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Artigo de periodico
Sterilized human skin graft with a dose of 25 kGy provides a privileged immune and collagen microenvironment in the adhesion of Nude mice wounds (2022)
Miranda, Jurandir Tomaz de; Bringel, Fabiana de Andrade; Velosa, Ana Paula Pereira; Protocevich, Veronica; Fernezlian, Sandra de Morais ; Silva, Pedro Leme; Capelozzi, Vera Luiza ; Mathor, Monica Beatriz; Teodoro, Walcy Rosolia
Fonte: PLOS ONE. Unidade: FM
Assuntos: METALOPROTEINASES, FERIMENTOS EM ANIMAL, PELES, CICATRIZAÇÃO
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ABNT
MIRANDA, Jurandir Tomaz de et al. Sterilized human skin graft with a dose of 25 kGy provides a privileged immune and collagen microenvironment in the adhesion of Nude mice wounds. PLOS ONE, v. 17, n. 1, 2022Tradução . . Disponível em: https://doi.org/10.1371/journal.pone.0262532. Acesso em: 21 ago. 2024.
APA
Miranda, J. T. de, Bringel, F. de A., Velosa, A. P. P., Protocevich, V., Fernezlian, S. de M., Silva, P. L., et al. (2022). Sterilized human skin graft with a dose of 25 kGy provides a privileged immune and collagen microenvironment in the adhesion of Nude mice wounds. PLOS ONE, 17( 1). doi:10.1371/journal.pone.0262532
NLM
Miranda JT de, Bringel F de A, Velosa APP, Protocevich V, Fernezlian S de M, Silva PL, Capelozzi VL, Mathor MB, Teodoro WR. Sterilized human skin graft with a dose of 25 kGy provides a privileged immune and collagen microenvironment in the adhesion of Nude mice wounds [Internet]. PLOS ONE. 2022 ; 17( 1):[citado 2024 ago. 21 ] Available from: https://doi.org/10.1371/journal.pone.0262532
Vancouver
Miranda JT de, Bringel F de A, Velosa APP, Protocevich V, Fernezlian S de M, Silva PL, Capelozzi VL, Mathor MB, Teodoro WR. Sterilized human skin graft with a dose of 25 kGy provides a privileged immune and collagen microenvironment in the adhesion of Nude mice wounds [Internet]. PLOS ONE. 2022 ; 17( 1):[citado 2024 ago. 21 ] Available from: https://doi.org/10.1371/journal.pone.0262532
Artigo de periodico
Circulating plasma miRNA and clinical/hemodynamic characteristics provide additional predictive information about acute pulmonary thromboembolism, chronic thromboembolic pulmonary hypertension and idiopathic pulmonary hypertension (2021)
Fabro, Alexandre Todorovic ; Machado-Rugolo, Juliana ; Baldavira, Camila Machado ; Prieto, Tabatha Gutierrez ; Farhat, Cecilia; Mangone, Flavia Regina Rotea; Batah, Sabrina Setembre ; Cruvinel, Heloísa Resende; Alda, Maiara Almeida; Monteiro, Jhonatas Sirino ; Padua, Adriana Inácio de; Morais, Sirlei Siani; Oliveira, Rogério Antônio de ; Santos, Marcel Koenigkam ; Martinez, José Antônio Baddini ; Setubal, João Carlos ; Rainho, Cláudia Aparecida ; Yoo, Hugo Hyung Bok ; Silva, Pedro Leme; Nagai, Maria Aparecida ; Capelozzi, Vera Luiza
Fonte: Frontiers in Pharmacology. Unidades: FMRP, IQ, FM, BIOINFORMÁTICA
Assuntos: MICRORNAS, SEQUENCIAMENTO GENÉTICO, PLASMA, HIPERTENSÃO PULMONAR, TROMBOEMBOLISMO
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FABRO, Alexandre Todorovic et al. Circulating plasma miRNA and clinical/hemodynamic characteristics provide additional predictive information about acute pulmonary thromboembolism, chronic thromboembolic pulmonary hypertension and idiopathic pulmonary hypertension. Frontiers in Pharmacology, v. 12, p. 1-12 art. 648769, 2021Tradução . . Disponível em: https://doi.org/10.3389/fphar.2021.648769. Acesso em: 21 ago. 2024.
APA
Fabro, A. T., Machado-Rugolo, J., Baldavira, C. M., Prieto, T. G., Farhat, C., Mangone, F. R. R., et al. (2021). Circulating plasma miRNA and clinical/hemodynamic characteristics provide additional predictive information about acute pulmonary thromboembolism, chronic thromboembolic pulmonary hypertension and idiopathic pulmonary hypertension. Frontiers in Pharmacology, 12, 1-12 art. 648769. doi:10.3389/fphar.2021.648769
NLM
Fabro AT, Machado-Rugolo J, Baldavira CM, Prieto TG, Farhat C, Mangone FRR, Batah SS, Cruvinel HR, Alda M A, Monteiro JS, Padua AI de, Morais SS, Oliveira RA de, Santos MK, Martinez JAB, Setubal JC, Rainho CA, Yoo HHB, Silva PL, Nagai MA, Capelozzi VL. Circulating plasma miRNA and clinical/hemodynamic characteristics provide additional predictive information about acute pulmonary thromboembolism, chronic thromboembolic pulmonary hypertension and idiopathic pulmonary hypertension [Internet]. Frontiers in Pharmacology. 2021 ; 12 1-12 art. 648769.[citado 2024 ago. 21 ] Available from: https://doi.org/10.3389/fphar.2021.648769
Vancouver
Fabro AT, Machado-Rugolo J, Baldavira CM, Prieto TG, Farhat C, Mangone FRR, Batah SS, Cruvinel HR, Alda M A, Monteiro JS, Padua AI de, Morais SS, Oliveira RA de, Santos MK, Martinez JAB, Setubal JC, Rainho CA, Yoo HHB, Silva PL, Nagai MA, Capelozzi VL. Circulating plasma miRNA and clinical/hemodynamic characteristics provide additional predictive information about acute pulmonary thromboembolism, chronic thromboembolic pulmonary hypertension and idiopathic pulmonary hypertension [Internet]. Frontiers in Pharmacology. 2021 ; 12 1-12 art. 648769.[citado 2024 ago. 21 ] Available from: https://doi.org/10.3389/fphar.2021.648769
Artigo de periodico
In situ evidence of collagen V and signaling pathway of found inflammatory zone 1 (FIZZ1) is associated with silicotic granuloma in lung mice (2020)
Martins, Vanessa; Silva, Adriana Lopes da; Teodoro, Walcy Paganelli Rosolia ; Velosa, Ana Paula Pereira; Balancin, Marcelo Luiz; Cruz, Fernanda Ferreira; Silva, Pedro Leme; Rocco, Patricia Rieken Macedo; Capelozzi, Vera Luiza
Fonte: Pathology research and practice. Unidade: FM
Assuntos: DIFERENCIAÇÃO CELULAR, COLÁGENO, FIBROBLASTOS, GRANULOMA, INFLAMAÇÃO, CAMUNDONGOS, FIBROSE PULMONAR
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ABNT
MARTINS, Vanessa et al. In situ evidence of collagen V and signaling pathway of found inflammatory zone 1 (FIZZ1) is associated with silicotic granuloma in lung mice. Pathology research and practice, v. 216, n. 9, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.prp.2020.153094. Acesso em: 21 ago. 2024.
APA
Martins, V., Silva, A. L. da, Teodoro, W. P. R., Velosa, A. P. P., Balancin, M. L., Cruz, F. F., et al. (2020). In situ evidence of collagen V and signaling pathway of found inflammatory zone 1 (FIZZ1) is associated with silicotic granuloma in lung mice. Pathology research and practice, 216( 9). doi:10.1016/j.prp.2020.153094
NLM
Martins V, Silva AL da, Teodoro WPR, Velosa APP, Balancin ML, Cruz FF, Silva PL, Rocco PRM, Capelozzi VL. In situ evidence of collagen V and signaling pathway of found inflammatory zone 1 (FIZZ1) is associated with silicotic granuloma in lung mice [Internet]. Pathology research and practice. 2020 ; 216( 9):[citado 2024 ago. 21 ] Available from: https://doi.org/10.1016/j.prp.2020.153094
Vancouver
Martins V, Silva AL da, Teodoro WPR, Velosa APP, Balancin ML, Cruz FF, Silva PL, Rocco PRM, Capelozzi VL. In situ evidence of collagen V and signaling pathway of found inflammatory zone 1 (FIZZ1) is associated with silicotic granuloma in lung mice [Internet]. Pathology research and practice. 2020 ; 216( 9):[citado 2024 ago. 21 ] Available from: https://doi.org/10.1016/j.prp.2020.153094
Artigo de periodico
Endotoxin-induced emphysema exacerbation: a novel model of chronic obstructive pulmonary disease exacerbations causing cardiopulmonary impairment and diaphragm dysfunction (2019)
Oliveira, Milena Vasconcellos de; Rocha, Nazareth de Novaes; Santos, Raquel Souza; Rocco, Marcella Rieken Macedo; Magalhaes, Raquel Ferreira de; Silva, Johnatas Dutra; Souza, Sergio Augusto Lopes; Capelozzi, Vera Luiza; Pelosi, Paolo; Silva, Pedro Leme
Fonte: Frontiers in physiology. Unidade: FM
Assuntos: PULMÃO, ARTÉRIA PULMONAR, ENFISEMA PULMONAR
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ABNT
OLIVEIRA, Milena Vasconcellos de et al. Endotoxin-induced emphysema exacerbation: a novel model of chronic obstructive pulmonary disease exacerbations causing cardiopulmonary impairment and diaphragm dysfunction. Frontiers in physiology, v. 10, 2019Tradução . . Disponível em: https://doi.org/10.3389/fphys.2019.00664. Acesso em: 21 ago. 2024.
APA
Oliveira, M. V. de, Rocha, N. de N., Santos, R. S., Rocco, M. R. M., Magalhaes, R. F. de, Silva, J. D., et al. (2019). Endotoxin-induced emphysema exacerbation: a novel model of chronic obstructive pulmonary disease exacerbations causing cardiopulmonary impairment and diaphragm dysfunction. Frontiers in physiology, 10. doi:10.3389/fphys.2019.00664
NLM
Oliveira MV de, Rocha N de N, Santos RS, Rocco MRM, Magalhaes RF de, Silva JD, Souza SAL, Capelozzi VL, Pelosi P, Silva PL. Endotoxin-induced emphysema exacerbation: a novel model of chronic obstructive pulmonary disease exacerbations causing cardiopulmonary impairment and diaphragm dysfunction [Internet]. Frontiers in physiology. 2019 ; 10[citado 2024 ago. 21 ] Available from: https://doi.org/10.3389/fphys.2019.00664
Vancouver
Oliveira MV de, Rocha N de N, Santos RS, Rocco MRM, Magalhaes RF de, Silva JD, Souza SAL, Capelozzi VL, Pelosi P, Silva PL. Endotoxin-induced emphysema exacerbation: a novel model of chronic obstructive pulmonary disease exacerbations causing cardiopulmonary impairment and diaphragm dysfunction [Internet]. Frontiers in physiology. 2019 ; 10[citado 2024 ago. 21 ] Available from: https://doi.org/10.3389/fphys.2019.00664
Artigo de periodico
Biological response to time-controlled adaptive ventilation depends on acute respiratory distress syndrome etiology (2018)
Silva, Pedro Leme; Capelozzi, Vera Luiza
Fonte: Critical care medicine. Unidade: FM
Assuntos: PULMÃO, MATRIZ EXTRACELULAR, PROTEOGLICANAS, SÍNDROME DO DESCONFORTO RESPIRATÓRIO EM ADULTOS, EXPRESSÃO GÊNICA
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SILVA, Pedro Leme e CAPELOZZI, Vera Luiza. Biological response to time-controlled adaptive ventilation depends on acute respiratory distress syndrome etiology. Critical care medicine, v. 46, n. 6, p. E609-E617, 2018Tradução . . Disponível em: https://doi.org/10.1097/CCM.0000000000003078. Acesso em: 21 ago. 2024.
APA
Silva, P. L., & Capelozzi, V. L. (2018). Biological response to time-controlled adaptive ventilation depends on acute respiratory distress syndrome etiology. Critical care medicine, 46( 6), E609-E617. doi:10.1097/CCM.0000000000003078
NLM
Silva PL, Capelozzi VL. Biological response to time-controlled adaptive ventilation depends on acute respiratory distress syndrome etiology [Internet]. Critical care medicine. 2018 ; 46( 6): E609-E617.[citado 2024 ago. 21 ] Available from: https://doi.org/10.1097/CCM.0000000000003078
Vancouver
Silva PL, Capelozzi VL. Biological response to time-controlled adaptive ventilation depends on acute respiratory distress syndrome etiology [Internet]. Critical care medicine. 2018 ; 46( 6): E609-E617.[citado 2024 ago. 21 ] Available from: https://doi.org/10.1097/CCM.0000000000003078
Artigo de periodico
Ghrelin therapy improves lung and cardiovascular function in experimental emphysema (2017)
Rocha, Nazareth de Novaes; Oliveira, Milena Vasconcellos de; Braga, Cássio Lisboa; Guimarães, Gabriela; Maia, Lígia de Albuquerque; Padilha, Gisele de Araújo; Silva, Johnatas Dutra; Takiya, Christina Maeda; Capelozzi, Vera Luiza; Silva, Pedro Leme; Rocco, Patricia Rieken Macedo
Fonte: Respiratory research. Unidade: FM
Assuntos: ENFISEMA PULMONAR, GRELINA, PULMÃO, CORAÇÃO
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ABNT
ROCHA, Nazareth de Novaes et al. Ghrelin therapy improves lung and cardiovascular function in experimental emphysema. Respiratory research, v. 18, 2017Tradução . . Disponível em: https://doi.org/10.1186/s12931-017-0668-9. Acesso em: 21 ago. 2024.
APA
Rocha, N. de N., Oliveira, M. V. de, Braga, C. L., Guimarães, G., Maia, L. de A., Padilha, G. de A., et al. (2017). Ghrelin therapy improves lung and cardiovascular function in experimental emphysema. Respiratory research, 18. doi:10.1186/s12931-017-0668-9
NLM
Rocha N de N, Oliveira MV de, Braga CL, Guimarães G, Maia L de A, Padilha G de A, Silva JD, Takiya CM, Capelozzi VL, Silva PL, Rocco PRM. Ghrelin therapy improves lung and cardiovascular function in experimental emphysema [Internet]. Respiratory research. 2017 ; 18[citado 2024 ago. 21 ] Available from: https://doi.org/10.1186/s12931-017-0668-9
Vancouver
Rocha N de N, Oliveira MV de, Braga CL, Guimarães G, Maia L de A, Padilha G de A, Silva JD, Takiya CM, Capelozzi VL, Silva PL, Rocco PRM. Ghrelin therapy improves lung and cardiovascular function in experimental emphysema [Internet]. Respiratory research. 2017 ; 18[citado 2024 ago. 21 ] Available from: https://doi.org/10.1186/s12931-017-0668-9
Artigo de periodico
Impact of Bacillus Calmette–Guérin Moreau vaccine on lung remodeling in experimental asthma (2013)
Samary, Cynthia dos Santos; Antunes, Mariana Alves; Silva, Johnatas Dutra; Silva, Adriana Lopes da; Araújo, Carla Cristina de; Bakker-Abreu, Ilka; Diaz, Bruno Lourenço; Fernezlian, Sandra; Parra, Edwin Roger; Capelozzi, Vera Luiza; Silva, Pedro Leme; Silva, José Roberto Lapa e; Rocco, Patricia Rieken Macedo
Fonte: Respiratory physiology & neurobiology. Unidade: FM
Assuntos: MATRIZ EXTRACELULAR, ASMA, VACINAS VIRAIS, TUBERCULOSE PULMONAR (IMUNOLOGIA;VIROLOGIA), DOENÇA CRÔNICA
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SAMARY, Cynthia dos Santos et al. Impact of Bacillus Calmette–Guérin Moreau vaccine on lung remodeling in experimental asthma. Respiratory physiology & neurobiology, v. 189, n. 3, p. 614-623, 2013Tradução . . Disponível em: https://doi.org/10.1016/j.resp.2013.07.025. Acesso em: 21 ago. 2024.
APA
Samary, C. dos S., Antunes, M. A., Silva, J. D., Silva, A. L. da, Araújo, C. C. de, Bakker-Abreu, I., et al. (2013). Impact of Bacillus Calmette–Guérin Moreau vaccine on lung remodeling in experimental asthma. Respiratory physiology & neurobiology, 189( 3), 614-623. doi:10.1016/j.resp.2013.07.025
NLM
Samary C dos S, Antunes MA, Silva JD, Silva AL da, Araújo CC de, Bakker-Abreu I, Diaz BL, Fernezlian S, Parra ER, Capelozzi VL, Silva PL, Silva JRL e, Rocco PRM. Impact of Bacillus Calmette–Guérin Moreau vaccine on lung remodeling in experimental asthma [Internet]. Respiratory physiology & neurobiology. 2013 ; 189( 3): 614-623.[citado 2024 ago. 21 ] Available from: https://doi.org/10.1016/j.resp.2013.07.025
Vancouver
Samary C dos S, Antunes MA, Silva JD, Silva AL da, Araújo CC de, Bakker-Abreu I, Diaz BL, Fernezlian S, Parra ER, Capelozzi VL, Silva PL, Silva JRL e, Rocco PRM. Impact of Bacillus Calmette–Guérin Moreau vaccine on lung remodeling in experimental asthma [Internet]. Respiratory physiology & neurobiology. 2013 ; 189( 3): 614-623.[citado 2024 ago. 21 ] Available from: https://doi.org/10.1016/j.resp.2013.07.025

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