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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
Source: Stem Cell Research and Therapy. Unidade: IQ
Subjects: CÉLULAS-TRONCO, IMUNOHISTOQUÍMICA, NEFROPATIAS
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ABNT
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: 18 nov. 2024.
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 2024 nov. 18 ] 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 2024 nov. 18 ] Available from: https://doi.org/10.1186/s13287-020-02060-4
Artigo de periodico
The alternatively spliced RECK transcript variant 3 is a predictor of poor survival for melanoma patients being upregulated in aggressive cell lines and modulating MMP gene expression in vitro (2020)
Jacomasso, Thiago; Ribas, Hennrique Taborda; Lima, Marina Trombetta ; Konig, Michelle Silberspitz; Trindade, Edvaldo da Silva; Martinez, Glaucia Regina ; Sogayar, Mari Cleide ; Winnischofer, Sheila Maria Brochado
Source: Melanoma Research. Unidade: IQ
Subjects: MELANOMA, EXPRESSÃO GÊNICA, METALOPROTEINASES
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JACOMASSO, Thiago et al. The alternatively spliced RECK transcript variant 3 is a predictor of poor survival for melanoma patients being upregulated in aggressive cell lines and modulating MMP gene expression in vitro. Melanoma Research, v. 30, n. 3, p. 223-234, 2020Tradução . . Disponível em: https://doi.org/10.1097/CMR.0000000000000650. Acesso em: 18 nov. 2024.
APA
Jacomasso, T., Ribas, H. T., Lima, M. T., Konig, M. S., Trindade, E. da S., Martinez, G. R., et al. (2020). The alternatively spliced RECK transcript variant 3 is a predictor of poor survival for melanoma patients being upregulated in aggressive cell lines and modulating MMP gene expression in vitro. Melanoma Research, 30( 3), 223-234. doi:10.1097/CMR.0000000000000650
NLM
Jacomasso T, Ribas HT, Lima MT, Konig MS, Trindade E da S, Martinez GR, Sogayar MC, Winnischofer SMB. The alternatively spliced RECK transcript variant 3 is a predictor of poor survival for melanoma patients being upregulated in aggressive cell lines and modulating MMP gene expression in vitro [Internet]. Melanoma Research. 2020 ; 30( 3): 223-234.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1097/CMR.0000000000000650
Vancouver
Jacomasso T, Ribas HT, Lima MT, Konig MS, Trindade E da S, Martinez GR, Sogayar MC, Winnischofer SMB. The alternatively spliced RECK transcript variant 3 is a predictor of poor survival for melanoma patients being upregulated in aggressive cell lines and modulating MMP gene expression in vitro [Internet]. Melanoma Research. 2020 ; 30( 3): 223-234.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1097/CMR.0000000000000650
Patente
Biologically active recombinant equine chorionic gonadotropin (RECG) and process for obtaining same, veterinary composition and use (2020)
Sogayar, Mari Cleide ; Nishiyama, Ana Claudia Oliveira Carreira ; Demasi, Marcos Angelo Almeida ; Camargo, Lauren; Coelho, Tatiane Maldonado
Unidades: IQ, FMVZ, BIOTECNOLOGIA
Assunto: GONADOTROFINA CORIÔNICA
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SOGAYAR, Mari Cleide et al. Biologically active recombinant equine chorionic gonadotropin (RECG) and process for obtaining same, veterinary composition and use. . Columbia: World Intellectual Property Organization/WIPO. . Acesso em: 18 nov. 2024. , 2020
APA
Sogayar, M. C., Nishiyama, A. C. O. C., Demasi, M. A. A., Camargo, L., & Coelho, T. M. (2020). Biologically active recombinant equine chorionic gonadotropin (RECG) and process for obtaining same, veterinary composition and use. Columbia: World Intellectual Property Organization/WIPO.
NLM
Sogayar MC, Nishiyama ACOC, Demasi MAA, Camargo L, Coelho TM. Biologically active recombinant equine chorionic gonadotropin (RECG) and process for obtaining same, veterinary composition and use. 2020 ;[citado 2024 nov. 18 ]
Vancouver
Sogayar MC, Nishiyama ACOC, Demasi MAA, Camargo L, Coelho TM. Biologically active recombinant equine chorionic gonadotropin (RECG) and process for obtaining same, veterinary composition and use. 2020 ;[citado 2024 nov. 18 ]
Artigo de periodico
Emerging roles and potential applications of non-coding RNAs in glioblastoma (2020)
DeOcesano-Pereira, Carlos ; Machado, Raquel Arminda Carvalho ; Tavassi, Ana Marisa Chudzinski; Sogayar, Mari Cleide
Source: International Journal of Molecular Sciences. Unidade: IQ
Subjects: RNA, EXPRESSÃO GÊNICA
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ABNT
DEOCESANO-PEREIRA, Carlos et al. Emerging roles and potential applications of non-coding RNAs in glioblastoma. International Journal of Molecular Sciences, v. 21, p. 1-27 art. 2611, 2020Tradução . . Disponível em: https://doi.org/10.3390/ijms21072611. Acesso em: 18 nov. 2024.
APA
DeOcesano-Pereira, C., Machado, R. A. C., Tavassi, A. M. C., & Sogayar, M. C. (2020). Emerging roles and potential applications of non-coding RNAs in glioblastoma. International Journal of Molecular Sciences, 21, 1-27 art. 2611. doi:10.3390/ijms21072611
NLM
DeOcesano-Pereira C, Machado RAC, Tavassi AMC, Sogayar MC. Emerging roles and potential applications of non-coding RNAs in glioblastoma [Internet]. International Journal of Molecular Sciences. 2020 ; 21 1-27 art. 2611.[citado 2024 nov. 18 ] Available from: https://doi.org/10.3390/ijms21072611
Vancouver
DeOcesano-Pereira C, Machado RAC, Tavassi AMC, Sogayar MC. Emerging roles and potential applications of non-coding RNAs in glioblastoma [Internet]. International Journal of Molecular Sciences. 2020 ; 21 1-27 art. 2611.[citado 2024 nov. 18 ] Available from: https://doi.org/10.3390/ijms21072611
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
Source: BMC Research Notes. Unidades: IME, EP, IQ, BIOTECNOLOGIA, FM
Subjects: BIOINFORMÁTICA, PROLIFERAÇÃO CELULAR
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ABNT
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: 18 nov. 2024.
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 2024 nov. 18 ] 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 2024 nov. 18 ] Available from: https://doi.org/10.1186/s13104-020-4914-8
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
Source: BMC Biotechnology. Unidades: IQ, BIOTECNOLOGIA
Subjects: PROLIFERAÇÃO CELULAR, CÉLULAS, PROTEÍNAS RECOMBINANTES
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ABNT
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: 18 nov. 2024.
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 2024 nov. 18 ] 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 2024 nov. 18 ] Available from: https://doi.org/10.1186/s12896-020-0600-0
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
Source: Frontiers in Bioengineering and Biotechnology. Unidades: IQ, FM
Subjects: ORGANELAS CELULARES, ENGENHARIA TECIDUAL, ORGANELAS CELULARES, INTESTINO DELGADO
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ABNT
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: 18 nov. 2024.
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 2024 nov. 18 ] 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 2024 nov. 18 ] Available from: https://doi.org/10.3389/fbioe.2020.00476

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