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Artigo de periodico
Functional polymorphisms in the promoter of the matrix metalloproteinase-9 (MMP-9) gene are not linked with significant plasma MMP-9 variations in healthy subjects (2008)
Demacq, Caroline; Vasconcellos, Vivian B.; Marcaccini, Andrea M.; Gerlach, Raquel Fernanda; Silva Júnior, Wilson Araújo da; Tanus-Santos, José Eduardo
Source: Clinical Chemistry and Laboratory Medicine. Unidades: FORP, FMRP
Subjects: POLIMORFISMO, METALOPROTEINASES
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ABNT
DEMACQ, Caroline et al. Functional polymorphisms in the promoter of the matrix metalloproteinase-9 (MMP-9) gene are not linked with significant plasma MMP-9 variations in healthy subjects. Clinical Chemistry and Laboratory Medicine, v. 46, n. 1, p. 57-63, 2008Tradução . . Disponível em: https://doi.org/10.1515/cclm.2008.014. Acesso em: 05 nov. 2024.
APA
Demacq, C., Vasconcellos, V. B., Marcaccini, A. M., Gerlach, R. F., Silva Júnior, W. A. da, & Tanus-Santos, J. E. (2008). Functional polymorphisms in the promoter of the matrix metalloproteinase-9 (MMP-9) gene are not linked with significant plasma MMP-9 variations in healthy subjects. Clinical Chemistry and Laboratory Medicine, 46( 1), 57-63. doi:10.1515/cclm.2008.014
NLM
Demacq C, Vasconcellos VB, Marcaccini AM, Gerlach RF, Silva Júnior WA da, Tanus-Santos JE. Functional polymorphisms in the promoter of the matrix metalloproteinase-9 (MMP-9) gene are not linked with significant plasma MMP-9 variations in healthy subjects [Internet]. Clinical Chemistry and Laboratory Medicine. 2008 ; 46( 1): 57-63.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1515/cclm.2008.014
Vancouver
Demacq C, Vasconcellos VB, Marcaccini AM, Gerlach RF, Silva Júnior WA da, Tanus-Santos JE. Functional polymorphisms in the promoter of the matrix metalloproteinase-9 (MMP-9) gene are not linked with significant plasma MMP-9 variations in healthy subjects [Internet]. Clinical Chemistry and Laboratory Medicine. 2008 ; 46( 1): 57-63.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1515/cclm.2008.014
Artigo de periodico
Prognostic factors and survival analysis in a sample of oral squamous cell carcinoma patients (2008)
Oliveira, Lucinei Roberto; Ribeiro-Silva, Alfredo; Costa, João Paulo Oliveira; Simões, Aguinaldo Luiz; Sala, Miguel Angel; Zucoloto, Sérgio
Source: Oral Surgery, Orla Medicine, Oral Pathology, Oral Radiology and Endodontics. Unidades: FMRP, FORP
Subjects: CARCINOMA, CÉLULAS
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ABNT
OLIVEIRA, Lucinei Roberto et al. Prognostic factors and survival analysis in a sample of oral squamous cell carcinoma patients. Oral Surgery, Orla Medicine, Oral Pathology, Oral Radiology and Endodontics, v. 106, n. 5, p. 685-695, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.tripleo.2008.07.002. Acesso em: 05 nov. 2024.
APA
Oliveira, L. R., Ribeiro-Silva, A., Costa, J. P. O., Simões, A. L., Sala, M. A., & Zucoloto, S. (2008). Prognostic factors and survival analysis in a sample of oral squamous cell carcinoma patients. Oral Surgery, Orla Medicine, Oral Pathology, Oral Radiology and Endodontics, 106( 5), 685-695. doi:10.1016/j.tripleo.2008.07.002
NLM
Oliveira LR, Ribeiro-Silva A, Costa JPO, Simões AL, Sala MA, Zucoloto S. Prognostic factors and survival analysis in a sample of oral squamous cell carcinoma patients [Internet]. Oral Surgery, Orla Medicine, Oral Pathology, Oral Radiology and Endodontics. 2008 ; 106( 5): 685-695.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1016/j.tripleo.2008.07.002
Vancouver
Oliveira LR, Ribeiro-Silva A, Costa JPO, Simões AL, Sala MA, Zucoloto S. Prognostic factors and survival analysis in a sample of oral squamous cell carcinoma patients [Internet]. Oral Surgery, Orla Medicine, Oral Pathology, Oral Radiology and Endodontics. 2008 ; 106( 5): 685-695.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1016/j.tripleo.2008.07.002
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: 05 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. 05 ] 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. 05 ] Available from: https://doi.org/10.1101/gr.2111304
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: 05 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. 05 ] 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. 05 ] Available from: https://doi.org/10.1034/j.1399-0004.2002.610511.x
Artigo de periodico
Distinct nonrandom patterns of chromosomal deletions in giant-cell lesions of bone (2002)
Baruffi, Marcelo Razera; Barbieri Neto, José; Pina Neto, João Monteiro de; Sverzut, Cassio Edvard; Casartelli, Cacilda
Source: Genetics and Molecular Biology. Unidades: FMRP, FORP
Subjects: GRANULOMA DE CÉLULAS GIGANTES, 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. Distinct nonrandom patterns of chromosomal deletions in giant-cell lesions of bone. Genetics and Molecular Biology, v. 25, n. 3, p. 265-270, 2002Tradução . . Disponível em: https://doi.org/10.1590/s1415-47572002000300002. Acesso em: 05 nov. 2024.
APA
Baruffi, M. R., Barbieri Neto, J., Pina Neto, J. M. de, Sverzut, C. E., & Casartelli, C. (2002). Distinct nonrandom patterns of chromosomal deletions in giant-cell lesions of bone. Genetics and Molecular Biology, 25( 3), 265-270. doi:10.1590/s1415-47572002000300002
NLM
Baruffi MR, Barbieri Neto J, Pina Neto JM de, Sverzut CE, Casartelli C. Distinct nonrandom patterns of chromosomal deletions in giant-cell lesions of bone [Internet]. Genetics and Molecular Biology. 2002 ; 25( 3): 265-270.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1590/s1415-47572002000300002
Vancouver
Baruffi MR, Barbieri Neto J, Pina Neto JM de, Sverzut CE, Casartelli C. Distinct nonrandom patterns of chromosomal deletions in giant-cell lesions of bone [Internet]. Genetics and Molecular Biology. 2002 ; 25( 3): 265-270.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1590/s1415-47572002000300002

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