Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Jazmin El-Hakeh"'
Autor:
Silvia, Danielian, Jazmin, El-Hakeh, Guillermo, Basílico, Matías, Oleastro, Sergio, Rosenzweig, Guillermina, Feldman, Liliana, Berozdnik, Miguel, Galicchio, Angela, Gallardo, Vera, Giraudi, Diana, Liberatore, Eva Maria, Rivas, Marta, Zelazko
Publikováno v:
Human mutation. 21(4)
The block in differentiation from pro-B to pre-B cells results in a selective defect in the humoral immune response characteristic of human X-linked agammaglobulinemia (XLA). Mutations of Bruton tyrosine kinase (BTK) gene have been identified as the
Autor:
Nora Basack, Felisa Molina, Silvia Danielian, Jazmin El-Hakeh, Eva María Rivas, Marta Zelazko, Liliana Berozdnik, Matías Oleastro, Sergio D. Rosenzweig
Publikováno v:
Human mutation. 19(2)
Wiskott-Aldrich syndrome (WAS), is an X-linked immunodeficiency disease caused by mutations of the WAS protein (WASP) gene, characterized by thrombocytopenia, eczema and recurrent infections. X-linked thrombocytopenia (XLT) is a milder form with only
Autor:
Guillermo Basílico, Silvia Danielian, Angela Magnolia Rios Gallardo, Guillermina Feldman, Vera Giraudi, Marta Zelazko, Diana Liberatore, Miguel Galicchio, Sergio D. Rosenzweig, Liliana Berozdnik, Jazmin El-Hakeh, Eva Maria Rivas, Matías Oleastro
Publikováno v:
Human Mutation. 21:451-451
The block in differentiation from pro-B to pre-B cells results in a selective defect in the humoral immune response characteristic of human X-linked agammaglobulinemia (XLA). Mutations of Bruton tyrosine kinase (BTK) gene have been identified as the