Improved PCR/nested PCR approaches with increased sensitivity and specificity for the detection of pathogens in hard ticks
Genetic diversity and linkage disequilibrium analysis in elite sugar beet breeding lines and wild beet accessions
Single nucleotide polymorphism genotyping using Kompetitive Allele Specific PCR (KASP): overview of the technology and its application in crop improvement
Single Nucleotide Polymorphism–based Genetic Diversity in the Reference Set of Peanut (spp.) by Developing and Applying Cost-Effective Kompetitive Allele Specific Polymerase Chain Reaction Genotyping Assays.
Common genetic variants at the 11q13. 3 renal cancer susceptibility locus influence binding of HIF to an enhancer of cyclin D1 expression
Evaluation of genes involved in limb development, angiogenesis, and coagulation as risk factors for congenital limb deficiencies
Significant association between body composition phenotypes and the osteocalcin genomic region in normative human population
Meta-analysis of genome-wide scans for total body BMD in children and adults reveals allelic heterogeneity and age-specific effects at the WNT16 locus
Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture
Use of a predictive model derived from in vivo endophenotype measurements to demonstrate associations with a complex locus, CYP2A6
Genetic and environmental factors influencing the placental growth factor (PGF) variation in two populations
Proteins involved in extracellular matrix dynamics are associated with respiratory syncytial virus disease severity
IL1RL1 Gene Variants and Nasopharyngeal IL1RL-a Levels Are Associated with Severe RSV Bronchiolitis: A Multicenter Cohort Study
PWE-166 Increasing VacA toxin activity alters Helicobacter pylori colonisation density and the nature of the acquired immune response in a mouse model of infection
Simultaneous monitoring of two fungal genotypes on plant roots by single nucleotide polymorphism quantification with an innovative KASPar quantitative PCR
Zinc transporter 8 autoantibodies and their association with SLC30A8 and HLA-DQ genes differ between immigrant and Swedish patients with newly diagnosed type 1 diabetes in the better diabetes diagnosis study
Contribution of common genetic variation to the risk of type 2 diabetes in the Mexican Mestizo population
Multiple genetic variants explain measurable variance in type 2 diabetes-related traits in Pakistanis
Reduced insulin secretion correlates with decreased expression of exocytotic genes in pancreatic islets from patients with type 2 diabetes
The effect of FOXA2 rs1209523 on glucose-related phenotypes and risk of type 2 diabetes in Danish individuals
Occurrence of Fusarium Head Blight species and Fusarium mycotoxins in winter wheat in the Netherlands in 2009
Reverse breeding in Arabidopsis thaliana generates homozygous parental lines from a heterozygous plant
North American Pulse Improvement Association (NAPIA) November 2-4, 2011 Meeting San Juan, Puerto Rico
Advances in genetics and molecular breeding of three legume crops of semi-arid tropics using next-generation sequencing and high-throughput genotyping technologies
Effects of polymorphisms in TRAILR1 and TNFR1A on the response to anti-TNF therapies in patients with rheumatoid and psoriatic arthritis
Effets des polymorphismes des gènes< i> TRAILR1 et< i> TNFR1A sur la réponse au traitement anti-TNF chez les patients atteints de polyarthrite rhumatoïde et de rhumatisme psoriasique.
TGFβ receptor gene variants in systemic sclerosis-related pulmonary arterial hypertension: results from a multicentre EUSTAR study of European Caucasian patients
Polymorphisms in the Interleukin 4, Interleukin 13, and Corresponding Receptor Genes Are Not Associated with Systemic Sclerosis and Do Not Influence Gene Expression
TRAF Family Member-Associated NF-KB Activator (TANK) Gene Polymorphism in Chronic Periodontitis and Peri-implantitis Patients
Analysis of RANKL gene polymorphism (rs9533156 and rs2277438) in Iranian patients with chronic periodontitis and periimplantitis
Impact of Loss-of-function Mutations in the Filaggrin Gene and Atopic Dermatitis on the Development of Occupational Irritant Contact Dermatitis
Clinical course of occupational irritant contact dermatitis of the hands in relation to filaggrin genotype status and atopy
