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massarray technology  (Sequenom)

 
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    Sequenom massarray technology
    Massarray Technology, 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/massarray+technology/massarray+platform/pm42263934-79-17-19
    Average 86 stars, based on 1 article reviews
    massarray technology - by Bioz Stars, 2026-09
    86/100 stars

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    Related Articles

    Software:

    Article Title: Sex-specific influence of DRD 2 on ADHD-type temperament in a large population-based birth cohort
    Article Snippet: Attention-deficit/hyperactivity disorder (ADHD) is a childhood-onset neurodevelopmental disorder with a significant public-health impact.. Previously, we described a candidate gene study in a population-based birth cohort that demonstrated an association with ADHD-affected males and the dopamine receptor D2 (DRD2).. The current study evaluates potential associations of dopamine receptor genes and Cloninger temperament traits within this same sample.

    HAT Assay:

    Article Title: Human Leukocyte Antigen-G: A Promising Prognostic Marker of Disease Progression to Improve the Control of Human African Trypanosomiasis.
    Article Snippet: .. They were genotyped in 309 individuals of the HAT cohort using Sequenom MassARRAY technology (functional genomics platform, Bordeaux, France). ..

    Functional Assay:

    Article Title: Human Leukocyte Antigen-G: A Promising Prognostic Marker of Disease Progression to Improve the Control of Human African Trypanosomiasis.
    Article Snippet: .. They were genotyped in 309 individuals of the HAT cohort using Sequenom MassARRAY technology (functional genomics platform, Bordeaux, France). ..

    other:

    Article Title: P.505 The potential role of BDNF and prolactin genotypes on antidepressant response in depressive patients
    Article Snippet: Participants provided buccal mucosa cells and were genotyped for GABRA6 rs3219151 and CNR1 rs776602 by Sequenom’s MassARRAY technology with IplexTM assay.



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    Mean of SUA among the 3 genotypes of SNPs ( SLC2A9 rs1014290, SLC22A12 rs559946 and SLC22A11 rs1783811). (A) The SUA were not significantly different across genotypes of rs1014290, rs559946, and rs1783811 in the total population ( P = .472, P = .498, P = .721); (B) the SUA were not significantly different across genotypes of rs1014290, rs559946, and rs1783811 in the hyperuricemia groups ( P = .922, P = .277, P = .549); (C) the SUA were not significantly different across genotypes of rs1014290, rs559946, and rs1783811 in the control groups ( P = .081, P = .591, P = .805). SLC2A9 = solute carrier family 2 member 9, SLC22A11 = solute carrier family 22 member 11, SLC22A12 = solute carrier family 22 member 12, <t>SNP</t> = single <t>nucleotide</t> polymorphism, SUA = serum uric acid. P < .05 indicates statistical significance.
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    Mean of SUA among the 3 genotypes of SNPs ( SLC2A9 rs1014290, SLC22A12 rs559946 and SLC22A11 rs1783811). (A) The SUA were not significantly different across genotypes of rs1014290, rs559946, and rs1783811 in the total population ( P = .472, P = .498, P = .721); (B) the SUA were not significantly different across genotypes of rs1014290, rs559946, and rs1783811 in the hyperuricemia groups ( P = .922, P = .277, P = .549); (C) the SUA were not significantly different across genotypes of rs1014290, rs559946, and rs1783811 in the control groups ( P = .081, P = .591, P = .805). SLC2A9 = solute carrier family 2 member 9, SLC22A11 = solute carrier family 22 member 11, SLC22A12 = solute carrier family 22 member 12, <t>SNP</t> = single <t>nucleotide</t> polymorphism, SUA = serum uric acid. P < .05 indicates statistical significance.
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    Mean of SUA among the 3 genotypes of SNPs ( SLC2A9 rs1014290, SLC22A12 rs559946 and SLC22A11 rs1783811). (A) The SUA were not significantly different across genotypes of rs1014290, rs559946, and rs1783811 in the total population ( P = .472, P = .498, P = .721); (B) the SUA were not significantly different across genotypes of rs1014290, rs559946, and rs1783811 in the hyperuricemia groups ( P = .922, P = .277, P = .549); (C) the SUA were not significantly different across genotypes of rs1014290, rs559946, and rs1783811 in the control groups ( P = .081, P = .591, P = .805). SLC2A9 = solute carrier family 2 member 9, SLC22A11 = solute carrier family 22 member 11, SLC22A12 = solute carrier family 22 member 12, SNP = single nucleotide polymorphism, SUA = serum uric acid. P < .05 indicates statistical significance.

    Journal: Medicine

    Article Title: Association of single-nucleotide polymorphisms in SLC2A9, SLC22A12 and SLC22A11 genes with hyperuricemia in the Chinese Tibetan population

    doi: 10.1097/MD.0000000000045023

    Figure Lengend Snippet: Mean of SUA among the 3 genotypes of SNPs ( SLC2A9 rs1014290, SLC22A12 rs559946 and SLC22A11 rs1783811). (A) The SUA were not significantly different across genotypes of rs1014290, rs559946, and rs1783811 in the total population ( P = .472, P = .498, P = .721); (B) the SUA were not significantly different across genotypes of rs1014290, rs559946, and rs1783811 in the hyperuricemia groups ( P = .922, P = .277, P = .549); (C) the SUA were not significantly different across genotypes of rs1014290, rs559946, and rs1783811 in the control groups ( P = .081, P = .591, P = .805). SLC2A9 = solute carrier family 2 member 9, SLC22A11 = solute carrier family 22 member 11, SLC22A12 = solute carrier family 22 member 12, SNP = single nucleotide polymorphism, SUA = serum uric acid. P < .05 indicates statistical significance.

    Article Snippet: DNA was extracted from whole blood samples using Sequenom MassARRAY® single nucleotide polymorphism (SNP) technology.

    Techniques: Control