mass-spectroscopy based, high-throughput massarray iplextm platform (Sequenom)
90
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Sequenom
mass-spectroscopy based, high-throughput massarray iplextm platform
Mass Spectroscopy Based, High Throughput Massarray Iplextm Platform, supplied by Sequenom, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/mass-spectroscopy+based%2C+high-throughput+massarray+iplextm+platform/sequenom+massarray/pm23312054-45-20-26
Average 90 stars, based on 1 article reviews
Mass Spectroscopy Based, High Throughput Massarray Iplextm Platform, supplied by Sequenom, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/mass-spectroscopy+based%2C+high-throughput+massarray+iplextm+platform/sequenom+massarray/pm23312054-45-20-26
Average 90 stars, based on 1 article reviews
mass-spectroscopy based, high-throughput massarray iplextm platform - by Bioz Stars,
2026-09
90/100 stars
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other:Article Title: Polymorphisms in apolipoprotein E and apolipoprotein A-V do not influence the lipid response to rosuvastatin but are associated with baseline lipid levels in Chinese patients with hyperlipidemia. Article Snippet: 1933-2874/$ see front matter 2012 doi:10.1016/j.jacl.2012.02.005 BACKGROUND: Apolipoprotein E (APOE) and APOA5 play an important role in lipid transport and metabolism.. Polymorphisms in APOE and APOA5 have been reported to be associated with baseline lipid levels and lipid responses to statins in different populations.. OBJECTIVE: This study evaluated associations of APOE and APOA5 genotype with baseline lipid levels and response to rosuvastatin in Chinese patients with hyperlipidemia. Article Title: Associations of polymorphisms in the apolipoprotein A1/C3/A4/A5 gene cluster with familial combined hyperlipidaemia in Hong Kong Chinese. Article Snippet: Background: Familial combined hyperlipidaemia (FCH) is the most common genetic dyslipidaemia associated with coronary artery disease.. Single nucleotide polymorphisms (SNPs) and haplotypes in the APOA1/C3/A4/A5 gene cluster are associated with FCH in Caucasians and with elevated triglycerides (TG) in various ethnic groups.. We examined these associations with FCH in Hong Kong Chinese. |