Endoplasmic reticulum retention is a common defect associated with tyrosinase-negative albinism

Proceedings of the National Academy of Sciences of the United States of America

Volumn 97, Issue 11, 2000, Pages 5889-5894

  Halaban, Ruth ^a   Svedine, Sherri ^b   Cheng, Elaine ^a   Smicun, Yoel ^a   Aron, Rebecca ^b   Hebert, Daniel N ^b  

^a YALE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b UNIVERSITY OF MASSACHUSETTS   (United States)

Author keywords

Calnexin; Protein folding; Quality control

Indexed keywords

CALNEXIN; CALRETICULIN; CHAPERONE; GLYCAN DERIVATIVE; GREEN FLUORESCENT PROTEIN; MELANIN; MONOPHENOL MONOOXYGENASE;

ANIMAL CELL; ARTICLE; CONTROLLED STUDY; ENDOPLASMIC RETICULUM; GENE MUTATION; GOLGI COMPLEX; HUMAN; HUMAN CELL; IMMUNOFLUORESCENCE; MELANOGENESIS; MOUSE; NONHUMAN; OCULOCUTANEOUS ALBINISM; PIGMENTATION; PRIORITY JOURNAL; PROTEIN FOLDING;

ALBINISM, OCULOCUTANEOUS; AMINO ACID SUBSTITUTION; ANIMALS; CALCIUM-BINDING PROTEINS; CALNEXIN; CALRETICULIN; CELLS, CULTURED; ENDOPLASMIC RETICULUM; GOLGI APPARATUS; HUMANS; MELANOCYTES; MELANOSOMES; MICE; MICE, MUTANT STRAINS; MICROSCOPY, FLUORESCENCE; MONOPHENOL MONOOXYGENASE; POINT MUTATION; PROTEIN BINDING; PROTEIN FOLDING; RECOMBINANT FUSION PROTEINS; RIBONUCLEOPROTEINS; TRANSFECTION;

EID: 0034705048     PISSN: 00278424     EISSN: None     Source Type: Journal    
DOI: 10.1073/pnas.97.11.5889     Document Type: Article

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