Ferritin—schwere Kette

Worwood M et al. (1985) Assignment of human ferritin genes to chromosomes 11 and 19q13.3----19qter.

Wu KJ et al. (1999) Coordinated regulation of iron-controlling genes, H-ferritin and IRP2, by c-MYC.

Courseaux A et al. (1996) Definition of the minimal MEN1 candidate area based on a 5-Mb integrated map of proximal 11q13. The European Consortium on Men1, (GENEM 1; Groupe d'Etude des Néoplasies Endocriniennes Multiples de type 1).

Harrison PM et al. (1996) The ferritins: molecular properties, iron storage function and cellular regulation.

Boyd D et al. (1984) Isolation and characterization of a cDNA clone for human ferritin heavy chain.

Murray MT et al. (1987) Conservation of ferritin heavy subunit gene structure: implications for the regulation of ferritin gene expression.

Youssoufian H et al. (1988) Association of a new chromosomal deletion [del(1)(q32q42)] with diaphragmatic hernia: assignment of a human ferritin gene.

Leibold EA et al. (1988) Cytoplasmic protein binds in vitro to a highly conserved sequence in the 5' untranslated region of ferritin heavy- and light-subunit mRNAs.

Costanzo F et al. (1986) Structure of gene and pseudogenes of human apoferritin H.

Gatti RA et al. (1987) Human ferritin genes: chromosomal assignments and polymorphisms.

Hasegawa S et al. (2013) Growth retardation and hair loss in transgenic mice overexpressing human H-ferritin gene.

Li L et al. (2010) Binding and uptake of H-ferritin are mediated by human transferrin receptor-1.

Yachou A et al. (1991) Mouse ferritin H sequences map to chromosomes 3, 6, and 19.

Faniello MC et al. (2006) Detection and functional analysis of an SNP in the promoter of the human ferritin H gene that modulates the gene expression.

Yachou AK et al. (1991) Mouse ferritin H multigene family is polymorphic and contains a single multiallelic functional gene located on chromosome 19.

Pham CG et al. (2004) Ferritin heavy chain upregulation by NF-kappaB inhibits TNFalpha-induced apoptosis by suppressing reactive oxygen species.

Papadopoulos P et al. (1992) A second human ferritin H locus on chromosome 11.

Ferreira C et al. (2001) H ferritin knockout mice: a model of hyperferritinemia in the absence of iron overload.

None (2000) Iron regulatory proteins and the molecular control of mammalian iron metabolism.

Ferreira C et al. (2000) Early embryonic lethality of H ferritin gene deletion in mice.

Mancias JD et al. (2014) Quantitative proteomics identifies NCOA4 as the cargo receptor mediating ferritinophagy.

Shi H et al. (2008) A cytosolic iron chaperone that delivers iron to ferritin.

Sammarco MC et al. (2008) Ferritin L and H subunits are differentially regulated on a post-transcriptional level.

Kato J et al. (2001) A mutation, in the iron-responsive element of H ferritin mRNA, causing autosomal dominant iron overload.

Caskey JH et al. (1983) Human ferritin gene is assigned to chromosome 19.

Cragg SJ et al. (1985) Genes for the 'H' subunit of human ferritin are present on a number of human chromosomes.

Hentze MW et al. (1986) Cloning, characterization, expression, and chromosomal localization of a human ferritin heavy-chain gene.

Orphanet article

NCBI article

OMIM.ORG article