Alymphoplasia is caused by a point mutation in the mouse gene encoding Nf-κb-inducing kinase-Reference-Cited by-同舟云学术

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Alymphoplasia is caused by a point mutation in the mouse gene encoding Nf-κb-inducing kinase

Published:1999-05 Issue:1 Volume:22 Page:74-77
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Shinkura Reiko,Kitada Kazuhiro,Matsuda Fumihiko,Tashiro Kei,Ikuta Koichi,Suzuki Misao,Kogishi Katsumi,Serikawa Tadao,Honjo Tasuku

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng0599_74.pdf

Reference28 articles.

1. Miyawaki, S. et al. A new mutation, aly, that induces a generalized lack of lymph nodes accompanied by immunodeficiency in mice. Eur. J. Immunol. 24, 429–434 ( 1994).

2. Shinkura, R. et al. Defects of somatic hypermutation and class switching in alymphoplasia (aly) mutant. Int. Immunol. 8, 1067 –1075 (1996).

3. Koike, R. et al. The splenic marginal zone is absent in alymphoplastic aly mutant mice. Eur. J. Immunol. 26, 669 –675 (1996).

4. Fütterer, A., Mink, K., Luz, A., Kosco-Vilbois, M.H. & Pfeffer, K. The lymphotoxin β receptor controls organogenesis and affinity maturation in peripheral lymphoid tissues. Immunity 9, 59–70 (1998 ).

5. Rennert, P.D., Browning, J.L., Mebius, R., Mackey, F. & Hochman, P.S. Surface lymphotoxin α/β complex is required for the development of peripheral lymphoid organs. J. Exp. Med. 184, 1999–2006 (1996).

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