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Registros recuperados : 27 | |
21. | ![Imagem marcado/desmarcado](/consulta/web/img/desmarcado.png) | BUSS, C. E.; AFONSO, J.; OLIVEIRA, P. S. N. DE; PETRINI, J.; TIZIOTO, P. C.; CESAR, A. S. M.; GUSTANI-BUSS, E. C.; CARDOSO, T. F.; ROVADOSKI, G. A.; DINIZ, W. J. DA S.; LIMA, A. O. DE; ROCHA, M. I. P.; ANDRADE, B. G. N.; WOLF, J. B.; COUTINHO, L. L.; MOURÃO, G. B.; REGITANO, L. C. de A. Bivariate GWAS reveals pleiotropic regions among feed efficiency and beef quality-related traits in Nelore cattle. Mammalian Genome, v. 34, p. 90-103, dec. 2022. Biblioteca(s): Embrapa Pecuária Sudeste. |
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22. | ![Imagem marcado/desmarcado](/consulta/web/img/desmarcado.png) | CARDOSO, T. F.; BRUSCADIN, J. J.; DINIZ, W. J. da S.; BANERJEE, P.; AFONSO, J.; ANDRADE, B. G. N. B; MALHEIROS, J. M.; ZERLOTINI NETO, A.; VIEIRA, D. da S.; FERNANDES, A. C.; CESAR, A. S. M.; MOURÃO, G. B.; COUTINHO, L. L.; REGITANO, L. C. de A. Integration of different omics layers with SNP-SNP interaction networks associated with methane emission in nelore cattle. In: BRAZILIAN CONGRESS OF GENETICS, 67., 2022, Natal. [Abstracts]. Ribeirão Preto: Sociedade Brasileira de Genética, 2022. p. 247. e-book. Na publicação: Adhemar Zerlotini. Biblioteca(s): Embrapa Agricultura Digital; Embrapa Pecuária Sudeste. |
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23. | ![Imagem marcado/desmarcado](/consulta/web/img/desmarcado.png) | LIMA, A. O. de; KOLTES, J. E.; DINIZ, W. J. S.; OLIVEIRA, P. S. N. de; CESAR, A. S. M.; TIZIOTO, P. L.; AFONSO, J.; SOUZA, M. de S.; PETRINI, J.; ROCHA, M. I. P.; CARDOSO, T. F.; ZERLOTINI NETO, A.; COUTINHO, L. L.; MOURÃO, G. B.; REGITANO, L. C. de A. Potential biomarkers for feed efficiency-related traits in nelore cattle identified by co-expression network and integrative genomics analyses. Frontiers in Genetics, v. 11, p. 1-14, Mar. 2020. Article 189. Na publicação: Luciana C. A. Regitano. Biblioteca(s): Embrapa Agricultura Digital; Embrapa Pecuária Sudeste. |
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24. | ![Imagem marcado/desmarcado](/consulta/web/img/desmarcado.png) | CARDOSO, T. F.; COUTINHO, L. L.; BRUSCADIN, J. J.; DINIZ, W. J. da S.; PETRINI, J.; ANDRADE, B. G. N.; OLIVEIRA, P. S. N. de; POLETI, M. D.; CESAR, A. S. M.; SILVEIRA, J. C. DA; CHIARATTI, M. R.; ZERLOTINI NETO, A.; MOURÃO, G. B.; REGITANO, L. C. de A. Multi-omics approach reveals miR-SNPs affecting muscle fatty acids profile in Nelore cattle. Genes, v. 12, n. 1, p. 1-18, Jan. 2021. Article 67. Na publicação: Adhemar Zerlotini. Biblioteca(s): Embrapa Agricultura Digital; Embrapa Pecuária Sudeste. |
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25. | ![Imagem marcado/desmarcado](/consulta/web/img/desmarcado.png) | MALHEIROS, J. M.; CORREIA, B. S. B.; CERIBELI, C.; BRUSCADIN, J. J.; DINIZ, W. J. S.; BANERJEE, P.; VIEIRA, D. S.; CARDOSO, T. F.; ANDRADE, B. G. N.; PETRINI, J.; CARDOSO, D. R.; COLNAGO, L. A.; BOGUSZ JUNIOR, S.; MOURÃO, G. B.; COUTINHO, L. L.; PALHARES, J. C. P.; MEDEIROS, S. R. de; BERNDT, A.; REGITANO, L. C. de A. Ruminal and feces metabolites associated with feed efciency, water intake and methane emission in Nelore bulls. Scientifc Reports, v. 13, 18001, 2023. 13 p. Biblioteca(s): Embrapa Instrumentação; Embrapa Pecuária Sudeste. |
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26. | ![Imagem marcado/desmarcado](/consulta/web/img/desmarcado.png) | AFONSO, J.; SHIM, W. J.; BODEN, M.; FORTES, M. R. S.; DINIZ, W. J. da S.; LIMA, A. O. de; ROCHA, M. I. P.; CARDOSO, T. F.; BRUSCADIN, J. J.; GROMBONI, C. F.; NOGUEIRA, A. R. A.; MOURÃO, G. B.; ZERLOTINI NETO, A.; COUTINHO, L. L.; REGITANO, L. C. de A. Repressive epigenetic mechanisms, such as the H3K27me3 histone modification, were predicted to affect muscle gene expression and its mineral content in Nelore cattle. Biochemistry and Biophysics Reports, v. 33, 101420, Mar. 2023. Biblioteca(s): Embrapa Agricultura Digital; Embrapa Pecuária Sudeste. |
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27. | ![Imagem marcado/desmarcado](/consulta/web/img/desmarcado.png) | ANDRADE, B. G. N.; DONATONI, F. A. B.; CUADRAT, R. R.; CARDOSO, T. F.; MALHEIROS, J. M.; OLIVEIRA, P. S. N. DE; PETRINI, J.; MOURÃO, G. B.; COUTINHO, L. L.; REECY, J. M.; KOLTES, J. E.; ZERLOTINI NETO, A.; MEDEIROS, S. R. de; BERNDT, A.; PALHARES, J. C. P.; AFLI, H.; REGITANO, L. C. de A. Stool and ruminal microbiome components associated with methane emission and feed efficiency in Nelore beef cattle. Frontiers in Genetics, v. 13, 812828, may, 2022. 12 p. Biblioteca(s): Embrapa Agricultura Digital; Embrapa Pecuária Sudeste. |
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Registros recuperados : 27 | |
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![](/consulta/web/img/deny.png) | Acesso ao texto completo restrito à biblioteca da Embrapa Cerrados. Para informações adicionais entre em contato com cpac.biblioteca@embrapa.br. |
Registro Completo
Biblioteca(s): |
Embrapa Cerrados. |
Data corrente: |
15/12/2014 |
Data da última atualização: |
15/12/2014 |
Tipo da produção científica: |
Artigo em Periódico Indexado |
Circulação/Nível: |
A - 2 |
Autoria: |
CUNHA, E. R. da; MARTINS, C. F.; SILVA, G. C.; CUMPA, H. C. B.; BAO, S. N. |
Afiliação: |
CARLOS FREDERICO MARTINS, CPAC; HEIDI CHRISTINA BESSLER CUMPA, CPAC. |
Título: |
Effects of prolonged in vitro culture and cryopreservation on viability, DNA Fragmentation, chromosome stability and ultrastructure of bovine cells from amniotic fluid and umbilical cord. |
Ano de publicação: |
2014 |
Fonte/Imprenta: |
Reproduction in Domestic Animals, v. 49, n. 5, p. 806-812, Oct. 2014. |
ISSN: |
0936-6768 |
DOI: |
10.1111/rda.12372 |
Idioma: |
Inglês |
Conteúdo: |
The objective of this work was to study cellular types that did not participated in the gastrulation process, amniotic fluid cells (AFCs) and umbilical cord cells (UCCs), in conditions of long-term culture and cryopreserved with different solutions. The AFCs and UCCs were used in a comparative study with ear fibroblast cells (EFCs) that were cultured in vitro until 20 cellular passages and cryopreserved in 10% dimethylsulphoxide (DMSO), 5% dimethyl formamide (DMF) and 7% glycerol (Gly) solutions. The cellular viability, ultrastructure, DNA fragmentation and chromosome stability were evaluated to determine the cellular type most resistant. In all cell types, it was possible to evaluate the AFCs until 15 passages and UCCs until 20 passages with different periods of cellular growth to reach the confluence phase. Solutions containing 10% DMSO ensured viability of 90.33 ± 5.58%, 90.56 ± 4.40% and 81.90 ± 3.31%, respectively for EFCs, AFCs and UCCs, being significantly more efficient and with less variation than other cryoprotectant solutions. The AFCs were more sensitive to cryopreservation and presented low viability rate at the passage 20 (17.2 ± 8.87%). There was no change in karyotype and nuclear fragmentation was low in all cellular passages studied. With the scanning electron analysis was possible the characterization of AFCs and UCCs in suspension. The three cellular types of cells presented different shapes and characteristics on the surface. The results demonstrate that bovine AFCs and UCCs can be isolated, cultured in vitro and cryopreserved in 10% DMSO, not causing damage to DNA and chromosomes. The UCCs were more resistant than AFCs in all aspects. MenosThe objective of this work was to study cellular types that did not participated in the gastrulation process, amniotic fluid cells (AFCs) and umbilical cord cells (UCCs), in conditions of long-term culture and cryopreserved with different solutions. The AFCs and UCCs were used in a comparative study with ear fibroblast cells (EFCs) that were cultured in vitro until 20 cellular passages and cryopreserved in 10% dimethylsulphoxide (DMSO), 5% dimethyl formamide (DMF) and 7% glycerol (Gly) solutions. The cellular viability, ultrastructure, DNA fragmentation and chromosome stability were evaluated to determine the cellular type most resistant. In all cell types, it was possible to evaluate the AFCs until 15 passages and UCCs until 20 passages with different periods of cellular growth to reach the confluence phase. Solutions containing 10% DMSO ensured viability of 90.33 ± 5.58%, 90.56 ± 4.40% and 81.90 ± 3.31%, respectively for EFCs, AFCs and UCCs, being significantly more efficient and with less variation than other cryoprotectant solutions. The AFCs were more sensitive to cryopreservation and presented low viability rate at the passage 20 (17.2 ± 8.87%). There was no change in karyotype and nuclear fragmentation was low in all cellular passages studied. With the scanning electron analysis was possible the characterization of AFCs and UCCs in suspension. The three cellular types of cells presented different shapes and characteristics on the surface. The results demonstrate that ... Mostrar Tudo |
Palavras-Chave: |
Cordão umbilical; Líquido aminiótico. |
Thesagro: |
Bovino; Criopreservação; Melhoramento genético animal. |
Thesaurus NAL: |
Amniotic fluid; Cattle; Cryopreservation; Genetic improvement; Umbilical cord. |
Categoria do assunto: |
G Melhoramento Genético |
Marc: |
LEADER 02681naa a2200313 a 4500 001 2002603 005 2014-12-15 008 2014 bl uuuu u00u1 u #d 022 $a0936-6768 024 7 $a10.1111/rda.12372$2DOI 100 1 $aCUNHA, E. R. da 245 $aEffects of prolonged in vitro culture and cryopreservation on viability, DNA Fragmentation, chromosome stability and ultrastructure of bovine cells from amniotic fluid and umbilical cord. 260 $c2014 520 $aThe objective of this work was to study cellular types that did not participated in the gastrulation process, amniotic fluid cells (AFCs) and umbilical cord cells (UCCs), in conditions of long-term culture and cryopreserved with different solutions. The AFCs and UCCs were used in a comparative study with ear fibroblast cells (EFCs) that were cultured in vitro until 20 cellular passages and cryopreserved in 10% dimethylsulphoxide (DMSO), 5% dimethyl formamide (DMF) and 7% glycerol (Gly) solutions. The cellular viability, ultrastructure, DNA fragmentation and chromosome stability were evaluated to determine the cellular type most resistant. In all cell types, it was possible to evaluate the AFCs until 15 passages and UCCs until 20 passages with different periods of cellular growth to reach the confluence phase. Solutions containing 10% DMSO ensured viability of 90.33 ± 5.58%, 90.56 ± 4.40% and 81.90 ± 3.31%, respectively for EFCs, AFCs and UCCs, being significantly more efficient and with less variation than other cryoprotectant solutions. The AFCs were more sensitive to cryopreservation and presented low viability rate at the passage 20 (17.2 ± 8.87%). There was no change in karyotype and nuclear fragmentation was low in all cellular passages studied. With the scanning electron analysis was possible the characterization of AFCs and UCCs in suspension. The three cellular types of cells presented different shapes and characteristics on the surface. The results demonstrate that bovine AFCs and UCCs can be isolated, cultured in vitro and cryopreserved in 10% DMSO, not causing damage to DNA and chromosomes. The UCCs were more resistant than AFCs in all aspects. 650 $aAmniotic fluid 650 $aCattle 650 $aCryopreservation 650 $aGenetic improvement 650 $aUmbilical cord 650 $aBovino 650 $aCriopreservação 650 $aMelhoramento genético animal 653 $aCordão umbilical 653 $aLíquido aminiótico 700 1 $aMARTINS, C. F. 700 1 $aSILVA, G. C. 700 1 $aCUMPA, H. C. B. 700 1 $aBAO, S. N. 773 $tReproduction in Domestic Animals$gv. 49, n. 5, p. 806-812, Oct. 2014.
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