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  1. 8561
    “…The matched peripheral blood mononuclear cells (PBMCs) were used for Sanger sequencing. The clinicopathologic information of the patients was retrospectively analyzed and the predictive abilities for postoperative recurrence of different clinicopathologic parameters and ctDNA were compared. …”
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    Circulating tumor DNA correlates with microvascular invasion and predicts tumor recurrence of hepatocellular carcinoma
  2. 8562
    “…We were also able to identify the androgen receptor (AR) point mutation T878A from 7.5 mL blood samples spiked with 50 LNCaP cells using RT-PCR and Sanger sequencing. Finally, CTCs were detected in 8 out of 8 samples from patients diagnosed with metastatic prostate cancer (mean ± SEM = 21 ± 2.957 CTCs/mL, median = 21 CTCs/mL), demonstrating the potential clinical utility of this device.…”
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    Characterization of a novel automated microfiltration device for the efficient isolation and analysis of circulating tumor cells from clinical blood samples
  3. 8563
    “…USP8 analysis was performed by Sanger sequencing in 50 tumors. Results. SST5 expression was positive in 26 (41.9%) pituitary tumors. …”
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    OR23-04 SST5 Expression and USP8 Mutation in Functioning and Silent Corticotroph Pituitary Tumors
  4. 8564
    “…The following tumors were identified: 11 ACTH-secreting, 49 GH-secreting (including 7 pluri-hormonal ones), 6 gonadotropinomas, 23 prolactinomas, 1 TSH-oma, and 43 non-secreting adenomas. Sanger sequencing was used for the assessment of AIP gene variants. …”
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    MON-300 AIP Gene Germline Mutations in Non-Selected Patients with Apparently Sporadic Pituitary Macrodenomas
  5. 8565
    “…Mutation status was determined either by Sanger sequencing or targeted next-generation sequencing. …”
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    SAT-554 Genetic Profile of Early-Onset Aldosterone-Producing Adenomas
  6. 8566
    “…We analysed the variability of resistance genes or candidate genes in this collection based on high-depth Illumina data or Sanger sequencing. Alleles previously shown to be associated with resistance were observed in 31 resistant accessions but not in any susceptible ones. …”
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    Allele mining unlocks the identification of RYMV resistance genes and alleles in African cultivated rice
  7. 8567
    “…Suspected variants were confirmed by Sanger sequencing. Protein levels were detected in patients with gene mutations by western blot. …”
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    Genetic heterogeneity of pediatric systemic lupus erythematosus with lymphoproliferation
  8. 8568
    “…We evaluated 14 tall cell carcinomas with reverse polarity (ten excision and five core needle biopsy specimens), 13 intraductal papillomas, 16 solid papillary carcinomas and five encapsulated papillary carcinomas by Sanger sequencing of the IDH2 R172 hotspot locus and of exons 9 and 20 of PIK3CA, and by immunohistochemistry using monoclonal antibodies (11C8B1) to the IDH2 R172S mutation. …”
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    Immunohistochemical Analysis of IDH2 R172 Hotspot Mutations in Breast Papillary Neoplasms: Applications in the Diagnosis of Tall Cell Carcinoma with Reverse Polarity
  9. 8569
    “…DNA of 154 CF patients, Russian by origin, in whom at least one mutant allele was not previously identified (164 CF alleles), was analyzed by Sanger sequencing followed by the multiplex ligase-dependent probe amplification (MLPA) method. …”
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    Analysis of CFTR Mutation Spectrum in Ethnic Russian Cystic Fibrosis Patients
  10. 8570
    “…We analyzed the clinical features and screened all coding exons of CFTR using a combination of Sanger sequencing and multiplex ligation-dependent probe amplification analysis. …”
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    Characterization of clinical and genetic spectrum of Chinese patients with cystic fibrosis
  11. 8571
    “…Whole‐exome sequencing (WES) was performed on a total of 13 affected individuals, 1 available unaffected relative, and 10 healthy unrelated individuals. Sanger sequencing was used to validate the screened mutations. …”
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    Identification of Novel EXT Mutations in Patients with Hereditary Multiple Exostoses Using Whole‐Exome Sequencing
  12. 8572
    “…Blood samples were randomly collected from 96 unrelated people from Al-Ahsa population, followed by DNA extraction then amplifying the NAT2 gene by polymerase chain reaction (PCR); finally, functional NAT2 gene (exon 2) was sequenced using the Sanger sequencing method. The well-known seven genetic variants of NAT2 gene are 191G>A, 282C>T, 341T>C, 481C>T, 590G>A, 803A>G, and 857G>A were detected with allele frequencies 1%, 35.4%, 42.7%, 41.1%, 29.2%, 51%, and 5.7%, respectively. …”
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    Study on Genotyping Polymorphism and Sequencing of N-Acetyltransferase 2 (NAT2) among Al-Ahsa Population
  13. 8573
    “…Traditional culture and serological testing produced negative results, while the mNGS assay revealed the presence of a potential pathogen, Enterococcus faecalis, in the urine specimen, which was further confirmed by both Sanger sequencing and qPCR analysis. A CT scan of the patient’s whole abdomen showed stones in the right kidney. …”
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    Identification of Enterococcus faecalis in a patient with urinary-tract infection based on metagenomic next-generation sequencing: a case report
  14. 8574
    “…Confirmation of carbapenemases was carried out by PCR and Sanger sequencing. The clonal lineages were assigned to selected isolates by multilocus sequence typing (MLST), and the plasmid analysis was done by PCR-based detection of the plasmid replicon typing. …”
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    Novel Carbapenem-Resistant Klebsiella pneumoniae ST147 Coharboring bla(NDM-1), bla(OXA-48) and Extended-Spectrum β-Lactamases from Pakistan
  15. 8575
    Publicado 2016
    “…Those harboring dasatinib highly-resistant mutations (T315I/A, F317L/V/C and V299L) were excluded based on BCR-ABL kinase domain mutation screening by Sanger sequencing at baseline. Hematologic, cytogenetic and molecular responses were evaluated regularly, and rates of progression-free-survival (PFS) and overall survival (OS) were analyzed. …”
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    BCR-ABL突变检测指导下的达沙替尼治疗伊马替尼耐药的慢性髓性白血病疗效分析
  16. 8576
    Publicado 2016
    “….-151G>T (rs1698852) by Sanger sequence. RESULTS: Of the 142 PNH patients, 21 (14.8%) patients had at least 1 episode of thrombotic event. …”
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    阵发性睡眠性血红蛋白尿症患者血栓易发因素的初步研究
  17. 8577
    “…Polymerase chain reaction (PCR) followed by Sanger sequencing was used to determine the polymorphisms in CYP2C8, CYP3A4 and pfmdr1 genes. …”
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    Plasmodium falciparum genetic factors rather than host factors are likely to drive resistance to ACT in Ghana
  18. 8578
    “…Polymerase chain reaction and Sanger sequencing therefore remain widely used as methods for characterizing gene sequences in many varieties of crops. …”
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    AutoCloner: automatic homologue-specific primer design for full-gene cloning in polyploids
  19. 8579
    “…METHODS: One thousand five hundred sixty-five infants with pathological jaundice were screened for G6PD variants by Sanger sequencing all of the 13 exons, and the junctions of exons and introns of the G6PD gene. …”
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    A novel G6PD deleterious variant identified in three families with severe glucose-6-phosphate dehydrogenase deficiency
  20. 8580
    “…In addition, 3 primary non-recurrent aGCTs and 9 aGCT recurrences were subjected to FOXL2 and TERT promoter Sanger sequencing analysis. All aGCTs harbored the FOXL2 C134W hotspot mutation. …”
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    Genomic profiling of primary and recurrent adult granulosa cell tumors of the ovary
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