Molecular and clinical correlates in iron overload associated with mutations in ferroportin. (Q43082361)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16885049%20AND%20SRC:MED&resulttype=core&format=json

28 December 2019

title

Molecular and clinical correlates in iron overload associated with mutations in ferroportin (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16885049%20AND%20SRC:MED&resulttype=core&format=json

28 December 2019

1 reference

4

Tomas Ganz

1 reference

13 November 2017

Ivana De Domenico

1

1 reference

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28 December 2019

Diane McVey Ward

2

1 reference

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28 December 2019

Elizabeta Nemeth

3

1 reference

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28 December 2019

Elena Corradini

5

1 reference

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28 December 2019

Francesca Ferrara

6

1 reference

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28 December 2019

Giovanni Musci

7

1 reference

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28 December 2019

Antonello Pietrangelo

8

1 reference

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28 December 2019

Jerry Kaplan

9

1 reference

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28 December 2019

Tomas Ganz

4

1 reference

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28 December 2019

publication date

1 August 2006

1 reference

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28 December 2019

1 reference

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28 December 2019

volume

91

1 reference

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28 December 2019

issue

8

1 reference

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28 December 2019

page(s)

1092-1095

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16885049%20AND%20SRC:MED&resulttype=core&format=json

The iron exporter ferroportin/Slc40a1 is essential for iron homeostasis

28 December 2019

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3718284

The molecular basis of ferroportin-linked hemochromatosis

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3718284

Functional consequences of ferroportin 1 mutations

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3718284

Resistance to hepcidin is conferred by hemochromatosis-associated mutations of ferroportin

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3718284

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

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3718284

Iron release from macrophages after erythrophagocytosis is up-regulated by ferroportin 1 overexpression and down-regulated by hepcidin

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3718284

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

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3718284

25 May 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=3718284

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

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3718284

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

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3718284

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

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3718284

Novel mutation in ferroportin1 is associated with autosomal dominant hemochromatosis

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3718284

Autosomal-dominant hemochromatosis is associated with a mutation in the ferroportin (SLC11A3) gene

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3718284

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

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3718284

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

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3718284

Positional cloning of zebrafish ferroportin1 identifies a conserved vertebrate iron exporter

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3718284

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

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3718284

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

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3718284

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

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3718284

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

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3718284

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

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3718284

Lack of enterocyte iron accumulation in the ferroportin disease

15 August 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/16885049

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Chediak-Higashi syndrome is not due to a defect in microtubule-based lysosomal mobility

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/16885049

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Hereditary hemochromatosis in adults without pathogenic mutations in the hemochromatosis gene

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/16885049

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16885049%20AND%20SRC:MED&resulttype=core&format=json

28 December 2019

1 reference