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Artigo de periodico
Novel Insights into the Pathophysiology and Treatment of Sickle Cell Disease (2023)
Araújo, Aderson da Silva; Pinto, Ana Cristina Silva ; Lobo, Clarisse Lopes de Castro; Figueiredo, Maria Stella ; Gualandro, Sandra Fátima Menosi ; Saad, Sara Teresinha Olalla ; Cançado, Rodolfo Delfini
Source: Hemoglobin. Unidades: FMRP, FM
Subjects: ANEMIA FALCIFORME, ADENOSINA, GLUTAMINA
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ABNT
ARAÚJO, Aderson da Silva et al. Novel Insights into the Pathophysiology and Treatment of Sickle Cell Disease. Hemoglobin, v. 47, n. 2, p. 71-79, 2023Tradução . . Disponível em: https://observatorio.fm.usp.br/handle/OPI/55991. Acesso em: 02 nov. 2024.
APA
Araújo, A. da S., Pinto, A. C. S., Lobo, C. L. de C., Figueiredo, M. S., Gualandro, S. F. M., Saad, S. T. O., & Cançado, R. D. (2023). Novel Insights into the Pathophysiology and Treatment of Sickle Cell Disease. Hemoglobin, 47( 2), 71-79. doi:10.1080/03630269.2023.2211771
NLM
Araújo A da S, Pinto ACS, Lobo CL de C, Figueiredo MS, Gualandro SFM, Saad STO, Cançado RD. Novel Insights into the Pathophysiology and Treatment of Sickle Cell Disease [Internet]. Hemoglobin. 2023 ; 47( 2): 71-79.[citado 2024 nov. 02 ] Available from: https://observatorio.fm.usp.br/handle/OPI/55991
Vancouver
Araújo A da S, Pinto ACS, Lobo CL de C, Figueiredo MS, Gualandro SFM, Saad STO, Cançado RD. Novel Insights into the Pathophysiology and Treatment of Sickle Cell Disease [Internet]. Hemoglobin. 2023 ; 47( 2): 71-79.[citado 2024 nov. 02 ] Available from: https://observatorio.fm.usp.br/handle/OPI/55991
Artigo de periodico
The P2X4 purinergic receptor has emerged as a potent regulator of hematopoietic stem/progenitor cell mobilization and homing-a novel view of P2X4 and P2X7 receptor interaction in orchestrating stem cell trafficking (2022)
Adamiak, Mateusz ; Bujko, Kamila ; Thapa, Arjun; Pensato, Valentina; Janus, Katarzyna Brzezniakiewicz ; Ratajczak, Janina; Davies, Daryl L ; Ulrich, Henning ; Kucia, Magda ; Ratajczak, Mariusz Z
Source: Leukemia. Unidade: IQ
Subjects: CÉLULAS-TRONCO, ADENOSINA
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ABNT
ADAMIAK, Mateusz et al. The P2X4 purinergic receptor has emerged as a potent regulator of hematopoietic stem/progenitor cell mobilization and homing-a novel view of P2X4 and P2X7 receptor interaction in orchestrating stem cell trafficking. Leukemia, v. 36, n. 1, p. 248-256, 2022Tradução . . Disponível em: https://doi.org/10.1038/s41375-021-01352-9. Acesso em: 02 nov. 2024.
APA
Adamiak, M., Bujko, K., Thapa, A., Pensato, V., Janus, K. B., Ratajczak, J., et al. (2022). The P2X4 purinergic receptor has emerged as a potent regulator of hematopoietic stem/progenitor cell mobilization and homing-a novel view of P2X4 and P2X7 receptor interaction in orchestrating stem cell trafficking. Leukemia, 36( 1), 248-256. doi:10.1038/s41375-021-01352-9
NLM
Adamiak M, Bujko K, Thapa A, Pensato V, Janus KB, Ratajczak J, Davies DL, Ulrich H, Kucia M, Ratajczak MZ. The P2X4 purinergic receptor has emerged as a potent regulator of hematopoietic stem/progenitor cell mobilization and homing-a novel view of P2X4 and P2X7 receptor interaction in orchestrating stem cell trafficking [Internet]. Leukemia. 2022 ; 36( 1): 248-256.[citado 2024 nov. 02 ] Available from: https://doi.org/10.1038/s41375-021-01352-9
Vancouver
Adamiak M, Bujko K, Thapa A, Pensato V, Janus KB, Ratajczak J, Davies DL, Ulrich H, Kucia M, Ratajczak MZ. The P2X4 purinergic receptor has emerged as a potent regulator of hematopoietic stem/progenitor cell mobilization and homing-a novel view of P2X4 and P2X7 receptor interaction in orchestrating stem cell trafficking [Internet]. Leukemia. 2022 ; 36( 1): 248-256.[citado 2024 nov. 02 ] Available from: https://doi.org/10.1038/s41375-021-01352-9
Artigo de periodico
The role of adenosine A1 receptor in the peripheral tramadol’s effect in the temporomandibular joint of rats (2021)
Abdalla, Henrique Ballassini; Napimoga, Marcelo Henrique; Maganin, Alexandre Gomes de Macedo; Lopes, Alexandre Hashimoto Pereira; Cunha, Thiago Mattar; Gill, Harvinder Singh; Napimoga, Juliana Trindade Clemente
Source: International Immunopharmacology. Unidade: FMRP
Subjects: ADENOSINA, ANALGÉSICOS, ANTI-INFLAMATÓRIOS, ARTRALGIA, MACRÓFAGOS, NOCICEPTIVIDADE
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ABNT
ABDALLA, Henrique Ballassini et al. The role of adenosine A1 receptor in the peripheral tramadol’s effect in the temporomandibular joint of rats. International Immunopharmacology, v. 97, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.intimp.2021.107680. Acesso em: 02 nov. 2024.
APA
Abdalla, H. B., Napimoga, M. H., Maganin, A. G. de M., Lopes, A. H. P., Cunha, T. M., Gill, H. S., & Napimoga, J. T. C. (2021). The role of adenosine A1 receptor in the peripheral tramadol’s effect in the temporomandibular joint of rats. International Immunopharmacology, 97. doi:10.1016/j.intimp.2021.107680
NLM
Abdalla HB, Napimoga MH, Maganin AG de M, Lopes AHP, Cunha TM, Gill HS, Napimoga JTC. The role of adenosine A1 receptor in the peripheral tramadol’s effect in the temporomandibular joint of rats [Internet]. International Immunopharmacology. 2021 ; 97[citado 2024 nov. 02 ] Available from: https://doi.org/10.1016/j.intimp.2021.107680
Vancouver
Abdalla HB, Napimoga MH, Maganin AG de M, Lopes AHP, Cunha TM, Gill HS, Napimoga JTC. The role of adenosine A1 receptor in the peripheral tramadol’s effect in the temporomandibular joint of rats [Internet]. International Immunopharmacology. 2021 ; 97[citado 2024 nov. 02 ] Available from: https://doi.org/10.1016/j.intimp.2021.107680
Artigo de periodico
Host ADP-ribosylation and the SARS-CoV-2 macrodomain (2021)
Hoch, Nicolas Carlos
Source: Biochemical Society Transactions. Unidade: IQ
Subjects: ADENOSINA, VIROLOGIA, COVID-19
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ABNT
HOCH, Nicolas Carlos. Host ADP-ribosylation and the SARS-CoV-2 macrodomain. Biochemical Society Transactions, v. 49, p. 1711–1721, 2021Tradução . . Disponível em: https://doi.org/10.1042/BST20201212. Acesso em: 02 nov. 2024.
APA
Hoch, N. C. (2021). Host ADP-ribosylation and the SARS-CoV-2 macrodomain. Biochemical Society Transactions, 49, 1711–1721. doi:10.1042/BST20201212
NLM
Hoch NC. Host ADP-ribosylation and the SARS-CoV-2 macrodomain [Internet]. Biochemical Society Transactions. 2021 ; 49 1711–1721.[citado 2024 nov. 02 ] Available from: https://doi.org/10.1042/BST20201212
Vancouver
Hoch NC. Host ADP-ribosylation and the SARS-CoV-2 macrodomain [Internet]. Biochemical Society Transactions. 2021 ; 49 1711–1721.[citado 2024 nov. 02 ] Available from: https://doi.org/10.1042/BST20201212
Artigo de periodico
Inhibition of the hypercapnic ventilatory response by adenosine in the retrotrapezoid nucleus in awake rats (2018)
Falquetto, Bárbara ; Santos, Luiz Marcelo Oliveira; Takakura, Ana Carolina ; Mulkey, Daniel K.; Moreira, Thiago dos Santos
Source: Neuropharmacology. Unidade: ICB
Subjects: ADENOSINA, RATOS, RESPIRAÇÃO ANIMAL, ASTRÓCITOS
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ABNT
FALQUETTO, Bárbara et al. Inhibition of the hypercapnic ventilatory response by adenosine in the retrotrapezoid nucleus in awake rats. Neuropharmacology, v. 138, p. 47-56, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.neuropharm.2018.05.029. Acesso em: 02 nov. 2024.
APA
Falquetto, B., Santos, L. M. O., Takakura, A. C., Mulkey, D. K., & Moreira, T. dos S. (2018). Inhibition of the hypercapnic ventilatory response by adenosine in the retrotrapezoid nucleus in awake rats. Neuropharmacology, 138, 47-56. doi:10.1016/j.neuropharm.2018.05.029
NLM
Falquetto B, Santos LMO, Takakura AC, Mulkey DK, Moreira T dos S. Inhibition of the hypercapnic ventilatory response by adenosine in the retrotrapezoid nucleus in awake rats [Internet]. Neuropharmacology. 2018 ; 138 47-56.[citado 2024 nov. 02 ] Available from: https://doi.org/10.1016/j.neuropharm.2018.05.029
Vancouver
Falquetto B, Santos LMO, Takakura AC, Mulkey DK, Moreira T dos S. Inhibition of the hypercapnic ventilatory response by adenosine in the retrotrapezoid nucleus in awake rats [Internet]. Neuropharmacology. 2018 ; 138 47-56.[citado 2024 nov. 02 ] Available from: https://doi.org/10.1016/j.neuropharm.2018.05.029
Artigo de periodico
Mining a differential sialotranscriptome of Rhipicephalus microplus guides antigen discovery to formulate a vaccine that reduces tick infestations (2017)
Maruyama, Sandra R.; Garcia, Gustavo R.; Teixeira, Felipe Roberti; Brandão, Lucinda Giampietro; Anderson, Jennifer M.; Ribeiro, José M. C.; Valenzuela, Jesus G.; Horackova, Jana; Veríssimo, Cecília J.; Katiki, Luciana M.; Banin, Tamy M.; Zangirolamo, Amanda F.; Gardinassi, Luiz G.; Ferreira, Beatriz Rossetti ; Santos, Isabel Kinney Ferreira de Miranda
Source: Parasites and Vectors. Unidades: EERP, FMRP
Subjects: ADENOSINA, CARRAPATOS, SALIVA, IXÓDIDAE, LINFÓCITOS T
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ABNT
MARUYAMA, Sandra R. et al. Mining a differential sialotranscriptome of Rhipicephalus microplus guides antigen discovery to formulate a vaccine that reduces tick infestations. Parasites and Vectors, v. 10, n. 1, 2017Tradução . . Disponível em: https://doi.org/10.1186/s13071-017-2136-2. Acesso em: 02 nov. 2024.
APA
Maruyama, S. R., Garcia, G. R., Teixeira, F. R., Brandão, L. G., Anderson, J. M., Ribeiro, J. M. C., et al. (2017). Mining a differential sialotranscriptome of Rhipicephalus microplus guides antigen discovery to formulate a vaccine that reduces tick infestations. Parasites and Vectors, 10( 1). doi:10.1186/s13071-017-2136-2
NLM
Maruyama SR, Garcia GR, Teixeira FR, Brandão LG, Anderson JM, Ribeiro JMC, Valenzuela JG, Horackova J, Veríssimo CJ, Katiki LM, Banin TM, Zangirolamo AF, Gardinassi LG, Ferreira BR, Santos IKF de M. Mining a differential sialotranscriptome of Rhipicephalus microplus guides antigen discovery to formulate a vaccine that reduces tick infestations [Internet]. Parasites and Vectors. 2017 ; 10( 1):[citado 2024 nov. 02 ] Available from: https://doi.org/10.1186/s13071-017-2136-2
Vancouver
Maruyama SR, Garcia GR, Teixeira FR, Brandão LG, Anderson JM, Ribeiro JMC, Valenzuela JG, Horackova J, Veríssimo CJ, Katiki LM, Banin TM, Zangirolamo AF, Gardinassi LG, Ferreira BR, Santos IKF de M. Mining a differential sialotranscriptome of Rhipicephalus microplus guides antigen discovery to formulate a vaccine that reduces tick infestations [Internet]. Parasites and Vectors. 2017 ; 10( 1):[citado 2024 nov. 02 ] Available from: https://doi.org/10.1186/s13071-017-2136-2
Artigo de periodico
Fructose 1,6-bisphosphate, a high-energy intermediate of glycolysis, attenuates experimental arthritis by activating anti-inflammatory adenosinergic pathway (2015)
Veras, Flávio P; Peres, Raphael S; Saraiva, André L. L; Pinto, Larissa G; Louzada Júnior, Paulo; Cunha, Thiago Mattar; Paschoal, Jonas Augusto Rizzato; Cunha, Fernando de Queiroz; Alves Filho, José Carlos Farias
Source: Scientific Reports. Unidades: FMRP, FCFRP
Subjects: ADENOSINA, GLICOSE, INFLAMAÇÃO, ARTRITE REUMATOIDE
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ABNT
VERAS, Flávio P et al. Fructose 1,6-bisphosphate, a high-energy intermediate of glycolysis, attenuates experimental arthritis by activating anti-inflammatory adenosinergic pathway. Scientific Reports, v. 5, 2015Tradução . . Disponível em: https://doi.org/10.1038/srep15171. Acesso em: 02 nov. 2024.
APA
Veras, F. P., Peres, R. S., Saraiva, A. L. L., Pinto, L. G., Louzada Júnior, P., Cunha, T. M., et al. (2015). Fructose 1,6-bisphosphate, a high-energy intermediate of glycolysis, attenuates experimental arthritis by activating anti-inflammatory adenosinergic pathway. Scientific Reports, 5. doi:10.1038/srep15171
NLM
Veras FP, Peres RS, Saraiva ALL, Pinto LG, Louzada Júnior P, Cunha TM, Paschoal JAR, Cunha F de Q, Alves Filho JCF. Fructose 1,6-bisphosphate, a high-energy intermediate of glycolysis, attenuates experimental arthritis by activating anti-inflammatory adenosinergic pathway [Internet]. Scientific Reports. 2015 ; 5[citado 2024 nov. 02 ] Available from: https://doi.org/10.1038/srep15171
Vancouver
Veras FP, Peres RS, Saraiva ALL, Pinto LG, Louzada Júnior P, Cunha TM, Paschoal JAR, Cunha F de Q, Alves Filho JCF. Fructose 1,6-bisphosphate, a high-energy intermediate of glycolysis, attenuates experimental arthritis by activating anti-inflammatory adenosinergic pathway [Internet]. Scientific Reports. 2015 ; 5[citado 2024 nov. 02 ] Available from: https://doi.org/10.1038/srep15171
Artigo de periodico
Pharmacological evidence for the mediation og the panicolytic effect of fluoxetine by dorsal periaqueductal gray matter μ-opioid receptors (2015)
Roncon, Camila Marroni; Almada, Rafael Carvalho; Maraschin, Jhonatan Christian; Audi, Elisabeth Aparecida; Zangrossi Junior, Helio; Graeff, Frederico Guilherme; Coimbra, Norberto Cysne
Source: Neuropharmacology. Unidades: FMRP, FFCLRP
Subjects: ADENOSINA, SUBSTÂNCIA CINZENTA PERIAQUEDUTAL, PÂNICO
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ABNT
RONCON, Camila Marroni et al. Pharmacological evidence for the mediation og the panicolytic effect of fluoxetine by dorsal periaqueductal gray matter μ-opioid receptors. Neuropharmacology, v. 99, p. 620-626, 2015Tradução . . Disponível em: https://doi.org/10.1016/j.neuropharm.2015.08.037. Acesso em: 02 nov. 2024.
APA
Roncon, C. M., Almada, R. C., Maraschin, J. C., Audi, E. A., Zangrossi Junior, H., Graeff, F. G., & Coimbra, N. C. (2015). Pharmacological evidence for the mediation og the panicolytic effect of fluoxetine by dorsal periaqueductal gray matter μ-opioid receptors. Neuropharmacology, 99, 620-626. doi:10.1016/j.neuropharm.2015.08.037
NLM
Roncon CM, Almada RC, Maraschin JC, Audi EA, Zangrossi Junior H, Graeff FG, Coimbra NC. Pharmacological evidence for the mediation og the panicolytic effect of fluoxetine by dorsal periaqueductal gray matter μ-opioid receptors [Internet]. Neuropharmacology. 2015 ; 99 620-626.[citado 2024 nov. 02 ] Available from: https://doi.org/10.1016/j.neuropharm.2015.08.037
Vancouver
Roncon CM, Almada RC, Maraschin JC, Audi EA, Zangrossi Junior H, Graeff FG, Coimbra NC. Pharmacological evidence for the mediation og the panicolytic effect of fluoxetine by dorsal periaqueductal gray matter μ-opioid receptors [Internet]. Neuropharmacology. 2015 ; 99 620-626.[citado 2024 nov. 02 ] Available from: https://doi.org/10.1016/j.neuropharm.2015.08.037
Artigo de periodico
Constrictor prostanoids and uridine adenosine tetraphosphate: vascular mediators and therapeutic targets in hypertension and diabetes (2015)
Matsumoto, Takayuki; Goulopoulou, Styliani; Taguchi, Kumiko; Tostes, Rita de Cássia Aleixo; Kobayashi, Tsuneo
Source: British Journal of Pharmacology. Unidade: FMRP
Subjects: ENDOTÉLIO VASCULAR, ADENOSINA, HIPERTENSÃO, DIABETES MELLITUS
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ABNT
MATSUMOTO, Takayuki et al. Constrictor prostanoids and uridine adenosine tetraphosphate: vascular mediators and therapeutic targets in hypertension and diabetes. British Journal of Pharmacology, v. 172, n. 16, p. 3980-4001, 2015Tradução . . Disponível em: https://doi.org/10.1111/bph.13205. Acesso em: 02 nov. 2024.
APA
Matsumoto, T., Goulopoulou, S., Taguchi, K., Tostes, R. de C. A., & Kobayashi, T. (2015). Constrictor prostanoids and uridine adenosine tetraphosphate: vascular mediators and therapeutic targets in hypertension and diabetes. British Journal of Pharmacology, 172( 16), 3980-4001. doi:10.1111/bph.13205
NLM
Matsumoto T, Goulopoulou S, Taguchi K, Tostes R de CA, Kobayashi T. Constrictor prostanoids and uridine adenosine tetraphosphate: vascular mediators and therapeutic targets in hypertension and diabetes [Internet]. British Journal of Pharmacology. 2015 ; 172( 16): 3980-4001.[citado 2024 nov. 02 ] Available from: https://doi.org/10.1111/bph.13205
Vancouver
Matsumoto T, Goulopoulou S, Taguchi K, Tostes R de CA, Kobayashi T. Constrictor prostanoids and uridine adenosine tetraphosphate: vascular mediators and therapeutic targets in hypertension and diabetes [Internet]. British Journal of Pharmacology. 2015 ; 172( 16): 3980-4001.[citado 2024 nov. 02 ] Available from: https://doi.org/10.1111/bph.13205
Artigo de periodico
Adenosine kinase from Schistosoma mansoni: structural basis for the differential incorporation of nucleoside analogues (2013)
Romanello, Larissa; Bachega, José Fernando Ruguiero; Cassago, Alexandre; Brandão Neto, José; De Marco, Ricardo; Garratt, Richard Charles ; Pereira, Humberto d'Muniz
Source: Acta Crystallographica D. Unidade: IFSC
Subjects: ADENOSINA, SCHISTOSOMA MANSONI, NUCLEOSÍDEOS
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ABNT
ROMANELLO, Larissa et al. Adenosine kinase from Schistosoma mansoni: structural basis for the differential incorporation of nucleoside analogues. Acta Crystallographica D, v. 69, n. Ja 2013, p. 126-136, 2013Tradução . . Disponível em: https://doi.org/10.1107/S0907444912044800. Acesso em: 02 nov. 2024.
APA
Romanello, L., Bachega, J. F. R., Cassago, A., Brandão Neto, J., De Marco, R., Garratt, R. C., & Pereira, H. d'M. (2013). Adenosine kinase from Schistosoma mansoni: structural basis for the differential incorporation of nucleoside analogues. Acta Crystallographica D, 69( Ja 2013), 126-136. doi:10.1107/S0907444912044800
NLM
Romanello L, Bachega JFR, Cassago A, Brandão Neto J, De Marco R, Garratt RC, Pereira H d'M. Adenosine kinase from Schistosoma mansoni: structural basis for the differential incorporation of nucleoside analogues [Internet]. Acta Crystallographica D. 2013 ; 69( Ja 2013): 126-136.[citado 2024 nov. 02 ] Available from: https://doi.org/10.1107/S0907444912044800
Vancouver
Romanello L, Bachega JFR, Cassago A, Brandão Neto J, De Marco R, Garratt RC, Pereira H d'M. Adenosine kinase from Schistosoma mansoni: structural basis for the differential incorporation of nucleoside analogues [Internet]. Acta Crystallographica D. 2013 ; 69( Ja 2013): 126-136.[citado 2024 nov. 02 ] Available from: https://doi.org/10.1107/S0907444912044800

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