A mutation of the Wilson disease protein, ATP7B, is degraded in the proteasomes and forms protein aggregates

Gastroenterology

Volumn 120, Issue 4, 2001, Pages 967-974

  Harada, Masaru ^a   Sakisaka, Shotaro ^a   Terada, Kunihiko ^a   Kimura, Rina ^a   Kawaguchi, Takumi ^a   Koga, Hironori ^a   Kim, Motoaki ^a   Taniguchi, Eitaro ^a   Hanada, Shinichiro ^a   Suganuma, Tatsuo ^a   Furuta, Koh ^a   Sugiyama, Toshihiro ^a   Sata, Michio ^a  

^a KURUME UNIVERSITY SCHOOL OF MEDICINE   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

COPPER; GENE PRODUCT; MUTANT PROTEIN; PROTEASOME; UNCLASSIFIED DRUG; WILSON DISEASE PROTEIN;

ARTICLE; CLINICAL FEATURE; CONTROLLED STUDY; CORRELATION FUNCTION; CYTOPLASM; ELECTRON MICROSCOPY; ENDOSOME; GENE MUTATION; GENETIC DISORDER; GENOTYPE; HUMAN; HUMAN CELL; LIVER CELL; MALLORY BODY; MICROTUBULE; PHENOTYPE; PRIORITY JOURNAL; PROTEIN AGGREGATION; PROTEIN DEGRADATION; PROTEIN EXPRESSION; PROTEIN LOCALIZATION; WILSON DISEASE;

EID: 0035126940     PISSN: 00165085     EISSN: None     Source Type: Journal    
DOI: 10.1053/gast.2001.22543     Document Type: Article

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