Characterization of SH2D1A Missense Mutations Identified in X-linked Lymphoproliferative Disease Patients

Journal of Biological Chemistry

Volumn 276, Issue 39, 2001, Pages 36809-36816

  Morra, Massimo ^a   Simarro Grande, Maria ^a   Martin, Margarita ^b   Chen, Alice Siau In ^a   Lanyi, Arpad ^c   Silander, Olin ^a   Calpe, Silvia ^a   Davis, Jack ^c   Pawson, Tony ^d   Eck, Michael J ^a   Sumegi, Janos ^c   Engel, Pablo ^b   Li, Shun Cheng ^e   Terhorst, Cox ^a  

^a HARVARD MEDICAL SCHOOL   (United States)

^b UNIVERSITY OF BARCELONA   (Spain)

^c UNIVERSITY OF NEBRASKA MEDICAL CENTER   (United States)

^d MOUNT SINAI HOSPITAL   (Canada)

^e UNIVERSITY OF WESTERN ONTARIO   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

DISEASES; GENES; PROTEINS; VIRUSES;

PHOSPHORYLATION;

MUTAGENESIS;

ANTIGEN; CD150 ANTIGEN; CD224 ANTIGEN; CD229 ANTIGEN; GENE PRODUCT; PHOSPHOTYROSINE; SIGNALING LYMPHOCYTE ACTIVATION MOLECULE ASSOCIATED PROTEIN; THREONINE; TYROSINE; UNCLASSIFIED DRUG; VALINE; AMINO ACID; CARRIER PROTEIN; SH2D1A PROTEIN, HUMAN; SIGNAL PEPTIDE;

ANIMAL CELL; ARTICLE; BINDING SITE; CLINICAL ARTICLE; CLINICAL FEATURE; ENVIRONMENTAL FACTOR; EPSTEIN BARR VIRUS; HALF LIFE TIME; HEREDITY; HUMAN; HUMAN CELL; HYDROPHOBICITY; IMMUNE DEFICIENCY; LYMPHOPROLIFERATIVE DISEASE; MISSENSE MUTATION; MOLECULAR INTERACTION; NATURAL KILLER CELL; NONHUMAN; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; PROTEIN DOMAIN; PROTEIN STRUCTURE; SIGNAL TRANSDUCTION; T LYMPHOCYTE; X CHROMOSOME LINKED DISORDER; AMINO ACID SEQUENCE; ANIMAL; CELL STRAIN COS1; CHEMICAL STRUCTURE; CHEMISTRY; DOSE RESPONSE; GENETIC TRANSFECTION; GENETICS; LEUKEMIA CELL LINE; METABOLISM; MOLECULAR CLONING; MOLECULAR GENETICS; MUTATION; PHENOTYPE; PHOSPHORYLATION; PLASMID; PROTEIN BINDING; PROTEIN TERTIARY STRUCTURE; SERODIAGNOSIS; SRC HOMOLOGY DOMAIN; WESTERN BLOTTING;

ANIMALIA; HUMAN HERPESVIRUS 4;

AMINO ACID SEQUENCE; AMINO ACIDS; ANIMALS; BLOTTING, WESTERN; CARRIER PROTEINS; CLONING, MOLECULAR; COS CELLS; DOSE-RESPONSE RELATIONSHIP, DRUG; HUMANS; INTRACELLULAR SIGNALING PEPTIDES AND PROTEINS; JURKAT CELLS; LYMPHOPROLIFERATIVE DISORDERS; MODELS, MOLECULAR; MOLECULAR SEQUENCE DATA; MUTATION; MUTATION, MISSENSE; PHENOTYPE; PHOSPHORYLATION; PLASMIDS; PRECIPITIN TESTS; PROTEIN BINDING; PROTEIN STRUCTURE, TERTIARY; SIGNAL TRANSDUCTION; SRC HOMOLOGY DOMAINS; TRANSFECTION;

EID: 0035965317     PISSN: 00219258     EISSN: None     Source Type: Journal    
DOI: 10.1074/jbc.M101305200     Document Type: Article

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