The Finnish type of the LDL receptor gene mutation: Molecular characterization of the deleted gene and the corresponding mRNA
Author:
Publisher
Wiley
Subject
Cell Biology,Genetics,Molecular Biology,Biochemistry,Structural Biology,Biophysics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1016/0014-5793(88)80127-3/fullpdf
Reference26 articles.
1. A Receptor-Mediated Pathway for Cholesterol Homeostasis
2. Coronary Artery Disease in 116 Kindred with Familial Type II Hyperlipoproteinemia
3. The human LDL receptor: A cysteine-rich protein with multiple Alu sequences in its mRNA
4. The LDL Receptor Gene: A Mosaic of Exons Shared with Different Proteins
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. Familial Hypercholesterolemia in Russia: Three Decades of Genetic Studies;Frontiers in Genetics;2020-12-17
2. Effects of a 9.6-kb deletion of the LDL receptor gene (FH Helsinki) on structure and levels of mRNA;Human Mutation;1998
3. Deletion of exon 15 of the LDL receptor gene is associated with a mild form of familial hypercholesterolemia. FH-Espoo.;Arteriosclerosis and Thrombosis: A Journal of Vascular Biology;1993-11
4. The Molecular Genetics of Pediatric Lipid Disorders: Recent Progress and Future Research Directions;Pediatric Research;1993-10
5. Identification of a splice-site mutation in the low density lipoprotein receptor gene by denaturing gradient gel electrophoresis;Human Genetics;1993-06
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