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Artigo de periodico
MIR146A and ADIPOQ genetic variants are associated with birth weight in relation to gestational age: a cohort study (2022)
Silva, Lívia Reis; Melo, Anderson Sanches de ; Salomão, Karina Bezerra ; Mazin, Suleimy Cristina; Tone, Luiz Gonzaga ; Cardoso, Viviane Cunha ; Reis, Rosana Maria dos ; Furtado, Cristiana Libardi Miranda ; Ferriani, Rui Alberto
Source: Journal of Assisted Reproduction and Genetics. Unidade: FMRP
Subjects: POLIMORFISMO, NUCLEOTÍDEOS, MICRORNAS, ADIPONECTINA, BEBÊS, IDADE GESTACIONAL
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ABNT
SILVA, Lívia Reis et al. MIR146A and ADIPOQ genetic variants are associated with birth weight in relation to gestational age: a cohort study. Journal of Assisted Reproduction and Genetics, v. 39, n. 8, p. 1873-1886, 2022Tradução . . Disponível em: https://doi.org/10.1007/s10815-022-02532-x. Acesso em: 09 nov. 2024.
APA
Silva, L. R., Melo, A. S. de, Salomão, K. B., Mazin, S. C., Tone, L. G., Cardoso, V. C., et al. (2022). MIR146A and ADIPOQ genetic variants are associated with birth weight in relation to gestational age: a cohort study. Journal of Assisted Reproduction and Genetics, 39( 8), 1873-1886. doi:10.1007/s10815-022-02532-x
NLM
Silva LR, Melo AS de, Salomão KB, Mazin SC, Tone LG, Cardoso VC, Reis RM dos, Furtado CLM, Ferriani RA. MIR146A and ADIPOQ genetic variants are associated with birth weight in relation to gestational age: a cohort study [Internet]. Journal of Assisted Reproduction and Genetics. 2022 ; 39( 8): 1873-1886.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1007/s10815-022-02532-x
Vancouver
Silva LR, Melo AS de, Salomão KB, Mazin SC, Tone LG, Cardoso VC, Reis RM dos, Furtado CLM, Ferriani RA. MIR146A and ADIPOQ genetic variants are associated with birth weight in relation to gestational age: a cohort study [Internet]. Journal of Assisted Reproduction and Genetics. 2022 ; 39( 8): 1873-1886.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1007/s10815-022-02532-x
Artigo de periodico
Effects of FTO and PPARγ variants on intrauterine growth restriction in a Brazilian birth cohort (2021)
Barbieri, Manuela Ramos; Fontes, Aparecida Maria ; Barbieri, Marco Antonio ; Saraiva, Maria da Conceição Pereira ; Simões, Vanda Maria Ferreira; Silva, A. A. M. da; Abraham, Kuruvilla Joseph ; Bettiol, Heloisa
Source: Brazilian Journal of Medical and Biological Research. Unidades: FMRP, FORP, ICMC
Subjects: ÍNDICE DE MASSA CORPORAL, ESTUDOS DE CASOS E CONTROLES, FETO, PREDISPOSIÇÃO GENÉTICA PARA DOENÇA, GENÓTIPOS, POLIMORFISMO
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ABNT
BARBIERI, Manuela Ramos et al. Effects of FTO and PPARγ variants on intrauterine growth restriction in a Brazilian birth cohort. Brazilian Journal of Medical and Biological Research, v. 54, n. 1, 2021Tradução . . Disponível em: https://doi.org/10.1590/1414-431X202010465. Acesso em: 09 nov. 2024.
APA
Barbieri, M. R., Fontes, A. M., Barbieri, M. A., Saraiva, M. da C. P., Simões, V. M. F., Silva, A. A. M. da, et al. (2021). Effects of FTO and PPARγ variants on intrauterine growth restriction in a Brazilian birth cohort. Brazilian Journal of Medical and Biological Research, 54( 1). doi:10.1590/1414-431X202010465
NLM
Barbieri MR, Fontes AM, Barbieri MA, Saraiva M da CP, Simões VMF, Silva AAM da, Abraham KJ, Bettiol H. Effects of FTO and PPARγ variants on intrauterine growth restriction in a Brazilian birth cohort [Internet]. Brazilian Journal of Medical and Biological Research. 2021 ; 54( 1):[citado 2024 nov. 09 ] Available from: https://doi.org/10.1590/1414-431X202010465
Vancouver
Barbieri MR, Fontes AM, Barbieri MA, Saraiva M da CP, Simões VMF, Silva AAM da, Abraham KJ, Bettiol H. Effects of FTO and PPARγ variants on intrauterine growth restriction in a Brazilian birth cohort [Internet]. Brazilian Journal of Medical and Biological Research. 2021 ; 54( 1):[citado 2024 nov. 09 ] Available from: https://doi.org/10.1590/1414-431X202010465
Artigo de periodico
Genetic variants of HIF1α are associated with right ventricular fibrotic load in repaired tetralogy of Fallot patients: a cardiovascular magnetic resonance study (2019)
Hoang, Thanh T.; Manso, Paulo Henrique ; Edman, Sharon; Mercer-Rosa, Laura; Mitchell, Laura E.; Sewda, Anshuman; Swartz, Michael D.; Fogel, Mark A.; Agopian, A. J.; Goldmuntz, Elizabeth
Source: Journal of Cardiovascular Magnetic Resonance. Unidade: FMRP
Subjects: RESSONÂNCIA MAGNÉTICA, CARDIOPATIAS, CARDIOPATIAS CONGÊNITAS, GENÉTICA, VENTRÍCULO CARDÍACO, POLIMORFISMO
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ABNT
HOANG, Thanh T. et al. Genetic variants of HIF1α are associated with right ventricular fibrotic load in repaired tetralogy of Fallot patients: a cardiovascular magnetic resonance study. Journal of Cardiovascular Magnetic Resonance, v. 21, n. 1, p. art. 51 [10], 2019Tradução . . Disponível em: https://doi.org/10.1186/s12968-019-0555-2. Acesso em: 09 nov. 2024.
APA
Hoang, T. T., Manso, P. H., Edman, S., Mercer-Rosa, L., Mitchell, L. E., Sewda, A., et al. (2019). Genetic variants of HIF1α are associated with right ventricular fibrotic load in repaired tetralogy of Fallot patients: a cardiovascular magnetic resonance study. Journal of Cardiovascular Magnetic Resonance, 21( 1), art. 51 [10]. doi:10.1186/s12968-019-0555-2
NLM
Hoang TT, Manso PH, Edman S, Mercer-Rosa L, Mitchell LE, Sewda A, Swartz MD, Fogel MA, Agopian AJ, Goldmuntz E. Genetic variants of HIF1α are associated with right ventricular fibrotic load in repaired tetralogy of Fallot patients: a cardiovascular magnetic resonance study [Internet]. Journal of Cardiovascular Magnetic Resonance. 2019 ; 21( 1): art. 51 [10].[citado 2024 nov. 09 ] Available from: https://doi.org/10.1186/s12968-019-0555-2
Vancouver
Hoang TT, Manso PH, Edman S, Mercer-Rosa L, Mitchell LE, Sewda A, Swartz MD, Fogel MA, Agopian AJ, Goldmuntz E. Genetic variants of HIF1α are associated with right ventricular fibrotic load in repaired tetralogy of Fallot patients: a cardiovascular magnetic resonance study [Internet]. Journal of Cardiovascular Magnetic Resonance. 2019 ; 21( 1): art. 51 [10].[citado 2024 nov. 09 ] Available from: https://doi.org/10.1186/s12968-019-0555-2
Artigo de periodico
Limits and patterns of cytomegalovirus genomic diversity in humans (2015)
Renzette, Nicholas; Pokalyuk, Cornelia; Gibson, Laura; Bhattacharjee, Bornali; Schleiss, Mark R.; Hamprecht, Klaus; Yamamoto, Aparecida Yulie; Mussi-Pinhata, Marisa Márcia; Britt, William J.; Jensen, Jeffrey D.; Kowalik, Timothy F.
Source: PNAS - Proceedings of the National Academy of Sciences of the United States of America. Unidade: FMRP
Subjects: CITOMEGALOVIRUS, DIVERSIDADE GENÉTICA, POLIMORFISMO
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ABNT
RENZETTE, Nicholas et al. Limits and patterns of cytomegalovirus genomic diversity in humans. PNAS - Proceedings of the National Academy of Sciences of the United States of America, v. 112, n. 30, p. E4120-E4128, 2015Tradução . . Disponível em: https://doi.org/10.1073/pnas.1501880112. Acesso em: 09 nov. 2024.
APA
Renzette, N., Pokalyuk, C., Gibson, L., Bhattacharjee, B., Schleiss, M. R., Hamprecht, K., et al. (2015). Limits and patterns of cytomegalovirus genomic diversity in humans. PNAS - Proceedings of the National Academy of Sciences of the United States of America, 112( 30), E4120-E4128. doi:10.1073/pnas.1501880112
NLM
Renzette N, Pokalyuk C, Gibson L, Bhattacharjee B, Schleiss MR, Hamprecht K, Yamamoto AY, Mussi-Pinhata MM, Britt WJ, Jensen JD, Kowalik TF. Limits and patterns of cytomegalovirus genomic diversity in humans [Internet]. PNAS - Proceedings of the National Academy of Sciences of the United States of America. 2015 ; 112( 30): E4120-E4128.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1073/pnas.1501880112
Vancouver
Renzette N, Pokalyuk C, Gibson L, Bhattacharjee B, Schleiss MR, Hamprecht K, Yamamoto AY, Mussi-Pinhata MM, Britt WJ, Jensen JD, Kowalik TF. Limits and patterns of cytomegalovirus genomic diversity in humans [Internet]. PNAS - Proceedings of the National Academy of Sciences of the United States of America. 2015 ; 112( 30): E4120-E4128.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1073/pnas.1501880112
Artigo de periodico
Pathogenesis of polycystic ovary syndrome: multifactorial assessment from the foetal stage to menopause (2015)
Melo, Anderson Sanches de; Dias, Sabrine Vilan; Cavalli, Ricardo de Carvalho; Cardoso, Viviane Cunha; Bettiol, Heloisa; Barbieri, Marco Antonio; Ferriani, Rui Alberto; Vieira, Carolina Sales
Source: Reproduction. Unidade: FMRP
Subjects: SÍNDROME DO OVÁRIO POLICÍSTICO, VARIAÇÃO GENÉTICA, POLIMORFISMO
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ABNT
MELO, Anderson Sanches de et al. Pathogenesis of polycystic ovary syndrome: multifactorial assessment from the foetal stage to menopause. Reproduction, v. 150, n. 1, p. R11-R24, 2015Tradução . . Disponível em: https://doi.org/10.1530/REP-14-0499. Acesso em: 09 nov. 2024.
APA
Melo, A. S. de, Dias, S. V., Cavalli, R. de C., Cardoso, V. C., Bettiol, H., Barbieri, M. A., et al. (2015). Pathogenesis of polycystic ovary syndrome: multifactorial assessment from the foetal stage to menopause. Reproduction, 150( 1), R11-R24. doi:10.1530/REP-14-0499
NLM
Melo AS de, Dias SV, Cavalli R de C, Cardoso VC, Bettiol H, Barbieri MA, Ferriani RA, Vieira CS. Pathogenesis of polycystic ovary syndrome: multifactorial assessment from the foetal stage to menopause [Internet]. Reproduction. 2015 ; 150( 1): R11-R24.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1530/REP-14-0499
Vancouver
Melo AS de, Dias SV, Cavalli R de C, Cardoso VC, Bettiol H, Barbieri MA, Ferriani RA, Vieira CS. Pathogenesis of polycystic ovary syndrome: multifactorial assessment from the foetal stage to menopause [Internet]. Reproduction. 2015 ; 150( 1): R11-R24.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1530/REP-14-0499
Trabalho de evento-resumo periodico
TNF-2 gene -308 polymorphism among women with preterm delivery from two Brazilian cohorts with different socioeconomic profiles (BRISA Birth Cohort, Brazil) (2015)
Freitas, Perla Lopes de; Cavalli, Ricardo de Carvalho; Silva, Antonio Augusto Moura da; Bettiol, Heloisa; Barbieri, Marco Antonio; Cardoso, Viviane Cunha; Batista, Rosângela Fernandes Lucena; Pereira, Silma Regina Ferreira
Source: Journal of Developmental Origins of Health and Disease. Conference titles: World Congress on Developmental Origins of Health and Disease. Unidade: FMRP
Subjects: POLIMORFISMO, GRAVIDEZ
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ABNT
FREITAS, Perla Lopes de et al. TNF-2 gene -308 polymorphism among women with preterm delivery from two Brazilian cohorts with different socioeconomic profiles (BRISA Birth Cohort, Brazil). Journal of Developmental Origins of Health and Disease. Cambridge: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 09 nov. 2024. , 2015
APA
Freitas, P. L. de, Cavalli, R. de C., Silva, A. A. M. da, Bettiol, H., Barbieri, M. A., Cardoso, V. C., et al. (2015). TNF-2 gene -308 polymorphism among women with preterm delivery from two Brazilian cohorts with different socioeconomic profiles (BRISA Birth Cohort, Brazil). Journal of Developmental Origins of Health and Disease. Cambridge: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Freitas PL de, Cavalli R de C, Silva AAM da, Bettiol H, Barbieri MA, Cardoso VC, Batista RFL, Pereira SRF. TNF-2 gene -308 polymorphism among women with preterm delivery from two Brazilian cohorts with different socioeconomic profiles (BRISA Birth Cohort, Brazil). Journal of Developmental Origins of Health and Disease. 2015 ; 6 S172.[citado 2024 nov. 09 ]
Vancouver
Freitas PL de, Cavalli R de C, Silva AAM da, Bettiol H, Barbieri MA, Cardoso VC, Batista RFL, Pereira SRF. TNF-2 gene -308 polymorphism among women with preterm delivery from two Brazilian cohorts with different socioeconomic profiles (BRISA Birth Cohort, Brazil). Journal of Developmental Origins of Health and Disease. 2015 ; 6 S172.[citado 2024 nov. 09 ]
Artigo de periodico
Lewis histo-blood group system phenotyping and genotyping reveal divergence in the association of Le(a-b-) phenotype and type 1 diabetes (2015)
Previato, M.; Borim, M. P.; Liberatore Junior, Raphael Del Roio; Pires, A. C.; Dias, M. A. F.; Mattos, C. C. Brandão de; Mattos, L. C.
Source: Vox Sanguinis. Unidade: FMRP
Subjects: DIABETES MELLITUS, GRUPOS SANGUÍNEOS, POLIMORFISMO, FENÓTIPOS
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ABNT
PREVIATO, M. et al. Lewis histo-blood group system phenotyping and genotyping reveal divergence in the association of Le(a-b-) phenotype and type 1 diabetes. Vox Sanguinis, v. 108, n. 3, p. 281-286, 2015Tradução . . Disponível em: https://doi.org/10.1111/vox.12211. Acesso em: 09 nov. 2024.
APA
Previato, M., Borim, M. P., Liberatore Junior, R. D. R., Pires, A. C., Dias, M. A. F., Mattos, C. C. B. de, & Mattos, L. C. (2015). Lewis histo-blood group system phenotyping and genotyping reveal divergence in the association of Le(a-b-) phenotype and type 1 diabetes. Vox Sanguinis, 108( 3), 281-286. doi:10.1111/vox.12211
NLM
Previato M, Borim MP, Liberatore Junior RDR, Pires AC, Dias MAF, Mattos CCB de, Mattos LC. Lewis histo-blood group system phenotyping and genotyping reveal divergence in the association of Le(a-b-) phenotype and type 1 diabetes [Internet]. Vox Sanguinis. 2015 ; 108( 3): 281-286.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1111/vox.12211
Vancouver
Previato M, Borim MP, Liberatore Junior RDR, Pires AC, Dias MAF, Mattos CCB de, Mattos LC. Lewis histo-blood group system phenotyping and genotyping reveal divergence in the association of Le(a-b-) phenotype and type 1 diabetes [Internet]. Vox Sanguinis. 2015 ; 108( 3): 281-286.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1111/vox.12211
Artigo de periodico
Genetic Predictors of Long-Term Response to Growth Hormone (GH) Therapy in Children With GH Deficiency and Turner Syndrome: the influence of a SOCS2 polymorphism (2014)
Braz, Adriana F.; Costalonga, Everlayny F.; Trarbach, Ericka B.; Scalco, Renata C.; Malaquias, Alexsandra C.; Guerra-Junior, Gil; Antonini, Sonir Roberto Rauber; Mendonça, Berenice Bilharinho de; Arnhold, Ivo J. P.; Jorge, Alexander Augusto de Lima
Source: Journal of clinical endocrinology and metabolism. Unidades: FMRP, FM
Subjects: CRIANÇAS, POLIMORFISMO, CIÊNCIA (TERAPIA)
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ABNT
BRAZ, Adriana F. et al. Genetic Predictors of Long-Term Response to Growth Hormone (GH) Therapy in Children With GH Deficiency and Turner Syndrome: the influence of a SOCS2 polymorphism. Journal of clinical endocrinology and metabolism, v. 99, n. 9, p. E1808-E1813, 2014Tradução . . Disponível em: https://doi.org/10.1210/jc.2014-1744. Acesso em: 09 nov. 2024.
APA
Braz, A. F., Costalonga, E. F., Trarbach, E. B., Scalco, R. C., Malaquias, A. C., Guerra-Junior, G., et al. (2014). Genetic Predictors of Long-Term Response to Growth Hormone (GH) Therapy in Children With GH Deficiency and Turner Syndrome: the influence of a SOCS2 polymorphism. Journal of clinical endocrinology and metabolism, 99( 9), E1808-E1813. doi:10.1210/jc.2014-1744
NLM
Braz AF, Costalonga EF, Trarbach EB, Scalco RC, Malaquias AC, Guerra-Junior G, Antonini SRR, Mendonça BB de, Arnhold IJP, Jorge AA de L. Genetic Predictors of Long-Term Response to Growth Hormone (GH) Therapy in Children With GH Deficiency and Turner Syndrome: the influence of a SOCS2 polymorphism [Internet]. Journal of clinical endocrinology and metabolism. 2014 ; 99( 9): E1808-E1813.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1210/jc.2014-1744
Vancouver
Braz AF, Costalonga EF, Trarbach EB, Scalco RC, Malaquias AC, Guerra-Junior G, Antonini SRR, Mendonça BB de, Arnhold IJP, Jorge AA de L. Genetic Predictors of Long-Term Response to Growth Hormone (GH) Therapy in Children With GH Deficiency and Turner Syndrome: the influence of a SOCS2 polymorphism [Internet]. Journal of clinical endocrinology and metabolism. 2014 ; 99( 9): E1808-E1813.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1210/jc.2014-1744
Artigo de periodico
A Novel ADIPOQ mutation (p.M40K) impairs assembly of high-molecular-weight adiponectin and is associated with early-onset obesity and metabolic syndrome (2014)
Bueno, Ana Carolina; Sun, Kai; Martins, Clarissa Silva; Elias Júnior, Jorge; Miranda, Wallace; Tao, Caroline; Foss-Freitas, Maria Cristina; Barbieri, Marco Antonio; Bettiol, Heloisa; Castro, Margaret de; Scherer, Philipp E.; Antonini, Sonir Roberto Rauber
Source: Journal of Clinical Endocrinology and Metabolism. Unidade: FMRP
Subjects: GENÉTICA, POLIMORFISMO, HORMÔNIOS (DEFICIÊNCIA), ENDOCRINOLOGIA (METABOLISMO)
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ABNT
BUENO, Ana Carolina et al. A Novel ADIPOQ mutation (p.M40K) impairs assembly of high-molecular-weight adiponectin and is associated with early-onset obesity and metabolic syndrome. Journal of Clinical Endocrinology and Metabolism, v. 99 n.4, p. E683-E693, 2014Tradução . . Disponível em: https://doi.org/10.1210/jc.2013-3009. Acesso em: 09 nov. 2024.
APA
Bueno, A. C., Sun, K., Martins, C. S., Elias Júnior, J., Miranda, W., Tao, C., et al. (2014). A Novel ADIPOQ mutation (p.M40K) impairs assembly of high-molecular-weight adiponectin and is associated with early-onset obesity and metabolic syndrome. Journal of Clinical Endocrinology and Metabolism, 99 n.4, E683-E693. doi:10.1210/jc.2013-3009
NLM
Bueno AC, Sun K, Martins CS, Elias Júnior J, Miranda W, Tao C, Foss-Freitas MC, Barbieri MA, Bettiol H, Castro M de, Scherer PE, Antonini SRR. A Novel ADIPOQ mutation (p.M40K) impairs assembly of high-molecular-weight adiponectin and is associated with early-onset obesity and metabolic syndrome [Internet]. Journal of Clinical Endocrinology and Metabolism. 2014 ; 99 n.4 E683-E693.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1210/jc.2013-3009
Vancouver
Bueno AC, Sun K, Martins CS, Elias Júnior J, Miranda W, Tao C, Foss-Freitas MC, Barbieri MA, Bettiol H, Castro M de, Scherer PE, Antonini SRR. A Novel ADIPOQ mutation (p.M40K) impairs assembly of high-molecular-weight adiponectin and is associated with early-onset obesity and metabolic syndrome [Internet]. Journal of Clinical Endocrinology and Metabolism. 2014 ; 99 n.4 E683-E693.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1210/jc.2013-3009
Artigo de periodico-carta/editorial
Comments to "A rational, non-radioactive strategy for the molecular diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency. [Carta] (2014)
Coeli-Lacchini, Fernanda Borchers; Turatti, Wendy; Elias, Paula Conde Lamparelli; Elias, Lucila Leico Kagohara; Martinelli Junior, Carlos Eduardo; Moreira, Ayrton Custódio; Antonini, Sonir Roberto Rauber; Castro, Margaret de
Source: Gene. Unidade: FMRP
Subjects: HIPERPLASIAS, DIAGNÓSTICO, MUTAÇÃO GENÉTICA, POLIMORFISMO
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ABNT
COELI-LACCHINI, Fernanda Borchers et al. Comments to "A rational, non-radioactive strategy for the molecular diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency. [Carta]. Gene. Amsterdam: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. Disponível em: https://doi.org/10.1016/j.gene.2013.09.109. Acesso em: 09 nov. 2024. , 2014
APA
Coeli-Lacchini, F. B., Turatti, W., Elias, P. C. L., Elias, L. L. K., Martinelli Junior, C. E., Moreira, A. C., et al. (2014). Comments to "A rational, non-radioactive strategy for the molecular diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency. [Carta]. Gene. Amsterdam: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. doi:10.1016/j.gene.2013.09.109
NLM
Coeli-Lacchini FB, Turatti W, Elias PCL, Elias LLK, Martinelli Junior CE, Moreira AC, Antonini SRR, Castro M de. Comments to "A rational, non-radioactive strategy for the molecular diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency. [Carta] [Internet]. Gene. 2014 ; 534( 2): 451-452.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1016/j.gene.2013.09.109
Vancouver
Coeli-Lacchini FB, Turatti W, Elias PCL, Elias LLK, Martinelli Junior CE, Moreira AC, Antonini SRR, Castro M de. Comments to "A rational, non-radioactive strategy for the molecular diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency. [Carta] [Internet]. Gene. 2014 ; 534( 2): 451-452.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1016/j.gene.2013.09.109
Artigo de periodico
NR3C1 polymorphisms in Brazilians of Caucasian, African, and Asian ancestry: glucocorticoid sensitivity and genotype association (2014)
Souza, Manoel Carlos L. A.; Martins, Clarissa S.; SilvaJúnior, Ivan M.; Chriguer, Rosangela S.; Bueno, Ana C.; Antonini, Sonir Roberto Rauber; Silva Júnior, Wilson Araújo da; Zago, Marco Antonio; Moreira, Ayrton Custódio; Castro, Margaret de
Source: Arquivos Brasileiros de Endocrinologia e Metabologia. Unidade: FMRP
Subjects: POLIMORFISMO, GENÉTICA DE POPULAÇÕES, SENSIBILIDADE E ESPECIFICIDADE, GENÓTIPOS (FREQUÊNCIA)
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ABNT
SOUZA, Manoel Carlos L. A. et al. NR3C1 polymorphisms in Brazilians of Caucasian, African, and Asian ancestry: glucocorticoid sensitivity and genotype association. Arquivos Brasileiros de Endocrinologia e Metabologia, v. 58, n. 1, p. 53-61, 2014Tradução . . Disponível em: https://doi.org/10.1590/0004-2730000002868. Acesso em: 09 nov. 2024.
APA
Souza, M. C. L. A., Martins, C. S., SilvaJúnior, I. M., Chriguer, R. S., Bueno, A. C., Antonini, S. R. R., et al. (2014). NR3C1 polymorphisms in Brazilians of Caucasian, African, and Asian ancestry: glucocorticoid sensitivity and genotype association. Arquivos Brasileiros de Endocrinologia e Metabologia, 58( 1), 53-61. doi:10.1590/0004-2730000002868
NLM
Souza MCLA, Martins CS, SilvaJúnior IM, Chriguer RS, Bueno AC, Antonini SRR, Silva Júnior WA da, Zago MA, Moreira AC, Castro M de. NR3C1 polymorphisms in Brazilians of Caucasian, African, and Asian ancestry: glucocorticoid sensitivity and genotype association [Internet]. Arquivos Brasileiros de Endocrinologia e Metabologia. 2014 ; 58( 1): 53-61.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1590/0004-2730000002868
Vancouver
Souza MCLA, Martins CS, SilvaJúnior IM, Chriguer RS, Bueno AC, Antonini SRR, Silva Júnior WA da, Zago MA, Moreira AC, Castro M de. NR3C1 polymorphisms in Brazilians of Caucasian, African, and Asian ancestry: glucocorticoid sensitivity and genotype association [Internet]. Arquivos Brasileiros de Endocrinologia e Metabologia. 2014 ; 58( 1): 53-61.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1590/0004-2730000002868
Artigo de periodico
Polymorphisms of the adiponectin gene in gestational hypertension and pre-eclampsia (2014)
Machado, J. S. R.; Palei, Ana Carolina Taveiros; Amaral, L. M.; Bueno, A. C.; Antonini, Sonir Roberto Rauber; Duarte, Geraldo; Tanus-Santos, José Eduardo; Sandrim, Valéria Cristina; Cavalli, Ricardo de Carvalho
Source: Journal of Human Hypertension. Unidade: FMRP
Subjects: ADIPONECTINA, HIPERTENSÃO NA GRAVIDEZ, POLIMORFISMO, PRÉ-ECLÂMPSIA
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ABNT
MACHADO, J. S. R. et al. Polymorphisms of the adiponectin gene in gestational hypertension and pre-eclampsia. Journal of Human Hypertension, v. 28, n. 2, p. 128-132, 2014Tradução . . Disponível em: https://doi.org/10.1038/jhh.2013.53. Acesso em: 09 nov. 2024.
APA
Machado, J. S. R., Palei, A. C. T., Amaral, L. M., Bueno, A. C., Antonini, S. R. R., Duarte, G., et al. (2014). Polymorphisms of the adiponectin gene in gestational hypertension and pre-eclampsia. Journal of Human Hypertension, 28( 2), 128-132. doi:10.1038/jhh.2013.53
NLM
Machado JSR, Palei ACT, Amaral LM, Bueno AC, Antonini SRR, Duarte G, Tanus-Santos JE, Sandrim VC, Cavalli R de C. Polymorphisms of the adiponectin gene in gestational hypertension and pre-eclampsia [Internet]. Journal of Human Hypertension. 2014 ; 28( 2): 128-132.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1038/jhh.2013.53
Vancouver
Machado JSR, Palei ACT, Amaral LM, Bueno AC, Antonini SRR, Duarte G, Tanus-Santos JE, Sandrim VC, Cavalli R de C. Polymorphisms of the adiponectin gene in gestational hypertension and pre-eclampsia [Internet]. Journal of Human Hypertension. 2014 ; 28( 2): 128-132.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1038/jhh.2013.53
Trabalho de evento-resumo
Commom polymorphisms in GHRd3, IGFBP3 and IGF1 genes do not explain GH-IGF-I dissociation in treated acromegalic patients (2013)
Kiminami, Daniel Ossamu Goldschmidt; Coeli-Lacchini, Fernanda Borchers; Roa, Silvia Ruiz; Castro, Margaret de; Antonini, Sonir Roberto Rauber; Moreira, Ayrton Custódio
Source: Abstracts. Conference titles: Annual Meeting and Expo of the Endocrine Society. Unidade: FMRP
Subjects: POLIMORFISMO, GENES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
KIMINAMI, Daniel Ossamu Goldschmidt et al. Commom polymorphisms in GHRd3, IGFBP3 and IGF1 genes do not explain GH-IGF-I dissociation in treated acromegalic patients. 2013, Anais.. San Francisco: Endocrine Society, 2013. . Acesso em: 09 nov. 2024.
APA
Kiminami, D. O. G., Coeli-Lacchini, F. B., Roa, S. R., Castro, M. de, Antonini, S. R. R., & Moreira, A. C. (2013). Commom polymorphisms in GHRd3, IGFBP3 and IGF1 genes do not explain GH-IGF-I dissociation in treated acromegalic patients. In Abstracts. San Francisco: Endocrine Society.
NLM
Kiminami DOG, Coeli-Lacchini FB, Roa SR, Castro M de, Antonini SRR, Moreira AC. Commom polymorphisms in GHRd3, IGFBP3 and IGF1 genes do not explain GH-IGF-I dissociation in treated acromegalic patients. Abstracts. 2013 ;[citado 2024 nov. 09 ]
Vancouver
Kiminami DOG, Coeli-Lacchini FB, Roa SR, Castro M de, Antonini SRR, Moreira AC. Commom polymorphisms in GHRd3, IGFBP3 and IGF1 genes do not explain GH-IGF-I dissociation in treated acromegalic patients. Abstracts. 2013 ;[citado 2024 nov. 09 ]
Trabalho de evento-resumo
Polimorfismo dos 14PB do HLA-G na transmissão materno infantil do HIV-1 (2013)
Sanches, Roberta Seron; Massaro, Juliana Doblas; Mendes Júnior, Celso Teixeira; Matos, Francielly Maiara da Penna; Martinez, Juliana; Kashima, Simone; Quintana, Silvana Maria; Cérvi, Maria Célia; Donadi, Eduardo Antônio; Fernandes, Ana Paula Morais
Source: Anais. Conference titles: Congresso Brasileiro de Genética Médica. Unidades: FFCLRP, FMRP, EERP
Subjects: POLIMORFISMO, HIV, CRIANÇAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SANCHES, Roberta Seron et al. Polimorfismo dos 14PB do HLA-G na transmissão materno infantil do HIV-1. 2013, Anais.. Florianópolis: SBGM, 2013. . Acesso em: 09 nov. 2024.
APA
Sanches, R. S., Massaro, J. D., Mendes Júnior, C. T., Matos, F. M. da P., Martinez, J., Kashima, S., et al. (2013). Polimorfismo dos 14PB do HLA-G na transmissão materno infantil do HIV-1. In Anais. Florianópolis: SBGM.
NLM
Sanches RS, Massaro JD, Mendes Júnior CT, Matos FM da P, Martinez J, Kashima S, Quintana SM, Cérvi MC, Donadi EA, Fernandes APM. Polimorfismo dos 14PB do HLA-G na transmissão materno infantil do HIV-1. Anais. 2013 ;[citado 2024 nov. 09 ]
Vancouver
Sanches RS, Massaro JD, Mendes Júnior CT, Matos FM da P, Martinez J, Kashima S, Quintana SM, Cérvi MC, Donadi EA, Fernandes APM. Polimorfismo dos 14PB do HLA-G na transmissão materno infantil do HIV-1. Anais. 2013 ;[citado 2024 nov. 09 ]
Artigo de periodico
The interactive effect of GHR-Exon 3 and −202 A/C IGFBP3 polymorphisms on rhGH responsiveness and treatment outcomes in patients with Turner Syndrome (2012)
Braz, Adriana F.; Costalonga, Everlayny F.; Montenegro, Luciana Ribeiro; Trarbach, Ericka B.; Antonini, Sonir Roberto Rauber; Malaquias, Alexsandra C.; Ramos, Ester Silveira; Mendonca, Berenice Bilharinho.; Arnhold, Ivo J. P.; Jorge, Alexander Augusto de Lima
Source: The journal of clinical endocrinology & metabolism. Unidades: FM, FMRP
Subjects: POLIMORFISMO, ENDOCRINOPATIAS (GENÉTICA;TERAPIA), ALELOPATIA (GENÉTICA), FATORES DE CRESCIMENTO (PATOLOGIA), GENÓTIPOS (ANÁLISE), PROTOCOLOS CLÍNICOS, BIOLOGIA MOLECULAR
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BRAZ, Adriana F. et al. The interactive effect of GHR-Exon 3 and −202 A/C IGFBP3 polymorphisms on rhGH responsiveness and treatment outcomes in patients with Turner Syndrome. The journal of clinical endocrinology & metabolism, v. 97, n. 4, p. E671-E677, 2012Tradução . . Disponível em: https://doi.org/10.1210/jc.2011-2521. Acesso em: 09 nov. 2024.
APA
Braz, A. F., Costalonga, E. F., Montenegro, L. R., Trarbach, E. B., Antonini, S. R. R., Malaquias, A. C., et al. (2012). The interactive effect of GHR-Exon 3 and −202 A/C IGFBP3 polymorphisms on rhGH responsiveness and treatment outcomes in patients with Turner Syndrome. The journal of clinical endocrinology & metabolism, 97( 4), E671-E677. doi:10.1210/jc.2011-2521
NLM
Braz AF, Costalonga EF, Montenegro LR, Trarbach EB, Antonini SRR, Malaquias AC, Ramos ES, Mendonca BB, Arnhold IJP, Jorge AA de L. The interactive effect of GHR-Exon 3 and −202 A/C IGFBP3 polymorphisms on rhGH responsiveness and treatment outcomes in patients with Turner Syndrome [Internet]. The journal of clinical endocrinology & metabolism. 2012 ; 97( 4): E671-E677.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1210/jc.2011-2521
Vancouver
Braz AF, Costalonga EF, Montenegro LR, Trarbach EB, Antonini SRR, Malaquias AC, Ramos ES, Mendonca BB, Arnhold IJP, Jorge AA de L. The interactive effect of GHR-Exon 3 and −202 A/C IGFBP3 polymorphisms on rhGH responsiveness and treatment outcomes in patients with Turner Syndrome [Internet]. The journal of clinical endocrinology & metabolism. 2012 ; 97( 4): E671-E677.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1210/jc.2011-2521
Artigo de periodico
A commentary on association of adiponectin polymorphism with cord blood adiponectin concetrations and intrauterine growth (2012)
Antonini, Sonir Roberto Rauber
Source: Journal of Human Genetics. Unidade: FMRP
Subjects: ADIPONECTINA (GENÉTICA), FETO (SANGUE;METABOLISMO), DESENVOLVIMENTO FETAL (GENÉTICA), POLIMORFISMO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ANTONINI, Sonir Roberto Rauber. A commentary on association of adiponectin polymorphism with cord blood adiponectin concetrations and intrauterine growth. Journal of Human Genetics, v. 57, n. 3, p. 157-158, 2012Tradução . . Disponível em: https://doi.org/10.1038/jhg.2011.149. Acesso em: 09 nov. 2024.
APA
Antonini, S. R. R. (2012). A commentary on association of adiponectin polymorphism with cord blood adiponectin concetrations and intrauterine growth. Journal of Human Genetics, 57( 3), 157-158. doi:10.1038/jhg.2011.149
NLM
Antonini SRR. A commentary on association of adiponectin polymorphism with cord blood adiponectin concetrations and intrauterine growth [Internet]. Journal of Human Genetics. 2012 ; 57( 3): 157-158.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1038/jhg.2011.149
Vancouver
Antonini SRR. A commentary on association of adiponectin polymorphism with cord blood adiponectin concetrations and intrauterine growth [Internet]. Journal of Human Genetics. 2012 ; 57( 3): 157-158.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1038/jhg.2011.149
Trabalho de evento-resumo periodico
Study of polymorphisms of the adiponectin gene in women with gestational hypertension and preeclampsia (2012)
Machado, J. S. R.; Cavalli, Ricardo de Carvalho; Sandrim, V. C.; Palei, A. C. T.; Amaral, L. M.; Bueno, A. C.; Antonini, Sonir Roberto Rauber; Tanus-Santos, José Eduardo; Duarte, Geraldo
Source: Pregnancy Hypertension. Conference titles: World Congress of the International Society for the Study of Hypertension in Pregnancy. Unidade: FMRP
Subjects: HIPERTENSÃO NA GRAVIDEZ, POLIMORFISMO, PRÉ-ECLÂMPSIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MACHADO, J. S. R. et al. Study of polymorphisms of the adiponectin gene in women with gestational hypertension and preeclampsia. Pregnancy Hypertension. Geneva: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 09 nov. 2024. , 2012
APA
Machado, J. S. R., Cavalli, R. de C., Sandrim, V. C., Palei, A. C. T., Amaral, L. M., Bueno, A. C., et al. (2012). Study of polymorphisms of the adiponectin gene in women with gestational hypertension and preeclampsia. Pregnancy Hypertension. Geneva: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Machado JSR, Cavalli R de C, Sandrim VC, Palei ACT, Amaral LM, Bueno AC, Antonini SRR, Tanus-Santos JE, Duarte G. Study of polymorphisms of the adiponectin gene in women with gestational hypertension and preeclampsia. Pregnancy Hypertension. 2012 ; 2( 3): 241.[citado 2024 nov. 09 ]
Vancouver
Machado JSR, Cavalli R de C, Sandrim VC, Palei ACT, Amaral LM, Bueno AC, Antonini SRR, Tanus-Santos JE, Duarte G. Study of polymorphisms of the adiponectin gene in women with gestational hypertension and preeclampsia. Pregnancy Hypertension. 2012 ; 2( 3): 241.[citado 2024 nov. 09 ]
Artigo de periodico
Fc'gama' receptor gene polymorphisms in childhood immune thrombocytopenic purpura (2012)
Amorim, Daniela Maria de Mendonça Caldas; Silveira, Vanessa da Silva; Scrideli, Carlos Alberto; Queiroz, Rosane Gomes de Paula; Tone, Luiz Gonzaga
Source: Journal of Pediatric Hematology Oncology. Unidade: FMRP
Subjects: DOENÇAS SANGUÍNEAS E LINFÁTICAS, POLIMORFISMO, REAÇÃO EM CADEIA POR POLIMERASE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
AMORIM, Daniela Maria de Mendonça Caldas et al. Fc'gama' receptor gene polymorphisms in childhood immune thrombocytopenic purpura. Journal of Pediatric Hematology Oncology, v. 34, n. 5, p. 349-352, 2012Tradução . . Disponível em: https://doi.org/10.1097/MPH.0b013e3182580908. Acesso em: 09 nov. 2024.
APA
Amorim, D. M. de M. C., Silveira, V. da S., Scrideli, C. A., Queiroz, R. G. de P., & Tone, L. G. (2012). Fc'gama' receptor gene polymorphisms in childhood immune thrombocytopenic purpura. Journal of Pediatric Hematology Oncology, 34( 5), 349-352. doi:10.1097/MPH.0b013e3182580908
NLM
Amorim DM de MC, Silveira V da S, Scrideli CA, Queiroz RG de P, Tone LG. Fc'gama' receptor gene polymorphisms in childhood immune thrombocytopenic purpura [Internet]. Journal of Pediatric Hematology Oncology. 2012 ; 34( 5): 349-352.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1097/MPH.0b013e3182580908
Vancouver
Amorim DM de MC, Silveira V da S, Scrideli CA, Queiroz RG de P, Tone LG. Fc'gama' receptor gene polymorphisms in childhood immune thrombocytopenic purpura [Internet]. Journal of Pediatric Hematology Oncology. 2012 ; 34( 5): 349-352.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1097/MPH.0b013e3182580908
Artigo de periodico
CYP3A5 and NAT2 gene polymorphisms: role in childhood acute lymphoblastic leukemia risk and treatment outcome (2012)
Silveira, Vanessa S.; Canalle, Renata; Scrideli, Carlos Alberto; Queiroz, Rosane Gomes de Paula; Lopes, Luiz Fernando; Tone, Luiz Gonzaga
Source: Molecular and Cellular Biochemistry. Unidade: FMRP
Subjects: POLIMORFISMO, RISCO, LEUCEMIA, INFÂNCIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SILVEIRA, Vanessa S. et al. CYP3A5 and NAT2 gene polymorphisms: role in childhood acute lymphoblastic leukemia risk and treatment outcome. Molecular and Cellular Biochemistry, 2012Tradução . . Disponível em: https://doi.org/10.1007/s11010-011-1220-8. Acesso em: 09 nov. 2024.
APA
Silveira, V. S., Canalle, R., Scrideli, C. A., Queiroz, R. G. de P., Lopes, L. F., & Tone, L. G. (2012). CYP3A5 and NAT2 gene polymorphisms: role in childhood acute lymphoblastic leukemia risk and treatment outcome. Molecular and Cellular Biochemistry. doi:10.1007/s11010-011-1220-8
NLM
Silveira VS, Canalle R, Scrideli CA, Queiroz RG de P, Lopes LF, Tone LG. CYP3A5 and NAT2 gene polymorphisms: role in childhood acute lymphoblastic leukemia risk and treatment outcome [Internet]. Molecular and Cellular Biochemistry. 2012 ;[citado 2024 nov. 09 ] Available from: https://doi.org/10.1007/s11010-011-1220-8
Vancouver
Silveira VS, Canalle R, Scrideli CA, Queiroz RG de P, Lopes LF, Tone LG. CYP3A5 and NAT2 gene polymorphisms: role in childhood acute lymphoblastic leukemia risk and treatment outcome [Internet]. Molecular and Cellular Biochemistry. 2012 ;[citado 2024 nov. 09 ] Available from: https://doi.org/10.1007/s11010-011-1220-8
Artigo de periodico
Mineralocorticoid receptor p.I180V polymorphism: association with body mass index and LDL-cholesterol levels (2010)
Fernandes Rosa, F. L.; Bueno, A. C.; Souza, R. Molina de; Castro, Margaret de; Santos, Jose Ernesto dos; Foss, Milton César; Zennaro, M. -C.; Bettiol, Heloisa; Barbieri, Marco Antonio; Antonini, Sonir Roberto Rauber
Source: Journal of Endocrinological Investigation. Unidade: FMRP
Subjects: HIPERTENSÃO, POLIMORFISMO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FERNANDES ROSA, F. L. et al. Mineralocorticoid receptor p.I180V polymorphism: association with body mass index and LDL-cholesterol levels. Journal of Endocrinological Investigation, v. 33, n. 7, p. 472-477, 2010Tradução . . Disponível em: https://doi.org/10.1007/bf03346627. Acesso em: 09 nov. 2024.
APA
Fernandes Rosa, F. L., Bueno, A. C., Souza, R. M. de, Castro, M. de, Santos, J. E. dos, Foss, M. C., et al. (2010). Mineralocorticoid receptor p.I180V polymorphism: association with body mass index and LDL-cholesterol levels. Journal of Endocrinological Investigation, 33( 7), 472-477. doi:10.1007/bf03346627
NLM
Fernandes Rosa FL, Bueno AC, Souza RM de, Castro M de, Santos JE dos, Foss MC, Zennaro M-C, Bettiol H, Barbieri MA, Antonini SRR. Mineralocorticoid receptor p.I180V polymorphism: association with body mass index and LDL-cholesterol levels [Internet]. Journal of Endocrinological Investigation. 2010 ; 33( 7): 472-477.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1007/bf03346627
Vancouver
Fernandes Rosa FL, Bueno AC, Souza RM de, Castro M de, Santos JE dos, Foss MC, Zennaro M-C, Bettiol H, Barbieri MA, Antonini SRR. Mineralocorticoid receptor p.I180V polymorphism: association with body mass index and LDL-cholesterol levels [Internet]. Journal of Endocrinological Investigation. 2010 ; 33( 7): 472-477.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1007/bf03346627

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