A novel association between a SNP in CYBRD1 and serum ferritin levels in a cohort study of HFE hereditary haemochromatosis.
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Exome sequencing in HFE C282Y homozygous men with extreme phenotypes identifies a GNPAT variant associated with severe iron overload.A novel test for gene-ancestry interactions in genome-wide association data.Genome-wide association study identifies genetic loci associated with iron deficiency.Genome-wide association study identifies variants in PMS1 associated with serum ferritin in a Chinese populationAssociations between single nucleotide polymorphisms in iron-related genes and iron status in multiethnic populations.Molecular diagnosis of hemochromatosis.In silico QTL mapping of basal liver iron levels in inbred mouse strainsFour variants in transferrin and HFE genes as potential markers of iron deficiency anaemia risk: an association study in menstruating women.Duodenal cytochrome b (DCYTB) in iron metabolism: an update on function and regulation.Signatures of Evolutionary Adaptation in Quantitative Trait Loci Influencing Trace Element Homeostasis in Liver.CYBRD1 as a modifier gene that modulates iron phenotype in HFE p.C282Y homozygous patients.Polymorphisms in iron homeostasis genes and urinary cadmium concentrations among nonsmoking women in Argentina and Bangladesh.The gut in iron homeostasis: role of HIF-2 under normal and pathological conditionsWhere genotype is not predictive of phenotype: towards an understanding of the molecular basis of reduced penetrance in human inherited disease.Diagnosis and treatment of hereditary hemochromatosis: an update.Genetic factors associated with iron storage in Australian blood donors.Analysis of polymorphism and hepatic expression of duodenal cytochrome b in chronic hepatitis C.Epistasis in iron metabolism: complex interactions between Cp, Mon1a, and Slc40a1 loci and tissue iron in mice.Duodenal cytochrome b (Cybrd1) ferric reductase functional studies in cells.Association of mRNA expression of iron metabolism-associated genes and progression of non-alcoholic steatohepatitis in rats.COMBINING INDIVIDUAL PARTICIPANT DATA AND SUMMARY STATISTICS FROM BOTH CONTINUOUSLY VALUED AND BINARY VARIABLES TO ESTIMATE REGRESSION PARAMETERS
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P2860
A novel association between a SNP in CYBRD1 and serum ferritin levels in a cohort study of HFE hereditary haemochromatosis.
description
article científic
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article scientifique
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articolo scientifico
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artigo científico
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bilimsel makale
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scientific article published on 10 August 2009
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
A novel association between a ...... E hereditary haemochromatosis.
@en
A novel association between a ...... E hereditary haemochromatosis.
@nl
type
label
A novel association between a ...... E hereditary haemochromatosis.
@en
A novel association between a ...... E hereditary haemochromatosis.
@nl
prefLabel
A novel association between a ...... E hereditary haemochromatosis.
@en
A novel association between a ...... E hereditary haemochromatosis.
@nl
P2093
P2860
P50
P1476
A novel association between a ...... E hereditary haemochromatosis.
@en
P2093
Andrew T McKie
Christine E McLaren
Clare C Constantine
Dorota M Gertig
Greg J Anderson
Heng Lin Yeap
Kenneth B Beckman
Martin B Delatycki
Melanie Bahlo
Nadine A Bertalli
P2860
P304
P356
10.1111/J.1365-2141.2009.07843.X
P407
P50
P577
2009-08-10T00:00:00Z