Functional consequences of ferroportin 1 mutations

Blood Cells, Molecules, and Diseases

Volumn 35, Issue 1, 2005, Pages 33-46

  Liu, Xiao Bing ^a,b   Yang, Funmei ^b   Haile, David J ^a,b  

^a SOUTH TEXAS VETERANS HEALTH CARE SYSTEM   (United States)

^b UNIVERSITY OF TEXAS HEALTH SCIENCE CENTER AT SAN ANTONIO   (United States)

Author keywords

Ferroportin 1; Hemochromatosis; Mutations

Indexed keywords

FERROPORTIN 1; HEPCIDIN; IRON;

ARTICLE; CELL SPECIFICITY; CELL TYPE; CONTROLLED STUDY; ENDOPLASMIC RETICULUM; GENE LOSS; GENE MUTATION; HEMOCHROMATOSIS; HUMAN; HUMAN CELL; IRON METABOLISM; IRON RESPONSIVE ELEMENT; PHENOTYPE; PRIORITY JOURNAL; PROTEIN DEGRADATION; PROTEIN EXPRESSION; PROTEIN FUNCTION; PROTEIN SYNTHESIS INHIBITION;

ANIMALS; ANTIMICROBIAL CATIONIC PEPTIDES; CATION TRANSPORT PROTEINS; CELL LINE; CELL MEMBRANE; HEMOCHROMATOSIS; HUMANS; IRON; MEMBRANE PROTEINS; MICE; PEPTIDE MAPPING; PROTEIN TRANSPORT; TRANSFECTION;

EID: 21544442328     PISSN: 10799796     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bcmd.2005.04.005     Document Type: Article

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