Novel Method Probe-based Real-Time PCR to Detect 2 Single-Nucleotide Polymorphisms Close to Each Other

2016 ◽  
Vol 24 (9) ◽  
pp. 673-678 ◽  
Author(s):  
Frederico S. V. Malta ◽  
Zilma N. Reis ◽  
Antônio C. V. Cabral
2005 ◽  
Vol 132 (3) ◽  
pp. 200-204 ◽  
Author(s):  
Tamara Čačev ◽  
Mladen Jokić ◽  
Radan Spaventi ◽  
Krešimir Pavelić ◽  
Sanja Kapitanović

2004 ◽  
Vol 18 (2) ◽  
pp. 117-122 ◽  
Author(s):  
Kenneth Petersen ◽  
Ulla Vogel ◽  
Eszter Rockenbauer ◽  
Kirsten Vang Nielsen ◽  
Steen Kølvraa ◽  
...  

2008 ◽  
Vol 46 (7) ◽  
pp. 2474-2474
Author(s):  
J. T. Foster ◽  
R. T. Okinaka ◽  
R. Svensson ◽  
K. Shaw ◽  
B. K. De ◽  
...  

Leukemia ◽  
2003 ◽  
Vol 17 (3) ◽  
pp. 630-633 ◽  
Author(s):  
F Maas ◽  
N Schaap ◽  
S Kolen ◽  
A Zoetbrood ◽  
I Buño ◽  
...  

PLoS ONE ◽  
2014 ◽  
Vol 9 (9) ◽  
pp. e107964 ◽  
Author(s):  
Dawn N. Birdsell ◽  
Amy J. Vogler ◽  
Jordan Buchhagen ◽  
Ashley Clare ◽  
Emily Kaufman ◽  
...  

Background The NLRP1gene is central to the NLR inflammasome. Variants to the NLRP1 gene are associated with vitiligo and other autoimmune diseases. We examined the effects of two single nucleotide polymorphisms (SNP) son cytokine levels and NLRP1 gene expression in 50 human volunteers. Methods NLRP1 was genotyped at SNPs rs2670660 and rs12150220, and participants who were homozygous at one or more SNP were analyzed. Plasma IL-18 and IL-1β levels were quantified using ELISA. NLRP1 gene expression was measured using real-time PCR. Results Participants with the risk genotype had significantly higher levels of plasma IL-18 than participants with protective genotype (0.439 ng/µL compared to 0.152 ng/µL, p = 0.024). Genotypes rs2670660 and rs12150220 were strongly linked in this population (p = 2.33 x 10-13). Conclusions Increased production of IL-18, suggests that at least one of the AA variants of rs2670660 or rs12150220 increases NLRP1 activity. rs2670660 and rs12150220 are strongly linked.


The Analyst ◽  
2018 ◽  
Vol 143 (14) ◽  
pp. 3292-3301 ◽  
Author(s):  
Huihui Mao ◽  
Guanghua Luo ◽  
Yuxia Zhan ◽  
Jun Zhang ◽  
Shuang Yao ◽  
...  

The base-quenched probe method for detecting single nucleotide polymorphisms (SNPs) relies on real-time PCR and melting-curve analysis, which might require only one pair of primers and one probe.


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