2001
DOI: 10.1016/s0021-9150(00)00765-6
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A multiplex PCR-based DNA assay for the detection of paraoxonase gene cluster polymorphisms

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Cited by 36 publications
(25 citation statements)
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“…Genomic DNA was extracted from peripheral blood lymphocytes, and primers for multiplex PCR amplification of PON1 55 and 192 were used according to Motti et al (2001).…”
Section: Methodsmentioning
confidence: 99%
“…Genomic DNA was extracted from peripheral blood lymphocytes, and primers for multiplex PCR amplification of PON1 55 and 192 were used according to Motti et al (2001).…”
Section: Methodsmentioning
confidence: 99%
“…The Q192R and L55M polymorphisms of the PON1 gene were simultaneously studied by the protocol described previously by Motti et al [14] with some modifications. In brief, a multiplex polymerase chain reaction (PCR) method using specific primers corresponding to the PON1 nucleotide sequence was carried out, and the PCR products were digested with HinfI and then electrophoresed on 4% agarose gels stained with ethidium bromide.…”
Section: Genotype Analysismentioning
confidence: 99%
“…DNA was extracted from peripheral blood cells using the Ultraclean Bloodspin kit (MoBio Laboratories, Carlsbad, CA, USA). PON-1 genotyping was carried out by a multiplex PCR assay (Motti et al, 2001). Amplification of 111 and 144 pb fragments was performed using a standard PCR for PON-1-Q192R and PON-1-L55M, respectively.…”
Section: Methodsmentioning
confidence: 99%