genetic analysis platform massarray (Sequenom)
90
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Sequenom
genetic analysis platform massarray
Genetic Analysis Platform Massarray, 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/genetic+analysis+system+massarray+platform/massarray+genetic+analysis+platform/pm26107754-48-1-5
Average 90 stars, based on 1 article reviews
Genetic Analysis Platform Massarray, 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/genetic+analysis+system+massarray+platform/massarray+genetic+analysis+platform/pm26107754-48-1-5
Average 90 stars, based on 1 article reviews
genetic analysis platform massarray - by Bioz Stars,
2026-09
90/100 stars
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other:Article Title: PHC-024 Renal Function Estimation by Different Methods (CKD-EPI,Cockcroft-Gault and MDRD4-IDMS) and Its Effect on the Dose of IV Dexketoprofen Article Snippet: Genomic DNA was analysed by a Article Title: Sequenom MassARRAY approach in the arrhythmogenic right ventricular cardiomyopathy post-mortem setting: clinical and forensic implications. Article Snippet: Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a rare cardiac disease characterized by myocardial fibrofatty replacement, which can lead to sudden death.. Previous studies have described a reduction of plakoglobin (PKG) protein at the level of intercalated disks as the hallmark of ARVC.. The main objective of this study was to investigate the involvement of desmosome mutations in the histological phenotype of ARVC. Article Title: SNPs and taxane toxicity in breast cancer patients. Article Snippet: 2014 Aim: In order to identify genetic variants associated with taxanes toxicity, a panel with 47 SNPs in 20 genes involved in taxane pathways was designed.. Patients & methods: Genomic DNA of 113 breast cancer patients was analyzed (70 taking docetaxel, 43 taking paclitaxel).. Results: Two SNPs associated with docetaxel toxicity were identified: CYP3A4*1B with infusion-related reactions; and ERCC1 Gln504Lys with mucositis (p ≤ 0.01). Article Title: Association of SNPs with the efficacy and safety of immunosuppressant therapy after heart transplantation. Article Snippet: 2015 Aim: Studying the possible influence of SNPs on efficacy and safety of calcineurin inhibitors upon heart transplantation.. Materials & methods: In 60 heart transplant patients treated with tacrolimus or cyclosporine, we studied a panel of 36 SNPs correlated with a series of clinical parameters during the first post-transplantation year.. Results: The presence of serious infections was correlated to ABCB1 rs1128503 (p = 0.012), CC genotype reduced the probability of infections being also associated with lower blood cyclosporine concentrations. Article Title: Impact of Single Nucleotide Polymorphisms (SNPs) on Immunosuppressive Therapy in Lung Transplantation Article Snippet: A Article Title: Increased hospital stay and allograft dysfunction in renal transplant recipients with Cyp2c19 AA variant in SNP rs4244285. Article Snippet: Pharmacogenetics correlates certain genetic variants, such as single nucleotide polymorphisms (SNPs), with blood drug levels, efficacy, and adverse effects of the treatment.. Tacrolimus is mainly metabolized via CYP3A4/5, whereas CYP2C19 and CYP3A4/5 are responsible for omeprazole metabolism.. Omeprazole inhibits tacrolimus metabolism via CYP3A5 in patients carrying variant alleles of CYP2C19, increasing tacrolimus blood concentrations. Mutagenesis:Article Title: EGFR Somatic Mutations in Lung Tumors: Radon Exposure and Passive-smoking in Former- and Never-smoking U.S. Women Article Snippet: .. Mayo Clinic EGFR mutations were analyzed at the Mayo Clinic as part of oncogene mutation screening using the Article Title: EGFR Somatic Mutations in Lung Tumors: Radon Exposure and Passive-smoking in Former- and Never-smoking U.S. Women Article Snippet: .. EGFR mutations were analyzed at the Mayo Clinic as part of oncogene mutation screening using the |