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Artigo de periodico
Emergence of Avian coronavirus escape mutants under suboptimal antibody titers (2022)
Brandão, Paulo Eduardo ; Berg, M; Silva, Sheila Oliveira de Souza ; Taniwaki, S. A
Source: Journal of Molecular Evolution. Unidade: FMVZ
Subjects: CORONAVIRUS, GALINHAS, MUTAÇÃO GENÉTICA, VACINAS
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BRANDÃO, Paulo Eduardo et al. Emergence of Avian coronavirus escape mutants under suboptimal antibody titers. Journal of Molecular Evolution, v. 90, p. 176-181, 2022Tradução . . Disponível em: https://doi.org/10.1007/s00239-022-10050-8. Acesso em: 16 out. 2024.
APA
Brandão, P. E., Berg, M., Silva, S. O. de S., & Taniwaki, S. A. (2022). Emergence of Avian coronavirus escape mutants under suboptimal antibody titers. Journal of Molecular Evolution, 90, 176-181. doi:10.1007/s00239-022-10050-8
NLM
Brandão PE, Berg M, Silva SO de S, Taniwaki SA. Emergence of Avian coronavirus escape mutants under suboptimal antibody titers [Internet]. Journal of Molecular Evolution. 2022 ; 90 176-181.[citado 2024 out. 16 ] Available from: https://doi.org/10.1007/s00239-022-10050-8
Vancouver
Brandão PE, Berg M, Silva SO de S, Taniwaki SA. Emergence of Avian coronavirus escape mutants under suboptimal antibody titers [Internet]. Journal of Molecular Evolution. 2022 ; 90 176-181.[citado 2024 out. 16 ] Available from: https://doi.org/10.1007/s00239-022-10050-8
Artigo de periodico
Exploring integument transcriptomes, cuticle ultrastructure, and cuticular hydrocarbons profiles in eusocial and solitary bee species displaying heterochronic adult cuticle maturation (2019)
Lopes, Tiago Falcon ; Pinheiro, Daniel G.; Ferreira-Caliman, Maria Juliana ; Turatti, Izabel Cristina Casanova; Abreu, Fabiano Carlos Pinto de; Galaschi-Teixeira, Juliana Stephanie ; Martins, Juliana Ramos ; Elias-Neto, Moysés; Soares, Michelle Prioli Miranda; Laure, Marcela Aparecida Framartino Bezerra; Figueiredo, Vera Lucia Castelo; Lopes, Norberto Peporine ; Simões, Zilá Luz Paulino ; Garófalo, Carlos Alberto ; Bitondi, Márcia Maria Gentile
Source: PLOS ONE. Unidades: FCFRP, FFCLRP, FMRP
Subjects: ABELHAS, EXPRESSÃO GÊNICA, MUTAÇÃO GENÉTICA, ESPECTROMETRIA DE MASSAS, QUITINA
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LOPES, Tiago Falcon et al. Exploring integument transcriptomes, cuticle ultrastructure, and cuticular hydrocarbons profiles in eusocial and solitary bee species displaying heterochronic adult cuticle maturation. PLOS ONE, v. 14, n. 3, p. [38] , 2019Tradução . . Disponível em: https://doi.org/10.1371/journal.pone.0213796. Acesso em: 16 out. 2024.
APA
Lopes, T. F., Pinheiro, D. G., Ferreira-Caliman, M. J., Turatti, I. C. C., Abreu, F. C. P. de, Galaschi-Teixeira, J. S., et al. (2019). Exploring integument transcriptomes, cuticle ultrastructure, and cuticular hydrocarbons profiles in eusocial and solitary bee species displaying heterochronic adult cuticle maturation. PLOS ONE, 14( 3), [38] . doi:10.1371/journal.pone.0213796
NLM
Lopes TF, Pinheiro DG, Ferreira-Caliman MJ, Turatti ICC, Abreu FCP de, Galaschi-Teixeira JS, Martins JR, Elias-Neto M, Soares MPM, Laure MAFB, Figueiredo VLC, Lopes NP, Simões ZLP, Garófalo CA, Bitondi MMG. Exploring integument transcriptomes, cuticle ultrastructure, and cuticular hydrocarbons profiles in eusocial and solitary bee species displaying heterochronic adult cuticle maturation [Internet]. PLOS ONE. 2019 ; 14( 3): [38] .[citado 2024 out. 16 ] Available from: https://doi.org/10.1371/journal.pone.0213796
Vancouver
Lopes TF, Pinheiro DG, Ferreira-Caliman MJ, Turatti ICC, Abreu FCP de, Galaschi-Teixeira JS, Martins JR, Elias-Neto M, Soares MPM, Laure MAFB, Figueiredo VLC, Lopes NP, Simões ZLP, Garófalo CA, Bitondi MMG. Exploring integument transcriptomes, cuticle ultrastructure, and cuticular hydrocarbons profiles in eusocial and solitary bee species displaying heterochronic adult cuticle maturation [Internet]. PLOS ONE. 2019 ; 14( 3): [38] .[citado 2024 out. 16 ] Available from: https://doi.org/10.1371/journal.pone.0213796
Artigo de periodico-dep/entr
Familial hypercholesterolaemia: PCSK9 inhibitors are coming [comentário] (2015)
Santos, Raul D.; Watts, Gerald F.
Source: Lancet. Unidade: FM
Subjects: FATORES DE RISCO, MUTAÇÃO GENÉTICA, DOENÇAS CARDIOVASCULARES (ETIOLOGIA), HIPERCOLESTEROLEMIA (COMPLICAÇÕES)
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SANTOS, Raul D. e WATTS, Gerald F. Familial hypercholesterolaemia: PCSK9 inhibitors are coming [comentário]. Lancet. London: Faculdade de Medicina, Universidade de São Paulo. Disponível em: https://doi.org/10.1016/S0140-6736(14)61702-5. Acesso em: 16 out. 2024. , 2015
APA
Santos, R. D., & Watts, G. F. (2015). Familial hypercholesterolaemia: PCSK9 inhibitors are coming [comentário]. Lancet. London: Faculdade de Medicina, Universidade de São Paulo. doi:10.1016/S0140-6736(14)61702-5
NLM
Santos RD, Watts GF. Familial hypercholesterolaemia: PCSK9 inhibitors are coming [comentário] [Internet]. Lancet. 2015 ; 385( 9965): 307-310.[citado 2024 out. 16 ] Available from: https://doi.org/10.1016/S0140-6736(14)61702-5
Vancouver
Santos RD, Watts GF. Familial hypercholesterolaemia: PCSK9 inhibitors are coming [comentário] [Internet]. Lancet. 2015 ; 385( 9965): 307-310.[citado 2024 out. 16 ] Available from: https://doi.org/10.1016/S0140-6736(14)61702-5
Artigo de periodico
Pre-operative role of BRAF in the guidance of the surgical approach and prognosis of differentiated thyroid carcinoma (2014)
Danilovic, Debora L. S.; Lima, Erika U.; Domingues, Regina B.; Brandao, Lenine G.; Hoff, Ana O.; Marui, Suemi
Source: European Journal of Endocrinology. Unidade: FM
Subjects: MUTAÇÃO GENÉTICA, NEOPLASIAS DA TIREOIDE (DIAGNÓSTICO), PROGNÓSTICO, CARCINOMA DE CÉLULAS ESCAMOSAS
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DANILOVIC, Debora L. S. et al. Pre-operative role of BRAF in the guidance of the surgical approach and prognosis of differentiated thyroid carcinoma. European Journal of Endocrinology, v. 170, n. 4, p. 619-625, 2014Tradução . . Disponível em: https://doi.org/10.1530/EJE-13-0944. Acesso em: 16 out. 2024.
APA
Danilovic, D. L. S., Lima, E. U., Domingues, R. B., Brandao, L. G., Hoff, A. O., & Marui, S. (2014). Pre-operative role of BRAF in the guidance of the surgical approach and prognosis of differentiated thyroid carcinoma. European Journal of Endocrinology, 170( 4), 619-625. doi:10.1530/EJE-13-0944
NLM
Danilovic DLS, Lima EU, Domingues RB, Brandao LG, Hoff AO, Marui S. Pre-operative role of BRAF in the guidance of the surgical approach and prognosis of differentiated thyroid carcinoma [Internet]. European Journal of Endocrinology. 2014 ; 170( 4): 619-625.[citado 2024 out. 16 ] Available from: https://doi.org/10.1530/EJE-13-0944
Vancouver
Danilovic DLS, Lima EU, Domingues RB, Brandao LG, Hoff AO, Marui S. Pre-operative role of BRAF in the guidance of the surgical approach and prognosis of differentiated thyroid carcinoma [Internet]. European Journal of Endocrinology. 2014 ; 170( 4): 619-625.[citado 2024 out. 16 ] Available from: https://doi.org/10.1530/EJE-13-0944
Artigo de periodico
Dosage Changes of a Segment at 17p13.1 Lead to Intellectual Disability and Microcephaly as a Result of Complex Genetic Interaction of Multiple Genes (2014)
Carvalho, Claudia M.B.; Vasanth, Shivakumar; Shinawi, Marwan; Russell, Chad; Ramocki, Melissa B.; Brown, Chester W.; Graakjaer, Jesper; Skytte, Anne-Bine; Patel, Gayle S.; Immken, LaDonna; Aleck, Kyrieckos; Lim, Cynthia; Cheung, Sau Wai; Rosenberg, Carla ; Katsanis, Nicholas; Lupski, James R.
Source: American Journal of Human Genetics. Unidade: IB
Subjects: GENES, MUTAÇÃO GENÉTICA
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CARVALHO, Claudia M.B. et al. Dosage Changes of a Segment at 17p13.1 Lead to Intellectual Disability and Microcephaly as a Result of Complex Genetic Interaction of Multiple Genes. American Journal of Human Genetics, v. 95, p. 565-578, 2014Tradução . . Disponível em: https://doi.org/10.1016/j.ajhg.2014.10.006. Acesso em: 16 out. 2024.
APA
Carvalho, C. M. B., Vasanth, S., Shinawi, M., Russell, C., Ramocki, M. B., Brown, C. W., et al. (2014). Dosage Changes of a Segment at 17p13.1 Lead to Intellectual Disability and Microcephaly as a Result of Complex Genetic Interaction of Multiple Genes. American Journal of Human Genetics, 95, 565-578. doi:10.1016/j.ajhg.2014.10.006
NLM
Carvalho CMB, Vasanth S, Shinawi M, Russell C, Ramocki MB, Brown CW, Graakjaer J, Skytte A-B, Patel GS, Immken LD, Aleck K, Lim C, Cheung SW, Rosenberg C, Katsanis N, Lupski JR. Dosage Changes of a Segment at 17p13.1 Lead to Intellectual Disability and Microcephaly as a Result of Complex Genetic Interaction of Multiple Genes [Internet]. American Journal of Human Genetics. 2014 ; 95 565-578.[citado 2024 out. 16 ] Available from: https://doi.org/10.1016/j.ajhg.2014.10.006
Vancouver
Carvalho CMB, Vasanth S, Shinawi M, Russell C, Ramocki MB, Brown CW, Graakjaer J, Skytte A-B, Patel GS, Immken LD, Aleck K, Lim C, Cheung SW, Rosenberg C, Katsanis N, Lupski JR. Dosage Changes of a Segment at 17p13.1 Lead to Intellectual Disability and Microcephaly as a Result of Complex Genetic Interaction of Multiple Genes [Internet]. American Journal of Human Genetics. 2014 ; 95 565-578.[citado 2024 out. 16 ] Available from: https://doi.org/10.1016/j.ajhg.2014.10.006
Trabalho de evento-resumo periodico
Epidermal growth factor receptor mutations in primary and metastatic adenocarcinomas from a tertiary hospital in São Paulo, Brazil (2013)
Sá, V. de; Nascimento, E.; Meireles, S.; Capelozzi, V.
Source: Virchows Archiv. Conference titles: European Society for Photobiology 2013 Congress. Unidade: FM
Subjects: MUTAÇÃO GENÉTICA, ADENOCARCINOMA, PULMÃO (PATOLOGIA), RESUMOS (EVENTOS)
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ABNT
SÁ, V. de et al. Epidermal growth factor receptor mutations in primary and metastatic adenocarcinomas from a tertiary hospital in São Paulo, Brazil. Virchows Archiv. Berlin: Faculdade de Medicina, Universidade de São Paulo. Disponível em: https://doi.org/10.1007/s00428-013-1444-y. Acesso em: 16 out. 2024. , 2013
APA
Sá, V. de, Nascimento, E., Meireles, S., & Capelozzi, V. (2013). Epidermal growth factor receptor mutations in primary and metastatic adenocarcinomas from a tertiary hospital in São Paulo, Brazil. Virchows Archiv. Berlin: Faculdade de Medicina, Universidade de São Paulo. doi:10.1007/s00428-013-1444-y
NLM
Sá V de, Nascimento E, Meireles S, Capelozzi V. Epidermal growth factor receptor mutations in primary and metastatic adenocarcinomas from a tertiary hospital in São Paulo, Brazil [Internet]. Virchows Archiv. 2013 ; 463( 2): 236.[citado 2024 out. 16 ] Available from: https://doi.org/10.1007/s00428-013-1444-y
Vancouver
Sá V de, Nascimento E, Meireles S, Capelozzi V. Epidermal growth factor receptor mutations in primary and metastatic adenocarcinomas from a tertiary hospital in São Paulo, Brazil [Internet]. Virchows Archiv. 2013 ; 463( 2): 236.[citado 2024 out. 16 ] Available from: https://doi.org/10.1007/s00428-013-1444-y
Artigo de periodico
Combined expression of BUB1B, DLG7, and PINK1 as predictors of poor outcome in adrenocortical tumors: validation in a Brazilian cohort of adult and pediatric patients (2012)
Fragoso, Maria Candida B. V.; Almeida, Madson Queiroz; Mazzuco, Tania L.; Mariani, Beatriz M. P.; Brito, Luciana P.; Gonçalves, Talita Cardoso; Alencar, Guilherme A.; Lima, Lorena de O.; Faria, Andre M.; Bourdeau, Isabelle; Lucon, Antonio M.; Freire, Daniel S.; Latronico, Ana Claudia; Mendonca, Berenice B.; Lacroix, Andre; Lerario, Antonio M.
Source: European Journal of Endocrinology. Unidade: FM
Subjects: MUTAÇÃO GENÉTICA, NEOPLASIAS DAS GLÂNDULAS SUPRARRENAIS, PROGNÓSTICO, CRIANÇAS, ADULTOS, EXPRESSÃO GÊNICA, ESTUDOS DE COORTES, BRASIL
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FRAGOSO, Maria Candida B. V. et al. Combined expression of BUB1B, DLG7, and PINK1 as predictors of poor outcome in adrenocortical tumors: validation in a Brazilian cohort of adult and pediatric patients. European Journal of Endocrinology, v. 166, n. 1, p. 61-67, 2012Tradução . . Disponível em: https://doi.org/10.1530/EJE-11-0964. Acesso em: 16 out. 2024.
APA
Fragoso, M. C. B. V., Almeida, M. Q., Mazzuco, T. L., Mariani, B. M. P., Brito, L. P., Gonçalves, T. C., et al. (2012). Combined expression of BUB1B, DLG7, and PINK1 as predictors of poor outcome in adrenocortical tumors: validation in a Brazilian cohort of adult and pediatric patients. European Journal of Endocrinology, 166( 1), 61-67. doi:10.1530/EJE-11-0964
NLM
Fragoso MCBV, Almeida MQ, Mazzuco TL, Mariani BMP, Brito LP, Gonçalves TC, Alencar GA, Lima L de O, Faria AM, Bourdeau I, Lucon AM, Freire DS, Latronico AC, Mendonca BB, Lacroix A, Lerario AM. Combined expression of BUB1B, DLG7, and PINK1 as predictors of poor outcome in adrenocortical tumors: validation in a Brazilian cohort of adult and pediatric patients [Internet]. European Journal of Endocrinology. 2012 ; 166( 1): 61-67.[citado 2024 out. 16 ] Available from: https://doi.org/10.1530/EJE-11-0964
Vancouver
Fragoso MCBV, Almeida MQ, Mazzuco TL, Mariani BMP, Brito LP, Gonçalves TC, Alencar GA, Lima L de O, Faria AM, Bourdeau I, Lucon AM, Freire DS, Latronico AC, Mendonca BB, Lacroix A, Lerario AM. Combined expression of BUB1B, DLG7, and PINK1 as predictors of poor outcome in adrenocortical tumors: validation in a Brazilian cohort of adult and pediatric patients [Internet]. European Journal of Endocrinology. 2012 ; 166( 1): 61-67.[citado 2024 out. 16 ] Available from: https://doi.org/10.1530/EJE-11-0964
Artigo de periodico-carta/editorial
Multiple, diffuse schwannomas in a RASopathy phenotype patient with germline KRAS mutation [Carta]: a causal relationship? (2012)
Bertola, D. R.; Pereira, A. C.; Brasil, A. S.; Suzuki, L.; Leite, C.; Falzoni, R.; Tannuri, U.; Poplawski, A. B.; Janowski, K. M.; Kim, C. A.; Messiaena, L. M.
Source: Clinical Genetics. Unidades: IB, FM
Subjects: MUTAÇÃO GENÉTICA, NEUROMA (GENÉTICA), FENÓTIPOS, FATORES DE RISCO, NEUROMA (DIAGNÓSTICO), MUTAÇÃO GENÉTICA, IMAGEM POR RESSONÂNCIA MAGNÉTICA, IMUNOHISTOQUÍMICA
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ABNT
BERTOLA, D. R. et al. Multiple, diffuse schwannomas in a RASopathy phenotype patient with germline KRAS mutation [Carta]: a causal relationship?. Clinical Genetics. Copenhagem: Instituto de Biociências, Universidade de São Paulo. Disponível em: https://doi.org/10.1111/j.1399-0004.2011.01764.x. Acesso em: 16 out. 2024. , 2012
APA
Bertola, D. R., Pereira, A. C., Brasil, A. S., Suzuki, L., Leite, C., Falzoni, R., et al. (2012). Multiple, diffuse schwannomas in a RASopathy phenotype patient with germline KRAS mutation [Carta]: a causal relationship? Clinical Genetics. Copenhagem: Instituto de Biociências, Universidade de São Paulo. doi:10.1111/j.1399-0004.2011.01764.x
NLM
Bertola DR, Pereira AC, Brasil AS, Suzuki L, Leite C, Falzoni R, Tannuri U, Poplawski AB, Janowski KM, Kim CA, Messiaena LM. Multiple, diffuse schwannomas in a RASopathy phenotype patient with germline KRAS mutation [Carta]: a causal relationship? [Internet]. Clinical Genetics. 2012 ; 81( 6): 595-597.[citado 2024 out. 16 ] Available from: https://doi.org/10.1111/j.1399-0004.2011.01764.x
Vancouver
Bertola DR, Pereira AC, Brasil AS, Suzuki L, Leite C, Falzoni R, Tannuri U, Poplawski AB, Janowski KM, Kim CA, Messiaena LM. Multiple, diffuse schwannomas in a RASopathy phenotype patient with germline KRAS mutation [Carta]: a causal relationship? [Internet]. Clinical Genetics. 2012 ; 81( 6): 595-597.[citado 2024 out. 16 ] Available from: https://doi.org/10.1111/j.1399-0004.2011.01764.x
Artigo de periodico
Molecular epidemiology of the SH (small hydrophobic) gene of human respiratory syncytial virus (HRSV), over 2 consecutive years (2012)
Lima, Hildenêr Nogueira; Botosso, Viviane Fongaro; Oliveira, Danielle Bruna Leal; Campos, Angélica Cristine de Almeida; Leal, Andrea Lima; Silva, Tereza Souza; Bosso, Patrícia Alves Ramos; Moraes, Claudia Trigo Pedroso; Silva Filho, Claudionor Gomes da; Vieira, Sandra Elisabete; Gilio, Alfredo Elias; Stewien, Klaus Eberhard; Durigon, Edison Luiz
Source: Virus Research. Unidades: FM, ICB
Subjects: GENES (ANÁLISE), DOENÇAS RESPIRATÓRIAS, PROTEÍNAS, NASOFARINGE (SECREÇÃO), APOPTOSE, VARIAÇÃO GENÉTICA, HOSPEDEIRO IMUNOCOMPROMETIDO, GENÓTIPOS, MUTAÇÃO GENÉTICA
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ABNT
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: 16 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. 16 ] 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. 16 ] Available from: https://doi.org/10.1016/j.virusres.2011.08.013
Artigo de periodico
Mutation and genomic amplification of the PIK3CA proto-oncogene in pituitary adenomas (2012)
Murat, C. B.; Braga, P. B. S.; Fortes, M. A. H. Z.; Bronstein, M. D.; Corrêa-Giannella, M. L. C.; Giorgi, R. R.
Source: Brazilian Journal of Medical and Biological Research. Unidade: FM
Subjects: ADENOMA, CARCINOMA, NEOPLASIAS DAS GLÂNDULAS SUPRARRENAIS, MUTAÇÃO GENÉTICA, GENÔMICA, PROTO-ONCOGENES, AMPLIFICAÇÃO DE GENES
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ABNT
MURAT, C. B. et al. Mutation and genomic amplification of the PIK3CA proto-oncogene in pituitary adenomas. Brazilian Journal of Medical and Biological Research, v. 45, n. 9, p. 851-855, 2012Tradução . . Disponível em: https://doi.org/10.1590/s0100-879x2012007500115. Acesso em: 16 out. 2024.
APA
Murat, C. B., Braga, P. B. S., Fortes, M. A. H. Z., Bronstein, M. D., Corrêa-Giannella, M. L. C., & Giorgi, R. R. (2012). Mutation and genomic amplification of the PIK3CA proto-oncogene in pituitary adenomas. Brazilian Journal of Medical and Biological Research, 45( 9), 851-855. doi:10.1590/s0100-879x2012007500115
NLM
Murat CB, Braga PBS, Fortes MAHZ, Bronstein MD, Corrêa-Giannella MLC, Giorgi RR. Mutation and genomic amplification of the PIK3CA proto-oncogene in pituitary adenomas [Internet]. Brazilian Journal of Medical and Biological Research. 2012 ; 45( 9): 851-855.[citado 2024 out. 16 ] Available from: https://doi.org/10.1590/s0100-879x2012007500115
Vancouver
Murat CB, Braga PBS, Fortes MAHZ, Bronstein MD, Corrêa-Giannella MLC, Giorgi RR. Mutation and genomic amplification of the PIK3CA proto-oncogene in pituitary adenomas [Internet]. Brazilian Journal of Medical and Biological Research. 2012 ; 45( 9): 851-855.[citado 2024 out. 16 ] Available from: https://doi.org/10.1590/s0100-879x2012007500115
Artigo de periodico
Impact of mutations in kisspeptin and neurokinin B signaling pathways on human reproduction (2010)
Silveira, Leticia Gontijo; Tusset, Cintia; Xavier, Ana Claudia Latronico
Source: Brain research. Unidade: FM
Subjects: REPRODUÇÃO, HIPOGONADISMO, PUBERDADE PRECOCE, MUTAÇÃO GENÉTICA
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SILVEIRA, Leticia Gontijo e TUSSET, Cintia e XAVIER, Ana Claudia Latronico. Impact of mutations in kisspeptin and neurokinin B signaling pathways on human reproduction. Brain research, v. 1364, p. 72-80, 2010Tradução . . Disponível em: https://doi.org/10.1016/j.brainres.2010.08.087. Acesso em: 16 out. 2024.
APA
Silveira, L. G., Tusset, C., & Xavier, A. C. L. (2010). Impact of mutations in kisspeptin and neurokinin B signaling pathways on human reproduction. Brain research, 1364, 72-80. doi:10.1016/j.brainres.2010.08.087
NLM
Silveira LG, Tusset C, Xavier ACL. Impact of mutations in kisspeptin and neurokinin B signaling pathways on human reproduction [Internet]. Brain research. 2010 ; 1364 72-80.[citado 2024 out. 16 ] Available from: https://doi.org/10.1016/j.brainres.2010.08.087
Vancouver
Silveira LG, Tusset C, Xavier ACL. Impact of mutations in kisspeptin and neurokinin B signaling pathways on human reproduction [Internet]. Brain research. 2010 ; 1364 72-80.[citado 2024 out. 16 ] Available from: https://doi.org/10.1016/j.brainres.2010.08.087
Artigo de periodico
A novel homozygous splice acceptor site mutation of KISS1R in two siblings with normosmic isolated hypogonadotropic hypogonadism (2010)
Teles, M. G.; Trarbach, E. B.; Noel, S. D.; Guerra Junior, G.; Beneduzzi, D.; Bianco, S. D.; Jorge, Alexander A. L.; Mukherjee, A.; Baptista, M. T.; Costa, E. M.; Castro, M. de; Mendonça, B. B.; Kaiser, U. B.; Latronico, A. C.
Source: European Journal of Endocrinology. Unidade: FM
Subjects: ENDOCRINOPATIAS (PATOLOGIA;FISIOPATOLOGIA), MUTAÇÃO GENÉTICA, DOENÇAS PULMONARES INTERSTICIAIS, SISTEMA IMUNE (FISIOPATOLOGIA)
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ABNT
TELES, M. G. et al. A novel homozygous splice acceptor site mutation of KISS1R in two siblings with normosmic isolated hypogonadotropic hypogonadism. European Journal of Endocrinology, v. 163, n. 1, p. 29-34, 2010Tradução . . Disponível em: https://doi.org/10.1530/EJE-10-0012. Acesso em: 16 out. 2024.
APA
Teles, M. G., Trarbach, E. B., Noel, S. D., Guerra Junior, G., Beneduzzi, D., Bianco, S. D., et al. (2010). A novel homozygous splice acceptor site mutation of KISS1R in two siblings with normosmic isolated hypogonadotropic hypogonadism. European Journal of Endocrinology, 163( 1), 29-34. doi:10.1530/EJE-10-0012
NLM
Teles MG, Trarbach EB, Noel SD, Guerra Junior G, Beneduzzi D, Bianco SD, Jorge AAL, Mukherjee A, Baptista MT, Costa EM, Castro M de, Mendonça BB, Kaiser UB, Latronico AC. A novel homozygous splice acceptor site mutation of KISS1R in two siblings with normosmic isolated hypogonadotropic hypogonadism [Internet]. European Journal of Endocrinology. 2010 ; 163( 1): 29-34.[citado 2024 out. 16 ] Available from: https://doi.org/10.1530/EJE-10-0012
Vancouver
Teles MG, Trarbach EB, Noel SD, Guerra Junior G, Beneduzzi D, Bianco SD, Jorge AAL, Mukherjee A, Baptista MT, Costa EM, Castro M de, Mendonça BB, Kaiser UB, Latronico AC. A novel homozygous splice acceptor site mutation of KISS1R in two siblings with normosmic isolated hypogonadotropic hypogonadism [Internet]. European Journal of Endocrinology. 2010 ; 163( 1): 29-34.[citado 2024 out. 16 ] Available from: https://doi.org/10.1530/EJE-10-0012
Artigo de periodico
The p.P56S mutation in the VAPB gene is not due to a single founder: first European case. [Letter to the editor] (2010)
Funke, A. D.; Esser, M.; Krüttgen, A.; Weis, J.; Mitne Neto, Miguel; Lazar, M.; Nishimura, A. L.; Sperfela, A. D.; Trillenberg, P.; Senderek, Jan; Krasnianski, M.; Zatz, Mayana ; Zierz, S.; Deschauer, M.
Source: Clinical Genetics. Unidade: IB
Assunto: MUTAÇÃO GENÉTICA
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ABNT
FUNKE, A. D. et al. The p.P56S mutation in the VAPB gene is not due to a single founder: first European case. [Letter to the editor]. Clinical Genetics, v. 77, n. 3, p. 302-303, 2010Tradução . . Acesso em: 16 out. 2024.
APA
Funke, A. D., Esser, M., Krüttgen, A., Weis, J., Mitne Neto, M., Lazar, M., et al. (2010). The p.P56S mutation in the VAPB gene is not due to a single founder: first European case. [Letter to the editor]. Clinical Genetics, 77( 3), 302-303.
NLM
Funke AD, Esser M, Krüttgen A, Weis J, Mitne Neto M, Lazar M, Nishimura AL, Sperfela AD, Trillenberg P, Senderek J, Krasnianski M, Zatz M, Zierz S, Deschauer M. The p.P56S mutation in the VAPB gene is not due to a single founder: first European case. [Letter to the editor]. Clinical Genetics. 2010 ; 77( 3): 302-303.[citado 2024 out. 16 ]
Vancouver
Funke AD, Esser M, Krüttgen A, Weis J, Mitne Neto M, Lazar M, Nishimura AL, Sperfela AD, Trillenberg P, Senderek J, Krasnianski M, Zatz M, Zierz S, Deschauer M. The p.P56S mutation in the VAPB gene is not due to a single founder: first European case. [Letter to the editor]. Clinical Genetics. 2010 ; 77( 3): 302-303.[citado 2024 out. 16 ]
Artigo de periodico
A novel STAT5B mutation causing GH insensitivity syndrome associated with hyperprolactinemia and immune dysfunction in two male siblings (2010)
Pires, Patricia N. Pugliese; Tonelli, Carlos A.; Dora, Jose M.; Silva, Paulo C. A.; Czepielewski, Mauro; Simoni, Genoir; Arnhold, Ivo J. P.; Jorge, Alexander A. L.
Source: European Journal of Endocrinology. Unidade: FM
Subjects: ENDOCRINOPATIAS (PATOLOGIA;FISIOPATOLOGIA), MUTAÇÃO GENÉTICA, DOENÇAS PULMONARES INTERSTICIAIS, SISTEMA IMUNE (FISIOPATOLOGIA), PROLACTINA (FISIOPATOLOGIA)
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ABNT
PIRES, Patricia N. Pugliese et al. A novel STAT5B mutation causing GH insensitivity syndrome associated with hyperprolactinemia and immune dysfunction in two male siblings. European Journal of Endocrinology, v. 163, n. 2, p. 349-355, 2010Tradução . . Disponível em: https://doi.org/10.1530/EJE-10-0272. Acesso em: 16 out. 2024.
APA
Pires, P. N. P., Tonelli, C. A., Dora, J. M., Silva, P. C. A., Czepielewski, M., Simoni, G., et al. (2010). A novel STAT5B mutation causing GH insensitivity syndrome associated with hyperprolactinemia and immune dysfunction in two male siblings. European Journal of Endocrinology, 163( 2), 349-355. doi:10.1530/EJE-10-0272
NLM
Pires PNP, Tonelli CA, Dora JM, Silva PCA, Czepielewski M, Simoni G, Arnhold IJP, Jorge AAL. A novel STAT5B mutation causing GH insensitivity syndrome associated with hyperprolactinemia and immune dysfunction in two male siblings [Internet]. European Journal of Endocrinology. 2010 ; 163( 2): 349-355.[citado 2024 out. 16 ] Available from: https://doi.org/10.1530/EJE-10-0272
Vancouver
Pires PNP, Tonelli CA, Dora JM, Silva PCA, Czepielewski M, Simoni G, Arnhold IJP, Jorge AAL. A novel STAT5B mutation causing GH insensitivity syndrome associated with hyperprolactinemia and immune dysfunction in two male siblings [Internet]. European Journal of Endocrinology. 2010 ; 163( 2): 349-355.[citado 2024 out. 16 ] Available from: https://doi.org/10.1530/EJE-10-0272
Artigo de periodico
Prevalence of GJB2 (connexin-26) and GJB6 (connexin-30) mutations in a cohort of 300 brazilian hearing-impaired individuals: implications for diagnosis and genetic counseling (2009)
Batissoco, Ana Carla; Abreu-Silva, Ronaldo Serafim; Braga, Maria Cristina Célia; Lezirovitz, Karina; Della Rosa, Valter Augusto; Tabith Jr, Alfredo; Otto, Paulo A ; Mingroni Netto, Regina Celia
Source: Ear and Hearing. Unidade: IB
Subjects: MUTAÇÃO GENÉTICA, ACONSELHAMENTO GENÉTICO
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ABNT
BATISSOCO, Ana Carla et al. Prevalence of GJB2 (connexin-26) and GJB6 (connexin-30) mutations in a cohort of 300 brazilian hearing-impaired individuals: implications for diagnosis and genetic counseling. Ear and Hearing, v. 30, n. 1, p. 1-7, 2009Tradução . . Acesso em: 16 out. 2024.
APA
Batissoco, A. C., Abreu-Silva, R. S., Braga, M. C. C., Lezirovitz, K., Della Rosa, V. A., Tabith Jr, A., et al. (2009). Prevalence of GJB2 (connexin-26) and GJB6 (connexin-30) mutations in a cohort of 300 brazilian hearing-impaired individuals: implications for diagnosis and genetic counseling. Ear and Hearing, 30( 1), 1-7.
NLM
Batissoco AC, Abreu-Silva RS, Braga MCC, Lezirovitz K, Della Rosa VA, Tabith Jr A, Otto PA, Mingroni Netto RC. Prevalence of GJB2 (connexin-26) and GJB6 (connexin-30) mutations in a cohort of 300 brazilian hearing-impaired individuals: implications for diagnosis and genetic counseling. Ear and Hearing. 2009 ; 30( 1): 1-7.[citado 2024 out. 16 ]
Vancouver
Batissoco AC, Abreu-Silva RS, Braga MCC, Lezirovitz K, Della Rosa VA, Tabith Jr A, Otto PA, Mingroni Netto RC. Prevalence of GJB2 (connexin-26) and GJB6 (connexin-30) mutations in a cohort of 300 brazilian hearing-impaired individuals: implications for diagnosis and genetic counseling. Ear and Hearing. 2009 ; 30( 1): 1-7.[citado 2024 out. 16 ]
Artigo de periodico
A novel association of a polymorphism in the first intron of adiponectin gene with type 2 diabetes, obesity and hypoadiponectinemia in Asian Indians (2008)
Lezirovitz, Karina; Maestrelli, Sylvia Regina Pedrosa; Cotrim, Nelson Henderson; Otto, Paulo A ; Pearson, Peter Lees; Mingroni Netto, Regina Celia
Source: Human Genetics. Unidade: IB
Subjects: DOENÇAS HEREDITÁRIAS, MUTAÇÃO GENÉTICA
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ABNT
LEZIROVITZ, Karina et al. A novel association of a polymorphism in the first intron of adiponectin gene with type 2 diabetes, obesity and hypoadiponectinemia in Asian Indians. Human Genetics, v. 123, n. 6, p. 625-631, 2008Tradução . . Acesso em: 16 out. 2024.
APA
Lezirovitz, K., Maestrelli, S. R. P., Cotrim, N. H., Otto, P. A., Pearson, P. L., & Mingroni Netto, R. C. (2008). A novel association of a polymorphism in the first intron of adiponectin gene with type 2 diabetes, obesity and hypoadiponectinemia in Asian Indians. Human Genetics, 123( 6), 625-631.
NLM
Lezirovitz K, Maestrelli SRP, Cotrim NH, Otto PA, Pearson PL, Mingroni Netto RC. A novel association of a polymorphism in the first intron of adiponectin gene with type 2 diabetes, obesity and hypoadiponectinemia in Asian Indians. Human Genetics. 2008 ; 123( 6): 625-631.[citado 2024 out. 16 ]
Vancouver
Lezirovitz K, Maestrelli SRP, Cotrim NH, Otto PA, Pearson PL, Mingroni Netto RC. A novel association of a polymorphism in the first intron of adiponectin gene with type 2 diabetes, obesity and hypoadiponectinemia in Asian Indians. Human Genetics. 2008 ; 123( 6): 625-631.[citado 2024 out. 16 ]
Artigo de periodico
Síndrome de Noonan: do Fenótipo à Terapêutica com Hormônio de Crescimento (2008)
Malaquias, Alexsandra C.; Ferreira, Lize V.; Souza, Silvia C.; Arnhold, Ivo J. P.; Mendonça, Berenice B.; Jorge, Alexander A. L.
Source: Arquivos Brasileiros de Endocrinologia e Metabologia. Unidade: FM
Subjects: HORMÔNIO DO CRESCIMENTO (USO TERAPÊUTICO), CONDUTAS TERAPÊUTICAS, INSUFICIÊNCIA DE CRESCIMENTO (TERAPIA;GENÉTICA;DIAGNÓSTICO), MUTAÇÃO GENÉTICA, FENÓTIPOS, DIAGNÓSTICO DIFERENCIAL
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ABNT
MALAQUIAS, Alexsandra C. et al. Síndrome de Noonan: do Fenótipo à Terapêutica com Hormônio de Crescimento. Arquivos Brasileiros de Endocrinologia e Metabologia, v. 52, n. 5, p. 800-808, 2008Tradução . . Disponível em: http://www.scielo.br/pdf/abem/v52n4/a19v52n4.pdf. Acesso em: 16 out. 2024.
APA
Malaquias, A. C., Ferreira, L. V., Souza, S. C., Arnhold, I. J. P., Mendonça, B. B., & Jorge, A. A. L. (2008). Síndrome de Noonan: do Fenótipo à Terapêutica com Hormônio de Crescimento. Arquivos Brasileiros de Endocrinologia e Metabologia, 52( 5), 800-808. Recuperado de http://www.scielo.br/pdf/abem/v52n4/a19v52n4.pdf
NLM
Malaquias AC, Ferreira LV, Souza SC, Arnhold IJP, Mendonça BB, Jorge AAL. Síndrome de Noonan: do Fenótipo à Terapêutica com Hormônio de Crescimento [Internet]. Arquivos Brasileiros de Endocrinologia e Metabologia. 2008 ; 52( 5): 800-808.[citado 2024 out. 16 ] Available from: http://www.scielo.br/pdf/abem/v52n4/a19v52n4.pdf
Vancouver
Malaquias AC, Ferreira LV, Souza SC, Arnhold IJP, Mendonça BB, Jorge AAL. Síndrome de Noonan: do Fenótipo à Terapêutica com Hormônio de Crescimento [Internet]. Arquivos Brasileiros de Endocrinologia e Metabologia. 2008 ; 52( 5): 800-808.[citado 2024 out. 16 ] Available from: http://www.scielo.br/pdf/abem/v52n4/a19v52n4.pdf
Artigo de periodico
A molecular analysis and long-term follow-up of two siblings with severe congenital hypothyroidism carrying the IVS30+1G>T intronic thyroglobulin mutation (2008)
Rubio, Ileana G. S.; Galrao, Ana Luiza; Pardo, Viviane; Knobel, Meyer; Possato, Roberta F.; Camargo, Rosalinda R. Y.; Ferreira, Marcelo A.; Kanamura, Cristina T.; Gomes, Simone A.; Medeiros-Neto, Geraldo
Source: Arquivos Brasileiros de Endocrinologia e Metabologia. Unidade: FM
Subjects: HORMÔNIOS TIREOIDIANOS (ANÁLISE), HIPOTIREOIDISMO (CONGÊNITO), DOENÇAS GENÉTICAS, MUTAÇÃO GENÉTICA, SEGUIMENTOS
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ABNT
RUBIO, Ileana G. S. et al. A molecular analysis and long-term follow-up of two siblings with severe congenital hypothyroidism carrying the IVS30+1G>T intronic thyroglobulin mutation. Arquivos Brasileiros de Endocrinologia e Metabologia, v. 52, n. 8, p. 1337-1344, 2008Tradução . . Disponível em: https://doi.org/10.1590/s0004-27302008000800022. Acesso em: 16 out. 2024.
APA
Rubio, I. G. S., Galrao, A. L., Pardo, V., Knobel, M., Possato, R. F., Camargo, R. R. Y., et al. (2008). A molecular analysis and long-term follow-up of two siblings with severe congenital hypothyroidism carrying the IVS30+1G>T intronic thyroglobulin mutation. Arquivos Brasileiros de Endocrinologia e Metabologia, 52( 8), 1337-1344. doi:10.1590/s0004-27302008000800022
NLM
Rubio IGS, Galrao AL, Pardo V, Knobel M, Possato RF, Camargo RRY, Ferreira MA, Kanamura CT, Gomes SA, Medeiros-Neto G. A molecular analysis and long-term follow-up of two siblings with severe congenital hypothyroidism carrying the IVS30+1G>T intronic thyroglobulin mutation [Internet]. Arquivos Brasileiros de Endocrinologia e Metabologia. 2008 ; 52( 8): 1337-1344.[citado 2024 out. 16 ] Available from: https://doi.org/10.1590/s0004-27302008000800022
Vancouver
Rubio IGS, Galrao AL, Pardo V, Knobel M, Possato RF, Camargo RRY, Ferreira MA, Kanamura CT, Gomes SA, Medeiros-Neto G. A molecular analysis and long-term follow-up of two siblings with severe congenital hypothyroidism carrying the IVS30+1G>T intronic thyroglobulin mutation [Internet]. Arquivos Brasileiros de Endocrinologia e Metabologia. 2008 ; 52( 8): 1337-1344.[citado 2024 out. 16 ] Available from: https://doi.org/10.1590/s0004-27302008000800022
Artigo de periodico
Central core disease due to recessive mutations in RYR1 gene: is it more common than described? (2007)
Kossugue, Patricia Mayumi; Paim, Julia F.; Navarro, Monica M.; Silva, Helga Cristina Almeida da; Pavanello, Rita de Cássia M.; Gurgel-Giannetti, Juliana; Zatz, Mayana ; Vainzof, Mariz
Source: Muscle & Nerve. Unidade: IB
Subjects: MIOPATIAS CONGÊNITAS ESTRUTURAIS, MUTAÇÃO GENÉTICA
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ABNT
KOSSUGUE, Patricia Mayumi et al. Central core disease due to recessive mutations in RYR1 gene: is it more common than described?. Muscle & Nerve, v. 35, n. 5, p. 670-674, 2007Tradução . . Disponível em: https://doi.org/10.1002/mus.20715. Acesso em: 16 out. 2024.
APA
Kossugue, P. M., Paim, J. F., Navarro, M. M., Silva, H. C. A. da, Pavanello, R. de C. M., Gurgel-Giannetti, J., et al. (2007). Central core disease due to recessive mutations in RYR1 gene: is it more common than described? Muscle & Nerve, 35( 5), 670-674. doi:10.1002/mus.20715
NLM
Kossugue PM, Paim JF, Navarro MM, Silva HCA da, Pavanello R de CM, Gurgel-Giannetti J, Zatz M, Vainzof M. Central core disease due to recessive mutations in RYR1 gene: is it more common than described? [Internet]. Muscle & Nerve. 2007 ; 35( 5): 670-674.[citado 2024 out. 16 ] Available from: https://doi.org/10.1002/mus.20715
Vancouver
Kossugue PM, Paim JF, Navarro MM, Silva HCA da, Pavanello R de CM, Gurgel-Giannetti J, Zatz M, Vainzof M. Central core disease due to recessive mutations in RYR1 gene: is it more common than described? [Internet]. Muscle & Nerve. 2007 ; 35( 5): 670-674.[citado 2024 out. 16 ] Available from: https://doi.org/10.1002/mus.20715
Artigo de periodico
Luteinizing hormone beta mutation and hypogonadism in men and women (2007)
Lofrano-Porto, Adriana; Barra, Gustavo Barcelos; Giacomini, Leonardo Abdala; Nascimento, Paula Pires; Latronico, Ana Claudia; Casulari, Luiz Augusto; Rocha Neves, Francisco de Assis da
Source: New England Journal of Medicine. Unidade: FM
Subjects: HOMENS, FENÓTIPOS, MUTAÇÃO GENÉTICA, MULHERES, INFERTILIDADE FEMININA
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ABNT
LOFRANO-PORTO, Adriana et al. Luteinizing hormone beta mutation and hypogonadism in men and women. New England Journal of Medicine, v. 356, n. 9, p. 897-904, 2007Tradução . . Disponível em: http://www.nejm.org/doi/full/10.1056/NEJMoa071999. Acesso em: 16 out. 2024.
APA
Lofrano-Porto, A., Barra, G. B., Giacomini, L. A., Nascimento, P. P., Latronico, A. C., Casulari, L. A., & Rocha Neves, F. de A. da. (2007). Luteinizing hormone beta mutation and hypogonadism in men and women. New England Journal of Medicine, 356( 9), 897-904. doi:10.1056/NEJMoa071999
NLM
Lofrano-Porto A, Barra GB, Giacomini LA, Nascimento PP, Latronico AC, Casulari LA, Rocha Neves F de A da. Luteinizing hormone beta mutation and hypogonadism in men and women [Internet]. New England Journal of Medicine. 2007 ; 356( 9): 897-904.[citado 2024 out. 16 ] Available from: http://www.nejm.org/doi/full/10.1056/NEJMoa071999
Vancouver
Lofrano-Porto A, Barra GB, Giacomini LA, Nascimento PP, Latronico AC, Casulari LA, Rocha Neves F de A da. Luteinizing hormone beta mutation and hypogonadism in men and women [Internet]. New England Journal of Medicine. 2007 ; 356( 9): 897-904.[citado 2024 out. 16 ] Available from: http://www.nejm.org/doi/full/10.1056/NEJMoa071999

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