Zobrazeno 1 - 10
of 42
pro vyhledávání: '"estudo de associação"'
Autor:
Trevisoli, Priscila Anchieta
Breeding has been the mainly responsible for the increase of poultry efficiency in the last decades. The breeding programs are geared towards higher meat yield and feed efficiency. Among the used genomic approaches, genome wide association studies (G
Publikováno v:
Revista Brasileira de Reumatologia, Vol 56, Iss 2, Pp 171-177 (2016)
ABSTRACT Rheumatoid Arthritis (RA) is an autoimmune inflammatory rheumatic disease which affects several organs and tissue, predominantly the synovial joints. Like many other autoimmune diseases, RA is a complex disease, where genetic variants, envir
Externí odkaz:
https://doaj.org/article/90bf52c15bc34111a63123e59e46519f
Publikováno v:
CES Medicina Veterinaria y Zootecnia, Volume: 16, Issue: 3, Pages: 62-95, Published: 18 APR 2022
Resumen La leche es un alimento esencial para los humanos y una de sus importancias radica en el contenido de proteínas lácteas. Las proteínas más frecuentes en este preciado líquido son las caseínas (αS1-caseína, αS2-caseína, β-caseína y
Association study between the Taq1A (rs1800497) polymorphism and schizophrenia in a Brazilian sample
Autor:
Quirino Cordeiro, Homero Vallada
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 72, Iss 8, Pp 582-586 (2014)
Schizophrenia is a severe psychotic disorder with recurrent relapse and functional impairment. It results from a poorly understood gene-environment interaction. The Taq1A polymorphism (located in the gene cluster NTAD) is a likely candidate for schiz
Externí odkaz:
https://doaj.org/article/177e7aaa2d494aa0a19c964b6c416216
Autor:
Gotardi, Leonardo Fioravante
Publikováno v:
LOCUS Repositório Institucional da UFV
Universidade Federal de Viçosa (UFV)
instacron:UFV
Universidade Federal de Viçosa (UFV)
instacron:UFV
Coordenação de Aperfeiçoamento de Pessoal de Nível Superior Os caracteres relacionados a qualidade do grão são de herança poligênica e de estrutura gênica complexa. As alfa-zeinas possuem relação com a capacidade de expansão do grão, enq
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3056::64a51c705e452e4f26611a078f197079
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 68, Iss 5, Pp 716-719 (2010)
Epidemiological studies have demonstrated that the genetic component is an important risk factor for the development of schizophrenia. The genes that codify the different compounds of the dopaminergic system have created interest for molecular invest
Externí odkaz:
https://doaj.org/article/030984c21bce4fd6b33366d22509742d
Publikováno v:
Acta Médica Portuguesa; v. 34, n. 6 (2021): Junho; 407-409
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3056::eefd32a98ca38cc36d6c9e625a28e9db
https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/16168
https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/16168
Autor:
Joel Lavinsky, Ricardo Ferreira Bento, Juemei Wang, Guilherme Kasperbauer, Rick A. Friedman, Hooman Allayee, Aline Mendonça, Amanda L. Crow
Publikováno v:
Repositório Institucional da UFRGS
Universidade Federal do Rio Grande do Sul (UFRGS)
instacron:UFRGS
Audiol Neurootol
Universidade Federal do Rio Grande do Sul (UFRGS)
instacron:UFRGS
Audiol Neurootol
Background: Although several candidate-gene association studies have been conducted to investigate noise-induced hearing loss (NIHL) in humans, most are underpowered, unreplicated, and account for only a fraction of the genetic risk. Mouse genome-wid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a727d353067fc7ba7c978bafa7e0e418
Autor:
Brito, Luciano Abreu
Fissura labial com ou sem fissura de palato não sindrômica (FL±P NS) é uma doença complexa que afeta 1:700 indivíduos no mundo. A busca das causas genéticas dessa malformação é dificultada pelo padrão multifatorial de herança e pela heter
Autor:
Nathália Gualberto Souza
Publikováno v:
Repositório Institucional da UFMG
Universidade Federal de Minas Gerais (UFMG)
instacron:UFMG
Universidade Federal de Minas Gerais (UFMG)
instacron:UFMG
CNPq - Conselho Nacional de Desenvolvimento Científico e Tecnológico FAPEMIG - Fundação de Amparo à Pesquisa do Estado de Minas Gerais CAPES - Coordenação de Aperfeiçoamento de Pessoal de Nível Superior Depression is characterized to change
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3056::51fbdb71fbec6a51949c384fc34bf96b