A novel mutation in the collagen domain of <scp>EDA</scp> results in hypohidrotic ectodermal dysplasia by impacting the receptor‐binding capability-Reference-Cited by-同舟云学术

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A novel mutation in the collagen domain of EDA results in hypohidrotic ectodermal dysplasia by impacting the receptor‐binding capability

Published:2022-11-29 Issue:4 Volume:11 Page:
ISSN:2324-9269
Container-title:Molecular Genetics & Genomic Medicine
language:en
Short-container-title:Molec Gen & Gen Med

Author:

Liu Xingyu¹^ORCID,Zhao Yuming¹,Zhu Junxia¹

Affiliation:

1. Department of Pediatric Dentistry, Peking University School and Hospital of Stomatology & National Center of Stomatology & National Clinical Research Center for Oral Diseases & National Engineering Laboratory for Digital and Material Technology of Stomatology & Central Laboratory Peking University School and Hospital of Stomatology Beijing China

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

Genetics (clinical),Genetics,Molecular Biology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mgg3.2119

Reference20 articles.

1. Only four genes (EDA1, EDAR, EDARADD, and WNT10A) account for 90% of hypohidrotic/anhidrotic ectodermal dysplasia cases

2. EDA Signaling and Skin Appendage Development

3. Gene defect in ectodermal dysplasia implicates a death domain adapter in development

Cited by 2 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. Transcriptomic and proteomic strategies to reveal the mechanism of Gymnocypris przewalskii scale development;BMC Genomics;2024-02-03

2. The EDA/EDAR/NF-κB pathway in non-syndromic tooth agenesis: A genetic perspective;Frontiers in Genetics;2023-04-03

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