Zobrazeno 1 - 6
of 6
pro vyhledávání: '"M S, Villela"'
Genomic signatures of divergent ecological strategies in a recent radiation of neotropical wild cats
Autor:
Jorge L. Ramirez, Jonas Lescroart, Henrique V. Figueiró, Juan Pablo Torres-Florez, Priscilla M. S. Villela, Luiz L. Coutinho, Patricia D. Freitas, Warren E. Johnson, Agostinho Antunes, Pedro M. Galetti, Eduardo Eizirik
Publikováno v:
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Molecular biology and evolution
Universidade de São Paulo (USP)
instacron:USP
Molecular biology and evolution
Ecological differentiation among diverging species is an important component of the evolutionary process and can be investigated in rapid and recent radiations. Here, we use whole genome sequences of five species from the genus Leopardus, a recently
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f233d3dd002851180dd84bcdd688d6c3
Autor:
Aline R. Martins, Aluana G. Abreu, Miklos M. Bajay, Priscilla M. S. Villela, Carlos E. A. Batista, Mariza Monteiro, Alessandro Alves-Pereira, Glyn M. Figueira, José B. Pinheiro, Beatriz Appezzato-Da-Glória, Maria I. Zucchi
Publikováno v:
Applications in Plant Sciences, Vol 1, Iss 6, p 1200507 (2013)
Premise of the study: A new set of microsatellite or simple sequence repeat (SSR) markers were developed for Smilax brasiliensis, which is popularly known as sarsaparilla and used in folk medicine as a tonic, antirheumatic, and antisyphilitic. Smilax
Externí odkaz:
https://doaj.org/article/5767cb3631a24ba6b49752912f71935d
Autor:
Eli Mansour, Solange Oliveira Rodrigues Valle, Anete Sevciovic Grumach, Alfeu Tavares França, Dewton de Moraes Vasconcelos, Eliana de Toledo, Jorge Pinto, M. M. S. Villela, Regis A. Campos
Publikováno v:
Journal of the European Academy of Dermatology and Venereology. 27:e338-e344
Background Hereditary Angio-oedema (HAE) is a serious medical condition caused by a rare autosomal dominant genetic disorder, in which C1 inhibitor (C1-INH) function is reduced. There is no organized information on the HAE patient population in Brazi
Autor:
A S, Grumach, S O R, Valle, E, Toledo, D, de Moraes Vasconcelos, M M S, Villela, E, Mansour, J A, Pinto, R A, Campos, A T, França
Publikováno v:
Journal of the European Academy of Dermatology and Venereology : JEADV. 27(3)
Hereditary Angio-oedema (HAE) is a serious medical condition caused by a rare autosomal dominant genetic disorder, in which C1 inhibitor (C1-INH) function is reduced. There is no organized information on the HAE patient population in Brazil.The Brazi
Publikováno v:
Revista do Instituto de Medicina Tropical de Sao Paulo. 28(5)
Publikováno v:
Revista brasileira de pesquisas medicas e biologicas. 10(4)
Quantative histochemical analysis of nerve degeneration in rats from zero to 192 hours was studied utilizing both Schiff reagent and PAS reaction. In addition, amylase digestion prior to PAS staining and aniline blockade of Schiff reactivity were emp