Secreted protease ADAMTS18 in development and disease
Author:
Funder
National Natural Science Foundation of China
Publisher
Elsevier BV
Subject
Genetics,General Medicine
Reference83 articles.
1. Cryptorchidism and infertility in rats with targeted disruption of the Adamts16 locus;Abdul-Majeed;PLoS One,2014
2. Identification of ADAMTS18 as a gene mutated in Knobloch syndrome;Aldahmesh;J. Med. Genet.,2011
3. The syndrome of microcornea, myopic chorioretinal atrophy, and telecanthus (MMCAT) is caused by mutations in ADAMTS18;Aldahmesh;Hum. Mutat.,2013
4. A disintegrin-like and metalloprotease (reprolysin-type) with thrombospondin type 1 motif (ADAMTS) superfamily: functions and mechanisms;Apte;J. Biol. Chem.,2009
5. Adamts18 deletion results in distinct developmental defects and provides a model for congenital disorders of lens, lung, and female reproductive tract development;Ataca;Biol. Open.,2016
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