massarray snp multiplex technology (Sequenom)
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Sequenom
massarray snp multiplex technology
Massarray Snp Multiplex 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+snp+multiplex/massarray+platform/pm41135865-88-1-0
Average 86 stars, based on 1 article reviews
Massarray Snp Multiplex 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+snp+multiplex/massarray+platform/pm41135865-88-1-0
Average 86 stars, based on 1 article reviews
massarray snp multiplex technology - by Bioz Stars,
2026-09
86/100 stars
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Multiplex Assay:Article Title: Molecular test of Paget's disease of bone in families not linked to SQSTM1 gene mutations Article Snippet: .. Genotyping of SNPs was done using the Sequenom Article Title: Genetic association study of Dickkopf-1 and sclerostin genes with paget disease of bone. Article Snippet: Increased expression of DKK1 gene was reported in pagetic osteoblasts and stromal cells, and increased serum levels of DKK1 and SOST proteins were reported in patients with Paget disease of bone (PDB).. This study aimed at identifying rare genetic variants of the DKK1 and SOST genes and at testing for genetic association with PDB in the French-Canadian population.. Exons, promoters, and exon–intron junctions of these genes were sequenced in patients with PDB and healthy controls. Article Title: Development of a molecular test of Paget's disease of bone. Article Snippet: .. Genotyping of SNPs relied on two different methods: Sanger sequencing or Sequenom Article Title: Identification of rare genetic variants in novel loci associated with Paget's disease of bone. Article Snippet: 15q24 locus.. We located 71 of these 126 rare variants in an intron, 30 in an exon and 9 in an untranslated region.. 60 % of these variants were located in functionally relevant gene regions. among the 12 missense rare variants in PDB, two (rs62620995 in TM7SF4; rs62641691 in CD276) were predicted to be damaging by in silico analysis tools. rs62620995, which altered a conserved amino acid (p.leu397Phe) in the TM7SF4 gene, encoding the DC-staMP protein involved in osteoclastogenesis through ranK signaling pathway, was found to have a marginal association with PDB (p = 0.09). rs35500845, located in the CTHRC1 gene, which encodes a regulator of collagen matrix deposition, was also associated with PDB in the French-Canadian population (p = 0.046). Article Title: Genetic association study of UCMA/GRP and OPTN genes ( PDB6 locus) with Paget's disease of bone Article Snippet: .. Genotyping of the Tag SNPs was performed by Sequenom Sequencing:Article Title: Molecular test of Paget's disease of bone in families not linked to SQSTM1 gene mutations Article Snippet: .. Genotyping of SNPs was done using the Sequenom Article Title: Genetic association study of Dickkopf-1 and sclerostin genes with paget disease of bone. Article Snippet: Increased expression of DKK1 gene was reported in pagetic osteoblasts and stromal cells, and increased serum levels of DKK1 and SOST proteins were reported in patients with Paget disease of bone (PDB).. This study aimed at identifying rare genetic variants of the DKK1 and SOST genes and at testing for genetic association with PDB in the French-Canadian population.. Exons, promoters, and exon–intron junctions of these genes were sequenced in patients with PDB and healthy controls. Article Title: Development of a molecular test of Paget's disease of bone. Article Snippet: .. Genotyping of SNPs relied on two different methods: Sanger sequencing or Sequenom Selection:Article Title: Identification of rare genetic variants in novel loci associated with Paget's disease of bone. Article Snippet: 15q24 locus.. We located 71 of these 126 rare variants in an intron, 30 in an exon and 9 in an untranslated region.. 60 % of these variants were located in functionally relevant gene regions. among the 12 missense rare variants in PDB, two (rs62620995 in TM7SF4; rs62641691 in CD276) were predicted to be damaging by in silico analysis tools. rs62620995, which altered a conserved amino acid (p.leu397Phe) in the TM7SF4 gene, encoding the DC-staMP protein involved in osteoclastogenesis through ranK signaling pathway, was found to have a marginal association with PDB (p = 0.09). rs35500845, located in the CTHRC1 gene, which encodes a regulator of collagen matrix deposition, was also associated with PDB in the French-Canadian population (p = 0.046). Control:Article Title: Identification of rare genetic variants in novel loci associated with Paget's disease of bone. Article Snippet: 15q24 locus.. We located 71 of these 126 rare variants in an intron, 30 in an exon and 9 in an untranslated region.. 60 % of these variants were located in functionally relevant gene regions. among the 12 missense rare variants in PDB, two (rs62620995 in TM7SF4; rs62641691 in CD276) were predicted to be damaging by in silico analysis tools. rs62620995, which altered a conserved amino acid (p.leu397Phe) in the TM7SF4 gene, encoding the DC-staMP protein involved in osteoclastogenesis through ranK signaling pathway, was found to have a marginal association with PDB (p = 0.09). rs35500845, located in the CTHRC1 gene, which encodes a regulator of collagen matrix deposition, was also associated with PDB in the French-Canadian population (p = 0.046). Variant Assay:Article Title: Identification of rare genetic variants in novel loci associated with Paget's disease of bone. Article Snippet: 15q24 locus.. We located 71 of these 126 rare variants in an intron, 30 in an exon and 9 in an untranslated region.. 60 % of these variants were located in functionally relevant gene regions. among the 12 missense rare variants in PDB, two (rs62620995 in TM7SF4; rs62641691 in CD276) were predicted to be damaging by in silico analysis tools. rs62620995, which altered a conserved amino acid (p.leu397Phe) in the TM7SF4 gene, encoding the DC-staMP protein involved in osteoclastogenesis through ranK signaling pathway, was found to have a marginal association with PDB (p = 0.09). rs35500845, located in the CTHRC1 gene, which encodes a regulator of collagen matrix deposition, was also associated with PDB in the French-Canadian population (p = 0.046). Mutagenesis:Article Title: Identification of rare genetic variants in novel loci associated with Paget's disease of bone. Article Snippet: 15q24 locus.. We located 71 of these 126 rare variants in an intron, 30 in an exon and 9 in an untranslated region.. 60 % of these variants were located in functionally relevant gene regions. among the 12 missense rare variants in PDB, two (rs62620995 in TM7SF4; rs62641691 in CD276) were predicted to be damaging by in silico analysis tools. rs62620995, which altered a conserved amino acid (p.leu397Phe) in the TM7SF4 gene, encoding the DC-staMP protein involved in osteoclastogenesis through ranK signaling pathway, was found to have a marginal association with PDB (p = 0.09). rs35500845, located in the CTHRC1 gene, which encodes a regulator of collagen matrix deposition, was also associated with PDB in the French-Canadian population (p = 0.046). |