Mutations in Mlph, encoding a member of the Rab effector family, cause the melanosome transport defects observed in leaden mice

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

Volumn 98, Issue 18, 2001, Pages 10238-10243

  Matesic, Lydia E ^a   Yip, Richard ^a   Reuss, Andreé E ^a   Swing, Deborah A ^a   O'Sullivan, T Norene ^a   Fletcher, Colin F ^a,b   Copeland, Neal G ^a   Jenkins, Nancy A ^a  

^a NATIONAL CANCER INSTITUTE   (United States)

^b GENOMICS INSTITUTE OF THE NOVARTIS RESEARCH FOUNDATION   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CALCIUM ION; CARRIER PROTEIN; CELL PROTEIN; GRANULOPHILIN; MELANOPHILIN; PROTEIN MYOVA; PROTEIN SLP3A; RAB PROTEIN; RAB27A PROTEIN; RABPHILIN 3A; UNCLASSIFIED DRUG;

ANIMAL TISSUE; ARTICLE; CALCIUM BINDING; CONTROLLED STUDY; GENE EXPRESSION REGULATION; GENE MUTATION; HAIR COLOR; INTRACELLULAR TRANSPORT; MELANOSOME; MOUSE; NONHUMAN; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; PROTEIN EXPRESSION; SKIN PIGMENTATION;

AMINO ACID SEQUENCE; ANIMALS; BASE SEQUENCE; CARRIER PROTEINS; CHROMOSOME MAPPING; CHROMOSOMES, ARTIFICIAL, BACTERIAL; DNA PRIMERS; GENETIC COMPLEMENTATION TEST; MELANOSOMES; MICE; MICE, INBRED C57BL; MICE, MUTANT STRAINS; MOLECULAR SEQUENCE DATA; MULTIGENE FAMILY; MUTATION; PIGMENTATION DISORDERS; RAB GTP-BINDING PROTEINS; SEQUENCE HOMOLOGY, AMINO ACID;

ANIMALIA; MAMMALIA; STAPHYLOCOCCUS PHAGE 3A;

EID: 0035964395     PISSN: 00278424     EISSN: None     Source Type: Journal    
DOI: 10.1073/pnas.181336698     Document Type: Article

References (58)