(Q22001443)

Transferrin receptor

1 reference

Beta-2-microglobulin

1 reference

Transferrin

1 reference

homeostatic iron regulator

1 reference

A Waheed

1

A

Waheed

1 reference

6 February 2023

S Parkkila

2

S

Parkkila

1 reference

6 February 2023

J Saarnio

3

J

Saarnio

1 reference

6 February 2023

R E Fleming

4

R E

Fleming

1 reference

6 February 2023

X Y Zhou

5

X Y

Zhou

1 reference

6 February 2023

S Tomatsu

6

S

Tomatsu

1 reference

6 February 2023

R S Britton

7

R S

Britton

1 reference

6 February 2023

B R Bacon

8

B R

Bacon

1 reference

6 February 2023

W S Sly

9

W S

Proceedings of the National Academy of Sciences of the United States of America

Sly

1 reference

6 February 2023

language of work or name

English

0 references

publication date

16 February 1999

0 references

published in

0 references

volume

96

0 references

issue

4

0 references

page(s)

1579-84

0 references

cites work

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=15523

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

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=15523

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

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=15523

Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=15523

Immunohistochemistry of carbonic anhydrase isozyme IX (MN/CA IX) in human gut reveals polarized expression in the epithelial cells with the highest proliferative capacity

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=15523

HFE gene knockout produces mouse model of hereditary hemochromatosis

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=15523

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

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=15523

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

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=15523

Nramp2 is mutated in the anemic Belgrade (b) rat: evidence of a role for Nramp2 in endosomal iron transport.

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=15523

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

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=15523

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

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=15523

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

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=15523

Uptake of iron by duodenal biopsy specimens from patients with iron-deficiency anaemia and primary haemochromatosis

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=15523

Control of iron absorption.

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=15523

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

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=15523

Characterization of isolated duodenal epithelial cells along a crypt-villus axis in rats fed diets with different iron content.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=15523

Iron absorption from the whole diet in men: how effective is the regulation of iron absorption?

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=15523

Mutation analysis in hereditary hemochromatosis.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=15523

Haemochromatosis and HLA-H.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=15523

The endocytosis of transferrin by rat intestinal epithelial cells

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=15523

Hereditary hemochromatosis. Phenotypic expression of the disease

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=15523

Correlation between genotype and phenotype in hereditary hemochromatosis: analysis of 61 cases

30 May 2018

1 reference

Crossref

https://api.crossref.org/works/10.1073%2FPNAS.96.4.1579

INTESTINAL MUCOSAL MECHANISMS CONTROLLING IRON ABSORPTION

21 January 2018

1 reference

12 December 2020

Regulation of the transferrin-independent iron transport system in cultured cells

1 reference

12 December 2020

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

1 reference

12 December 2020

Hereditary haemochromatosis

1 reference

12 December 2020

Prevalence of Hemochromatosis among 11,065 Presumably Healthy Blood Donors

1 reference

12 December 2020

Haemochromatosis and HLA-H

1 reference

12 December 2020

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

1 reference

12 December 2020

How little we know about the absorption of iron

1 reference

12 December 2020

Ethnic differences in the HFE codon 282 (Cys/Tyr) polymorphism

1 reference

12 December 2020

Predominance of the HLA-H Cys282Tyr mutation in Austrian patients with genetic haemochromatosis

1 reference

12 December 2020

Iron is hot: an update on the pathophysiology of hemochromatosis

1 reference

12 December 2020

Experience with isotonic 2.2% glycine as distension medium for hysteroscopic endomyometrial resection

1 reference

Crossref

https://api.crossref.org/works/10.1073%2FPNAS.96.4.1579

7 January 2021

inferred from DOI database lookup

Identifiers

DOI

10.1073/PNAS.96.4.1579

1 reference

4418414

ADS bibcode

1999PNAS...96.1579W

0 references

4418414

1 reference

1 reference

1 reference