Common variants in TMPRSS6 are associated with iron status and erythrocyte volume. - Wikidata - wikimedia - TriplyDB

Common variants in TMPRSS6 are associated with iron status and erythrocyte volume.

Common variants in TMPRSS6 are associated with iron status and erythrocyte volume.

http://www.wikidata.org/entity/Q35102503

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Hemojuvelin and bone morphogenetic protein (BMP) signaling in iron homeostasis SNPs associated with cerebrospinal fluid phospho-tau levels influence rate of decline in Alzheimer's disease Natural selection on EPAS1 (HIF2alpha) associated with low hemoglobin concentration in Tibetan highlanders The role of TMPRSS6/matriptase-2 in iron regulation and anemia Hepcidin and iron regulation, 10 years later.The Brisbane Systems Genetics Study: genetical genomics meets complex trait genetics Serum iron levels and the risk of Parkinson disease: a Mendelian randomization study.Candidate gene sequencing of SLC11A2 and TMPRSS6 in a family with severe anaemia: common SNPs, rare haplotypes, no causative mutation Serum ferritin levels are associated with a distinct phenotype of chronic hepatitis C poorly responding to pegylated interferon-alpha and ribavirin therapy.Is the adiposity-associated FTO gene variant related to all-cause mortality independent of adiposity? Meta-analysis of data from 169,551 Caucasian adults Targeting the hepcidin-ferroportin axis in the diagnosis and treatment of anemias A genome-wide association study of red blood cell traits using the electronic medical record.Pica associated with iron deficiency or depletion: clinical and laboratory correlates in 262 non-pregnant adult outpatients Pathophysiological consequences and benefits of HFE mutations: 20 years of research.Down-regulation of Bmp/Smad signaling by Tmprss6 is required for maintenance of systemic iron homeostasis Physiology of iron metabolism Genome-wide association study identifies genetic loci associated with iron deficiency.Membrane-anchored serine proteases in vertebrate cell and developmental biology Identification of nine novel loci associated with white blood cell subtypes in a Japanese population.Genome-wide association study identifies variants in PMS1 associated with serum ferritin in a Chinese population Genetic determinants for body iron store and type 2 diabetes risk in US men and women.Systems Epidemiology: A New Direction in Nutrition and Metabolic Disease Research Demographic correlates of low hemoglobin deferral among prospective whole blood donors.Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosis Novel association to the proprotein convertase PCSK7 gene locus revealed by analysing soluble transferrin receptor (sTfR) levels.Inter-ethnic differences in genetic variants within the transmembrane protease, serine 6 (TMPRSS6) gene associated with iron status indicators: a systematic review with meta-analyses.The A736V TMPRSS6 polymorphism influences hepcidin and iron metabolism in chronic hemodialysis patients: TMPRSS6 and hepcidin in hemodialysis.Identification of a common variant in the TFR2 gene implicated in the physiological regulation of serum iron levels.Tmprss6 is a genetic modifier of the Hfe-hemochromatosis phenotype in mice.Inflammation regulates TMPRSS6 expression via STAT5.Genome-wide admixture and association study of serum iron, ferritin, transferrin saturation and total iron binding capacity in African Americans.Regulation of TMPRSS6 by BMP6 and iron in human cells and mice.The National Heart, Lung, and Blood Institute Recipient Epidemiology and Donor Evaluation Study (REDS-III): a research program striving to improve blood donor and transfusion recipient outcomes Four variants in transferrin and HFE genes as potential markers of iron deficiency anaemia risk: an association study in menstruating women.GWAS of butyrylcholinesterase activity identifies four novel loci, independent effects within BCHE and secondary associations with metabolic risk factors Silencing of RhoA nucleotide exchange factor, ARHGEF3, reveals its unexpected role in iron uptake.Association of genetic variants with response to iron supplements in pregnancy Laboratory and genetic assessment of iron deficiency in blood donors Iron and hepcidin as risk factors in atherosclerosis: what do the genes say?Common TMPRSS6 mutations and iron, erythrocyte, and pica phenotypes in 48 women with iron deficiency or depletion.

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P2860

Common variants in TMPRSS6 are associated with iron status and erythrocyte volume.

http://www.wikidata.org/entity/Q35102503

description

2009 nî lūn-bûn

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2009 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2009 թվականի հոտեմբերին հրատարակված գիտական հոդված

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2009年の論文

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2009年論文

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2009年論文

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2009年論文

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2009年論文

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2009年論文

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2009年论文

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name

Common variants in TMPRSS6 are associated with iron status and erythrocyte volume.

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Common variants in TMPRSS6 are associated with iron status and erythrocyte volume.

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type

label

Common variants in TMPRSS6 are associated with iron status and erythrocyte volume.

@ast

Common variants in TMPRSS6 are associated with iron status and erythrocyte volume.

@en

prefLabel

Common variants in TMPRSS6 are associated with iron status and erythrocyte volume.

@ast

Common variants in TMPRSS6 are associated with iron status and erythrocyte volume.

@en

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Nature Genetics

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Common variants in TMPRSS6 are associated with iron status and erythrocyte volume.

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P2093

Brian P McEvoy

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John B Whitfield

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Manuel A R Ferreira

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Megan J Campbell

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Rita P S Middelberg

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Scott Gordon

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P2860

Mutations in TMPRSS6 cause iron-refractory iron deficiency anemia (IRIDA)

Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder

PLINK: a tool set for whole-genome association and population-based linkage analyses

The serine protease matriptase-2 (TMPRSS6) inhibits hepcidin activation by cleaving membrane hemojuvelin

Mapping the genetic architecture of gene expression in human liver

Genome-wide association of major depression: description of samples for the GAIN Major Depressive Disorder Study: NTR and NESDA biobank projects.

Effects of HFE C282Y and H63D polymorphisms and polygenic background on iron stores in a large community sample of twins.

Interaction of the hereditary hemochromatosis protein HFE with transferrin receptor 2 is required for transferrin-induced hepcidin expression.

Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels.

Fine tuning of hepcidin expression by positive and negative regulators.

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1173-1175

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10.1038/NG.456

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11

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41

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Gonneke Willemsen

Jouke-Jan Hottenga

Peter M. Visscher

Anjali K. Henders

Grant W. Montgomery

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2009-10-11T00:00:00Z

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26886443

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19820699

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3135421

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