Filaggrin gene mutations in hand eczema patients in the Indian subcontinent: A prospective case‐control study
Author:
Affiliation:
1. Department of Dermatology, Venereology, and LeprologyPostgraduate Institute of Medical Education and Research Chandigarh India
2. Department of BiochemistryPostgraduate Institute of Medical Education and Research Chandigarh India
Publisher
Wiley
Subject
Dermatology,Immunology and Allergy
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1111/cod.13233
Reference24 articles.
1. Prevalent and Rare Mutations in the Gene Encoding Filaggrin Cause Ichthyosis Vulgaris and Predispose Individuals to Atopic Dermatitis
2. Common loss-of-function variants of the epidermal barrier protein filaggrin are a major predisposing factor for atopic dermatitis
3. Filaggrin loss‐of‐function mutations and atopic dermatitis as risk factors for hand eczema in apprentice nurses: part II of a prospective cohort study
4. Filaggrin null mutations increase the risk and persistence of hand eczema in subjects with atopic dermatitis: results from a general population study
5. Filaggrin mutations may confer susceptibility to chronic hand eczema characterized by combined allergic and irritant contact dermatitis
Cited by 22 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. Educational and psychological interventions for managing atopic dermatitis (eczema);Cochrane Database of Systematic Reviews;2024-08-12
2. Increased loss‐of‐function filaggrin gene mutation prevalence in atopic dermatitis patients across northern latitudes indicates genetic fitness: A systematic review and meta‐analysis;Experimental Dermatology;2024-07
3. Exploring filaggrin gene polymorphisms in Indian children with atopic dermatitis: Hitherto an unchartered territory;Indian Journal of Dermatology, Venereology and Leprology;2023-10-28
4. In silico analysis of the profilaggrin sequence indicates alterations in the stability, degradation route, and intracellular protein fate in filaggrin null mutation carriers;Frontiers in Molecular Biosciences;2023-05-02
5. Filaggrin gene polymorphisms in Indian children with atopic dermatitis: A cross-sectional multicentre study;Indian Journal of Dermatology, Venereology and Leprology;2023-04-01
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