Assessing the role of HLA-linked and unlinked determinants of disease.
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Increasing incidence of Type 1 diabetes--role for genes?Linkage analysis of HLA and candidate genes for celiac disease in a North American family-based studyHow many more breast cancer predisposition genes are there?The genetics of rheumatoid arthritis and the need for animal models to find and understand the underlying genesGenetic, household and spatial clustering of leprosy on an island in Indonesia: a population-based study.Environmental risk factors for multiple sclerosis: a review with a focus on molecular mechanismsSeven regions of the genome show evidence of linkage to type 1 diabetes in a consensus analysis of 767 multiplex families.HLA DPA1, DPB1 alleles and haplotypes contribute to the risk associated with type 1 diabetes: analysis of the type 1 diabetes genetics consortium families.The role of HLA class II genes in insulin-dependent diabetes mellitus: molecular analysis of 180 Caucasian, multiplex familiesInsulin-dependent diabetes mellitus: a model for the study of multifactorial disordersGenetic heterogeneity, modes of inheritance, and risk estimates for a joint study of Caucasians with insulin-dependent diabetes mellitusGenetic analysis of type 1 diabetes using whole genome approachesGenome-wide association analyses identify 13 new susceptibility loci for generalized vitiligoA genome-wide association study of Hodgkin's lymphoma identifies new susceptibility loci at 2p16.1 (REL), 8q24.21 and 10p14 (GATA3)Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility.Follow-up analysis of genome-wide association data identifies novel loci for type 1 diabetes.Targeted Deep Sequencing in Multiple-Affected Sibships of European Ancestry Identifies Rare Deleterious Variants in PTPN22 That Confer Risk for Type 1 Diabetes.HLA DR-DQ haplotypes and genotypes and type 1 diabetes risk: analysis of the type 1 diabetes genetics consortium familiesHLA genotyping in the international Type 1 Diabetes Genetics ConsortiumAssociation analysis of SNPs in the IL4R locus with type I diabetes.Efficient study designs for test of genetic association using sibship data and unrelated cases and controls.Discovery, linkage disequilibrium and association analyses of polymorphisms of the immune complement inhibitor, decay-accelerating factor gene (DAF/CD55) in type 1 diabetesY chromosome lineage- and village-specific genes on chromosomes 1p22 and 6q27 control visceral leishmaniasis in Sudan.From disease association to risk assessment: an optimistic view from genome-wide association studies on type 1 diabetes.Occurrence of rheumatoid arthritis is not increased in the first degree relatives of a population based inception cohort of inflammatory polyarthritisEvidence for association of the TCF7 locus with type I diabetes.Genetics and pathogenesis of type 1 diabetes: prospects for prevention and interventionThe aggregation of the 5' insulin gene polymorphism in insulin dependent (type I) diabetes mellitus families.Approaches in type 1 diabetes research: A status report.Linkage of rheumatoid arthritis to the candidate gene NRAMP1 on 2q35The genetics of primary nocturnal enuresis: inheritance and suggestion of a second major gene on chromosome 12q.Multiple sclerosis: it epidemiological, genetic, and health care impactWorldwide differences in the incidence of type I diabetes are associated with amino acid variation at position 57 of the HLA-DQ beta chainGerminal centre frequency is decreased in pancreatic lymph nodes from individuals with recent-onset type 1 diabetes.PARP alleles within the linked chromosomal region are associated with systemic lupus erythematosusAssociation and interaction of the IL4R, IL4, and IL13 loci with type 1 diabetes among Filipinos.Genome scan meta-analysis of schizophrenia and bipolar disorder, part I: Methods and power analysis.Joint modeling of linkage and association: identifying SNPs responsible for a linkage signalA genomewide scan for type 1-diabetes susceptibility in Scandinavian families: identification of new loci with evidence of interactions.Complex HLA-DR and -DQ interactions confer risk of narcolepsy-cataplexy in three ethnic groups
P2860
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P2860
Assessing the role of HLA-linked and unlinked determinants of disease.
description
1987 nî lūn-bûn
@nan
1987年の論文
@ja
1987年論文
@yue
1987年論文
@zh-hant
1987年論文
@zh-hk
1987年論文
@zh-mo
1987年論文
@zh-tw
1987年论文
@wuu
1987年论文
@zh
1987年论文
@zh-cn
name
Assessing the role of HLA-linked and unlinked determinants of disease.
@en
type
label
Assessing the role of HLA-linked and unlinked determinants of disease.
@en
prefLabel
Assessing the role of HLA-linked and unlinked determinants of disease.
@en
P2860
P1476
Assessing the role of HLA-linked and unlinked determinants of disease.
@en
P2093
P2860
P407
P577
1987-01-01T00:00:00Z