Epigenetic silencing of the adhesion molecule ADAM23 is highly frequent in breast tumors (2004)
- Authors:
- Costa, Fabrício F.
- Verbisck, Newton Valério
- Salim, Anna Christina de Matos
- Ierardi, Daniela Filippini
- Pires, Lilian Campos Pires
- Sasahara, Regina Maki
- Sogayar, Mari Cleide
- Zanata, Silvio Marques - Universidade Federal do Paraná (UFPR)
- Mackay, Alan
- O'Hare, Michael
- Soares, Fernando Augusto
- Simpson, Andrew John George
- Camargo, Anamaria Aranha
- Autor USP: SOGAYAR, MARI CLEIDE - IQ
- Unidade: IQ
- DOI: 10.1038/sj.onc.1207263
- Subjects: GENES SUPRESSORES DE TUMOR; EXPRESSÃO GÊNICA
- Language: Inglês
- Imprenta:
- Publisher place: Basingstoke
- Date published: 2004
- Source:
- Este periódico é de assinatura
- Este artigo é de acesso aberto
- URL de acesso aberto
- Cor do Acesso Aberto: bronze
-
ABNT
COSTA, Fabrício F.; VERBISCK, Newton Valério; SALIM, Anna Christina de Matos; et al. Epigenetic silencing of the adhesion molecule ADAM23 is highly frequent in breast tumors. Oncogene, Basingstoke, v. 23, n. 7, p. 1481-1488, 2004. DOI: 10.1038/sj.onc.1207263. -
APA
Costa, F. F., Verbisck, N. V., Salim, A. C. de M., Ierardi, D. F., Pires, L. C. P., Sasahara, R. M., et al. (2004). Epigenetic silencing of the adhesion molecule ADAM23 is highly frequent in breast tumors. Oncogene, 23( 7), 1481-1488. doi:10.1038/sj.onc.1207263 -
NLM
Costa FF, Verbisck NV, Salim AC de M, Ierardi DF, Pires LCP, Sasahara RM, Sogayar MC, Zanata SM, Mackay A, O'Hare M, Soares FA, Simpson AJG, Camargo AA. Epigenetic silencing of the adhesion molecule ADAM23 is highly frequent in breast tumors. Oncogene. 2004 ; 23( 7): 1481-1488. -
Vancouver
Costa FF, Verbisck NV, Salim AC de M, Ierardi DF, Pires LCP, Sasahara RM, Sogayar MC, Zanata SM, Mackay A, O'Hare M, Soares FA, Simpson AJG, Camargo AA. Epigenetic silencing of the adhesion molecule ADAM23 is highly frequent in breast tumors. Oncogene. 2004 ; 23( 7): 1481-1488. - Three-dimensional islet-cell structures as a new source for cell-based biabetes therapy
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Informações sobre o DOI: 10.1038/sj.onc.1207263 (Fonte: oaDOI API)
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