Placental microstructure and efficiency in cloned bovines: a design-based stereological approach (2008)
- Authors:
- USP affiliated authors: RIBEIRO, ANTONIO AUGUSTO COPPI MACIEL - FMVZ ; BALIEIRO, JÚLIO CÉSAR DE CARVALHO - FZEA
- Unidades: FMVZ; FZEA
- DOI: 10.1007/s00441-008-0626-4
- Subjects: CLONAGEM ANIMAL; EMBRIÃO DE ANIMAL; BOVINOS; PLACENTA
- Language: Inglês
- Imprenta:
- Source:
- Título: Cell and Tissue Research
- ISSN: 0302-766X
- Volume/Número/Paginação/Ano: v. 333, n. 1, p. 105-114, July 2008
- Este artigo possui versão em acesso aberto
- URL de acesso aberto
- Versão do Documento: Versão submetida (Pré-print)
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Status: Artigo possui versão em acesso aberto em repositório (Green Open Access) -
ABNT
RIBEIRO, Antonio Augusto Coppi Maciel et al. Placental microstructure and efficiency in cloned bovines: a design-based stereological approach. Cell and Tissue Research, v. 333, n. 1, p. 105-114, 2008Tradução . . Disponível em: https://doi.org/10.1007/s00441-008-0626-4. Acesso em: 14 mar. 2026. -
APA
Ribeiro, A. A. C. M., Lacerda, P. M. de O., Melo, M. P. de, Balieiro, J. C. de C., & Souza, R. R. de. (2008). Placental microstructure and efficiency in cloned bovines: a design-based stereological approach. Cell and Tissue Research, 333( 1), 105-114. doi:10.1007/s00441-008-0626-4 -
NLM
Ribeiro AACM, Lacerda PM de O, Melo MP de, Balieiro JC de C, Souza RR de. Placental microstructure and efficiency in cloned bovines: a design-based stereological approach [Internet]. Cell and Tissue Research. 2008 ; 333( 1): 105-114.[citado 2026 mar. 14 ] Available from: https://doi.org/10.1007/s00441-008-0626-4 -
Vancouver
Ribeiro AACM, Lacerda PM de O, Melo MP de, Balieiro JC de C, Souza RR de. Placental microstructure and efficiency in cloned bovines: a design-based stereological approach [Internet]. Cell and Tissue Research. 2008 ; 333( 1): 105-114.[citado 2026 mar. 14 ] Available from: https://doi.org/10.1007/s00441-008-0626-4 - Partial urethral obstruction of rabbit urinary bladder: stereological evidence that the increase in muscle content is mostly driven by changes in number, rather than size, of smooth muscle cells
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