The hereditary hemochromatosis gene (HFE): a MHC class I-like gene that functions in the regulation of iron homeostasis (Q33784079)

29 July 2017

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title

The hereditary hemochromatosis gene (HFE): a MHC class I-like gene that functions in the regulation of iron homeostasis (English)

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29 July 2017

Feder JN

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29 July 2017

publication date

1 January 1999

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29 July 2017

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29 July 2017

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29 July 2017

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29 July 2017

page(s)

175-185

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Hereditary hemochromatosis. Analysis of laboratory expression of the disease by genotype in 18 pedigrees

29 July 2017

cites work

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Crossref

https://api.crossref.org/works/10.1007%2FBF02786472

Transferrin receptors in the human gastrointestinal tract. Relationship to body iron stores.

21 January 2018

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12 December 2020

Localization of the hemochromatosis disease gene: linkage disequilibrium analysis using an American patient collection

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12 December 2020

Haemochromatosis and HLA-H.

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12 December 2020

The three-dimensional structure of HLA-B27 at 2.1 A resolution suggests a general mechanism for tight peptide binding to MHC

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12 December 2020

Localization of the hemochromatosis gene close to D6S105.

1 reference

12 December 2020

A 1.1-Mb transcript map of the hereditary hemochromatosis locus

1 reference

12 December 2020

Microcytic anaemia mice have a mutation in Nramp2, a candidate iron transporter gene

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12 December 2020

Global prevalence of putative haemochromatosis mutations

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12 December 2020

Regulation of intestinal iron absorption and mucosal iron kinetics in hereditary hemochromatosis

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12 December 2020

Mutations in the MHC class I-like candidate gene for hemochromatosis in French patients

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12 December 2020

The hemochromatosis 845 G-->A and 187 C-->G mutations: prevalence in non-Caucasian populations

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12 December 2020

The hemochromatosis founder mutation in HLA-H disrupts beta2-microglobulin interaction and cell surface expression

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12 December 2020

Prevalence of Hemochromatosis among 11,065 Presumably Healthy Blood Donors

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12 December 2020

HLA-H and Associated Proteins in Patients with Hemochromatosis

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12 December 2020

Comparative studies of the binding and growth-supportive ability of mammalian transferrins in human cells

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12 December 2020

The hemochromatosis gene product complexes with the transferrin receptor and lowers its affinity for ligand binding

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12 December 2020

A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis

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12 December 2020

Structure of the human class I histocompatibility antigen, HLA-A2

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12 December 2020

Hereditary hemochromatosis: effects of C282Y and H63D mutations on association with beta2-microglobulin, intracellular processing, and cell surface expression of the HFE protein in COS-7 cells

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12 December 2020

Association of HLA-A3 and HLA-B14 antigens with idiopathic haemochromatosis

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12 December 2020

Beta 2-microglobulin deficient mice lack CD4-8+ cytolytic T cells.

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12 December 2020

Regulation of MHC gene expression

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12 December 2020

The significance of transferrin for intestinal iron absorption.

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12 December 2020

Rapid diagnosis of the HLA-H gene Cys 282 Tyr mutation in hemochromatosis by polymerase chain reaction--a very rare mutation in the Chinese population

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12 December 2020

Mutation analysis in hereditary hemochromatosis

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12 December 2020

Haemochromatosis and HLA-H

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12 December 2020

Transferrin receptor mutation analysis in hereditary hemochromatosis patients

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12 December 2020

Construction and validation of yeast artificial chromosome contig maps by RecA-assisted restriction endonuclease cleavage

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12 December 2020

Association of the transferrin receptor in human placenta with HFE, the protein defective in hereditary hemochromatosis

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12 December 2020

A haplotype and linkage disequilibrium analysis of the hereditary hemochromatosis gene region

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12 December 2020

Crystal structure of the hemochromatosis protein HFE and characterization of its interaction with transferrin receptor

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12 December 2020

Identification of a mouse homolog for the human hereditary haemochromatosis candidate gene

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12 December 2020

Immunohistochemistry of HLA-H, the protein defective in patients with hereditary hemochromatosis, reveals unique pattern of expression in gastrointestinal tract

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12 December 2020

Iron overload in β2-microglobulin-deficient mice

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12 December 2020

The significance of the 187G (H63D) mutation in hemochromatosis

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12 December 2020

Haemochromatosis, HFE and genetic complexity

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12 December 2020

Prevalence of heterozygotes for hemochromatosis in the white population of the United States

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12 December 2020

Mutation analysis of the HLA-H gene in Italian hemochromatosis patients

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12 December 2020

HFE gene knockout produces mouse model of hereditary hemochromatosis

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12 December 2020

Clone-contig and STS maps of the hereditary hemochromatosis region on human chromosome 6p21.3-p22.

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12 December 2020

Cloning and characterization of a mammalian proton-coupled metal-ion transporter

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12 December 2020

Co-trafficking of HFE, a nonclassical major histocompatibility complex class I protein, with the transferrin receptor implies a role in intracellular iron regulation

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12 December 2020

Exon/intron organization and complete nucleotide sequence of an HLA gene

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12 December 2020

Identifiers

DOI

10.1007/BF02786472

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Dimensions Publication ID

29 July 2017

1020712083

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