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Artigo de periodico
Autism spectrum disorder: signaling pathways and prospective therapeutic targets (2021)
Baranova, Juliana; Dragunas, Guilherme ; Botellho, Mayara C. S ; Ayub, Ana Luísa P ; Alves, Rebeca Bueno ; Alencar, Rebeca Rodrigues de ; Papaiz, Debora D; Sogayar, Mari Cleide ; Ulrich, Henning ; Correa, Ricardo G
Fonte: Cellular and Molecular Neurobiology. Unidades: IQ, ICB
Assunto: TRANSTORNO DO ESPECTRO AUTISTA
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ABNT
BARANOVA, Juliana et al. Autism spectrum disorder: signaling pathways and prospective therapeutic targets. Cellular and Molecular Neurobiology, v. 41, p. 619–649, 2021Tradução . . Disponível em: https://doi.org/10.1007/s10571-020-00882-7. Acesso em: 04 nov. 2025.
APA
Baranova, J., Dragunas, G., Botellho, M. C. S., Ayub, A. L. P., Alves, R. B., Alencar, R. R. de, et al. (2021). Autism spectrum disorder: signaling pathways and prospective therapeutic targets. Cellular and Molecular Neurobiology, 41, 619–649. doi:10.1007/s10571-020-00882-7
NLM
Baranova J, Dragunas G, Botellho MCS, Ayub ALP, Alves RB, Alencar RR de, Papaiz DD, Sogayar MC, Ulrich H, Correa RG. Autism spectrum disorder: signaling pathways and prospective therapeutic targets [Internet]. Cellular and Molecular Neurobiology. 2021 ; 41 619–649.[citado 2025 nov. 04 ] Available from: https://doi.org/10.1007/s10571-020-00882-7
Vancouver
Baranova J, Dragunas G, Botellho MCS, Ayub ALP, Alves RB, Alencar RR de, Papaiz DD, Sogayar MC, Ulrich H, Correa RG. Autism spectrum disorder: signaling pathways and prospective therapeutic targets [Internet]. Cellular and Molecular Neurobiology. 2021 ; 41 619–649.[citado 2025 nov. 04 ] Available from: https://doi.org/10.1007/s10571-020-00882-7
Artigo de periodico
Therapeutic potential of human induced pluripotent stem cells and renal progenitor cells in experimental chronic kidney disease (2020)
Ribeiro, Patrícia de Carvalho; Lojudice, Fernando Henrique ; Charpiot, Ida Maria Maximina Fernandes; Baptista, Maria Alice Sperto Ferreira ; Araujo, Stanley de Almeida; Mendes, Glória Elisa Florido; Sogayar, Mari Cleide ; Abbud Filho, Mario ; Caldas, Heloisa Cristina
Fonte: Stem Cell Research and Therapy. Unidade: IQ
Assuntos: CÉLULAS-TRONCO, IMUNOHISTOQUÍMICA, NEFROPATIAS
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RIBEIRO, Patrícia de Carvalho et al. Therapeutic potential of human induced pluripotent stem cells and renal progenitor cells in experimental chronic kidney disease. Stem Cell Research and Therapy, v. 11, p. 1-10 art. 530, 2020Tradução . . Disponível em: https://doi.org/10.1186/s13287-020-02060-4. Acesso em: 04 nov. 2025.
APA
Ribeiro, P. de C., Lojudice, F. H., Charpiot, I. M. M. F., Baptista, M. A. S. F., Araujo, S. de A., Mendes, G. E. F., et al. (2020). Therapeutic potential of human induced pluripotent stem cells and renal progenitor cells in experimental chronic kidney disease. Stem Cell Research and Therapy, 11, 1-10 art. 530. doi:10.1186/s13287-020-02060-4
NLM
Ribeiro P de C, Lojudice FH, Charpiot IMMF, Baptista MASF, Araujo S de A, Mendes GEF, Sogayar MC, Abbud Filho M, Caldas HC. Therapeutic potential of human induced pluripotent stem cells and renal progenitor cells in experimental chronic kidney disease [Internet]. Stem Cell Research and Therapy. 2020 ; 11 1-10 art. 530.[citado 2025 nov. 04 ] Available from: https://doi.org/10.1186/s13287-020-02060-4
Vancouver
Ribeiro P de C, Lojudice FH, Charpiot IMMF, Baptista MASF, Araujo S de A, Mendes GEF, Sogayar MC, Abbud Filho M, Caldas HC. Therapeutic potential of human induced pluripotent stem cells and renal progenitor cells in experimental chronic kidney disease [Internet]. Stem Cell Research and Therapy. 2020 ; 11 1-10 art. 530.[citado 2025 nov. 04 ] Available from: https://doi.org/10.1186/s13287-020-02060-4
Artigo de periodico
Fluorescence-based method is more accurate than counting-based methods for plotting growth curves of adherent cells (2020)
Pereira, Túlio Felipe; Levin, Gabriel ; DeOcesano-Pereira, Carlos ; Caodaglio, Amanda Schiersner ; Fujita, André ; Tonso, Aldo ; Sogayar, Mari Cleide
Fonte: BMC Research Notes. Unidades: IME, EP, IQ, Interunidades em Biotecnologia, FM
Assuntos: BIOINFORMÁTICA, PROLIFERAÇÃO CELULAR
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PEREIRA, Túlio Felipe et al. Fluorescence-based method is more accurate than counting-based methods for plotting growth curves of adherent cells. BMC Research Notes, v. 13, n. 1, p. 1-7, 2020Tradução . . Disponível em: https://doi.org/10.1186/s13104-020-4914-8. Acesso em: 04 nov. 2025.
APA
Pereira, T. F., Levin, G., DeOcesano-Pereira, C., Caodaglio, A. S., Fujita, A., Tonso, A., & Sogayar, M. C. (2020). Fluorescence-based method is more accurate than counting-based methods for plotting growth curves of adherent cells. BMC Research Notes, 13( 1), 1-7. doi:10.1186/s13104-020-4914-8
NLM
Pereira TF, Levin G, DeOcesano-Pereira C, Caodaglio AS, Fujita A, Tonso A, Sogayar MC. Fluorescence-based method is more accurate than counting-based methods for plotting growth curves of adherent cells [Internet]. BMC Research Notes. 2020 ;13( 1): 1-7.[citado 2025 nov. 04 ] Available from: https://doi.org/10.1186/s13104-020-4914-8
Vancouver
Pereira TF, Levin G, DeOcesano-Pereira C, Caodaglio AS, Fujita A, Tonso A, Sogayar MC. Fluorescence-based method is more accurate than counting-based methods for plotting growth curves of adherent cells [Internet]. BMC Research Notes. 2020 ;13( 1): 1-7.[citado 2025 nov. 04 ] Available from: https://doi.org/10.1186/s13104-020-4914-8
Artigo de periodico
R-Spondin 1 (RSPO1) increases mouse intestinal organoid unit size and survival in vitro and improves tissue-engineered small intestine formation in vivo (2020)
Levin, Gabriel ; Zuber, Samuel M; Squillaro, Anthony I; Sogayar, Mari Cleide ; Grikscheit, Tracy C; Carreira, Ana Claudia Oliveira
Fonte: Frontiers in Bioengineering and Biotechnology. Unidades: IQ, FM
Assuntos: ORGANELAS CELULARES, ENGENHARIA TECIDUAL, ORGANELAS CELULARES, INTESTINO DELGADO
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LEVIN, Gabriel et al. R-Spondin 1 (RSPO1) increases mouse intestinal organoid unit size and survival in vitro and improves tissue-engineered small intestine formation in vivo. Frontiers in Bioengineering and Biotechnology, v. 8, p. 1-13 art. 476, 2020Tradução . . Disponível em: https://doi.org/10.3389/fbioe.2020.00476. Acesso em: 04 nov. 2025.
APA
Levin, G., Zuber, S. M., Squillaro, A. I., Sogayar, M. C., Grikscheit, T. C., & Carreira, A. C. O. (2020). R-Spondin 1 (RSPO1) increases mouse intestinal organoid unit size and survival in vitro and improves tissue-engineered small intestine formation in vivo. Frontiers in Bioengineering and Biotechnology, 8, 1-13 art. 476. doi:10.3389/fbioe.2020.00476
NLM
Levin G, Zuber SM, Squillaro AI, Sogayar MC, Grikscheit TC, Carreira ACO. R-Spondin 1 (RSPO1) increases mouse intestinal organoid unit size and survival in vitro and improves tissue-engineered small intestine formation in vivo [Internet]. Frontiers in Bioengineering and Biotechnology. 2020 ; 8 1-13 art. 476.[citado 2025 nov. 04 ] Available from: https://doi.org/10.3389/fbioe.2020.00476
Vancouver
Levin G, Zuber SM, Squillaro AI, Sogayar MC, Grikscheit TC, Carreira ACO. R-Spondin 1 (RSPO1) increases mouse intestinal organoid unit size and survival in vitro and improves tissue-engineered small intestine formation in vivo [Internet]. Frontiers in Bioengineering and Biotechnology. 2020 ; 8 1-13 art. 476.[citado 2025 nov. 04 ] Available from: https://doi.org/10.3389/fbioe.2020.00476
Artigo de periodico
Production, purification and characterization of recombinant human R-spondin1 (RSPO1) protein stably expressed in human HEK293 cells (2020)
Levin, Gabriel ; Koga, Bruna Andrade Aguiar; Belchior, Gustavo Gross; Carreira, Ana Claudia Oliveira ; Sogayar, Mari Cleide
Fonte: BMC Biotechnology. Unidades: IQ, Interunidades em Biotecnologia
Assuntos: PROLIFERAÇÃO CELULAR, CÉLULAS, PROTEÍNAS RECOMBINANTES
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LEVIN, Gabriel et al. Production, purification and characterization of recombinant human R-spondin1 (RSPO1) protein stably expressed in human HEK293 cells. BMC Biotechnology, v. 20, n. 5, p. 1-14 , 2020Tradução . . Disponível em: https://doi.org/10.1186/s12896-020-0600-0. Acesso em: 04 nov. 2025.
APA
Levin, G., Koga, B. A. A., Belchior, G. G., Carreira, A. C. O., & Sogayar, M. C. (2020). Production, purification and characterization of recombinant human R-spondin1 (RSPO1) protein stably expressed in human HEK293 cells. BMC Biotechnology, 20( 5), 1-14 . doi:10.1186/s12896-020-0600-0
NLM
Levin G, Koga BAA, Belchior GG, Carreira ACO, Sogayar MC. Production, purification and characterization of recombinant human R-spondin1 (RSPO1) protein stably expressed in human HEK293 cells [Internet]. BMC Biotechnology. 2020 ; 20( 5): 1-14 .[citado 2025 nov. 04 ] Available from: https://doi.org/10.1186/s12896-020-0600-0
Vancouver
Levin G, Koga BAA, Belchior GG, Carreira ACO, Sogayar MC. Production, purification and characterization of recombinant human R-spondin1 (RSPO1) protein stably expressed in human HEK293 cells [Internet]. BMC Biotechnology. 2020 ; 20( 5): 1-14 .[citado 2025 nov. 04 ] Available from: https://doi.org/10.1186/s12896-020-0600-0
Artigo de periodico
CHD7 promotes glioblastoma cell motility and invasiveness through transcriptional modulation of an invasion signature (2019)
Machado, Raquel Arminda Carvalho ; Schneider, Hannah; DeOcesano-Pereira, Carlos ; Lichtenstein, Flávio ; Andrade, Fernando; Fujita, André ; Lima, Marina Trombetta ; Weller, Michael; Bowman-Colin, Christian ; Sogayar, Mari Cleide
Fonte: Scientific Reports. Unidades: IME, IQ, FM
Assunto: BIOINFORMÁTICA
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MACHADO, Raquel Arminda Carvalho et al. CHD7 promotes glioblastoma cell motility and invasiveness through transcriptional modulation of an invasion signature. Scientific Reports, v. 9, p. 1-13 art. 3952, 2019Tradução . . Disponível em: https://doi.org/10.1038/s41598-019-39564-w. Acesso em: 04 nov. 2025.
APA
Machado, R. A. C., Schneider, H., DeOcesano-Pereira, C., Lichtenstein, F., Andrade, F., Fujita, A., et al. (2019). CHD7 promotes glioblastoma cell motility and invasiveness through transcriptional modulation of an invasion signature. Scientific Reports, 9, 1-13 art. 3952. doi:10.1038/s41598-019-39564-w
NLM
Machado RAC, Schneider H, DeOcesano-Pereira C, Lichtenstein F, Andrade F, Fujita A, Lima MT, Weller M, Bowman-Colin C, Sogayar MC. CHD7 promotes glioblastoma cell motility and invasiveness through transcriptional modulation of an invasion signature [Internet]. Scientific Reports. 2019 ; 9 1-13 art. 3952.[citado 2025 nov. 04 ] Available from: https://doi.org/10.1038/s41598-019-39564-w
Vancouver
Machado RAC, Schneider H, DeOcesano-Pereira C, Lichtenstein F, Andrade F, Fujita A, Lima MT, Weller M, Bowman-Colin C, Sogayar MC. CHD7 promotes glioblastoma cell motility and invasiveness through transcriptional modulation of an invasion signature [Internet]. Scientific Reports. 2019 ; 9 1-13 art. 3952.[citado 2025 nov. 04 ] Available from: https://doi.org/10.1038/s41598-019-39564-w
Artigo de periodico
NOD-like receptors: major players (and targets) in the interface between innate immunity and cancer (2019)
Velloso, Fernando Janczur; Trombetta-Lima, Marina; Anschau, Valesca; Sogayar, Mari Cleide ; Correa, Ricardo Garcia
Fonte: Bioscience Reports. Unidade: IQ
Assuntos: NEOPLASIAS, SISTEMA IMUNE, RECEPTORES
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VELLOSO, Fernando Janczur et al. NOD-like receptors: major players (and targets) in the interface between innate immunity and cancer. Bioscience Reports, v. 39, n. 4, p. 1-21 art. BSR20181709, 2019Tradução . . Disponível em: https://doi.org/10.1042/BSR20181709. Acesso em: 04 nov. 2025.
APA
Velloso, F. J., Trombetta-Lima, M., Anschau, V., Sogayar, M. C., & Correa, R. G. (2019). NOD-like receptors: major players (and targets) in the interface between innate immunity and cancer. Bioscience Reports, 39( 4), 1-21 art. BSR20181709. doi:10.1042/BSR20181709
NLM
Velloso FJ, Trombetta-Lima M, Anschau V, Sogayar MC, Correa RG. NOD-like receptors: major players (and targets) in the interface between innate immunity and cancer [Internet]. Bioscience Reports. 2019 ; 39( 4): 1-21 art. BSR20181709.[citado 2025 nov. 04 ] Available from: https://doi.org/10.1042/BSR20181709
Vancouver
Velloso FJ, Trombetta-Lima M, Anschau V, Sogayar MC, Correa RG. NOD-like receptors: major players (and targets) in the interface between innate immunity and cancer [Internet]. Bioscience Reports. 2019 ; 39( 4): 1-21 art. BSR20181709.[citado 2025 nov. 04 ] Available from: https://doi.org/10.1042/BSR20181709
Artigo de periodico
Where do we aspire to publish? A position paper on scientific communication in biochemistry and molecular biology (2019)
Baptista, Mauricio da Silva ; Alves, Maria Júlia Manso ; Arantes, Guilherme Menegon ; Armelin, Hugo Aguirre ; Augusto, Ohara ; Baldini, Regina Lúcia ; Bassères, Daniela Sanchez ; Bechara, Etelvino José Henriques ; Bruni-Cardoso, Alexandre ; Chaimovich Guralnik, Hernan ; Colepicolo, Pio ; Colli, Walter ; Cuccovia, Iolanda Midea ; Da Silva, Aline Maria ; Di Mascio, Paolo ; Farah, Chuck Shaker ; Ferreira, Clélia ; Forti, Fábio Luís ; Giordano, Ricardo José ; Gomes, Suely Lopes ; Gueiros Filho, Frederico José ; Hoch, Nicolas Carlos ; Hotta, Carlos Takeshi ; Labriola, Leticia ; Lameu, Claudiana ; Machini, Maria Teresa ; Malnic, Bettina ; Marana, Sandro Roberto ; Medeiros, Marisa Helena Gennari de ; Meotti, Flávia Carla ; Miyamoto, Sayuri ; Oliveira, Carla Columbano de ; Souza-Pinto, Nadja Cristhina de ; Reis, Eduardo Moraes ; Ronsein, Graziella Eliza ; Salinas, Roberto Kopke ; Schechtman, Deborah ; Schreier, Shirley ; Setubal, João Carlos ; Sogayar, Mari Cleide ; Souza, Gláucia Mendes ; Terra, Walter Ribeiro ; Truzzi, Daniela Ramos ; Ulrich, Henning ; Verjovski-Almeida, Sergio ; Winck, Flavia Vischi ; Zingales, Bianca ; Kowaltowski, Alicia Juliana
Fonte: Brazilian Journal of Medical and Biological Research. Unidade: IQ
Assuntos: PERIÓDICOS CIENTÍFICOS, PRÉ-IMPRESSOS
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BAPTISTA, Mauricio da Silva et al. Where do we aspire to publish? A position paper on scientific communication in biochemistry and molecular biology. Brazilian Journal of Medical and Biological Research, v. 52, n. 9, p. 1-5 art. e8935, 2019Tradução . . Disponível em: https://doi.org/10.1590/1414-431x20198935. Acesso em: 04 nov. 2025.
APA
Baptista, M. da S., Alves, M. J. M., Arantes, G. M., Armelin, H. A., Augusto, O., Baldini, R. L., et al. (2019). Where do we aspire to publish? A position paper on scientific communication in biochemistry and molecular biology. Brazilian Journal of Medical and Biological Research, 52( 9), 1-5 art. e8935. doi:10.1590/1414-431x20198935
NLM
Baptista M da S, Alves MJM, Arantes GM, Armelin HA, Augusto O, Baldini RL, Bassères DS, Bechara EJH, Bruni-Cardoso A, Chaimovich Guralnik H, Colepicolo P, Colli W, Cuccovia IM, Da Silva AM, Di Mascio P, Farah CS, Ferreira C, Forti FL, Giordano RJ, Gomes SL, Gueiros Filho FJ, Hoch NC, Hotta CT, Labriola L, Lameu C, Machini MT, Malnic B, Marana SR, Medeiros MHG de, Meotti FC, Miyamoto S, Oliveira CC de, Souza-Pinto NC de, Reis EM, Ronsein GE, Salinas RK, Schechtman D, Schreier S, Setubal JC, Sogayar MC, Souza GM, Terra WR, Truzzi DR, Ulrich H, Verjovski-Almeida S, Winck FV, Zingales B, Kowaltowski AJ. Where do we aspire to publish? A position paper on scientific communication in biochemistry and molecular biology [Internet]. Brazilian Journal of Medical and Biological Research. 2019 ; 52( 9): 1-5 art. e8935.[citado 2025 nov. 04 ] Available from: https://doi.org/10.1590/1414-431x20198935
Vancouver
Baptista M da S, Alves MJM, Arantes GM, Armelin HA, Augusto O, Baldini RL, Bassères DS, Bechara EJH, Bruni-Cardoso A, Chaimovich Guralnik H, Colepicolo P, Colli W, Cuccovia IM, Da Silva AM, Di Mascio P, Farah CS, Ferreira C, Forti FL, Giordano RJ, Gomes SL, Gueiros Filho FJ, Hoch NC, Hotta CT, Labriola L, Lameu C, Machini MT, Malnic B, Marana SR, Medeiros MHG de, Meotti FC, Miyamoto S, Oliveira CC de, Souza-Pinto NC de, Reis EM, Ronsein GE, Salinas RK, Schechtman D, Schreier S, Setubal JC, Sogayar MC, Souza GM, Terra WR, Truzzi DR, Ulrich H, Verjovski-Almeida S, Winck FV, Zingales B, Kowaltowski AJ. Where do we aspire to publish? A position paper on scientific communication in biochemistry and molecular biology [Internet]. Brazilian Journal of Medical and Biological Research. 2019 ; 52( 9): 1-5 art. e8935.[citado 2025 nov. 04 ] Available from: https://doi.org/10.1590/1414-431x20198935
Artigo de periodico
Proteome profiling of triple negative breast cancer cells overexpressing NOD1 and NOD2 receptors unveils molecular signatures of malignant cell proliferation (2019)
Velloso, Fernando Janczur; Campos, Alexandre R; Sogayar, Mari Cleide ; Correa, Ricardo Garcia
Fonte: BMC Genomics. Unidade: IQ
Assuntos: PROTEÔMICA, NEOPLASIAS MAMÁRIAS
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VELLOSO, Fernando Janczur et al. Proteome profiling of triple negative breast cancer cells overexpressing NOD1 and NOD2 receptors unveils molecular signatures of malignant cell proliferation. BMC Genomics, v. 20, n. 1, p. 1-20 art. 152, 2019Tradução . . Disponível em: https://doi.org/10.1186/s12864-019-5523-6. Acesso em: 04 nov. 2025.
APA
Velloso, F. J., Campos, A. R., Sogayar, M. C., & Correa, R. G. (2019). Proteome profiling of triple negative breast cancer cells overexpressing NOD1 and NOD2 receptors unveils molecular signatures of malignant cell proliferation. BMC Genomics, 20( 1), 1-20 art. 152. doi:10.1186/s12864-019-5523-6
NLM
Velloso FJ, Campos AR, Sogayar MC, Correa RG. Proteome profiling of triple negative breast cancer cells overexpressing NOD1 and NOD2 receptors unveils molecular signatures of malignant cell proliferation [Internet]. BMC Genomics. 2019 ; 20( 1): 1-20 art. 152.[citado 2025 nov. 04 ] Available from: https://doi.org/10.1186/s12864-019-5523-6
Vancouver
Velloso FJ, Campos AR, Sogayar MC, Correa RG. Proteome profiling of triple negative breast cancer cells overexpressing NOD1 and NOD2 receptors unveils molecular signatures of malignant cell proliferation [Internet]. BMC Genomics. 2019 ; 20( 1): 1-20 art. 152.[citado 2025 nov. 04 ] Available from: https://doi.org/10.1186/s12864-019-5523-6
Artigo de periodico
High CD90 (THY-1) expression positively correlates with cell transformation and worse prognosis in basal-like breast cancer tumors (2018)
Lobba, Aline Ramos Maia ; Carreira, Ana Claudia Oliveira ; Cerqueira, Otto Luiz Dutra; Fujita, André ; DeOcesano-Pereira, Carlos ; Osorio, Cynthia Aparecida Bueno ; Soares, Fernando Augusto ; Rameshwar, Pranela ; Sogayar, Mari Cleide
Fonte: PLOS ONE. Unidades: IME, FO, IQ, FM
Assuntos: BIOINFORMÁTICA, NEOPLASIAS
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ABNT
LOBBA, Aline Ramos Maia et al. High CD90 (THY-1) expression positively correlates with cell transformation and worse prognosis in basal-like breast cancer tumors. PLOS ONE, v. 13, n. 6, p. 1-21, 2018Tradução . . Disponível em: https://doi.org/10.1371/journal.pone.0199254. Acesso em: 04 nov. 2025.
APA
Lobba, A. R. M., Carreira, A. C. O., Cerqueira, O. L. D., Fujita, A., DeOcesano-Pereira, C., Osorio, C. A. B., et al. (2018). High CD90 (THY-1) expression positively correlates with cell transformation and worse prognosis in basal-like breast cancer tumors. PLOS ONE, 13( 6), 1-21. doi:10.1371/journal.pone.0199254
NLM
Lobba ARM, Carreira ACO, Cerqueira OLD, Fujita A, DeOcesano-Pereira C, Osorio CAB, Soares FA, Rameshwar P, Sogayar MC. High CD90 (THY-1) expression positively correlates with cell transformation and worse prognosis in basal-like breast cancer tumors [Internet]. PLOS ONE. 2018 ; 13( 6): 1-21.[citado 2025 nov. 04 ] Available from: https://doi.org/10.1371/journal.pone.0199254
Vancouver
Lobba ARM, Carreira ACO, Cerqueira OLD, Fujita A, DeOcesano-Pereira C, Osorio CAB, Soares FA, Rameshwar P, Sogayar MC. High CD90 (THY-1) expression positively correlates with cell transformation and worse prognosis in basal-like breast cancer tumors [Internet]. PLOS ONE. 2018 ; 13( 6): 1-21.[citado 2025 nov. 04 ] Available from: https://doi.org/10.1371/journal.pone.0199254
Artigo de periodico
RECK is not an independent prognostic marker for breast cancer (2015)
Gomes, Luciana Rodrigues; Fujita, André ; Mott, Joni D ; Soares, Fernando Augusto ; Labriola, Leticia ; Sogayar, Mari Cleide
Fonte: BMC Cancer. Unidades: IME, FO, IQ
Assuntos: IMUNOHISTOQUÍMICA, NEOPLASIAS MAMÁRIAS
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ABNT
GOMES, Luciana Rodrigues et al. RECK is not an independent prognostic marker for breast cancer. BMC Cancer, v. 15, p. 1-11 art. 660, 2015Tradução . . Disponível em: https://doi.org/10.1186/s12885-015-1666-2. Acesso em: 04 nov. 2025.
APA
Gomes, L. R., Fujita, A., Mott, J. D., Soares, F. A., Labriola, L., & Sogayar, M. C. (2015). RECK is not an independent prognostic marker for breast cancer. BMC Cancer, 15, 1-11 art. 660. doi:10.1186/s12885-015-1666-2
NLM
Gomes LR, Fujita A, Mott JD, Soares FA, Labriola L, Sogayar MC. RECK is not an independent prognostic marker for breast cancer [Internet]. BMC Cancer. 2015 ; 15 1-11 art. 660.[citado 2025 nov. 04 ] Available from: https://doi.org/10.1186/s12885-015-1666-2
Vancouver
Gomes LR, Fujita A, Mott JD, Soares FA, Labriola L, Sogayar MC. RECK is not an independent prognostic marker for breast cancer [Internet]. BMC Cancer. 2015 ; 15 1-11 art. 660.[citado 2025 nov. 04 ] Available from: https://doi.org/10.1186/s12885-015-1666-2
Artigo de periodico
A quantitative and humane tail bleeding assay for efficacy evaluation of antihaemophilic factors in haemophilia A mice (2014)
Molina, Erika de Simone ; Fujita, André ; Sogayar, Mari Cleide ; Demasi, Marcos Angelo Almeida
Fonte: Haemophilia. Unidades: IME, IQ, Interunidades em Biotecnologia
Assuntos: BIOINFORMÁTICA, HEMOFILIA
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ABNT
MOLINA, Erika de Simone et al. A quantitative and humane tail bleeding assay for efficacy evaluation of antihaemophilic factors in haemophilia A mice. Haemophilia, v. 20, p. e392-e398, 2014Tradução . . Disponível em: https://doi.org/10.1111/hae.12484. Acesso em: 04 nov. 2025.
APA
Molina, E. de S., Fujita, A., Sogayar, M. C., & Demasi, M. A. A. (2014). A quantitative and humane tail bleeding assay for efficacy evaluation of antihaemophilic factors in haemophilia A mice. Haemophilia, 20, e392-e398. doi:10.1111/hae.12484
NLM
Molina E de S, Fujita A, Sogayar MC, Demasi MAA. A quantitative and humane tail bleeding assay for efficacy evaluation of antihaemophilic factors in haemophilia A mice [Internet]. Haemophilia. 2014 ; 20 e392-e398.[citado 2025 nov. 04 ] Available from: https://doi.org/10.1111/hae.12484
Vancouver
Molina E de S, Fujita A, Sogayar MC, Demasi MAA. A quantitative and humane tail bleeding assay for efficacy evaluation of antihaemophilic factors in haemophilia A mice [Internet]. Haemophilia. 2014 ; 20 e392-e398.[citado 2025 nov. 04 ] Available from: https://doi.org/10.1111/hae.12484
Artigo de periodico
New insights in osteogenic differentiation revealed by mass spectrometric assessment of phosphorylated substrates in murine skin mesenchymal cells (2013)
Halcsik, Erik; Forni, Maria Fernanda ; Fujita, André ; Verano-Braga, Thiago ; Jensen, Ole Norregaard ; Sogayar, Mari Cleide
Fonte: BMC Cell Biology. Unidades: IME, IQ
Assunto: BIOLOGIA CELULAR
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ABNT
HALCSIK, Erik et al. New insights in osteogenic differentiation revealed by mass spectrometric assessment of phosphorylated substrates in murine skin mesenchymal cells. BMC Cell Biology, v. 14, p. 1-19, 2013Tradução . . Disponível em: https://doi.org/10.1186/1471-2121-14-47. Acesso em: 04 nov. 2025.
APA
Halcsik, E., Forni, M. F., Fujita, A., Verano-Braga, T., Jensen, O. N., & Sogayar, M. C. (2013). New insights in osteogenic differentiation revealed by mass spectrometric assessment of phosphorylated substrates in murine skin mesenchymal cells. BMC Cell Biology, 14, 1-19. doi:10.1186/1471-2121-14-47
NLM
Halcsik E, Forni MF, Fujita A, Verano-Braga T, Jensen ON, Sogayar MC. New insights in osteogenic differentiation revealed by mass spectrometric assessment of phosphorylated substrates in murine skin mesenchymal cells [Internet]. BMC Cell Biology. 2013 ; 14 1-19.[citado 2025 nov. 04 ] Available from: https://doi.org/10.1186/1471-2121-14-47
Vancouver
Halcsik E, Forni MF, Fujita A, Verano-Braga T, Jensen ON, Sogayar MC. New insights in osteogenic differentiation revealed by mass spectrometric assessment of phosphorylated substrates in murine skin mesenchymal cells [Internet]. BMC Cell Biology. 2013 ; 14 1-19.[citado 2025 nov. 04 ] Available from: https://doi.org/10.1186/1471-2121-14-47
Artigo de periodico
Unveiling novel genes upregulated by both rhBMP2 and rhBMP7 during early osteoblastic transdifferentiation of C2C12 cells (2011)
Bustus-Valenzuela, Juan C.; Fujita, André ; Halcsik, Erik; Granjeiro, José Mauro ; Sogayar, Mari Cleide
Fonte: BMC Research Notes. Unidades: IME, IQ
Assunto: BIOQUÍMICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BUSTUS-VALENZUELA, Juan C. et al. Unveiling novel genes upregulated by both rhBMP2 and rhBMP7 during early osteoblastic transdifferentiation of C2C12 cells. BMC Research Notes, v. 4, p. 1-15, 2011Tradução . . Disponível em: https://doi.org/10.1186/1756-0500-4-370. Acesso em: 04 nov. 2025.
APA
Bustus-Valenzuela, J. C., Fujita, A., Halcsik, E., Granjeiro, J. M., & Sogayar, M. C. (2011). Unveiling novel genes upregulated by both rhBMP2 and rhBMP7 during early osteoblastic transdifferentiation of C2C12 cells. BMC Research Notes, 4, 1-15. doi:10.1186/1756-0500-4-370
NLM
Bustus-Valenzuela JC, Fujita A, Halcsik E, Granjeiro JM, Sogayar MC. Unveiling novel genes upregulated by both rhBMP2 and rhBMP7 during early osteoblastic transdifferentiation of C2C12 cells [Internet]. BMC Research Notes. 2011 ; 4 1-15.[citado 2025 nov. 04 ] Available from: https://doi.org/10.1186/1756-0500-4-370
Vancouver
Bustus-Valenzuela JC, Fujita A, Halcsik E, Granjeiro JM, Sogayar MC. Unveiling novel genes upregulated by both rhBMP2 and rhBMP7 during early osteoblastic transdifferentiation of C2C12 cells [Internet]. BMC Research Notes. 2011 ; 4 1-15.[citado 2025 nov. 04 ] Available from: https://doi.org/10.1186/1756-0500-4-370
Artigo de periodico
GEDI: a user-friendly toolbox for analysis of large-scale gene expression data (2007)
Fujita, André ; Sato, João Ricardo; Ferreira, Carlos Eduardo ; Sogayar, Mari Cleide
Fonte: BMC Bioinformatics. Unidades: IME, IQ, Interunidades em Bioinformática
Assuntos: EXPRESSÃO GÊNICA, BIOQUÍMICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FUJITA, André et al. GEDI: a user-friendly toolbox for analysis of large-scale gene expression data. BMC Bioinformatics, v. 8, n. art. 457, p. 1-7, 2007Tradução . . Disponível em: https://doi.org/10.1186/1471-2105-8-457. Acesso em: 04 nov. 2025.
APA
Fujita, A., Sato, J. R., Ferreira, C. E., & Sogayar, M. C. (2007). GEDI: a user-friendly toolbox for analysis of large-scale gene expression data. BMC Bioinformatics, 8( art. 457), 1-7. doi:10.1186/1471-2105-8-457
NLM
Fujita A, Sato JR, Ferreira CE, Sogayar MC. GEDI: a user-friendly toolbox for analysis of large-scale gene expression data [Internet]. BMC Bioinformatics. 2007 ; 8( art. 457): 1-7.[citado 2025 nov. 04 ] Available from: https://doi.org/10.1186/1471-2105-8-457
Vancouver
Fujita A, Sato JR, Ferreira CE, Sogayar MC. GEDI: a user-friendly toolbox for analysis of large-scale gene expression data [Internet]. BMC Bioinformatics. 2007 ; 8( art. 457): 1-7.[citado 2025 nov. 04 ] Available from: https://doi.org/10.1186/1471-2105-8-457
Artigo de periodico
Modeling gene expression regulatory networks with the sparse vector autoregressive model (2007)
Fujita, André ; Sato, João Ricardo; Garay-Malpartida, Humberto Miguel; Yamaguchi, Rui; Miyano, Satoru; Sogayar, Mari Cleide ; Ferreira, Carlos Eduardo
Fonte: BMC Systems Biology. Unidades: IQ, IME, Interunidades em Bioinformática
Assuntos: EXPRESSÃO GÊNICA, BIOQUÍMICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FUJITA, André et al. Modeling gene expression regulatory networks with the sparse vector autoregressive model. BMC Systems Biology, v. 1, n. 39, p. 1-11, 2007Tradução . . Disponível em: https://doi.org/10.1186/1752-0509-1-39. Acesso em: 04 nov. 2025.
APA
Fujita, A., Sato, J. R., Garay-Malpartida, H. M., Yamaguchi, R., Miyano, S., Sogayar, M. C., & Ferreira, C. E. (2007). Modeling gene expression regulatory networks with the sparse vector autoregressive model. BMC Systems Biology, 1( 39), 1-11. doi:10.1186/1752-0509-1-39
NLM
Fujita A, Sato JR, Garay-Malpartida HM, Yamaguchi R, Miyano S, Sogayar MC, Ferreira CE. Modeling gene expression regulatory networks with the sparse vector autoregressive model [Internet]. BMC Systems Biology. 2007 ; 1( 39): 1-11.[citado 2025 nov. 04 ] Available from: https://doi.org/10.1186/1752-0509-1-39
Vancouver
Fujita A, Sato JR, Garay-Malpartida HM, Yamaguchi R, Miyano S, Sogayar MC, Ferreira CE. Modeling gene expression regulatory networks with the sparse vector autoregressive model [Internet]. BMC Systems Biology. 2007 ; 1( 39): 1-11.[citado 2025 nov. 04 ] Available from: https://doi.org/10.1186/1752-0509-1-39
Artigo de periodico
Time-varying modeling of gene expression regulatory networks using the wavelet dynamic vector autoregressive method (2007)
Fujita, André ; Sato, João Ricardo ; Garay-Malpartida, Humberto Miguel ; Morettin, Pedro Alberto ; Sogayar, Mari Cleide ; Ferreira, Carlos Eduardo
Fonte: Bioinformatics. Unidades: IME, IQ, Interunidades em Bioinformática
Assuntos: EXPRESSÃO GÊNICA, BIOQUÍMICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FUJITA, André et al. Time-varying modeling of gene expression regulatory networks using the wavelet dynamic vector autoregressive method. Bioinformatics, v. 23, n. 13, p. 1623-1630, 2007Tradução . . Disponível em: https://doi.org/10.1093/bioinformatics/btm151. Acesso em: 04 nov. 2025.
APA
Fujita, A., Sato, J. R., Garay-Malpartida, H. M., Morettin, P. A., Sogayar, M. C., & Ferreira, C. E. (2007). Time-varying modeling of gene expression regulatory networks using the wavelet dynamic vector autoregressive method. Bioinformatics, 23( 13), 1623-1630. doi:10.1093/bioinformatics/btm151
NLM
Fujita A, Sato JR, Garay-Malpartida HM, Morettin PA, Sogayar MC, Ferreira CE. Time-varying modeling of gene expression regulatory networks using the wavelet dynamic vector autoregressive method [Internet]. Bioinformatics. 2007 ; 23( 13): 1623-1630.[citado 2025 nov. 04 ] Available from: https://doi.org/10.1093/bioinformatics/btm151
Vancouver
Fujita A, Sato JR, Garay-Malpartida HM, Morettin PA, Sogayar MC, Ferreira CE. Time-varying modeling of gene expression regulatory networks using the wavelet dynamic vector autoregressive method [Internet]. Bioinformatics. 2007 ; 23( 13): 1623-1630.[citado 2025 nov. 04 ] Available from: https://doi.org/10.1093/bioinformatics/btm151

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