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BRAGHINI, CAROLINA AYUMI ; NESHICH, IZABELLA AGOSTINHO PENA ; NESHICH, GORAN ; SOARDI, FERNANDA CAROLINE ; DE MELLO, MARICILDA PALANDI ; COSTA, Vital Paulino ; DE VASCONCELLOS, JOSÉ PAULO CABRAL ; DE MELO, MÔNICA BARBOSA . New mutation in the myocilin gene segregates with juvenile-onset open-angle glaucoma in a Brazilian family. Gene (Amsterdam) , v. 523, p. 50-57, 2013.
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Menaa F ; Braghini, CA ; VASCONCELLOS, José Paulo Cabral de ; Menaa, B. ; COSTA, Vital Paulino ; Figueiredo, ES ; MELO, Mônica Barbosa de . Keeping an eye on myocilin: a complex molecule associated with primary open-angle glaucoma susceptibility.. Molecules (Basel. Online) , v. 16, p. 5402-5421, 2011.
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PAOLERA, Maurício Della ; VASCONCELLOS, José Paulo Cabral de ; Caixeta-Umbelino, C ; KASAHARA, Niro ; ROCHA, Mylene Neves ; RICHETI, Flávio ; COSTA, Vital Paulino ; TAVARES, Anderson ; MELO, Mônica Barbosa de . CYP1B1 gene analysis in primary congenital glaucoma Brazilian patients: novel mutations and association with poor prognosis. Journal of Glaucoma , v. 19, p. 176-182, 2010.
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OLIVEIRA, André Lima de ; RODRIGUES, Fábio ; Santos, R.E. ; Aoki, T. ; ROCHA, Mylene Neves ; LONGUI, Carlos Alberto ; MELO, Mônica Barbosa de . GSTT1, GSTM1, and GSTP1 polymorphisms and chemotherapy response in locally advanced breast cancer. Genetics and Molecular Research , v. 9, p. 1045-1053, 2010.
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Caixeta-Umbelino, C ; VASCONCELLOS, José Paulo Cabral de ; KASAHARA, Niro ; PAOLERA, Maurício Della ; ALMEIDA, Geraldo Viecente de ; COHEN, Ralph ; MANDIA JR, C. ; COSTA, Vital Paulino ; ROCHA, Mylene Neves ; RICHETI, Flávio ; LONGUI, Carlos Alberto ; MELO, Mônica Barbosa de . Lack of association between optineurin gene variants T34T, E50K, M98K, 691_692insAG and R545Q and primary open angle glaucoma in Brazilian patients. Ophthalmic Genetics , v. 30, p. 13-18, 2009.
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SANTANA, Alessandro ; WAISWOL, M ; ARCIERI, ES ; VASCONCELLOS, José Paulo Cabral de ; MELO, Mônica Barbosa de . Mutation analysis of CRYAA, CRYGC and CRYGD genes associated with autosomal dominant congenital cataract in Brazilian families. Molecular Vision , v. 15, p. 793-800, 2009.
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CUNHA AF ; BRUGNEROTTO AF ; CORAT, MA ; DEVLIN, EE ; GIMENES AP ; MELO, Mônica Barbosa de ; PASSOS, LA ; BODINE, D ; SAAD, S. T. O. ; COSTA, Fernando Ferreira . High levels of human gamma-globin are expressed in adult mice carrying a transgene of the Brazilian type of hereditary persistence of fetal hemoglobin ((A)gamma -195).. Hemoglobin , v. 33, p. 439-447, 2009.
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SANTOS, A. D. S. ; Prado RAA ; MELO, Mônica Barbosa de ; MELO, Murilo Rezende ; LONGUI, Carlos Alberto . Structural evaluation of type 3 dopaminergic receptor gene (DRD3) in chronic anovulatory women. Genetics and Molecular Research , v. 7, p. 140-151, 2008.
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Rodrigues, F. F. O. ; Santos, R.E. ; MELO, Mônica Barbosa de ; Silva, M.A.L.G. ; OLIVEIRA, André Lima de ; Rosenowicz, R.L. ; Ulson, L.B. ; Aoki, T. . Correlation of polymorphism C3435T of the MDR-1 gene and the response of primary chemotherapy in women wityh locally advanced breast cancer. Genetics and Molecular Research , v. 7, p. 177-183, 2008.
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Cury AN ; LONGUI, Carlos Alberto ; KOCHI, Cristiane ; CALLIARI, Luís Eduardo Procópio ; Scalissi N ; Salles JE ; ROCHA, Mylene Neves ; MELO, Mônica Barbosa de ; MELO, Murilo Rezende ; MONTE, Osmar . Graves' disease in Brazilian children and adults: lack of genetic association with CTLA-4 +49A>G polymorphism. Hormone Research , v. 70, p. 36-41, 2008.
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KOCHI, Cristiane ; LONGUI, Carlos Alberto ; LEMOSMARINI, Sofia H V ; GUERRAJR, Gili ; MELO, Mônica Barbosa de ; CALLIARI, Luís Eduardo Procópio ; MONTE, Osmar . The influence of parental origin of X chromosme genes on the stature of patients with 45X Turner syndrome, no prelo. GENETICS AND MOLECULAR RESEARCH , Brasil, v. 6, p. 1-7, 2007.
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RICHETI, Flávio ; NORONHA, Renata Maria ; WAETGE, Ricardo Temudo Lessa ; VASCONCELLOS, José Paulo Cabral de ; SOUZA, Osías Francisco de ; KNEIPP, Bianca ; ASSIS, Nilma ; ROCHA, Mylene Neves ; CALLIARI, Luís Eduardo Procópio ; LONGUI, Carlos Alberto ; MONTE, Osmar ; MELO, Mônica Barbosa de . Evaluation of AC(n) and C(-106)T polymorphisms of the aldose reductase gene in Brazilian patients with DM1 and susceptibility to diabetic retinopathy, aceito para publicação. Molecular Vision , EUA, v. 13, p. 740-745, 2007.
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CALLIARI, Luís Eduardo Procópio ; LONGUI, Carlos Alberto ; ROCHA, Mylene Neves ; FARIA, Cláudia Dutra Costantin ; KOCHI, Cristiane ; MELO, Murilo Resende ; MELO, Mônica Barbosa de ; MONTE, Osmar . A novel mutation in DAX1 gene causing different phenotypes in three siblings with adrenal hypoplasia congenita. Genetics and Molecular Research , v. 6, p. 177-183, 2007.
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CELLA, Wener ; VASCONCELLOS, José Paulo Cabral de ; MELO, Mônica Barbosa de ; KNEIPP, Bianca ; COSTA, Fernando Ferreira ; LONGUI, Carlos Alberto ; COSTA, Vital Paulino . Structural assessment of PITX2, FOXC1, CYP1B1 and GJA1 genes in patients with Axenfeld-Rieger syndrome with developmental glaucoma. Investigative Ophtalmology & Visual Science , Estados Unidos, v. 47, n.5, p. 1803-1809, 2006.
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MOURA, Mônica Souza Filho ; MELO, Mônica Barbosa de ; LONGUI, Carlos Alberto ; ROCHA, Mylene Neves ; MONTE, Osmar . Triagem de mutações nos receptores de angiotensina II, AGTR1 e AGTR2 e avaliação dos polimorfismos C573T e A1166C do gene AGTR1 em pacientes com adrenarca precoce idiopática. Arquivos Brasileiros de Endocrinologia & Metabologia , Brasil, v. 50, n.5, p. 893-900, 2006.
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VASCONCELLOS, José Paulo Cabral de ; MELO, Mônica Barbosa de ; SCHIMITI, Rui Barroso ; BRESSANIM, Norisvaldo César ; COSTA, Fernando Ferreira ; COSTA, Vital Paulino . A novel mutation in the GJA1 gene in a family with oculodentodigital dysplasia. Archives of Ophthalmology , Estados Unidos, v. 123, n.10, p. 1422-1426, 2005.
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MELO, Mônica Barbosa de ; BORDIN, S. ; DUARTE, A. S. S. ; OGO, S. H. ; TORSONI, M. A. ; SAAD, S. T. O. ; COSTA, Fernando Ferreira . Molecular characterization of hemoglobin alpha-D chains from Geochelone carbonaria and Geochelone denticulata land turtles. Comparative Biochemistry and Physiology. Part B: Biochemistry & Molecular Biology (Print) , Irlanda, v. 134, p. 389-395, 2003.
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ORTEGA, M. M. ; NASCIMENTO, H. ; MELO, Mônica Barbosa de ; TEORI, M. T. ; COSTA, Fernando Ferreira ; LIMA, C. S. P. . Polymorphisms of glutathione s-transferase mu1 (GSTM1) and theta 1 (GSTT1) genes in multiple myeloma. Acta Haematologica , República Tcheca, v. 109, p. 108-109, 2003.
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ORTEGA, M. M. ; MELO, Mônica Barbosa de ; SOUZA, C. A. ; LORAND-METZE, I. ; COSTA, Fernando Ferreira ; LIMA, C. S. P. . A possible role of the p53 gene deletion as a prognostic factor in multiple myeloma. Annals of Hematology , Alemanha, v. 82, p. 405-409, 2003.
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MELO, Mônica Barbosa de ; AHMAD, N. N. ; LIMA, C. S. P. ; PAGNANO, K. B. B. ; BORDIN, S. ; LORANDMETZE, I. ; SAAD, S. T. O. ; COSTA, Fernando Ferreira . Mutations in the p53 gene in acute myeloid leukemia patients correlate with poor prognosis. Hematology , Suiça, v. 7, n.1, p. 13-19, 2002.
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STOILOV, I. ; COSTA, Vital Paulino ; VASCONCELLOS, José Paulo Cabral de ; MELO, Mônica Barbosa de ; BETINJANE, A. J. ; CARANI, J. C. E. ; OLTROGGE, W. ; SARFARAZI, M. . Molecular genetics of primary congenital glaucoma in Brazil. Investigative Ophtalmology & Visual Science , EUA, v. 43, n.6, p. 1820-1827, 2002.
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HORTA, L. S. G. ; LONGUI, Carlos Alberto ; SOARES, E. S. ; D'OSWALDO, A. F. ; FULLER, C. R. ; ROCHA, Mylene Neves ; MELO, Mônica Barbosa de ; MONTE, Osmar . Methylation of the androgen receptor gene in cryptorchid boys. The Journal Of Endocrine Genetics, EUA, v. 3, p. 27-31, 2002.
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LONGUI, Carlos Alberto ; ROCHA, Mylene Neves ; MARTINHO, L. C. A. P. ; GOMES, G. G. ; MIRANDA, R. E. ; LIMA, T. A. S. ; MELO, Mônica Barbosa de ; MONTE, Osmar . Molecular Detection of X0 - Turner Syndrome. Genetics And Molecular Research, Brasil, v. 1, n.3, p. 266-270, 2002.
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ARRUDA, V. R. ; LIMA, C. S. P. ; GRIGNOLI, C. R. E. ; MELO, Mônica Barbosa de ; LORAND-METZE, I. ; ALBERTO, F. L. ; SAAD, S. T. O. ; COSTA, Fernando Ferreira . Increased risk for acute myeloid leukaemia in individuals with glutathione S-transferase mu 1 (GSTM1) and theta 1 (GSTT1) gene defects. European Journal of Haematology , Inglaterra, v. 66, n.6, p. 383-388, 2001.
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CAMARGO, A. A. ; MELO, Mônica Barbosa de ; et al . The contribution of 700,000 ORF sequence tags to the definition of the human transcripome. PNAS. Proceedings of the National Academy of Sciences of the United States of America , Estados Unidos, v. 98, n.21, p. 12103-12108, 2001.
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VASCONCELLOS, José Paulo Cabral de ; MELO, Mônica Barbosa de ; COSTA, Vital Paulino ; TSUKUMO, D. M. L. ; BASSÈRES, D. S. ; BORDIN, S. ; SAAD, S. T. O. ; COSTA, Fernando Ferreira . Novel mutation in the MYOC gene in primary open angle glaucoma patients. Journal of Medical Genetics , Inglaterra, v. 37, p. 301-303, 2000.
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AHMAD, N. N. ; MELO, Mônica Barbosa de ; SINGH, A. D. ; DONOSO, L. A. ; SHIELDS, J. A. . A possible hot spot in exon 21 of the RB gene predisposing to a low penetrant retinoblastoma phenotype?. Ophthalmic Genetics, Estados Unidos, v. 20, n.4, p. 225-231, 1999.
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VASCONCELLOS, José Paulo Cabral de ; MELO, Mônica Barbosa de ; MENEZES, F. ; TSUKUMO, D. M. L. ; COSTA, Vital Paulino ; KARA-JOSE, N. ; COSTA, Fernando Ferreira . Mutações no gene MYOC/TIGR em uma população brasileira com glaucoma juvenil e glaucoma primário de ângulo aberto. Arquivos Brasileiros de Oftalmologia , Brasil, v. 61, n.6, p. 690-694, 1998.
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BORDIN, S. ; MARTINS, J. T. ; GONÇALVES, M. S. ; MELO, Mônica Barbosa de ; SAAD, S. T. O. ; COSTA, Fernando Ferreira . Haplotype analysis and gamma A gene polymorphism associated with the Brazilian type of hereditary persistence of fetal hemoglobin.. American Journal of Hematology , Estados Unidos, v. 58, n.1, p. 49-54, 1998.
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MELO, Mônica Barbosa de ; COSTA, Fernando Ferreira ; SAAD, S. T. O. ; LORAND-METZE, I. ; BORDIN, S. ; AHMAD, N. N. . Molecular analysis of the retinoblastoma (RB1) gene in acute myeloid leukemia patients.. LEUKEMIA RESEARCH , Inglaterra, v. 22, n.9, p. 787-792, 1998.
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MELO, Mônica Barbosa de ; LORAND-METZE, I. ; LIMA, C. S. P. ; SAAD, S. T. O. ; COSTA, Fernando Ferreira . N-ras gene point mutations in Brazilian acute myelogenous leukemia patients correlate with a poor prognosis. LEUKEMIA & LYMPHOMA , República Tcheca, v. 24, p. 309-317, 1997.
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NUNES, M. V. ; MELO, Mônica Barbosa de ; COSTA, Fernando Ferreira ; VARELLAGARCIA, M. . A simple technique for isolation of DNA suitable for PCR amplification from cytogenetic preparations.. Brazilian Journal Of Genetics, Brasil, v. 18, n.3, p. 489-490, 1995.
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MELO, Mônica Barbosa de ; SALES, T. S. I. ; LORAND-METZE, I. ; COSTA, Fernando Ferreira . Rapid method for isolation of DNA from glass slide smears for PCR. Acta Haematologica , Inglaterra, v. 87, p. 214-215, 1992.
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VASCONCELLOS, José Paulo Cabral de ; MELO, Mônica Barbosa de ; SCHIMITI, R. ; COSTA, Vital Paulino ; COSTA, Fernando Ferreira . Estudo da mutação CYS433ARG no gene MYOC em família com glaucoma primário de ângulo aberto. Arquivos Brasileiros de Oftalmologia , Brasil, v. 64, n.4, p. 74, 2001.