Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Augene Park"'
Publikováno v:
Journal of Men's Health, Vol 18, Iss 2, p 044 (2022)
Background and objective: A growing body of literature suggests modulated expression of members of the opiorphin family of genes (PROL1, SMR3A and SMR3B) is associated with cancer. Recently, overexpression of PROL1 was shown to be associated with pro
Externí odkaz:
https://doaj.org/article/243c2dd13eea4b1798524b431056883d
Publikováno v:
Future Oncology
Background: We describe the first studies investigating a role for opiorphin genes ( PROL1, SMR3A and SMR3B) in prostate cancer (PrCa). Materials & methods: Databases and PrCa tissue arrays were screened for opiorphin expression. Xenografted tumor gr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6fb089eba7d1245a23fe31f8a5aebdb5
https://doi.org/10.2217/fon-2020-1299
https://doi.org/10.2217/fon-2020-1299
Background The opiorphin family of genes (represented in humans by ProL1, hSMR3A and hSMR3B) encode peptides which act as potent neutral endopeptidase (NEP) inhibitors. Because modulated NEP activity is associated with cancer development it has been
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c927b6e2be11914bfbf5161ac5116ccb
https://doi.org/10.21203/rs.3.rs-30262/v2
https://doi.org/10.21203/rs.3.rs-30262/v2
Publikováno v:
Journal of Men's Health. 18:44
Background and objective: A growing body of literature suggests modulated expression of members of the opiorphin family of genes (PROL1, SMR3A and SMR3B) is associated with cancer. Recently, overexpression of PROL1 was shown to be associated with pro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7e363d58492cdfd6622722c445de05a3
https://doi.org/10.31083/jomh.2021.131
https://doi.org/10.31083/jomh.2021.131
Publikováno v:
Journal of Urology. 199
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::66fdfc5fa7d5dbd703da7526036acfff
https://doi.org/10.1016/j.juro.2018.02.2324
https://doi.org/10.1016/j.juro.2018.02.2324