about
A CLEC16A variant confers risk for juvenile idiopathic arthritis and anti-cyclic citrullinated peptide antibody negative rheumatoid arthritisConstruction and analysis of tag single nucleotide polymorphism maps for six human-mouse orthologous candidate genes in type 1 diabetesAn additional susceptibility gene for juvenile idiopathic arthritis in the HLA class I region on several DR-DQ haplotypesAssociation of the T-cell regulatory gene CTLA4 with susceptibility to autoimmune diseaseAutoimmune adrenocortical failure in Norway autoantibodies and human leukocyte antigen class II associations related to clinical featuresAssessing the validity of the association between the SUMO4 M55V variant and risk of type 1 diabetesCurrent guidelines for BRCA testing of breast cancer patients are insufficient to detect all mutation carriersDetection of a low-grade enteroviral infection in the islets of langerhans of living patients newly diagnosed with type 1 diabetes.HLA complex genes in type 1 diabetes and other autoimmune diseases. Which genes are involved?A common haplotype in NAPEPLD is associated with severe obesity in a Norwegian population-based cohort (the HUNT study).Polymorphisms in the gene encoding thymus-specific serine protease in the extended HLA complex: a potential candidate gene for autoimmune and HLA-associated diseases.Application and interpretation of transmission/disequilibrium tests: transmission of HLA-DQ haplotypes to unaffected siblings in 526 families with type 1 diabetes.DNA methylation and gene expression changes in monozygotic twins discordant for psoriasis: identification of epigenetically dysregulated genesCommon variants in the regulatory region of the insulin gene are associated with fasting plasma insulin levels in juvenile obesity.Linkage disequilibrium mapping of a type 1 diabetes susceptibility gene (IDDM7) to chromosome 2q31-q33.Fine mapping of the diabetes-susceptibility locus, IDDM4, on chromosome 11q13.The predisposition to type 1 diabetes linked to the human leukocyte antigen complex includes at least one non-class II gene.HLA-encoded genetic predisposition in IDDM: DR4 subtypes may be associated with different degrees of protection.Association analysis in type 1 diabetes of the PRSS16 gene encoding a thymus-specific serine protease.Relative predispositional effects of HLA class II DRB1-DQB1 haplotypes and genotypes on type 1 diabetes: a meta-analysis.Polymorphisms in the cathepsin L2 (CTSL2) gene show association with type 1 diabetes and early-onset myasthenia gravis.Polymorphisms in CLEC16A and CIITA at 16p13 are associated with primary adrenal insufficiency.Association of autoimmune Addison's disease with alleles of STAT4 and GATA3 in European cohorts.Extensive variation and low heritability of DNA methylation identified in a twin study.A mild form of Mucopolysaccharidosis IIIB diagnosed with targeted next-generation sequencing of linked genomic regions.A conserved eEF2 coding variant in SCA26 leads to loss of translational fidelity and increased susceptibility to proteostatic insultJoint effects of HLA, INS, PTPN22 and CTLA4 genes on the risk of type 1 diabetesSLC9A6 mutations cause X-linked mental retardation, microcephaly, epilepsy, and ataxia, a phenotype mimicking Angelman syndrome.Clinical and molecular genetic spectrum of congenital deficiency of the leptin receptor.Intra-individual changes in DNA methylation not mediated by cell-type composition are correlated with aging during childhood.Lack of association of the Ala(45)Thr polymorphism and other common variants of the NeuroD gene with type 1 diabetes.Association of intercellular adhesion molecule-1 gene with type 1 diabetes.DR- and DQ-associated protection from type 1A diabetes: comparison of DRB1*1401 and DQA1*0102-DQB1*0602*.The HLA associated predisposition to type 1 diabetes and other autoimmune diseases.Insulin gene region-encoded susceptibility to type 1 diabetes is not restricted to HLA-DR4-positive individuals.Evidence by allelic association-dependent methods for a type 1 diabetes polygene (IDDM6) on chromosome 18q21.No difference in the parental origin of susceptibility HLA class II haplotypes among Norwegian patients with insulin-dependent diabetes mellitus.An inverse association between history of childhood eczema and subsequent risk of type 1 diabetes that is not likely to be explained by HLA-DQ, PTPN22, or CTLA4 polymorphisms.Clinical, immunological, and genetic features of autoimmune primary adrenal insufficiency: observations from a Norwegian registry.X-linked congenital adrenal hypoplasia with hypogonadotropic hypogonadism caused by an inversion disrupting a conserved noncoding element upstream of the NR0B1 (DAX1) gene.
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P50
description
Noors bioloog
@nl
Norwegian biologist and professor
@en
ahli biologi asal Norwegia
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bitheolaí agus ollamh Ioruach
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norsk professor
@nb
استاد دانشگاه و زیستشناس نروژی
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name
Dag Erik Undlien
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Dag Undlien
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Dag Undlien
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Dag Undlien
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Dag Undlien
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Dag Undlien
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Dag Undlien
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Dag Undlien
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Dag Undlien
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Dag Undlien
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type
label
Dag Erik Undlien
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Dag Undlien
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Dag Undlien
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Dag Undlien
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Dag Undlien
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Dag Undlien
@en
Dag Undlien
@es
Dag Undlien
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Dag Undlien
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Dag Undlien
@id
altLabel
Dag E Undlien
@en
Dag E. Undlien
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Dag Undlien
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prefLabel
Dag Erik Undlien
@nb
Dag Undlien
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Dag Undlien
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Dag Undlien
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Dag Undlien
@de
Dag Undlien
@en
Dag Undlien
@es
Dag Undlien
@fr
Dag Undlien
@ga
Dag Undlien
@id
P21
P214
1997149108673168780003
P2287
P27
P31
P569
1964-06-12T00:00:00Z
P734
P7859
viaf-1997149108673168780003