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| Registros recuperados : 35 | |
| 21. |  | NICIURA, S. C. M.; FERREIRA, C. R.; CHIARATTI, M. R.; MEIRELLES, F. V.; REGITANO, L. C. de A.; ALENCAR, M. M. de; BARBOSA, P. F. Caracterização do genótipo mitocondrial de um rebanho da raça bovina Canchim. In: REUNIÃO ANUAL DA SOCIEDADE BRASILEIRA DE ZOOTECNIA, 45., 2008, Lavras. Anais... Lavras: UFLA; SBZ, 2008. 1 CD-ROM| Biblioteca(s): Embrapa Pecuária Sudeste. |
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| 22. | | FERREIRA, C. R.; BURGSTALLER, J. P.; PERECIN, F.; GARCIA, J. M.; CHIARATTI, M. R.; MÉO, S. C.; MULLER, M.; SMITH, L. C.; MEIRELLES, F. V.; STEINBORN, R. Pronounced segregation of donor mitochondria introduced by bovine Ooplasmic tranfer to the female germ-line. Biology of Reproduction, v. 82, n. 03, p. 563-571, mar. 2010.| Biblioteca(s): Embrapa Pecuária Sudeste. |
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| 23. | | ALEXANDRE, P. A.; GOMES, R. da C.; SANTANA, M. H. A.; SILVA, S. L.; LEMES, P. R.; MUDADU, M. de A.; REGITANO, L. C. de A.; MEIRELLES, F. V.; FERRAZ, J. B. S.; FUKUMASU, H. Bovine NR1I3 gene polymorphisms and its association with feed efficiency traits in Nellore cattle. Meta Gene, v. 2, p. 206-217, dec. 2014.| Biblioteca(s): Embrapa Pecuária Sudeste. |
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| 24. | | CARVALHO, M. E.; ELER, J. P.; CUCCO, D. C.; REZENDE, F. M. de; FERRAZ, J. B. S.; MEIRELLES, F. V.; REGITANO, L. C. de A.; BALIEIRO, J. C. C. Efeito médio de substituição alélica para os polimorfismos CAPN4753 e UOGCAST no gene da calpaína e calpastatina. In: SIMPÓSIO BRASILEIRO DE MELHORAMENTO ANIMAL, 7., 2008, São Carlos, SP. Anais... São Carlos, SBMA, 2008.| Biblioteca(s): Embrapa Pecuária Sudeste. |
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| 25. | | CHIARATTI, M. R.; FERREIRA, C. R.; PERECIN, F.; NICIURA, S. C. M.; SANGALLI, J. R.; MESQUITA, L. G.; BALIEIRO, J. C. de C.; SMITH, L. C.; GARCIA, J. M.; MEIRELLES, F. V. Ooplast-mediated developmental rescue of bovine oocytes exposed to ethidium bromide. Reproductive BioMedicine Online v. 22, n. 22, p. 172-183, 2011.| Biblioteca(s): Embrapa Pecuária Sudeste. |
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| 26. | | MIGLINO, M. A.; PEREIRA, F. T. V.; VISINTIN, J. A.; GARCIA, J. M.; MEIRELLES, F. V.; RUMPF, R.; AMBRÓSIO, C. E.; PAPA, P. C.; SANTOS, T. C.; CARVALHO, A. F.; LEISER, R.; CARTER, A. M. Placentation in cloned cattle: structure and microvascular architecture. Theriogenology, v. 68, p. 604-617, 2007.| Biblioteca(s): Embrapa Recursos Genéticos e Biotecnologia. |
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| 27. | | CARVALHO, M. E.; ELER, J. P.; BONIN, M. N.; REZENDE, F. M.; BIASE, F. H.; MEIRELLES, F. V.; REGITANO, L. C. de A.; COUTINHO, L. L.; BALIEIRO, J. C. C.; FERRAZ, J. B. S. Genotypic and allelic frequencies of gene polymorphisms associated with meat tenderness in Nellore beef cattle. Genetics and Molecular Research, v. 16, n. 1, p. 1-15, 2017.| Biblioteca(s): Embrapa Pecuária Sudeste. |
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| 28. | | PERECIN, F.; YAMAZAKI, W.; FERREIRA, C. R.; MÉO, S. C.; BIASE, F. H.; MERIGHE, G. K. F.; SARAIVA, N. Z.; TETZNER, T. A. D.; MEIRELLES, F. V.; GARCIA, J. M. Efeito do protocolo de sincronização celular na produção de clones bovinos. Acta Scientiae Veterinariae, v. 35, supl. 3, p. s1181, 2007. In: REUNIÃO ANUAL DA SOCIEDADE BRASILEIRA DE TECNOLOGIA DE EMBRIÕES, 21., 2007, Salvador. Anais... Salvador: UFRGS, 2007. p. 1267| Biblioteca(s): Embrapa Pecuária Sudeste. |
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| 29. | | FADEL, L.; VIANA, B. R.; FEITOSA, M. L. T.; ERCOLIN, A. C. M.; ROBALLO, K. C. S.; CASALS, J. B.; PIERI, N. C. G.; MEIRELLES, F. V.; MARTINS, D. dos S.; MIGLINO, M. A.; AMBRÓSIO, C. E. Protocols for obtainment and isolation of two mesenchymal stem cell sources in sheep. Acta Cirurgica Brasileira, v. 26, n. 4, p. 267-273, 2011.| Biblioteca(s): Embrapa Caprinos e Ovinos. |
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| 30. | | GOMES, R. da C.; SILVA, S. L.; CARVALHO, M. E.; REZENDE, F. M.; PINTO, L. F. B.; SANTANA, M. H. A.; STELLA, T. R.; MEIRELLES, F. V.; ROSSI JÚNIOR, P.; LEME, P. R.; FERRAZ, J. B. S. Protein synthesis and degradation gene SNPs related to feed intake, feed efficiency, growth, and ultrasound carcass traits in Nellore cattle. Genetics and Molecular Research, v. 12, n. 3, p. 2923-2936, 2013.| Biblioteca(s): Embrapa Gado de Corte. |
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| 31. | | PERECIN, F.; YAMAZAKI, W.; FERREIRA, C. R.; MÉO, S. C.; BIASE, F. H.; MERIGHE, G. K. F.; SARAIVA, N. Z.; TETZNER, T. A. D.; MEIRELLES, F. V.; GARCIA, J. M. Expressão de DNA metiltransferases em blastocistos bovinos produzidos in vivo e in vitro. Acta Scientiae Veterinariae, v. 35, supl. 3, p. 1181, 2007.| Biblioteca(s): Embrapa Pecuária Sudeste. |
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| 32. | | SANTOS BIASE, W. K. F.; BIASE, F. H.; BURATINI JÚNIOR, J.; BALIEIRO, J.; WATANABE, Y. F.; ACCORSI, M. F.; FERREIRA, C. R.; STRANIERI, P.; CAETANO, A. R.; MEIRELLES, F. V. Single nucleotide polymorphisms in the bovine genome are associated with the number of oocytes collected during ovum pick up. Animal Reproduction Science, v. 134, p. 141-149, 2012.| Biblioteca(s): Embrapa Recursos Genéticos e Biotecnologia. |
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| 33. | | NICIURA, S. C. M.; FERREIRA, C. R.; PERECIN, F.; SARAIVA, N. Z.; TETZNER, T. A. D.; BORGES, J. C.; YAMAZAKI, W.; LEAL, C. L. V.; MEIRELLES, F. V.; GARCIA, J. M. Troca de carioplasto entre zigotos ativados com estrôncio ou 6-DMAP. Acta Scientiae Veterinariae, Porto Alegre, v. 35, Supl. 3, 2007. p. s1269. Edição de anais da 21a. Reunião Anual da Sociedade Brasileira de Tecnologia de Embriões, Salvador, 2007.| Biblioteca(s): Embrapa Pecuária Sudeste. |
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| 34. | | CHIARATTI, M. R.; FERREIRA, C. R.; MEIRELLES, F. V.; MÉO, S. C.; PERECIN, F.; SMITH, L. C.; FERRAZ, M. L.; SÁ FILHO, M. F. de; GIMENES, L. U.; BARUSELLI, P. S.; GASPARRINI, B.; GARCIA, J. M. Xenooplasmic transfer between buffalo and bovine enables development of homoplasmic offspring. Cellular Reprogramming, v. 12, n. 2, 2010.| Biblioteca(s): Embrapa Pecuária Sudeste. |
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| 35. | | RECCHIA, K.; MACHADO, L. S.; BOTIGELLI, R. C.; PIERI, N. C. G.; BARBOSA, G.; CASTRO, R. V. G. de; MARQUES, M. G.; PESSÔA, L. V. de F.; FANTINATO NETO, P.; MEIRELLES, F. V.; SOUZA, A. F. de; MARTINS, S. M. M. K.; BRESSAN, F. F. In vitro induced pluripotency from urine-derived cells in porcine. World Journal of Stem Cells, v. 14, n. 3, p. 231-244, 2022.| Biblioteca(s): Embrapa Suínos e Aves. |
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| Registros recuperados : 35 | |
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Registro Completo
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Biblioteca(s): |
Embrapa Suínos e Aves. |
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Data corrente: |
21/12/2022 |
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Data da última atualização: |
21/12/2022 |
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Tipo da produção científica: |
Artigo em Periódico Indexado |
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Circulação/Nível: |
B - 3 |
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Autoria: |
RECCHIA, K.; MACHADO, L. S.; BOTIGELLI, R. C.; PIERI, N. C. G.; BARBOSA, G.; CASTRO, R. V. G. de; MARQUES, M. G.; PESSÔA, L. V. de F.; FANTINATO NETO, P.; MEIRELLES, F. V.; SOUZA, A. F. de; MARTINS, S. M. M. K.; BRESSAN, F. F. |
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Afiliação: |
KAIANA RECCHIA, Universidade de São Paulo; LUCAS SIMÕES MACHADO, Universidade de São Paulo; RAMON CESAR BOTIGELLI, Universidade Estadual Paulista; NAIRA CAROLINE GODOY PIERI, Universidade de São Paulo; GABRIELA BARBOSA, Universidade de São Paulo; RAQUEL VASCONCELOS GUIMARÃES DE CASTRO, Universidade de São Paulo; MARIANA GROKE MARQUES, CNPSA; LAÍS VICARI DE FIGUEIREDO PESSÔA, Universidade de São Paulo; PAULO FANTINATO NETO, Universidade de São Paulo; FLÁVIO VIEIRA MEIRELLES, Universidade de São Paulo; ALINE FERNANDA DE SOUZA, Universidade de São Paulo; SIMONE MARIA MASSAMI KITAMURA MARTINS, Universidade de São Paulo; FABIANA FERNANDES BRESSAN, Universidade de São Paulo. |
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Título: |
In vitro induced pluripotency from urine-derived cells in porcine. |
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Ano de publicação: |
2022 |
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Fonte/Imprenta: |
World Journal of Stem Cells, v. 14, n. 3, p. 231-244, 2022. |
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DOI: |
https://doi.org/10.4252/wjsc.v14.i3.231 |
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Idioma: |
Inglês |
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Conteúdo: |
Methods: The UDCs were reprogrammed in vitro using human or murine octamer-binding transcription factor 4 (OCT4), SRY-box2 (SOX2), Kruppel-like factor 4 (KLF4), and C-MYC, and cultured with basic fibroblast growth factor (bFGF) supplementation. To characterize the putative porcine iPSCs three clonal lineages were submitted to immunocytochemistry for alkaline phosphatase (AP), OCT4, SOX2, NANOG, TRA1 81 and SSEA 1 detection. Endogenous transcripts related to the pluripotency (OCT4, SOX2 and NANOG) were analyzed via reverse transcription quantitative real-time polymerase chain reaction in different time points during the culture, and all three lineages formed embryoid bodies (EBs) when cultured in suspension without bFGF supplementation. Results: The UDCs were isolated from swine urine samples and when at passage 2 submitted to in vitro reprogramming. Colonies of putative iPSCs were obtained only from UDCs transduced with the murine factors (mOSKM), but not from human factors (hOSKM). Three clonal lineages were isolated and further cultured for at least 28 passages, all the lineages were positive for AP detection, the OCT4, SOX2, NANOG markers, albeit the immunocytochemical analysis also revealed heterogeneous phenotypic profiles among lineages and passages for NANOG and SSEA1, similar results were observed in the abundance of the endogenous transcripts related to pluripotent state. All the clonal lineages when cultured in suspension without bFGF were able to form EBs expressing ectoderm and mesoderm layers transcripts. Conclusion: For the first time UDCs were isolated in the swine model and reprogrammed into a pluripotent-like state, enabling new numerous applications in both human or veterinary regenerative medicine. MenosMethods: The UDCs were reprogrammed in vitro using human or murine octamer-binding transcription factor 4 (OCT4), SRY-box2 (SOX2), Kruppel-like factor 4 (KLF4), and C-MYC, and cultured with basic fibroblast growth factor (bFGF) supplementation. To characterize the putative porcine iPSCs three clonal lineages were submitted to immunocytochemistry for alkaline phosphatase (AP), OCT4, SOX2, NANOG, TRA1 81 and SSEA 1 detection. Endogenous transcripts related to the pluripotency (OCT4, SOX2 and NANOG) were analyzed via reverse transcription quantitative real-time polymerase chain reaction in different time points during the culture, and all three lineages formed embryoid bodies (EBs) when cultured in suspension without bFGF supplementation. Results: The UDCs were isolated from swine urine samples and when at passage 2 submitted to in vitro reprogramming. Colonies of putative iPSCs were obtained only from UDCs transduced with the murine factors (mOSKM), but not from human factors (hOSKM). Three clonal lineages were isolated and further cultured for at least 28 passages, all the lineages were positive for AP detection, the OCT4, SOX2, NANOG markers, albeit the immunocytochemical analysis also revealed heterogeneous phenotypic profiles among lineages and passages for NANOG and SSEA1, similar results were observed in the abundance of the endogenous transcripts related to pluripotent state. All the clonal lineages when cultured in suspension without bFGF were able to form EBs expressi... Mostrar Tudo |
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Palavras-Chave: |
Células-tronco; IPSC; Noninvasive; Pluripotência; Pluripotency; Reprogramming. |
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Thesagro: |
Suíno; Urina. |
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Thesaurus NAL: |
Induced pluripotent stem cells; Swine; Urine. |
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Categoria do assunto: |
-- |
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URL: |
https://ainfo.cnptia.embrapa.br/digital/bitstream/doc/1150134/1/10084.pdf
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Marc: |
LEADER 02880naa a2200409 a 4500
001 2150134
005 2022-12-21
008 2022 bl uuuu u00u1 u #d
024 7 $ahttps://doi.org/10.4252/wjsc.v14.i3.231$2DOI
100 1 $aRECCHIA, K.
245 $aIn vitro induced pluripotency from urine-derived cells in porcine.$h[electronic resource]
260 $c2022
520 $aMethods: The UDCs were reprogrammed in vitro using human or murine octamer-binding transcription factor 4 (OCT4), SRY-box2 (SOX2), Kruppel-like factor 4 (KLF4), and C-MYC, and cultured with basic fibroblast growth factor (bFGF) supplementation. To characterize the putative porcine iPSCs three clonal lineages were submitted to immunocytochemistry for alkaline phosphatase (AP), OCT4, SOX2, NANOG, TRA1 81 and SSEA 1 detection. Endogenous transcripts related to the pluripotency (OCT4, SOX2 and NANOG) were analyzed via reverse transcription quantitative real-time polymerase chain reaction in different time points during the culture, and all three lineages formed embryoid bodies (EBs) when cultured in suspension without bFGF supplementation. Results: The UDCs were isolated from swine urine samples and when at passage 2 submitted to in vitro reprogramming. Colonies of putative iPSCs were obtained only from UDCs transduced with the murine factors (mOSKM), but not from human factors (hOSKM). Three clonal lineages were isolated and further cultured for at least 28 passages, all the lineages were positive for AP detection, the OCT4, SOX2, NANOG markers, albeit the immunocytochemical analysis also revealed heterogeneous phenotypic profiles among lineages and passages for NANOG and SSEA1, similar results were observed in the abundance of the endogenous transcripts related to pluripotent state. All the clonal lineages when cultured in suspension without bFGF were able to form EBs expressing ectoderm and mesoderm layers transcripts. Conclusion: For the first time UDCs were isolated in the swine model and reprogrammed into a pluripotent-like state, enabling new numerous applications in both human or veterinary regenerative medicine.
650 $aInduced pluripotent stem cells
650 $aSwine
650 $aUrine
650 $aSuíno
650 $aUrina
653 $aCélulas-tronco
653 $aIPSC
653 $aNoninvasive
653 $aPluripotência
653 $aPluripotency
653 $aReprogramming
700 1 $aMACHADO, L. S.
700 1 $aBOTIGELLI, R. C.
700 1 $aPIERI, N. C. G.
700 1 $aBARBOSA, G.
700 1 $aCASTRO, R. V. G. de
700 1 $aMARQUES, M. G.
700 1 $aPESSÔA, L. V. de F.
700 1 $aFANTINATO NETO, P.
700 1 $aMEIRELLES, F. V.
700 1 $aSOUZA, A. F. de
700 1 $aMARTINS, S. M. M. K.
700 1 $aBRESSAN, F. F.
773 $tWorld Journal of Stem Cells$gv. 14, n. 3, p. 231-244, 2022.
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Embrapa Suínos e Aves (CNPSA) |
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