(Q33870226)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10728794%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

review article

1 reference

title

Haemochromatosis in the new millennium (English)

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10728794%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

2

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5 November 2019

author name string

L W Powell

series ordinal

1

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10728794%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

T R Yapp

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10728794%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

publication date

1 January 2000

1 reference

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5 November 2019

published in

Journal of Hepatology

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10728794%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

volume

32

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10728794%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

page(s)

48-62

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10728794%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

issue

1 Suppl

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10728794%20AND%20SRC:MED&resulttype=core&format=json

Value of hepatic iron measurements in early hemochromatosis and determination of the critical iron level associated with fibrosis

5 November 2019

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7 January 2021

Gluconate metabolism of Pasteurellapestis

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7 January 2021

Hemosiderosis in cirrhosis: a study of 447 native livers

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7 January 2021

End-stage liver disease without hemochromatosis associated with elevated hepatic iron index

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7 January 2021

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

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7 January 2021

The relationship between iron overload, clinical symptoms, and age in 410 patients with genetic hemochromatosis

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7 January 2021

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

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7 January 2021

Hemochromatosis in two young sisters. Case studies and a family survey

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7 January 2021

Juvenile idiopathic haemochromatosis: a life-threatening disorder presenting as hypogonadotropic hypogonadism

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7 January 2021

Juvenile hemochromatosis locus maps to chromosome 1q.

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7 January 2021

Perinatal hemochromatosis: entity or end result?

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7 January 2021

Recurrence of neonatal haemochromatosis in half sibs born of unaffected mothers

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7 January 2021

Association of HLA-A3 and HLA-B14 antigens with idiopathic haemochromatosis

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7 January 2021

Letter: HLA antigens in haemochromatosis.

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7 January 2021

Heredity of idiopathic haemochromatosis: a study of 106 families

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7 January 2021

Idiopathic haemochromatosis in the Australian population: HLA linkage and recessivity

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7 January 2021

HLA as a marker of the hemochromatosis gene in Sweden

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7 January 2021

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

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7 January 2021

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

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7 January 2021

Haemochromatosis and HLA-H.

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7 January 2021

Haemochromatosis and HLA-H

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7 January 2021

A simple genetic test identifies 90% of UK patients with haemochromatosis. The UK Haemochromatosis Consortium

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7 January 2021

Molecular medicine and hemochromatosis: at the crossroads

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7 January 2021

A novel mutation of HFE explains the classical phenotype of genetic hemochromatosis in a C282Y heterozygote

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7 January 2021

Prevalence of Hemochromatosis among 11,065 Presumably Healthy Blood Donors

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7 January 2021

Prevalence of haemochromatosis amongst asymptomatic Australians

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7 January 2021

Global prevalence of putative haemochromatosis mutations

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7 January 2021

Multicentric origin of hemochromatosis gene (HFE) mutations

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7 January 2021

Increased frequency of the haemochromatosis Cys282Tyr mutation in sporadic porphyria cutanea tarda

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7 January 2021

High prevalence of the His63Asp HFE mutation in italian patients with porphyria cutanea tarda

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7 January 2021

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

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7 January 2021

Spectrum of mutations in the HFE gene implicated in haemochromatosis and porphyria.

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7 January 2021

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

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7 January 2021

Iron and the sex difference in heart disease risk

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7 January 2021

Iron stores and the international variation in mortality from coronary artery disease

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7 January 2021

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

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7 January 2021

Hemochromatosis: association of severity of iron overload with genetic markers.

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7 January 2021

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

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7 January 2021

Prevalence of abnormal iron studies in heterozygotes for hereditary hemochromatosis: an analysis of 255 heterozygotes

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7 January 2021

Clinical and biochemical abnormalities in people heterozygous for hemochromatosis

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7 January 2021

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

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7 January 2021

Correlation between genotype and phenotype in hereditary hemochromatosis: analysis of 61 cases

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7 January 2021

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

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7 January 2021

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

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7 January 2021

Cloning, sequencing and characterization of the rat hereditary hemochromatosis promoter: comparison of the human, mouse and rat HFE promoter regions.

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7 January 2021

Uptake of iron by duodenal biopsy specimens from patients with iron-deficiency anaemia and primary haemochromatosis

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7 January 2021

A duodenal mucosal abnormality in the reduction of Fe(III) in patients with genetic haemochromatosis

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7 January 2021

Intestinal mucosal uptake of iron and iron retention in idiopathic haemochromatosis as evidence for a mucosal abnormality

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7 January 2021

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

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7 January 2021

The hereditary hemochromatosis protein, HFE, specifically regulates transferrin-mediated iron uptake in HeLa cells

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7 January 2021

Association of HFE protein with transferrin receptor in crypt enterocytes of human duodenum

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7 January 2021

Co-trafficking of HFE, a nonclassical major histocompatibility complex class I protein, with the transferrin receptor implies a role in intracellular iron regulation.

1 reference

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7 January 2021

Transferrin receptor is negatively modulated by the hemochromatosis protein HFE: implications for cellular iron homeostasis

1 reference

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7 January 2021

The transferrin receptor binding site on HFE, the class I MHC-related protein mutated in hereditary hemochromatosis

1 reference

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7 January 2021

https://api.crossref.org/works/10.1016%2FS0168-8278%2800%2980415-8

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7 January 2021

Cloning and characterization of a mammalian proton-coupled metal-ion transporter

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7 January 2021

Molecular control of vertebrate iron metabolism: mRNA-based regulatory circuits operated by iron, nitric oxide, and oxidative stress

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7 January 2021

Lack of hepatic transferrin receptor expression in hemochromatosis

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7 January 2021

Regulation of the hepatic transferrin receptor in hereditary hemochromatosis

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7 January 2021

Regulation of transferrin, transferrin receptor, and ferritin genes in human duodenum

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7 January 2021

Hephaestin, a ceruloplasmin homologue implicated in intestinal iron transport, is defective in the sla mouse

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https://api.crossref.org/works/10.1016%2FS0168-8278%2800%2980415-8

7 January 2021

Lipid peroxidation and associated hepatic organelle dysfunction in iron overload

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7 January 2021

Antioxidant status and lipid peroxidation in hereditary haemochromatosis

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7 January 2021

Hepatic stellate cell activation in genetic haemochromatosis. Lobular distribution, effect of increasing hepatic iron and response to phlebotomy.

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7 January 2021

Malondialdehyde and 4-hydroxynonenal protein adducts in plasma and liver of rats with iron overload

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7 January 2021

Proliferation of hepatic stellate cells is inhibited by phosphorylation of CREB on serine 133.

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7 January 2021

Excess iron induces hepatic oxidative stress and transforming growth factor beta1 in genetic hemochromatosis.

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7 January 2021

Alcohol and iron: a radical combination?

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7 January 2021

The significance of the 187G (H63D) mutation in hemochromatosis

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7 January 2021

Polymorphism in intron 4 of HFE may cause overestimation of C282Y homozygote prevalence in haemochromatosis

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7 January 2021

Genetic irony beyond haemochromatosis: clinical effects of HLA-H mutations

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7 January 2021

Compound heterozygotes for hemochromatosis gene mutations: may they help to understand the pathophysiology of the disease?

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7 January 2021

Haemochromatosis, HFE and genetic complexity

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7 January 2021

Crystal structure of the hemochromatosis protein HFE and characterization of its interaction with transferrin receptor

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7 January 2021

Hereditary hemochromatosis: effects of C282Y and H63D mutations on association with beta2-microglobulin, intracellular processing, and cell surface expression of the HFE protein in COS-7 cells

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7 January 2021

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

1 reference

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7 January 2021

Transferrin receptor distribution and regulation in the rat small intestine. Effect of iron stores and erythropoiesis

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7 January 2021

Transferrin receptors in the human gastrointestinal tract. Relationship to body iron stores.

1 reference

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7 January 2021

Genetic hemochromatosis

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7 January 2021

Noninvasive prediction of fibrosis in C282Y homozygous hemochromatosis

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2800%2980415-8

7 January 2021

Implications of genotyping of spouses to limit investigation of children in genetic hemochromatosis

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2800%2980415-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0168-8278%2800%2980415-8

7 January 2021

Long-term survival in patients with hereditary hemochromatosis

1 reference

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7 January 2021

Survival and causes of death in cirrhotic and in noncirrhotic patients with primary hemochromatosis

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7 January 2021

Familial iron overload with possible autosomal dominant inheritance

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7 January 2021

10.1016/S0168-8278(00)80415-8

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10728794%20AND%20SRC:MED&resulttype=core&format=json

release_a5uop2rjavgh5pe7dbhw73f3se

5 November 2019

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/a5uop2rjavgh5pe7dbhw73f3se

24 November 2022

mapped directly with Wikidata item

1 reference