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Artigo de periodico
Impact of early enzyme-replacement therapy for mucopolysaccharidosis VI: results of a long-term follow-up of Brazilian siblings (2016)
Franco, J. F.; Soares, D. C.; Torres, L. C.; Leal, G. N.; Cunha, M. T.; Honjo, R. S.; Bertola, D. R.; Kim, C. A.
Source: Genetics and Molecular Research. Unidades: IB, FM
Subjects: PREVENÇÃO DE DOENÇAS, ENZIMAS, GLICOSAMINOGLICANAS, BIOTECNOLOGIA DE PLANTAS, BRASIL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FRANCO, J. F. et al. Impact of early enzyme-replacement therapy for mucopolysaccharidosis VI: results of a long-term follow-up of Brazilian siblings. Genetics and Molecular Research, v. 15, n. 1, p. 7 , 2016Tradução . . Disponível em: https://doi.org/10.4238/gmr.15017850. Acesso em: 18 nov. 2024.
APA
Franco, J. F., Soares, D. C., Torres, L. C., Leal, G. N., Cunha, M. T., Honjo, R. S., et al. (2016). Impact of early enzyme-replacement therapy for mucopolysaccharidosis VI: results of a long-term follow-up of Brazilian siblings. Genetics and Molecular Research, 15( 1), 7 . doi:10.4238/gmr.15017850
NLM
Franco JF, Soares DC, Torres LC, Leal GN, Cunha MT, Honjo RS, Bertola DR, Kim CA. Impact of early enzyme-replacement therapy for mucopolysaccharidosis VI: results of a long-term follow-up of Brazilian siblings [Internet]. Genetics and Molecular Research. 2016 ; 15( 1): 7 .[citado 2024 nov. 18 ] Available from: https://doi.org/10.4238/gmr.15017850
Vancouver
Franco JF, Soares DC, Torres LC, Leal GN, Cunha MT, Honjo RS, Bertola DR, Kim CA. Impact of early enzyme-replacement therapy for mucopolysaccharidosis VI: results of a long-term follow-up of Brazilian siblings [Internet]. Genetics and Molecular Research. 2016 ; 15( 1): 7 .[citado 2024 nov. 18 ] Available from: https://doi.org/10.4238/gmr.15017850
Artigo de periodico
Development and characterization of microsatellite loci for Tabebuia cassinoides (Bignoniaceae) (2014)
Pretti, V.Q; Françoso, E; Sforça, D. A; Pinheiro, F; Meyer, Diogo ; Lohmann, Lucia G
Source: Genetics and Molecular Research. Unidade: IB
Subjects: ÁRVORES, BOTÂNICA (CLASSIFICAÇÃO), MARCADOR MOLECULAR, GENOMAS, BIOGEOGRAFIA, GENÉTICA DE POPULAÇÕES, MADEIRA (DURABILIDADE;ASPECTOS ECONÔMICOS)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PRETTI, V.Q et al. Development and characterization of microsatellite loci for Tabebuia cassinoides (Bignoniaceae). Genetics and Molecular Research, n. 3, p. 5601-5605, 2014Tradução . . Disponível em: https://doi.org/10.4238/2014.July.25.15. Acesso em: 18 nov. 2024.
APA
Pretti, V. Q., Françoso, E., Sforça, D. A., Pinheiro, F., Meyer, D., & Lohmann, L. G. (2014). Development and characterization of microsatellite loci for Tabebuia cassinoides (Bignoniaceae). Genetics and Molecular Research, ( 3), 5601-5605. doi:10.4238/2014.July.25.15
NLM
Pretti VQ, Françoso E, Sforça DA, Pinheiro F, Meyer D, Lohmann LG. Development and characterization of microsatellite loci for Tabebuia cassinoides (Bignoniaceae) [Internet]. Genetics and Molecular Research. 2014 ;( 3): 5601-5605.[citado 2024 nov. 18 ] Available from: https://doi.org/10.4238/2014.July.25.15
Vancouver
Pretti VQ, Françoso E, Sforça DA, Pinheiro F, Meyer D, Lohmann LG. Development and characterization of microsatellite loci for Tabebuia cassinoides (Bignoniaceae) [Internet]. Genetics and Molecular Research. 2014 ;( 3): 5601-5605.[citado 2024 nov. 18 ] Available from: https://doi.org/10.4238/2014.July.25.15
Artigo de periodico
Johanson-Blizzard syndrome: a report of gender-discordant twins with a novel UBR1 mutation (2014)
Quaio, C. R.; Koda, Y. K.; Bertola, D. R.; Sukalo, M.; Zenker, M.; Kim, C. A.
Source: Genetics and Molecular Research. Unidades: FM, IB
Subjects: GÊMEOS, EXPRESSÃO GÊNICA, PANCREATOPATIAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
QUAIO, C. R. et al. Johanson-Blizzard syndrome: a report of gender-discordant twins with a novel UBR1 mutation. Genetics and Molecular Research, v. 13, n. 2, p. 4159-4164, 2014Tradução . . Disponível em: https://doi.org/10.4238/2014.June.9.2. Acesso em: 18 nov. 2024.
APA
Quaio, C. R., Koda, Y. K., Bertola, D. R., Sukalo, M., Zenker, M., & Kim, C. A. (2014). Johanson-Blizzard syndrome: a report of gender-discordant twins with a novel UBR1 mutation. Genetics and Molecular Research, 13( 2), 4159-4164. doi:10.4238/2014.June.9.2
NLM
Quaio CR, Koda YK, Bertola DR, Sukalo M, Zenker M, Kim CA. Johanson-Blizzard syndrome: a report of gender-discordant twins with a novel UBR1 mutation [Internet]. Genetics and Molecular Research. 2014 ; 13( 2): 4159-4164.[citado 2024 nov. 18 ] Available from: https://doi.org/10.4238/2014.June.9.2
Vancouver
Quaio CR, Koda YK, Bertola DR, Sukalo M, Zenker M, Kim CA. Johanson-Blizzard syndrome: a report of gender-discordant twins with a novel UBR1 mutation [Internet]. Genetics and Molecular Research. 2014 ; 13( 2): 4159-4164.[citado 2024 nov. 18 ] Available from: https://doi.org/10.4238/2014.June.9.2
Artigo de periodico
Variable expressivity of osteogenesis imperfecta in a Brazilian family due to p.G1079S mutation in the COL1A1 gene (2012)
Moraes, M. V. D.; Milanez, M.; Almada, B.V.P.; Zatz, Mayana
Source: Genetics and Molecular Research. Unidade: IB
Subjects: OSTEOGÊNESE, MUTAÇÃO GENÉTICA, GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MORAES, M. V. D. et al. Variable expressivity of osteogenesis imperfecta in a Brazilian family due to p.G1079S mutation in the COL1A1 gene. Genetics and Molecular Research, v. 11, n. 3, p. 3246-3255. 2012. online, 2012Tradução . . Disponível em: https://doi.org/10.4238/2012.September.12.7. Acesso em: 18 nov. 2024.
APA
Moraes, M. V. D., Milanez, M., Almada, B. V. P., & Zatz, M. (2012). Variable expressivity of osteogenesis imperfecta in a Brazilian family due to p.G1079S mutation in the COL1A1 gene. Genetics and Molecular Research, 11( 3), 3246-3255. 2012. online. doi:10.4238/2012.September.12.7
NLM
Moraes MVD, Milanez M, Almada BVP, Zatz M. Variable expressivity of osteogenesis imperfecta in a Brazilian family due to p.G1079S mutation in the COL1A1 gene [Internet]. Genetics and Molecular Research. 2012 ; 11( 3): 3246-3255. 2012. online.[citado 2024 nov. 18 ] Available from: https://doi.org/10.4238/2012.September.12.7
Vancouver
Moraes MVD, Milanez M, Almada BVP, Zatz M. Variable expressivity of osteogenesis imperfecta in a Brazilian family due to p.G1079S mutation in the COL1A1 gene [Internet]. Genetics and Molecular Research. 2012 ; 11( 3): 3246-3255. 2012. online.[citado 2024 nov. 18 ] Available from: https://doi.org/10.4238/2012.September.12.7
Artigo de periodico
Morphometric and genetic changes in a population of Apis mellifera after 34 years of Africanization (2009)
Francoy, Tiago Maurício; Wittmann, Dieter; Steinhage, Volker (Institut für Informatik III, Universität Bonn, Bonn, Germany); Müller, S.; Cunha, D. R.; Nascimento, A. M.; Figueiredo, Vera Lucia Castelo; Simões, Zilá Luz Paulino; De Jong, David; Arias, Maria Cristina ; Gonçalves, Lionel Segui
Source: Genetics and Molecular Research. Unidades: FFCLRP, FMRP, IB
Subjects: ABELHAS, BIODIVERSIDADE
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ABNT
FRANCOY, Tiago Maurício et al. Morphometric and genetic changes in a population of Apis mellifera after 34 years of Africanization. Genetics and Molecular Research, v. 8, n. 2, p. 709-717, 2009Tradução . . Disponível em: https://doi.org/10.4238/vol8-2kerr019. Acesso em: 18 nov. 2024.
APA
Francoy, T. M., Wittmann, D., Müller, S., Cunha, D. R., Nascimento, A. M., Figueiredo, V. L. C., et al. (2009). Morphometric and genetic changes in a population of Apis mellifera after 34 years of Africanization. Genetics and Molecular Research, 8( 2), 709-717. doi:10.4238/vol8-2kerr019
NLM
Francoy TM, Wittmann D, Müller S, Cunha DR, Nascimento AM, Figueiredo VLC, Simões ZLP, De Jong D, Arias MC, Gonçalves LS. Morphometric and genetic changes in a population of Apis mellifera after 34 years of Africanization [Internet]. Genetics and Molecular Research. 2009 ; 8( 2): 709-717.[citado 2024 nov. 18 ] Available from: https://doi.org/10.4238/vol8-2kerr019
Vancouver
Francoy TM, Wittmann D, Müller S, Cunha DR, Nascimento AM, Figueiredo VLC, Simões ZLP, De Jong D, Arias MC, Gonçalves LS. Morphometric and genetic changes in a population of Apis mellifera after 34 years of Africanization [Internet]. Genetics and Molecular Research. 2009 ; 8( 2): 709-717.[citado 2024 nov. 18 ] Available from: https://doi.org/10.4238/vol8-2kerr019
Artigo de periodico-carta/editorial
Comments to the paper by Ambrósio CE, Fadel L, Gaiad TP, Martins DS, et al. [Identification of three distinguishable phenotypes in golden retriever muscular dystrophy (Genet. Mol. Res. 2009 Apr 7;8 (2): 389-396)] (2009)
Zucconi, E; Jazedje, T; Valadares, M C; Zatz, Mayana
Source: Genetics and Molecular Research. Unidade: IB
Subjects: DISTROFIA MUSCULAR ANIMAL, GENÉTICA ANIMAL, CÃO GOLDEN RETRIEVER, MUTAÇÃO GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ZUCCONI, E et al. Comments to the paper by Ambrósio CE, Fadel L, Gaiad TP, Martins DS, et al. [Identification of three distinguishable phenotypes in golden retriever muscular dystrophy (Genet. Mol. Res. 2009 Apr 7;8 (2): 389-396)]. Genetics and Molecular Research. Ribeirão Preto: Instituto de Biociências, Universidade de São Paulo. Disponível em: https://doi.org/10.4238/vol8-3gmrCarta01. Acesso em: 18 nov. 2024. , 2009
APA
Zucconi, E., Jazedje, T., Valadares, M. C., & Zatz, M. (2009). Comments to the paper by Ambrósio CE, Fadel L, Gaiad TP, Martins DS, et al. [Identification of three distinguishable phenotypes in golden retriever muscular dystrophy (Genet. Mol. Res. 2009 Apr 7;8 (2): 389-396)]. Genetics and Molecular Research. Ribeirão Preto: Instituto de Biociências, Universidade de São Paulo. doi:10.4238/vol8-3gmrCarta01
NLM
Zucconi E, Jazedje T, Valadares MC, Zatz M. Comments to the paper by Ambrósio CE, Fadel L, Gaiad TP, Martins DS, et al. [Identification of three distinguishable phenotypes in golden retriever muscular dystrophy (Genet. Mol. Res. 2009 Apr 7;8 (2): 389-396)] [Internet]. Genetics and Molecular Research. 2009 ; 8( 3): 818-821.[citado 2024 nov. 18 ] Available from: https://doi.org/10.4238/vol8-3gmrCarta01
Vancouver
Zucconi E, Jazedje T, Valadares MC, Zatz M. Comments to the paper by Ambrósio CE, Fadel L, Gaiad TP, Martins DS, et al. [Identification of three distinguishable phenotypes in golden retriever muscular dystrophy (Genet. Mol. Res. 2009 Apr 7;8 (2): 389-396)] [Internet]. Genetics and Molecular Research. 2009 ; 8( 3): 818-821.[citado 2024 nov. 18 ] Available from: https://doi.org/10.4238/vol8-3gmrCarta01
Artigo de periodico
A novel COL1A1 gene-splicing mutation (c.1875+1G>C) in a Brazilian patient with osteogenesis imperfecta (2009)
Barbirato, C; Almeida, M. G; Milanez, M; Sipolatti, V; Rebouças, M. R. G. O; Akel Jr., A. N; Nunes, V. R. R; Perrone, A. M. S.; Zatz, Mayana ; Louro, I. D; Paula, F
Source: Genetics and Molecular Research. Unidade: IB
Subjects: OSTEOGÊNESE, MUTAÇÃO GENÉTICA, FENÓTIPOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BARBIRATO, C et al. A novel COL1A1 gene-splicing mutation (c.1875+1G>C) in a Brazilian patient with osteogenesis imperfecta. Genetics and Molecular Research, v. 8, n. 1, p. 173-178, 2009Tradução . . Disponível em: https://doi.org/10.4238/vol8-1gmr563. Acesso em: 18 nov. 2024.
APA
Barbirato, C., Almeida, M. G., Milanez, M., Sipolatti, V., Rebouças, M. R. G. O., Akel Jr., A. N., et al. (2009). A novel COL1A1 gene-splicing mutation (c.1875+1G>C) in a Brazilian patient with osteogenesis imperfecta. Genetics and Molecular Research, 8( 1), 173-178. doi:10.4238/vol8-1gmr563
NLM
Barbirato C, Almeida MG, Milanez M, Sipolatti V, Rebouças MRGO, Akel Jr. AN, Nunes VRR, Perrone AMS, Zatz M, Louro ID, Paula F. A novel COL1A1 gene-splicing mutation (c.1875+1G>C) in a Brazilian patient with osteogenesis imperfecta [Internet]. Genetics and Molecular Research. 2009 ; 8( 1): 173-178.[citado 2024 nov. 18 ] Available from: https://doi.org/10.4238/vol8-1gmr563
Vancouver
Barbirato C, Almeida MG, Milanez M, Sipolatti V, Rebouças MRGO, Akel Jr. AN, Nunes VRR, Perrone AMS, Zatz M, Louro ID, Paula F. A novel COL1A1 gene-splicing mutation (c.1875+1G>C) in a Brazilian patient with osteogenesis imperfecta [Internet]. Genetics and Molecular Research. 2009 ; 8( 1): 173-178.[citado 2024 nov. 18 ] Available from: https://doi.org/10.4238/vol8-1gmr563
Artigo de periodico
A framework for modeling of juxtacrine signaling systems (2007)
Rozante, Luiz Carlos da Silva; Gubitoso, Marco Dimas ; Matioli, Sergio Russo
Source: Genetics and Molecular Research. Unidades: IME, IB, BIOINFORMÁTICA
Subjects: RECEPTORES CELULARES, DROSOPHILA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ROZANTE, Luiz Carlos da Silva e GUBITOSO, Marco Dimas e MATIOLI, Sergio Russo. A framework for modeling of juxtacrine signaling systems. Genetics and Molecular Research, v. 6, n. 4, p. 821-845, 2007Tradução . . Disponível em: http://www.funpecrp.com.br/gmr/year2007/vol4-6/pdf/Xm0006.pdf. Acesso em: 18 nov. 2024.
APA
Rozante, L. C. da S., Gubitoso, M. D., & Matioli, S. R. (2007). A framework for modeling of juxtacrine signaling systems. Genetics and Molecular Research, 6( 4), 821-845. Recuperado de http://www.funpecrp.com.br/gmr/year2007/vol4-6/pdf/Xm0006.pdf
NLM
Rozante LC da S, Gubitoso MD, Matioli SR. A framework for modeling of juxtacrine signaling systems [Internet]. Genetics and Molecular Research. 2007 ; 6( 4): 821-845.[citado 2024 nov. 18 ] Available from: http://www.funpecrp.com.br/gmr/year2007/vol4-6/pdf/Xm0006.pdf
Vancouver
Rozante LC da S, Gubitoso MD, Matioli SR. A framework for modeling of juxtacrine signaling systems [Internet]. Genetics and Molecular Research. 2007 ; 6( 4): 821-845.[citado 2024 nov. 18 ] Available from: http://www.funpecrp.com.br/gmr/year2007/vol4-6/pdf/Xm0006.pdf

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