Targeted mutagenesis of the murine transferrin receptor-2 gene produces hemochromatosis (Q24533580)

5 July 2017

Targeted mutagenesis of the murine transferrin receptor-2 gene produces hemochromatosis (English)

1 reference

5 July 2017

Robert E Fleming

1

1 reference

5 July 2017

John R Ahmann

2

1 reference

5 July 2017

Mary C Migas

3

1 reference

5 July 2017

Abdul Waheed

4

1 reference

5 July 2017

H Phillip Koeffler

5

1 reference

5 July 2017

Hiroshi Kawabata

6

1 reference

5 July 2017

Robert S Britton

7

1 reference

5 July 2017

Bruce R Bacon

8

1 reference

5 July 2017

William S Sly

9

1 reference

5 July 2017

language of work or name

English

0 references

publication date

19 July 2002

1 reference

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

5 July 2017

1 reference

5 July 2017

99

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5 July 2017

10653-10658

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5 July 2017

16

1 reference

Autosomal-dominant hemochromatosis is associated with a mutation in the ferroportin (SLC11A3) gene

5 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=125003

Molecular cloning of transferrin receptor 2. A new member of the transferrin receptor-like family

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=125003

Transferrin receptor is necessary for development of erythrocytes and the nervous system

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=125003

A study of genes that may modulate the expression of hereditary hemochromatosis: transferrin receptor-1, ferroportin, ceruloplasmin, ferritin light and heavy chains, iron regulatory proteins (IRP)-1 and -2, and hepcidin

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=125003

Hemochromatosis caused by mutations in the iron-regulatory proteins ferroportin and H ferritin

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=125003

A new mouse liver-specific gene, encoding a protein homologous to human antimicrobial peptide hepcidin, is overexpressed during iron overload

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=125003

Comparison of the interactions of transferrin receptor and transferrin receptor 2 with transferrin and the hereditary hemochromatosis protein HFE

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=125003

Transferrin receptor 2-alpha supports cell growth both in iron-chelated cultured cells and in vivo

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=125003

Transferrin receptor 2: continued expression in mouse liver in the face of iron overload and in hereditary hemochromatosis

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=125003

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

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=125003

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

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=125003

Aceruloplasminemia: an inherited neurodegenerative disease with impairment of iron homeostasis

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=125003

HFE gene knockout produces mouse model of hereditary hemochromatosis

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=125003

Lack of hepcidin gene expression and severe tissue iron overload in upstream stimulatory factor 2 (USF2) knockout mice

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=125003

Expression of transferrin receptor 2 in normal and neoplastic hematopoietic cells

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=125003

New mutations inactivating transferrin receptor 2 in hemochromatosis type 3.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=125003

The gene TFR2 is mutated in a new type of haemochromatosis mapping to 7q22.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=125003

Targeting genes for self-excision in the germ line

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=125003

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

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=125003

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

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=125003

Regulators of iron balance in humans

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=125003

Haplotype analysis in Australian hemochromatosis patients: evidence for a predominant ancestral haplotype exclusively associated with hemochromatosis

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=125003

Efficient clearance of non-transferrin-bound iron by rat liver. Implications for hepatic iron loading in iron overload states

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=125003

Regulation of expression of murine transferrin receptor 2.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=125003

Transferrin receptor-2 gene and non-C282Y homozygous patients with hemochromatosis.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=125003

30 May 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.162360699

Transferrin receptor-2 (TFR2) mutation Y250X in Alabama Caucasian and African American subjects with and without primary iron overload

21 January 2018

1 reference

12 December 2020

Clinical and pathologic findings in hemochromatosis type 3 due to a novel mutation in transferrin receptor 2 gene

1 reference

12 December 2020

Evidence that iron stores regulate iron absorption--a setpoint theory

1 reference

12 December 2020

Iron overload in β2-microglobulin-deficient mice

1 reference

12 December 2020

New Food and Drug Administration-based oversight over genetic testing

1 reference

Crossref

https://api.crossref.org/works/10.1073%2FPNAS.162360699

7 January 2021

inferred from DOI database lookup

Autosomal-dominant hemochrom-atosis is associated with a mutation in the ferroportin (SLC11A3) gene

1 reference

Crossref

https://api.crossref.org/works/10.1073%2FPNAS.162360699

7 January 2021

inferred from DOI database lookup

Identifiers

DOI

10.1073/PNAS.162360699

1 reference

OpenCitations bibliographic resource ID

5 July 2017

0 references

4209579

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference

5 July 2017

1 reference