A missense mutation in pstpip2 is associated with the murine autoinflammatory disorder chronic multifocal osteomyelitis

Bone

Volumn 38, Issue 1, 2006, Pages 41-47

  Ferguson, Polly J ^a   Bing, Xinyu ^a   Vasef, Mohammed A ^a   Ochoa, Luis A ^a   Mahgoub, Amar ^a   Waldschmidt, Thomas J ^a   Tygrett, Lorraine T ^a   Schlueter, Annette J ^a   El Shanti, Hatem ^a  

^a UNIVERSITY OF IOWA   (United States)

Author keywords

Autoinflammatory; CRMO; Osteomyelitis; Psoriasis; pstpip2

Indexed keywords

AMINO ACID; LEUCINE; PROLINE; PROLINE SERINE THREONINE PHOSPHATASE INTERACTING PROTEIN 1; PROLINE SERINE THREONINE PHOSPHATASE INTERACTING PROTEIN 2; PROTEIN; UNCLASSIFIED DRUG;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; AUTOINFLAMMATORY DISEASE; BACKCROSSING; BONE; CARTILAGE; CHROMOSOME 18; CONTROLLED STUDY; FEMALE; GENE LOCUS; GENE SEQUENCE; MISSENSE MUTATION; MOUSE; NONHUMAN; OSTEOMYELITIS; PAPA SYNDROME; PHENOTYPE; SEQUENCE HOMOLOGY; SKIN;

ADAPTOR PROTEINS, SIGNAL TRANSDUCING; AMINO ACID SEQUENCE; AMINO ACID SUBSTITUTION; ANIMALS; AUTOIMMUNE DISEASES; CHROMOSOME MAPPING; CHROMOSOMES, MAMMALIAN; CHRONIC DISEASE; CROSSES, GENETIC; CYTOSKELETAL PROTEINS; DNA MUTATIONAL ANALYSIS; EXONS; FEMALE; GENETIC MARKERS; INFLAMMATION; MALE; MICE; MICE, INBRED BALB C; MICE, INBRED C57BL; MICROSATELLITE REPEATS; MOLECULAR SEQUENCE DATA; MUTATION, MISSENSE; OSTEOMYELITIS; PROLINE;

EID: 29344448820     PISSN: 87563282     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bone.2005.07.009     Document Type: Article

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