Oxidative Refolding of Amyloidogenic Variants of Human Lysozyme
Author:
Publisher
Elsevier BV
Subject
Molecular Biology,Structural Biology
Reference32 articles.
1. Human lysozyme gene mutations cause hereditary systemic amyloidosis;Pepys;Nature,1993
2. Hereditary renal amyloidosis caused by a new variant lysozyme W64R in a French family;Valleix;Kidney Int.,2002
3. A novel lysozyme mutation Phe57Ile associated with hereditary renal amyloidosis;Yazaki;Kidney Int.,2003
4. Instability, unfolding and aggregation of human lysozyme variants underlying amyloid fibrillogenesis;Booth;Nature,1997
5. Mechanistic studies of the folding of human lysozyme and the origin of amyloidogenic behavior in its disease-related variants;Canet;Biochemistry,1999
Cited by 12 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. Lysozyme amyloidosis—a report on a large German cohort and the characterisation of a novel amyloidogenic lysozyme gene variant;Amyloid;2022-05-09
2. A New Folding Kinetic Mechanism for Human Transthyretin and the Influence of the Amyloidogenic V30M Mutation;International Journal of Molecular Sciences;2016-08-31
3. A Nanobody Binding to Non-Amyloidogenic Regions of the Protein Human Lysozyme Enhances Partial Unfolding but Inhibits Amyloid Fibril Formation;The Journal of Physical Chemistry B;2013-09-24
4. Small Molecules That Target Protein Misfolding;Journal of Medicinal Chemistry;2012-11-01
5. Disease‐related amyloidogenic variants of human lysozyme trigger the unfolded protein response and disturb eye development inDrosophila melanogaster;The FASEB Journal;2011-09-29
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