Flow cytometric analysis of Wiskott-Aldrich syndrome (WAS) protein in lymphocytes from WAS patients and their familial carriers.
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M. Yamada | I. Kobayashi | T. Ariga | Y. Sakiyama | K. Kobayashi | D. Nelson | N. Kawamura | M. Ohtsu | N. Ishikawa | S. Tsuruta | M. Anakura | Ichiro Kobayashi | Tadashi Ariga | Yukio Sakiyama | Nobuyoshi Ishikawa | Kunihiko Kobayashi | David L. Nelson | Satoshi Tsuruta | Michiya Anakura
[1] M. Kurimoto,et al. Deficient expression of Bruton's tyrosine kinase in monocytes from X-linked agammaglobulinemia as evaluated by a flow cytometric analysis and its clinical application to carrier detection. , 1998, Blood.
[2] M. Yamada,et al. Mutation Analysis of Five Japanese Families with Wiskott-Aldrich Syndrome and Determination of the Family Members' Carrier Status Using Three Different Methods , 1997, Pediatric Research.
[3] L. Notarangelo,et al. Studies of the expression of the Wiskott-Aldrich syndrome protein. , 1996, The Journal of clinical investigation.
[4] F. Rosen,et al. Nonrandom inactivation of the X chromosome in early lineage hematopoietic cells in carriers of Wiskott-Aldrich syndrome. , 1995, Blood.
[5] K. Sullivan,et al. A multiinstitutional survey of the Wiskott-Aldrich syndrome. , 1994, The Journal of pediatrics.
[6] Aldrich Ra,et al. Pedigree demonstrating a sex-linked recessive condition characterized by draining ears, eczematoid dermatitis and bloody diarrhea. , 1954 .