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Artigo de periodico
Perfluorooctanoate (PFOA) cell-autonomously promotes thermogenic and adipogenic differentiation of brown and white adipocytes (2024)
Reckziegel, Patricia ; Petrovic, Natasa ; Cannon, Barbara; Nedergaard, Jan
Source: Ecotoxicology and Environmental Safety. Unidade: FCF
Subjects: TERMOGÊNESE, POLUIÇÃO AMBIENTAL
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ABNT
RECKZIEGEL, Patricia et al. Perfluorooctanoate (PFOA) cell-autonomously promotes thermogenic and adipogenic differentiation of brown and white adipocytes. Ecotoxicology and Environmental Safety, v. 271, p. 1-12 art. 115955, 2024Tradução . . Disponível em: https://dx.doi.org/10.1016/j.ecoenv.2024.115955. Acesso em: 10 jun. 2024.
APA
Reckziegel, P., Petrovic, N., Cannon, B., & Nedergaard, J. (2024). Perfluorooctanoate (PFOA) cell-autonomously promotes thermogenic and adipogenic differentiation of brown and white adipocytes. Ecotoxicology and Environmental Safety, 271, 1-12 art. 115955. doi:10.1016/j.ecoenv.2024.115955
NLM
Reckziegel P, Petrovic N, Cannon B, Nedergaard J. Perfluorooctanoate (PFOA) cell-autonomously promotes thermogenic and adipogenic differentiation of brown and white adipocytes [Internet]. Ecotoxicology and Environmental Safety. 2024 ; 271 1-12 art. 115955.[citado 2024 jun. 10 ] Available from: https://dx.doi.org/10.1016/j.ecoenv.2024.115955
Vancouver
Reckziegel P, Petrovic N, Cannon B, Nedergaard J. Perfluorooctanoate (PFOA) cell-autonomously promotes thermogenic and adipogenic differentiation of brown and white adipocytes [Internet]. Ecotoxicology and Environmental Safety. 2024 ; 271 1-12 art. 115955.[citado 2024 jun. 10 ] Available from: https://dx.doi.org/10.1016/j.ecoenv.2024.115955
Artigo de periodico
Carcinogenicity of perfluorooctanoic acid and perfluorooctanesulfonic acid (2024)
Zahm, Shelia ; Bonde, Jens Peter ; Chiu, Weihsueh A ; Hoppin, Jane ; Kanno, Jun ; Abdallah, Mohamed; Blystone, Chad R ; Calkins, Miriam M ; Dong, Guang Hui ; Dorman, David C; Fry, Rebecca; Guo, Huan; Haug, Line Småstuen ; Hofmann, Jonathan N. ; Iwasaki, Motoki; Machala, Miroslav ; Mancini, Francesca Romana ; Maria-Engler, Silvya Stuchi ; Møller, Peter Rsak ; Ng, Jack Chakmeng; Pallardy, Marc ; Post, Gloria B ; Salihovic, Samira ; Schlezinger, Jennifer ; Soshilov, Anatoly; Steenland, Kyle ; Steffensen, Inger Lise ; Tryndyak, Volodymyr ; White, Alexandra; Woskie, Susan
Source: The Lancet Oncology. Unidade: FCF
Subjects: CARCINOGÊNESE, PRODUTOS QUÍMICOS
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ABNT
ZAHM, Shelia et al. Carcinogenicity of perfluorooctanoic acid and perfluorooctanesulfonic acid. The Lancet Oncology, v. 25, n. 1, p. 16-17, 2024Tradução . . Disponível em: https://dx.doi.org/10.1016/S1470-2045(23)00622-8. Acesso em: 10 jun. 2024.
APA
Zahm, S., Bonde, J. P., Chiu, W. A., Hoppin, J., Kanno, J., Abdallah, M., et al. (2024). Carcinogenicity of perfluorooctanoic acid and perfluorooctanesulfonic acid. The Lancet Oncology, 25( 1), 16-17. doi:10.1016/S1470-2045(23)00622-8
NLM
Zahm S, Bonde JP, Chiu WA, Hoppin J, Kanno J, Abdallah M, Blystone CR, Calkins MM, Dong GH, Dorman DC, Fry R, Guo H, Haug LS, Hofmann JN, Iwasaki M, Machala M, Mancini FR, Maria-Engler SS, Møller PR, Ng JC, Pallardy M, Post GB, Salihovic S, Schlezinger J, Soshilov A, Steenland K, Steffensen IL, Tryndyak V, White A, Woskie S. Carcinogenicity of perfluorooctanoic acid and perfluorooctanesulfonic acid [Internet]. The Lancet Oncology. 2024 ; 25( 1): 16-17.[citado 2024 jun. 10 ] Available from: https://dx.doi.org/10.1016/S1470-2045(23)00622-8
Vancouver
Zahm S, Bonde JP, Chiu WA, Hoppin J, Kanno J, Abdallah M, Blystone CR, Calkins MM, Dong GH, Dorman DC, Fry R, Guo H, Haug LS, Hofmann JN, Iwasaki M, Machala M, Mancini FR, Maria-Engler SS, Møller PR, Ng JC, Pallardy M, Post GB, Salihovic S, Schlezinger J, Soshilov A, Steenland K, Steffensen IL, Tryndyak V, White A, Woskie S. Carcinogenicity of perfluorooctanoic acid and perfluorooctanesulfonic acid [Internet]. The Lancet Oncology. 2024 ; 25( 1): 16-17.[citado 2024 jun. 10 ] Available from: https://dx.doi.org/10.1016/S1470-2045(23)00622-8
Artigo de periodico
Ripe papaya pectins inhibit the proliferation of colon cancer spheroids and the formation of chemically induced aberrant crypts in rats colons (2024)
Donadio, Janaina Lombello Santos ; Prado, Samira Bernardino Ramos do; Soares, Caroline Giacomelli ; Tamarossi, Rodrigo Invernort; Heidor, Renato ; Moreno, Fernando Salvador ; Fabi, João Paulo
Source: Carbohydrate Polymers. Unidade: FCF
Subjects: PECTINA, MAMÃO, ANTINEOPLÁSICOS
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ABNT
DONADIO, Janaina Lombello Santos et al. Ripe papaya pectins inhibit the proliferation of colon cancer spheroids and the formation of chemically induced aberrant crypts in rats colons. Carbohydrate Polymers, v. 331, p. 1-15, 2024Tradução . . Disponível em: https://dx.doi.org/10.1016/j.carbpol.2024.121878. Acesso em: 10 jun. 2024.
APA
Donadio, J. L. S., Prado, S. B. R. do, Soares, C. G., Tamarossi, R. I., Heidor, R., Moreno, F. S., & Fabi, J. P. (2024). Ripe papaya pectins inhibit the proliferation of colon cancer spheroids and the formation of chemically induced aberrant crypts in rats colons. Carbohydrate Polymers, 331, 1-15. doi:10.1016/j.carbpol.2024.121878
NLM
Donadio JLS, Prado SBR do, Soares CG, Tamarossi RI, Heidor R, Moreno FS, Fabi JP. Ripe papaya pectins inhibit the proliferation of colon cancer spheroids and the formation of chemically induced aberrant crypts in rats colons [Internet]. Carbohydrate Polymers. 2024 ; 331 1-15.[citado 2024 jun. 10 ] Available from: https://dx.doi.org/10.1016/j.carbpol.2024.121878
Vancouver
Donadio JLS, Prado SBR do, Soares CG, Tamarossi RI, Heidor R, Moreno FS, Fabi JP. Ripe papaya pectins inhibit the proliferation of colon cancer spheroids and the formation of chemically induced aberrant crypts in rats colons [Internet]. Carbohydrate Polymers. 2024 ; 331 1-15.[citado 2024 jun. 10 ] Available from: https://dx.doi.org/10.1016/j.carbpol.2024.121878
Artigo de periodico
Baseline gene signatures of reactogenicity to Ebola vaccination: a machine learning approach across multiple cohorts (2023)
Carvalho, Patrícia Conceição Gonzalez Dias; Hirata, Thiago Dominguez Crespo ; Alves, Leandro Yukio Mano ; Moscardini, Isabelle Franco; Nascimento, Ana Paula Barbosa do; Martins, André Guilherme Costa ; Sorgi, Sara; Harandi, Ali M; Ferreira, Daniela M ; Vianello, Eleonora ; Haks, Marielle C ; Ottenhoff, Tom H. M; Santoro, Francesco ; Murillo, Paola Martinez; Huttner, Angela; Siegrist, Claire Anne ; Medaglini, Donata ; Nakaya, Helder Takashi Imoto
Source: Frontiers in Immunology. Unidade: FCF
Subjects: GENÉTICA, VACINAÇÃO
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ABNT
CARVALHO, Patrícia Conceição Gonzalez Dias et al. Baseline gene signatures of reactogenicity to Ebola vaccination: a machine learning approach across multiple cohorts. Frontiers in Immunology, v. 14, p. 1-10 art. 1259197, 2023Tradução . . Disponível em: https://dx.doi.org/10.3389/fimmu.2023.1259197. Acesso em: 10 jun. 2024.
APA
Carvalho, P. C. G. D., Hirata, T. D. C., Alves, L. Y. M., Moscardini, I. F., Nascimento, A. P. B. do, Martins, A. G. C., et al. (2023). Baseline gene signatures of reactogenicity to Ebola vaccination: a machine learning approach across multiple cohorts. Frontiers in Immunology, 14, 1-10 art. 1259197. doi:10.3389/fimmu.2023.1259197
NLM
Carvalho PCGD, Hirata TDC, Alves LYM, Moscardini IF, Nascimento APB do, Martins AGC, Sorgi S, Harandi AM, Ferreira DM, Vianello E, Haks MC, Ottenhoff THM, Santoro F, Murillo PM, Huttner A, Siegrist CA, Medaglini D, Nakaya HTI. Baseline gene signatures of reactogenicity to Ebola vaccination: a machine learning approach across multiple cohorts [Internet]. Frontiers in Immunology. 2023 ; 14 1-10 art. 1259197.[citado 2024 jun. 10 ] Available from: https://dx.doi.org/10.3389/fimmu.2023.1259197
Vancouver
Carvalho PCGD, Hirata TDC, Alves LYM, Moscardini IF, Nascimento APB do, Martins AGC, Sorgi S, Harandi AM, Ferreira DM, Vianello E, Haks MC, Ottenhoff THM, Santoro F, Murillo PM, Huttner A, Siegrist CA, Medaglini D, Nakaya HTI. Baseline gene signatures of reactogenicity to Ebola vaccination: a machine learning approach across multiple cohorts [Internet]. Frontiers in Immunology. 2023 ; 14 1-10 art. 1259197.[citado 2024 jun. 10 ] Available from: https://dx.doi.org/10.3389/fimmu.2023.1259197
Artigo de periodico
Cold acclimation and pioglitazone combined increase thermogenic capacity of brown and white adipose tissues but this does not translate into higher energy expenditure in mice (2023)
Valdivia, Luís Felipe Galvão ; Castro, Érique ; Eichler, Rosangela Aparecida dos Santos ; Moreno, Mayara Franzoi ; Sousa, Érica de; Jardim, Giovanna Freitas Rodrigues; Peixoto, Álbert Souza ; Moraes, Maria Nathália ; Castrucci, Ana Maria de Lauro ; Nedergaard, Jan ; Petrovic, Natasa ; Reckziegel, Patrícia ; Festuccia, William Tadeu Lara
Source: American Journal of Physiology-Endocrinology and Metabolism. Unidades: ICB, IB, FCF
Subjects: FISIOLOGIA, TERMOGÊNESE, TECIDO ADIPOSO, ACLIMATAÇÃO, GLICOSE, CAMUNDONGOS, PEROXISSOMOS, TEMPERATURA ANIMAL, PROTEÍNAS DA MEMBRANA
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ABNT
VALDIVIA, Luís Felipe Galvão et al. Cold acclimation and pioglitazone combined increase thermogenic capacity of brown and white adipose tissues but this does not translate into higher energy expenditure in mice. American Journal of Physiology-Endocrinology and Metabolism, v. 324, n. 4, p. E289-E373, 2023Tradução . . Disponível em: https://doi.org/10.1152/ajpendo.00217.202. Acesso em: 10 jun. 2024.
APA
Valdivia, L. F. G., Castro, É., Eichler, R. A. dos S., Moreno, M. F., Sousa, É. de, Jardim, G. F. R., et al. (2023). Cold acclimation and pioglitazone combined increase thermogenic capacity of brown and white adipose tissues but this does not translate into higher energy expenditure in mice. American Journal of Physiology-Endocrinology and Metabolism, 324( 4), E289-E373. doi:10.1152/ajpendo.00217.202
NLM
Valdivia LFG, Castro É, Eichler RA dos S, Moreno MF, Sousa É de, Jardim GFR, Peixoto ÁS, Moraes MN, Castrucci AM de L, Nedergaard J, Petrovic N, Reckziegel P, Festuccia WTL. Cold acclimation and pioglitazone combined increase thermogenic capacity of brown and white adipose tissues but this does not translate into higher energy expenditure in mice [Internet]. American Journal of Physiology-Endocrinology and Metabolism. 2023 ; 324( 4): E289-E373.[citado 2024 jun. 10 ] Available from: https://doi.org/10.1152/ajpendo.00217.202
Vancouver
Valdivia LFG, Castro É, Eichler RA dos S, Moreno MF, Sousa É de, Jardim GFR, Peixoto ÁS, Moraes MN, Castrucci AM de L, Nedergaard J, Petrovic N, Reckziegel P, Festuccia WTL. Cold acclimation and pioglitazone combined increase thermogenic capacity of brown and white adipose tissues but this does not translate into higher energy expenditure in mice [Internet]. American Journal of Physiology-Endocrinology and Metabolism. 2023 ; 324( 4): E289-E373.[citado 2024 jun. 10 ] Available from: https://doi.org/10.1152/ajpendo.00217.202
Artigo de periodico
Resolving taxonomic confusion: establishing the genus Phytobacter on the list of clinically relevant Enterobacteriaceae (2022)
Smits, Theo H. M ; Arend, Lavinia N. V. S ; Cardew, Sofia; Hallbäck, Erika Tång ; Mira, Marcelo T ; Moore, Edward R. B ; Sampaio, Jorge Luiz Mello ; Rezzonico, Fabio ; Pillonetto, Marcelo
Source: European Journal of Clinical Microbiology & Infectious Diseases. Unidade: FCF
Subjects: ENTEROBACTERIACEAE, GENÔMICA, GENÔMICA, ZOOLOGIA (CLASSIFICAÇÃO)
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ABNT
SMITS, Theo H. M et al. Resolving taxonomic confusion: establishing the genus Phytobacter on the list of clinically relevant Enterobacteriaceae. European Journal of Clinical Microbiology & Infectious Diseases, v. 41, p. 547–558, 2022Tradução . . Disponível em: https://doi.org/10.1007/s10096-022-04413-8. Acesso em: 10 jun. 2024.
APA
Smits, T. H. M., Arend, L. N. V. S., Cardew, S., Hallbäck, E. T., Mira, M. T., Moore, E. R. B., et al. (2022). Resolving taxonomic confusion: establishing the genus Phytobacter on the list of clinically relevant Enterobacteriaceae. European Journal of Clinical Microbiology & Infectious Diseases, 41, 547–558. doi:10.1007/s10096-022-04413-8
NLM
Smits THM, Arend LNVS, Cardew S, Hallbäck ET, Mira MT, Moore ERB, Sampaio JLM, Rezzonico F, Pillonetto M. Resolving taxonomic confusion: establishing the genus Phytobacter on the list of clinically relevant Enterobacteriaceae [Internet]. European Journal of Clinical Microbiology & Infectious Diseases. 2022 ; 41 547–558.[citado 2024 jun. 10 ] Available from: https://doi.org/10.1007/s10096-022-04413-8
Vancouver
Smits THM, Arend LNVS, Cardew S, Hallbäck ET, Mira MT, Moore ERB, Sampaio JLM, Rezzonico F, Pillonetto M. Resolving taxonomic confusion: establishing the genus Phytobacter on the list of clinically relevant Enterobacteriaceae [Internet]. European Journal of Clinical Microbiology & Infectious Diseases. 2022 ; 41 547–558.[citado 2024 jun. 10 ] Available from: https://doi.org/10.1007/s10096-022-04413-8
Artigo de periodico
Pharmacogenomics of statins: lipid response and other outcomes in Brazilian cohorts (2022)
Hernandez, Carolina Dagli ; Zhou, Yitian; Lauschke, Volker Martin; Genvigir, Fabiana Dalla Vecchia ; Hirata, Thiago Dominguez Crespo ; Hirata, Mario Hiroyuki ; Hirata, Rosario Dominguez Crespo
Source: Pharmacological Reports. Unidade: FCF
Subjects: ESTATINAS, FARMACOGENÉTICA
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ABNT
HERNANDEZ, Carolina Dagli et al. Pharmacogenomics of statins: lipid response and other outcomes in Brazilian cohorts. Pharmacological Reports, v. 74, p. 47–66, 2022Tradução . . Disponível em: https://doi.org/10.1007/s43440-021-00319-y. Acesso em: 10 jun. 2024.
APA
Hernandez, C. D., Zhou, Y., Lauschke, V. M., Genvigir, F. D. V., Hirata, T. D. C., Hirata, M. H., & Hirata, R. D. C. (2022). Pharmacogenomics of statins: lipid response and other outcomes in Brazilian cohorts. Pharmacological Reports, 74, 47–66. doi:10.1007/s43440-021-00319-y
NLM
Hernandez CD, Zhou Y, Lauschke VM, Genvigir FDV, Hirata TDC, Hirata MH, Hirata RDC. Pharmacogenomics of statins: lipid response and other outcomes in Brazilian cohorts [Internet]. Pharmacological Reports. 2022 ; 74 47–66.[citado 2024 jun. 10 ] Available from: https://doi.org/10.1007/s43440-021-00319-y
Vancouver
Hernandez CD, Zhou Y, Lauschke VM, Genvigir FDV, Hirata TDC, Hirata MH, Hirata RDC. Pharmacogenomics of statins: lipid response and other outcomes in Brazilian cohorts [Internet]. Pharmacological Reports. 2022 ; 74 47–66.[citado 2024 jun. 10 ] Available from: https://doi.org/10.1007/s43440-021-00319-y
Artigo de periodico
Genetic deficiency of indoleamine 2,3-dioxygenase aggravates vascular but not liver disease in a nonalcoholic steatohepatitis and atherosclerosis comorbidity model (2022)
Arora, Aastha ; Tripodi, Gustavo Luis; Kareinen, Ilona ; Berg, Martin; Forteza, Maria Josefa ; Gisterå, Anton ; Griepke, Silke; Casagrande, Felipe Beccaria ; Martins, Joilson de Oliveira ; Abdalla, Dulcinéia Saes Parra ; Cole, Jennifer ; Monaco, Claudia ; Ketelhuth, Daniel Francisco Jacon
Source: Intional Journal of Molecular Sciences. Unidade: FCF
Subjects: ARTERIOSCLEROSE, INFLAMAÇÃO
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ABNT
ARORA, Aastha et al. Genetic deficiency of indoleamine 2,3-dioxygenase aggravates vascular but not liver disease in a nonalcoholic steatohepatitis and atherosclerosis comorbidity model. Intional Journal of Molecular Sciences, v. 23, p. 1-17 art. 5203, 2022Tradução . . Disponível em: https://doi.org/10.3390/ijms23095203. Acesso em: 10 jun. 2024.
APA
Arora, A., Tripodi, G. L., Kareinen, I., Berg, M., Forteza, M. J., Gisterå, A., et al. (2022). Genetic deficiency of indoleamine 2,3-dioxygenase aggravates vascular but not liver disease in a nonalcoholic steatohepatitis and atherosclerosis comorbidity model. Intional Journal of Molecular Sciences, 23, 1-17 art. 5203. doi:10.3390/ijms23095203
NLM
Arora A, Tripodi GL, Kareinen I, Berg M, Forteza MJ, Gisterå A, Griepke S, Casagrande FB, Martins J de O, Abdalla DSP, Cole J, Monaco C, Ketelhuth DFJ. Genetic deficiency of indoleamine 2,3-dioxygenase aggravates vascular but not liver disease in a nonalcoholic steatohepatitis and atherosclerosis comorbidity model [Internet]. Intional Journal of Molecular Sciences. 2022 ; 23 1-17 art. 5203.[citado 2024 jun. 10 ] Available from: https://doi.org/10.3390/ijms23095203
Vancouver
Arora A, Tripodi GL, Kareinen I, Berg M, Forteza MJ, Gisterå A, Griepke S, Casagrande FB, Martins J de O, Abdalla DSP, Cole J, Monaco C, Ketelhuth DFJ. Genetic deficiency of indoleamine 2,3-dioxygenase aggravates vascular but not liver disease in a nonalcoholic steatohepatitis and atherosclerosis comorbidity model [Internet]. Intional Journal of Molecular Sciences. 2022 ; 23 1-17 art. 5203.[citado 2024 jun. 10 ] Available from: https://doi.org/10.3390/ijms23095203
Artigo de periodico
Effects of pectins on colorectal cancer: targeting hallmarks as a support for future clinical trials (2022)
Donadio, Janaina Lombello Santos ; Prado, Samira Bernardino Ramos do; Rogero, Marcelo Macedo ; Fabi, João Paulo
Source: Food and Function Review. Unidades: FSP, FCF
Subjects: NEOPLASIAS COLORRETAIS, PECTINA
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ABNT
DONADIO, Janaina Lombello Santos et al. Effects of pectins on colorectal cancer: targeting hallmarks as a support for future clinical trials. Food and Function Review, v. 13, n. 22, p. 11438-11454, 2022Tradução . . Disponível em: https://doi.org/10.1039/D2FO01995G. Acesso em: 10 jun. 2024.
APA
Donadio, J. L. S., Prado, S. B. R. do, Rogero, M. M., & Fabi, J. P. (2022). Effects of pectins on colorectal cancer: targeting hallmarks as a support for future clinical trials. Food and Function Review, 13( 22), 11438-11454. doi:10.1039/D2FO01995G
NLM
Donadio JLS, Prado SBR do, Rogero MM, Fabi JP. Effects of pectins on colorectal cancer: targeting hallmarks as a support for future clinical trials [Internet]. Food and Function Review. 2022 ; 13( 22): 11438-11454.[citado 2024 jun. 10 ] Available from: https://doi.org/10.1039/D2FO01995G
Vancouver
Donadio JLS, Prado SBR do, Rogero MM, Fabi JP. Effects of pectins on colorectal cancer: targeting hallmarks as a support for future clinical trials [Internet]. Food and Function Review. 2022 ; 13( 22): 11438-11454.[citado 2024 jun. 10 ] Available from: https://doi.org/10.1039/D2FO01995G
Artigo de periodico
Genetic variant ABCC1 rs45511401 is Associated with increased response to statins in patients with familial hypercholesterolemia (2022)
Hernandez, Carolina Dagli ; Borges, Jéssica Bassani ; Marçal, Elisangela da Silva Rodrigues; Freitas, Renata Caroline Costa de ; Mori, Augusto Akira ; Gonçalves, Rodrigo Marques; Faludi, André Arpad ; Oliveira, Victor Fernandes de ; Ferreira, Glaucio Monteiro ; Bastos, Gisele Medeiros ; Zhou, Yitian ; Lauschke, Volker Martin ; Cerda, Alvaro ; Hirata, Mario Hiroyuki ; Hirata, Rosario Dominguez Crespo
Source: Pharmaceutics. Unidade: FCF
Subjects: HIPERCOLESTEROLEMIA, ESTATINAS, VARIAÇÃO GENÉTICA, FARMACOGENÉTICA, MEDICAMENTO
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ABNT
HERNANDEZ, Carolina Dagli et al. Genetic variant ABCC1 rs45511401 is Associated with increased response to statins in patients with familial hypercholesterolemia. Pharmaceutics, v. 14, p. 1-20 art. 944, 2022Tradução . . Disponível em: https://doi.org/10.3390/pharmaceutics14050944. Acesso em: 10 jun. 2024.
APA
Hernandez, C. D., Borges, J. B., Marçal, E. da S. R., Freitas, R. C. C. de, Mori, A. A., Gonçalves, R. M., et al. (2022). Genetic variant ABCC1 rs45511401 is Associated with increased response to statins in patients with familial hypercholesterolemia. Pharmaceutics, 14, 1-20 art. 944. doi:10.3390/pharmaceutics14050944
NLM
Hernandez CD, Borges JB, Marçal E da SR, Freitas RCC de, Mori AA, Gonçalves RM, Faludi AA, Oliveira VF de, Ferreira GM, Bastos GM, Zhou Y, Lauschke VM, Cerda A, Hirata MH, Hirata RDC. Genetic variant ABCC1 rs45511401 is Associated with increased response to statins in patients with familial hypercholesterolemia [Internet]. Pharmaceutics. 2022 ; 14 1-20 art. 944.[citado 2024 jun. 10 ] Available from: https://doi.org/10.3390/pharmaceutics14050944
Vancouver
Hernandez CD, Borges JB, Marçal E da SR, Freitas RCC de, Mori AA, Gonçalves RM, Faludi AA, Oliveira VF de, Ferreira GM, Bastos GM, Zhou Y, Lauschke VM, Cerda A, Hirata MH, Hirata RDC. Genetic variant ABCC1 rs45511401 is Associated with increased response to statins in patients with familial hypercholesterolemia [Internet]. Pharmaceutics. 2022 ; 14 1-20 art. 944.[citado 2024 jun. 10 ] Available from: https://doi.org/10.3390/pharmaceutics14050944
Artigo de periodico
Aporphine and isoquinoline derivatives block glioblastoma cell stemness and enhance temozolomide cytotoxicity (2022)
Rodrigues Junior, Dorival Mendes ; Raminelli, Cristiano ; Hassanie, Haifa ; Trossini, Gustavo Henrique Goulart ; Perecim, Givago Prado; Puigsubira, Laia Caja ; Moustakas, Aristidis ; Vettore, André Luiz
Source: Scientific Reports. Unidade: FCF
Subjects: NEOPLASIAS CEREBRAIS, QUIMIOTERAPIA, RADIOTERAPIA
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ABNT
RODRIGUES JUNIOR, Dorival Mendes et al. Aporphine and isoquinoline derivatives block glioblastoma cell stemness and enhance temozolomide cytotoxicity. Scientific Reports, v. 12, p. 1-17, 2022Tradução . . Disponível em: https://doi.org/10.1038/s41598-022-25534-2. Acesso em: 10 jun. 2024.
APA
Rodrigues Junior, D. M., Raminelli, C., Hassanie, H., Trossini, G. H. G., Perecim, G. P., Puigsubira, L. C., et al. (2022). Aporphine and isoquinoline derivatives block glioblastoma cell stemness and enhance temozolomide cytotoxicity. Scientific Reports, 12, 1-17. doi:10.1038/s41598-022-25534-2
NLM
Rodrigues Junior DM, Raminelli C, Hassanie H, Trossini GHG, Perecim GP, Puigsubira LC, Moustakas A, Vettore AL. Aporphine and isoquinoline derivatives block glioblastoma cell stemness and enhance temozolomide cytotoxicity [Internet]. Scientific Reports. 2022 ; 12 1-17.[citado 2024 jun. 10 ] Available from: https://doi.org/10.1038/s41598-022-25534-2
Vancouver
Rodrigues Junior DM, Raminelli C, Hassanie H, Trossini GHG, Perecim GP, Puigsubira LC, Moustakas A, Vettore AL. Aporphine and isoquinoline derivatives block glioblastoma cell stemness and enhance temozolomide cytotoxicity [Internet]. Scientific Reports. 2022 ; 12 1-17.[citado 2024 jun. 10 ] Available from: https://doi.org/10.1038/s41598-022-25534-2
Artigo de periodico
Cardiovascular pharmacogenomics: an update on clinical studies of antithrombotic drugs in Brazilian patients (2021)
Hirata, Thiago Dominguez Crespo ; Hernandez, Carolina Dagli ; Genvigir, Fabiana Dalla Vecchia ; Lauschke, Volker Martin ; Zhou, Yitian ; Hirata, Mario Hiroyuki ; Hirata, Rosario Dominguez Crespo
Source: Molecular Diagnosis and Therapy. Unidade: FCF
Subjects: ANTICOAGULANTES, DOENÇAS CARDIOVASCULARES, TROMBOSE
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ABNT
HIRATA, Thiago Dominguez Crespo et al. Cardiovascular pharmacogenomics: an update on clinical studies of antithrombotic drugs in Brazilian patients. Molecular Diagnosis and Therapy, v. 25, p. 735–755, 2021Tradução . . Disponível em: https://doi.org/10.1007/s40291-021-00549-z. Acesso em: 10 jun. 2024.
APA
Hirata, T. D. C., Hernandez, C. D., Genvigir, F. D. V., Lauschke, V. M., Zhou, Y., Hirata, M. H., & Hirata, R. D. C. (2021). Cardiovascular pharmacogenomics: an update on clinical studies of antithrombotic drugs in Brazilian patients. Molecular Diagnosis and Therapy, 25, 735–755. doi:10.1007/s40291-021-00549-z
NLM
Hirata TDC, Hernandez CD, Genvigir FDV, Lauschke VM, Zhou Y, Hirata MH, Hirata RDC. Cardiovascular pharmacogenomics: an update on clinical studies of antithrombotic drugs in Brazilian patients [Internet]. Molecular Diagnosis and Therapy. 2021 ; 25 735–755.[citado 2024 jun. 10 ] Available from: https://doi.org/10.1007/s40291-021-00549-z
Vancouver
Hirata TDC, Hernandez CD, Genvigir FDV, Lauschke VM, Zhou Y, Hirata MH, Hirata RDC. Cardiovascular pharmacogenomics: an update on clinical studies of antithrombotic drugs in Brazilian patients [Internet]. Molecular Diagnosis and Therapy. 2021 ; 25 735–755.[citado 2024 jun. 10 ] Available from: https://doi.org/10.1007/s40291-021-00549-z
Artigo de periodico
XPR1 mediates the pancreatic β-Cell phosphate flush (2021)
Barker, Christopher J; Tessaro, Fernando Henrique Galvão; Ferreira, Sabrina de Souza; Simas, Rafael; Ayala, Thais S; Köhler, Martin; Rajasekaran, Subu Surendran; Martins, Joilson de Oliveira ; Darè, Elisabetta; Berggren, Per-Olof
Source: Diabetes. Unidade: FCF
Subjects: INSULINA, FOSFATOS, CÉLULAS, ILHOTAS DE LANGERHANS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BARKER, Christopher J et al. XPR1 mediates the pancreatic β-Cell phosphate flush. Diabetes, v. 70, n. 1, p. 111–118, 2021Tradução . . Disponível em: https://doi.org/10.2337/db19-0633. Acesso em: 10 jun. 2024.
APA
Barker, C. J., Tessaro, F. H. G., Ferreira, S. de S., Simas, R., Ayala, T. S., Köhler, M., et al. (2021). XPR1 mediates the pancreatic β-Cell phosphate flush. Diabetes, 70( 1), 111–118. doi:10.2337/db19-0633
NLM
Barker CJ, Tessaro FHG, Ferreira S de S, Simas R, Ayala TS, Köhler M, Rajasekaran SS, Martins J de O, Darè E, Berggren P-O. XPR1 mediates the pancreatic β-Cell phosphate flush [Internet]. Diabetes. 2021 ; 70( 1): 111–118.[citado 2024 jun. 10 ] Available from: https://doi.org/10.2337/db19-0633
Vancouver
Barker CJ, Tessaro FHG, Ferreira S de S, Simas R, Ayala TS, Köhler M, Rajasekaran SS, Martins J de O, Darè E, Berggren P-O. XPR1 mediates the pancreatic β-Cell phosphate flush [Internet]. Diabetes. 2021 ; 70( 1): 111–118.[citado 2024 jun. 10 ] Available from: https://doi.org/10.2337/db19-0633
Artigo de periodico
A metal-free blue chromophore derived from plant pigments (2020)
Freitas-Dörr, Barbara Coelho de ; Machado, Caroline de Oliveira ; Pinheiro, Amanda Capistrano ; Fernandes, Arthur Bonfá ; Dörr, Felipe Augusto ; Pinto, Ernani ; Lopes-Ferreira, Mônica ; Abdellah, Mohamed ; Sa, Jacinto ; Russo, Lilian Cristina ; Forti, Fabio Luis ; Gonçalves, Letícia Christina Pires ; Bastos, Erick Leite
Source: Science Advances. Unidades: FCF, CENA, IQ
Subjects: PIGMENTOS VEGETAIS, BIOLOGIA CELULAR
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FREITAS-DÖRR, Barbara Coelho de et al. A metal-free blue chromophore derived from plant pigments. Science Advances, v. 6, n. 14, p. 1-8 art. eaaz0421, 2020Tradução . . Disponível em: https://doi.org/10.1126/sciadv.aaz0421. Acesso em: 10 jun. 2024.
APA
Freitas-Dörr, B. C. de, Machado, C. de O., Pinheiro, A. C., Fernandes, A. B., Dörr, F. A., Pinto, E., et al. (2020). A metal-free blue chromophore derived from plant pigments. Science Advances, 6( 14), 1-8 art. eaaz0421. doi:10.1126/sciadv.aaz0421
NLM
Freitas-Dörr BC de, Machado C de O, Pinheiro AC, Fernandes AB, Dörr FA, Pinto E, Lopes-Ferreira M, Abdellah M, Sa J, Russo LC, Forti FL, Gonçalves LCP, Bastos EL. A metal-free blue chromophore derived from plant pigments [Internet]. Science Advances. 2020 ; 6( 14): 1-8 art. eaaz0421.[citado 2024 jun. 10 ] Available from: https://doi.org/10.1126/sciadv.aaz0421
Vancouver
Freitas-Dörr BC de, Machado C de O, Pinheiro AC, Fernandes AB, Dörr FA, Pinto E, Lopes-Ferreira M, Abdellah M, Sa J, Russo LC, Forti FL, Gonçalves LCP, Bastos EL. A metal-free blue chromophore derived from plant pigments [Internet]. Science Advances. 2020 ; 6( 14): 1-8 art. eaaz0421.[citado 2024 jun. 10 ] Available from: https://doi.org/10.1126/sciadv.aaz0421
Artigo de periodico
Proinflammatory action of a new electronegative low-density lipoprotein epitope (2019)
Faulin, Tanize do Espírito Santo; Kazuma, Soraya Megumi; Tripodi, Gustavo Luis; Cavalcante, Marcela Frota; Wakasuqui, Felipe; Oliveira, Cristiano Luis Pinto de; Degenhardt, Maximilia Frazão de Souza; Michaloski, Jussara; Giordano, Ricardo José ; Ketelhuth, Daniel Francisco Jacon; Abdalla, Dulcinéia Saes Parra
Source: Biomolecules. Unidades: IF, IQ, FCF
Subjects: ARTERIOSCLEROSE, MACRÓFAGOS, LIPOPROTEÍNAS LDL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FAULIN, Tanize do Espírito Santo et al. Proinflammatory action of a new electronegative low-density lipoprotein epitope. Biomolecules, v. 9, n. 8, p. 1-17 art. 386, 2019Tradução . . Disponível em: https://doi.org/10.3390/biom9080386. Acesso em: 10 jun. 2024.
APA
Faulin, T. do E. S., Kazuma, S. M., Tripodi, G. L., Cavalcante, M. F., Wakasuqui, F., Oliveira, C. L. P. de, et al. (2019). Proinflammatory action of a new electronegative low-density lipoprotein epitope. Biomolecules, 9( 8), 1-17 art. 386. doi:10.3390/biom9080386
NLM
Faulin T do ES, Kazuma SM, Tripodi GL, Cavalcante MF, Wakasuqui F, Oliveira CLP de, Degenhardt MF de S, Michaloski J, Giordano RJ, Ketelhuth DFJ, Abdalla DSP. Proinflammatory action of a new electronegative low-density lipoprotein epitope [Internet]. Biomolecules. 2019 ; 9( 8): 1-17 art. 386.[citado 2024 jun. 10 ] Available from: https://doi.org/10.3390/biom9080386
Vancouver
Faulin T do ES, Kazuma SM, Tripodi GL, Cavalcante MF, Wakasuqui F, Oliveira CLP de, Degenhardt MF de S, Michaloski J, Giordano RJ, Ketelhuth DFJ, Abdalla DSP. Proinflammatory action of a new electronegative low-density lipoprotein epitope [Internet]. Biomolecules. 2019 ; 9( 8): 1-17 art. 386.[citado 2024 jun. 10 ] Available from: https://doi.org/10.3390/biom9080386
Artigo de periodico
Protein kinase- and lipase inhibitors of inositide metabolism deplete IP7 indirectly in pancreatic β-cells: Off-target effects on cellular bioenergetics and direct effects on IP6K activity (2018)
Rajasekaran, Subu Surendran; Illies, Christopher; Shears, Stephen B; Wang, Huanchen; Ayala, Thais S; Martins, Joilson de Oliveira ; Daré, Elisabetta; Berggren, Per-Olof; Barker, Christopher J
Source: Cellular Signalling. Unidade: FCF
Subjects: PROTEÍNAS QUINASES, LIPASE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RAJASEKARAN, Subu Surendran et al. Protein kinase- and lipase inhibitors of inositide metabolism deplete IP7 indirectly in pancreatic β-cells: Off-target effects on cellular bioenergetics and direct effects on IP6K activity. Cellular Signalling, v. 42, p. 127-133, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.cellsig.2017.10.008. Acesso em: 10 jun. 2024.
APA
Rajasekaran, S. S., Illies, C., Shears, S. B., Wang, H., Ayala, T. S., Martins, J. de O., et al. (2018). Protein kinase- and lipase inhibitors of inositide metabolism deplete IP7 indirectly in pancreatic β-cells: Off-target effects on cellular bioenergetics and direct effects on IP6K activity. Cellular Signalling, 42, 127-133. doi:10.1016/j.cellsig.2017.10.008
NLM
Rajasekaran SS, Illies C, Shears SB, Wang H, Ayala TS, Martins J de O, Daré E, Berggren P-O, Barker CJ. Protein kinase- and lipase inhibitors of inositide metabolism deplete IP7 indirectly in pancreatic β-cells: Off-target effects on cellular bioenergetics and direct effects on IP6K activity [Internet]. Cellular Signalling. 2018 ; 42 127-133.[citado 2024 jun. 10 ] Available from: https://doi.org/10.1016/j.cellsig.2017.10.008
Vancouver
Rajasekaran SS, Illies C, Shears SB, Wang H, Ayala TS, Martins J de O, Daré E, Berggren P-O, Barker CJ. Protein kinase- and lipase inhibitors of inositide metabolism deplete IP7 indirectly in pancreatic β-cells: Off-target effects on cellular bioenergetics and direct effects on IP6K activity [Internet]. Cellular Signalling. 2018 ; 42 127-133.[citado 2024 jun. 10 ] Available from: https://doi.org/10.1016/j.cellsig.2017.10.008
Artigo de periodico
Inositol hexakisphosphate kinase 1 is a metabolic sensor in pancreatic beta-cells (2018)
Rajasekaran, Subu Surendran; Kim, Jaeyoon; Gaboardi, Gian Carlo; Gromada, Jesper; Shears, Stephen B; Santos, Karen Tiago dos; Nolasco, Eduardo Lima; Ferreira, Sabrina de Souza; Illies, Christopher; Köhler, Martin; Gu, Chunfang; Ryu, Sung Ho; Martins, Joilson de Oliveira ; Daré, Elisabetta; Barker, Christopher J; Berggren, Per Olof
Source: Cellular Signalling. Unidade: FCF
Subjects: DIABETES MELLITUS NÃO INSULINO-DEPENDENTE, INSULINA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RAJASEKARAN, Subu Surendran et al. Inositol hexakisphosphate kinase 1 is a metabolic sensor in pancreatic beta-cells. Cellular Signalling, v. 46, p. 120-128, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.cellsig.2018.03.001. Acesso em: 10 jun. 2024.
APA
Rajasekaran, S. S., Kim, J., Gaboardi, G. C., Gromada, J., Shears, S. B., Santos, K. T. dos, et al. (2018). Inositol hexakisphosphate kinase 1 is a metabolic sensor in pancreatic beta-cells. Cellular Signalling, 46, 120-128. doi:10.1016/j.cellsig.2018.03.001
NLM
Rajasekaran SS, Kim J, Gaboardi GC, Gromada J, Shears SB, Santos KT dos, Nolasco EL, Ferreira S de S, Illies C, Köhler M, Gu C, Ryu SH, Martins J de O, Daré E, Barker CJ, Berggren PO. Inositol hexakisphosphate kinase 1 is a metabolic sensor in pancreatic beta-cells [Internet]. Cellular Signalling. 2018 ; 46 120-128.[citado 2024 jun. 10 ] Available from: https://doi.org/10.1016/j.cellsig.2018.03.001
Vancouver
Rajasekaran SS, Kim J, Gaboardi GC, Gromada J, Shears SB, Santos KT dos, Nolasco EL, Ferreira S de S, Illies C, Köhler M, Gu C, Ryu SH, Martins J de O, Daré E, Barker CJ, Berggren PO. Inositol hexakisphosphate kinase 1 is a metabolic sensor in pancreatic beta-cells [Internet]. Cellular Signalling. 2018 ; 46 120-128.[citado 2024 jun. 10 ] Available from: https://doi.org/10.1016/j.cellsig.2018.03.001
Artigo de periodico
Adverse Effects of Plant Food Supplements and Plants Consumed as Food: results from the Poisons Centres-Based PlantLIBRA Study (2016)
Lüde, Saskia; Vecchio, Sarah; Tellier, Sandra Sinno; Dopter, Aymeric; Mustonen, Harriet; Vucinic, Slavica; Jonsson, Birgitta; Müller, Dieter; Fruchtengarten, Ligia Veras Gimenez; Hruby, Karl; Nascimento, Elizabeth de Souza; Di Lorenzo, Chiara; Restani, Patrizia; Kupferschmidt, Hugo; Ceschi, Alessandro
Source: Phytotherapy Research. Unidade: FCF
Subjects: SUPLEMENTAÇÃO ALIMENTAR, PLANTAS ALIMENTÍCIAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LÜDE, Saskia et al. Adverse Effects of Plant Food Supplements and Plants Consumed as Food: results from the Poisons Centres-Based PlantLIBRA Study. Phytotherapy Research, v. 30, n. 6, p. 988 -996, 2016Tradução . . Disponível em: https://doi.org/10.1002/ptr.5604. Acesso em: 10 jun. 2024.
APA
Lüde, S., Vecchio, S., Tellier, S. S., Dopter, A., Mustonen, H., Vucinic, S., et al. (2016). Adverse Effects of Plant Food Supplements and Plants Consumed as Food: results from the Poisons Centres-Based PlantLIBRA Study. Phytotherapy Research, 30( 6), 988 -996. doi:10.1002/ptr.5604
NLM
Lüde S, Vecchio S, Tellier SS, Dopter A, Mustonen H, Vucinic S, Jonsson B, Müller D, Fruchtengarten LVG, Hruby K, Nascimento E de S, Di Lorenzo C, Restani P, Kupferschmidt H, Ceschi A. Adverse Effects of Plant Food Supplements and Plants Consumed as Food: results from the Poisons Centres-Based PlantLIBRA Study [Internet]. Phytotherapy Research. 2016 ; 30( 6): 988 -996.[citado 2024 jun. 10 ] Available from: https://doi.org/10.1002/ptr.5604
Vancouver
Lüde S, Vecchio S, Tellier SS, Dopter A, Mustonen H, Vucinic S, Jonsson B, Müller D, Fruchtengarten LVG, Hruby K, Nascimento E de S, Di Lorenzo C, Restani P, Kupferschmidt H, Ceschi A. Adverse Effects of Plant Food Supplements and Plants Consumed as Food: results from the Poisons Centres-Based PlantLIBRA Study [Internet]. Phytotherapy Research. 2016 ; 30( 6): 988 -996.[citado 2024 jun. 10 ] Available from: https://doi.org/10.1002/ptr.5604

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