TGF-β activates APC through Cdh1 binding for Cks1 and Skp2 proteasomal destruction stabilizing p27kip1 for normal endometrial growth (2016)
- Authors:
- Autor USP: GAMA, PATRICIA - ICB
- Unidade: ICB
- DOI: 10.1080/15384101.2016.1150393
- Subjects: CICLO CELULAR; ENDOMÉTRIO; ONCOLOGIA
- Language: Inglês
- Imprenta:
- Publisher place: Philadelphia
- Date published: 2016
- Source:
- Título do periódico: Cell Cycle
- ISSN: 1551-4005
- Volume/Número/Paginação/Ano: v. 15, n. 7, p. 931-947, 2016
- Este periódico é de assinatura
- Este artigo é de acesso aberto
- URL de acesso aberto
- Cor do Acesso Aberto: bronze
-
ABNT
PAVLIDES, Savvas C et al. TGF-β activates APC through Cdh1 binding for Cks1 and Skp2 proteasomal destruction stabilizing p27kip1 for normal endometrial growth. Cell Cycle, v. 15, n. 7, p. 931-947, 2016Tradução . . Disponível em: https://doi.org/10.1080/15384101.2016.1150393. Acesso em: 19 abr. 2024. -
APA
Pavlides, S. C., Lecanda, J., Daubriac, J., Pandya, U. M., Gama, P., Blank, S., et al. (2016). TGF-β activates APC through Cdh1 binding for Cks1 and Skp2 proteasomal destruction stabilizing p27kip1 for normal endometrial growth. Cell Cycle, 15( 7), 931-947. doi:10.1080/15384101.2016.1150393 -
NLM
Pavlides SC, Lecanda J, Daubriac J, Pandya UM, Gama P, Blank S, Mittal K, Shukla P, Gold LI. TGF-β activates APC through Cdh1 binding for Cks1 and Skp2 proteasomal destruction stabilizing p27kip1 for normal endometrial growth [Internet]. Cell Cycle. 2016 ; 15( 7): 931-947.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1080/15384101.2016.1150393 -
Vancouver
Pavlides SC, Lecanda J, Daubriac J, Pandya UM, Gama P, Blank S, Mittal K, Shukla P, Gold LI. TGF-β activates APC through Cdh1 binding for Cks1 and Skp2 proteasomal destruction stabilizing p27kip1 for normal endometrial growth [Internet]. Cell Cycle. 2016 ; 15( 7): 931-947.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1080/15384101.2016.1150393 - Transforming growth factor 'beta' and celll cycle regulation in endometrial carconomas
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Informações sobre o DOI: 10.1080/15384101.2016.1150393 (Fonte: oaDOI API)
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