Measurement of serum hepcidin-25 levels as a potential test for diagnosing hemochromatosis and related disorders (Q84373935)

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5 February 2020

title

Measurement of serum hepcidin-25 levels as a potential test for diagnosing hemochromatosis and related disorders (English)

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3

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author name string

Yoshibumi Kaneko

1

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Hiroaki Miyajima

2

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5 February 2020

Naohisa Tomosugi

4

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5 February 2020

Hisao Hayashi

5

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5 February 2020

Natsuko Morotomi

6

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Ken-ichi Tsuchida

7

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5 February 2020

Takaaki Ikeda

8

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Akihisa Ishikawa

9

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Yusuke Ota

10

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5 February 2020

Shinya Wakusawa

11

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Kentaro Yoshioka

12

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Satoshi Kono

13

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Sara Pelucchi

14

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Ai Hattori

15

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Yasuaki Tatsumi

16

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Toshihide Okada

17

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Masakazu Yamagishi

18

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publication date

9 June 2010

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Journal of Gastroenterology

5 February 2020

published in

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volume

45

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issue

11

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page(s)

1163-1171

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Hepcidin in iron overload disorders

5 February 2020

cites work

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12 December 2020

Mutant antimicrobial peptide hepcidin is associated with severe juvenile hemochromatosis

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12 December 2020

Serum prohepcidin levels correlate with hepatic iron stores in chronic hepatitis C patients

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12 December 2020

Hepcidin is decreased in TFR2 hemochromatosis

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12 December 2020

A mutation in SLC11A3 is associated with autosomal dominant hemochromatosis

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12 December 2020

Liver hepcidin mRNA correlates with iron stores, but not inflammation, in patients with chronic hepatitis C.

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12 December 2020

Regulation of transferrin receptor 2 protein levels by transferrin

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12 December 2020

Global prevalence of putative haemochromatosis mutations

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12 December 2020

Simple and sensitive quantification of bioactive peptides in biological matrices using liquid chromatography/selected reaction monitoring mass spectrometry coupled with trichloroacetic acid clean-up

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12 December 2020

Primary iron overload with inappropriate hepcidin expression in V162del ferroportin disease

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12 December 2020

Hepcidin, a putative mediator of anemia of inflammation, is a type II acute-phase protein

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12 December 2020

Disrupted hepcidin regulation in HFE-associated haemochromatosis and the liver as a regulator of body iron homoeostasis.

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12 December 2020

Iron overload and cofactors with special reference to alcohol, hepatitis C virus infection and steatosis/insulin resistance

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12 December 2020

Iron chelation therapy in aceruloplasminaemia: study of a patient with a novel missense mutation.

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12 December 2020

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

1 reference

12 December 2020

Familial apoceruloplasmin deficiency associated with blepharospasm and retinal degeneration

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12 December 2020

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

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12 December 2020

Two novel mutations, L490R and V561X, of the transferrin receptor 2 gene in Japanese patients with hemochromatosis.

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12 December 2020

Novel mutation in ferroportin 1 gene is associated with autosomal dominant iron overload

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12 December 2020

In vitro functional analysis of human ferroportin (FPN) and hemochromatosis-associated FPN mutations

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12 December 2020

Immunoassay for human serum hepcidin

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12 December 2020

Iron and chronic viral hepatitis

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12 December 2020

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

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12 December 2020

Serum hepcidin level and erythropoietic activity after hematopoietic stem cell transplantation

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12 December 2020

Resistance to hepcidin is conferred by hemochromatosis-associated mutations of ferroportin

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12 December 2020

Suppression of hepcidin during anemia requires erythropoietic activity

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12 December 2020

Serum hepcidin levels are innately low in HFE-related haemochromatosis but differ between C282Y-homozygotes with elevated and normal ferritin levels

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12 December 2020

Iron overload in the Asian community.

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12 December 2020

A Japanese family with ferroportin disease caused by a novel mutation of SLC40A1 gene: hyperferritinemia associated with a relatively low transferrin saturation of iron

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12 December 2020

LEAP-1, a novel highly disulfide-bonded human peptide, exhibits antimicrobial activity

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12 December 2020

Quantitation of hepcidin from human and mouse serum using liquid chromatography tandem mass spectrometry

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12 December 2020

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

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12 December 2020

Aceruloplasminemia: molecular characterization of this disorder of iron metabolism

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12 December 2020

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

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12 December 2020

Ferroportin 1 (SCL40A1) variant associated with iron overload in African-Americans

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12 December 2020

The fascinating but deceptive ferritin: to measure it or not to measure it in chronic kidney disease?

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12 December 2020

Autosomal dominant reticuloendothelial iron overload (HFE type 4) due to a new missense mutation in the FERROPORTIN 1 gene (SLC11A3) in a large French-Canadian family

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12 December 2020

AVAQ 594-597 deletion of the TfR2 gene in a Japanese family with hemochromatosis

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12 December 2020

The solution structure of human hepcidin, a peptide hormone with antimicrobial activity that is involved in iron uptake and hereditary hemochromatosis

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12 December 2020

Diferric transferrin regulates transferrin receptor 2 protein stability

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12 December 2020

Patients with chronic hepatitis C achieving a sustained virological response to peginterferon and ribavirin therapy recover from impaired hepcidin secretion

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12 December 2020

Hepcidin, a urinary antimicrobial peptide synthesized in the liver

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12 December 2020

Hepcidin, an antimicrobial peptide is downregulated in ceruloplasmin-deficient mice

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12 December 2020

Ferroxidase activity is required for the stability of cell surface ferroportin in cells expressing GPI-ceruloplasmin

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12 December 2020

Three patients with middle-age-onset hemochromatosis caused by novel mutations in the hemojuvelin gene

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12 December 2020

Mutations in HFE2 cause iron overload in chromosome 1q-linked juvenile hemochromatosis

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12 December 2020

The molecular basis of ferroportin-linked hemochromatosis

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12 December 2020

Genetic and clinical heterogeneity of ferroportin disease.

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12 December 2020

Reduced serum hepcidin levels in patients with chronic hepatitis C.

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12 December 2020

Hepcidin regulates cellular iron efflux by binding to ferroportin and inducing its internalization

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12 December 2020

10.1007/S00535-010-0259-8

Identifiers

DOI

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5 February 2020

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