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Artigo de periodico
The A61 G EGF polymorphism is associated with development of extraaxial nervous system tumors but not with overall survival (2010)
Almeida, Luciana Oliveira de; Custódio, Aline Cadurin; Santos, Marcelo José dos; Almeida, José R. W.; Clara, Carlos Afonso; Pinto, Giovanny Rebouças; Rey, Juan A.; Casartelli, Cacilda
Source: Cancer Genetics and Cytogenetics. Unidade: FMRP
Subjects: POLIMORFISMO, NEOPLASIAS CEREBRAIS
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ABNT
ALMEIDA, Luciana Oliveira de et al. The A61 G EGF polymorphism is associated with development of extraaxial nervous system tumors but not with overall survival. Cancer Genetics and Cytogenetics, v. 198, n. 1, p. 15-21, 2010Tradução . . Disponível em: https://doi.org/10.1016/j.cancergencyto.2009.11.013. Acesso em: 28 set. 2024.
APA
Almeida, L. O. de, Custódio, A. C., Santos, M. J. dos, Almeida, J. R. W., Clara, C. A., Pinto, G. R., et al. (2010). The A61 G EGF polymorphism is associated with development of extraaxial nervous system tumors but not with overall survival. Cancer Genetics and Cytogenetics, 198( 1), 15-21. doi:10.1016/j.cancergencyto.2009.11.013
NLM
Almeida LO de, Custódio AC, Santos MJ dos, Almeida JRW, Clara CA, Pinto GR, Rey JA, Casartelli C. The A61 G EGF polymorphism is associated with development of extraaxial nervous system tumors but not with overall survival [Internet]. Cancer Genetics and Cytogenetics. 2010 ; 198( 1): 15-21.[citado 2024 set. 28 ] Available from: https://doi.org/10.1016/j.cancergencyto.2009.11.013
Vancouver
Almeida LO de, Custódio AC, Santos MJ dos, Almeida JRW, Clara CA, Pinto GR, Rey JA, Casartelli C. The A61 G EGF polymorphism is associated with development of extraaxial nervous system tumors but not with overall survival [Internet]. Cancer Genetics and Cytogenetics. 2010 ; 198( 1): 15-21.[citado 2024 set. 28 ] Available from: https://doi.org/10.1016/j.cancergencyto.2009.11.013
Artigo de periodico
Genomic deletions at 1p and 14p are associated with an abnormal cDNA microarray gene expression pattern in meningiomas but not it schwannomas (2010)
Martínez-Glez, Victor; Alvarez, Luis; Franco-Hernández, Carmen; Torres-Martin, Miguel; Campos, Jose M. de; Isla, Alberto; Vaquero, Jesús; Lassaletta, Luis; Castresana, Javier S.; Casartelli, Cacilda; Rey, Juan A.
Source: Cancer Genetics and Cytogenetics. Unidade: FMRP
Subjects: MENINGIOMA, EXPRESSÃO GÊNICA
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ABNT
MARTÍNEZ-GLEZ, Victor et al. Genomic deletions at 1p and 14p are associated with an abnormal cDNA microarray gene expression pattern in meningiomas but not it schwannomas. Cancer Genetics and Cytogenetics, v. 196, n. 1, p. 1-6, 2010Tradução . . Disponível em: https://doi.org/10.1016/j.cancergencyto.2009.08.003. Acesso em: 28 set. 2024.
APA
Martínez-Glez, V., Alvarez, L., Franco-Hernández, C., Torres-Martin, M., Campos, J. M. de, Isla, A., et al. (2010). Genomic deletions at 1p and 14p are associated with an abnormal cDNA microarray gene expression pattern in meningiomas but not it schwannomas. Cancer Genetics and Cytogenetics, 196( 1), 1-6. doi:10.1016/j.cancergencyto.2009.08.003
NLM
Martínez-Glez V, Alvarez L, Franco-Hernández C, Torres-Martin M, Campos JM de, Isla A, Vaquero J, Lassaletta L, Castresana JS, Casartelli C, Rey JA. Genomic deletions at 1p and 14p are associated with an abnormal cDNA microarray gene expression pattern in meningiomas but not it schwannomas [Internet]. Cancer Genetics and Cytogenetics. 2010 ; 196( 1): 1-6.[citado 2024 set. 28 ] Available from: https://doi.org/10.1016/j.cancergencyto.2009.08.003
Vancouver
Martínez-Glez V, Alvarez L, Franco-Hernández C, Torres-Martin M, Campos JM de, Isla A, Vaquero J, Lassaletta L, Castresana JS, Casartelli C, Rey JA. Genomic deletions at 1p and 14p are associated with an abnormal cDNA microarray gene expression pattern in meningiomas but not it schwannomas [Internet]. Cancer Genetics and Cytogenetics. 2010 ; 196( 1): 1-6.[citado 2024 set. 28 ] Available from: https://doi.org/10.1016/j.cancergencyto.2009.08.003
Artigo de periodico
Meningiomas and schwannomas: molecular subgroup classification found by expression arrays (2009)
Martinez-Glez, Victor; Franco-Hernandez, Carmen; Alvarez, Luis; Campos, Jose M. de; Isla, Alberto; Vaquero, Jesus; Lassaletta, Luis; Casartelli, Cacilda; Rey, Juan A.
Source: International Journal of Oncology. Unidade: FMRP
Subjects: EXPRESSÃO GÊNICA, MENINGIOMA
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ABNT
MARTINEZ-GLEZ, Victor et al. Meningiomas and schwannomas: molecular subgroup classification found by expression arrays. International Journal of Oncology, v. 34, n. 2, p. 493-504, 2009Tradução . . Disponível em: https://doi.org/10.3892/ijo_00000174. Acesso em: 28 set. 2024.
APA
Martinez-Glez, V., Franco-Hernandez, C., Alvarez, L., Campos, J. M. de, Isla, A., Vaquero, J., et al. (2009). Meningiomas and schwannomas: molecular subgroup classification found by expression arrays. International Journal of Oncology, 34( 2), 493-504. doi:10.3892/ijo_00000174
NLM
Martinez-Glez V, Franco-Hernandez C, Alvarez L, Campos JM de, Isla A, Vaquero J, Lassaletta L, Casartelli C, Rey JA. Meningiomas and schwannomas: molecular subgroup classification found by expression arrays [Internet]. International Journal of Oncology. 2009 ; 34( 2): 493-504.[citado 2024 set. 28 ] Available from: https://doi.org/10.3892/ijo_00000174
Vancouver
Martinez-Glez V, Franco-Hernandez C, Alvarez L, Campos JM de, Isla A, Vaquero J, Lassaletta L, Casartelli C, Rey JA. Meningiomas and schwannomas: molecular subgroup classification found by expression arrays [Internet]. International Journal of Oncology. 2009 ; 34( 2): 493-504.[citado 2024 set. 28 ] Available from: https://doi.org/10.3892/ijo_00000174
Artigo de periodico
Allelic status of 1p and 19q in oligodendrogliomas and glioblastomas: multiplex ligation-dependent probe amplification versus loss of heterozygosity (2009)
Franco-Hernández, Carmen; Martínez-Glez, Victor; Campos, Jose M. de; Isla, Alberto; Vaquero, Jesús; Gutiérrez, Manuel; Casartelli, Cacilda; Rey, Juan A.
Source: Cancer Genetics and Cytogenetics. Unidade: FMRP
Subjects: NEOPLASIAS, GENÉTICA
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ABNT
FRANCO-HERNÁNDEZ, Carmen et al. Allelic status of 1p and 19q in oligodendrogliomas and glioblastomas: multiplex ligation-dependent probe amplification versus loss of heterozygosity. Cancer Genetics and Cytogenetics, v. 190, n. 2, p. 93-96, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.cancergencyto.2008.09.017. Acesso em: 28 set. 2024.
APA
Franco-Hernández, C., Martínez-Glez, V., Campos, J. M. de, Isla, A., Vaquero, J., Gutiérrez, M., et al. (2009). Allelic status of 1p and 19q in oligodendrogliomas and glioblastomas: multiplex ligation-dependent probe amplification versus loss of heterozygosity. Cancer Genetics and Cytogenetics, 190( 2), 93-96. doi:10.1016/j.cancergencyto.2008.09.017
NLM
Franco-Hernández C, Martínez-Glez V, Campos JM de, Isla A, Vaquero J, Gutiérrez M, Casartelli C, Rey JA. Allelic status of 1p and 19q in oligodendrogliomas and glioblastomas: multiplex ligation-dependent probe amplification versus loss of heterozygosity [Internet]. Cancer Genetics and Cytogenetics. 2009 ; 190( 2): 93-96.[citado 2024 set. 28 ] Available from: https://doi.org/10.1016/j.cancergencyto.2008.09.017
Vancouver
Franco-Hernández C, Martínez-Glez V, Campos JM de, Isla A, Vaquero J, Gutiérrez M, Casartelli C, Rey JA. Allelic status of 1p and 19q in oligodendrogliomas and glioblastomas: multiplex ligation-dependent probe amplification versus loss of heterozygosity [Internet]. Cancer Genetics and Cytogenetics. 2009 ; 190( 2): 93-96.[citado 2024 set. 28 ] Available from: https://doi.org/10.1016/j.cancergencyto.2008.09.017
Artigo de periodico
WRN Cys1367Arg SNP is not associated with risk and prognosis of gliomas in Southeast Brasil (2008)
Pinto, Giovanny Rebouças; Yoshioka, France Keiko Nascimento; Clara, Carlos Afonso; Santos, Marcelo José dos; Almeida, José Reynaldo Walther de; Burbano, Rommel Rodríguez; Rey, Juan A.; Casartelli, Cacilda
Source: Journal of Neuro-Oncology. Unidade: FMRP
Subjects: MUTAÇÃO GENÉTICA, PROGNÓSTICO, GENÉTICA MÉDICA
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ABNT
PINTO, Giovanny Rebouças et al. WRN Cys1367Arg SNP is not associated with risk and prognosis of gliomas in Southeast Brasil. Journal of Neuro-Oncology, v. 90, n. 3, p. 253-258, 2008Tradução . . Disponível em: https://doi.org/10.1007/s11060-008-9664-8. Acesso em: 28 set. 2024.
APA
Pinto, G. R., Yoshioka, F. K. N., Clara, C. A., Santos, M. J. dos, Almeida, J. R. W. de, Burbano, R. R., et al. (2008). WRN Cys1367Arg SNP is not associated with risk and prognosis of gliomas in Southeast Brasil. Journal of Neuro-Oncology, 90( 3), 253-258. doi:10.1007/s11060-008-9664-8
NLM
Pinto GR, Yoshioka FKN, Clara CA, Santos MJ dos, Almeida JRW de, Burbano RR, Rey JA, Casartelli C. WRN Cys1367Arg SNP is not associated with risk and prognosis of gliomas in Southeast Brasil [Internet]. Journal of Neuro-Oncology. 2008 ; 90( 3): 253-258.[citado 2024 set. 28 ] Available from: https://doi.org/10.1007/s11060-008-9664-8
Vancouver
Pinto GR, Yoshioka FKN, Clara CA, Santos MJ dos, Almeida JRW de, Burbano RR, Rey JA, Casartelli C. WRN Cys1367Arg SNP is not associated with risk and prognosis of gliomas in Southeast Brasil [Internet]. Journal of Neuro-Oncology. 2008 ; 90( 3): 253-258.[citado 2024 set. 28 ] Available from: https://doi.org/10.1007/s11060-008-9664-8
Artigo de periodico
Methylation status of ANAPC1, CDKN2A and TP53 promoter genes in individuals with gastric cancer (2008)
Lima, E. M.; Leal, M. F.; Burbano, R. R.; Khayat, A. S.; Assumpção, P. P.; Bello, M. J.; Rey, J. A.; Smith, M. A. C.; Casartelli, Cacilda
Source: Brazilian Journal of Medical and Biological Research. Unidade: FMRP
Subjects: NEOPLASIAS GÁSTRICAS, DNA
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ABNT
LIMA, E. M. et al. Methylation status of ANAPC1, CDKN2A and TP53 promoter genes in individuals with gastric cancer. Brazilian Journal of Medical and Biological Research, v. 41, n. 6, p. 539-543, 2008Tradução . . Disponível em: https://doi.org/10.1590/s0100-879x2008000600017. Acesso em: 28 set. 2024.
APA
Lima, E. M., Leal, M. F., Burbano, R. R., Khayat, A. S., Assumpção, P. P., Bello, M. J., et al. (2008). Methylation status of ANAPC1, CDKN2A and TP53 promoter genes in individuals with gastric cancer. Brazilian Journal of Medical and Biological Research, 41( 6), 539-543. doi:10.1590/s0100-879x2008000600017
NLM
Lima EM, Leal MF, Burbano RR, Khayat AS, Assumpção PP, Bello MJ, Rey JA, Smith MAC, Casartelli C. Methylation status of ANAPC1, CDKN2A and TP53 promoter genes in individuals with gastric cancer [Internet]. Brazilian Journal of Medical and Biological Research. 2008 ; 41( 6): 539-543.[citado 2024 set. 28 ] Available from: https://doi.org/10.1590/s0100-879x2008000600017
Vancouver
Lima EM, Leal MF, Burbano RR, Khayat AS, Assumpção PP, Bello MJ, Rey JA, Smith MAC, Casartelli C. Methylation status of ANAPC1, CDKN2A and TP53 promoter genes in individuals with gastric cancer [Internet]. Brazilian Journal of Medical and Biological Research. 2008 ; 41( 6): 539-543.[citado 2024 set. 28 ] Available from: https://doi.org/10.1590/s0100-879x2008000600017
Artigo de periodico-carta/editorial
Mutation analysis of the CITED4 gene in glioblastomas. [Carta] (2008)
Torres-Martín; Franco-Hernandez, Carmen; Matinez-Glez, Victor; Campos, Jose M. de; Isla, Alberto; Casartelli, Cacilda; Rey, Juan A.
Source: Cancer Genetics and Cytogenetics. Unidade: FMRP
Subjects: POLIMORFISMO, NEOPLASIAS
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ABNT
TORRES-MARTÍN, et al. Mutation analysis of the CITED4 gene in glioblastomas. [Carta]. Cancer Genetics and Cytogenetics. New York: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 28 set. 2024. , 2008
APA
Torres-Martín,, Franco-Hernandez, C., Matinez-Glez, V., Campos, J. M. de, Isla, A., Casartelli, C., & Rey, J. A. (2008). Mutation analysis of the CITED4 gene in glioblastomas. [Carta]. Cancer Genetics and Cytogenetics. New York: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Torres-Martín, Franco-Hernandez C, Matinez-Glez V, Campos JM de, Isla A, Casartelli C, Rey JA. Mutation analysis of the CITED4 gene in glioblastomas. [Carta]. Cancer Genetics and Cytogenetics. 2008 ; 185( 2): 114-116.[citado 2024 set. 28 ]
Vancouver
Torres-Martín, Franco-Hernandez C, Matinez-Glez V, Campos JM de, Isla A, Casartelli C, Rey JA. Mutation analysis of the CITED4 gene in glioblastomas. [Carta]. Cancer Genetics and Cytogenetics. 2008 ; 185( 2): 114-116.[citado 2024 set. 28 ]
Artigo de periodico
DAPK1 promoter hypermethylaiton in brain metastases and peripheral blood (2007)
Martinez-Glez, V.; Franco-Hernandez, C.; Gonzalez-Gomez, P.; Isla, A.; Campos, J. M. de; Vaquero, J.; Gutierrez, M.; Casartelli, Cacilda; Rey, J. A.
Source: Neoplasma. Unidade: FMRP
Assunto: METÁSTASE NEOPLÁSICA
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ABNT
MARTINEZ-GLEZ, V. et al. DAPK1 promoter hypermethylaiton in brain metastases and peripheral blood. Neoplasma, v. 54, n. 2, p. 123-126, 2007Tradução . . Acesso em: 28 set. 2024.
APA
Martinez-Glez, V., Franco-Hernandez, C., Gonzalez-Gomez, P., Isla, A., Campos, J. M. de, Vaquero, J., et al. (2007). DAPK1 promoter hypermethylaiton in brain metastases and peripheral blood. Neoplasma, 54( 2), 123-126.
NLM
Martinez-Glez V, Franco-Hernandez C, Gonzalez-Gomez P, Isla A, Campos JM de, Vaquero J, Gutierrez M, Casartelli C, Rey JA. DAPK1 promoter hypermethylaiton in brain metastases and peripheral blood. Neoplasma. 2007 ; 54( 2): 123-126.[citado 2024 set. 28 ]
Vancouver
Martinez-Glez V, Franco-Hernandez C, Gonzalez-Gomez P, Isla A, Campos JM de, Vaquero J, Gutierrez M, Casartelli C, Rey JA. DAPK1 promoter hypermethylaiton in brain metastases and peripheral blood. Neoplasma. 2007 ; 54( 2): 123-126.[citado 2024 set. 28 ]
Artigo de periodico
An intronic variant in the TP53 gene in a Brazilian woman with breast cancer (2005)
Lacerda, Leandra Linhares; Serrano, Sérgio Vicente; Mathes, Ângelo do Carmo da Silva; Rey, Juan A.; Bello, Maria Josefa; Casartelli, Cacilda
Source: Cancer Genetics and Cytogenetics. Unidade: FMRP
Subjects: NEOPLASIAS MAMÁRIAS, MUTAÇÃO GENÉTICA
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ABNT
LACERDA, Leandra Linhares et al. An intronic variant in the TP53 gene in a Brazilian woman with breast cancer. Cancer Genetics and Cytogenetics, v. 160, p. 160-163, 2005Tradução . . Disponível em: https://doi.org/10.1016/j.cancergencyto.2004.11.014. Acesso em: 28 set. 2024.
APA
Lacerda, L. L., Serrano, S. V., Mathes, Â. do C. da S., Rey, J. A., Bello, M. J., & Casartelli, C. (2005). An intronic variant in the TP53 gene in a Brazilian woman with breast cancer. Cancer Genetics and Cytogenetics, 160, 160-163. doi:10.1016/j.cancergencyto.2004.11.014
NLM
Lacerda LL, Serrano SV, Mathes Â do C da S, Rey JA, Bello MJ, Casartelli C. An intronic variant in the TP53 gene in a Brazilian woman with breast cancer [Internet]. Cancer Genetics and Cytogenetics. 2005 ; 160 160-163.[citado 2024 set. 28 ] Available from: https://doi.org/10.1016/j.cancergencyto.2004.11.014
Vancouver
Lacerda LL, Serrano SV, Mathes Â do C da S, Rey JA, Bello MJ, Casartelli C. An intronic variant in the TP53 gene in a Brazilian woman with breast cancer [Internet]. Cancer Genetics and Cytogenetics. 2005 ; 160 160-163.[citado 2024 set. 28 ] Available from: https://doi.org/10.1016/j.cancergencyto.2004.11.014
Artigo de periodico
Molecular study of the tumour suppressor gene PTEN in gastric adenocarcinoma in Brazil (2005)
Lima, E. M.; Araújo, J. J.; Harada, M. L.; Assumpção, P. P.; Burbano, R. R.; Casartelli, Cacilda
Source: Clinical and Experimental Medicine. Unidade: FMRP
Subjects: NEOPLASIAS GÁSTRICAS, GENÉTICA MÉDICA
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ABNT
LIMA, E. M. et al. Molecular study of the tumour suppressor gene PTEN in gastric adenocarcinoma in Brazil. Clinical and Experimental Medicine, v. 5, p. 129-132, 2005Tradução . . Disponível em: https://doi.org/10.1007/s10238-005-0077-0. Acesso em: 28 set. 2024.
APA
Lima, E. M., Araújo, J. J., Harada, M. L., Assumpção, P. P., Burbano, R. R., & Casartelli, C. (2005). Molecular study of the tumour suppressor gene PTEN in gastric adenocarcinoma in Brazil. Clinical and Experimental Medicine, 5, 129-132. doi:10.1007/s10238-005-0077-0
NLM
Lima EM, Araújo JJ, Harada ML, Assumpção PP, Burbano RR, Casartelli C. Molecular study of the tumour suppressor gene PTEN in gastric adenocarcinoma in Brazil [Internet]. Clinical and Experimental Medicine. 2005 ; 5 129-132.[citado 2024 set. 28 ] Available from: https://doi.org/10.1007/s10238-005-0077-0
Vancouver
Lima EM, Araújo JJ, Harada ML, Assumpção PP, Burbano RR, Casartelli C. Molecular study of the tumour suppressor gene PTEN in gastric adenocarcinoma in Brazil [Internet]. Clinical and Experimental Medicine. 2005 ; 5 129-132.[citado 2024 set. 28 ] Available from: https://doi.org/10.1007/s10238-005-0077-0
Artigo de periodico
Hypermethylation of the DNA repair gene MGMT: association with TP53 G:C to A:T transitions in a series of 469 nervous system tumors (2004)
Bello, M. Josefa; Alonso, M. Eva; Amiñoso, Cinthia; Anselmo, Nilson P.; Arjona, Dolores; Gonzalez-Gomez, Pilar; Lopez-Marin, Isabel; Campos, José M. de; Gutierrez, Manuel; Isla, Alberto; Kusak, M. Elena; Lassaletta, Luis; Sarasa, José L.; Vaquero, Jesus; Casartelli, Cacilda
Source: Mutation Research. Unidade: FMRP
Subjects: GENÉTICA MÉDICA, PROCESSOS NEOPLÁSICOS
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ABNT
BELLO, M. Josefa et al. Hypermethylation of the DNA repair gene MGMT: association with TP53 G:C to A:T transitions in a series of 469 nervous system tumors. Mutation Research, v. 554, p. 23-32, 2004Tradução . . Disponível em: https://doi.org/10.1016/j.mrfmmm.2004.02.011. Acesso em: 28 set. 2024.
APA
Bello, M. J., Alonso, M. E., Amiñoso, C., Anselmo, N. P., Arjona, D., Gonzalez-Gomez, P., et al. (2004). Hypermethylation of the DNA repair gene MGMT: association with TP53 G:C to A:T transitions in a series of 469 nervous system tumors. Mutation Research, 554, 23-32. doi:10.1016/j.mrfmmm.2004.02.011
NLM
Bello MJ, Alonso ME, Amiñoso C, Anselmo NP, Arjona D, Gonzalez-Gomez P, Lopez-Marin I, Campos JM de, Gutierrez M, Isla A, Kusak ME, Lassaletta L, Sarasa JL, Vaquero J, Casartelli C. Hypermethylation of the DNA repair gene MGMT: association with TP53 G:C to A:T transitions in a series of 469 nervous system tumors [Internet]. Mutation Research. 2004 ; 554 23-32.[citado 2024 set. 28 ] Available from: https://doi.org/10.1016/j.mrfmmm.2004.02.011
Vancouver
Bello MJ, Alonso ME, Amiñoso C, Anselmo NP, Arjona D, Gonzalez-Gomez P, Lopez-Marin I, Campos JM de, Gutierrez M, Isla A, Kusak ME, Lassaletta L, Sarasa JL, Vaquero J, Casartelli C. Hypermethylation of the DNA repair gene MGMT: association with TP53 G:C to A:T transitions in a series of 469 nervous system tumors [Internet]. Mutation Research. 2004 ; 554 23-32.[citado 2024 set. 28 ] Available from: https://doi.org/10.1016/j.mrfmmm.2004.02.011
Artigo de periodico
Conventional cytogenetic characterization of a new cell line, ACPO1, established from a primary human gastric tumor (2004)
Lima, E. M.; Rissino, J. D.; Harada, M. L.; Assumpção, P. P.; Demachki, S.; Guimarães, A. C.; Casartelli, Cacilda; Smith, M. A. C.; Burbano, R. R.
Source: Brazilian Journal of Medical and Biological Research. Unidade: FMRP
Subjects: GENÉTICA MÉDICA, NEOPLASIAS
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ABNT
LIMA, E. M. et al. Conventional cytogenetic characterization of a new cell line, ACPO1, established from a primary human gastric tumor. Brazilian Journal of Medical and Biological Research, v. 37, n. 12, p. 1831-1838, 2004Tradução . . Disponível em: https://doi.org/10.1590/s0100-879x2004001200008. Acesso em: 28 set. 2024.
APA
Lima, E. M., Rissino, J. D., Harada, M. L., Assumpção, P. P., Demachki, S., Guimarães, A. C., et al. (2004). Conventional cytogenetic characterization of a new cell line, ACPO1, established from a primary human gastric tumor. Brazilian Journal of Medical and Biological Research, 37( 12), 1831-1838. doi:10.1590/s0100-879x2004001200008
NLM
Lima EM, Rissino JD, Harada ML, Assumpção PP, Demachki S, Guimarães AC, Casartelli C, Smith MAC, Burbano RR. Conventional cytogenetic characterization of a new cell line, ACPO1, established from a primary human gastric tumor [Internet]. Brazilian Journal of Medical and Biological Research. 2004 ; 37( 12): 1831-1838.[citado 2024 set. 28 ] Available from: https://doi.org/10.1590/s0100-879x2004001200008
Vancouver
Lima EM, Rissino JD, Harada ML, Assumpção PP, Demachki S, Guimarães AC, Casartelli C, Smith MAC, Burbano RR. Conventional cytogenetic characterization of a new cell line, ACPO1, established from a primary human gastric tumor [Internet]. Brazilian Journal of Medical and Biological Research. 2004 ; 37( 12): 1831-1838.[citado 2024 set. 28 ] Available from: https://doi.org/10.1590/s0100-879x2004001200008
Artigo de periodico
Cytogenetic description of breast fibroadenomas: alterations related solely to proliferation ? (2001)
Burbano, R. R.; Lima, E. M.; Khayat, A. S.; Barbieri Neto, José; Cabral, I. R.; Bastos Júnior, L.; Bahia, Marcelo de Oliveira; Casartelli, Cacilda
Source: Brazilian Journal of Medical and Biological. Unidade: FMRP
Subjects: NEOPLASIAS MAMÁRIAS, CITOGENÉTICA
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ABNT
BURBANO, R. R. et al. Cytogenetic description of breast fibroadenomas: alterations related solely to proliferation ?. Brazilian Journal of Medical and Biological, v. 34, p. 1003-1006, 2001Tradução . . Disponível em: https://doi.org/10.1590/s0100-879x2001000800005. Acesso em: 28 set. 2024.
APA
Burbano, R. R., Lima, E. M., Khayat, A. S., Barbieri Neto, J., Cabral, I. R., Bastos Júnior, L., et al. (2001). Cytogenetic description of breast fibroadenomas: alterations related solely to proliferation ? Brazilian Journal of Medical and Biological, 34, 1003-1006. doi:10.1590/s0100-879x2001000800005
NLM
Burbano RR, Lima EM, Khayat AS, Barbieri Neto J, Cabral IR, Bastos Júnior L, Bahia M de O, Casartelli C. Cytogenetic description of breast fibroadenomas: alterations related solely to proliferation ? [Internet]. Brazilian Journal of Medical and Biological. 2001 ; 34 1003-1006.[citado 2024 set. 28 ] Available from: https://doi.org/10.1590/s0100-879x2001000800005
Vancouver
Burbano RR, Lima EM, Khayat AS, Barbieri Neto J, Cabral IR, Bastos Júnior L, Bahia M de O, Casartelli C. Cytogenetic description of breast fibroadenomas: alterations related solely to proliferation ? [Internet]. Brazilian Journal of Medical and Biological. 2001 ; 34 1003-1006.[citado 2024 set. 28 ] Available from: https://doi.org/10.1590/s0100-879x2001000800005
Artigo de periodico
Analysis of p73 gene in meningiomas with deletion at 1p (2001)
Lomas, Jesus; Bello, Josefa; Arjona, Dolores; Gonzales-Gomez, Pilar; Alonso, M. Eva; Campos, José M. de; Vaquero, Jesus; Ruiz-Barnes, Pedro; Sarasa, José L.; Casartelli, Cacilda; Rey, Juan A.
Source: Cancer Genetics and Cytogenetics. Unidade: FMRP
Assunto: MENINGIOMA
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ABNT
LOMAS, Jesus et al. Analysis of p73 gene in meningiomas with deletion at 1p. Cancer Genetics and Cytogenetics, v. 129, p. 88-91, 2001Tradução . . Disponível em: https://doi.org/10.1016/s0165-4608(01)00430-7. Acesso em: 28 set. 2024.
APA
Lomas, J., Bello, J., Arjona, D., Gonzales-Gomez, P., Alonso, M. E., Campos, J. M. de, et al. (2001). Analysis of p73 gene in meningiomas with deletion at 1p. Cancer Genetics and Cytogenetics, 129, 88-91. doi:10.1016/s0165-4608(01)00430-7
NLM
Lomas J, Bello J, Arjona D, Gonzales-Gomez P, Alonso ME, Campos JM de, Vaquero J, Ruiz-Barnes P, Sarasa JL, Casartelli C, Rey JA. Analysis of p73 gene in meningiomas with deletion at 1p [Internet]. Cancer Genetics and Cytogenetics. 2001 ; 129 88-91.[citado 2024 set. 28 ] Available from: https://doi.org/10.1016/s0165-4608(01)00430-7
Vancouver
Lomas J, Bello J, Arjona D, Gonzales-Gomez P, Alonso ME, Campos JM de, Vaquero J, Ruiz-Barnes P, Sarasa JL, Casartelli C, Rey JA. Analysis of p73 gene in meningiomas with deletion at 1p [Internet]. Cancer Genetics and Cytogenetics. 2001 ; 129 88-91.[citado 2024 set. 28 ] Available from: https://doi.org/10.1016/s0165-4608(01)00430-7
Artigo de periodico
Deletion 5p11 accompanied by multiple numerical changes in testicular lymphoma (2001)
Espinoza, Luis A.; Barbieri Neto, José; Popescu, Nicholas C.; Casartelli, Cacilda
Source: Cancer Genetics and Cytogenetics. Unidade: FMRP
Subjects: LINFOMA, TESTÍCULO, GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ESPINOZA, Luis A. et al. Deletion 5p11 accompanied by multiple numerical changes in testicular lymphoma. Cancer Genetics and Cytogenetics, v. 131, p. 79-81, 2001Tradução . . Disponível em: https://doi.org/10.1016/s0165-4608(01)00495-2. Acesso em: 28 set. 2024.
APA
Espinoza, L. A., Barbieri Neto, J., Popescu, N. C., & Casartelli, C. (2001). Deletion 5p11 accompanied by multiple numerical changes in testicular lymphoma. Cancer Genetics and Cytogenetics, 131, 79-81. doi:10.1016/s0165-4608(01)00495-2
NLM
Espinoza LA, Barbieri Neto J, Popescu NC, Casartelli C. Deletion 5p11 accompanied by multiple numerical changes in testicular lymphoma [Internet]. Cancer Genetics and Cytogenetics. 2001 ; 131 79-81.[citado 2024 set. 28 ] Available from: https://doi.org/10.1016/s0165-4608(01)00495-2
Vancouver
Espinoza LA, Barbieri Neto J, Popescu NC, Casartelli C. Deletion 5p11 accompanied by multiple numerical changes in testicular lymphoma [Internet]. Cancer Genetics and Cytogenetics. 2001 ; 131 79-81.[citado 2024 set. 28 ] Available from: https://doi.org/10.1016/s0165-4608(01)00495-2
Artigo de periodico
Aneurysmal bone cyst with chromosomal changes involving 7q and 16p (2001)
Baruffi, Marcelo Razera; Barbieri Neto, José; Barbieri, Claudio Henrique; Casartelli, Cacilda
Source: Cancer Genetics and Cytogenetics. Unidade: FMRP
Subjects: CISTOS, OSSO E OSSOS, CITOGENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BARUFFI, Marcelo Razera et al. Aneurysmal bone cyst with chromosomal changes involving 7q and 16p. Cancer Genetics and Cytogenetics, v. 129, p. 177-180, 2001Tradução . . Disponível em: https://doi.org/10.1016/s0165-4608(01)00453-8. Acesso em: 28 set. 2024.
APA
Baruffi, M. R., Barbieri Neto, J., Barbieri, C. H., & Casartelli, C. (2001). Aneurysmal bone cyst with chromosomal changes involving 7q and 16p. Cancer Genetics and Cytogenetics, 129, 177-180. doi:10.1016/s0165-4608(01)00453-8
NLM
Baruffi MR, Barbieri Neto J, Barbieri CH, Casartelli C. Aneurysmal bone cyst with chromosomal changes involving 7q and 16p [Internet]. Cancer Genetics and Cytogenetics. 2001 ; 129 177-180.[citado 2024 set. 28 ] Available from: https://doi.org/10.1016/s0165-4608(01)00453-8
Vancouver
Baruffi MR, Barbieri Neto J, Barbieri CH, Casartelli C. Aneurysmal bone cyst with chromosomal changes involving 7q and 16p [Internet]. Cancer Genetics and Cytogenetics. 2001 ; 129 177-180.[citado 2024 set. 28 ] Available from: https://doi.org/10.1016/s0165-4608(01)00453-8
Artigo de periodico
Osteoid osteomas with chromosome alterations involving 22q (2001)
Baruffi, Marcelo Razera; Volpon, José Batista; Barbieri Neto, José; Casartelli, Cacilda
Source: Cancer Genetics and Cytogenetics. Unidade: FMRP
Subjects: ONCOLOGIA, OSSO E OSSOS (CIRURGIA), CITOGENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BARUFFI, Marcelo Razera et al. Osteoid osteomas with chromosome alterations involving 22q. Cancer Genetics and Cytogenetics, v. 124, p. 127-131, 2001Tradução . . Disponível em: https://doi.org/10.1016/s0165-4608(00)00327-7. Acesso em: 28 set. 2024.
APA
Baruffi, M. R., Volpon, J. B., Barbieri Neto, J., & Casartelli, C. (2001). Osteoid osteomas with chromosome alterations involving 22q. Cancer Genetics and Cytogenetics, 124, 127-131. doi:10.1016/s0165-4608(00)00327-7
NLM
Baruffi MR, Volpon JB, Barbieri Neto J, Casartelli C. Osteoid osteomas with chromosome alterations involving 22q [Internet]. Cancer Genetics and Cytogenetics. 2001 ; 124 127-131.[citado 2024 set. 28 ] Available from: https://doi.org/10.1016/s0165-4608(00)00327-7
Vancouver
Baruffi MR, Volpon JB, Barbieri Neto J, Casartelli C. Osteoid osteomas with chromosome alterations involving 22q [Internet]. Cancer Genetics and Cytogenetics. 2001 ; 124 127-131.[citado 2024 set. 28 ] Available from: https://doi.org/10.1016/s0165-4608(00)00327-7
Artigo de periodico
Trisomy 4 in a case of gynecomastia (2000)
Burbano, Rommel Rodríguez; Barbieri Neto, José; Philbert, Paulo Meyer de Paula; Lemos, José Alexandre; Bahia, Marcelo; Casartelli, Cacilda
Source: Cancer Genetics Cytogenetics. Unidade: FMRP
Subjects: GENÉTICA MÉDICA, ONCOLOGIA, NEOPLASIAS, MAMA, DOENÇAS DOS GENITAIS FEMININOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BURBANO, Rommel Rodríguez et al. Trisomy 4 in a case of gynecomastia. Cancer Genetics Cytogenetics, v. 117, p. 143-145, 2000Tradução . . Disponível em: http://probe.usp.br/cgi-bin/sciserv.pl?collection=journals&journal=01654608&issue=v117i0002&article=143_t4iacog&form=pdf&file=file.pdf. Acesso em: 28 set. 2024.
APA
Burbano, R. R., Barbieri Neto, J., Philbert, P. M. de P., Lemos, J. A., Bahia, M., & Casartelli, C. (2000). Trisomy 4 in a case of gynecomastia. Cancer Genetics Cytogenetics, 117, 143-145. Recuperado de http://probe.usp.br/cgi-bin/sciserv.pl?collection=journals&journal=01654608&issue=v117i0002&article=143_t4iacog&form=pdf&file=file.pdf
NLM
Burbano RR, Barbieri Neto J, Philbert PM de P, Lemos JA, Bahia M, Casartelli C. Trisomy 4 in a case of gynecomastia [Internet]. Cancer Genetics Cytogenetics. 2000 ; 117 143-145.[citado 2024 set. 28 ] Available from: http://probe.usp.br/cgi-bin/sciserv.pl?collection=journals&journal=01654608&issue=v117i0002&article=143_t4iacog&form=pdf&file=file.pdf
Vancouver
Burbano RR, Barbieri Neto J, Philbert PM de P, Lemos JA, Bahia M, Casartelli C. Trisomy 4 in a case of gynecomastia [Internet]. Cancer Genetics Cytogenetics. 2000 ; 117 143-145.[citado 2024 set. 28 ] Available from: http://probe.usp.br/cgi-bin/sciserv.pl?collection=journals&journal=01654608&issue=v117i0002&article=143_t4iacog&form=pdf&file=file.pdf
Artigo de periodico
Cytogenetics of epithelial hyperplasias of the human breast (2000)
Burbano, Rommel Rodríguez; Medeiros, Arnaldo; Amorim, Marucia Irena Medeiros de; Lima, Eleonidas Moura; Mello, Adriano; Barbieri Neto, José; Casartelli, Cacilda
Source: Cancer Genetics Cytogenetics. Unidade: FMRP
Subjects: GENÉTICA MÉDICA, ONCOLOGIA, MAMA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BURBANO, Rommel Rodríguez et al. Cytogenetics of epithelial hyperplasias of the human breast. Cancer Genetics Cytogenetics, v. 119, p. 62-66, 2000Tradução . . Disponível em: http://probe.usp.br/cgi-bin/sciserv.pl?collection=journals&journal=01654608&issue=v119i0001&article=62_coehothb&form=pdf&file=file.pdf. Acesso em: 28 set. 2024.
APA
Burbano, R. R., Medeiros, A., Amorim, M. I. M. de, Lima, E. M., Mello, A., Barbieri Neto, J., & Casartelli, C. (2000). Cytogenetics of epithelial hyperplasias of the human breast. Cancer Genetics Cytogenetics, 119, 62-66. Recuperado de http://probe.usp.br/cgi-bin/sciserv.pl?collection=journals&journal=01654608&issue=v119i0001&article=62_coehothb&form=pdf&file=file.pdf
NLM
Burbano RR, Medeiros A, Amorim MIM de, Lima EM, Mello A, Barbieri Neto J, Casartelli C. Cytogenetics of epithelial hyperplasias of the human breast [Internet]. Cancer Genetics Cytogenetics. 2000 ; 119 62-66.[citado 2024 set. 28 ] Available from: http://probe.usp.br/cgi-bin/sciserv.pl?collection=journals&journal=01654608&issue=v119i0001&article=62_coehothb&form=pdf&file=file.pdf
Vancouver
Burbano RR, Medeiros A, Amorim MIM de, Lima EM, Mello A, Barbieri Neto J, Casartelli C. Cytogenetics of epithelial hyperplasias of the human breast [Internet]. Cancer Genetics Cytogenetics. 2000 ; 119 62-66.[citado 2024 set. 28 ] Available from: http://probe.usp.br/cgi-bin/sciserv.pl?collection=journals&journal=01654608&issue=v119i0001&article=62_coehothb&form=pdf&file=file.pdf
Artigo de periodico
Investigation of single-strand conformational polymorphism of the TP53 gene in women with a family history of breast cancer (2000)
Burbano, R. R.; Medeiros, A. C.; Mello, A. A.; Lemos, José Alexandre; Bahia, Marcelo de Oliveira; Casartelli, Cacilda
Source: Brazilian Journal of Medical and Biological Research. Unidade: FMRP
Subjects: GENÉTICA MÉDICA, ONCOLOGIA, MAMA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BURBANO, R. R. et al. Investigation of single-strand conformational polymorphism of the TP53 gene in women with a family history of breast cancer. Brazilian Journal of Medical and Biological Research, v. 33, n. 11, p. 1325-1328, 2000Tradução . . Disponível em: https://doi.org/10.1590/s0100-879x2000001100010. Acesso em: 28 set. 2024.
APA
Burbano, R. R., Medeiros, A. C., Mello, A. A., Lemos, J. A., Bahia, M. de O., & Casartelli, C. (2000). Investigation of single-strand conformational polymorphism of the TP53 gene in women with a family history of breast cancer. Brazilian Journal of Medical and Biological Research, 33( 11), 1325-1328. doi:10.1590/s0100-879x2000001100010
NLM
Burbano RR, Medeiros AC, Mello AA, Lemos JA, Bahia M de O, Casartelli C. Investigation of single-strand conformational polymorphism of the TP53 gene in women with a family history of breast cancer [Internet]. Brazilian Journal of Medical and Biological Research. 2000 ; 33( 11): 1325-1328.[citado 2024 set. 28 ] Available from: https://doi.org/10.1590/s0100-879x2000001100010
Vancouver
Burbano RR, Medeiros AC, Mello AA, Lemos JA, Bahia M de O, Casartelli C. Investigation of single-strand conformational polymorphism of the TP53 gene in women with a family history of breast cancer [Internet]. Brazilian Journal of Medical and Biological Research. 2000 ; 33( 11): 1325-1328.[citado 2024 set. 28 ] Available from: https://doi.org/10.1590/s0100-879x2000001100010

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