Sequence-based prediction of pathological mutations
Author:
Publisher
Wiley
Subject
Molecular Biology,Biochemistry,Structural Biology
Reference52 articles.
1. Characterization of single-nucleotide polymorphisms in coding regions of human genes
2. . . .to a future of genetic medicine
3. Predicting the functional consequences of non-synonymous single nucleotide polymorphisms: structure-based assessment of amino acid variation11Edited by F. Cohen
4. Predicting Deleterious Amino Acid Substitutions
5. Prediction of deleterious human alleles
Cited by 150 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. A New Set of in Silico Tools to Support the Interpretation of ATM Missense Variants Using Graphical Analysis;The Journal of Molecular Diagnostics;2024-01
2. Role of deleterious nsSNPs of klotho protein and their drug response: a computational mechanical insights;Journal of Biomolecular Structure and Dynamics;2023-05-22
3. High-Throughput Prediction of the Impact of Genetic Variability on Drug Sensitivity and Resistance Patterns for Clinically Relevant Epidermal Growth Factor Receptor Mutations from Atomistic Simulations;Journal of Chemical Information and Modeling;2022-12-28
4. Prediction Of The Impact Of Genetic Variability On Drug Sensitivity For Clinically Relevant EGFR Mutations;2022-04-25
5. Missense mutations involvement in COX-2 structure, and protein-substrate binding affinity: in-silico study;Nucleosides, Nucleotides & Nucleic Acids;2021-10-11
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