Type II Collagen Mutations in Rare and Common
Author:
Publisher
Informa UK Limited
Subject
General Medicine
Link
http://www.tandfonline.com/doi/pdf/10.3109/07853899409147337
Reference60 articles.
1. PREDISPOSITION TO FAMILIAL OSTEOARTHROSIS LINKED TO TYPE II COLLAGEN GENE
2. Genetic Linkage of a Polymorphism in the Type II Procollagen Gene (COL2A1) to Primary Osteoarthritis Associated with Mild Chondrodysplasia
3. News for the practitioner
4. Mutations in collagen genes: causes of rare and some common diseases in humans
5. Osteogenesis Imperfecta
Cited by 59 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. CHD7 regulates craniofacial cartilage development via controlling HTR2B expression;Journal of Bone and Mineral Research;2024-02-04
2. Development of cartilage tissue using a stirred bioreactor and human iPSC-derived limb bud mesenchymal cells;Biochemical and Biophysical Research Communications;2023-12
3. Control of craniofacial development by the collagen receptor, discoidin domain receptor 2;eLife;2023-01-19
4. The value of undenatured collagen for the normalization of the function of the cartilaginous tissue of the joints;Meditsinskiy sovet = Medical Council;2022-08-12
5. The optimal way to fill the deficiency of essential substances for the well-being of the joints;Meditsinskiy sovet = Medical Council;2022-07-06
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