Literature for peptidase S01.159: prostasin
(References are filtered for relevance to Mutation. To remove the filter click here. See explanation.)
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Szabo,R. and Bugge,T.H.
Loss of HAI-2 in mice with decreased prostasin activity leads to an early-onset intestinal failure resembling congenital tufting enteropathy
PLoS ONE13, e0194660-e0194660. PubMed Europe PubMed DOI M -
Frateschi,S., Keppner,A., Malsure,S., Iwaszkiewicz,J., Sergi,C., Merillat,A.M., Fowler-Jaeger,N., Randrianarison,N., Planes,C. and Hummler,E.
Mutations of the serine protease CAP1/Prss8 lead to reduced embryonic viability, skin defects, and decreased ENaC activity
Am J Pathol181, 605-615. PubMed Europe PubMed DOI M -
Spacek,D.V., Perez,A.F., Ferranti,K.M., Wu,L.K., Moy,D.M., Magnan,D.R. and King,T.R.
The mouse frizzy (fr) and rat 'hairless' (frCR) mutations are natural variants of protease serine S1 family member 8 (Prss8)
Exp Dermatol19, 527-532. PubMed Europe PubMed DOI M
2018
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2010
