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X-LINKED LYMPHOPROLIFERATIVE DISEASE


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    Sinopse

    High Quality Content by WIKIPEDIA articles! X-linked lymphoproliferative disease is a lymphoproliferative disorder. THere is a mutation on the X chromosome that has been found to be associated with a T and NK cell lymphoproliferative disorder. THe mutation is on the long arm of the chromosome, at position 25, which is denoted as Xq25. AT this position, there is a deletion in the SH2D1A gene, which codes for an SH2 domain on a signal transducing protein called SLAM-associated protein (SAP). THe term SH2 domain stands for src-homology 2 domain, which is a three-dimensional domain structure of about 100 amino acid residues. THese domains are present in many signaling proteins because they permit specific, non-covalent bonding to proteins that contain phosphotyrosines. THe amino acid residues adjacent to the phosphotyrosine on the target protein are what determine the unique binding specificity.

    Detalhes do Produto

      • Ano:  2010
      • País de Produção: Germany
      • Código de Barras:  9786130569594
      • ISBN:  6130569599
      • Encadernação:  BROCHURA
      • Nº de Páginas:  80

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