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Artigo de periodico
Silencing of IGF1R by Small Interfering RNA (siRNA) in an Adrenocortical Tumor Cell Line (2012)
Ribeiro, Tamaya C.; Montenegro, Luciana; Jorge, Alexander A.; Nishi, Miriam Y.; Latronico, Ana C.; Mendonca, Berenice B.
Fonte: Endocrine Reviews. Nome do evento: ENDO 2012: The Endocrine Society's 94th Annual Meeting & Expo. Unidade: FM
Assuntos: EXPRESSÃO GÊNICA, NEOPLASIAS DAS GLÂNDULAS SUPRARRENAIS, REAÇÃO EM CADEIA POR POLIMERASE, WESTERN BLOTTING, RESUMOS (EVENTOS)
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ABNT
RIBEIRO, Tamaya C. et al. Silencing of IGF1R by Small Interfering RNA (siRNA) in an Adrenocortical Tumor Cell Line. Endocrine Reviews, v. 33, 2012Tradução . . Disponível em: http://edrv.endojournals.org/cgi/content/meeting_abstract/33/03_MeetingAbstracts/SUN-496. Acesso em: 23 ago. 2024.
APA
Ribeiro, T. C., Montenegro, L., Jorge, A. A., Nishi, M. Y., Latronico, A. C., & Mendonca, B. B. (2012). Silencing of IGF1R by Small Interfering RNA (siRNA) in an Adrenocortical Tumor Cell Line. Endocrine Reviews, 33. Recuperado de http://edrv.endojournals.org/cgi/content/meeting_abstract/33/03_MeetingAbstracts/SUN-496
NLM
Ribeiro TC, Montenegro L, Jorge AA, Nishi MY, Latronico AC, Mendonca BB. Silencing of IGF1R by Small Interfering RNA (siRNA) in an Adrenocortical Tumor Cell Line [Internet]. Endocrine Reviews. 2012 ; 33[citado 2024 ago. 23 ] Available from: http://edrv.endojournals.org/cgi/content/meeting_abstract/33/03_MeetingAbstracts/SUN-496
Vancouver
Ribeiro TC, Montenegro L, Jorge AA, Nishi MY, Latronico AC, Mendonca BB. Silencing of IGF1R by Small Interfering RNA (siRNA) in an Adrenocortical Tumor Cell Line [Internet]. Endocrine Reviews. 2012 ; 33[citado 2024 ago. 23 ] Available from: http://edrv.endojournals.org/cgi/content/meeting_abstract/33/03_MeetingAbstracts/SUN-496
Trabalho de evento
Screening of PTPN11 mutations in brazilian patients with noonan syndrome:: identification of a novel mutation (N58D) (2003)
Souza, Silvia C. A. L.; Jorge, Alexander A.; Ferreira, Lize V.; Arnhold, Ivo J. P.; Mendonça, Berenice B.
Fonte: Resumos. Nome do evento: ENDO - The Endocrine Society's Annual Meeting. Unidade: FM
Assunto: ENDOCRINOLOGIA
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ABNT
SOUZA, Silvia C. A. L. et al. Screening of PTPN11 mutations in brazilian patients with noonan syndrome:: identification of a novel mutation (N58D). 2003, Anais.. Philadelphia: Faculdade de Medicina, Universidade de São Paulo, 2003. . Acesso em: 23 ago. 2024.
APA
Souza, S. C. A. L., Jorge, A. A., Ferreira, L. V., Arnhold, I. J. P., & Mendonça, B. B. (2003). Screening of PTPN11 mutations in brazilian patients with noonan syndrome:: identification of a novel mutation (N58D). In Resumos. Philadelphia: Faculdade de Medicina, Universidade de São Paulo.
NLM
Souza SCAL, Jorge AA, Ferreira LV, Arnhold IJP, Mendonça BB. Screening of PTPN11 mutations in brazilian patients with noonan syndrome:: identification of a novel mutation (N58D). Resumos. 2003 ;[citado 2024 ago. 23 ]
Vancouver
Souza SCAL, Jorge AA, Ferreira LV, Arnhold IJP, Mendonça BB. Screening of PTPN11 mutations in brazilian patients with noonan syndrome:: identification of a novel mutation (N58D). Resumos. 2003 ;[citado 2024 ago. 23 ]
Trabalho de evento
Screening for GHR mutations in children with idiopathic short stature (ISS):: identification of two novel mutations (N103S and R368C) (2003)
Jorge, Alexander A.; Lin, Chin J.; Souza, Silvia C. A. L.; Arnhold, Ivo J. P.; Mendonça, Berenice B.
Fonte: Resumos. Nome do evento: ENDO - The Endocrine Society's Annual Meeting. Unidade: FM
Assunto: ENDOCRINOLOGIA
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ABNT
JORGE, Alexander A. et al. Screening for GHR mutations in children with idiopathic short stature (ISS):: identification of two novel mutations (N103S and R368C). 2003, Anais.. Philadelphia: Faculdade de Medicina, Universidade de São Paulo, 2003. . Acesso em: 23 ago. 2024.
APA
Jorge, A. A., Lin, C. J., Souza, S. C. A. L., Arnhold, I. J. P., & Mendonça, B. B. (2003). Screening for GHR mutations in children with idiopathic short stature (ISS):: identification of two novel mutations (N103S and R368C). In Resumos. Philadelphia: Faculdade de Medicina, Universidade de São Paulo.
NLM
Jorge AA, Lin CJ, Souza SCAL, Arnhold IJP, Mendonça BB. Screening for GHR mutations in children with idiopathic short stature (ISS):: identification of two novel mutations (N103S and R368C). Resumos. 2003 ;[citado 2024 ago. 23 ]
Vancouver
Jorge AA, Lin CJ, Souza SCAL, Arnhold IJP, Mendonça BB. Screening for GHR mutations in children with idiopathic short stature (ISS):: identification of two novel mutations (N103S and R368C). Resumos. 2003 ;[citado 2024 ago. 23 ]
Artigo de periodico
An unusual phenotype of fraiser syndrome due to IVS9 +4C>T mutation in the WT1 gene: predominantly male ambiguous genitalia and absence of gonadal dysgenesis (2002)
Melo, Karla F. S.; Martin, Regina M.; Costa, Elaine M. F.; Carvalho, Filomena; Jorge, Alexander A.; Arnhold, Ivo J. P.; Mendonça, Berenice B.
Fonte: The Journal of Clinical Endocrinology & Metabolism. Unidade: FM
Assuntos: ENDOCRINOLOGIA, ANATOMIA PATOLÓGICA
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ABNT
MELO, Karla F. S. et al. An unusual phenotype of fraiser syndrome due to IVS9 +4C>T mutation in the WT1 gene: predominantly male ambiguous genitalia and absence of gonadal dysgenesis. The Journal of Clinical Endocrinology & Metabolism, v. 87, n. 6, p. 2500-2505, 2002Tradução . . Acesso em: 23 ago. 2024.
APA
Melo, K. F. S., Martin, R. M., Costa, E. M. F., Carvalho, F., Jorge, A. A., Arnhold, I. J. P., & Mendonça, B. B. (2002). An unusual phenotype of fraiser syndrome due to IVS9 +4C>T mutation in the WT1 gene: predominantly male ambiguous genitalia and absence of gonadal dysgenesis. The Journal of Clinical Endocrinology & Metabolism, 87( 6), 2500-2505.
NLM
Melo KFS, Martin RM, Costa EMF, Carvalho F, Jorge AA, Arnhold IJP, Mendonça BB. An unusual phenotype of fraiser syndrome due to IVS9 +4C>T mutation in the WT1 gene: predominantly male ambiguous genitalia and absence of gonadal dysgenesis. The Journal of Clinical Endocrinology & Metabolism. 2002 ; 87( 6): 2500-2505.[citado 2024 ago. 23 ]
Vancouver
Melo KFS, Martin RM, Costa EMF, Carvalho F, Jorge AA, Arnhold IJP, Mendonça BB. An unusual phenotype of fraiser syndrome due to IVS9 +4C>T mutation in the WT1 gene: predominantly male ambiguous genitalia and absence of gonadal dysgenesis. The Journal of Clinical Endocrinology & Metabolism. 2002 ; 87( 6): 2500-2505.[citado 2024 ago. 23 ]
Trabalho de evento-resumo
An unusual phenotype in a male patient with frasler syndrome dueto IVS9DS+4C>T mutation: perineal hypospadias (2000)
Melo, Karla F. S.; Martin, Regina M.; Costa, Elaine Maria Frade; Jorge, Alexander A.; Arnhold, Ivo Jorge Prado; Mendonça, Berenice Bilharinho de
Nome do evento: Annual Meeting of the Endocrine Society's. Unidade: FM
Assunto: MEDICINA INTERNA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MELO, Karla F. S. et al. An unusual phenotype in a male patient with frasler syndrome dueto IVS9DS+4C>T mutation: perineal hypospadias. 2000, Anais.. Toronto: Faculdade de Medicina, Universidade de São Paulo, 2000. . Acesso em: 23 ago. 2024.
APA
Melo, K. F. S., Martin, R. M., Costa, E. M. F., Jorge, A. A., Arnhold, I. J. P., & Mendonça, B. B. de. (2000). An unusual phenotype in a male patient with frasler syndrome dueto IVS9DS+4C>T mutation: perineal hypospadias. In . Toronto: Faculdade de Medicina, Universidade de São Paulo.
NLM
Melo KFS, Martin RM, Costa EMF, Jorge AA, Arnhold IJP, Mendonça BB de. An unusual phenotype in a male patient with frasler syndrome dueto IVS9DS+4C>T mutation: perineal hypospadias. 2000 ;[citado 2024 ago. 23 ]
Vancouver
Melo KFS, Martin RM, Costa EMF, Jorge AA, Arnhold IJP, Mendonça BB de. An unusual phenotype in a male patient with frasler syndrome dueto IVS9DS+4C>T mutation: perineal hypospadias. 2000 ;[citado 2024 ago. 23 ]

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