Literature DB >> 10498911

Inherited disorders of iron storage and transport.

W J Griffiths1, A L Kelly, T M Cox.   

Abstract

Diverse hereditary disorders associated with iron accumulation cause widespread organ damage. New insights into cellular pathways of iron transport have emerged from the identification of molecules implicated in heritable defects of iron metabolism. Unravelling the genetic basis of rare variants of haemochromatosis should provide vital functional information to further our mechanistic understanding of iron homeostasis.

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Year:  1999        PMID: 10498911     DOI: 10.1016/s1357-4310(99)01541-5

Source DB:  PubMed          Journal:  Mol Med Today        ISSN: 1357-4310


  1 in total

1.  Menkes Copper ATPase (Atp7a) is a novel metal-responsive gene in rat duodenum, and immunoreactive protein is present on brush-border and basolateral membrane domains.

Authors:  Jennifer J Ravia; Renu M Stephen; Fayez K Ghishan; James F Collins
Journal:  J Biol Chem       Date:  2005-08-04       Impact factor: 5.157

  1 in total

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