Mouse strain differences determine severity of iron accumulation in Hfe knockout model of hereditary hemochromatosis (Q34486746)

2 August 2017

title

Mouse strain differences determine severity of iron accumulation in Hfe knockout model of hereditary hemochromatosis (English)

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2 August 2017

5

E M Brunt

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2 August 2017

R E Fleming

1

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2 August 2017

C C Holden

2

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2 August 2017

S Tomatsu

3

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2 August 2017

A Waheed

4

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2 August 2017

R S Britton

6

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2 August 2017

B R Bacon

7

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2 August 2017

D C Roopenian

8

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2 August 2017

W S Sly

9

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2 August 2017

language of work or name

English

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publication date

1 February 2001

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Proceedings of the National Academy of Sciences of the United States of America

2 August 2017

published in

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2 August 2017

volume

98

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2 August 2017

issue

5

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2 August 2017

page(s)

2707-2711

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EASL International Consensus Conference on Haemochromatosis

2 August 2017

cites work

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The effect of HFE genotypes on measurements of iron overload in patients attending a health appraisal clinic

6 July 2018

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Histological evaluation of iron in liver biopsies: relationship to HFE mutations.

6 July 2018

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Genes that modify the hemochromatosis phenotype in mice

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6 July 2018

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Effects of HFE C282Y and H63D polymorphisms and polygenic background on iron stores in a large community sample of twins

6 July 2018

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Experimental hemochromatosis due to MHC class I HFE deficiency: immune status and iron metabolism

6 July 2018

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A population-based study of the clinical expression of the hemochromatosis gene

6 July 2018

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The C282Y mutation causing hereditary hemochromatosis does not produce a null allele

6 July 2018

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A genetic developmental model of iron deficiency: biological aspects

6 July 2018

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Mechanism of increased iron absorption in murine model of hereditary hemochromatosis: increased duodenal expression of the iron transporter DMT1

6 July 2018

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HFE gene knockout produces mouse model of hereditary hemochromatosis

6 July 2018

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

6 July 2018

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Evidence for heterogeneity in hereditary hemochromatosis. Evaluation of 174 persons in nine families

6 July 2018

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6 July 2018

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Expression of HLA-linked hemochromatosis in subjects homozygous or heterozygous for the C282Y mutation

21 January 2018

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Population-based screening for hemochromatosis using phenotypic and DNA testing among employees of health maintenance organizations in Springfield, Missouri

21 January 2018

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HFE genotype in patients with hemochromatosis and other liver diseases.

21 January 2018

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Hemochromatosis: association of severity of iron overload with genetic markers

21 January 2018

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Concordance of iron storage in siblings with genetic hemochromatosis: evidence for a predominantly genetic effect on iron storage

21 January 2018

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Population screening for hemochromatosis: a comparison of unbound iron-binding capacity, transferrin saturation, and C282Y genotyping in 5,211 voluntary blood donors

27 October 2018

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12 December 2020

Genetic variation of basal iron status, ferritin and iron regulatory protein in mice: potential for modulation of oxidative stress

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12 December 2020

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12 December 2020

Reticuloendothelial iron stores and hereditary hemochromatosis: a paradox

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https://pubmed.ncbi.nlm.nih.gov/11226304

12 December 2020

Dissociation between tissue iron concentrations and transferrin saturation among inbred mouse strains

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https://pubmed.ncbi.nlm.nih.gov/11226304

12 December 2020

Genetic and clinical description of hemochromatosis probands and heterozygotes: evidence that multiple genes linked to the major histocompatibility complex are responsible for hemochromatosis

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https://pubmed.ncbi.nlm.nih.gov/11226304

12 December 2020

Molecular medicine and hemochromatosis: at the crossroads

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12 December 2020

Linkage disequilibrium analysis in Australian haemochromatosis patients indicates bipartite association with clinical expression

1 reference

https://pubmed.ncbi.nlm.nih.gov/11226304

12 December 2020

Identifiers

DOI

10.1073/PNAS.051630898

1 reference

2 August 2017

0 references

1 reference

2 August 2017

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