Single nucleotide polymorphisms in TNFSF15 confer susceptibility to Crohn's disease-Reference-Cited by-同舟云学术

Single nucleotide polymorphisms in TNFSF15 confer susceptibility to Crohn's disease

Published:2005-10-13 Issue:22 Volume:14 Page:3499-3506
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Yamazaki Keiko,McGovern Dermot,Ragoussis Jiannis,Paolucci Marta,Butler Helen,Jewell Derek,Cardon Lon,Takazoe Masakazu,Tanaka Torao,Ichimori Toshiki,Saito Susumu,Sekine Akihiro,Iida Aritoshi,Takahashi Atsushi,Tsunoda Tatsuhiko,Lathrop Mark,Nakamura Yusuke

Publisher

Oxford University Press (OUP)

Subject

Genetics(clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/14/22/3499/13922821/ddi379.pdf

Reference37 articles.

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2. Brant, S.R. and Shugart, Y.Y. (2004) Inflammatory bowel disease gene hunting by linkage analysis: rationale, methodology, and present status of the field. Inflamm. Bowel. Dis., 10, 300–311.

3. Hugot, J.P., Chamaillard, M., Zouali, H., Lesage, S., Cezard, J.P., Belaiche, J., Almer, S., Tysk, C., O'Morain, C.A., Gassull, M. et al. (2001) Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease. Nature, 411, 599–603.

4. Ogura, Y., Bonen, D.K., Inohara, N., Nicolae, D.L., Chen, F.F., Ramos, R., Britton, H., Moran, T., Karaliuskas, R., Duerr, R.H. et al. (2001) A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease. Nature, 411, 603–606.

5. Lesage, S., Zouali, H., Cezard, J.P., Colombel, J.F., Belaiche, J., Almer, S., Tysk, C., O'Morain, C., Gassull, M., Binder, V. et al. (2002) CARD15/NOD2 mutational analysis and genotype–phenotype correlation in 612 patients with inflammatory bowel disease. Am. J. Hum. Genet., 70, 845–857.

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