Agents Against Carbapenem-Resistant Enterobacterales With and Without Carbapenemases, ATLAS Global Surveillance Program, 2017–2021
  13. 8373
    “…Isolates resistant to meropenem were screened for acquired β-lactamases by multiplex PCR/Sanger sequencing. RESULTS: In total, 97.1% of the 68 CRE isolates were inhibited by ≤16 µg/mL of cefepime-taniborbactam. …”
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    2150. In Vitro Activity of Cefepime-Taniborbactam and Comparators Against Genotypically Characterized Carbapenem-Resistant Enterobacterales (CRE) and Carbapenem-Resistant Pseudomonas aeruginosa (CRPA) from the United States, 2018-2021
  14. 8374
    por Kobayashi, Genki
    Publicado 2023
    “…Assembly from publicly available NGS reads would help design specific primers for the mitochondrial gene sequences of species, whose mitochondrial genes are hard to amplify by Sanger sequencing using universal primers.…”
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    Buried treasure in a public repository: Mining mitochondrial genes of 32 annelid species from sequence reads deposited in the Sequence Read Archive (SRA)
  15. 8375
    por Velasco, Riccardo, Zharkikh, Andrey, Troggio, Michela, Cartwright, Dustin A., Cestaro, Alessandro, Pruss, Dmitry, Pindo, Massimo, FitzGerald, Lisa M., Vezzulli, Silvia, Reid, Julia, Malacarne, Giulia, Iliev, Diana, Coppola, Giuseppina, Wardell, Bryan, Micheletti, Diego, Macalma, Teresita, Facci, Marco, Mitchell, Jeff T., Perazzolli, Michele, Eldredge, Glenn, Gatto, Pamela, Oyzerski, Rozan, Moretto, Marco, Gutin, Natalia, Stefanini, Marco, Chen, Yang, Segala, Cinzia, Davenport, Christine, Demattè, Lorenzo, Mraz, Amy, Battilana, Juri, Stormo, Keith, Costa, Fabrizio, Tao, Quanzhou, Si-Ammour, Azeddine, Harkins, Tim, Lackey, Angie, Perbost, Clotilde, Taillon, Bruce, Stella, Alessandra, Solovyev, Victor, Fawcett, Jeffrey A., Sterck, Lieven, Vandepoele, Klaas, Grando, Stella M., Toppo, Stefano, Moser, Claudio, Lanchbury, Jerry, Bogden, Robert, Skolnick, Mark, Sgaramella, Vittorio, Bhatnagar, Satish K., Fontana, Paolo, Gutin, Alexander, Van de Peer, Yves, Salamini, Francesco, Viola, Roberto
    Publicado 2007
    “…The relative age of grape duplicated genes was estimated and this made possible to reveal a relatively recent Vitis-specific large scale duplication event concerning at least 10 chromosomes (duplication not reported before). CONCLUSIONS: Sanger shotgun sequencing and highly efficient sequencing by synthesis (SBS), together with dedicated assembly programs, resolved a complex heterozygous genome. …”
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    A High Quality Draft Consensus Sequence of the Genome of a Heterozygous Grapevine Variety
  16. 8376
    “…The majority of known miRNAs were discovered by conventional cloning and a Sanger sequencing approach. The next-generation sequencing (NGS) technologies enable in-depth characterization of the global repertoire of miRNAs, and different protocols for miRNA library construction have been developed. …”
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    Sequencing bias: comparison of different protocols of MicroRNA library construction
  17. 8377
    “…RESULTS: A catalogue of 103,000 Sanger ESTs was assembled into 28,024 unigenes from which 18.6% presented one or more SSR motifs. …”
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    A fast and cost-effective approach to develop and map EST-SSR markers: oak as a case study
  18. 8378
    “…The first alfalfa (Medicago sativa) gene index (MSGI 1.0) was assembled using the Sanger ESTs available from GenBank, the GS FLX Titanium EST sequences, and the de novo assembled Illumina sequences. …”
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    Using RNA-Seq for gene identification, polymorphism detection and transcript profiling in two alfalfa genotypes with divergent cell wall composition in stems
  19. 8379
    “…The p.N321S variant in PCMTD1 could not be confirmed by the Sanger method. Sequencing RNF213 in 42 index cases confirmed p.R4810K and revealed it to be the only unregistered variant. …”
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    Identification of RNF213 as a Susceptibility Gene for Moyamoya Disease and Its Possible Role in Vascular Development
  20. 8380
    “…RESULTS: We designed a custom GoldenGate assay for 1,536 SNPs detected through the resequencing of gene fragments (707 in vitro SNPs/Indels) and from Sanger-derived Expressed Sequenced Tags assembled into a unigene set (829 in silico SNPs/Indels). …”
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    Development and implementation of a highly-multiplexed SNP array for genetic mapping in maritime pine and comparative mapping with loblolly pine
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