(Q28585417)

English

Mechanism of increased iron absorption in murine model of hereditary hemochromatosis: increased duodenal expression of the iron transporter DMT1

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scholarly article

1 reference

PubMed publication ID

31 January 2017

Mechanism of increased iron absorption in murine model of hereditary hemochromatosis: increased duodenal expression of the iron transporter DMT1 (English)

1 reference

PubMed publication ID

31 January 2017

Homeostatic iron regulator

1 reference

GOA release 2020-03-11

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1 reference

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inferred from title

author name string

R. E. Fleming

1

1 reference

PubMed publication ID

31 January 2017

M. C. Migas

2

1 reference

PubMed publication ID

31 January 2017

X. Zhou

3

1 reference

PubMed publication ID

31 January 2017

J. Jiang

4

1 reference

PubMed publication ID

31 January 2017

R. S. Britton

5

1 reference

PubMed publication ID

31 January 2017

E. M. Brunt

6

1 reference

PubMed publication ID

31 January 2017

S. Tomatsu

7

1 reference

PubMed publication ID

31 January 2017

A. Waheed

8

1 reference

PubMed publication ID

31 January 2017

B. R. Bacon

9

1 reference

PubMed publication ID

31 January 2017

W. S. Sly

10

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PubMed publication ID

31 January 2017

language of work or name

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publication date

16 March 1999

1 reference

PubMed publication ID

31 January 2017

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

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PubMed publication ID

31 January 2017

96

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PubMed publication ID

31 January 2017

6

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PubMed publication ID

31 January 2017

3143–3148

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PubMed publication ID

31 January 2017

describes a project that uses

1 reference

Europe PubMed Central

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC15909/fullTextXML

based on heuristic

inferred from PubMed Central ID database lookup

Association of HFE protein with transferrin receptor in crypt enterocytes of human duodenum

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=15909

17 March 2017

The human Nramp2 gene: characterization of the gene structure, alternative splicing, promoter region and polymorphisms

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=15909

17 March 2017

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=15909

17 March 2017

HFE gene knockout produces mouse model of hereditary hemochromatosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=15909

17 March 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=15909

17 March 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=15909

17 March 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=15909

17 March 2017

THE ABSORPTION OF NONFERROUS METALS IN IRON DEFICIENCY.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=15909

29 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=15909

29 September 2017

Regulation of intestinal non-haem iron absorption

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=15909

29 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=15909

29 September 2017

Hemochromatosis: genetics and pathogenesis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=15909

29 September 2017

Iron regulatory elements (IREs): a family of mRNA non-coding sequences

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=15909

29 September 2017

Various rat adult tissues express only one major mRNA species from the glyceraldehyde-3-phosphate-dehydrogenase multigenic family

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=15909

29 September 2017

Primary hemochromatosis in children: report of three newly diagnosed cases and review of the pediatric literature

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=15909

29 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=15909

3 June 2018

Control of iron absorption.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=15909

3 June 2018

Blood lead concentrations in hereditary hemochromatosis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=15909

3 June 2018

Identification and characterization of a second mouse Nramp gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=15909

3 June 2018

Intestinal mucosal uptake of iron and iron retention in idiopathic haemochromatosis as evidence for a mucosal abnormality

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=15909

3 June 2018

Differential expression of transferrin receptor in duodenal mucosa in iron overload. Evidence for a site-specific defect in genetic hemochromatosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=15909

3 June 2018

Hereditary hemochromatosis. Phenotypic expression of the disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=15909

3 June 2018

Taurocholate transport by liver plasma membrane vesicles is not altered in cirrhotic rats.

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.96.6.3143

21 January 2018

Comparative effects of iron deficiency induced by bleeding and a low-iron diet on the intestinal absorptive interactions of iron, cobalt, manganese, zinc, lead and cadmium

1 reference

https://pubmed.ncbi.nlm.nih.gov/10077651

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Liver manganese in hemochromatosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/10077651

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Alteration in cobalt absorption in patients with disorders of iron metabolism

1 reference

https://pubmed.ncbi.nlm.nih.gov/10077651

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Iron absorption in idiopathic haemochromatosis and its measurement using a whole-body counter

1 reference

https://pubmed.ncbi.nlm.nih.gov/10077651

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prevalence of Hemochromatosis among 11,065 Presumably Healthy Blood Donors

1 reference

https://pubmed.ncbi.nlm.nih.gov/10077651

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Regulation of the hepatic transferrin receptor in hereditary hemochromatosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/10077651

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Reticuloendothelial iron stores and hereditary hemochromatosis: a paradox

1 reference

https://pubmed.ncbi.nlm.nih.gov/10077651

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary haemochromatosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/10077651

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Immunohistochemical evidence for a lack of ferritin in duodenal absorptive epithelial cells in idiopathic hemochromatosis.

1 reference

https://pubmed.ncbi.nlm.nih.gov/10077651

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Food iron absorption in idiopathic hemochromatosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/10077651

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/10077651

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Duodenal ferritin synthesis in genetic hemochromatosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/10077651

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Iron-responsive element-binding protein in hemochromatosis liver and intestine

1 reference

https://pubmed.ncbi.nlm.nih.gov/10077651

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Diphtheria toxin-mediated ablation of parietal cells in the stomach of transgenic mice

1 reference

https://pubmed.ncbi.nlm.nih.gov/10077651

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Inappropriately high iron regulatory protein activity in monocytes of patients with genetic hemochromatosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/10077651

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cellular expression and regulation of iron transport and storage proteins in genetic haemochromatosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/10077651

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary hemochromatosis--sometimes having a real complex can be a good thing

1 reference

https://pubmed.ncbi.nlm.nih.gov/10077651

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

INTESTINAL MUCOSAL MECHANISMS CONTROLLING IRON ABSORPTION

1 reference

https://pubmed.ncbi.nlm.nih.gov/10077651

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Diagnosis of hemochromatosis in young subjects: predictive accuracy of biochemical screening tests

1 reference

https://pubmed.ncbi.nlm.nih.gov/10077651

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1073/PNAS.96.6.3143

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1999PNAS...96.3143F

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OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

PMC publication ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

PubMed publication ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

ResearchGate publication ID

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