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Filtros : "Indexado na Base de Dados MEDLINE" "Passos-Bueno, Maria Rita" Removidos: "University of Pennsylvania (UP)" "Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)" "ASHG" Limpar

Filtros

USP affiliated authors
- bueno, maria rita dos santos e passos (~2)
- alonso, nivaldo (~1)
- menck, carlos frederico martins (~1)
- rocha, katia maria da (~1)
Date published
- 2013 (~2)
Subjects
- biologia molecular (1)
- craniossinostose (genética) (1)
- fatores de crescimento (deficiência) (1)
- fenótipos (1)
- genótipos (1)

Artigo de periodico
Susceptibility to DNA damage as a molecular mechanism for non-syndromic cleft lip and palate (2013)
Kobayashi, Gerson Shigeru; Alvizi, Lucas; Sunaga, Daniele Yumi; Francis-West, Philippa; Kuta, Anna; Almada, Bruno Vinícius Pimenta; Ferreira, Simone Gomes; Andrade-Lima, Leonardo Carmo de; Bueno, Daniela Franco; Raposo-Amaral, Cássio Eduardo; Menck, Carlos Frederico Martins ; Passos-Bueno, Maria Rita
Source: PLOS ONE. Unidades: ICB, IB
Assunto: MICROBIOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
KOBAYASHI, Gerson Shigeru et al. Susceptibility to DNA damage as a molecular mechanism for non-syndromic cleft lip and palate. PLOS ONE, v. 8, n. 6, p. 1-11, 2013Tradução . . Disponível em: https://doi.org/10.1371/journal.pone.0065677. Acesso em: 10 nov. 2024.
APA
Kobayashi, G. S., Alvizi, L., Sunaga, D. Y., Francis-West, P., Kuta, A., Almada, B. V. P., et al. (2013). Susceptibility to DNA damage as a molecular mechanism for non-syndromic cleft lip and palate. PLOS ONE, 8( 6), 1-11. doi:10.1371/journal.pone.0065677
NLM
Kobayashi GS, Alvizi L, Sunaga DY, Francis-West P, Kuta A, Almada BVP, Ferreira SG, Andrade-Lima LC de, Bueno DF, Raposo-Amaral CE, Menck CFM, Passos-Bueno MR. Susceptibility to DNA damage as a molecular mechanism for non-syndromic cleft lip and palate [Internet]. PLOS ONE. 2013 ; 8( 6): 1-11.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1371/journal.pone.0065677
Vancouver
Kobayashi GS, Alvizi L, Sunaga DY, Francis-West P, Kuta A, Almada BVP, Ferreira SG, Andrade-Lima LC de, Bueno DF, Raposo-Amaral CE, Menck CFM, Passos-Bueno MR. Susceptibility to DNA damage as a molecular mechanism for non-syndromic cleft lip and palate [Internet]. PLOS ONE. 2013 ; 8( 6): 1-11.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1371/journal.pone.0065677
Artigo de periodico
Novel Molecular Pathways Elicited by Mutant FGFR2 May Account for Brain Abnormalities in Apert Syndrome (2013)
Yeh, Erika; Fanganiello, Roberto D.; Sunaga, Daniele Y.; Zhou, Xueyan; Holmes, Gregory; Rocha, Katia M.; Alonso, Nivaldo; Matushita, Hamilton; Wang, Yingli; Jabs, Ethylin W.; Passos-Bueno, Maria Rita
Source: PLOS ONE. Unidades: FM, IB
Subjects: FATORES DE CRESCIMENTO (DEFICIÊNCIA), MUTAÇÃO GENÉTICA, FENÓTIPOS, GENÓTIPOS, BIOLOGIA MOLECULAR, CRANIOSSINOSTOSE (GENÉTICA)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
YEH, Erika et al. Novel Molecular Pathways Elicited by Mutant FGFR2 May Account for Brain Abnormalities in Apert Syndrome. PLOS ONE, v. 8, n. 4, p. 7 , 2013Tradução . . Disponível em: http://www.plosone.org/article/info%3Adoi%2F10.1371%2Fjournal.pone.0060439. Acesso em: 10 nov. 2024.
APA
Yeh, E., Fanganiello, R. D., Sunaga, D. Y., Zhou, X., Holmes, G., Rocha, K. M., et al. (2013). Novel Molecular Pathways Elicited by Mutant FGFR2 May Account for Brain Abnormalities in Apert Syndrome. PLOS ONE, 8( 4), 7 . doi:10.1371/journal.pone.0060439
NLM
Yeh E, Fanganiello RD, Sunaga DY, Zhou X, Holmes G, Rocha KM, Alonso N, Matushita H, Wang Y, Jabs EW, Passos-Bueno MR. Novel Molecular Pathways Elicited by Mutant FGFR2 May Account for Brain Abnormalities in Apert Syndrome [Internet]. PLOS ONE. 2013 ; 8( 4): 7 .[citado 2024 nov. 10 ] Available from: http://www.plosone.org/article/info%3Adoi%2F10.1371%2Fjournal.pone.0060439
Vancouver
Yeh E, Fanganiello RD, Sunaga DY, Zhou X, Holmes G, Rocha KM, Alonso N, Matushita H, Wang Y, Jabs EW, Passos-Bueno MR. Novel Molecular Pathways Elicited by Mutant FGFR2 May Account for Brain Abnormalities in Apert Syndrome [Internet]. PLOS ONE. 2013 ; 8( 4): 7 .[citado 2024 nov. 10 ] Available from: http://www.plosone.org/article/info%3Adoi%2F10.1371%2Fjournal.pone.0060439

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