ReP USP - Resultado da busca

Artigo de periodico
Validation and measurement uncertainty of an UPLC-PDA stability indicating method applied to degradation kinetics of caspofungin (2014)
Ghisleni, Daniela Dal Molim ; Okamoto, Rogério Takao; Lourenço, Felipe Rebello ; Pinto, Terezinha de Jesus Andreoli
Source: Current Pharmaceutical Analysis. Unidade: FCF
Assunto: ESTABILIDADE DOS MEDICAMENTOS
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ABNT
GHISLENI, Daniela Dal Molim et al. Validation and measurement uncertainty of an UPLC-PDA stability indicating method applied to degradation kinetics of caspofungin. Current Pharmaceutical Analysis, v. 10, n. 3, p. 193-202, 2014Tradução . . Acesso em: 16 nov. 2024.
APA
Ghisleni, D. D. M., Okamoto, R. T., Lourenço, F. R., & Pinto, T. de J. A. (2014). Validation and measurement uncertainty of an UPLC-PDA stability indicating method applied to degradation kinetics of caspofungin. Current Pharmaceutical Analysis, 10( 3), 193-202.
NLM
Ghisleni DDM, Okamoto RT, Lourenço FR, Pinto T de JA. Validation and measurement uncertainty of an UPLC-PDA stability indicating method applied to degradation kinetics of caspofungin. Current Pharmaceutical Analysis. 2014 ; 10( 3): 193-202.[citado 2024 nov. 16 ]
Vancouver
Ghisleni DDM, Okamoto RT, Lourenço FR, Pinto T de JA. Validation and measurement uncertainty of an UPLC-PDA stability indicating method applied to degradation kinetics of caspofungin. Current Pharmaceutical Analysis. 2014 ; 10( 3): 193-202.[citado 2024 nov. 16 ]
Artigo de periodico
Determination of ethinylestradiol and levo-norgestrel using microemulsion electrokinetic chromatography (2014)
Silva, Claudinei Alves da; Aurora-Prado, Maria Segunda ; Tavares, Marina Franco Maggi
Source: Current Analytical Chemistry. Unidades: FCF, IQ
Subjects: ELETROFORESE (MÉTODO DE SEPARAÇÃO), ESTEROIDES
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ABNT
SILVA, Claudinei Alves da e AURORA-PRADO, Maria Segunda e TAVARES, Marina Franco Maggi. Determination of ethinylestradiol and levo-norgestrel using microemulsion electrokinetic chromatography. Current Analytical Chemistry, v. 10, n. 2, p. 216-224, 2014Tradução . . Disponível em: http://apps.webofknowledge.com/full_record.do?product=UA&search_mode=GeneralSearch&qid=5&SID=4Bj4Ns2BRnXmDjyUQki&page=1&doc=2. Acesso em: 16 nov. 2024.
APA
Silva, C. A. da, Aurora-Prado, M. S., & Tavares, M. F. M. (2014). Determination of ethinylestradiol and levo-norgestrel using microemulsion electrokinetic chromatography. Current Analytical Chemistry, 10( 2), 216-224. Recuperado de http://apps.webofknowledge.com/full_record.do?product=UA&search_mode=GeneralSearch&qid=5&SID=4Bj4Ns2BRnXmDjyUQki&page=1&doc=2
NLM
Silva CA da, Aurora-Prado MS, Tavares MFM. Determination of ethinylestradiol and levo-norgestrel using microemulsion electrokinetic chromatography [Internet]. Current Analytical Chemistry. 2014 ; 10( 2): 216-224.[citado 2024 nov. 16 ] Available from: http://apps.webofknowledge.com/full_record.do?product=UA&search_mode=GeneralSearch&qid=5&SID=4Bj4Ns2BRnXmDjyUQki&page=1&doc=2
Vancouver
Silva CA da, Aurora-Prado MS, Tavares MFM. Determination of ethinylestradiol and levo-norgestrel using microemulsion electrokinetic chromatography [Internet]. Current Analytical Chemistry. 2014 ; 10( 2): 216-224.[citado 2024 nov. 16 ] Available from: http://apps.webofknowledge.com/full_record.do?product=UA&search_mode=GeneralSearch&qid=5&SID=4Bj4Ns2BRnXmDjyUQki&page=1&doc=2
Artigo de periodico
Chimeric proteins combining phosphatase and cellulose binding activities: proof of concept and application in the hydrolysis of paraoxon (2014)
Gonçalves, Larissa Martins; Chaimovich Guralnik, Hernan ; Cuccovia, Iolanda Midea ; Marana, Sandro Roberto
Source: Protein & Peptide Letters. Unidade: IQ
Subjects: CARBOIDRATOS, HIDRÓLISE
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ABNT
GONÇALVES, Larissa Martins et al. Chimeric proteins combining phosphatase and cellulose binding activities: proof of concept and application in the hydrolysis of paraoxon. Protein & Peptide Letters, v. 21, n. 8, p. 488-475, 2014Tradução . . Acesso em: 16 nov. 2024.
APA
Gonçalves, L. M., Chaimovich Guralnik, H., Cuccovia, I. M., & Marana, S. R. (2014). Chimeric proteins combining phosphatase and cellulose binding activities: proof of concept and application in the hydrolysis of paraoxon. Protein & Peptide Letters, 21( 8), 488-475.
NLM
Gonçalves LM, Chaimovich Guralnik H, Cuccovia IM, Marana SR. Chimeric proteins combining phosphatase and cellulose binding activities: proof of concept and application in the hydrolysis of paraoxon. Protein & Peptide Letters. 2014 ; 21( 8): 488-475.[citado 2024 nov. 16 ]
Vancouver
Gonçalves LM, Chaimovich Guralnik H, Cuccovia IM, Marana SR. Chimeric proteins combining phosphatase and cellulose binding activities: proof of concept and application in the hydrolysis of paraoxon. Protein & Peptide Letters. 2014 ; 21( 8): 488-475.[citado 2024 nov. 16 ]
Artigo de periodico
New tuberculostatic agents targeting nucleic acid biosynthesis: drug design using QSAR approaches (2014)
Bueno, Renata Vieria; Braga, Rodolpho de Campos; Segretti, Natanael Dante; Ferreira, Elizabeth Igne ; Trossini, Gustavo Henrique Goulart ; Andrade, Carolina Horta
Source: Current Pharmaceutical Design. Unidade: FCF
Subjects: TUBERCULOSE, ÁCIDOS NUCLEICOS
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ABNT
BUENO, Renata Vieria et al. New tuberculostatic agents targeting nucleic acid biosynthesis: drug design using QSAR approaches. Current Pharmaceutical Design, v. 20, n. 27, p. 4474-4485, 2014Tradução . . Acesso em: 16 nov. 2024.
APA
Bueno, R. V., Braga, R. de C., Segretti, N. D., Ferreira, E. I., Trossini, G. H. G., & Andrade, C. H. (2014). New tuberculostatic agents targeting nucleic acid biosynthesis: drug design using QSAR approaches. Current Pharmaceutical Design, 20( 27), 4474-4485.
NLM
Bueno RV, Braga R de C, Segretti ND, Ferreira EI, Trossini GHG, Andrade CH. New tuberculostatic agents targeting nucleic acid biosynthesis: drug design using QSAR approaches. Current Pharmaceutical Design. 2014 ; 20( 27): 4474-4485.[citado 2024 nov. 16 ]
Vancouver
Bueno RV, Braga R de C, Segretti ND, Ferreira EI, Trossini GHG, Andrade CH. New tuberculostatic agents targeting nucleic acid biosynthesis: drug design using QSAR approaches. Current Pharmaceutical Design. 2014 ; 20( 27): 4474-4485.[citado 2024 nov. 16 ]
Artigo de periodico
Neuroimmune interactions and psychologycal stress induced by cohabitation with a sick partner: a review (2014)
Palermo-Neto, João; Alves, Glaucie Jussilane
Source: Current Pharmaceutical Design. Unidade: FMVZ
Subjects: NEUROIMUNOMODULAÇÃO, ESTRESSE PSICOLÓGICO, TUMOR DE EHRLICH ANIMAL, SISTEMA NERVOSO SIMPÁTICO
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ABNT
PALERMO-NETO, João e ALVES, Glaucie Jussilane. Neuroimmune interactions and psychologycal stress induced by cohabitation with a sick partner: a review. Current Pharmaceutical Design, v. 20, n. 29, p. 4629-4641, 2014Tradução . . Disponível em: https://doi.org/10.2174/1381612820666140130204657. Acesso em: 16 nov. 2024.
APA
Palermo-Neto, J., & Alves, G. J. (2014). Neuroimmune interactions and psychologycal stress induced by cohabitation with a sick partner: a review. Current Pharmaceutical Design, 20( 29), 4629-4641. doi:10.2174/1381612820666140130204657
NLM
Palermo-Neto J, Alves GJ. Neuroimmune interactions and psychologycal stress induced by cohabitation with a sick partner: a review [Internet]. Current Pharmaceutical Design. 2014 ; 20( 29): 4629-4641.[citado 2024 nov. 16 ] Available from: https://doi.org/10.2174/1381612820666140130204657
Vancouver
Palermo-Neto J, Alves GJ. Neuroimmune interactions and psychologycal stress induced by cohabitation with a sick partner: a review [Internet]. Current Pharmaceutical Design. 2014 ; 20( 29): 4629-4641.[citado 2024 nov. 16 ] Available from: https://doi.org/10.2174/1381612820666140130204657
Artigo de periodico
Molecular modeling and docking application to evaluate cruzain inhibitory activity by chalcones and hydrazides (2014)
Vital, Drielli Gomes; Arribas, Marco; Trossini, Gustavo Henrique Goulart
Source: Letters in Drug Design & Discovery. Unidade: FCF
Subjects: MODELAGEM MOLECULAR, DOENÇA DE CHAGAS
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ABNT
VITAL, Drielli Gomes e ARRIBAS, Marco e TROSSINI, Gustavo Henrique Goulart. Molecular modeling and docking application to evaluate cruzain inhibitory activity by chalcones and hydrazides. Letters in Drug Design & Discovery, v. 11, n. 3, p. 249-255, 2014Tradução . . Acesso em: 16 nov. 2024.
APA
Vital, D. G., Arribas, M., & Trossini, G. H. G. (2014). Molecular modeling and docking application to evaluate cruzain inhibitory activity by chalcones and hydrazides. Letters in Drug Design & Discovery, 11( 3), 249-255.
NLM
Vital DG, Arribas M, Trossini GHG. Molecular modeling and docking application to evaluate cruzain inhibitory activity by chalcones and hydrazides. Letters in Drug Design & Discovery. 2014 ; 11( 3): 249-255.[citado 2024 nov. 16 ]
Vancouver
Vital DG, Arribas M, Trossini GHG. Molecular modeling and docking application to evaluate cruzain inhibitory activity by chalcones and hydrazides. Letters in Drug Design & Discovery. 2014 ; 11( 3): 249-255.[citado 2024 nov. 16 ]
Artigo de periodico
The survey of the use of QSAR methods to determine intestinal absorption and oral bioavailability during drug design (2014)
Silva, Fredson Torres; Trossini, Gustavo Henrique Goulart
Source: Medicinal Chemistry. Unidade: FCF
Subjects: BIODISPONIBILIDADE, RELAÇÕES QUANTITATIVAS ENTRE ESTRUTURA QUÍMICA E ATIVIDADE BIOLÓGICA
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ABNT
SILVA, Fredson Torres e TROSSINI, Gustavo Henrique Goulart. The survey of the use of QSAR methods to determine intestinal absorption and oral bioavailability during drug design. Medicinal Chemistry, v. 10, n. 5, p. 441-448, 2014Tradução . . Acesso em: 16 nov. 2024.
APA
Silva, F. T., & Trossini, G. H. G. (2014). The survey of the use of QSAR methods to determine intestinal absorption and oral bioavailability during drug design. Medicinal Chemistry, 10( 5), 441-448.
NLM
Silva FT, Trossini GHG. The survey of the use of QSAR methods to determine intestinal absorption and oral bioavailability during drug design. Medicinal Chemistry. 2014 ; 10( 5): 441-448.[citado 2024 nov. 16 ]
Vancouver
Silva FT, Trossini GHG. The survey of the use of QSAR methods to determine intestinal absorption and oral bioavailability during drug design. Medicinal Chemistry. 2014 ; 10( 5): 441-448.[citado 2024 nov. 16 ]
Artigo de periodico
Structure based design, synthesis, and evaluation of potential inhibitors of steroid sulfatase (2014)
Costa, E. V.; Sousa, E.; Choosang, K.; Singh, S.; Rocha, J.; Lima, R. T.; Pakkong, P.; Ahmed, S.; Vasconcelos, M. H.; Montanari, Carlos Alberto ; Pinto, M. M.
Source: Current Topics in Medicinal Chemistry. Unidade: IQSC
Assunto: QUÍMICA MÉDICA
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ABNT
COSTA, E. V. et al. Structure based design, synthesis, and evaluation of potential inhibitors of steroid sulfatase. Current Topics in Medicinal Chemistry, v. 14, n. 8, p. 1033-1044, 2014Tradução . . Disponível em: https://repositorio.usp.br/directbitstream/9681e089-d632-4260-8666-e505cc746359/P15026.pdf. Acesso em: 16 nov. 2024.
APA
Costa, E. V., Sousa, E., Choosang, K., Singh, S., Rocha, J., Lima, R. T., et al. (2014). Structure based design, synthesis, and evaluation of potential inhibitors of steroid sulfatase. Current Topics in Medicinal Chemistry, 14( 8), 1033-1044. Recuperado de https://repositorio.usp.br/directbitstream/9681e089-d632-4260-8666-e505cc746359/P15026.pdf
NLM
Costa EV, Sousa E, Choosang K, Singh S, Rocha J, Lima RT, Pakkong P, Ahmed S, Vasconcelos MH, Montanari CA, Pinto MM. Structure based design, synthesis, and evaluation of potential inhibitors of steroid sulfatase [Internet]. Current Topics in Medicinal Chemistry. 2014 ; 14( 8): 1033-1044.[citado 2024 nov. 16 ] Available from: https://repositorio.usp.br/directbitstream/9681e089-d632-4260-8666-e505cc746359/P15026.pdf
Vancouver
Costa EV, Sousa E, Choosang K, Singh S, Rocha J, Lima RT, Pakkong P, Ahmed S, Vasconcelos MH, Montanari CA, Pinto MM. Structure based design, synthesis, and evaluation of potential inhibitors of steroid sulfatase [Internet]. Current Topics in Medicinal Chemistry. 2014 ; 14( 8): 1033-1044.[citado 2024 nov. 16 ] Available from: https://repositorio.usp.br/directbitstream/9681e089-d632-4260-8666-e505cc746359/P15026.pdf
Artigo de periodico
Antifungal activity of a library of cyclitols and related compounds (2014)
Bellomo, Ana; Bertucci, Ana; Sovera, Victoria de la; Carrau, Gonzalo; Raimondi, Marcela; Zacchino, Susana; Stefani, Hélio Alexandre ; Gonzalez, David
Source: Letters in Drug Design & Discovery. Unidade: FCF
Subjects: ANTIFÚNGICOS, AMINOÁCIDOS
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ABNT
BELLOMO, Ana et al. Antifungal activity of a library of cyclitols and related compounds. Letters in Drug Design & Discovery, v. 11, n. 1, p. 67-75, 2014Tradução . . Disponível em: http://www.ingentaconnect.com/content/ben/lddd/2013/00000011/00000001/art00011. Acesso em: 16 nov. 2024.
APA
Bellomo, A., Bertucci, A., Sovera, V. de la, Carrau, G., Raimondi, M., Zacchino, S., et al. (2014). Antifungal activity of a library of cyclitols and related compounds. Letters in Drug Design & Discovery, 11( 1), 67-75. Recuperado de http://www.ingentaconnect.com/content/ben/lddd/2013/00000011/00000001/art00011
NLM
Bellomo A, Bertucci A, Sovera V de la, Carrau G, Raimondi M, Zacchino S, Stefani HA, Gonzalez D. Antifungal activity of a library of cyclitols and related compounds [Internet]. Letters in Drug Design & Discovery. 2014 ; 11( 1): 67-75.[citado 2024 nov. 16 ] Available from: http://www.ingentaconnect.com/content/ben/lddd/2013/00000011/00000001/art00011
Vancouver
Bellomo A, Bertucci A, Sovera V de la, Carrau G, Raimondi M, Zacchino S, Stefani HA, Gonzalez D. Antifungal activity of a library of cyclitols and related compounds [Internet]. Letters in Drug Design & Discovery. 2014 ; 11( 1): 67-75.[citado 2024 nov. 16 ] Available from: http://www.ingentaconnect.com/content/ben/lddd/2013/00000011/00000001/art00011

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