about
sameAs
Analyses of pig genomes provide insight into porcine demography and evolutionRNA sequencing: current and prospective uses in metabolic researchIncreased Melatonin Signaling Is a Risk Factor for Type 2 DiabetesA Variant of GJD2, Encoding for Connexin 36, Alters the Function of Insulin Producing β-CellsExpression of phosphofructokinase in skeletal muscle is influenced by genetic variation and associated with insulin sensitivityThe diabetes susceptibility gene Clec16a regulates mitophagyThe genetic architecture of type 2 diabetesA central role for GRB10 in regulation of islet function in man.A snapshot of CNVs in the pig genomeCopy number variation in the bovine genomeGlobal assessment of genomic variation in cattle by genome resequencing and high-throughput genotyping.Genomic position mapping discrepancies of commercial SNP chips.Global genomic and transcriptomic analysis of human pancreatic islets reveals novel genes influencing glucose metabolismGenetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility lociTCF7L2 is a master regulator of insulin production and processing.Serotonin (5-HT) receptor 2b activation augments glucose-stimulated insulin secretion in human and mouse islets of Langerhans.The CTRB1/2 locus affects diabetes susceptibility and treatment via the incretin pathway.A Low-Frequency Inactivating AKT2 Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk.Leveraging cross-species transcription factor binding site patterns: from diabetes risk loci to disease mechanisms.A systems genetics approach identifies genes and pathways for type 2 diabetes in human islets.LoFtool: a gene intolerance score based on loss-of-function variants in 60 706 individuals.MafA-Controlled Nicotinic Receptor Expression Is Essential for Insulin Secretion and Is Impaired in Patients with Type 2 Diabetes.Glucose-induced Changes in Gene Expression in Human Pancreatic Islets - Causes or Consequences of Chronic Hyperglycemia.Altered DNA methylation and differential expression of genes influencing metabolism and inflammation in adipose tissue from subjects with type 2 diabetes.Loss of TFB1M results in mitochondrial dysfunction that leads to impaired insulin secretion and diabetes.Sequence data and association statistics from 12,940 type 2 diabetes cases and controls.Genome-wide association study of Hirschsprung disease detects a novel low-frequency variant at the RET locus.Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls.Expression profiling of cell cycle genes in human pancreatic islets with and without type 2 diabetes.Controllability in an islet specific regulatory network identifies the transcriptional factor NFATC4, which regulates Type 2 Diabetes associated genes.Genome-wide meta-analysis identifies BARX1 and EML4-MTA3 as new loci associated with infantile hypertrophic pyloric stenosisVariants in the fetal genome near pro-inflammatory cytokine genes on 2q13 are associated with gestational duration
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