Literature DB >> 12123233

A valine deletion of ferroportin 1: a common mutation in hemochromastosis type 4.

Antonella Roetto, Alison T Merryweather-Clarke, Filomena Daraio, Karen Livesey, Jennifer J Pointon, Giuliana Barbabietola, Antonio Piga, Peter H Mackie, Kathryn J H Robson, Clara Camaschella.   

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Year:  2002        PMID： 12123233     DOI： 10.1182/blood-2002-03-0693

Source DB:  PubMed          Journal:  Blood        ISSN： 0006-4971            Impact factor:   22.113


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  23 in total

1.  Identification of ferroportin disease in the Indian subcontinent.

Authors:  D F Wallace; P Browett; P Wong; H Kua; R Ameratunga; V N Subramaniam
Journal:  Gut       Date:  2005-04       Impact factor: 23.059

2.  Ferroportin disease due to the A77D mutation in Australia.

Authors:  V N Subramaniam; D F Wallace; J L Dixon; L M Fletcher; D H Crawford
Journal:  Gut       Date:  2005-07       Impact factor: 23.059

3.  SLC40A1 Q248H allele frequencies and Q248H-associated risk of non-HFE iron overload in persons of sub-Saharan African descent.

Authors:  James C Barton; Ronald T Acton; Pauline L Lee; Carol West
Journal:  Blood Cells Mol Dis       Date:  2007-05-09       Impact factor: 3.039

4.  Ferroportin deficiency in erythroid cells causes serum iron deficiency and promotes hemolysis due to oxidative stress.

Authors:  De-Liang Zhang; Manik C Ghosh; Hayden Ollivierre; Yan Li; Tracey A Rouault
Journal:  Blood       Date:  2018-09-13       Impact factor: 22.113

5.  Ferroportin/IREG-1/MTP-1/SLC40A1 modulates the uptake of iron at the apical membrane of enterocytes.

Authors:  C Thomas; P S Oates
Journal:  Gut       Date:  2004-01       Impact factor: 23.059

Review 6.  Hepcidin and its role in iron absorption.

Authors:  K J Robson
Journal:  Gut       Date:  2004-05       Impact factor: 23.059

Review 7.  The SLC40 basolateral iron transporter family (IREG1/ferroportin/MTP1).

Authors:  Andrew T McKie; David J Barlow
Journal:  Pflugers Arch       Date:  2003-06-27       Impact factor: 3.657

8.  Analysis of genes implicated in iron regulation in individuals presenting with primary iron overload.

Authors:  Monique G Zaahl; Alison T Merryweather-Clarke; Maritha J Kotze; Schalk van der Merwe; Louise Warnich; Kathryn J H Robson
Journal:  Hum Genet       Date:  2004-08-24       Impact factor: 4.132

Review 9.  Is genetic screening for hemochromatosis worthwhile?

Authors:  Omer T Njajou; Behrooz Z Alizadeh; Cornelia M van Duijn
Journal:  Eur J Epidemiol       Date:  2004       Impact factor: 8.082

10.  A novel mutation in ferroportin1 is associated with haemochromatosis in a Solomon Islands patient.

Authors:  K E Arden; D F Wallace; J L Dixon; L Summerville; J W Searle; G J Anderson; G A Ramm; L W Powell; V N Subramaniam
Journal:  Gut       Date:  2003-08       Impact factor: 23.059
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