2013
DOI: 10.1371/journal.pone.0078142
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A Fast and Cost-Effective Method for Identifying a Polymorphism of Interleukin 28B Related to Hepatitis C

Abstract: Approximately 170 million people are chronic carriers of hepatitis C virus (HCV). Patients with chronic hepatitis C are currently treated with pegylated interferon and ribavirin (PEG-IFN/RBV). A genome-wide association with PEG-IFN/RBV treatment response and a single nucleotide polymorphism (rs12979860) has been identified near the interleukin 28B gene that encodes interferon-λ-3. In this paper, we describe an innovative, fast, and low-cost multiplex polymerase chain reaction with confronting two-pair primers … Show more

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Cited by 5 publications
(4 citation statements)
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“…The single-nucleotide polymorphism (SNP) rs12979860 in the region of the interleukin 28B (IL28B) gene was analyzed using confronting two-pair primers as previously described 13 .…”
Section: Testing For Snps Of Il28bmentioning
confidence: 99%
“…The single-nucleotide polymorphism (SNP) rs12979860 in the region of the interleukin 28B (IL28B) gene was analyzed using confronting two-pair primers as previously described 13 .…”
Section: Testing For Snps Of Il28bmentioning
confidence: 99%
“…Frozen whole blood was used for IL-28B genotyping after genomic DNA extraction using QIAamp DNA Blood Mini kit (Qiagen). IL-28B genotyping was performed by PCR with confronting two-pair primers (CTPP) PCR as described previously [15]. The primer sequences used for IL-28B were (F1: GACGAGAGGGCGTTAGAGCG, R1: GGAGTGCAATTCAACCCTGGTTCG; F2: GAGCTCCCCGAAGGCGT, R2: AACGCAGGCTCAGGGTCAAT) [15].…”
Section: Methodsmentioning
confidence: 99%
“…IL-28B genotyping was performed by PCR with confronting two-pair primers (CTPP) PCR as described previously [15]. The primer sequences used for IL-28B were (F1: GACGAGAGGGCGTTAGAGCG, R1: GGAGTGCAATTCAACCCTGGTTCG; F2: GAGCTCCCCGAAGGCGT, R2: AACGCAGGCTCAGGGTCAAT) [15]. The reactions consisted of a total volume of 50 µl containing 1·5 U Hotstart DNA polymerase (Takara, China), 0·5 µ m of primers F1, F2, and R2, 0·75 µ m of primer R1, 1·0 µ m dNTP and 50 ng genomic DNA.…”
Section: Methodsmentioning
confidence: 99%
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