Hermansky-Pudlak syndrome: A disease of protein trafficking and organelle function

Pigment Cell Research

Volumn 19, Issue 1, 2006, Pages 19-42

  Wei, Maria L ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

Hermansky Pudlak; Melanocyte; Melanosome; Oculocutaneous albinism; Pigment disorder

Indexed keywords

HPS 1 PROTEIN; HPS 2 PROTEIN; HPS 3 PROTEIN; HPS 4 PROTEIN; HPS 5 PROTEIN; HPS 6 PROTEIN; HPS 7 PROTEIN; HPS 8 PROTEIN; MULTIPROTEIN COMPLEX; UNCLASSIFIED DRUG;

ACANTHOSIS NIGRICANS; ALBINISM; BLEEDING; CHEDIAK HIGASHI SYNDROME; CHEMICAL ANALYSIS; COLITIS; CONGENITAL HIP DISLOCATION; CYTOLOGY; ENTERITIS; FIBROSIS; GENE; GENETIC POLYMORPHISM; HPS 1 GENE; HPS 2 GENE; HPS 3 GENE; HPS 4 GENE; HPS 5 GENE; HPS 6 GENE; HPS 7 GENE; HPS 8 GENE; HUMAN; HYPERTRICHOSIS; LUNG DISEASE; MELANOCYTE; NEUTROPENIA; NONHUMAN; NONSENSE MUTATION; NYSTAGMUS; OCULAR ALBINISM; OTITIS MEDIA; PROTEIN STRUCTURE; REVIEW; SKIN PIGMENTATION; UPPER RESPIRATORY TRACT INFECTION;

ADAPTOR PROTEIN COMPLEX 3; ADAPTOR PROTEIN COMPLEX BETA SUBUNITS; ANIMALS; BIOLOGICAL TRANSPORT; CARRIER PROTEINS; DISEASE MODELS, ANIMAL; HERMANSKI-PUDLAK SYNDROME; HUMANS; INTRACELLULAR SIGNALING PEPTIDES AND PROTEINS; MELANOCYTES; MEMBRANE PROTEINS; MEMBRANE TRANSPORT PROTEINS; MUTATION; ORGANELLES; PROTEINS;

EID: 33645057693     PISSN: 08935785     EISSN: 16000749     Source Type: Journal    
DOI: 10.1111/j.1600-0749.2005.00289.x     Document Type: Review

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