(Q28188379)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14647275%20AND%20SRC:MED&resulttype=core&format=json

21 December 2019

title

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

1 reference

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21 December 2019

0 references

1 reference

6

1 reference

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21 December 2019

George Papanikolaou

1

1 reference

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21 December 2019

Marcia L E MacDonald

4

1 reference

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21 December 2019

Tomas Ganz

22

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21 December 2019

Michael R. Hayden

23

1 reference

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21 December 2019

author name string

Mark E Samuels

2

1 reference

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21 December 2019

Erwin H Ludwig

3

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21 December 2019

Patrick L Franchini

5

1 reference

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21 December 2019

Lisa Andres

7

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21 December 2019

Julie MacFarlane

8

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21 December 2019

Nikos Sakellaropoulos

9

1 reference

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21 December 2019

Marianna Politou

10

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21 December 2019

Elizabeta Nemeth

11

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21 December 2019

Jay Thompson

12

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21 December 2019

Jenni K Risler

13

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21 December 2019

Catherine Zaborowska

14

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21 December 2019

Ryan Babakaiff

15

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21 December 2019

Christopher C Radomski

16

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21 December 2019

Terry D Pape

17

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21 December 2019

Owen Davidas

18

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21 December 2019

John Christakis

19

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21 December 2019

Pierre Brissot

20

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21 December 2019

Gillian Lockitch

21

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21 December 2019

Y Paul Goldberg

24

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21 December 2019

language of work or name

English

0 references

publication date

30 November 2003

1 reference

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21 December 2019

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21 December 2019

volume

36

1 reference

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21 December 2019

issue

1

1 reference

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21 December 2019

page(s)

77-82

1 reference

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Natural history of juvenile haemochromatosis

21 December 2019

cites work

1 reference

7 January 2021

Juvenile hemochromatosis.

1 reference

7 January 2021

Juvenile hemochromatosis locus maps to chromosome 1q.

1 reference

7 January 2021

Genetic heterogeneity underlies juvenile hemochromatosis phenotype: analysis of three families of northern Greek origin

1 reference

7 January 2021

Linkage to chromosome 1q in Greek families with juvenile hemochromatosis

1 reference

7 January 2021

Juvenile hemochromatosis locus maps to chromosome 1q in a French Canadian population

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

Hepcidin, a new iron regulatory peptide

1 reference

7 January 2021

Mutant antimicrobial peptide hepcidin is associated with severe juvenile hemochromatosis

1 reference

7 January 2021

Hepcidin, a urinary antimicrobial peptide synthesized in the liver

1 reference

7 January 2021

Hepcidin: a putative iron-regulatory hormone relevant to hereditary hemochromatosis and the anemia of chronic disease

1 reference

7 January 2021

Hepcidin, a key regulator of iron metabolism and mediator of anemia of inflammation

1 reference

7 January 2021

RGM is a repulsive guidance molecule for retinal axons

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

Decreased liver hepcidin expression in the Hfe knockout mouse

1 reference

7 January 2021

Regulatory defects in liver and intestine implicate abnormal hepcidin and Cybrd1 expression in mouse hemochromatosis

1 reference

7 January 2021

Severe iron deficiency anemia in transgenic mice expressing liver hepcidin

1 reference

7 January 2021

Inappropriate expression of hepcidin is associated with iron refractory anemia: implications for the anemia of chronic disease

1 reference

7 January 2021

2002 E. Mead Johnson Award for Research in Pediatrics Lecture: the molecular biology of the anemia of chronic disease: a hypothesis

1 reference

7 January 2021

The anaemia of infection

1 reference

7 January 2021

Pathogenesis and treatment of anaemia of chronic disease

1 reference

7 January 2021

Digenic inheritance of mutations in HAMP and HFE results in different types of haemochromatosis

1 reference

7 January 2021

Hereditary hemochromatosis: HFE mutation analysis in Greeks reveals genetic heterogeneity

1 reference

7 January 2021

PedCheck: a program for identification of genotype incompatibilities in linkage analysis

1 reference

7 January 2021

PolyPhred: automating the detection and genotyping of single nucleotide substitutions using fluorescence-based resequencing

1 reference

7 January 2021

Base-calling of automated sequencer traces using phred. I. Accuracy assessment

1 reference

7 January 2021

BLAST 2 Sequences, a new tool for comparing protein and nucleotide sequences

1 reference

7 January 2021

Identifiers

DOI

10.1038/NG1274

2 references

Consolidated OpenCitations Corpus – April 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14647275%20AND%20SRC:MED&resulttype=core&format=json

21 December 2019

1 reference

Consolidated OpenCitations Corpus – April 2017

2 references

Consolidated OpenCitations Corpus – April 2017