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Blood

Volumn 124, Issue 8, 2014, Pages 1212-1213

How mutant HFE causes hereditary hemochromatosis

(1) Muckenthaler, Martina U a

a UNIVERSITY OF HEIDELBERG (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

BETA 2 MICROGLOBULIN; BONE MORPHOGENETIC PROTEIN 6; BONE MORPHOGENETIC PROTEIN RECEPTOR 1; BONE MORPHOGENETIC PROTEIN RECEPTOR 1A; BONE MORPHOGENETIC PROTEIN RECEPTOR 2; FERROPORTIN; HEMOJUVELIN; HEPCIDIN; HFE PROTEIN; MESSENGER RNA; SMAD6 PROTEIN; SMAD7 PROTEIN; TRANSFERRIN; TRANSFERRIN RECEPTOR 2;

CELL MEMBRANE; CELL SURFACE; COMPLEX FORMATION; GENETIC DISORDER; HEMOCHROMATOSIS; HEREDITARY HEMOCHROMATOSIS; HUMAN; LIVER CELL; LIVER CELL NUCLEUS; MISSENSE MUTATION; NONHUMAN; NOTE; POINT MUTATION; PRIORITY JOURNAL; PROTEIN DEGRADATION; PROTEIN EXPRESSION; PROTEIN PHOSPHORYLATION; PROTEIN PROTEIN INTERACTION; SIGNAL TRANSDUCTION; UBIQUITINATION;

ANIMALS; BONE MORPHOGENETIC PROTEIN RECEPTORS, TYPE I; GENE EXPRESSION REGULATION; HEPCIDINS; HISTOCOMPATIBILITY ANTIGENS CLASS I; HUMANS; MEMBRANE PROTEINS;

EID: 84907357104 PISSN: 00064971 EISSN: 15280020 Source Type: Journal
DOI: 10.1182/blood-2014-07-581744 Document Type: Note

Times cited : (16)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.