sequenom iplexmassarray platform (Sequenom)
86
Structured Review
Sequenom
sequenom iplexmassarray platform
Sequenom Iplexmassarray Platform, supplied by Sequenom, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/sequenom+platform/iplexmassarray+platform+sequenom/pm41231379-5-13-13
Average 86 stars, based on 1 article reviews
Sequenom Iplexmassarray Platform, supplied by Sequenom, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/sequenom+platform/iplexmassarray+platform+sequenom/pm41231379-5-13-13
Average 86 stars, based on 1 article reviews
sequenom iplexmassarray platform - by Bioz Stars,
2026-10
86/100 stars
Images
Related Articles
other:Article Title: AMHR2 c.-482A > G and serum basal FSH as predictors of ovarian response to stimulation. Article Snippet: Purpose Ovarian stimulation (OS) is a critical component of assisted reproduction techniques (ART), in which gonadotropins are administered to induce follicular development and maturation to improve the chances of conception.. It has been reported that ovarian response to OS can be affected by certain genetic factors.. This study explores the relationship among SNVs of AMHR2 (c.-482A > G/rs2002555 and c.1749C > T/rs2071558), basal FSH and estradiol levels, gonadotropin dosage, and ovarian response to identify predictive indicators. Article Title: Expression quantitative trait loci for PVT1 contributes to the prognosis of hepatocellular carcinoma Article Snippet: Then, we use the Sequenom Mass ARRAY iPLEX platform (Sequenom Inc) to genotype the SNP rs4733586. Mass Spectrometry:Article Title: Immune-related genes STIM1, ITPKC and PELI1 polymorphisms are associated with risk of colorectal cancer Article Snippet: Results The minor alleles of rs3794050, rs3750996 and rs2607420 were associated with an increased CRC risk (P < 0.05).. In contrast, the minor allele of rs329497 was correlated with reduced disease risk (P = 0.025).. Genetic model analysis showed that rs3794050 was related to an increased risk of disease in recessive and log-additive models (P < 0.05); rs3750996 had a strong correlation with CRC risk under all genetic models (P < 0.02); rs2607420 was correlated with an increased risk of disease in dominant and log-additive models (P < 0.01); whereas the protective effect of rs329497 on CRC risk was observed in dominant and log-additive models (P < 0.05). DNA Amplification:Article Title: A case-control study provides evidence of association for a common SNP rs974819 in PDGFD to coronary heart disease and suggests a sex-dependent effect. Article Snippet: Contents lists available at SciVerse ScienceDirect Thrombosis Research j ourna l homepage: www.e lsev ie r .com/ locate / thromres Regular Article A case-control study provides evidence of association for a common SNP rs974819 in PDGFD to coronary heart disease and suggests a sex-dependent effect Jianqing Zhou a,1, Yi Huang b,1, R. Stephanie Huang c, Feiming Wang d, Limin Xu b, Yanping Le b, Xi Yang a, Weifeng Xu a, Xiaoyan Huang a, Jiangfang Lian a,⁎, Shiwei Duan b,⁎ a Ningbo Medical Center, Lihuili hospital, Ningbo University, Ningbo, Zhejiang 315041, China b School of Medicine, Ningbo University, Ningbo, Zhejiang 315211, China c Department of Medicine, University of Chicago, IL 60637, USA d Zhejiang Zhenhai Middle School, Ningbo, Zhejiang 315200, China Abbreviations: SNP, Single nucleotide polymorphism LIPA, lipase A; PDGFD, Platelet-derived growth factor D librium; GWAS, genome-wide association studies; MI, m ⁎ Corresponding authors.. E-mail addresses: hjmpin@163.com (J. Lian), duansh 1 JZ and YH are co-first authors of this work.. 0049-3848/$ – see front matter. |