The flatiron mutation in mouse ferroportin acts as a dominant negative to cause ferroportin disease (Q24678328)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17289807%20AND%20SRC:MED&resulttype=core&format=json

25 December 2019

title

The flatiron mutation in mouse ferroportin acts as a dominant negative to cause ferroportin disease (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17289807%20AND%20SRC:MED&resulttype=core&format=json

25 December 2019

0 references

3

1 reference

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25 December 2019

Lee Niswander

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17289807%20AND%20SRC:MED&resulttype=core&format=json

25 December 2019

author name string

Irene E Zohn

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17289807%20AND%20SRC:MED&resulttype=core&format=json

25 December 2019

Ivana De Domenico

2

1 reference

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25 December 2019

Diane McVey Ward

4

1 reference

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25 December 2019

Jessica F Goodman

5

1 reference

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25 December 2019

Xiayun Liang

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17289807%20AND%20SRC:MED&resulttype=core&format=json

25 December 2019

Amaru J Sanchez

7

1 reference

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25 December 2019

Jerry Kaplan

9

1 reference

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25 December 2019

language of work or name

English

0 references

publication date

8 February 2007

1 reference

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25 December 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17289807%20AND%20SRC:MED&resulttype=core&format=json

25 December 2019

volume

109

1 reference

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25 December 2019

page(s)

4174-4180

1 reference

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25 December 2019

issue

10

1 reference

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The role of LIP5 and CHMP5 in multivesicular body formation and HIV-1 budding in mammalian cells

25 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=1885502

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

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1885502

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

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1885502

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

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1885502

A phenotype-based screen for embryonic lethal mutations in the mouse

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1885502

Impaired iron transport activity of ferroportin 1 in hereditary iron overload

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1885502

Presence of the iron exporter ferroportin at the plasma membrane of macrophages is enhanced by iron loading and down-regulated by hepcidin

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1885502

The iron exporter ferroportin/Slc40a1 is essential for iron homeostasis

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1885502

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

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1885502

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

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1885502

7 April 2017

The ferroportin disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1885502

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

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1885502

Positional cloning of zebrafish ferroportin1 identifies a conserved vertebrate iron exporter

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1885502

Analysis of mouse embryonic patterning and morphogenesis by forward genetics

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1885502

Evidence for the multimeric structure of ferroportin

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1885502

Hemochromatosis: genetics and pathophysiology

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1885502

Using genomewide mutagenesis screens to identify the genes required for neural tube closure in the mouse

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1885502

The molecular basis of ferroportin-linked hemochromatosis

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1885502

Functional consequences of ferroportin 1 mutations

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1885502

Hereditary hemochromatosis--a new look at an old disease

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1885502

Wild-type and mutant ferroportins do not form oligomers in transfected cells.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1885502

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

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1885502

Ferroportin is a monomer in vivo in mice.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1885502

Primary iron overload with inappropriate hepcidin expression in V162del ferroportin disease

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1885502

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

28 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/17289807

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

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

1 reference

Crossref

https://api.crossref.org/works/10.1182%2FBLOOD-2007-01-066068

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1182/BLOOD-2007-01-066068

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17289807%20AND%20SRC:MED&resulttype=core&format=json

25 December 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17289807%20AND%20SRC:MED&resulttype=core&format=json

25 December 2019

1 reference