massarray assaydesign 3.1 software (Sequenom)
90
Structured Review
Sequenom
massarray assaydesign 3.1 software
Massarray Assaydesign 3.1 Software, 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/massarray+assaydesign+software/massarray+assay+design+3+0+software/10__1097_slash_md__0000000000021390-76-6-10
Average 90 stars, based on 1 article reviews
Massarray Assaydesign 3.1 Software, 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/massarray+assaydesign+software/massarray+assay+design+3+0+software/10__1097_slash_md__0000000000021390-76-6-10
Average 90 stars, based on 1 article reviews
massarray assaydesign 3.1 software - by Bioz Stars,
2026-10
90/100 stars
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Software:Article Title: A human ALDH1A2 gene variant is associated with increased newborn kidney size and serum retinoic acid. Article Snippet: .. Primers for SNP detection were designed using Article Title: A Common Variant of thePAX2Gene Is Associated with Reduced Newborn Kidney Size Article Snippet: .. Primers for SNP detection were designed using Article Title: A CommonRETVariant Is Associated with Reduced Newborn Kidney Size and Function Article Snippet: .. Primers for SNP detection were designed using Article Title: A Common RET Variant Is Associated with Reduced Newborn Kidney Size and Function Article Snippet: .. Primers for SNP detection were designed using Article Title: A variant OSR1 allele which disturbs OSR1 mRNA expression in renal progenitor cells is associated with reduction of newborn kidney size and function. Article Snippet: McGill University Department of Human Genetics’ and McGill University Department of Paediatrics, Montreal Children’s Hospital Research Institute, Montreal, Canada, McGill Department of Experimental Surgery, Lady Davis Research Institute, Montreal Jewish General Hospital, Montreal, Canada and Excellence Centre for Research, Transfer and High Education DENOthe, University of Florence and Meyer Children’s Hospital, Florence, Italy Article Title: A novel intronic polymorphism of ABCA1 gene reveals risk for sporadic Alzheimer's disease in Chinese. Article Snippet: Leung Wing Chu, Yan Li, Zhong Li, Alan YB Tang, Bernard MY Cheung, Raymond YH Leung, Ping-Yiu Yik, Dong-Yan Jin, and You-Qiang Song* Department of Medicine, The University of Hong Kong, Hong Kong Department of Biochemistry, The University of Hong Kong, Hong Kong Neurology Department, The first affiliated hospital of Sun Yat-sen University, Guangzhou, China The Genome Research Centre, The University of Hong Kong, Hong Kong Department of Orthopaedic Surgery, The University of Hong Kong, Hong Kong Article Title: Association of ICAM3 Genetic Variant with Severe Acute Respiratory Syndrome Article Snippet: Genotyping of the initial SARS samples (309 cases) and HCW control subjects was done by Sequenom. .. Article Title: p21 gene polymorphisms in systemic lupus erythematosus. Article Snippet: Mass spectrometric data was automatically imported into the SpectroTYPER (Sequenom) database for data analysis including noise normalization and peak area analysis. .. The expected molecular weights of all relevant peaks were calculated by the Amplification:Article Title: A novel intronic polymorphism of ABCA1 gene reveals risk for sporadic Alzheimer's disease in Chinese. Article Snippet: Leung Wing Chu, Yan Li, Zhong Li, Alan YB Tang, Bernard MY Cheung, Raymond YH Leung, Ping-Yiu Yik, Dong-Yan Jin, and You-Qiang Song* Department of Medicine, The University of Hong Kong, Hong Kong Department of Biochemistry, The University of Hong Kong, Hong Kong Neurology Department, The first affiliated hospital of Sun Yat-sen University, Guangzhou, China The Genome Research Centre, The University of Hong Kong, Hong Kong Department of Orthopaedic Surgery, The University of Hong Kong, Hong Kong Article Title: Association of ICAM3 Genetic Variant with Severe Acute Respiratory Syndrome Article Snippet: Genotyping of the initial SARS samples (309 cases) and HCW control subjects was done by Sequenom. .. |