A novel primary human immunodeficiency due to deficiency in the WASP-interacting protein WIP

Journal of Experimental Medicine

Volumn 209, Issue 1, 2012, Pages 29-34

  Lanzi, Gaetana ^a   Moratto, Daniele ^a   Vairo, Donatella ^a   Masneri, Stefania ^a   Delmonte, Ottavia ^b   Paganini, Tiziana ^a   Parolini, Silvia ^a   Tabellini, Giovanna ^a   Mazza, Cinzia ^a   Savoldi, Gianfranco ^a   Montin, Davide ^b   Martino, Silvana ^b   Tovo, Pierangelo ^b   Pessach, Itai M ^c   Massaad, Michel J ^c   Ramesh, Narayanaswamy ^c   Porta, Fulvio ^d   Plebani, Alessandro ^a   Notarangelo, Luigi D ^c   Geha, Raif S ^c   Giliani, Silvia ^a   more..

^a UNIVERSITY OF BRESCIA   (Italy)

^b UNIVERSITY OF TURIN   (Italy)

^c BOSTON CHILDREN S HOSPITAL   (United States)

^d Division of Hematology and Oncology   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

C REACTIVE PROTEIN; CELL PROTEIN; MESSENGER RNA; UNCLASSIFIED DRUG; WASP INTERACTING PROTEIN;

ARTICLE; BONE MARROW TRANSPLANTATION; CASE REPORT; CELL FUNCTION; CELL PROLIFERATION; CHEMOTAXIS; CHILD; CODON; CONTROLLED STUDY; CORD BLOOD STEM CELL TRANSPLANTATION; DISEASE COURSE; ECZEMA; ENTERITIS; FEMALE; GENE MUTATION; GENETIC CODE; HOMOZYGOTE; HUMAN; HUMAN CELL; HUMAN TISSUE; INFECTION PREVENTION; MOUTH ULCER; NATURAL KILLER CELL; PHENOTYPE; PRIORITY JOURNAL; PROTEIN EXPRESSION; PROTEIN STABILITY; RECURRENT INFECTION; SCHOOL CHILD; SEQUENCE ANALYSIS; SKIN DEFECT; T LYMPHOCYTE; THROMBOCYTOPENIA; WEIGHT REDUCTION; WISKOTT ALDRICH SYNDROME;

BASE SEQUENCE; CYTOSKELETAL PROTEINS; FEMALE; GENE EXPRESSION REGULATION; GENE ORDER; HUMANS; INFANT, NEWBORN; INTRACELLULAR SIGNALING PEPTIDES AND PROTEINS; MUTATION; T-LYMPHOCYTES; WISKOTT-ALDRICH SYNDROME; WISKOTT-ALDRICH SYNDROME PROTEIN;

EID: 84856946231     PISSN: 00221007     EISSN: 15409538     Source Type: Journal    
DOI: 10.1084/jem.20110896     Document Type: Article

References (15)

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