The haemochromatosis protein hfe induces an apparent iron-deficient phenotype in H1299 cells that is not corrected by co-expression of β2-microglobulin

Biochemical Journal

Volumn 370, Issue 3, 2003, Pages 891-899

  Wang, Jian ^a   Chen, Guohua ^a   Pantopoulos, Kostas ^a,b  

^a MCGILL UNIVERSITY   (Canada)

^b MCGILL UNIVERSITY   (Canada)

Author keywords

Ferritin; Iron regulatory protein; Iron responsive element; Transferrin receptor

Indexed keywords

BLOOD; CELL CULTURE; CLONING; IRON; PROTEINS;

IRON METABOLISM;

METABOLISM;

BETA 2 MICROGLOBULIN; COMPLEMENTARY DNA; FERRITIN; IRON 55; IRON BINDING PROTEIN; IRON REGULATORY FACTOR; REGULATOR PROTEIN; TETRACYCLINE; TRANSFERRIN RECEPTOR; UNCLASSIFIED DRUG;

ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CANCER CELL; CONTROLLED STUDY; GENE EXPRESSION; GENETIC DISORDER; HEMOCHROMATOSIS; HUMAN; HUMAN CELL; IRON DEFICIENCY; IRON METABOLISM; IRON RESPONSIVE ELEMENT; LUNG CANCER; PHENOTYPE; PLASMID; PRIORITY JOURNAL; PROMOTER REGION; PROTEIN EXPRESSION;

BETA 2-MICROGLOBULIN; HEMOCHROMATOSIS; HISTOCOMPATIBILITY ANTIGENS CLASS I; HUMANS; IRON; MEMBRANE PROTEINS; PHENOTYPE; POINT MUTATION; PROTEIN SYNTHESIS INHIBITORS; RECEPTORS, TRANSFERRIN; TETRACYCLINE; TRANSFERRIN; TUMOR CELLS, CULTURED;

EID: 0037444795     PISSN: 02646021     EISSN: None     Source Type: Journal    
DOI: 10.1042/BJ20021607     Document Type: Article

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