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Artigo de periodico
Unexpected role of SIX1 variants in craniosynostosis: expanding the phenotype of SIX1-related disorders (2021)
Calpena, Eduardo; Wurmser, Maud; McGowan, Simon J; Atique, Rodrigo; Bertola, Débora R; Cunningham , Michael L; Gustafson, Jonas A; Johnson, David; Morton, Jenny E. V; Passos-Bueno, Maria Rita ; Timberlake, Andre T; Lifton, Richa P; Wall, Steven A; Twigg, Stephen R. F; Maire, Pascal; Wilkie, Andrew O. M
Source: Journal of Medical Genetics. Unidade: IB
Subjects: CRANIOSSINOSTOSE, ANORMALIDADES CRANIOFACIAIS, DOENÇAS CONGÊNITAS, MUTAÇÃO GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CALPENA, Eduardo et al. Unexpected role of SIX1 variants in craniosynostosis: expanding the phenotype of SIX1-related disorders. Journal of Medical Genetics, 2021Tradução . . Disponível em: https://doi.org/10.1136/jmedgenet-2020-107459. Acesso em: 10 nov. 2024.
APA
Calpena, E., Wurmser, M., McGowan, S. J., Atique, R., Bertola, D. R., Cunningham , M. L., et al. (2021). Unexpected role of SIX1 variants in craniosynostosis: expanding the phenotype of SIX1-related disorders. Journal of Medical Genetics. doi:10.1136/jmedgenet-2020-107459
NLM
Calpena E, Wurmser M, McGowan SJ, Atique R, Bertola DR, Cunningham ML, Gustafson JA, Johnson D, Morton JEV, Passos-Bueno MR, Timberlake AT, Lifton RP, Wall SA, Twigg SRF, Maire P, Wilkie AOM. Unexpected role of SIX1 variants in craniosynostosis: expanding the phenotype of SIX1-related disorders [Internet]. Journal of Medical Genetics. 2021 ;[citado 2024 nov. 10 ] Available from: https://doi.org/10.1136/jmedgenet-2020-107459
Vancouver
Calpena E, Wurmser M, McGowan SJ, Atique R, Bertola DR, Cunningham ML, Gustafson JA, Johnson D, Morton JEV, Passos-Bueno MR, Timberlake AT, Lifton RP, Wall SA, Twigg SRF, Maire P, Wilkie AOM. Unexpected role of SIX1 variants in craniosynostosis: expanding the phenotype of SIX1-related disorders [Internet]. Journal of Medical Genetics. 2021 ;[citado 2024 nov. 10 ] Available from: https://doi.org/10.1136/jmedgenet-2020-107459
Artigo de periodico
Craniosynostosis in 10q26 deletion patients: a consequence of brain underdevelopment or altered suture biology? (2015)
Faria, Ágatha Cristhina; Rabbi-Bortolini, Eliete; Reboucas, Maria R. G. O; Pereira, Andreia L. A. de S. Thiago; Frasson, Milena G. Tonini; Atique, Rodrigo; Lourenço, Naila Cristina Vilaça; Rosenberg, Carla ; Kobayashi, Gerson Shigeru; Passos-Bueno, Maria Rita ; Errera, Flávia Imbroisi Valle
Source: American Journal of Medical Genetics Part A. Unidade: IB
Subjects: CRANIOSSINOSTOSE, ANORMALIDADES CRANIOFACIAIS, GENÉTICA MOLECULAR, DOENÇAS GENÉTICAS, CÉREBRO (DESENVOLVIMENTO), MUTAÇÃO GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FARIA, Ágatha Cristhina et al. Craniosynostosis in 10q26 deletion patients: a consequence of brain underdevelopment or altered suture biology?. American Journal of Medical Genetics Part A, v. No 2015, p. 1-7, 2015Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.37448. Acesso em: 10 nov. 2024.
APA
Faria, Á. C., Rabbi-Bortolini, E., Reboucas, M. R. G. O., Pereira, A. L. A. de S. T., Frasson, M. G. T., Atique, R., et al. (2015). Craniosynostosis in 10q26 deletion patients: a consequence of brain underdevelopment or altered suture biology? American Journal of Medical Genetics Part A, No 2015, 1-7. doi:10.1002/ajmg.a.37448
NLM
Faria ÁC, Rabbi-Bortolini E, Reboucas MRGO, Pereira ALA de ST, Frasson MGT, Atique R, Lourenço NCV, Rosenberg C, Kobayashi GS, Passos-Bueno MR, Errera FIV. Craniosynostosis in 10q26 deletion patients: a consequence of brain underdevelopment or altered suture biology? [Internet]. American Journal of Medical Genetics Part A. 2015 ; No 2015 1-7.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1002/ajmg.a.37448
Vancouver
Faria ÁC, Rabbi-Bortolini E, Reboucas MRGO, Pereira ALA de ST, Frasson MGT, Atique R, Lourenço NCV, Rosenberg C, Kobayashi GS, Passos-Bueno MR, Errera FIV. Craniosynostosis in 10q26 deletion patients: a consequence of brain underdevelopment or altered suture biology? [Internet]. American Journal of Medical Genetics Part A. 2015 ; No 2015 1-7.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1002/ajmg.a.37448
Artigo de periodico
Optimization of parameters for a more efficient use of adipose-derived stem cells in regenerative medicine therapies (2012)
Aguena, Meire; Fanganiello, Roberto Dalto; Tissiani, Luiz Alexandre Lorico; Ishiy, Felipe Augusto André; Atique, Rodrigo; Alonso, Nivaldo; Passos-Bueno, Maria Rita
Source: Stem Cells International. Unidades: FM, IB
Subjects: TECIDO ADIPOSO, CÉLULAS-TRONCO, TRANSPLANTE AUTÓLOGO, CIRURGIA PLÁSTICA, IMUNOFENOTIPAGEM, CITOMETRIA DE FLUXO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
AGUENA, Meire et al. Optimization of parameters for a more efficient use of adipose-derived stem cells in regenerative medicine therapies. Stem Cells International, p. 7 , 2012Tradução . . Disponível em: https://doi.org/10.1155/2012/303610. Acesso em: 10 nov. 2024.
APA
Aguena, M., Fanganiello, R. D., Tissiani, L. A. L., Ishiy, F. A. A., Atique, R., Alonso, N., & Passos-Bueno, M. R. (2012). Optimization of parameters for a more efficient use of adipose-derived stem cells in regenerative medicine therapies. Stem Cells International, 7 . doi:10.1155/2012/303610
NLM
Aguena M, Fanganiello RD, Tissiani LAL, Ishiy FAA, Atique R, Alonso N, Passos-Bueno MR. Optimization of parameters for a more efficient use of adipose-derived stem cells in regenerative medicine therapies [Internet]. Stem Cells International. 2012 ; 7 .[citado 2024 nov. 10 ] Available from: https://doi.org/10.1155/2012/303610
Vancouver
Aguena M, Fanganiello RD, Tissiani LAL, Ishiy FAA, Atique R, Alonso N, Passos-Bueno MR. Optimization of parameters for a more efficient use of adipose-derived stem cells in regenerative medicine therapies [Internet]. Stem Cells International. 2012 ; 7 .[citado 2024 nov. 10 ] Available from: https://doi.org/10.1155/2012/303610
Artigo de periodico
FGFR2 mutation confers a less drastic gain of function in mesenchymal stem cells than in fibroblasts (2012)
Yeh, Erika; Atique, Rodrigo; Ishiy, Felipe Augusto André; Fanganiello, Roberto Dalto; Alonso, Nivaldo; Matushita, Hamilton; Rocha, Kátia Maria da; Passos-Bueno, Maria Rita
Source: Stem Cell Reviews and Reports. Unidades: FM, IB
Subjects: CÉLULAS-TRONCO, FIBROBLASTOS, CRANIOSSINOSTOSE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
YEH, Erika et al. FGFR2 mutation confers a less drastic gain of function in mesenchymal stem cells than in fibroblasts. Stem Cell Reviews and Reports, v. No 2011, p. on-line, 2012Tradução . . Disponível em: https://doi.org/10.1007/s12015-011-9327-6. Acesso em: 10 nov. 2024.
APA
Yeh, E., Atique, R., Ishiy, F. A. A., Fanganiello, R. D., Alonso, N., Matushita, H., et al. (2012). FGFR2 mutation confers a less drastic gain of function in mesenchymal stem cells than in fibroblasts. Stem Cell Reviews and Reports, No 2011, on-line. doi:10.1007/s12015-011-9327-6
NLM
Yeh E, Atique R, Ishiy FAA, Fanganiello RD, Alonso N, Matushita H, Rocha KM da, Passos-Bueno MR. FGFR2 mutation confers a less drastic gain of function in mesenchymal stem cells than in fibroblasts [Internet]. Stem Cell Reviews and Reports. 2012 ; No 2011 on-line.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1007/s12015-011-9327-6
Vancouver
Yeh E, Atique R, Ishiy FAA, Fanganiello RD, Alonso N, Matushita H, Rocha KM da, Passos-Bueno MR. FGFR2 mutation confers a less drastic gain of function in mesenchymal stem cells than in fibroblasts [Internet]. Stem Cell Reviews and Reports. 2012 ; No 2011 on-line.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1007/s12015-011-9327-6

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