LEKTI proteolytic processing in human primary keratinocytes, tissue distribution and defective expression in Netherton syndrome
Author:
Publisher
Oxford University Press (OUP)
Subject
Genetics(clinical),Genetics,Molecular Biology,General Medicine
Link
http://academic.oup.com/hmg/article-pdf/12/19/2417/6948045/ddg247.pdf
Cited by 181 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. Comparative analyses of Netherton syndrome patients and Spink5 conditional knock-out mice uncover disease-relevant pathways;Communications Biology;2024-02-05
2. Proteolytic and Antiproteolytic Activity in the Skin: Gluing the Pieces Together;Journal of Investigative Dermatology;2023-10
3. Netherton Syndrome Caused by Heterozygous Frameshift Mutation Combined with Homozygous c.1258A>G Polymorphism in SPINK5 Gene;Genes;2023-05-14
4. Netherton-Syndrom bei einer bulgarischen Patientin;Wiener Medizinische Wochenschrift;2023-01-25
5. Multiplex Proteomic Evaluation in Inborn Errors with Deregulated IgE Response;Biomedicines;2023-01-13
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