Endocardial cushion defect in a patient with Crouzon syndrome carrying a mutation in the fibroblast growth factor receptor (FGFR)-2 gene
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.2007.00861.x/fullpdf
Reference10 articles.
1. Mutation associated with Crouzon syndrome causes ligand-independent dimerization and activation of FGF receptor-2;Mangasarian;J Cell Physiol,1997
2. Attenuation of signaling pathways stimulated by pathologically activated FGF-receptor 2 mutants prevents craniosynostosis;Eswarakumar;Proc Natl Acad Sci U S A,2006
3. Craniosynostosis syndromes: from genes to premature fusion of skull bones;Hehr;Mol Genet Metabol,1999
4. Clinical spectrum of fibroblast growth factor receptor mutations;Passos-Bueno;Hum Mutat,1999
5. Cellular signaling by fibroblast growth factor receptors;Eswarakumar;Cytokine Growth Factor Rev,2005
Cited by 6 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. Crouzon Syndrome Associated with Congenital Coarctation of Aorta;Chinese Medical Journal;2018-06-20
2. Crouzon Syndrome: a Comprehensive Review;Balkan Journal of Dental Medicine;2018-03-01
3. Effects of FGFR Signaling on Cell Proliferation and Differentiation of Apert Dental Cells;Cells Tissues Organs;2015-11-28
4. Ascorbic acid regulates osterix expression in osteoblasts by activation of prolyl hydroxylase and ubiquitination-mediated proteosomal degradation pathway;Physiological Genomics;2011-06
5. Achados neuropsicolinguísticos na síndrome de Crouzon: relato de caso;Revista da Sociedade Brasileira de Fonoaudiologia;2010-12
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