XIAP deficiency in humans causes an X-linked lymphoproliferative syndrome-Reference-Cited by-同舟云学术

XIAP deficiency in humans causes an X-linked lymphoproliferative syndrome

Published:2006-11 Issue:7115 Volume:444 Page:110-114
ISSN:0028-0836
Container-title:Nature
language:en
Short-container-title:Nature

Author:

Rigaud Stéphanie,Fondanèche Marie-Claude,Lambert Nathalie,Pasquier Benoit,Mateo Véronique,Soulas Pauline,Galicier Lionel,Le Deist Françoise,Rieux-Laucat Frédéric,Revy Patrick,Fischer Alain,de Saint Basile Geneviève,Latour Sylvain

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

Link

http://www.nature.com/articles/nature05257.pdf

Reference21 articles.

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2. Rathmell, J. C. & Thompson, C. B. Pathways of apoptosis in lymphocyte development, homeostasis, and disease. Cell 109, (Suppl.)S97–107 (2002)

3. Purtilo, D. T., Cassel, C. K., Yang, J. P. & Harper, R. X-linked recessive progressive combined variable immunodeficiency (Duncan's disease). Lancet 1, 935–940 (1975)

4. Nichols, K. E., Ma, C. S., Cannons, J. L., Schwartzberg, P. L. & Tangye, S. G. Molecular and cellular pathogenesis of X-linked lymphoproliferative disease. Immunol. Rev. 203, 180–199 (2005)

5. Gaspar, H. B., Sharifi, R., Gilmour, K. C. & Thrasher, A. J. X-linked lymphoproliferative disease: clinical, diagnostic and molecular perspective. Br. J. Haematol. 119, 585–595 (2002)

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