Mutation spectrum of genes associated with steroid-resistant nephrotic syndrome in Chinese children-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Mutation spectrum of genes associated with steroid-resistant nephrotic syndrome in Chinese children

Published:2017-08 Issue: Volume:625 Page:15-20
ISSN:0378-1119
Container-title:Gene
language:en
Short-container-title:Gene

Author:

Wang Ying,Dang Xiqiang,He Qingnan,Zhen Yan,He Xiaoxie,Yi Zhuwen,Zhu Kuichun

Funder

Ministry of Science and Technology of the People's Republic of China

Central South University

Publisher

Elsevier BV

Subject

Genetics,General Medicine

Reference36 articles.

1. Binczak-Kuleta A, Rubik J, Litwin M, Ryder M, Lewandowska K, Taryma-Lesniak O, et al. Retrospective mutational analysis of NPHS1, NPHS2, WT1 and LAMB2 in children with steroid-resistant focal segmental glomerulosclerosis - a single-centre experience. Bosn J Basic Med Sci. 2014;14(2):89–93. Epub 2014/05/27. PubMed PMID: 24856380; PubMed Central PMCID: PMC4333957.

2. Bullich G, Trujillano D, Santin S, Ossowski S, Mendizabal S, Fraga G, et al. Targeted next-generation sequencing in steroid-resistant nephrotic syndrome: mutations in multiple glomerular genes may influence disease severity. Eur. J. Hum. Genet. 2015;23(9):1192–9. Epub 2014/11/20. doi: 10.1038/ejhg.2014.252 ejhg2014252 [pii]. PubMed PMID: 25407002; PubMed Central PMCID: PMC4538209.

3. Buscher AK, Kranz B, Buscher R, Hildebrandt F, Dworniczak B, Pennekamp P, et al. Immunosuppression and renal outcome in congenital and pediatric steroid-resistant nephrotic syndrome. Clin. J. Am. Soc. Nephrol. 2010;5(11):2075–84. Epub 2010/08/28. doi: 10.2215/CJN.01190210 CJN.01190210 [pii]. PubMed PMID: 20798252; PubMed Central PMCID: PMC3001773.

4. Choi Y, Sims GE, Murphy S, Miller JR, Chan AP. Predicting the functional effect of amino acid substitutions and indels. PLoS One. 2012;7(10):e46688. doi:10.1371/journal.pone.0046688. PubMed PMID: 23056405; PubMed Central PMCID: PMCPMC3466303.

5. Deltas C, Savva I, Voskarides K, Papazachariou L, Pierides A. Carriers of autosomal recessive Alport syndrome with thin basement membrane nephropathy presenting as focal segmental glomerulosclerosis in later life. Nephron 2015;130(4):271–80. Epub 2015/07/24. doi: 10.1159/000435789 000435789 [pii]. PubMed PMID: 26201269.

Cited by 18 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. Review of genetic testing in kidney disease patients: Diagnostic yield of single nucleotide variants and copy number variations evaluated across and within kidney phenotype groups;American Journal of Medical Genetics Part C: Seminars in Medical Genetics;2022-09

2. Study on Large-Scale Promotion of Prefabricated Buildings in Anhui Province Based on SEM and IoT;Scientific Programming;2022-01-18

3. Genetic Variations and Clinical Features of NPHS1-Related Nephrotic Syndrome in Chinese Children: A Multicenter, Retrospective Study;Frontiers in Medicine;2021-11-11

4. Case Report: The Monogenic Familial Steroid-Resistant Nephrotic Syndrome Caused by a Novel Missense Mutation of NPHS2 Gene A593C in a Chinese Family;Frontiers in Pediatrics;2021-09-23

5. Inferring clonal composition from multiple tumor biopsies;npj Systems Biology and Applications;2020-08-25

同舟云学术

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