Association of caspase-9 and RUNX3 with inflammatory bowel disease-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Association of caspase-9 and RUNX3 with inflammatory bowel disease

Published:2010-09-30 Issue:1 Volume:77 Page:23-29
ISSN:0001-2815
Container-title:Tissue Antigens
language:en
Short-container-title:

Author:

Guo C.,Ahmad T.,Beckly J.,Cummings J. R. F.,Hancock L.,Geremia A.,Cooney R.,Pathan S.,Jewell D. P.

Publisher

Wiley

Subject

Genetics,Biochemistry,Immunology,General Medicine,Immunology and Allergy

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0039.2010.01569.x/fullpdf

Reference49 articles.

1. Genetics of Crohn disease, an archetypal inflammatory barrier disease.;Schreiber;Nat Rev Genet,2005

2. Identification of novel susceptibility loci for inflammatory bowel disease on chromosomes 1p, 3q, and 4q: evidence for epistasis between 1p and IBD1.;Cho;Proc Nat Acad Sci U S A,1998

3. Linkage and linkage disequilibrium in chromosome band 1p36 in American Chaldeans with inflammatory bowel disease.;Cho;Hum Mol Genet,2000

4. Perspectives on RUNX genes: an update;Cohen;Am J Med Genet A,2009

5. Molecular pathology of RUNX3 in human carcinogenesis.;Subramaniam;Biochim Biophys Acta,2009

Cited by 15 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. N-ethyl-N-nitrosourea (ENU)-induced C-terminal truncation of Runx3 results in autoimmune colitis associated with Th17/Treg imbalance;Immunology Letters;2024-08

2. Genetic Variants Associated with Biological Treatment Response in Inflammatory Bowel Disease: A Systematic Review;International Journal of Molecular Sciences;2024-03-27

3. Variants of the CASP9 gene as candidate markers for primary response to anti-TNF therapy in Crohn’s disease patients;Journal of Applied Genetics;2023-09-02

4. Variants of the CASP9 gene as candidate markers for primary response to anti-TNF therapy in Crohn's disease patients;2023-08-16

5. Abatacept as an alternative therapy for the treatment of drug-intolerant lupus nephritis: A case of underlying monosomy 1p36 deletion syndrome;Clinical Nephrology;2022-05-01

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线，采集、加工和组织学术论文而形成的新型学术文献查询和分析系统，可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容，当前同舟云学术共收录了国内外主流学术期刊6万余种，收集的期刊论文及会议论文总量共计约1.5亿篇，并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询！咨询电话：010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号京ICP备18003416号-3