Hereditary haemochromatosis: diagnosis and management in the gene era. (Q33603907)

28 July 2017

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title

Hereditary haemochromatosis: diagnosis and management in the gene era. (English)

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ORCID Public Data File 2021

28 July 2017

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author name string

J K Olynyk

series ordinal

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28 July 2017

publication date

1 April 1999

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28 July 2017

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28 July 2017

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28 July 2017

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28 July 2017

page(s)

73-80

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

28 July 2017

cites work

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https://api.crossref.org/works/10.1111%2FJ.1478-3231.1999.TB00014.X

Mutation analysis in hereditary hemochromatosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1478-3231.1999.TB00014.X

Haemochromatosis and HLA-H.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1478-3231.1999.TB00014.X

HFE gene knockout produces mouse model of hereditary hemochromatosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1478-3231.1999.TB00014.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1478-3231.1999.TB00014.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1478-3231.1999.TB00014.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1478-3231.1999.TB00014.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1478-3231.1999.TB00014.X

The hemochromatosis gene product complexes with the transferrin receptor and lowers its affinity for ligand binding

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1478-3231.1999.TB00014.X

Mutation analysis of the HFE gene associated with hereditary hemochromatosis in African Americans

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1478-3231.1999.TB00014.X

The hemochromatosis 845 G-->A and 187 C-->G mutations: prevalence in non-Caucasian populations

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1478-3231.1999.TB00014.X

Increased hepatic iron concentration in nonalcoholic steatohepatitis is associated with increased fibrosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1478-3231.1999.TB00014.X

The C282Y mutation in the haemochromatosis gene (HFE) and hepatitis C virus infection are independent cofactors for porphyria cutanea tarda in Australian patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1478-3231.1999.TB00014.X

Heterozygosity for hereditary hemochromatosis is associated with more fibrosis in chronic hepatitis C.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1478-3231.1999.TB00014.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1478-3231.1999.TB00014.X

Genotypic/phenotypic correlations in genetic hemochromatosis: evolution of diagnostic criteria.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1478-3231.1999.TB00014.X

The arthritis of hemochromatosis. A review of 25 cases with special reference to chondrocalcinosis, and a comparison with patients with primary hyperparathyroidism and controls

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1478-3231.1999.TB00014.X

Screening for genetic haemochromatosis in a rheumatology clinic

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1478-3231.1999.TB00014.X

Acetaldehyde-induced stimulation of collagen synthesis and gene expression is dependent on conditions of cell culture: studies with rat lipocytes and fibroblasts

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1478-3231.1999.TB00014.X

Oval cell numbers in human chronic liver diseases are directly related to disease severity.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1478-3231.1999.TB00014.X

Distribution of transferrin saturation in an Australian population: Relevance to the early diagnosis of hemochromatosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1478-3231.1999.TB00014.X

Dexamethasone inhibits the proliferation of hepatocytes and oval cells but not bile duct cells in rat liver

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1478-3231.1999.TB00014.X

Hereditary hemochromatosis: gene discovery and its implications for population-based screening

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1478-3231.1999.TB00014.X

Cost-effectiveness of screening for hereditary hemochromatosis

21 January 2018

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https://api.crossref.org/works/10.1111%2FJ.1478-3231.1999.TB00014.X

Blood pressure, stroke, and coronary heart disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1478-3231.1999.TB00014.X

10.1111/J.1478-3231.1999.TB00014.X

21 January 2018

Identifiers

DOI

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28 July 2017

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