Genetic and clinical heterogeneity of ferroportin disease. (Q50335665)

5 March 2018

title

Genetic and clinical heterogeneity of ferroportin disease. (English)

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5 March 2018

author

Daniela Pietra

8

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5 March 2018

author name string

L Cremonesi

1

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5 March 2018

Gian Luca Forni

2

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5 March 2018

Nadia Soriani

3

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5 March 2018

Martina Lamagna

4

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5 March 2018

Isabella Fermo

5

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5 March 2018

Filomena Daraio

6

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5 March 2018

Anna Galli

7

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5 March 2018

Luca Malcovati

9

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5 March 2018

Maurizio Ferrari

10

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5 March 2018

Clara Camaschella

11

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5 March 2018

Mario Cazzola

12

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5 March 2018

language of work or name

English

0 references

publication date

1 December 2005

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5 March 2018

British Journal of Haematology

published in

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5 March 2018

volume

131

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5 March 2018

page(s)

663-670

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issue

5

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5 March 2018

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

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2141.2005.05815.X

Hemochromatosis and iron-overload screening in a racially diverse population.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2141.2005.05815.X

The evaluation of hyperferritinemia: an updated strategy based on advances in detecting genetic abnormalities.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2141.2005.05815.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2141.2005.05815.X

Ferroportin 1 (SCL40A1) variant associated with iron overload in African-Americans

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2141.2005.05815.X

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/10.1111%2FJ.1365-2141.2005.05815.X

The molecular basis of ferroportin-linked hemochromatosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2141.2005.05815.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2141.2005.05815.X

Positional cloning of zebrafish ferroportin1 identifies a conserved vertebrate iron exporter

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2141.2005.05815.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2141.2005.05815.X

Ferroportin1 is required for normal iron cycling in zebrafish

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2141.2005.05815.X

Iron overload in Africans and African-Americans and a common mutation in the SCL40A1 (ferroportin 1) gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2141.2005.05815.X

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/10.1111%2FJ.1365-2141.2005.05815.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2141.2005.05815.X

Iron loading and erythrophagocytosis increase ferroportin 1 (FPN1) expression in J774 macrophages.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2141.2005.05815.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2141.2005.05815.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2141.2005.05815.X

Hepcidin, a putative mediator of anemia of inflammation, is a type II acute-phase protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2141.2005.05815.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2141.2005.05815.X

Hepcidin is decreased in TFR2 hemochromatosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2141.2005.05815.X

A mutation in SLC11A3 is associated with autosomal dominant hemochromatosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2141.2005.05815.X

Hepcidin in iron overload disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2141.2005.05815.X

21 January 2018

The ferroportin disease

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2141.2005.05815.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2141.2005.05815.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2141.2005.05815.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2141.2005.05815.X

Ferroportin disease due to the A77D mutation in Australia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2141.2005.05815.X

Novel mutation in ferroportin1 is associated with autosomal dominant hemochromatosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2141.2005.05815.X

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/10.1111%2FJ.1365-2141.2005.05815.X

Identification of ferroportin disease in the Indian subcontinent.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2141.2005.05815.X

10.1111/J.1365-2141.2005.05815.X

21 January 2018

Identifiers

DOI

1 reference

5 March 2018

release_sybzlhu53fd6dncs5fitwdoxya

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/sybzlhu53fd6dncs5fitwdoxya

mapped directly with Wikidata item

24 November 2022

based on heuristic

PubMed ID

16351644

1 reference

5 March 2018