about
Post genome-wide association studies of novel genes associated with type 2 diabetes show gene-gene interaction and high predictive valueChromosomal mapping of the human and murine orphan receptors ERRalpha (ESRRA) and ERRbeta (ESRRB) and identification of a novel human ERRalpha-related pseudogeneIdentification of a gene causing human cytochrome c oxidase deficiency by integrative genomics.Reduced fat mass in mice lacking orphan nuclear receptor estrogen-related receptor alphaFunctional classes of bronchial mucosa genes that are differentially expressed in asthmaInsulin storage and glucose homeostasis in mice null for the granule zinc transporter ZnT8 and studies of the type 2 diabetes-associated variantsNew genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes riskA genome-wide association study identifies novel risk loci for type 2 diabetesThe growth factor midkine is modulated by both glucocorticoid and retinoid in fetal lung developmentPlacental abnormalities in mouse embryos lacking the orphan nuclear receptor ERR-betaAssociation of levels of fasting glucose and insulin with rare variants at the chromosome 11p11.2-MADD locus: Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium Targeted Sequencing StudyA genome-wide association search for type 2 diabetes genes in African AmericansTFCat: the curated catalog of mouse and human transcription factorsGenetic variation in GIPR influences the glucose and insulin responses to an oral glucose challengeMolecular diagnosis of neonatal diabetes mellitus using next-generation sequencing of the whole exome.Convex lens-induced nanoscale templating.Characterization of variability in large-scale gene expression data: implications for study design.Analysis of beta-cell gene expression reveals inflammatory signaling and evidence of dedifferentiation following human islet isolation and cultureA methodology for global validation of microarray experiments.Differential allelic expression in the human genome: a robust approach to identify genetic and epigenetic cis-acting mechanisms regulating gene expression.Small deletion variants have stable breakpoints commonly associated with alu elements.A genome-wide association study reveals variants in ARL15 that influence adiponectin levels.Increased subcutaneous adipose tissue expression of genes involved in glycerolipid-fatty acid cycling in obese insulin-resistant versus -sensitive individualsMultilevel space-time aggregation for bright field cell microscopy segmentation and trackingOrphan nuclear receptors: an emerging family of metabolic regulators.A new highly penetrant form of obesity due to deletions on chromosome 16p11.2.Mapping of a chromosome 12 region associated with airway hyperresponsiveness in a recombinant congenic mouse strain and selection of potential candidate genes by expression and sequence variation analyses.The protein kinase PKR: a molecular clock that sequentially activates survival and death programs.Control genes and variability: absence of ubiquitous reference transcripts in diverse mammalian expression studies.An N-ethyl-N-nitrosourea (ENU)-induced dominant negative mutation in the JAK3 kinase protects against cerebral malariaNovel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals.Common variants at 10 genomic loci influence hemoglobin A₁(C) levels via glycemic and nonglycemic pathwaysA variant near MTNR1B is associated with increased fasting plasma glucose levels and type 2 diabetes risk.A Mendelian randomization study of the effect of type-2 diabetes on coronary heart disease.Pancreatic β-Cell Dysfunction in Diet-Induced Obese Mice: Roles of AMP-Kinase, Protein Kinase Cε, Mitochondrial and Cholesterol Metabolism, and Alterations in Gene ExpressionElucidating cis- and trans-regulatory variation using genetical genomics.Comparison of the effects of Leishmania major or Leishmania donovani infection on macrophage gene expression.The orphan nuclear receptor estrogen-related receptor alpha is a transcriptional regulator of the human medium-chain acyl coenzyme A dehydrogenase gene.Rare MTNR1B variants impairing melatonin receptor 1B function contribute to type 2 diabetesGenetic variant in HK1 is associated with a proanemic state and A1C but not other glycemic control-related traits.
P50
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P50
description
hulumtues
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Robert Sladek
@ast
Robert Sladek
@en
Robert Sladek
@es
Robert Sladek
@nl
Robert Sladek
@sl
type
label
Robert Sladek
@ast
Robert Sladek
@en
Robert Sladek
@es
Robert Sladek
@nl
Robert Sladek
@sl
prefLabel
Robert Sladek
@ast
Robert Sladek
@en
Robert Sladek
@es
Robert Sladek
@nl
Robert Sladek
@sl
P106
P21
P2798
P31
P496
0000-0002-2730-1204