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COLABARDINI, Ana Cristina. Análise funcional dos genes que codificam as proteínas quinases pkcA e ypkA de Aspergillus nidulans. 2014. Tese (Doutorado) – Universidade de São Paulo, Ribeirão Preto, 2014. . Acesso em: 03 out. 2024.
APA
Colabardini, A. C. (2014). Análise funcional dos genes que codificam as proteínas quinases pkcA e ypkA de Aspergillus nidulans (Tese (Doutorado). Universidade de São Paulo, Ribeirão Preto.
NLM
Colabardini AC. Análise funcional dos genes que codificam as proteínas quinases pkcA e ypkA de Aspergillus nidulans. 2014 ;[citado 2024 out. 03 ]
Vancouver
Colabardini AC. Análise funcional dos genes que codificam as proteínas quinases pkcA e ypkA de Aspergillus nidulans. 2014 ;[citado 2024 out. 03 ]
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BIAGI, Diogo G. et al. A negative screen for mutations in calstabin 1 and 2 genes in patients with dilated cardiomyopathy. Journal of Negative Results in BioMedicine, v. 11, n. 4, p. (online) 1-5, 2012Tradução . . Disponível em: https://doi.org/10.1186/1477-5751-11-4. Acesso em: 03 out. 2024.
APA
Biagi, D. G., Mill, J. G., Mansur, A. J., Krieger, J. E., & Pereira, A. C. (2012). A negative screen for mutations in calstabin 1 and 2 genes in patients with dilated cardiomyopathy. Journal of Negative Results in BioMedicine, 11( 4), (online) 1-5. doi:10.1186/1477-5751-11-4
NLM
Biagi DG, Mill JG, Mansur AJ, Krieger JE, Pereira AC. A negative screen for mutations in calstabin 1 and 2 genes in patients with dilated cardiomyopathy [Internet]. Journal of Negative Results in BioMedicine. 2012 ; 11( 4): (online) 1-5.[citado 2024 out. 03 ] Available from: https://doi.org/10.1186/1477-5751-11-4
Vancouver
Biagi DG, Mill JG, Mansur AJ, Krieger JE, Pereira AC. A negative screen for mutations in calstabin 1 and 2 genes in patients with dilated cardiomyopathy [Internet]. Journal of Negative Results in BioMedicine. 2012 ; 11( 4): (online) 1-5.[citado 2024 out. 03 ] Available from: https://doi.org/10.1186/1477-5751-11-4
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ALCALDE, Rosana et al. Clinical, epidemiological and molecular features of the HIV-1 subtype C and recombinant forms that are circulating in the city of São Paulo, Brazil. Virology Journal, v. 9, n. 156, p. 1-10 (online), 2012Tradução . . Disponível em: https://doi.org/10.1186/1743-422x-9-156. Acesso em: 03 out. 2024.
APA
Alcalde, R., Guimarães, M. L., Duarte, A. J. S., & Casseb, J. S. do R. (2012). Clinical, epidemiological and molecular features of the HIV-1 subtype C and recombinant forms that are circulating in the city of São Paulo, Brazil. Virology Journal, 9( 156), 1-10 (online). doi:10.1186/1743-422x-9-156
NLM
Alcalde R, Guimarães ML, Duarte AJS, Casseb JS do R. Clinical, epidemiological and molecular features of the HIV-1 subtype C and recombinant forms that are circulating in the city of São Paulo, Brazil [Internet]. Virology Journal. 2012 ; 9( 156): 1-10 (online).[citado 2024 out. 03 ] Available from: https://doi.org/10.1186/1743-422x-9-156
Vancouver
Alcalde R, Guimarães ML, Duarte AJS, Casseb JS do R. Clinical, epidemiological and molecular features of the HIV-1 subtype C and recombinant forms that are circulating in the city of São Paulo, Brazil [Internet]. Virology Journal. 2012 ; 9( 156): 1-10 (online).[citado 2024 out. 03 ] Available from: https://doi.org/10.1186/1743-422x-9-156
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LIMA, Hildenêr Nogueira et al. Molecular epidemiology of the SH (small hydrophobic) gene of human respiratory syncytial virus (HRSV), over 2 consecutive years. Virus Research, v. 163, n. 1, p. 82-86, 2012Tradução . . Disponível em: https://doi.org/10.1016/j.virusres.2011.08.013. Acesso em: 03 out. 2024.
APA
Lima, H. N., Botosso, V. F., Oliveira, D. B. L., Campos, A. C. de A., Leal, A. L., Silva, T. S., et al. (2012). Molecular epidemiology of the SH (small hydrophobic) gene of human respiratory syncytial virus (HRSV), over 2 consecutive years. Virus Research, 163( 1), 82-86. doi:10.1016/j.virusres.2011.08.013
NLM
Lima HN, Botosso VF, Oliveira DBL, Campos AC de A, Leal AL, Silva TS, Bosso PAR, Moraes CTP, Silva Filho CG da, Vieira SE, Gilio AE, Stewien KE, Durigon EL. Molecular epidemiology of the SH (small hydrophobic) gene of human respiratory syncytial virus (HRSV), over 2 consecutive years [Internet]. Virus Research. 2012 ; 163( 1): 82-86.[citado 2024 out. 03 ] Available from: https://doi.org/10.1016/j.virusres.2011.08.013
Vancouver
Lima HN, Botosso VF, Oliveira DBL, Campos AC de A, Leal AL, Silva TS, Bosso PAR, Moraes CTP, Silva Filho CG da, Vieira SE, Gilio AE, Stewien KE, Durigon EL. Molecular epidemiology of the SH (small hydrophobic) gene of human respiratory syncytial virus (HRSV), over 2 consecutive years [Internet]. Virus Research. 2012 ; 163( 1): 82-86.[citado 2024 out. 03 ] Available from: https://doi.org/10.1016/j.virusres.2011.08.013
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PAULO, Sabrina Soares. Análise dos genes SHH e GLI2 em pacientes com hipopituitarismo e/ou defeitos de linha média cerebral. 2012. Tese (Doutorado) – Universidade de São Paulo, Ribeirão Preto, 2012. . Acesso em: 03 out. 2024.
APA
Paulo, S. S. (2012). Análise dos genes SHH e GLI2 em pacientes com hipopituitarismo e/ou defeitos de linha média cerebral (Tese (Doutorado). Universidade de São Paulo, Ribeirão Preto.
NLM
Paulo SS. Análise dos genes SHH e GLI2 em pacientes com hipopituitarismo e/ou defeitos de linha média cerebral. 2012 ;[citado 2024 out. 03 ]
Vancouver
Paulo SS. Análise dos genes SHH e GLI2 em pacientes com hipopituitarismo e/ou defeitos de linha média cerebral. 2012 ;[citado 2024 out. 03 ]
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MOREIRA, Ricardo P. P. et al. Impact of Glucocorticoid Receptor Gene Polymorphisms on the Metabolic Profile of Adult Patients with the Classical Form of 21-Hydroxylase Deficiency. PLOS ONE, v. 7, n. 92, p. 7 art., 2012Tradução . . Disponível em: https://doi.org/10.1371/journal.pone.0044893. Acesso em: 03 out. 2024.
APA
Moreira, R. P. P., Gomes, L. G., Mendonca, B. B., & Bachega, T. A. S. S. B. (2012). Impact of Glucocorticoid Receptor Gene Polymorphisms on the Metabolic Profile of Adult Patients with the Classical Form of 21-Hydroxylase Deficiency. PLOS ONE, 7( 92), 7 art. doi:10.1371/journal.pone.0044893
NLM
Moreira RPP, Gomes LG, Mendonca BB, Bachega TASSB. Impact of Glucocorticoid Receptor Gene Polymorphisms on the Metabolic Profile of Adult Patients with the Classical Form of 21-Hydroxylase Deficiency [Internet]. PLOS ONE. 2012 ; 7( 92): 7 art.[citado 2024 out. 03 ] Available from: https://doi.org/10.1371/journal.pone.0044893
Vancouver
Moreira RPP, Gomes LG, Mendonca BB, Bachega TASSB. Impact of Glucocorticoid Receptor Gene Polymorphisms on the Metabolic Profile of Adult Patients with the Classical Form of 21-Hydroxylase Deficiency [Internet]. PLOS ONE. 2012 ; 7( 92): 7 art.[citado 2024 out. 03 ] Available from: https://doi.org/10.1371/journal.pone.0044893
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PONTILLO, Alessandra et al. Polymorphisms in inflammasome' genes and susceptibility to HIV-1 infection. Journal of acquired immune deficiency syndromes, v. 59, n. 2, p. 121-125, 2012Tradução . . Disponível em: https://doi.org/10.1097/QAI.0b013e3182392ebe. Acesso em: 03 out. 2024.
APA
Pontillo, A., Oshiro, T. M., Girardelli, M., Kamada, A. J., Crovella, S., & Duarte, A. J. S. (2012). Polymorphisms in inflammasome' genes and susceptibility to HIV-1 infection. Journal of acquired immune deficiency syndromes, 59( 2), 121-125. doi:10.1097/QAI.0b013e3182392ebe
NLM
Pontillo A, Oshiro TM, Girardelli M, Kamada AJ, Crovella S, Duarte AJS. Polymorphisms in inflammasome' genes and susceptibility to HIV-1 infection [Internet]. Journal of acquired immune deficiency syndromes. 2012 ; 59( 2): 121-125.[citado 2024 out. 03 ] Available from: https://doi.org/10.1097/QAI.0b013e3182392ebe
Vancouver
Pontillo A, Oshiro TM, Girardelli M, Kamada AJ, Crovella S, Duarte AJS. Polymorphisms in inflammasome' genes and susceptibility to HIV-1 infection [Internet]. Journal of acquired immune deficiency syndromes. 2012 ; 59( 2): 121-125.[citado 2024 out. 03 ] Available from: https://doi.org/10.1097/QAI.0b013e3182392ebe
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MARUI, Suemi et al. GH-Releasing hormone receptor gene: a novel splice-disrupting mutation and study of founder effects. Hormone research in paediatrics, v. 78, n. 3, p. 165-172, 2012Tradução . . Disponível em: https://doi.org/10.1159/000342760. Acesso em: 03 out. 2024.
APA
Marui, S., Trabach, E. b., Boguszewski, M. C. S., França, M. M., Jorge, A. A. L., Inoue, H., et al. (2012). GH-Releasing hormone receptor gene: a novel splice-disrupting mutation and study of founder effects. Hormone research in paediatrics, 78( 3), 165-172. doi:10.1159/000342760
NLM
Marui S, Trabach E b., Boguszewski MCS, França MM, Jorge AAL, Inoue H, Nishi MY, Lacerda Filho L de, Aguiar-Oliveira MH, Mendonça BB, Arnhold IJP. GH-Releasing hormone receptor gene: a novel splice-disrupting mutation and study of founder effects [Internet]. Hormone research in paediatrics. 2012 ;78( 3): 165-172.[citado 2024 out. 03 ] Available from: https://doi.org/10.1159/000342760
Vancouver
Marui S, Trabach E b., Boguszewski MCS, França MM, Jorge AAL, Inoue H, Nishi MY, Lacerda Filho L de, Aguiar-Oliveira MH, Mendonça BB, Arnhold IJP. GH-Releasing hormone receptor gene: a novel splice-disrupting mutation and study of founder effects [Internet]. Hormone research in paediatrics. 2012 ;78( 3): 165-172.[citado 2024 out. 03 ] Available from: https://doi.org/10.1159/000342760
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BENEDUZZI, Daiane et al. Novel mutation in the gonadotropin-releasing hormone receptor (GNRHR) gene in a patient with normosmic isolated hypogonadotropic hypogonadism. Arquivos Brasileiros de Endocrinologia & Metabologia, v. 56, n. 8, p. 540-544, 2012Tradução . . Disponível em: https://doi.org/10.1590/s0004-27302012000800013. Acesso em: 03 out. 2024.
APA
Beneduzzi, D., Trarbach, E. B., Xavier, A. C. L., Mendonça, B. B. de, & Silveira, L. F. G. (2012). Novel mutation in the gonadotropin-releasing hormone receptor (GNRHR) gene in a patient with normosmic isolated hypogonadotropic hypogonadism. Arquivos Brasileiros de Endocrinologia & Metabologia, 56( 8), 540-544. doi:10.1590/s0004-27302012000800013
NLM
Beneduzzi D, Trarbach EB, Xavier ACL, Mendonça BB de, Silveira LFG. Novel mutation in the gonadotropin-releasing hormone receptor (GNRHR) gene in a patient with normosmic isolated hypogonadotropic hypogonadism [Internet]. Arquivos Brasileiros de Endocrinologia & Metabologia. 2012 ; 56( 8): 540-544.[citado 2024 out. 03 ] Available from: https://doi.org/10.1590/s0004-27302012000800013
Vancouver
Beneduzzi D, Trarbach EB, Xavier ACL, Mendonça BB de, Silveira LFG. Novel mutation in the gonadotropin-releasing hormone receptor (GNRHR) gene in a patient with normosmic isolated hypogonadotropic hypogonadism [Internet]. Arquivos Brasileiros de Endocrinologia & Metabologia. 2012 ; 56( 8): 540-544.[citado 2024 out. 03 ] Available from: https://doi.org/10.1590/s0004-27302012000800013
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ZAMBONI, A. et al. A Novel Heterozygous Missense Variant on FGFR2 Gene in Two 46,XY Sisters with Non-syndromic Partial Gonadal Dysgenesis. Hormone Research in Paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo. Disponível em: http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowPDF&ArtikelNr=330526&Ausgabe=255433&ProduktNr=224036&filename=330526.pdf. Acesso em: 03 out. 2024. , 2011
APA
Zamboni, A., Gerdulo, M., Nishi, M. Y., Pontual, M., Frade, E., Mendonça. B.,, & Domenice, S. (2011). A Novel Heterozygous Missense Variant on FGFR2 Gene in Two 46,XY Sisters with Non-syndromic Partial Gonadal Dysgenesis. Hormone Research in Paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo. Recuperado de http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowPDF&ArtikelNr=330526&Ausgabe=255433&ProduktNr=224036&filename=330526.pdf
NLM
Zamboni A, Gerdulo M, Nishi MY, Pontual M, Frade E, Mendonça. B., Domenice S. A Novel Heterozygous Missense Variant on FGFR2 Gene in Two 46,XY Sisters with Non-syndromic Partial Gonadal Dysgenesis [Internet]. Hormone Research in Paediatrics. 2011 ; 76( suppl. 4): 4.[citado 2024 out. 03 ] Available from: http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowPDF&ArtikelNr=330526&Ausgabe=255433&ProduktNr=224036&filename=330526.pdf
Vancouver
Zamboni A, Gerdulo M, Nishi MY, Pontual M, Frade E, Mendonça. B., Domenice S. A Novel Heterozygous Missense Variant on FGFR2 Gene in Two 46,XY Sisters with Non-syndromic Partial Gonadal Dysgenesis [Internet]. Hormone Research in Paediatrics. 2011 ; 76( suppl. 4): 4.[citado 2024 out. 03 ] Available from: http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowPDF&ArtikelNr=330526&Ausgabe=255433&ProduktNr=224036&filename=330526.pdf
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SALATHIEL, Adriana Shikiera Martinelli et al. Genotipagem HLA DR e DQ em familiares de gêmeas monozigóticas com pênfigo vulgar. 2011, Anais.. Florianópolis: SBD, 2011. . Acesso em: 03 out. 2024.
APA
Salathiel, A. S. M., Deghaide, N. H. S., Donadi, E. A., & Roselino, A. M. F. (2011). Genotipagem HLA DR e DQ em familiares de gêmeas monozigóticas com pênfigo vulgar. In Resumos. Florianópolis: SBD.
NLM
Salathiel ASM, Deghaide NHS, Donadi EA, Roselino AMF. Genotipagem HLA DR e DQ em familiares de gêmeas monozigóticas com pênfigo vulgar. Resumos. 2011 ;[citado 2024 out. 03 ]
Vancouver
Salathiel ASM, Deghaide NHS, Donadi EA, Roselino AMF. Genotipagem HLA DR e DQ em familiares de gêmeas monozigóticas com pênfigo vulgar. Resumos. 2011 ;[citado 2024 out. 03 ]
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GUILHERME, L. et al. Genes, autoimmunity and pathogenesis of rheumatic heart disease. Annals of Pediatric Cardiology, v. 4, n. 1, p. 13-21, 2011Tradução . . Disponível em: https://doi.org/10.4103/0974-2069.79617. Acesso em: 03 out. 2024.
APA
Guilherme, L., Köhler, K. F., Postol, E., & Kalil, J. (2011). Genes, autoimmunity and pathogenesis of rheumatic heart disease. Annals of Pediatric Cardiology, 4( 1), 13-21. doi:10.4103/0974-2069.79617
NLM
Guilherme L, Köhler KF, Postol E, Kalil J. Genes, autoimmunity and pathogenesis of rheumatic heart disease [Internet]. Annals of Pediatric Cardiology. 2011 ; 4( 1): 13-21.[citado 2024 out. 03 ] Available from: https://doi.org/10.4103/0974-2069.79617
Vancouver
Guilherme L, Köhler KF, Postol E, Kalil J. Genes, autoimmunity and pathogenesis of rheumatic heart disease [Internet]. Annals of Pediatric Cardiology. 2011 ; 4( 1): 13-21.[citado 2024 out. 03 ] Available from: https://doi.org/10.4103/0974-2069.79617
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FRANÇA, M. et al. Analyses of the GLI2 Gene in Patients with Congenital Isolated GH Deficiency (IGHD) or Associated to Other Pituitary Hormone Deficiencies (CPHD) Without Holoprosencephaly (HPE). Hormone Research in Paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo. Disponível em: http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowPDF&ArtikelNr=330526&Ausgabe=255433&ProduktNr=224036&filename=330526.pdf. Acesso em: 03 out. 2024. , 2011
APA
França, M., Jorge, A., Carvalho, L., Otto, A., Corrêa, F., Costalonga, E., et al. (2011). Analyses of the GLI2 Gene in Patients with Congenital Isolated GH Deficiency (IGHD) or Associated to Other Pituitary Hormone Deficiencies (CPHD) Without Holoprosencephaly (HPE). Hormone Research in Paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo. Recuperado de http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowPDF&ArtikelNr=330526&Ausgabe=255433&ProduktNr=224036&filename=330526.pdf
NLM
França M, Jorge A, Carvalho L, Otto A, Corrêa F, Costalonga E, Mendonça. B., Arnhold I. Analyses of the GLI2 Gene in Patients with Congenital Isolated GH Deficiency (IGHD) or Associated to Other Pituitary Hormone Deficiencies (CPHD) Without Holoprosencephaly (HPE) [Internet]. Hormone Research in Paediatrics. 2011 ; 76( suppl. 4): 1.[citado 2024 out. 03 ] Available from: http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowPDF&ArtikelNr=330526&Ausgabe=255433&ProduktNr=224036&filename=330526.pdf
Vancouver
França M, Jorge A, Carvalho L, Otto A, Corrêa F, Costalonga E, Mendonça. B., Arnhold I. Analyses of the GLI2 Gene in Patients with Congenital Isolated GH Deficiency (IGHD) or Associated to Other Pituitary Hormone Deficiencies (CPHD) Without Holoprosencephaly (HPE) [Internet]. Hormone Research in Paediatrics. 2011 ; 76( suppl. 4): 1.[citado 2024 out. 03 ] Available from: http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowPDF&ArtikelNr=330526&Ausgabe=255433&ProduktNr=224036&filename=330526.pdf
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EWALD, Ingrid P. et al. Prevalence of the BRCA1 founder mutation c.5266dupin Brazilian individuals at-risk for the hereditary breast and ovarian cancer syndrome. Hereditary Cancer in Clinical Practice, v. 9, n. 1, p. (online), 2011Tradução . . Disponível em: https://doi.org/10.1186/1897-4287-9-12. Acesso em: 03 out. 2024.
APA
Ewald, I. P., Izetti, P., Vargas, F. R., Moreira, M. A. M., Moreira, A. S., Moreira-Filho, C. A., et al. (2011). Prevalence of the BRCA1 founder mutation c.5266dupin Brazilian individuals at-risk for the hereditary breast and ovarian cancer syndrome. Hereditary Cancer in Clinical Practice, 9( 1), (online). doi:10.1186/1897-4287-9-12
NLM
Ewald IP, Izetti P, Vargas FR, Moreira MAM, Moreira AS, Moreira-Filho CA, Cunha DR, Hamaguchi S, Camey SA, Schmidt A, Caleffi M, Koehler-Santos P, Giugliani R, Ashton-Prolla P. Prevalence of the BRCA1 founder mutation c.5266dupin Brazilian individuals at-risk for the hereditary breast and ovarian cancer syndrome [Internet]. Hereditary Cancer in Clinical Practice. 2011 ; 9( 1): (online).[citado 2024 out. 03 ] Available from: https://doi.org/10.1186/1897-4287-9-12
Vancouver
Ewald IP, Izetti P, Vargas FR, Moreira MAM, Moreira AS, Moreira-Filho CA, Cunha DR, Hamaguchi S, Camey SA, Schmidt A, Caleffi M, Koehler-Santos P, Giugliani R, Ashton-Prolla P. Prevalence of the BRCA1 founder mutation c.5266dupin Brazilian individuals at-risk for the hereditary breast and ovarian cancer syndrome [Internet]. Hereditary Cancer in Clinical Practice. 2011 ; 9( 1): (online).[citado 2024 out. 03 ] Available from: https://doi.org/10.1186/1897-4287-9-12
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PIRES, Patricia N. Pugliese et al. Novel inactivating mutations in the GH secretagogue receptor gene in patients with constitutional delay of growth and puberty. European journal of endocrinology, v. 165, n. 2, p. 233-241, 2011Tradução . . Disponível em: https://doi.org/10.1530/EJE-11-016. Acesso em: 03 out. 2024.
APA
Pires, P. N. P., Fortin, J. -P., Arthur, T., Xavier, A. C. L., Mendonça, B. B. de, Villares, S. M. F., et al. (2011). Novel inactivating mutations in the GH secretagogue receptor gene in patients with constitutional delay of growth and puberty. European journal of endocrinology, 165( 2), 233-241. doi:10.1530/EJE-11-016
NLM
Pires PNP, Fortin J-P, Arthur T, Xavier ACL, Mendonça BB de, Villares SMF, Arnhold IJP, Kopin AS, Jorge AA de L. Novel inactivating mutations in the GH secretagogue receptor gene in patients with constitutional delay of growth and puberty [Internet]. European journal of endocrinology. 2011 ; 165( 2): 233-241.[citado 2024 out. 03 ] Available from: https://doi.org/10.1530/EJE-11-016
Vancouver
Pires PNP, Fortin J-P, Arthur T, Xavier ACL, Mendonça BB de, Villares SMF, Arnhold IJP, Kopin AS, Jorge AA de L. Novel inactivating mutations in the GH secretagogue receptor gene in patients with constitutional delay of growth and puberty [Internet]. European journal of endocrinology. 2011 ; 165( 2): 233-241.[citado 2024 out. 03 ] Available from: https://doi.org/10.1530/EJE-11-016
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LIBORIO, Tatiana N. et al. In situ hybridization detection of homeobox genes reveals distinct expression patterns in oral squamous cell carcinomas. Histopatology, v. 58, n. 2, p. 225-233, 2011Tradução . . Disponível em: http://onlinelibrary.wiley.com/doi/10.1111/j.1365-2559.2011.03751.x/pdf. Acesso em: 03 out. 2024.
APA
Liborio, T. N., Acquafreda, T., Matizonkas-Antonio, L. F., Silva-Valenzuela, M. G., Ferraz, A. R., & Nunes, F. D. (2011). In situ hybridization detection of homeobox genes reveals distinct expression patterns in oral squamous cell carcinomas. Histopatology, 58( 2), 225-233. doi:10.1111/j.1365-2559.2011.03751.x
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BANDO, Silvia Y. et al. Hippocampal CA3 Transcriptome Signature Correlates with Initial Precipitating Injury in Refractory Mesial Temporal Lobe Epilepsy. PLOS ONE, v. 6, n. 10, 2011Tradução . . Disponível em: https://doi.org/10.1371/journal.pone.0026268. Acesso em: 03 out. 2024.
APA
Bando, S. Y., Alegro, M. de C., Amaro, E., Silva, A. V., Castro, L. H. M., Wen, H. -T., et al. (2011). Hippocampal CA3 Transcriptome Signature Correlates with Initial Precipitating Injury in Refractory Mesial Temporal Lobe Epilepsy. PLOS ONE, 6( 10). doi:10.1371/journal.pone.0026268
NLM
Bando SY, Alegro M de C, Amaro E, Silva AV, Castro LHM, Wen H-T, Lima L de A, Brentani H, Moreira-Filho CA. Hippocampal CA3 Transcriptome Signature Correlates with Initial Precipitating Injury in Refractory Mesial Temporal Lobe Epilepsy [Internet]. PLOS ONE. 2011 ; 6( 10):[citado 2024 out. 03 ] Available from: https://doi.org/10.1371/journal.pone.0026268
Vancouver
Bando SY, Alegro M de C, Amaro E, Silva AV, Castro LHM, Wen H-T, Lima L de A, Brentani H, Moreira-Filho CA. Hippocampal CA3 Transcriptome Signature Correlates with Initial Precipitating Injury in Refractory Mesial Temporal Lobe Epilepsy [Internet]. PLOS ONE. 2011 ; 6( 10):[citado 2024 out. 03 ] Available from: https://doi.org/10.1371/journal.pone.0026268
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VIEIRA, Suzana M. et al. Association of genetic variants in the promoter region of genes encoding p22phox (CYBA) and glutamate cysteine ligase catalytic subunit (GCLC) and renal disease in patients with type 1 diabetes mellitus. BMC Medical Genetics, v. 12, n. 129, p. 1-6, 2011Tradução . . Disponível em: https://doi.org/10.1186/1471-2350-12-129. Acesso em: 03 out. 2024.
APA
Vieira, S. M., Monteiro, M. B., Marques, T., Luna, A. M., Fortes, M. A., Nery, M., et al. (2011). Association of genetic variants in the promoter region of genes encoding p22phox (CYBA) and glutamate cysteine ligase catalytic subunit (GCLC) and renal disease in patients with type 1 diabetes mellitus. BMC Medical Genetics, 12( 129), 1-6. doi:10.1186/1471-2350-12-129
NLM
Vieira SM, Monteiro MB, Marques T, Luna AM, Fortes MA, Nery M, Queiroz M, Dib SA, Vendramini MF, Azevedo MJ, Canani LH, Parisi MC, Pavin EJ, Giannella-Neto D, Corrêa-Giannella ML. Association of genetic variants in the promoter region of genes encoding p22phox (CYBA) and glutamate cysteine ligase catalytic subunit (GCLC) and renal disease in patients with type 1 diabetes mellitus [Internet]. BMC Medical Genetics. 2011 ; 12( 129): 1-6.[citado 2024 out. 03 ] Available from: https://doi.org/10.1186/1471-2350-12-129
Vancouver
Vieira SM, Monteiro MB, Marques T, Luna AM, Fortes MA, Nery M, Queiroz M, Dib SA, Vendramini MF, Azevedo MJ, Canani LH, Parisi MC, Pavin EJ, Giannella-Neto D, Corrêa-Giannella ML. Association of genetic variants in the promoter region of genes encoding p22phox (CYBA) and glutamate cysteine ligase catalytic subunit (GCLC) and renal disease in patients with type 1 diabetes mellitus [Internet]. BMC Medical Genetics. 2011 ; 12( 129): 1-6.[citado 2024 out. 03 ] Available from: https://doi.org/10.1186/1471-2350-12-129
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MASCHIETTO, Mariana et al. Gene expression analysis of blastemal component reveals genes associated with relapse mechanism in Wilms tumour. European journal of cancer, v. 47, n. 18, p. 2715\20132722, 2011Tradução . . Disponível em: https://doi.org/10.1016/j.ejca.2011.05.024. Acesso em: 03 out. 2024.
APA
Maschietto, M., Piccoli, F. S., Costa, C. M. L., Camargo, L. P., Neves, J. I., Grundy, P. E., et al. (2011). Gene expression analysis of blastemal component reveals genes associated with relapse mechanism in Wilms tumour. European journal of cancer, 47( 18), 2715\20132722. doi:10.1016/j.ejca.2011.05.024
NLM
Maschietto M, Piccoli FS, Costa CML, Camargo LP, Neves JI, Grundy PE, Brentani HP, Soares FA, Camargo B de, Carraro DM. Gene expression analysis of blastemal component reveals genes associated with relapse mechanism in Wilms tumour [Internet]. European journal of cancer. 2011 ; 47( 18): 2715\20132722.[citado 2024 out. 03 ] Available from: https://doi.org/10.1016/j.ejca.2011.05.024
Vancouver
Maschietto M, Piccoli FS, Costa CML, Camargo LP, Neves JI, Grundy PE, Brentani HP, Soares FA, Camargo B de, Carraro DM. Gene expression analysis of blastemal component reveals genes associated with relapse mechanism in Wilms tumour [Internet]. European journal of cancer. 2011 ; 47( 18): 2715\20132722.[citado 2024 out. 03 ] Available from: https://doi.org/10.1016/j.ejca.2011.05.024
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FRANÇA, Marcela et al. Considerable frequency of novel GLI2 missense witations in patientes with hypopituitarism without holoprosencephaly. . Basel: Faculdade de Medicina, Universidade de São Paulo. Disponível em: http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowPDF&ArtikelNr=334325&Ausgabe=255336&ProduktNr=224036&filename=334325.pdf. Acesso em: 03 out. 2024. , 2011
APA
França, M., Jorge, A., Otto, A., Carvalho, L., Mendonça, B. B. de, & Arnhold, I. J. P. (2011). Considerable frequency of novel GLI2 missense witations in patientes with hypopituitarism without holoprosencephaly. Basel: Faculdade de Medicina, Universidade de São Paulo. Recuperado de http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowPDF&ArtikelNr=334325&Ausgabe=255336&ProduktNr=224036&filename=334325.pdf
NLM
França M, Jorge A, Otto A, Carvalho L, Mendonça BB de, Arnhold IJP. Considerable frequency of novel GLI2 missense witations in patientes with hypopituitarism without holoprosencephaly [Internet]. 2011 ; 76 25.[citado 2024 out. 03 ] Available from: http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowPDF&ArtikelNr=334325&Ausgabe=255336&ProduktNr=224036&filename=334325.pdf
Vancouver
França M, Jorge A, Otto A, Carvalho L, Mendonça BB de, Arnhold IJP. Considerable frequency of novel GLI2 missense witations in patientes with hypopituitarism without holoprosencephaly [Internet]. 2011 ; 76 25.[citado 2024 out. 03 ] Available from: http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowPDF&ArtikelNr=334325&Ausgabe=255336&ProduktNr=224036&filename=334325.pdf