ReP USP - Resultado da busca

Artigo de periodico
Single immunizations of self-amplifying or non-replicating mRNA-LNP vaccines control HPV-associated tumors in mice (2023)
Silva, Jamile Ramos da ; Rodrigues, Karine Bitencourt ; Pelegrin, Guilherme Formoso ; Sales, Natiely Silva ; Muramatsu, Hiromi ; Silva, Mariângela de Oliveira ; Porchia, Bruna Felício Milazzotto Maldonado ; Moreno, Ana Carolina Ramos ; Aps, Luana Raposo M. M. ; Carvalho, Aléxia Adrianne Venceslau ; Tombácz, István ; Fotoran, Wesley Luzetti ; Karikó, Katalin ; Lin, Paulo J. C.; Tam, Ying K. ; Diniz, Mariana de Oliveira ; Pardi, Norbert ; Ferreira, Luís Carlos de Souza
Source: Science Translational Medicine. Unidades: ICB, BIOTECNOLOGIA
Subjects: MICROBIOLOGIA, VACINAS VIRAIS, MODELOS ANIMAIS DE DOENÇAS, CAMUNDONGOS, PAPILLOMAVIRUS, HPV, INFECÇÕES POR PAPILLOMAVIRUS, NEOPLASIAS DO COLO UTERINO, PROTEÍNAS RECOMBINANTES, NANOPARTÍCULAS, NUCLEOSÍDEOS, GLICOPROTEÍNAS
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ABNT
SILVA, Jamile Ramos da et al. Single immunizations of self-amplifying or non-replicating mRNA-LNP vaccines control HPV-associated tumors in mice. Science Translational Medicine, v. 15, n. 686, p. 1-18, 2023Tradução . . Disponível em: https://doi.org/10.1126/scitranslmed.abn3464. Acesso em: 01 nov. 2024.
APA
Silva, J. R. da, Rodrigues, K. B., Pelegrin, G. F., Sales, N. S., Muramatsu, H., Silva, M. de O., et al. (2023). Single immunizations of self-amplifying or non-replicating mRNA-LNP vaccines control HPV-associated tumors in mice. Science Translational Medicine, 15( 686), 1-18. doi:10.1126/scitranslmed.abn3464
NLM
Silva JR da, Rodrigues KB, Pelegrin GF, Sales NS, Muramatsu H, Silva M de O, Porchia BFMM, Moreno ACR, Aps LRMM, Carvalho AAV, Tombácz I, Fotoran WL, Karikó K, Lin PJC, Tam YK, Diniz M de O, Pardi N, Ferreira LC de S. Single immunizations of self-amplifying or non-replicating mRNA-LNP vaccines control HPV-associated tumors in mice [Internet]. Science Translational Medicine. 2023 ; 15( 686): 1-18.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1126/scitranslmed.abn3464
Vancouver
Silva JR da, Rodrigues KB, Pelegrin GF, Sales NS, Muramatsu H, Silva M de O, Porchia BFMM, Moreno ACR, Aps LRMM, Carvalho AAV, Tombácz I, Fotoran WL, Karikó K, Lin PJC, Tam YK, Diniz M de O, Pardi N, Ferreira LC de S. Single immunizations of self-amplifying or non-replicating mRNA-LNP vaccines control HPV-associated tumors in mice [Internet]. Science Translational Medicine. 2023 ; 15( 686): 1-18.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1126/scitranslmed.abn3464
Artigo de periodico
Fetal lung underdevelopment is rescued by administration of amniotic fluid stem cell extracellular vesicles in rodents (2021)
Antounians, Lina; Catania, Vincenzo D.; Montalva, Louise; Liu, Benjamin D.; Hou, Huayun; Chan, Cadia; Matei, Andreea C.; Tzanetakis, Areti; Li, Bo; Figueira, Rebeca L.; Costa, Karina Miura da ; Wong, Amy P.; Mitchell, Robert; David, Anna L.; Patel, Ketan; De Coppi, Paolo; Sbragia, Lourenço; Wilson, Michael D.; Rossant, Janet; Zani, Augusto
Source: Science Translational Medicine. Unidade: FMRP
Subjects: BIOLOGIA CELULAR, PULMÃO, RODENTIA, CÉLULAS-TRONCO
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ABNT
ANTOUNIANS, Lina et al. Fetal lung underdevelopment is rescued by administration of amniotic fluid stem cell extracellular vesicles in rodents. Science Translational Medicine, v. 13, n. 590, 2021Tradução . . Disponível em: https://doi.org/10.1126/scitranslmed.aax5941. Acesso em: 01 nov. 2024.
APA
Antounians, L., Catania, V. D., Montalva, L., Liu, B. D., Hou, H., Chan, C., et al. (2021). Fetal lung underdevelopment is rescued by administration of amniotic fluid stem cell extracellular vesicles in rodents. Science Translational Medicine, 13( 590). doi:10.1126/scitranslmed.aax5941
NLM
Antounians L, Catania VD, Montalva L, Liu BD, Hou H, Chan C, Matei AC, Tzanetakis A, Li B, Figueira RL, Costa KM da, Wong AP, Mitchell R, David AL, Patel K, De Coppi P, Sbragia L, Wilson MD, Rossant J, Zani A. Fetal lung underdevelopment is rescued by administration of amniotic fluid stem cell extracellular vesicles in rodents [Internet]. Science Translational Medicine. 2021 ; 13( 590):[citado 2024 nov. 01 ] Available from: https://doi.org/10.1126/scitranslmed.aax5941
Vancouver
Antounians L, Catania VD, Montalva L, Liu BD, Hou H, Chan C, Matei AC, Tzanetakis A, Li B, Figueira RL, Costa KM da, Wong AP, Mitchell R, David AL, Patel K, De Coppi P, Sbragia L, Wilson MD, Rossant J, Zani A. Fetal lung underdevelopment is rescued by administration of amniotic fluid stem cell extracellular vesicles in rodents [Internet]. Science Translational Medicine. 2021 ; 13( 590):[citado 2024 nov. 01 ] Available from: https://doi.org/10.1126/scitranslmed.aax5941
Artigo de periodico
CRISPR-engineered human brown-like adipocytes prevent diet-induced obesity and ameliorate metabolic syndrome in mice (2020)
Wang, Chih-Hao; Lundh, Morten; Fu, Accalia; Kriszt, Rókus; Huang, Tian Lian; Lynes, Matthew D.; Leiria, Luiz Osório Silveira ; Shamsi, Farnaz; Darcy, Justin; Greenwood, Bennett P.; Narain, Niven R.; Tolstikov, Vladimir; Smith, Kyle L.; Emanuelli, Brice; Chang, Young-Tae; Hagen, Susan; Danial, Nika N.; Kiebish, Michael A.; Tseng, Yu-Hua
Source: Science Translational Medicine. Unidade: FMRP
Subjects: TECIDO ADIPOSO, DIETA, OBESIDADE, TERMOGÊNESE
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ABNT
WANG, Chih-Hao et al. CRISPR-engineered human brown-like adipocytes prevent diet-induced obesity and ameliorate metabolic syndrome in mice. Science Translational Medicine, v. 12, n. 558, 2020Tradução . . Disponível em: https://doi.org/10.1126/scitranslmed.aaz8664. Acesso em: 01 nov. 2024.
APA
Wang, C. -H., Lundh, M., Fu, A., Kriszt, R., Huang, T. L., Lynes, M. D., et al. (2020). CRISPR-engineered human brown-like adipocytes prevent diet-induced obesity and ameliorate metabolic syndrome in mice. Science Translational Medicine, 12( 558). doi:10.1126/scitranslmed.aaz8664
NLM
Wang C-H, Lundh M, Fu A, Kriszt R, Huang TL, Lynes MD, Leiria LOS, Shamsi F, Darcy J, Greenwood BP, Narain NR, Tolstikov V, Smith KL, Emanuelli B, Chang Y-T, Hagen S, Danial NN, Kiebish MA, Tseng Y-H. CRISPR-engineered human brown-like adipocytes prevent diet-induced obesity and ameliorate metabolic syndrome in mice [Internet]. Science Translational Medicine. 2020 ; 12( 558):[citado 2024 nov. 01 ] Available from: https://doi.org/10.1126/scitranslmed.aaz8664
Vancouver
Wang C-H, Lundh M, Fu A, Kriszt R, Huang TL, Lynes MD, Leiria LOS, Shamsi F, Darcy J, Greenwood BP, Narain NR, Tolstikov V, Smith KL, Emanuelli B, Chang Y-T, Hagen S, Danial NN, Kiebish MA, Tseng Y-H. CRISPR-engineered human brown-like adipocytes prevent diet-induced obesity and ameliorate metabolic syndrome in mice [Internet]. Science Translational Medicine. 2020 ; 12( 558):[citado 2024 nov. 01 ] Available from: https://doi.org/10.1126/scitranslmed.aaz8664
Artigo de periodico
The peptidomimetic vasotide targets two retinal VEGF receptors and reduces pathological angiogenesis in murine and nonhuman primate models of retinal disease (2015)
Sidman, Richard L; Li, Jianxue; Lawrence, Matthew; Hu, Wenzheng; Musso, Gary F; Giordano, Ricardo José ; Cardó-Vila, Marina; Pasqualini, Renata; Arap, Wadih
Source: Science Translational Medicine. Unidade: IQ
Subjects: DOENÇAS RETINIANAS, RECEPTORES
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ABNT
SIDMAN, Richard L et al. The peptidomimetic vasotide targets two retinal VEGF receptors and reduces pathological angiogenesis in murine and nonhuman primate models of retinal disease. Science Translational Medicine, v. 7, p. 1-15 art. 309, 2015Tradução . . Disponível em: https://doi.org/10.1126/scitranslmed.aac4882. Acesso em: 01 nov. 2024.
APA
Sidman, R. L., Li, J., Lawrence, M., Hu, W., Musso, G. F., Giordano, R. J., et al. (2015). The peptidomimetic vasotide targets two retinal VEGF receptors and reduces pathological angiogenesis in murine and nonhuman primate models of retinal disease. Science Translational Medicine, 7, 1-15 art. 309. doi:10.1126/scitranslmed.aac4882
NLM
Sidman RL, Li J, Lawrence M, Hu W, Musso GF, Giordano RJ, Cardó-Vila M, Pasqualini R, Arap W. The peptidomimetic vasotide targets two retinal VEGF receptors and reduces pathological angiogenesis in murine and nonhuman primate models of retinal disease [Internet]. Science Translational Medicine. 2015 ; 7 1-15 art. 309.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1126/scitranslmed.aac4882
Vancouver
Sidman RL, Li J, Lawrence M, Hu W, Musso GF, Giordano RJ, Cardó-Vila M, Pasqualini R, Arap W. The peptidomimetic vasotide targets two retinal VEGF receptors and reduces pathological angiogenesis in murine and nonhuman primate models of retinal disease [Internet]. Science Translational Medicine. 2015 ; 7 1-15 art. 309.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1126/scitranslmed.aac4882
Artigo de periodico
A Wnt-TGFβ2 axis induces a fibrogenic program in muscle stem cells from dystrophic mice (2014)
Biressi, Stefano; Miyabara, Elen Haruka ; Gopinath, Suchitra D.; Carlig, Poppy M. M.; Rando, Thomas A.
Source: Science Translational Medicine. Unidade: ICB
Assunto: ANATOMIA
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ABNT
BIRESSI, Stefano et al. A Wnt-TGFβ2 axis induces a fibrogenic program in muscle stem cells from dystrophic mice. Science Translational Medicine, v. 6, n. 267, p. 1-12, 2014Tradução . . Disponível em: https://doi.org/10.1126/scitranslmed.3008411. Acesso em: 01 nov. 2024.
APA
Biressi, S., Miyabara, E. H., Gopinath, S. D., Carlig, P. M. M., & Rando, T. A. (2014). A Wnt-TGFβ2 axis induces a fibrogenic program in muscle stem cells from dystrophic mice. Science Translational Medicine, 6( 267), 1-12. doi:10.1126/scitranslmed.3008411
NLM
Biressi S, Miyabara EH, Gopinath SD, Carlig PMM, Rando TA. A Wnt-TGFβ2 axis induces a fibrogenic program in muscle stem cells from dystrophic mice [Internet]. Science Translational Medicine. 2014 ; 6( 267): 1-12.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1126/scitranslmed.3008411
Vancouver
Biressi S, Miyabara EH, Gopinath SD, Carlig PMM, Rando TA. A Wnt-TGFβ2 axis induces a fibrogenic program in muscle stem cells from dystrophic mice [Internet]. Science Translational Medicine. 2014 ; 6( 267): 1-12.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1126/scitranslmed.3008411
Artigo de periodico
Evaluation of DNA from the Papanicolaou Test to Detect Ovarian and Endometrial Cancers (2013)
Kinde, Isaac; Bettegowda, Chetan; Wang, Yuxuan; Wu, Jian; Agrawal, Nishant; Shih, Ie-Ming; Kurman, Robert; Dao, Fanny; Levine, Douglas A.; Giuntoli, Robert; Roden, Richard; Eshleman, James R.; Carvalho, Jesus Paula; Marie, Suely Kazue Nagahashi; Papadopoulos, Nickolas; Kinzler, Kenneth W.; Vogelstein, Bert; Diaz Jr., Luis A.
Source: Science Translational Medicine. Unidade: FM
Subjects: DNA (AVALIAÇÃO), GENÓTIPOS, NEOPLASIAS OVARIANAS, ENDOMÉTRIO (PATOLOGIA), NEOPLASIAS UTERINAS
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ABNT
KINDE, Isaac et al. Evaluation of DNA from the Papanicolaou Test to Detect Ovarian and Endometrial Cancers. Science Translational Medicine, v. 5, n. 167, p. 167ra4, 2013Tradução . . Disponível em: https://doi.org/10.1126/scitranslmed.3004952. Acesso em: 01 nov. 2024.
APA
Kinde, I., Bettegowda, C., Wang, Y., Wu, J., Agrawal, N., Shih, I. -M., et al. (2013). Evaluation of DNA from the Papanicolaou Test to Detect Ovarian and Endometrial Cancers. Science Translational Medicine, 5( 167), 167ra4. doi:10.1126/scitranslmed.3004952
NLM
Kinde I, Bettegowda C, Wang Y, Wu J, Agrawal N, Shih I-M, Kurman R, Dao F, Levine DA, Giuntoli R, Roden R, Eshleman JR, Carvalho JP, Marie SKN, Papadopoulos N, Kinzler KW, Vogelstein B, Diaz Jr. LA. Evaluation of DNA from the Papanicolaou Test to Detect Ovarian and Endometrial Cancers [Internet]. Science Translational Medicine. 2013 ; 5( 167): 167ra4.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1126/scitranslmed.3004952
Vancouver
Kinde I, Bettegowda C, Wang Y, Wu J, Agrawal N, Shih I-M, Kurman R, Dao F, Levine DA, Giuntoli R, Roden R, Eshleman JR, Carvalho JP, Marie SKN, Papadopoulos N, Kinzler KW, Vogelstein B, Diaz Jr. LA. Evaluation of DNA from the Papanicolaou Test to Detect Ovarian and Endometrial Cancers [Internet]. Science Translational Medicine. 2013 ; 5( 167): 167ra4.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1126/scitranslmed.3004952
Artigo de periodico
Challenges in Using Stem Cells for Cardiac Repair (2010)
Mummery, Christine L.; Davis, Richard P.; Krieger, José Eduardo
Source: Science Translational Medicine. Unidade: FM
Subjects: CÉLULAS-TRONCO (USO TERAPÊUTICO), PROCEDIMENTOS CIRÚRGICOS CARDÍACOS
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ABNT
MUMMERY, Christine L. e DAVIS, Richard P. e KRIEGER, José Eduardo. Challenges in Using Stem Cells for Cardiac Repair. Science Translational Medicine, v. 2, n. 27, p. 27ps17, 2010Tradução . . Disponível em: https://doi.org/10.1126/scitranslmed.3000558. Acesso em: 01 nov. 2024.
APA
Mummery, C. L., Davis, R. P., & Krieger, J. E. (2010). Challenges in Using Stem Cells for Cardiac Repair. Science Translational Medicine, 2( 27), 27ps17. doi:10.1126/scitranslmed.3000558
NLM
Mummery CL, Davis RP, Krieger JE. Challenges in Using Stem Cells for Cardiac Repair [Internet]. Science Translational Medicine. 2010 ; 2( 27): 27ps17.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1126/scitranslmed.3000558
Vancouver
Mummery CL, Davis RP, Krieger JE. Challenges in Using Stem Cells for Cardiac Repair [Internet]. Science Translational Medicine. 2010 ; 2( 27): 27ps17.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1126/scitranslmed.3000558

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