Genetic basis of potential therapeutic strategies for craniosynostosis
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Reference97 articles.
1. Apert syndrome mutations in fibroblast growth factor receptor 2 exhibit increased affinity for FGF ligand;Anderson;Hum Mol Genet,1998
2. A population-based study of craniosynostosis in metropolitan Atlanta, 1989-2003;Boulet;Am J Med Genet Part A,2008
3. The variable expressivity and incomplete penetrance of the twist-null heterozygous mouse phenotype resemble those of human Saethre-Chotzen syndrome;Bourgeois;Hum Mol Genet,1998
4. Craniosynostosis in Twist heterozygous mice: A model for Saethre-Chotzen syndrome;Carver;Anat Rec,2002
5. Activation of extracellular signal-regulated kinases 1 and 2 (ERK1 and ERK2) by FGF-2 and PDGF-BB in normal human osteoblastic and bone marrow stromal cells: Differences in mobility and in-gel renaturation of ERK1 in human, rat, and mouse osteoblastic cells;Chaudhary;Biochem Biophys Res Commun,1997
Cited by 66 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. The spontaneous mouse mutant low set ears (Lse) is caused by tandem duplication of Fgf3 and Fgf4;Mammalian Genome;2023-06-21
2. Molecular Mechanisms Involved in Craniosynostosis;In Vivo;2023
3. Clinical and Diagnostic Anatomy;Cleft Maxillary Reconstruction;2023
4. Clinical and Genetic Studies of the First Monozygotic Twins with Pfeiffer Syndrome;Genes;2022-10-13
5. Craniofacial sutures: Signaling centres integrating mechanosensation, cell signaling, and cell differentiation;European Journal of Cell Biology;2022-06
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