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Iron homeostasis: insights from genetics and animal models
scientific article published on 01 December 2000
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scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
11252750
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11252750%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 November 2019
review article
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Europe PubMed Central
title
Iron homeostasis: insights from genetics and animal models
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
11252750
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11252750%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 November 2019
author
Nancy Andrews
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ORCID Public Data File 2021
author name string
N C Andrews
series ordinal
1
1 reference
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Europe PubMed Central
PubMed ID
11252750
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11252750%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 November 2019
publication date
1 December 2000
1 reference
stated in
Europe PubMed Central
PubMed ID
11252750
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11252750%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 November 2019
published in
Nature Reviews Genetics
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Europe PubMed Central
PubMed ID
11252750
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11252750%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 November 2019
volume
1
1 reference
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Europe PubMed Central
PubMed ID
11252750
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11252750%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 November 2019
page(s)
208-217
1 reference
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Europe PubMed Central
PubMed ID
11252750
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11252750%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 November 2019
issue
3
1 reference
stated in
Europe PubMed Central
PubMed ID
11252750
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11252750%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 November 2019
exact match
https://scigraph.springernature.com/pub.10.1038/35042073
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Crossref
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7 January 2021
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Malabsorption and defective utilization of iron in three siblings
1 reference
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7 January 2021
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Microcytic anemia with iron malabsorption: an inherited disorder of iron metabolism
1 reference
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7 January 2021
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Ferrokinetics in the syndrome of familial hypoferremic microcytic anemia with iron malabsorption
1 reference
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7 January 2021
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An Iron-binding Component in Human Blood Plasma
1 reference
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Crossref
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7 January 2021
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The molecular defect in hypotransferrinemic mice
1 reference
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7 January 2021
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Regulation of the distribution of tissue iron. Lessons learned from the hypotransferrinemic mouse
1 reference
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7 January 2021
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Tissue iron loading and histopathological changes in hypotransferrinaemic mice
1 reference
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Crossref
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7 January 2021
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Congenital Atransferrinemia A Case Report and Review of the Literature
1 reference
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Crossref
reference URL
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7 January 2021
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Defect of Intestinal Mucosal Iron Uptake in Mice with Hereditary Microcytic Anemia
1 reference
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7 January 2021
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Characterization and partial purification of a ferrireductase from human duodenal microvillus membranes
1 reference
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1 reference
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Cloning and characterization of a mammalian proton-coupled metal-ion transporter
1 reference
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A thalassemia-like disorder in Belgrade laboratory rats
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7 January 2021
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Nramp2 is mutated in the anemic Belgrade (b) rat: evidence of a role for Nramp2 in endosomal iron transport.
1 reference
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Crossref
reference URL
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7 January 2021
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The iron transport protein NRAMP2 is an integral membrane glycoprotein that colocalizes with transferrin in recycling endosomes
1 reference
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Crossref
reference URL
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retrieved
7 January 2021
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malvolio, the Drosophila homologue of mouse NRAMP-1 (Bcg), is expressed in macrophages and in the nervous system and is required for normal taste behaviour.
1 reference
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Crossref
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7 January 2021
based on heuristic
inferred from DOI database lookup
Iron deficiency anaemia in newborn sla mice: a genetic defect of placental iron transport
1 reference
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Crossref
reference URL
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7 January 2021
based on heuristic
inferred from DOI database lookup
Hereditary defect of intestinal iron transport in mice with sex-linked anemia
1 reference
stated in
Crossref
reference URL
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7 January 2021
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inferred from DOI database lookup
Iron metabolism and absorption studies in the X-linked anaemia of mice
1 reference
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Crossref
reference URL
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7 January 2021
based on heuristic
inferred from DOI database lookup
Hephaestin, a ceruloplasmin homologue implicated in intestinal iron transport, is defective in the sla mouse
1 reference
stated in
Crossref
reference URL
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retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Positional cloning of zebrafish ferroportin1 identifies a conserved vertebrate iron exporter
1 reference
stated in
Crossref
reference URL
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7 January 2021
based on heuristic
inferred from DOI database lookup
A novel duodenal iron-regulated transporter, IREG1, implicated in the basolateral transfer of iron to the circulation
1 reference
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Crossref
reference URL
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7 January 2021
based on heuristic
inferred from DOI database lookup
A novel mammalian iron-regulated protein involved in intracellular iron metabolism
1 reference
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Crossref
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7 January 2021
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inferred from DOI database lookup
The ferritins: molecular properties, iron storage function and cellular regulation
1 reference
stated in
Crossref
reference URL
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7 January 2021
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Inactivation of the Friedreich ataxia mouse gene leads to early embryonic lethality without iron accumulation
1 reference
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Early embryonic lethality of H ferritin gene deletion in mice.
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A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis
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Crystal structure of the hemochromatosis protein HFE and characterization of its interaction with transferrin receptor
1 reference
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Association of the transferrin receptor in human placenta with HFE, the protein defective in hereditary hemochromatosis
1 reference
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Crossref
reference URL
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7 January 2021
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Crystal structure of the hereditary haemochromatosis protein HFE complexed with transferrin receptor
1 reference
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7 January 2021
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Experimental hemochromatosis due to MHC class I HFE deficiency: immune status and iron metabolism
1 reference
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7 January 2021
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HFE gene knockout produces mouse model of hereditary hemochromatosis
1 reference
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Crossref
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7 January 2021
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Genes that modify the hemochromatosis phenotype in mice
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7 January 2021
based on heuristic
inferred from DOI database lookup
Iron metabolism in copper-deficient swine
1 reference
stated in
Crossref
reference URL
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7 January 2021
based on heuristic
inferred from DOI database lookup
Aceruloplasminemia: an inherited neurodegenerative disease with impairment of iron homeostasis
1 reference
stated in
Crossref
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https://api.crossref.org/works/10.1038%2F35042073
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7 January 2021
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inferred from DOI database lookup
Aceruloplasminemia: molecular characterization of this disorder of iron metabolism
1 reference
stated in
Crossref
reference URL
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retrieved
7 January 2021
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inferred from DOI database lookup
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1 reference
stated in
Crossref
reference URL
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7 January 2021
based on heuristic
inferred from DOI database lookup
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1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35042073
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Targeted gene disruption reveals an essential role for ceruloplasmin in cellular iron efflux
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35042073
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7 January 2021
based on heuristic
inferred from DOI database lookup
Transferrin receptor is necessary for development of erythrocytes and the nervous system
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35042073
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
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1 reference
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Crossref
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7 January 2021
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The gene TFR2 is mutated in a new type of haemochromatosis mapping to 7q22.
1 reference
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Crossref
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7 January 2021
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1 reference
stated in
Crossref
reference URL
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retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
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1 reference
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Crossref
reference URL
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retrieved
7 January 2021
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inferred from DOI database lookup
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1 reference
stated in
Crossref
reference URL
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7 January 2021
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inferred from DOI database lookup
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1 reference
stated in
Crossref
reference URL
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7 January 2021
based on heuristic
inferred from DOI database lookup
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1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35042073
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
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1 reference
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Crossref
reference URL
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7 January 2021
based on heuristic
inferred from DOI database lookup
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1 reference
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Crossref
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7 January 2021
based on heuristic
inferred from DOI database lookup
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1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35042073
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Molecular pathogenesis of Friedreich ataxia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F35042073
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1038/35042073
1 reference
stated in
Europe PubMed Central
PubMed ID
11252750
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11252750%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 November 2019
Dimensions Publication ID
1007436683
0 references
PubMed ID
11252750
1 reference
stated in
Europe PubMed Central
PubMed ID
11252750
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11252750%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 November 2019
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