The molecular basis of ferroportin-linked hemochromatosis (Q33863312)

29 July 2017

The molecular basis of ferroportin-linked hemochromatosis (English)

1 reference

29 July 2017

Tomas Ganz

6

0 references

author name string

Ivana De Domenico

1

1 reference

29 July 2017

Diane McVey Ward

2

1 reference

29 July 2017

Elizabeta Nemeth

3

1 reference

29 July 2017

Michael B Vaughn

4

1 reference

29 July 2017

Giovanni Musci

5

1 reference

29 July 2017

Jerry Kaplan

7

1 reference

29 July 2017

language of work or name

English

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publication date

13 June 2005

1 reference

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

29 July 2017

1 reference

29 July 2017

102

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29 July 2017

25

1 reference

29 July 2017

8955-8960

1 reference

In vitro functional analysis of human ferroportin (FPN) and hemochromatosis-associated FPN mutations

29 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1157058

Iron homeostasis in neuronal cells: a role for IREG1

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1157058

Hepcidin regulates cellular iron efflux by binding to ferroportin and inducing its internalization

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1157058

Expression of hepcidin is down-regulated in TfR2 mutant mice manifesting a phenotype of hereditary hemochromatosis

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1157058

IL-6 mediates hypoferremia of inflammation by inducing the synthesis of the iron regulatory hormone hepcidin

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1157058

5 July 2018

The ferroportin disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1157058

A novel mutation in ferroportin1 is associated with haemochromatosis in a Solomon Islands patient

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1157058

Hepcidin, a key regulator of iron metabolism and mediator of anemia of inflammation

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1157058

C/EBPalpha regulates hepatic transcription of hepcidin, an antimicrobial peptide and regulator of iron metabolism. Cross-talk between C/EBP pathway and iron metabolism

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1157058

A valine deletion of ferroportin 1: a common mutation in hemochromastosis type 4

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1157058

Autosomal dominant reticuloendothelial iron overload associated with a 3-base pair deletion in the ferroportin 1 gene (SLC11A3)

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1157058

Novel mutation in ferroportin1 is associated with autosomal dominant hemochromatosis

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1157058

A novel duodenal iron-regulated transporter, IREG1, implicated in the basolateral transfer of iron to the circulation

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1157058

A novel mammalian iron-regulated protein involved in intracellular iron metabolism

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1157058

Positional cloning of zebrafish ferroportin1 identifies a conserved vertebrate iron exporter

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1157058

Hepcidin is decreased in TFR2 hemochromatosis

5 July 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0503804102

Hepcidin, a candidate modifier of the hemochromatosis phenotype in mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0503804102

Autosomal dominant hereditary hemochromatosis associated with a novel ferroportin mutation and unique clinical features

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0503804102

Autosomal dominant iron overload due to a novel mutation of ferroportin1 associated with parenchymal iron loading and cirrhosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0503804102

Molecular analyses of patients with hyperferritinemia and normal serum iron values reveal both L ferritin IRE and 3 new ferroportin (slc11A3) mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0503804102

Dominant hemochromatosis due to N144H mutation of SLC11A3: clinical and biological characteristics

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0503804102

Genetic hyperferritinaemia and reticuloendothelial iron overload associated with a three base pair deletion in the coding region of the ferroportin gene (SLC11A3).

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0503804102

Novel mutation in ferroportin 1 gene is associated with autosomal dominant iron overload

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0503804102

Hepcidin, a new iron regulatory peptide

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/15956209

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Genetic disorders of iron overload and the novel "ferroportin disease"

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/15956209

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1073/PNAS.0503804102

1 reference

29 July 2017

0 references

1 reference

29 July 2017

1 reference