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| Registros recuperados : 6 | |
| 1. |  | BORGES, A. M. C. M.; SILVA, L. G.; NOGUEIRA, M. F.; OLIVEIRA, A. C. S.; SEGRI, N. J.; FERREIRA, F.; WITTER, R.; AGUIAR, D. M. The Brazilian Pantanal remains at a great risk of Equine Infectious Anemia. Virus Reviews & Research, v. 17, n. 2, p. 71-72, 2012. Supplement 1. Trabalho apresentado no XXIII Congresso Brasileiro de Virologia & VII Reunião do Mercosul de Virologia, Foz do Iguaçu, PR. VV1107.| Biblioteca(s): Embrapa Pantanal. |
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| 2. | | SPOHR, K. A. H.; BORGES, A. M. C. M.; RIBEIRO, T. M. P.; JAYME, V. S.; GODOY, I.; NAKAZATO, L.; DUTRA, V.; AGUIAR, D. M. Fatores de risco associados à prevalência de anticorpos anti-Sarcocystis neurona, Neospora spp. e Toxoplasma gondii em equinos de Roraima, Amazônia. Pesquisa Veterinária Brasileira, Rio de Janeiro, v. 38, n. 7, p. 1337-1343, julho 2018 Título em inglês: Risk factors associated to the prevalence of anti-Sarcocystis neurona, Neospora spp. and Toxoplasma gondii antibodies in horses from Roraima, Brazilian Amazon.| Biblioteca(s): Embrapa Unidades Centrais. |
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| 4. | | BORGES, A. M. C. M.; SILVA, L. G.; NOGUEIRA, M. F.; OLIVEIRA, A. C. S.; SEGRI, N. J.; FERREIRA, F.; WITTER, R.; AGUIAR, D. M. Prevalence and risk factors for Equine Infectious Anemia in Poconé municipality, northern Brazilian Pantanal. Research in Veterinary Science, v. 95, n. 1, p. 76-81, 2013. 6p.| Biblioteca(s): Embrapa Pantanal. |
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| 5. | | MALOSSI, C. D.; FIORATTI, E. G.; CARDOSO, J. F.; MAGRO, A. J.; KROON, E. G.; AGUIAR, D. M. de; BORGES, A. M. C. M; NOGUEIRA, M. F.; ULLMANN, L. S.; ARAUJO JUNIOR, J. P. High genomic variability in Equine Infectious Anemia Virus obtained from naturally infected horses in Pantanal, Brazil: an endemic region case. Viruses, v. 12, n. 2, 207, p. 1-15, 2020.| Biblioteca(s): Embrapa Pantanal. |
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| 6. | | NOGUEIRA, M. F.; AGUIAR, D. M.; OLIVEIRA, J. M.; SANTOS, C. J. S.; BORGES, A. M. C. M.; SILVA, L. G.; MONTEZUMA, E. S.; OLIVEIRA, A. L. C.; REIS, J. K. P. Performance of rgp90 Elisa in the serodiagnosis of Equine Infectious Anemia in the Brazilian Pantanal. Virus Reviews & Research, v. 17, n. 2, p. 70-71, 2012. Supplement 1. Trabalho apresentado no XXIII Congresso Brasileiro de Virologia & VII Reunião do Mercosul de Virologia, Foz do Iguaçu, PR. VV1101.| Biblioteca(s): Embrapa Pantanal. |
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 | Acesso ao texto completo restrito à biblioteca da Embrapa Amazônia Oriental. Para informações adicionais entre em contato com cpatu.biblioteca@embrapa.br. |
Registro Completo
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Biblioteca(s): |
Embrapa Amazônia Oriental; Embrapa Gado de Leite. |
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Data corrente: |
30/03/2016 |
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Data da última atualização: |
09/08/2022 |
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Tipo da produção científica: |
Artigo em Periódico Indexado |
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Circulação/Nível: |
B - 1 |
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Autoria: |
OLIVEIRA, C. S.; SARAIVA, N. Z.; LIMA, M. R. de; OLIVEIRA, L. Z.; SERAPIÃO, R. V.; GARCIA, J. M.; BORGES, C. A. V.; CAMARGO, L. S. de A. |
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Afiliação: |
CLARA SLADE OLIVEIRA, CNPGL; NAIARA ZOCCAL SARAIVA, CPATU; Universidade de São Paulo; Universidade de São Paulo; Pesagro; Universidade de São Paulo; CRISTIANO AMANCIO VIEIRA BORGES, CNPGL; LUIZ SERGIO DE ALMEIDA CAMARGO, CNPGL. |
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Título: |
Cell death is involved in sexual dimorphism during preimplantation development. |
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Ano de publicação: |
2016 |
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Fonte/Imprenta: |
Mechanisms of Development v. 139, p. 42-50, 2016. |
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DOI: |
http://dx.doi.org/10.1016/j.mod.2015.12.001 |
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Idioma: |
Inglês |
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Conteúdo: |
In bovine preimplantation development, female embryos progress at lower rates and originate smaller blastocysts than male counterparts. Although sex-specific gene expression patterns are reported, when and how sex dimorphism is established is not clear. Differences among female and male early development can be useful for human assisted reproductive medicine, when X-linked disorders risk is detected, and for genetic breeding programs, especially in dairy cattle, which requires female animals for milk production. The aim of this study was to characterize the development of female and male embryos, attempting to identify sex effects during preimplantation development and the role of cell death in this process. Using sex-sorted semen from three different bulls for fertilization, we compared kinetics of bovine sex-specific embryos in six time points, and cell death was assessed in viable embryos. For kinetics analysis, we detected an increased population of female embryos arrested at 48 and 120 h.p.i., suggesting this time points as delicate stages of development for female embryos that should be considered for testing improvement strategies for assisted reproductive technologies. Assessing viable embryos quality, we found 144 h.p.i. is the first time point when viable embryos are phenotypically distinct: cell number is decreased, and apoptosis and cell fragmentation are increased in female embryos at this stage. These new results lead us to propose that sex dimorphism in viable embryos is established during morula-blastocyst transition, and cell death is involved in this process. MenosIn bovine preimplantation development, female embryos progress at lower rates and originate smaller blastocysts than male counterparts. Although sex-specific gene expression patterns are reported, when and how sex dimorphism is established is not clear. Differences among female and male early development can be useful for human assisted reproductive medicine, when X-linked disorders risk is detected, and for genetic breeding programs, especially in dairy cattle, which requires female animals for milk production. The aim of this study was to characterize the development of female and male embryos, attempting to identify sex effects during preimplantation development and the role of cell death in this process. Using sex-sorted semen from three different bulls for fertilization, we compared kinetics of bovine sex-specific embryos in six time points, and cell death was assessed in viable embryos. For kinetics analysis, we detected an increased population of female embryos arrested at 48 and 120 h.p.i., suggesting this time points as delicate stages of development for female embryos that should be considered for testing improvement strategies for assisted reproductive technologies. Assessing viable embryos quality, we found 144 h.p.i. is the first time point when viable embryos are phenotypically distinct: cell number is decreased, and apoptosis and cell fragmentation are increased in female embryos at this stage. These new results lead us to propose that sex dimorphism in viable... Mostrar Tudo |
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Palavras-Chave: |
Dimorfismo sexual. |
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Thesagro: |
Bovino; Embrião. |
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Categoria do assunto: |
L Ciência Animal e Produtos de Origem Animal |
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Marc: |
LEADER 02355naa a2200253 a 4500
001 2062957
005 2022-08-09
008 2016 bl uuuu u00u1 u #d
024 7 $ahttp://dx.doi.org/10.1016/j.mod.2015.12.001$2DOI
100 1 $aOLIVEIRA, C. S.
245 $aCell death is involved in sexual dimorphism during preimplantation development.$h[electronic resource]
260 $c2016
520 $aIn bovine preimplantation development, female embryos progress at lower rates and originate smaller blastocysts than male counterparts. Although sex-specific gene expression patterns are reported, when and how sex dimorphism is established is not clear. Differences among female and male early development can be useful for human assisted reproductive medicine, when X-linked disorders risk is detected, and for genetic breeding programs, especially in dairy cattle, which requires female animals for milk production. The aim of this study was to characterize the development of female and male embryos, attempting to identify sex effects during preimplantation development and the role of cell death in this process. Using sex-sorted semen from three different bulls for fertilization, we compared kinetics of bovine sex-specific embryos in six time points, and cell death was assessed in viable embryos. For kinetics analysis, we detected an increased population of female embryos arrested at 48 and 120 h.p.i., suggesting this time points as delicate stages of development for female embryos that should be considered for testing improvement strategies for assisted reproductive technologies. Assessing viable embryos quality, we found 144 h.p.i. is the first time point when viable embryos are phenotypically distinct: cell number is decreased, and apoptosis and cell fragmentation are increased in female embryos at this stage. These new results lead us to propose that sex dimorphism in viable embryos is established during morula-blastocyst transition, and cell death is involved in this process.
650 $aBovino
650 $aEmbrião
653 $aDimorfismo sexual
700 1 $aSARAIVA, N. Z.
700 1 $aLIMA, M. R. de
700 1 $aOLIVEIRA, L. Z.
700 1 $aSERAPIÃO, R. V.
700 1 $aGARCIA, J. M.
700 1 $aBORGES, C. A. V.
700 1 $aCAMARGO, L. S. de A.
773 $tMechanisms of Development$gv. 139, p. 42-50, 2016.
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