The use of MassARRAY technology for high throughput genotyping.
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Common NFKBIL2 polymorphisms and susceptibility to pneumococcal disease: a genetic association studyVariants in the SP110 gene are associated with genetic susceptibility to tuberculosis in West AfricaGenetic design and statistical power of nested association mapping in maizeTransforming single DNA molecules into fluorescent magnetic particles for detection and enumeration of genetic variationsSARS transmission pattern in Singapore reassessed by viral sequence variation analysisSynaptic P-Rex1 signaling regulates hippocampal long-term depression and autism-like social behaviorGenetic association between intronic variants in AS3MT and arsenic methylation efficiency is focused on a large linkage disequilibrium cluster in chromosome 10A Mal functional variant is associated with protection against invasive pneumococcal disease, bacteremia, malaria and tuberculosisSusceptibility loci associated with specific and shared subtypes of lymphoid malignanciesIdentification of two independent risk factors for lupus within the MHC in United Kingdom families.RNase T1 mediated base-specific cleavage and MALDI-TOF MS for high-throughput comparative sequence analysisCardiac myosin binding protein C and MAP-kinase activating death domain-containing gene polymorphisms and diastolic heart failure.KCNN2 polymorphisms and cardiac tachyarrhythmias.Empirical comparison of Simple Sequence Repeats and single nucleotide polymorphisms in assessment of maize diversity and relatedness.Investigation of 89 candidate gene variants for effects on all-cause mortality following acute coronary syndromeMannose-binding lectin genotypes: lack of association with susceptibility to thoracic empyema.Obesity and diabetes genes are associated with being born small for gestational age: results from the Auckland Birthweight Collaborative study.The NOD-like receptor signalling pathway in Helicobacter pylori infection and related gastric cancer: a case-control study and gene expression analyses.Genetic variants in the transcription regulatory region of MEGF10 are associated with autism in Chinese Han population.ENU mutagenesis identifies mice with morbid obesity and severe hyperinsulinemia caused by a novel mutation in leptinPositive replication and linkage disequilibrium mapping of the chromosome 21q22.1 malaria susceptibility locus.Future of personalized medicine in oncology: a systems biology approach.Analysis of MMP2 promoter polymorphisms in childhood obesity.Large-scale single-nucleotide polymorphism (SNP) and haplotype analyses, using dense SNP Maps, of 199 drug-related genes in 752 subjects: the analysis of the association between uncommon SNPs within haplotype blocks and the haplotypes constructed wiNovel pathway analysis of genomic polymorphism-cancer risk interaction in the Breast Cancer Prevention Trial.Multiplex protein detection with DNA readout via mass spectrometry.Reduced genetic influence on childhood obesity in small for gestational age children.NFKBIZ polymorphisms and susceptibility to pneumococcal disease in European and African populations.SNPflow: a lightweight application for the processing, storing and automatic quality checking of genotyping assays.The role of TLR2, TLR4 and CD14 genetic polymorphisms in gastric carcinogenesis: a case-control study and meta-analysis.Genetic variants of MARCO are associated with susceptibility to pulmonary tuberculosis in a Gambian population.The evidence for association of ATP2B2 polymorphisms with autism in Chinese Han populationInterleukin-10 polymorphism in position -1082 and acute respiratory distress syndrome.Whole-exome sequencing for the identification of susceptibility genes of Kashin-Beck diseaseA multi-detection assay for malaria transmitting mosquitoes.Identification of the genetic basis for complex disorders by use of pooling-based genomewide single-nucleotide-polymorphism association studiesSchizophrenia Related Variants in CACNA1C also Confer Risk of Autism.The strength of selection on ultraconserved elements in the human genomeMetallothionein genes: no association with Crohn's disease in a New Zealand population.Polymorphisms at Locus 4p14 of Toll-Like Receptors TLR-1 and TLR-10 Confer Susceptibility to Gastric Carcinoma in Helicobacter pylori Infection
P2860
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P2860
The use of MassARRAY technology for high throughput genotyping.
description
2002 nî lūn-bûn
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2002 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2002 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2002年の論文
@ja
2002年論文
@yue
2002年論文
@zh-hant
2002年論文
@zh-hk
2002年論文
@zh-mo
2002年論文
@zh-tw
2002年论文
@wuu
name
The use of MassARRAY technology for high throughput genotyping.
@ast
The use of MassARRAY technology for high throughput genotyping.
@en
type
label
The use of MassARRAY technology for high throughput genotyping.
@ast
The use of MassARRAY technology for high throughput genotyping.
@en
prefLabel
The use of MassARRAY technology for high throughput genotyping.
@ast
The use of MassARRAY technology for high throughput genotyping.
@en
P2093
P1476
The use of MassARRAY technology for high throughput genotyping.
@en
P2093
Charles R Cantor
Christian Jurinke
Dirk van den Boom
Hubert Köster
P577
2002-01-01T00:00:00Z