Hereditary hemochromatosis and transferrin receptor 2
Keywords: TfR2; HFE; Hepcidin; Hemojuvelin; BMP; Ferroportin;
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Research ReportBrain transcriptome perturbations in the Hfeâ/â mouse model of genetic iron loading
Keywords: Iron; Hemochromatosis; HFE; Microarray; Mouse model;
Uptake and release of metal ions by transferrin and interaction with receptor 1
Keywords: T; apotransferrin; TC; the C-lobe of apotransferrin in an unknown state of charge and protonation; TCFe; C-site-loaded monoferric transferrin; TFe2; TAl2, TGa2, TCo2, TBi2, metal-saturated transferrins; Ur; uranyl (UO22+); TUr2; uranyl-saturated transferr
Iron stores and HFE genotypes are not related to increased risk of first-time myocardial infarction
Keywords: Myocardial Infarction; Iron; Ferritin; HFE; Prospective;
Plasma ferritin levels, genetic variations in HFE gene, and coronary heart disease in Chinese: A case-control study
Keywords: Coronary heart disease; HFE; Ferritin;
Polymorphisms of hemochromatosis, and alpha-1 antitrypsin genes in Egyptian HCV patients with and without hepatocellular carcinoma
Keywords: A1AT; alpha-1 antitrypsin; AFP; alpha-fetoprotein; ALT; alanine aminotransferase; AST; aspartate aminotransferase; CLD; chronic liver disease; ER; endoplasmic reticulum; HBsAg; hepatitis B surface antigen; HCC; hepatocellular carcinoma; HCV; hepatitis C v
Haemochromatosis
Keywords: ferroportin; haemochromatosis; hepcidin; HFE; iron; liver
Hereditary hemochromatosis: Mutations in genes involved in iron homeostasis in Brazilian patients
Keywords: Hemochromatosis; HFE; Primary iron overload; Sequencing
Gastrins, iron homeostasis and colorectal cancer
Keywords: CCK; cholecystokinin; CRC; colorectal carcinoma; Dcytb; a duodenal cytochrome b-like ferric reductase; DMT-1; divalent metal transporter 1; ECL; enterochromaffin-like; Fpn; ferroportin; Ggly; glycine-extended gastrin17; Gamide; amidated gastrin17; HFE; th
Research ArticleHemochromatosis gene and nonalcoholic fatty liver disease: A systematic review and meta-analysis
Keywords: Iron; Steatosis; Hemochromatosis; Case-control studies; Meta-analysis; NALFD; nonalcoholic fatty liver disease; C282Y; cysteine-to-tyrosine substitution at the amino acid 282; H63D; histidine-to-aspartate change at the amino acid 63; HFE; hemochromatosis
ER stress impairs MHC Class I surface expression and increases susceptibility of thyroid cells to NK-mediated cytotoxicity
Keywords: BiP; binding protein (GRP78); ER; endoplasmic reticulum; ERAD; ER associated degradation; GRP94; glucose regulated protein 94; HFE; hereditary hemochromatosis protein; HLA-I; human leukocyte antigen-I; IFN-γ; interferon-γ; IL-2; interleukin-2; MHC-I; ma
Gene-Air Pollution Interaction and Cardiovascular Disease: A Review
Keywords: ACE; angiotensin-I converting enzyme; ADRB2; β2-adrenergic receptor; AGT; angiotensinogen; AGTR1; type 1 angiotensin II receptor; ALOX15; arachidonate 15-lipoxygenase; APOE; apolipoprotein E; BC; black carbon; BP; blood pressure; CRP; C-reactive protein;
HFE polymorphisms affect cellular glutamate regulation
Keywords: HFE; Iron; Glutamate
Expression of the HFE allelic variant H63D in SH-SY5Y cells affects tau phosphorylation at serine residues
Keywords: HFE; Iron; Tau; Phosphorylation; GSK-3β; Oxidative stress; Alzheimer's disease
Genetic and metabolic factors are associated with increased hepatic iron stores in a selected population of p.Cys282Tyr heterozygotes
Keywords: Hemochromatosis; HFE; Transferrin saturation; Hepatic iron overload; Steatosis
HFE gene mutations in patients with primary iron overload: Is there a significant improvement in molecular diagnosis yield with HFE sequencing?
Keywords: Hemochromatosis; HFE; Sequencing; Primary iron overload; Molecular modeling
Les gènes des hémochromatoses
Keywords: Surcharge en fer; Hémochromatose génétique; HFE; Récepteur à la transferrine; Hepcidine; Bone morphogenic proteins; Hémojuvéline; FerroportineIron overload; Genetic hemochromatosis; HFE; Type 2 transferrin receptor; Hepcidin; Bone morphogenic proteins; He
Hemochromatosis (HFE) genotype and atherosclerosis: Increased susceptibility to iron-induced vascular damage in C282Y carriers?
Keywords: C282Y mutation; HFE; Iron; Atherosclerosis
Prolyl-peptidyl isomerase, Pin1, phosphorylation is compromised in association with the expression of the HFE polymorphic allele, H63D
Keywords: Pin1; Iron; HFE; Oxidative stress; Phosphorylation; Neurodegenerative disease; Transgenic mice
Research ArticleBeta-globin mutations are associated with parenchymal siderosis and fibrosis in patients with non-alcoholic fatty liver disease
Keywords: AAT; alpha1-antitrypsin; ALT; alanine transaminase; BMI; body mass index; CI; confidence interval; FPN; ferroportin-1; GGT; gamma-glutamyl-transferase; Hb; hemoglobin; HDL; high density lipoprotein; HFE; hemochromatosis gene; HOMA-IR; homeostasis metaboli
Surcharges héréditaires en fer
Keywords: Surcharge en fer; Hémochromatose; HFE; Hepcidine; Ferroportine; Hémojuvéline; Fer non lié à la transferrineIron overload; Haemochromatosis; HFE; Hepcidin; Ferroportin; Haemojuvelin; Transferrin receptor; Non-transferrin bound iron
BMP6 Treatment Compensates for the Molecular Defect and Ameliorates Hemochromatosis in Hfe Knockout Mice
Keywords: Hemochromatosis; HFE; Bone Morphogenetic ProteinBMP, bone morphogenetic protein; BMP6 Ab, BMP6 antibody; CHB, Children's Hospital Boston; Hamp, Hepcidin mRNA; Hfe−/−, Hfe knockout mice; Hfe Tg, Hfe transgenic mice; HJV, hemojuvelin; MGH, Massachusetts Gen
Hereditary Hemochromatosis: Pathogenesis, Diagnosis, and Treatment
Keywords: Iron Metabolism; Hereditary Disorders; Micronutrients; Hepcidin; HFE; BMP; bone morphogenic protein; FPN; ferroportin; HAMP; hepcidin gene; HJV; hemojuvelin; RGM; repulsive guidance molecule; TfR; transferrin receptor; TS; transferrin saturation;
Predicting Iron Overload in Hyperferritinemia
Keywords: HFE; hemochromatosis gene product; HH; hereditary hemochromatosis; HIC; hepatic iron concentration; TRS; transferrin saturation;
CAT53 and HFE alleles in Alzheimer's disease: A putative protective role of the C282Y HFE mutation
Keywords: CAT53; HFE; C282Y; MHC; Alzheimer's disease;
A novel HFE mutation (c.del478) results in nonsense-mediated decay of the mutant transcript in a hemochromatosis patient
Keywords: Hemochromatosis; HFE; c.del478; Nonsense-mediated decay; Haploinsufficiency;
Knockdown of β2-microglobulin perturbs the subcellular distribution of HFE and hepcidin
Keywords: β2-microglobulin; HFE; Hepcidin; Hereditary Haemochromatosis; Late endosomes
Cancer cell iron metabolism and the development of potent iron chelators as anti-tumour agents
Keywords: 311; 2-hydroxy-1-naphthylaldehyde isonicotinoyl hydrazone; BpT; 2-benzoylpyridine thiosemicarbazone; CDK; cyclin-dependent kinase; CDKi; cyclin-dependent kinase inhibitor; DFO; desferrioxamine; DMT1; divalent metal ion transporter 1; DpT; di-2-pyridylketo
Mutations in the hemochromatosis gene and the clinical outcome of multiple sclerosis
Keywords: Multiple sclerosis; Genetics; Outcome; HFE; Iron
A novel (Leu183Pro-)mutation in the HFE-gene co-inherited with the Cys282Tyr mutation in two unrelated Dutch hemochromatosis patients
Keywords: Hemochromatosis; HFE; Iron; Genotype;
Iron metabolism in the mononuclear phagocyte system
Keywords: Mononuclear phagocyte system; CD163; Natural resistance-associated macrophage protein 1; Divalent metal transporter 1; HFE; Ferroportin 1; Hepcidin
Current approach to hemochromatosis
Keywords: Hemochromatosis; Iron overload; HFE; Hepcidin; Hemojuvelin; Ferroportin; Transferrin receptor 2; Transferrin; Saturation ferritin; Venesection
Root Cause Analysis
Keywords: ACR; American College of Radiology; HFE; human factors engineering; JCAHO; Joint Commission on the Accreditation of Healthcare Organizations; RCA; root cause analysis; SAC; Safety Assessment Code;
Hepcidin, transferrin (exon 7), and hemochromatosis genotyping suggests that haplotype block analysis is the best strategy for predicting iron deficiency phenotype in women
Keywords: Hepcidin; HAMP; Transferrin; HFE; Haplotype; Iron deficiency; Iron deficiency anemia; Women
Overexpression of HFE in HepG2 cells reveals differences in intracellular distribution and co-localization of wt- and mutated forms
Keywords: HFE; TFR1; Liver; Iron; UPR
Hexachlorobenzene stimulates uroporphyria in low affinity AHR mice without increasing CYP1A2
Keywords: AHR; aryl hydrocarbon receptor; ALA; 5-aminolevulinate; CYP; cytochrome P450; HCB; hexachlorobenzene; Fe; iron; HFE; protein regulating iron uptake by intestinal cells and release by Kupffer cells; PCT; porphyria cutanea tarda; TCDD; 2,3,7,8-tetrachloro-p
Hepatic iron metabolism gene expression profiles in HFE associated Hereditary Hemochromatosis
Keywords: HFE; Hepcidin; Hemojuvelin; TfR2; Ferroportin
The Hereditary Hemochromatosis protein HFE and its chaperone β2-microglobulin localise predominantly to the endosomal-recycling compartment
Keywords: HFE; β2-Microglobulin; Hereditary Hemochromatosis; Transferrin; Endosomal-recycling compartment; Rab11
African Americans at Risk for Increased Iron Stores or Liver Disease
Keywords: African Americans; Serum ferritin; Transferrin saturation; HFE; Liver disease; Increased iron stores;
Iron dysregulation in Alzheimer's disease: Multimodal brain permeable iron chelating drugs, possessing neuroprotective-neurorescue and amyloid precursor protein-processing regulatory activities as therapeutic agents
Keywords: AD; Alzheimer's disease; ALS; amyotrophic lateral sclerosis; APP; amyloid precursor protein; BDNF; brain-derived neurotrophic factor; Aβ; beta-amyloid peptide; β-CTF; beta-C-terminal fragment; EGCG; epigallocatechin gallate; DFO; desferrioxamine; ERK1/2
Mutations du gène HFE chez des β-thalassémiques majeurs tunisiens et surcharge en fer
Keywords: Hémochromatose; Gènes; HFE; TunisiensHemochromatosis; Genes; HFE; Tunisians
Magnetic resonance imaging to identify classic and nonclassic forms of ferroportin disease
Keywords: Iron overload; Hemochromatosis; Ferroportin; Magnetic resonance imaging; HFE
Haemochromatosis gene (HFE) mutations in viral-associated neoplasia: Linkage to cervical cancer
Keywords: C282Y; Cervical carcinoma; H63D; HFE; HPV; Viral neoplasia
Hepcidin generated by hepatoma cells inhibits iron export from co-cultured THP1 monocytes
Keywords: Ferroportin; Hemochromatosis; Anemia of chronic disease; HFE; Hemojuvelin
Revisiting Hereditary Hemochromatosis: Current Concepts and Progress
Keywords: Hemochromatosis; Iron overload; HFE; C282Y
Les hémochromatoses héréditaires : partie II. L'hémochromatose héréditaire liée au HFE (HFE1)
Keywords: Hémochromatose; HFE; HFE1; Hemochromatosis; HFE; HFE1;
Hereditary hemochromatosis
Keywords: Iron overload; HFE; Hepcidin; Ferroportin; Hemojuvelin; Transferrin receptor 2
A compartmental model of iron regulation in the mouse
Keywords: Iron regulation; Hepcidin; Ferroportin; HFE; Hemochromatosis;
Anesthetic and non-anesthetic effects on interfacial lipids around an ion channel
Keywords: DMPC; dimyristoylphosphatidylcholine; gA; gramicidin A; HFE; hexafluoroethane; MD; molecular dynamics; NAMD program; not-another-molecular-dynamic program; Molecular dynamics simulations; Mechanisms of general anesthesia; Anesthetics; Non-anesthetics; Ord
Autosomal dominant hereditary hemochromatosis associated with a novel ferroportin mutation and unique clinical features
Keywords: Hemochromatosis; HFE; Iron; Transferrin saturation; Hepatocyte; Macrophage; Liver;