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Artigo de periodico
Zika virus impairs neurogenesis and synaptogenesis pathways in human neural stem cells and neurons (2019)
Fernandes, Livia Rosa ; Cugola, Fernanda Rodrigues ; Russo, Fabiele Baldino ; Sakuma, Rebeca Kawahara ; Freire, Caio Cesar de Melo ; Leite, Paulo Emílio Corrêa ; Stern, Ana Carolina Bassi; Pascale, Claudia Blanes Angeli ; Durigon, Danielle Bruna Leal de Oliveira ; Melo, Stella Rezende; Zanotto, Paolo Marinho de Andrade ; Durigon, Edison Luiz ; Larsen, Martin Røsse ; Beltrão-Braga, Patrícia ; Palmisano, Giuseppe
Source: Frontiers in Cellular Neuroscience. Unidades: ICB, EACH
Subjects: MICROBIOLOGIA, PARASITOLOGIA, ZIKA VÍRUS, CÉLULAS-TRONCO, MICROCEFALIA, NEUROGENÉTICA, MALFORMAÇÕES, PROTEÔMICA, ESPECTROMETRIA DE MASSAS
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ABNT
FERNANDES, Livia Rosa et al. Zika virus impairs neurogenesis and synaptogenesis pathways in human neural stem cells and neurons. Frontiers in Cellular Neuroscience, v. 13, p. 16 , 2019Tradução . . Disponível em: https://doi.org/10.3389/fncel.2019.00064. Acesso em: 14 nov. 2024.
APA
Fernandes, L. R., Cugola, F. R., Russo, F. B., Sakuma, R. K., Freire, C. C. de M., Leite, P. E. C., et al. (2019). Zika virus impairs neurogenesis and synaptogenesis pathways in human neural stem cells and neurons. Frontiers in Cellular Neuroscience, 13, 16 . doi:10.3389/fncel.2019.00064
NLM
Fernandes LR, Cugola FR, Russo FB, Sakuma RK, Freire CC de M, Leite PEC, Stern ACB, Pascale CBA, Durigon DBL de O, Melo SR, Zanotto PM de A, Durigon EL, Larsen MR, Beltrão-Braga P, Palmisano G. Zika virus impairs neurogenesis and synaptogenesis pathways in human neural stem cells and neurons [Internet]. Frontiers in Cellular Neuroscience. 2019 ; 13 16 .[citado 2024 nov. 14 ] Available from: https://doi.org/10.3389/fncel.2019.00064
Vancouver
Fernandes LR, Cugola FR, Russo FB, Sakuma RK, Freire CC de M, Leite PEC, Stern ACB, Pascale CBA, Durigon DBL de O, Melo SR, Zanotto PM de A, Durigon EL, Larsen MR, Beltrão-Braga P, Palmisano G. Zika virus impairs neurogenesis and synaptogenesis pathways in human neural stem cells and neurons [Internet]. Frontiers in Cellular Neuroscience. 2019 ; 13 16 .[citado 2024 nov. 14 ] Available from: https://doi.org/10.3389/fncel.2019.00064
Artigo de periodico
On the relationship of anthranilic derivatives structure and the FXR (Farnesoid X receptor) agonist activity (2018)
Kronenberger, Thales ; Windshügel, Björn ; Wrenger, Carsten ; Honório, Káthia Maria ; Maltarollo, Vinícius Gonçalves
Source: Journal of Biomolecular Structure & Dynamics. Unidades: ICB, EACH
Subjects: PARASITOLOGIA, HOMEOSTASE, DOENÇAS METABÓLICAS
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KRONENBERGER, Thales et al. On the relationship of anthranilic derivatives structure and the FXR (Farnesoid X receptor) agonist activity. Journal of Biomolecular Structure & Dynamics, v. 36, n. 16, p. 4378–4391, 2018Tradução . . Disponível em: https://doi.org/10.1080/07391102.2017.1417161. Acesso em: 14 nov. 2024.
APA
Kronenberger, T., Windshügel, B., Wrenger, C., Honório, K. M., & Maltarollo, V. G. (2018). On the relationship of anthranilic derivatives structure and the FXR (Farnesoid X receptor) agonist activity. Journal of Biomolecular Structure & Dynamics, 36( 16), 4378–4391. doi:10.1080/07391102.2017.1417161
NLM
Kronenberger T, Windshügel B, Wrenger C, Honório KM, Maltarollo VG. On the relationship of anthranilic derivatives structure and the FXR (Farnesoid X receptor) agonist activity [Internet]. Journal of Biomolecular Structure & Dynamics. 2018 ; 36( 16): 4378–4391.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1080/07391102.2017.1417161
Vancouver
Kronenberger T, Windshügel B, Wrenger C, Honório KM, Maltarollo VG. On the relationship of anthranilic derivatives structure and the FXR (Farnesoid X receptor) agonist activity [Internet]. Journal of Biomolecular Structure & Dynamics. 2018 ; 36( 16): 4378–4391.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1080/07391102.2017.1417161
Artigo de periodico
Advances and challenges in drug design of PPARδ ligands (2018)
Maltarollo, Vinícius Gonçalves ; Kronenberger, Thales ; Windshuegel, Bjoern ; Wrenger, Carsten ; Trossini, Gustavo Henrique Goulart ; Honório, Káthia Maria
Source: Current Drug Targets. Unidades: ICB, FCF, EACH
Subjects: DIABETES MELLITUS NÃO INSULINO-DEPENDENTE, SÍNDROME X METABÓLICA, ÁCIDOS GRAXOS, DOENÇAS METABÓLICAS, PARASITOLOGIA
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MALTAROLLO, Vinícius Gonçalves et al. Advances and challenges in drug design of PPARδ ligands. Current Drug Targets, v. 19, n. 2, p. 144-154, 2018Tradução . . Disponível em: https://doi.org/10.2174/1389450118666170414113159. Acesso em: 14 nov. 2024.
APA
Maltarollo, V. G., Kronenberger, T., Windshuegel, B., Wrenger, C., Trossini, G. H. G., & Honório, K. M. (2018). Advances and challenges in drug design of PPARδ ligands. Current Drug Targets, 19( 2), 144-154. doi:10.2174/1389450118666170414113159
NLM
Maltarollo VG, Kronenberger T, Windshuegel B, Wrenger C, Trossini GHG, Honório KM. Advances and challenges in drug design of PPARδ ligands [Internet]. Current Drug Targets. 2018 ; 19( 2): 144-154.[citado 2024 nov. 14 ] Available from: https://doi.org/10.2174/1389450118666170414113159
Vancouver
Maltarollo VG, Kronenberger T, Windshuegel B, Wrenger C, Trossini GHG, Honório KM. Advances and challenges in drug design of PPARδ ligands [Internet]. Current Drug Targets. 2018 ; 19( 2): 144-154.[citado 2024 nov. 14 ] Available from: https://doi.org/10.2174/1389450118666170414113159
Artigo de periodico
Current trends in quantitative structure-activity relationship validation and applications on drug discovery (2017)
Maltarollo, Vinicius G.; Kronenberger, Thales; Wrenger, Carsten ; Honorio, Káthia Maria
Source: Future Science OA. Unidades: EACH, ICB
Subjects: RELAÇÕES QUANTITATIVAS ENTRE ESTRUTURA QUÍMICA E ATIVIDADE BIOLÓGICA, PLANEJAMENTO DE FÁRMACOS, FÁRMACOS
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ABNT
MALTAROLLO, Vinicius G. et al. Current trends in quantitative structure-activity relationship validation and applications on drug discovery. Future Science OA, v. 3, n. 4, p. FSO214-FSO216, 2017Tradução . . Disponível em: https://doi.org/10.4155/fsoa-2017-0052. Acesso em: 14 nov. 2024.
APA
Maltarollo, V. G., Kronenberger, T., Wrenger, C., & Honorio, K. M. (2017). Current trends in quantitative structure-activity relationship validation and applications on drug discovery. Future Science OA, 3( 4), FSO214-FSO216. doi:10.4155/fsoa-2017-0052
NLM
Maltarollo VG, Kronenberger T, Wrenger C, Honorio KM. Current trends in quantitative structure-activity relationship validation and applications on drug discovery [Internet]. Future Science OA. 2017 ; 3( 4): FSO214-FSO216.[citado 2024 nov. 14 ] Available from: https://doi.org/10.4155/fsoa-2017-0052
Vancouver
Maltarollo VG, Kronenberger T, Wrenger C, Honorio KM. Current trends in quantitative structure-activity relationship validation and applications on drug discovery [Internet]. Future Science OA. 2017 ; 3( 4): FSO214-FSO216.[citado 2024 nov. 14 ] Available from: https://doi.org/10.4155/fsoa-2017-0052
Artigo de periodico
Studies of Staphylococcus aureus FabI inhibitors: fragment-based approach based on holographic structure–activity relationship analyses (2017)
Kronenberger, Thales; Asse Junior, Leonardo Rander; Wrenger, Carsten ; Trossini, Gustavo Henrique Goulart ; Honorio, Kathia Maria; Maltarollo, Vinícius Gonçalves
Source: Future Medicinal Chemistry. Unidades: EACH, ICB, FCF
Subjects: STAPHYLOCOCCUS, RELAÇÕES QUANTITATIVAS ENTRE ESTRUTURA QUÍMICA E ATIVIDADE BIOLÓGICA, MODELAGEM MOLECULAR
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ABNT
KRONENBERGER, Thales et al. Studies of Staphylococcus aureus FabI inhibitors: fragment-based approach based on holographic structure–activity relationship analyses. Future Medicinal Chemistry, v. 9, n. 2, p. 135-151, 2017Tradução . . Disponível em: https://doi.org/10.4155/fmc-2016-0179. Acesso em: 14 nov. 2024.
APA
Kronenberger, T., Asse Junior, L. R., Wrenger, C., Trossini, G. H. G., Honorio, K. M., & Maltarollo, V. G. (2017). Studies of Staphylococcus aureus FabI inhibitors: fragment-based approach based on holographic structure–activity relationship analyses. Future Medicinal Chemistry, 9( 2), 135-151. doi:10.4155/fmc-2016-0179
NLM
Kronenberger T, Asse Junior LR, Wrenger C, Trossini GHG, Honorio KM, Maltarollo VG. Studies of Staphylococcus aureus FabI inhibitors: fragment-based approach based on holographic structure–activity relationship analyses [Internet]. Future Medicinal Chemistry. 2017 ; 9( 2): 135-151.[citado 2024 nov. 14 ] Available from: https://doi.org/10.4155/fmc-2016-0179
Vancouver
Kronenberger T, Asse Junior LR, Wrenger C, Trossini GHG, Honorio KM, Maltarollo VG. Studies of Staphylococcus aureus FabI inhibitors: fragment-based approach based on holographic structure–activity relationship analyses [Internet]. Future Medicinal Chemistry. 2017 ; 9( 2): 135-151.[citado 2024 nov. 14 ] Available from: https://doi.org/10.4155/fmc-2016-0179
Artigo de periodico
Structure-activity relationship of Trp-containing analogs of the antimicrobial peptide gomesin (2014)
Domingues, Tatiana Moreira; Buri, Marcus Vinicius; Daffre, Sirlei; Campana, Patrícia Targon; Riske, Karin do Amaral; Miranda, Antônio Basílio C.
Source: Journal of Peptide Science. Unidades: ICB, EACH
Assunto: PEPTÍDEOS
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ABNT
DOMINGUES, Tatiana Moreira et al. Structure-activity relationship of Trp-containing analogs of the antimicrobial peptide gomesin. Journal of Peptide Science, v. 20, n. 6, p. 421-428, 2014Tradução . . Disponível em: https://doi.org/10.1002/psc.2632. Acesso em: 14 nov. 2024.
APA
Domingues, T. M., Buri, M. V., Daffre, S., Campana, P. T., Riske, K. do A., & Miranda, A. B. C. (2014). Structure-activity relationship of Trp-containing analogs of the antimicrobial peptide gomesin. Journal of Peptide Science, 20( 6), 421-428. doi:10.1002/psc.2632
NLM
Domingues TM, Buri MV, Daffre S, Campana PT, Riske K do A, Miranda ABC. Structure-activity relationship of Trp-containing analogs of the antimicrobial peptide gomesin [Internet]. Journal of Peptide Science. 2014 ; 20( 6): 421-428.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1002/psc.2632
Vancouver
Domingues TM, Buri MV, Daffre S, Campana PT, Riske K do A, Miranda ABC. Structure-activity relationship of Trp-containing analogs of the antimicrobial peptide gomesin [Internet]. Journal of Peptide Science. 2014 ; 20( 6): 421-428.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1002/psc.2632

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