In silico prediction of the functional consequences of nsSNPs in human beta-catenin gene
Author:
Publisher
Elsevier BV
Subject
Genetics
Reference77 articles.
1. A method and server for predicting damaging missense mutations;Adzhubei;Nat. Methods,2010
2. A profound computational study to prioritize the disease-causing mutations in PRPS1 gene;Agrahari;Metab. Brain Dis.,2018
3. Association of single nucleotide polymorphisms in Wnt signaling pathway genes with breast cancer in Saudi patients;Alanazi;PLoS One,2013
4. Stabilizing mutation of CTNNB1/beta-catenin and protein accumulation analyzed in a large series of parathyroid tumors of Swedish patients;Bjorklund;Mol. Cancer,2008
5. Sequence- and structure-based prediction of eukaryotic protein phosphorylation sites;Blom;J. Mol. Biol.,1999
Cited by 3 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. Comprehensive in silico prioritization of pathogenic nsSNPs in human β-adducin gene towards finding its relation with cancer;Human Gene;2022-12
2. In silico analyses of Wnt1 nsSNPs reveal structurally destabilizing variants, altered interactions with Frizzled receptors and its deregulation in tumorigenesis;Scientific Reports;2022-09-02
3. Genetic determinants of lung cancer: Understanding the oncogenic potential of somatic missense mutations;Genomics;2022-07
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