Fonte: Hormone research. Nome do evento: Annual meeting of the sociedad latino-americana de endocrinología pediátrica - SLEP. Unidade: FM
Assuntos: MUTATAÇÃO GENÉTICA, APOPTOSE, NEOPLASIAS DAS GLÂNDULAS SUPRARRENAIS
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ALMEIDA, M. Queiroz et al. Mutation in PTPN11 gene are a common cause of noonan syndrome (NS) but are not a selective IGF-1 receptor kinase inhibitor (NVP-AEW541) suppresses proliferation of the human adrenocortical cancer cell line NCI H295 due to apoptosis induction. Hormone research, v. 68, p. 24, 2007Tradução . . Acesso em: 24 out. 2025.APA
Almeida, M. Q., Gerdulo, M., Jorge, A. L. A., Nishi, M. Y., Lerario, A., Fragoso, M. B. V., et al. (2007). Mutation in PTPN11 gene are a common cause of noonan syndrome (NS) but are not a selective IGF-1 receptor kinase inhibitor (NVP-AEW541) suppresses proliferation of the human adrenocortical cancer cell line NCI H295 due to apoptosis induction. Hormone research, 68, 24.NLM
Almeida MQ, Gerdulo M, Jorge ALA, Nishi MY, Lerario A, Fragoso MBV, Mendonça BB de, Xavier ACL. Mutation in PTPN11 gene are a common cause of noonan syndrome (NS) but are not a selective IGF-1 receptor kinase inhibitor (NVP-AEW541) suppresses proliferation of the human adrenocortical cancer cell line NCI H295 due to apoptosis induction. Hormone research. 2007 ; 68 24.[citado 2025 out. 24 ]Vancouver
Almeida MQ, Gerdulo M, Jorge ALA, Nishi MY, Lerario A, Fragoso MBV, Mendonça BB de, Xavier ACL. Mutation in PTPN11 gene are a common cause of noonan syndrome (NS) but are not a selective IGF-1 receptor kinase inhibitor (NVP-AEW541) suppresses proliferation of the human adrenocortical cancer cell line NCI H295 due to apoptosis induction. Hormone research. 2007 ; 68 24.[citado 2025 out. 24 ]
