HAI-1 is required for the novel role of FGFBP1 in maintenance of cell morphology and F-actin rearrangement in human keratinocytes
Author:
Funder
National Cancer Institute
Ministry of National Defense Medical Affairs Bureau, Taiwan
Chi Mei Medical Center
Publisher
Springer Science and Business Media LLC
Subject
Cancer Research,Cell Biology
Link
https://link.springer.com/content/pdf/10.1007/s13577-023-00906-6.pdf
Reference43 articles.
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3. Avrahami L, Maas S, Pasmanik-Chor M, Rainshtein L, Magal N, Smitt JHS, et al. Autosomal recessive ichthyosis with hypotrichosis syndrome: Further delineation of the phenotype. Clin Genet. 2008;74:47–53.
4. Basel-Vanagaite L, Attia R, Ishida-Yamamoto A, Rainshtein L, Ben Amitai D, Lurie R, et al. Autosomal recessive ichthyosis with hypotrichosis caused by a mutation in ST14, encoding type II transmembrane serine protease matriptase. Am J Hum Genet. 2007;80:467–77.
5. List K, Haudenschild CC, Szabo R, Chen WJ, Wahl SM, Swaim W, et al. Matriptase/MT-SP1 is required for postnatal survival, epidermal barrier function, hair follicle development, and thymic homeostasis. Oncogene. 2002;21:3765–79.
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