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Artigo de periodico
The non-coding RNA BC1 is down-regulated in the hippocampus of wistar audiogenic rat (WAR) strain after audiogenic kindling (2011)
Gitaí, Daniel Leite Goes; Fachin, Ana Lucia; Mello, Stephano Spanó; Elias, Carol Fuzachi; Bittencourt, Jackson Cioni ; Leite, João Pereira; Passos, Geraldo Aleixo Silva; Garcia-Cairasco, Norberto; Paçó-Larson, Maria Luísa
Source: Brain Research. Unidades: ICB, FMRP, FORP
Subjects: EXPRESSÃO GÊNICA, EPILEPSIA
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ABNT
GITAÍ, Daniel Leite Goes et al. The non-coding RNA BC1 is down-regulated in the hippocampus of wistar audiogenic rat (WAR) strain after audiogenic kindling. Brain Research, v. 1367, p. 114-121, 2011Tradução . . Disponível em: https://doi.org/10.1016/j.brainres.2010.10.069. Acesso em: 06 nov. 2024.
APA
Gitaí, D. L. G., Fachin, A. L., Mello, S. S., Elias, C. F., Bittencourt, J. C., Leite, J. P., et al. (2011). The non-coding RNA BC1 is down-regulated in the hippocampus of wistar audiogenic rat (WAR) strain after audiogenic kindling. Brain Research, 1367, 114-121. doi:10.1016/j.brainres.2010.10.069
NLM
Gitaí DLG, Fachin AL, Mello SS, Elias CF, Bittencourt JC, Leite JP, Passos GAS, Garcia-Cairasco N, Paçó-Larson ML. The non-coding RNA BC1 is down-regulated in the hippocampus of wistar audiogenic rat (WAR) strain after audiogenic kindling [Internet]. Brain Research. 2011 ;1367 114-121.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1016/j.brainres.2010.10.069
Vancouver
Gitaí DLG, Fachin AL, Mello SS, Elias CF, Bittencourt JC, Leite JP, Passos GAS, Garcia-Cairasco N, Paçó-Larson ML. The non-coding RNA BC1 is down-regulated in the hippocampus of wistar audiogenic rat (WAR) strain after audiogenic kindling [Internet]. Brain Research. 2011 ;1367 114-121.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1016/j.brainres.2010.10.069
Artigo de periodico
The effect of TAK-778 on gene expression of osteoblastic cells is mediated through estrogen receptor (2009)
Bellesini, Larissa Sverzut; Beloti, Márcio Mateus; Crippa, Grasiele Edilaine; Prado, Karina Fittipaldi Bombonato; Junta, Cristina Moraes; Marques, Márcia Martins; Passos, Geraldo Aleixo Silva; Rosa, Adalberto Luiz
Source: Experimental Biology and Medicine. Unidades: FORP, FO
Subjects: EXPRESSÃO GÊNICA, CÉLULAS DO OSSO ALVEOLAR, OSTEOBLASTO
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ABNT
BELLESINI, Larissa Sverzut et al. The effect of TAK-778 on gene expression of osteoblastic cells is mediated through estrogen receptor. Experimental Biology and Medicine, v. 234, n. 2, p. 190-199, 2009Tradução . . Acesso em: 06 nov. 2024.
APA
Bellesini, L. S., Beloti, M. M., Crippa, G. E., Prado, K. F. B., Junta, C. M., Marques, M. M., et al. (2009). The effect of TAK-778 on gene expression of osteoblastic cells is mediated through estrogen receptor. Experimental Biology and Medicine, 234( 2), 190-199.
NLM
Bellesini LS, Beloti MM, Crippa GE, Prado KFB, Junta CM, Marques MM, Passos GAS, Rosa AL. The effect of TAK-778 on gene expression of osteoblastic cells is mediated through estrogen receptor. Experimental Biology and Medicine. 2009 ; 234( 2): 190-199.[citado 2024 nov. 06 ]
Vancouver
Bellesini LS, Beloti MM, Crippa GE, Prado KFB, Junta CM, Marques MM, Passos GAS, Rosa AL. The effect of TAK-778 on gene expression of osteoblastic cells is mediated through estrogen receptor. Experimental Biology and Medicine. 2009 ; 234( 2): 190-199.[citado 2024 nov. 06 ]
Artigo de periodico
Occurrence of TRGV-BJ hybrid gene in SV40-transformed fibroblast cell lines (2009)
D'Arce, L. P. G.; Bassi, C. L.; Fachin, A. L.; Passos, Geraldo Aleixo Silva; Sakamoto-Hojo, Elza Tiemi
Source: Genética. Unidades: FORP, FFCLRP
Subjects: RADIAÇÃO IONIZANTE, FIBROBLASTOS, DOENÇAS GENÉTICAS, DISCINESIAS
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ABNT
D'ARCE, L. P. G. et al. Occurrence of TRGV-BJ hybrid gene in SV40-transformed fibroblast cell lines. Genética, v. 136, n. 3, p. 471-478, 2009Tradução . . Disponível em: https://doi.org/10.1007/s10709-008-9348-5. Acesso em: 06 nov. 2024.
APA
D'Arce, L. P. G., Bassi, C. L., Fachin, A. L., Passos, G. A. S., & Sakamoto-Hojo, E. T. (2009). Occurrence of TRGV-BJ hybrid gene in SV40-transformed fibroblast cell lines. Genética, 136( 3), 471-478. doi:10.1007/s10709-008-9348-5
NLM
D'Arce LPG, Bassi CL, Fachin AL, Passos GAS, Sakamoto-Hojo ET. Occurrence of TRGV-BJ hybrid gene in SV40-transformed fibroblast cell lines [Internet]. Genética. 2009 ; 136( 3): 471-478.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1007/s10709-008-9348-5
Vancouver
D'Arce LPG, Bassi CL, Fachin AL, Passos GAS, Sakamoto-Hojo ET. Occurrence of TRGV-BJ hybrid gene in SV40-transformed fibroblast cell lines [Internet]. Genética. 2009 ; 136( 3): 471-478.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1007/s10709-008-9348-5
Artigo de periodico
A transcript finishing initiative for closing gaps in the human transcriptome (2004)
Bettoni, Fabiana; Carraro, Maria Dirce; Pires, Lilian Campos Pires; Parmigiani, Rafael B; Ferreira, Elisa N; Moreira, Eloísa de Sá; Latorre, Maria do Rosário Dias de Oliveira; Simpson, Andrew J. G; Camargo, Anamaria A; Cruz, Luciana Oliveira; Degaki, Theri Leica; Festa, Fernanda; Massirer, Katlin B; Sogayar, Mari Cleide ; Camargo Filho, Fernando; Camargo, Luiz Paulo; Cunha, Marco A. V; De Souza, Sandro J; Faria Júnior, Milton; Giuliatti, Silvana; Kopp, Leonardo; Oliveira, Paulo. S. L; Paiva, Paulo B; Pereira, Anderson A; Pinheiro, Daniel G; Puga, Renato D; Souza, Jorge Estefano S; Albuquerque, Dulcineia M; Andrade, Luís E. C; Baia, Gilson S; Cavaleiro-Luna, Ana M. S; Cerutti, Janete M; Costa, Fernando F; Costanzi-Strauss, Eugenia ; Espreafico, Enilza Maria; Ferrasi, Adriana C; Ferro, Emer Suavinho ; Fortes, Maria A. H. Z; Furchi, Joelma R. F; Gianella-Neto, Daniel; Goldman, Gustavo Henrique; Goldman, Maria Helena de Souza; Gruber, Arthur ; Guimarães, Gustavo S; Hackel, Christine; Henrique-Silva, Flávio; Kimura, Edna Teruko ; Leoni, Suzana G; Macedo, Cláudia; Malnic, Bettina ; Manzini B., Carina V; Marie, Suely Kazue Nagahashi; Martinez-Rossi, Nilce Maria; Menossi, Marcelo; Miracca, Elisabete C; Nagai, Maria Aparecida; Nobrega, Francisco Gorgonio da; Nobrega, Marina Pasetto; Oba-Shinjo, Sueli M; Oliveira, Márika K; Orabona, Guilherme M; Otsuka, Audrey Y; Paço-Larson, Maria Luiza; Paixão, Beatriz M. C; Pandolfi, José R. C; Pardini, Maria I. M. C; Passos-Bueno, Maria Rita ; Passos, Geraldo Aleixo Silva; Pesquero, João B; Pessoa, Juliana G; Rahal, Paula; Rainho, Cláudia A; Reis, Caroline P; Ricca, Tatiana I; Rodrigues, Vanderlei; Rogatto, Silvia R; Romano, Camila M; Romeiro, Janaína G; Rossi, Antonio; Sá, Renata G; Sales, Magaly M; Sant'Anna, Simone C; Santarosa, Patrícia L; Segato, Fernando; Silva Júnior, Wilson Araújo da; Silva, Ismael D. C. G; Silva, Neusa P; Soares-Costa, Andrea; Sonati, Maria F; Strauss, Brian E; Tajara, Eloiza H; Valentini, Sandro R; Villanova, Fabiola V; Ward, Laura S; Zanette, Dalila L
Source: Genome Research. Unidades: FSP, IQ, ICB, FMRP, FCFRP, FORP, FMVZ, FM, IB
Assunto: HISTOLOGIA
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ABNT
BETTONI, Fabiana et al. A transcript finishing initiative for closing gaps in the human transcriptome. Genome Research, v. 14, p. 1413-1423, 2004Tradução . . Disponível em: https://doi.org/10.1101/gr.2111304. Acesso em: 06 nov. 2024.
APA
Bettoni, F., Carraro, M. D., Pires, L. C. P., Parmigiani, R. B., Ferreira, E. N., Moreira, E. de S., et al. (2004). A transcript finishing initiative for closing gaps in the human transcriptome. Genome Research, 14, 1413-1423. doi:10.1101/gr.2111304
NLM
Bettoni F, Carraro MD, Pires LCP, Parmigiani RB, Ferreira EN, Moreira E de S, Latorre M do RD de O, Simpson AJG, Camargo AA, Cruz LO, Degaki TL, Festa F, Massirer KB, Sogayar MC, Camargo Filho F, Camargo LP, Cunha MAV, De Souza SJ, Faria Júnior M, Giuliatti S, Kopp L, Oliveira PSL, Paiva PB, Pereira AA, Pinheiro DG, Puga RD, Souza JES, Albuquerque DM, Andrade LEC, Baia GS, Cavaleiro-Luna AMS, Cerutti JM, Costa FF, Costanzi-Strauss E, Espreafico EM, Ferrasi AC, Ferro ES, Fortes MAHZ, Furchi JRF, Gianella-Neto D, Goldman GH, Goldman MH de S, Gruber A, Guimarães GS, Hackel C, Henrique-Silva F, Kimura ET, Leoni SG, Macedo C, Malnic B, Manzini B. CV, Marie SKN, Martinez-Rossi NM, Menossi M, Miracca EC, Nagai MA, Nobrega FG da, Nobrega MP, Oba-Shinjo SM, Oliveira MK, Orabona GM, Otsuka AY, Paço-Larson ML, Paixão BMC, Pandolfi JRC, Pardini MIMC, Passos-Bueno MR, Passos GAS, Pesquero JB, Pessoa JG, Rahal P, Rainho CA, Reis CP, Ricca TI, Rodrigues V, Rogatto SR, Romano CM, Romeiro JG, Rossi A, Sá RG, Sales MM, Sant'Anna SC, Santarosa PL, Segato F, Silva Júnior WA da, Silva IDCG, Silva NP, Soares-Costa A, Sonati MF, Strauss BE, Tajara EH, Valentini SR, Villanova FV, Ward LS, Zanette DL. A transcript finishing initiative for closing gaps in the human transcriptome [Internet]. Genome Research. 2004 ; 14 1413-1423.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1101/gr.2111304
Vancouver
Bettoni F, Carraro MD, Pires LCP, Parmigiani RB, Ferreira EN, Moreira E de S, Latorre M do RD de O, Simpson AJG, Camargo AA, Cruz LO, Degaki TL, Festa F, Massirer KB, Sogayar MC, Camargo Filho F, Camargo LP, Cunha MAV, De Souza SJ, Faria Júnior M, Giuliatti S, Kopp L, Oliveira PSL, Paiva PB, Pereira AA, Pinheiro DG, Puga RD, Souza JES, Albuquerque DM, Andrade LEC, Baia GS, Cavaleiro-Luna AMS, Cerutti JM, Costa FF, Costanzi-Strauss E, Espreafico EM, Ferrasi AC, Ferro ES, Fortes MAHZ, Furchi JRF, Gianella-Neto D, Goldman GH, Goldman MH de S, Gruber A, Guimarães GS, Hackel C, Henrique-Silva F, Kimura ET, Leoni SG, Macedo C, Malnic B, Manzini B. CV, Marie SKN, Martinez-Rossi NM, Menossi M, Miracca EC, Nagai MA, Nobrega FG da, Nobrega MP, Oba-Shinjo SM, Oliveira MK, Orabona GM, Otsuka AY, Paço-Larson ML, Paixão BMC, Pandolfi JRC, Pardini MIMC, Passos-Bueno MR, Passos GAS, Pesquero JB, Pessoa JG, Rahal P, Rainho CA, Reis CP, Ricca TI, Rodrigues V, Rogatto SR, Romano CM, Romeiro JG, Rossi A, Sá RG, Sales MM, Sant'Anna SC, Santarosa PL, Segato F, Silva Júnior WA da, Silva IDCG, Silva NP, Soares-Costa A, Sonati MF, Strauss BE, Tajara EH, Valentini SR, Villanova FV, Ward LS, Zanette DL. A transcript finishing initiative for closing gaps in the human transcriptome [Internet]. Genome Research. 2004 ; 14 1413-1423.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1101/gr.2111304
Artigo de periodico
Systemic lupus erythematosus patients under immunosuppressive treatment express high levels of the immunoglobulin lambda variable IGLV8S1 gene with silent somatic mutations (2002)
Tamia-Ferreira, Márcia Cristina; Trevisan, Glauce Lunardelli; Carvalho, Ivan Fiore de; Passos, Geraldo Aleixo Silva
Source: Biochimica et Biophysica Acta. Unidades: FMRP, FORP
Subjects: DOENÇAS IMUNOLÓGICAS, MUTAÇÃO GENÉTICA
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ABNT
TAMIA-FERREIRA, Márcia Cristina et al. Systemic lupus erythematosus patients under immunosuppressive treatment express high levels of the immunoglobulin lambda variable IGLV8S1 gene with silent somatic mutations. Biochimica et Biophysica Acta, v. 1586, p. 108-112, 2002Tradução . . Acesso em: 06 nov. 2024.
APA
Tamia-Ferreira, M. C., Trevisan, G. L., Carvalho, I. F. de, & Passos, G. A. S. (2002). Systemic lupus erythematosus patients under immunosuppressive treatment express high levels of the immunoglobulin lambda variable IGLV8S1 gene with silent somatic mutations. Biochimica et Biophysica Acta, 1586, 108-112.
NLM
Tamia-Ferreira MC, Trevisan GL, Carvalho IF de, Passos GAS. Systemic lupus erythematosus patients under immunosuppressive treatment express high levels of the immunoglobulin lambda variable IGLV8S1 gene with silent somatic mutations. Biochimica et Biophysica Acta. 2002 ; 1586 108-112.[citado 2024 nov. 06 ]
Vancouver
Tamia-Ferreira MC, Trevisan GL, Carvalho IF de, Passos GAS. Systemic lupus erythematosus patients under immunosuppressive treatment express high levels of the immunoglobulin lambda variable IGLV8S1 gene with silent somatic mutations. Biochimica et Biophysica Acta. 2002 ; 1586 108-112.[citado 2024 nov. 06 ]
Artigo de periodico
Chromosomal rearrangements involving telomeric DNA sequences in Balb/3T3 cells transfected with the Ha-ras oncogene (2002)
Peitl, Paulo; Mello, Sthephano S.; Camparoto, Marjori Leiva; Passos, Geraldo Aleixo Silva; Hande, Manoor P.; Cardoso, Renato S.; Sakamoto-Hojo, Elza Tiemi
Source: Mutagenesis. Unidades: FORP, FFCLRP
Subjects: DNA, ONCOGENES
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ABNT
PEITL, Paulo et al. Chromosomal rearrangements involving telomeric DNA sequences in Balb/3T3 cells transfected with the Ha-ras oncogene. Mutagenesis, v. 17, n. 1, p. 67-72, 2002Tradução . . Disponível em: https://doi.org/10.1093/mutage/17.1.67. Acesso em: 06 nov. 2024.
APA
Peitl, P., Mello, S. S., Camparoto, M. L., Passos, G. A. S., Hande, M. P., Cardoso, R. S., & Sakamoto-Hojo, E. T. (2002). Chromosomal rearrangements involving telomeric DNA sequences in Balb/3T3 cells transfected with the Ha-ras oncogene. Mutagenesis, 17( 1), 67-72. doi:10.1093/mutage/17.1.67
NLM
Peitl P, Mello SS, Camparoto ML, Passos GAS, Hande MP, Cardoso RS, Sakamoto-Hojo ET. Chromosomal rearrangements involving telomeric DNA sequences in Balb/3T3 cells transfected with the Ha-ras oncogene [Internet]. Mutagenesis. 2002 ; 17( 1): 67-72.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1093/mutage/17.1.67
Vancouver
Peitl P, Mello SS, Camparoto ML, Passos GAS, Hande MP, Cardoso RS, Sakamoto-Hojo ET. Chromosomal rearrangements involving telomeric DNA sequences in Balb/3T3 cells transfected with the Ha-ras oncogene [Internet]. Mutagenesis. 2002 ; 17( 1): 67-72.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1093/mutage/17.1.67
Artigo de periodico
Recurrent 22q11.2 deletion in a sibship suggestive of parental germline mosaicism in velocardiofacial syndrome (2002)
Sandrin Garcia, P; Macedo, C; Martelli, Lúcia Regina; Ramos, Ester Silveira; Guion Almeida, Maria Leine; Richieri Costa, Antônio; Passos, Geraldo Aleixo Silva
Source: Clinical genetics. Unidades: FMRP, HRAC, FORP
Subjects: GENÉTICA, DNA
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ABNT
SANDRIN GARCIA, P et al. Recurrent 22q11.2 deletion in a sibship suggestive of parental germline mosaicism in velocardiofacial syndrome. Clinical genetics, v. 61, n. 5, p. 380-383, 2002Tradução . . Disponível em: https://doi.org/10.1034/j.1399-0004.2002.610511.x. Acesso em: 06 nov. 2024.
APA
Sandrin Garcia, P., Macedo, C., Martelli, L. R., Ramos, E. S., Guion Almeida, M. L., Richieri Costa, A., & Passos, G. A. S. (2002). Recurrent 22q11.2 deletion in a sibship suggestive of parental germline mosaicism in velocardiofacial syndrome. Clinical genetics, 61( 5), 380-383. doi:10.1034/j.1399-0004.2002.610511.x
NLM
Sandrin Garcia P, Macedo C, Martelli LR, Ramos ES, Guion Almeida ML, Richieri Costa A, Passos GAS. Recurrent 22q11.2 deletion in a sibship suggestive of parental germline mosaicism in velocardiofacial syndrome [Internet]. Clinical genetics. 2002 ; 61( 5): 380-383.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1034/j.1399-0004.2002.610511.x
Vancouver
Sandrin Garcia P, Macedo C, Martelli LR, Ramos ES, Guion Almeida ML, Richieri Costa A, Passos GAS. Recurrent 22q11.2 deletion in a sibship suggestive of parental germline mosaicism in velocardiofacial syndrome [Internet]. Clinical genetics. 2002 ; 61( 5): 380-383.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1034/j.1399-0004.2002.610511.x
Artigo de periodico
Differential gene expression in 'gama'-irradiated BALB/3T3 fibroblast under the influence of 3-aminobenzamide, an inhibitior of parp enzyme (2002)
Cardoso, R. S.; Espanhol, Aline R.; Passos, Geraldo Aleixo Silva; Sakamoto-Hojo, Elza Tiemi
Source: Mutation Research: Fundamental and Molecular Mechanisms of Mutagenesis. Unidades: FORP, FFCLRP
Subjects: BIOLOGIA CELULAR, GENES
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ABNT
CARDOSO, R. S. et al. Differential gene expression in 'gama'-irradiated BALB/3T3 fibroblast under the influence of 3-aminobenzamide, an inhibitior of parp enzyme. Mutation Research: Fundamental and Molecular Mechanisms of Mutagenesis, v. 508, n. 1, p. 33-40, 2002Tradução . . Disponível em: https://doi.org/10.1016/s0027-5107(02)00141-0. Acesso em: 06 nov. 2024.
APA
Cardoso, R. S., Espanhol, A. R., Passos, G. A. S., & Sakamoto-Hojo, E. T. (2002). Differential gene expression in 'gama'-irradiated BALB/3T3 fibroblast under the influence of 3-aminobenzamide, an inhibitior of parp enzyme. Mutation Research: Fundamental and Molecular Mechanisms of Mutagenesis, 508( 1), 33-40. doi:10.1016/s0027-5107(02)00141-0
NLM
Cardoso RS, Espanhol AR, Passos GAS, Sakamoto-Hojo ET. Differential gene expression in 'gama'-irradiated BALB/3T3 fibroblast under the influence of 3-aminobenzamide, an inhibitior of parp enzyme [Internet]. Mutation Research: Fundamental and Molecular Mechanisms of Mutagenesis. 2002 ; 508( 1): 33-40.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1016/s0027-5107(02)00141-0
Vancouver
Cardoso RS, Espanhol AR, Passos GAS, Sakamoto-Hojo ET. Differential gene expression in 'gama'-irradiated BALB/3T3 fibroblast under the influence of 3-aminobenzamide, an inhibitior of parp enzyme [Internet]. Mutation Research: Fundamental and Molecular Mechanisms of Mutagenesis. 2002 ; 508( 1): 33-40.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1016/s0027-5107(02)00141-0
Artigo de periodico
The human immunoglobulin variable lambda locus IGLV9 gene is a monomorphic marker in the urban Brazilian population (1999)
Silva, Maria Isabel; Passos, Geraldo Aleixo Silva
Source: Immunology Letters. Unidade: FORP
Assunto: IMUNOGENÉTICA
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ABNT
SILVA, Maria Isabel e PASSOS, Geraldo Aleixo Silva. The human immunoglobulin variable lambda locus IGLV9 gene is a monomorphic marker in the urban Brazilian population. Immunology Letters, 1999Tradução . . Disponível em: https://doi.org/10.1016/s0165-2478(99)00109-1. Acesso em: 06 nov. 2024.
APA
Silva, M. I., & Passos, G. A. S. (1999). The human immunoglobulin variable lambda locus IGLV9 gene is a monomorphic marker in the urban Brazilian population. Immunology Letters. doi:10.1016/s0165-2478(99)00109-1
NLM
Silva MI, Passos GAS. The human immunoglobulin variable lambda locus IGLV9 gene is a monomorphic marker in the urban Brazilian population [Internet]. Immunology Letters. 1999 ;[citado 2024 nov. 06 ] Available from: https://doi.org/10.1016/s0165-2478(99)00109-1
Vancouver
Silva MI, Passos GAS. The human immunoglobulin variable lambda locus IGLV9 gene is a monomorphic marker in the urban Brazilian population [Internet]. Immunology Letters. 1999 ;[citado 2024 nov. 06 ] Available from: https://doi.org/10.1016/s0165-2478(99)00109-1

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