HFE gene knockout produces mouse model of hereditary hemochromatosis (Q28263309)

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9 November 2019

title

HFE gene knockout produces mouse model of hereditary hemochromatosis (English)

1 reference

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9 November 2019

X Y Zhou

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9 November 2019

S Tomatsu

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9 November 2019

R E Fleming

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9 November 2019

A Waheed

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9 November 2019

J Jiang

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9 November 2019

Y Fei

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9 November 2019

D A Ruddy

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C E Prass

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9 November 2019

R C Schatzman

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9 November 2019

R O'Neill

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9 November 2019

R S Britton

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9 November 2019

B R Bacon

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9 November 2019

W S Sly

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9 November 2019

language of work or name

English

0 references

publication date

1 March 1998

1 reference

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

9 November 2019

published in

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volume

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issue

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9 November 2019

page(s)

2492-2497

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Association of the transferrin receptor in human placenta with HFE, the protein defective in hereditary hemochromatosis

9 November 2019

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19387

The hemochromatosis founder mutation in HLA-H disrupts beta2-microglobulin interaction and cell surface expression

20 March 2017

1 reference

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

20 March 2017

1 reference

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A mouse model for beta 0-thalassemia

20 March 2017

1 reference

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Heme oxygenase 1 is required for mammalian iron reutilization

20 March 2017

1 reference

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Hereditary hemochromatosis: Effects of C282Y and H63D mutations on association with β 2 -microglobulin, intracellular processing, and cell surface expression of the HFE protein in COS-7 cells

29 September 2017

1 reference

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Immunohistochemistry of HLA-H, the protein defective in patients with hereditary hemochromatosis, reveals unique pattern of expression in gastrointestinal tract

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19387

Mutation analysis of the HLA-H gene in Italian hemochromatosis patients

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19387

Defective iron homeostasis in beta 2-microglobulin knockout mice recapitulates hereditary hemochromatosis in man.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19387

beta2 knockout mice develop parenchymal iron overload: A putative role for class I genes of the major histocompatibility complex in iron metabolism

29 September 2017

1 reference

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Hemochromatosis: the genetic disorder of the twenty-first century

29 September 2017

1 reference

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Animal models in liver research: iron overload.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19387

Recent experiments with MHC knock-out mice: more questions than answers

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19387

Tissue distribution and clearance kinetics of non-transferrin-bound iron in the hypotransferrinemic mouse: a rodent model for hemochromatosis

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19387

Mutation analysis in hereditary hemochromatosis

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19387

Haemochromatosis and HLA-H.

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19387

Mouse model for the lysosomal disorder galactosialidosis and correction of the phenotype with overexpressing erythroid precursor cells

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19387

Genetic and phenotypic expression of hemochromatosis in Canadians

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19387

Hereditary hemochromatosis. Phenotypic expression of the disease

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19387

Identification of a mouse homolog for the human hereditary haemochromatosis candidate gene

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19387

Mutations in the MHC class I-like candidate gene for hemochromatosis in French patients

27 November 2018

1 reference

12 December 2020

Inappropriately high iron regulatory protein activity in monocytes of patients with genetic hemochromatosis

1 reference

12 December 2020

Transferrin receptors in hemochromatosis

1 reference

12 December 2020

Prevalence of Hemochromatosis among 11,065 Presumably Healthy Blood Donors

1 reference

12 December 2020

Iron overload in β2-microglobulin-deficient mice

1 reference

12 December 2020

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

1 reference

12 December 2020

Haemochromatosis: strike while the iron is hot

1 reference

12 December 2020

Haemochromatosis and HLA-H

1 reference

12 December 2020

Identifiers

DOI

10.1073/PNAS.95.5.2492

2 references

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9 November 2019

ADS bibcode

1998PNAS...95.2492Z

0 references

1 reference

2 references

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9 November 2019

PubMed publication ID

9482913

2 references

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9482913%20AND%20SRC:MED&resulttype=core&format=json