Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Juliano B. Carregal"'
Autor:
Tamiris Maria de Assis, Letícia C. Assis, Alexandre A. de Castro, Ingrid Guarnetti Prandi, Teodorico C. Ramalho, Ranylson Marcello Leal Savedra, Juliano B. Carregal, Daiana T. Mancini, Elaine F. F. da Cunha, Juliana O. S. de Giacoppo
Publikováno v:
Journal of Molecular Modeling. 24
The serine/threonine protein phosphatase type 5 (PP5) is a promising target for designing new antitumor drugs. This enzyme is a member of the PPP phosphatases gene family, which catalyzes a dephosphorylation reaction: a regulatory process in the sign
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1739704f89e5ff8b6a5ca9f3ebefaaef
https://doi.org/10.1007/s00894-018-3837-y
https://doi.org/10.1007/s00894-018-3837-y
Autor:
Letícia C, Assis, Alexandre A, de Castro, Ingrid G, Prandi, Daiana T, Mancini, Juliana O S, de Giacoppo, Ranylson M L, Savedra, Tamiris M, de Assis, Juliano B, Carregal, Elaine F F, da Cunha, Teodorico Castro, Ramalho
Publikováno v:
Journal of molecular modeling. 24(10)
The serine/threonine protein phosphatase type 5 (PP5) is a promising target for designing new antitumor drugs. This enzyme is a member of the PPP phosphatases gene family, which catalyzes a dephosphorylation reaction: a regulatory process in the sign
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b1f0831b1e5735075849343438021d6b
https://pubmed.ncbi.nlm.nih.gov/30280322
https://pubmed.ncbi.nlm.nih.gov/30280322
Publikováno v:
Revista Processos Químicos. 9:40-44
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2c1580eedc7d03536647e8fb26eda0a2
https://doi.org/10.19142/rpq.v9i18.251
https://doi.org/10.19142/rpq.v9i18.251
Autor:
Bianca dos Reis Santos, Juliano B. Carregal, Alisson Marques Silva, Ana Paula Carregal, Alex Gutterres Taranto, Flávia V. Maciel
Publikováno v:
Journal of molecular modeling. 23(4)
The demand for new therapies has encouraged the development of faster and cheaper methods of drug design. Considering the number of potential biological targets for new drugs, the docking-based virtual screening (DBVS) approach has occupied a promine
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::608b6dd9e31bff3ea77964bc99268093
https://pubmed.ncbi.nlm.nih.gov/28285443
https://pubmed.ncbi.nlm.nih.gov/28285443
Autor:
Teodorico C. Ramalho, Moacyr C. Junior, Juliana O. S. Giacoppo, Juliano B. Carregal, Elaine F. F. da Cunha
Aedes aegypti is an important vector of arboviruses such as dengue, yellow fever, chikungunya and Zika. Among the various types of insecticides used to combat this vector, the insect growth regulators have been developed and recommended for control o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::21aaf9b85370dca60ba1ced3ebb48ce8
