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A mouse model of juvenile hemochromatosis
scientific article
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scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
16075059
retrieved
4 July 2017
title
A mouse model of juvenile hemochromatosis
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
16075059
retrieved
4 July 2017
author
Nancy Andrews
series ordinal
5
1 reference
stated in
Europe PubMed Central
PubMed ID
16075059
retrieved
4 July 2017
Mark D Fleming
object named as
Mark D Fleming
series ordinal
4
0 references
Geraldine Pinkus
series ordinal
3
object named as
Geraldine S Pinkus
0 references
author name string
Franklin W Huang
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
16075059
retrieved
4 July 2017
Jack L Pinkus
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed ID
16075059
retrieved
4 July 2017
language of work or name
English
0 references
publication date
1 August 2005
1 reference
stated in
Europe PubMed Central
PubMed ID
16075059
retrieved
4 July 2017
published in
Journal of Clinical Investigation
1 reference
stated in
Europe PubMed Central
PubMed ID
16075059
retrieved
4 July 2017
volume
115
1 reference
stated in
Europe PubMed Central
PubMed ID
16075059
retrieved
4 July 2017
issue
8
1 reference
stated in
Europe PubMed Central
PubMed ID
16075059
retrieved
4 July 2017
page(s)
2187-2191
1 reference
stated in
Europe PubMed Central
PubMed ID
16075059
retrieved
4 July 2017
cites work
Hepcidin regulates cellular iron efflux by binding to ferroportin and inducing its internalization
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180543
retrieved
24 March 2017
Mutant antimicrobial peptide hepcidin is associated with severe juvenile hemochromatosis
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180543
retrieved
24 March 2017
Autosomal dominant reticuloendothelial iron overload associated with a 3-base pair deletion in the ferroportin 1 gene (SLC11A3)
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180543
retrieved
24 March 2017
Severe iron deficiency anemia in transgenic mice expressing liver hepcidin
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180543
retrieved
24 March 2017
Autosomal-dominant hemochromatosis is associated with a mutation in the ferroportin (SLC11A3) gene
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180543
retrieved
24 March 2017
A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180543
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24 March 2017
Transferrin receptor is necessary for development of erythrocytes and the nervous system
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180543
retrieved
24 March 2017
The iron exporter ferroportin/Slc40a1 is essential for iron homeostasis
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180543
retrieved
24 March 2017
In vitro functional analysis of human ferroportin (FPN) and hemochromatosis-associated FPN mutations
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180543
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24 March 2017
RGM and its receptor neogenin regulate neuronal survival
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180543
retrieved
24 March 2017
DRAGON: a member of the repulsive guidance molecule-related family of neuronal- and muscle-expressed membrane proteins is regulated by DRG11 and has neuronal adhesive properties
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180543
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24 March 2017
Repulsive guidance molecule (RGM) gene function is required for neural tube closure but not retinal topography in the mouse visual system
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180543
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24 March 2017
Mutations in HFE2 cause iron overload in chromosome 1q-linked juvenile hemochromatosis
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180543
retrieved
24 March 2017
RGM is a repulsive guidance molecule for retinal axons
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180543
retrieved
24 March 2017
A mutation in SLC11A3 is associated with autosomal dominant hemochromatosis
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180543
retrieved
24 March 2017
Positional cloning of zebrafish ferroportin1 identifies a conserved vertebrate iron exporter
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180543
retrieved
24 March 2017
The C282Y mutation causing hereditary hemochromatosis does not produce a null allele
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180543
retrieved
24 March 2017
Lack of hepcidin gene expression and severe tissue iron overload in upstream stimulatory factor 2 (USF2) knockout mice
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180543
retrieved
24 March 2017
Balancing acts: molecular control of mammalian iron metabolism
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180543
retrieved
7 April 2017
Spectrum of hemojuvelin gene mutations in 1q-linked juvenile hemochromatosis.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180543
retrieved
27 September 2017
A novel mutation in ferroportin1 is associated with haemochromatosis in a Solomon Islands patient
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180543
retrieved
27 September 2017
The gene TFR2 is mutated in a new type of haemochromatosis mapping to 7q22.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180543
retrieved
27 September 2017
Genes that modify the hemochromatosis phenotype in mice
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180543
retrieved
27 September 2017
Deregulation of proteins involved in iron metabolism in hepcidin-deficient mice.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180543
retrieved
29 November 2018
Hepatic and extrahepatic expression of the new iron regulatory protein hemojuvelin.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180543
retrieved
29 November 2018
Hepcidin is decreased in TFR2 hemochromatosis
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180543
retrieved
29 November 2018
The repulsive guidance molecule RGMa is involved in the formation of afferent connections in the dentate gyrus.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180543
retrieved
29 November 2018
Comparative analysis of mouse hepcidin 1 and 2 genes: evidence for different patterns of expression and co‐inducibility during iron overload1
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180543
retrieved
29 November 2018
Disrupted hepcidin regulation in HFE-associated haemochromatosis and the liver as a regulator of body iron homoeostasis.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180543
retrieved
29 November 2018
Dominant hemochromatosis due to N144H mutation of SLC11A3: clinical and biological characteristics
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180543
retrieved
29 November 2018
Mouse mutant embryos lacking huntingtin are rescued from lethality by wild-type extraembryonic tissues.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180543
retrieved
29 November 2018
The molecular defect in hypotransferrinemic mice
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/16075059
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1172/JCI25049
1 reference
stated in
Europe PubMed Central
PubMed ID
16075059
retrieved
4 July 2017
OpenCitations bibliographic resource ID
523588
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
523588
PMCID
1180543
1 reference
stated in
Europe PubMed Central
PubMed ID
16075059
retrieved
4 July 2017
PubMed ID
16075059
1 reference
stated in
Europe PubMed Central
PubMed ID
16075059
retrieved
4 July 2017
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