Molecular aspects of iron absorption and HFE expression.
about
Pathophysiology of hereditary hemochromatosisGlobal transcriptional response to Hfe deficiency and dietary iron overload in mouse liver and duodenumRegulation of transferrin-mediated iron uptake by HFE, the protein defective in hereditary hemochromatosis.Iron uptake from plasma transferrin by the duodenum is impaired in the Hfe knockout mouse.Hemochromatosis. Common genes, uncommon illness?Erythroblast iron metabolism in sideroblastic and sideropenic states.Occult celiac disease prevents penetrance of hemochromatosis.HFE gene mutation and oxidative damage biomarkers in patients with myelodysplastic syndromes and its relation to transfusional iron overload: an observational cross-sectional studyIron, anaemia, and inflammatory bowel diseases.Levodopa Responsive Parkinsonism in Patients with Hemochromatosis: Case Presentation and Literature Review.Beta2-microglobulin-dependent bacterial clearance and survival during murine Klebsiella pneumoniae bacteremia.The risk of new-onset cancer associated with HFE C282Y and H63D mutations: evidence from 87,028 participantsHIV-associated sensory neuropathy: risk factors and genetics.Iron-related transcriptomic variations in CaCo-2 cells, an in vitro model of intestinal absorptive cells.Correction of the iron overload defect in beta-2-microglobulin knockout mice by lactoferrin abolishes their increased susceptibility to tuberculosis.Associations of common variants in HFE and TMPRSS6 with iron parameters are independent of serum hepcidin in a general population: a replication study.High prevalence of non-HFE gene-associated haemochromatosis in patients from southern Italy.Association between HFE polymorphisms and susceptibility to Alzheimer's disease: a meta-analysis of 22 studies including 4,365 cases and 8,652 controls.The hemochromatosis C282Y allele: a risk factor for hepatic veno-occlusive disease after hematopoietic stem cell transplantation.Therapeutic complications in a patient with high-risk acute lymphoblastic leukemia and undiagnosed hereditary hemochromatosis.Lack of association of primary iron overload and common HFE gene mutations with liver cirrhosis in adult Indian population.Liver transplantation normalizes serum hepcidin level and cures iron metabolism alterations in HFE hemochromatosis.
P2860
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P2860
Molecular aspects of iron absorption and HFE expression.
description
2001 nî lūn-bûn
@nan
2001 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2001年の論文
@ja
2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
@wuu
name
Molecular aspects of iron absorption and HFE expression.
@ast
Molecular aspects of iron absorption and HFE expression.
@en
Molecular aspects of iron absorption and HFE expression.
@nl
type
label
Molecular aspects of iron absorption and HFE expression.
@ast
Molecular aspects of iron absorption and HFE expression.
@en
Molecular aspects of iron absorption and HFE expression.
@nl
prefLabel
Molecular aspects of iron absorption and HFE expression.
@ast
Molecular aspects of iron absorption and HFE expression.
@en
Molecular aspects of iron absorption and HFE expression.
@nl
P2093
P356
P1433
P1476
Molecular aspects of iron absorption and HFE expression.
@en
P2093
R E Fleming
R S Britton
S Parkkila
P304
P356
10.1053/GAST.2001.29617
P407
P577
2001-12-01T00:00:00Z