Literature for peptidase S01.514: PRSS56 peptidase

(Topics flags: M Mutation. To select only the references relevant to a single topic, click the link above. See explanation.)

2023
1. Li,D., Xia,L., Huang,P., Wang,Z., Guo,Q., Huang,C., Leng,W. and Qin,S.
   Serine protease PRSS56, a novel cancer-testis antigen activated by DNA hypomethylation, promotes colorectal and gastric cancer progression via PI3K/AKT axis
   Cell Biosci13, 124-124. PubMed  Europe PubMed DOI
2. Ota,J., Inooka,T., Okado,S., Maeda,N., Koyanagi,Y., Kominami,T., Nishiguchi,K.M. and Ueno,S.
   Pathogenic variants of MFRP and PRSS56 genes are major causes of nanophthalmos in Japanese patients
   Ophthalmic Genet44, 423-429. PubMed  Europe PubMed DOI
2022
3. Wu,W., Xu,J., Yin,H., Fu,C., Yao,K. and Chen,X.
   Heterozygous variants c.781G>A and c.1066dup of serine protease 56 cause familial nanophthalmos by impairing serine-type endopeptidase activity
   Br J Ophthalmol PubMed  Europe PubMed DOI
2021
4. Koli,S., Labelle-Dumais,C., Zhao,Y., Paylakhi,S. and Nair,K.S.
   Identification of MFRP and the secreted serine proteases PRSS56 and ADAMTS19 as part of a molecular network involved in ocular growth regulation
   PLoS Genet17, e1009458-e1009458. PubMed  Europe PubMed DOI
2020
5. Labelle-Dumais,C., Pyatla,G., Paylakhi,S., Tolman,N.G., Hameed,S., Seymens,Y., Dang,E., Mandal,A.K., Senthil,S., Khanna,R.C., Kabra,M., Kaur,I., John,S.W.M., Chakrabarti,S. and Nair,K.S.
   Loss of PRSS56 function leads to ocular angle defects and increased susceptibility to high intraocular pressure
   Dis Model Mech PubMed  Europe PubMed DOI
2018
6. Wittmann,G. and Lechan,R.M.
   Prss56 expression in the rodent hypothalamus: inverse correlation with pro-opiomelanocortin suggests oscillatory gene expression in adult rat tanycytes
   J Comp Neurol526, 2444-2461. PubMed  Europe PubMed DOI
2016
7. Jourdon,A., Gresset,A., Spassky,N., Charnay,P., Topilko,P. and Santos,R.
   Prss56, a novel marker of adult neurogenesis in the mouse brain
   Brain Struct Funct221, 4411-4427. PubMed  Europe PubMed DOI
2011
8. Gal,A., Rau,I., El Matri,L., Kreienkamp,H.J., Fehr,S., Baklouti,K., Chouchane,I., Li,Y., Rehbein,M., Fuchs,J., Fledelius,H.C., Vilhelmsen,K., Schorderet,D.F., Munier,F.L., Ostergaard,E., Thompson,D.A. and Rosenberg,T.
   Autosomal-recessive posterior microphthalmos is caused by mutations in PRSS56, a gene encoding a trypsin-like serine protease
   Am J Hum Genet88, 382-390. PubMed  Europe PubMed DOI  M
9. Nair,K.S., Hmani-Aifa,M., Ali,Z., Kearney,A.L., Salem,S.B., Macalinao,D.G., Cosma,I.M., Bouassida,W., Hakim,B., Benzina,Z., Soto,I., Soderkvist,P., Howell,G.R., Smith,R.S., Ayadi,H. and John,S.W.
   Alteration of the serine protease PRSS56 causes angle-closure glaucoma in mice and posterior microphthalmia in humans and mice
   Nat Genet43, 579-584. PubMed  Europe PubMed DOI  M
10. Orr,A., Dube,M.P., Zenteno,J.C., Jiang,H., Asselin,G., Evans,S.C., Caqueret,A., Lakosha,H., Letourneau,L., Marcadier,J., Matsuoka,M., MacGillivray,C., Nightingale,M., Papillon-Cavanagh,S., Perry,S., Provost,S., Ludman,M., Guernsey,D.L. and Samuels,M.E.
    Mutations in a novel serine protease PRSS56 in families with nanophthalmos
    Mol Vis17, 1850-1861. PubMed  Europe PubMed  M