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Artigo de periodico
Antennal sensilla of specialist and generalist Anastrepha species (2023)
Perre, Paula; Bassan, Márcio; Perondini, André Luiz Paranhos ; Selivon, Denise
Source: Bulletin of Insectology. Unidade: IB
Subjects: DIPTERA, MOSCA-DAS-FRUTAS, ANATOMIA ANIMAL
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ABNT
PERRE, Paula et al. Antennal sensilla of specialist and generalist Anastrepha species. Bulletin of Insectology, v. 76, n. 1, p. 63-71, 2023Tradução . . Disponível em: http://www.bulletinofinsectology.org/pdfarticles/vol76-2023-063-071perre.pdf. Acesso em: 17 nov. 2024.
APA
Perre, P., Bassan, M., Perondini, A. L. P., & Selivon, D. (2023). Antennal sensilla of specialist and generalist Anastrepha species. Bulletin of Insectology, 76( 1), 63-71. Recuperado de http://www.bulletinofinsectology.org/pdfarticles/vol76-2023-063-071perre.pdf
NLM
Perre P, Bassan M, Perondini ALP, Selivon D. Antennal sensilla of specialist and generalist Anastrepha species [Internet]. Bulletin of Insectology. 2023 ; 76( 1): 63-71.[citado 2024 nov. 17 ] Available from: http://www.bulletinofinsectology.org/pdfarticles/vol76-2023-063-071perre.pdf
Vancouver
Perre P, Bassan M, Perondini ALP, Selivon D. Antennal sensilla of specialist and generalist Anastrepha species [Internet]. Bulletin of Insectology. 2023 ; 76( 1): 63-71.[citado 2024 nov. 17 ] Available from: http://www.bulletinofinsectology.org/pdfarticles/vol76-2023-063-071perre.pdf
Artigo de periodico
Correction to: effects of low-intensity training on the brain and muscle in the congenital muscular dystrophy 1D model (2022)
Comim, Clarissa M; Soares, Jaime A; Alberti, Adriano; Freiberger, Viviane; Ventura, Letícia; Dias, Paula; Schactae, Aryadnne L; Grigollo, Leoberto R; Steckert, Amanda V; Martins, Daniel F; Nodari Junior, Rudy J; Vainzof, Mariz ; Quevedo, João
Source: Neurological Sciences. Unidade: IB
Subjects: DISTROFIA MUSCULAR, DOENÇAS NEUROMUSCULARES, MIOPATIAS CONGÊNITAS ESTRUTURAIS
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ABNT
COMIM, Clarissa M et al. Correction to: effects of low-intensity training on the brain and muscle in the congenital muscular dystrophy 1D model. Neurological Sciences, v. 153, 2022Tradução . . Disponível em: https://doi.org/10.1007/s10072-022-05999-9. Acesso em: 17 nov. 2024.
APA
Comim, C. M., Soares, J. A., Alberti, A., Freiberger, V., Ventura, L., Dias, P., et al. (2022). Correction to: effects of low-intensity training on the brain and muscle in the congenital muscular dystrophy 1D model. Neurological Sciences, 153. doi:10.1007/s10072-022-05999-9
NLM
Comim CM, Soares JA, Alberti A, Freiberger V, Ventura L, Dias P, Schactae AL, Grigollo LR, Steckert AV, Martins DF, Nodari Junior RJ, Vainzof M, Quevedo J. Correction to: effects of low-intensity training on the brain and muscle in the congenital muscular dystrophy 1D model [Internet]. Neurological Sciences. 2022 ; 153[citado 2024 nov. 17 ] Available from: https://doi.org/10.1007/s10072-022-05999-9
Vancouver
Comim CM, Soares JA, Alberti A, Freiberger V, Ventura L, Dias P, Schactae AL, Grigollo LR, Steckert AV, Martins DF, Nodari Junior RJ, Vainzof M, Quevedo J. Correction to: effects of low-intensity training on the brain and muscle in the congenital muscular dystrophy 1D model [Internet]. Neurological Sciences. 2022 ; 153[citado 2024 nov. 17 ] Available from: https://doi.org/10.1007/s10072-022-05999-9
Artigo de periodico
Effects of low-intensity training on the brain and muscle in the congenital muscular dystrophy 1D model (2022)
Comim, Clarissa M; Soares, Jaime A; Alberti, Adriano; Freiberger, Viviane; Ventura, Letícia; Dias, Paula; Schactae, Aryadnne L; Grigollo, Leoberto R; Steckert, Amanda V; Martins, Daniel F; Nodari Junior, Rudy J; Vainzof, Mariz ; Quevedo, João
Source: Neurological Sciences. Unidade: IB
Subjects: DISTROFIA MUSCULAR, DOENÇAS NEUROMUSCULARES, MIOPATIAS CONGÊNITAS ESTRUTURAIS
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ABNT
COMIM, Clarissa M et al. Effects of low-intensity training on the brain and muscle in the congenital muscular dystrophy 1D model. Neurological Sciences, v. 153, 2022Tradução . . Disponível em: https://doi.org/10.1007/s10072-022-05928-w. Acesso em: 17 nov. 2024.
APA
Comim, C. M., Soares, J. A., Alberti, A., Freiberger, V., Ventura, L., Dias, P., et al. (2022). Effects of low-intensity training on the brain and muscle in the congenital muscular dystrophy 1D model. Neurological Sciences, 153. doi:10.1007/s10072-022-05928-w
NLM
Comim CM, Soares JA, Alberti A, Freiberger V, Ventura L, Dias P, Schactae AL, Grigollo LR, Steckert AV, Martins DF, Nodari Junior RJ, Vainzof M, Quevedo J. Effects of low-intensity training on the brain and muscle in the congenital muscular dystrophy 1D model [Internet]. Neurological Sciences. 2022 ; 153[citado 2024 nov. 17 ] Available from: https://doi.org/10.1007/s10072-022-05928-w
Vancouver
Comim CM, Soares JA, Alberti A, Freiberger V, Ventura L, Dias P, Schactae AL, Grigollo LR, Steckert AV, Martins DF, Nodari Junior RJ, Vainzof M, Quevedo J. Effects of low-intensity training on the brain and muscle in the congenital muscular dystrophy 1D model [Internet]. Neurological Sciences. 2022 ; 153[citado 2024 nov. 17 ] Available from: https://doi.org/10.1007/s10072-022-05928-w
Artigo de periodico
Dominant or recessive mutations in the RYR1 gene causing central core myopathy in Brazilian patients (2020)
Leão, Leonardo Galleni; Souza, Lucas Santos; Nogueira, Letícia; Pavanello, Rita de Cássia Mingroni; Gurgel-Giannetti, Juliana; Reed, Umbertina C; Oliveira, Acary S.B; Cuperman, Thais; Cotta, Ana; Paim, Julia F; Zatz, Mayana ; Vainzof, Mariz
Source: Acta Myologica. Unidades: FM, IB
Subjects: DOENÇAS NEUROMUSCULARES, MUTAÇÃO GENÉTICA, MIOPATIAS CONGÊNITAS ESTRUTURAIS
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ABNT
LEÃO, Leonardo Galleni et al. Dominant or recessive mutations in the RYR1 gene causing central core myopathy in Brazilian patients. Acta Myologica, v. 39, n. 4, p. 274–282, 2020Tradução . . Disponível em: https://doi.org/10.36185/2532-1900-030. Acesso em: 17 nov. 2024.
APA
Leão, L. G., Souza, L. S., Nogueira, L., Pavanello, R. de C. M., Gurgel-Giannetti, J., Reed, U. C., et al. (2020). Dominant or recessive mutations in the RYR1 gene causing central core myopathy in Brazilian patients. Acta Myologica, 39( 4), 274–282. doi:10.36185/2532-1900-030
NLM
Leão LG, Souza LS, Nogueira L, Pavanello R de CM, Gurgel-Giannetti J, Reed UC, Oliveira ASB, Cuperman T, Cotta A, Paim JF, Zatz M, Vainzof M. Dominant or recessive mutations in the RYR1 gene causing central core myopathy in Brazilian patients [Internet]. Acta Myologica. 2020 ; 39( 4): 274–282.[citado 2024 nov. 17 ] Available from: https://doi.org/10.36185/2532-1900-030
Vancouver
Leão LG, Souza LS, Nogueira L, Pavanello R de CM, Gurgel-Giannetti J, Reed UC, Oliveira ASB, Cuperman T, Cotta A, Paim JF, Zatz M, Vainzof M. Dominant or recessive mutations in the RYR1 gene causing central core myopathy in Brazilian patients [Internet]. Acta Myologica. 2020 ; 39( 4): 274–282.[citado 2024 nov. 17 ] Available from: https://doi.org/10.36185/2532-1900-030
Artigo de periodico
Antiproliferative in vitro effects of BI 2536-mediated PLK1 imhibition on cervical adenocarcinoma cells (2013)
Pezuk, Julia Alejandra; Brassesco, Maria Sol; Oliveira, Jaqueline Carvalho de; Morales, Andressa Gois; Montaldi, Ana Paula; Sakamoto-Hojo, Elza Tiemi; Scrideli, Carlos Alberto; Tone, Luiz Gonzaga
Source: Clinical and Experimental Medicine. Unidades: IB, FFCLRP, FMRP
Subjects: ANTINEOPLÁSICOS (ESTUDO IN VITRO), APOPTOSE, NEOPLASIAS DO COLO UTERINO
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ABNT
PEZUK, Julia Alejandra et al. Antiproliferative in vitro effects of BI 2536-mediated PLK1 imhibition on cervical adenocarcinoma cells. Clinical and Experimental Medicine, v. 13, n. 1, p. 75-80, 2013Tradução . . Disponível em: https://doi.org/10.1007/s10238-011-0166-1. Acesso em: 17 nov. 2024.
APA
Pezuk, J. A., Brassesco, M. S., Oliveira, J. C. de, Morales, A. G., Montaldi, A. P., Sakamoto-Hojo, E. T., et al. (2013). Antiproliferative in vitro effects of BI 2536-mediated PLK1 imhibition on cervical adenocarcinoma cells. Clinical and Experimental Medicine, 13( 1), 75-80. doi:10.1007/s10238-011-0166-1
NLM
Pezuk JA, Brassesco MS, Oliveira JC de, Morales AG, Montaldi AP, Sakamoto-Hojo ET, Scrideli CA, Tone LG. Antiproliferative in vitro effects of BI 2536-mediated PLK1 imhibition on cervical adenocarcinoma cells [Internet]. Clinical and Experimental Medicine. 2013 ; 13( 1): 75-80.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1007/s10238-011-0166-1
Vancouver
Pezuk JA, Brassesco MS, Oliveira JC de, Morales AG, Montaldi AP, Sakamoto-Hojo ET, Scrideli CA, Tone LG. Antiproliferative in vitro effects of BI 2536-mediated PLK1 imhibition on cervical adenocarcinoma cells [Internet]. Clinical and Experimental Medicine. 2013 ; 13( 1): 75-80.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1007/s10238-011-0166-1
Trabalho de evento-resumo periodico
Fukutin-related protein localizes on the endoplasmic reticulum and perinuclear region in muscle of distrophic animal models (2010)
Martins-Machado, Poliana Cristina; Ayub-Guerrieri, Danielle; Onofre-Oliveira, Paula; Monteiro, Gisele ; Santos, André F; Zilbersztajn-Gotlieb, Dinorah; Netto, Luis Eduardo Soares ; Vainzof, Mariz
Source: Acta Myologica. Conference titles: International Congress on Neuromuscular Diseases (ICNMD). Unidades: FCF, IB
Subjects: DISTROFIA MUSCULAR ANIMAL, PROTEÍNAS, MODELOS ANIMAIS DE DOENÇAS
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ABNT
MARTINS-MACHADO, Poliana Cristina et al. Fukutin-related protein localizes on the endoplasmic reticulum and perinuclear region in muscle of distrophic animal models. Acta Myologica. Ospedaletto: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo. . Acesso em: 17 nov. 2024. , 2010
APA
Martins-Machado, P. C., Ayub-Guerrieri, D., Onofre-Oliveira, P., Monteiro, G., Santos, A. F., Zilbersztajn-Gotlieb, D., et al. (2010). Fukutin-related protein localizes on the endoplasmic reticulum and perinuclear region in muscle of distrophic animal models. Acta Myologica. Ospedaletto: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo.
NLM
Martins-Machado PC, Ayub-Guerrieri D, Onofre-Oliveira P, Monteiro G, Santos AF, Zilbersztajn-Gotlieb D, Netto LES, Vainzof M. Fukutin-related protein localizes on the endoplasmic reticulum and perinuclear region in muscle of distrophic animal models. Acta Myologica. 2010 ; 29 136.[citado 2024 nov. 17 ]
Vancouver
Martins-Machado PC, Ayub-Guerrieri D, Onofre-Oliveira P, Monteiro G, Santos AF, Zilbersztajn-Gotlieb D, Netto LES, Vainzof M. Fukutin-related protein localizes on the endoplasmic reticulum and perinuclear region in muscle of distrophic animal models. Acta Myologica. 2010 ; 29 136.[citado 2024 nov. 17 ]
Trabalho de evento-resumo periodico
Mitochondrial cardioencephalomyopathy: new SCO2 gene mutations in a Brazilian patiente (2010)
Gurgel-Giannetti, Juliana; Lara, M T; Concentino, E L C; Martins-Machado, M C P; Yamamoto, L U; Onofre-Oliveira, Poliana; Vainzof, Mariz
Source: Acta Myologica. Conference titles: International Congress on Neuromuscular Diseases (ICNMD). Unidade: IB
Subjects: MUTAÇÃO GENÉTICA, GENÉTICA MÉDICA
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ABNT
GURGEL-GIANNETTI, Juliana et al. Mitochondrial cardioencephalomyopathy: new SCO2 gene mutations in a Brazilian patiente. Acta Myologica. Ospedaletto: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 17 nov. 2024. , 2010
APA
Gurgel-Giannetti, J., Lara, M. T., Concentino, E. L. C., Martins-Machado, M. C. P., Yamamoto, L. U., Onofre-Oliveira, P., & Vainzof, M. (2010). Mitochondrial cardioencephalomyopathy: new SCO2 gene mutations in a Brazilian patiente. Acta Myologica. Ospedaletto: Instituto de Biociências, Universidade de São Paulo.
NLM
Gurgel-Giannetti J, Lara MT, Concentino ELC, Martins-Machado MCP, Yamamoto LU, Onofre-Oliveira P, Vainzof M. Mitochondrial cardioencephalomyopathy: new SCO2 gene mutations in a Brazilian patiente. Acta Myologica. 2010 ; 29 240.[citado 2024 nov. 17 ]
Vancouver
Gurgel-Giannetti J, Lara MT, Concentino ELC, Martins-Machado MCP, Yamamoto LU, Onofre-Oliveira P, Vainzof M. Mitochondrial cardioencephalomyopathy: new SCO2 gene mutations in a Brazilian patiente. Acta Myologica. 2010 ; 29 240.[citado 2024 nov. 17 ]
Trabalho de evento-resumo periodico
Systemic transplantation of human adipose-derived stem cells into the Golden Retriever dystrophic dog (2010)
Vieira, Natássia; Bueno Júnior, Carlos Roberto ; Brandalise, Vanessa; Caetano, H. V. A; Zucconi, E; Secco, Mariane; Vainzof, Mariz ; Zatz, Mayana
Source: Acta Myologica. Conference titles: International Congress on Neuromuscular Diseases (ICNMD). Unidade: IB
Subjects: DISTROFIA MUSCULAR ANIMAL, CÉLULAS-TRONCO, CÃO GOLDEN RETRIEVER
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ABNT
VIEIRA, Natássia et al. Systemic transplantation of human adipose-derived stem cells into the Golden Retriever dystrophic dog. Acta Myologica. Ospedaletto: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 17 nov. 2024. , 2010
APA
Vieira, N., Bueno Júnior, C. R., Brandalise, V., Caetano, H. V. A., Zucconi, E., Secco, M., et al. (2010). Systemic transplantation of human adipose-derived stem cells into the Golden Retriever dystrophic dog. Acta Myologica. Ospedaletto: Instituto de Biociências, Universidade de São Paulo.
NLM
Vieira N, Bueno Júnior CR, Brandalise V, Caetano HVA, Zucconi E, Secco M, Vainzof M, Zatz M. Systemic transplantation of human adipose-derived stem cells into the Golden Retriever dystrophic dog. Acta Myologica. 2010 ; 29 268.[citado 2024 nov. 17 ]
Vancouver
Vieira N, Bueno Júnior CR, Brandalise V, Caetano HVA, Zucconi E, Secco M, Vainzof M, Zatz M. Systemic transplantation of human adipose-derived stem cells into the Golden Retriever dystrophic dog. Acta Myologica. 2010 ; 29 268.[citado 2024 nov. 17 ]
Trabalho de evento-resumo periodico
The value of cardiovascular magnetic resonance in the follow-up of Duchenne/Becker muscular dystrophy (2010)
Gurgel-Giannetti, Juliana; Silva, Marly; Meira, Zilda; Ferreira, R. A; Yamamoto, L U; Vainzof, Mariz ; Zatz, Mayana ; Rochitte, C E
Source: Acta Myologica. Conference titles: International Congress on Neuromuscular Diseases (ICNMD). Unidade: IB
Subjects: DISTROFIA MUSCULAR, RESSONÂNCIA MAGNÉTICA
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ABNT
GURGEL-GIANNETTI, Juliana et al. The value of cardiovascular magnetic resonance in the follow-up of Duchenne/Becker muscular dystrophy. Acta Myologica. Ospedaletto: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 17 nov. 2024. , 2010
APA
Gurgel-Giannetti, J., Silva, M., Meira, Z., Ferreira, R. A., Yamamoto, L. U., Vainzof, M., et al. (2010). The value of cardiovascular magnetic resonance in the follow-up of Duchenne/Becker muscular dystrophy. Acta Myologica. Ospedaletto: Instituto de Biociências, Universidade de São Paulo.
NLM
Gurgel-Giannetti J, Silva M, Meira Z, Ferreira RA, Yamamoto LU, Vainzof M, Zatz M, Rochitte CE. The value of cardiovascular magnetic resonance in the follow-up of Duchenne/Becker muscular dystrophy. Acta Myologica. 2010 ; 29 99 res.S6.PP2.[citado 2024 nov. 17 ]
Vancouver
Gurgel-Giannetti J, Silva M, Meira Z, Ferreira RA, Yamamoto LU, Vainzof M, Zatz M, Rochitte CE. The value of cardiovascular magnetic resonance in the follow-up of Duchenne/Becker muscular dystrophy. Acta Myologica. 2010 ; 29 99 res.S6.PP2.[citado 2024 nov. 17 ]
Trabalho de evento-resumo periodico
Mice models deficient for two muscle proteins helping to understand protein complexes organization and function (2010)
Vainzof, Mariz ; Martins-Machado, P C M; Onofre-Oliveira, P C G; Ayub-Guerrieri, D; Gotlieb, D; Fernandes, A; Lopes, V; Yamamoto, L U
Source: Acta Myologica. Conference titles: International Congress on Neuromuscular Diseases (ICNMD). Unidade: IB
Subjects: MODELOS ANIMAIS DE DOENÇAS, DOENÇAS NEUROMUSCULARES, PROTEÍNAS
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ABNT
VAINZOF, Mariz et al. Mice models deficient for two muscle proteins helping to understand protein complexes organization and function. Acta Myologica. Ospedaletto: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 17 nov. 2024. , 2010
APA
Vainzof, M., Martins-Machado, P. C. M., Onofre-Oliveira, P. C. G., Ayub-Guerrieri, D., Gotlieb, D., Fernandes, A., et al. (2010). Mice models deficient for two muscle proteins helping to understand protein complexes organization and function. Acta Myologica. Ospedaletto: Instituto de Biociências, Universidade de São Paulo.
NLM
Vainzof M, Martins-Machado PCM, Onofre-Oliveira PCG, Ayub-Guerrieri D, Gotlieb D, Fernandes A, Lopes V, Yamamoto LU. Mice models deficient for two muscle proteins helping to understand protein complexes organization and function. Acta Myologica. 2010 ; 29 262.[citado 2024 nov. 17 ]
Vancouver
Vainzof M, Martins-Machado PCM, Onofre-Oliveira PCG, Ayub-Guerrieri D, Gotlieb D, Fernandes A, Lopes V, Yamamoto LU. Mice models deficient for two muscle proteins helping to understand protein complexes organization and function. Acta Myologica. 2010 ; 29 262.[citado 2024 nov. 17 ]
Artigo de periodico
Cytogenetic characterization of Metynnis maculatus (Teleostei; Characiformes): the description in Serrasalminae of a small B chromosome bearing inactive NOR-like sequences (2009)
Baroni, Sabrina; Lopes, Carlos E; Almeida-Toledo, Lurdes Foresti de
Source: Caryologia. Unidade: IB
Subjects: CHARACIFORMES, CITOGENÉTICA, DNA RECOMBINANTE
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ABNT
BARONI, Sabrina e LOPES, Carlos E e ALMEIDA-TOLEDO, Lurdes Foresti de. Cytogenetic characterization of Metynnis maculatus (Teleostei; Characiformes): the description in Serrasalminae of a small B chromosome bearing inactive NOR-like sequences. Caryologia, v. 62, n. 2, p. 95-101, 2009Tradução . . Disponível em: https://doi.org/10.1080/00087114.2004.10589674. Acesso em: 17 nov. 2024.
APA
Baroni, S., Lopes, C. E., & Almeida-Toledo, L. F. de. (2009). Cytogenetic characterization of Metynnis maculatus (Teleostei; Characiformes): the description in Serrasalminae of a small B chromosome bearing inactive NOR-like sequences. Caryologia, 62( 2), 95-101. doi:10.1080/00087114.2004.10589674
NLM
Baroni S, Lopes CE, Almeida-Toledo LF de. Cytogenetic characterization of Metynnis maculatus (Teleostei; Characiformes): the description in Serrasalminae of a small B chromosome bearing inactive NOR-like sequences [Internet]. Caryologia. 2009 ; 62( 2): 95-101.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1080/00087114.2004.10589674
Vancouver
Baroni S, Lopes CE, Almeida-Toledo LF de. Cytogenetic characterization of Metynnis maculatus (Teleostei; Characiformes): the description in Serrasalminae of a small B chromosome bearing inactive NOR-like sequences [Internet]. Caryologia. 2009 ; 62( 2): 95-101.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1080/00087114.2004.10589674
Artigo de periodico
Hoplosternum littorale (Teleostei, Callichthyidae) from a coastal river basin in Brazil: cytogenetic analysis and gene mapping of 5S and 18S rDNA (2005)
Pazza, Rubens; Almeida-Toledo, Lurdes Foresti de
Source: Caryologia. Unidade: IB
Subjects: PEIXES, OSTEICHTHYES, CITOGENÉTICA (ANÁLISE)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PAZZA, Rubens e ALMEIDA-TOLEDO, Lurdes Foresti de. Hoplosternum littorale (Teleostei, Callichthyidae) from a coastal river basin in Brazil: cytogenetic analysis and gene mapping of 5S and 18S rDNA. Caryologia, v. 58, n. 4, p. 339-344, 2005Tradução . . Disponível em: https://doi.org/10.1080/00087114.2005.10589472. Acesso em: 17 nov. 2024.
APA
Pazza, R., & Almeida-Toledo, L. F. de. (2005). Hoplosternum littorale (Teleostei, Callichthyidae) from a coastal river basin in Brazil: cytogenetic analysis and gene mapping of 5S and 18S rDNA. Caryologia, 58( 4), 339-344. doi:10.1080/00087114.2005.10589472
NLM
Pazza R, Almeida-Toledo LF de. Hoplosternum littorale (Teleostei, Callichthyidae) from a coastal river basin in Brazil: cytogenetic analysis and gene mapping of 5S and 18S rDNA [Internet]. Caryologia. 2005 ; 58( 4): 339-344.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1080/00087114.2005.10589472
Vancouver
Pazza R, Almeida-Toledo LF de. Hoplosternum littorale (Teleostei, Callichthyidae) from a coastal river basin in Brazil: cytogenetic analysis and gene mapping of 5S and 18S rDNA [Internet]. Caryologia. 2005 ; 58( 4): 339-344.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1080/00087114.2005.10589472
Artigo de periodico
CFTR, PRSS1 and SPINK1 mutations in the development of pancreatitis in brazilian patients (2003)
Bernardino, Andréa Liliane Ferreira; Guarita, Dulce Reis; Mott, Carlos de Barros; Pedroso, Martha Regina Arcon; Machado, Marcel Cerqueira César; Laudanna, Antônio Atílio; Tani, Claudia Megume; Almeida, Fatima Lovatti; Zatz, Mayana
Source: Journal of the Pancreas. Unidades: IB, FM
Subjects: MUTAÇÃO GENÉTICA, FIBROSE CÍSTICA
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ABNT
BERNARDINO, Andréa Liliane Ferreira et al. CFTR, PRSS1 and SPINK1 mutations in the development of pancreatitis in brazilian patients. Journal of the Pancreas, v. 4, n. 5, p. 169-177, 2003Tradução . . Disponível em: http://www.joplink.net. Acesso em: 17 nov. 2024.
APA
Bernardino, A. L. F., Guarita, D. R., Mott, C. de B., Pedroso, M. R. A., Machado, M. C. C., Laudanna, A. A., et al. (2003). CFTR, PRSS1 and SPINK1 mutations in the development of pancreatitis in brazilian patients. Journal of the Pancreas, 4( 5), 169-177. Recuperado de http://www.joplink.net
NLM
Bernardino ALF, Guarita DR, Mott C de B, Pedroso MRA, Machado MCC, Laudanna AA, Tani CM, Almeida FL, Zatz M. CFTR, PRSS1 and SPINK1 mutations in the development of pancreatitis in brazilian patients [Internet]. Journal of the Pancreas. 2003 ; 4( 5): 169-177.[citado 2024 nov. 17 ] Available from: http://www.joplink.net
Vancouver
Bernardino ALF, Guarita DR, Mott C de B, Pedroso MRA, Machado MCC, Laudanna AA, Tani CM, Almeida FL, Zatz M. CFTR, PRSS1 and SPINK1 mutations in the development of pancreatitis in brazilian patients [Internet]. Journal of the Pancreas. 2003 ; 4( 5): 169-177.[citado 2024 nov. 17 ] Available from: http://www.joplink.net
Artigo de periodico
Synaptonemal complex analysis in the fish species Piaractus mesopotamicus and Colossoma macropomum, and in their interspecific hybrid (2002)
Santos, Vera Habda dos; Foresti, Fausto; Oliveira, Claudio; Almeida-Toledo, Lurdes Foresti de; Toledo Filho, Sílvio de Almeida; Bernardino, Geraldo
Source: Caryologia. Unidade: IB
Subjects: CROMOSSOMOS (EVOLUÇÃO), PEIXES, MEIOSE
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ABNT
SANTOS, Vera Habda dos et al. Synaptonemal complex analysis in the fish species Piaractus mesopotamicus and Colossoma macropomum, and in their interspecific hybrid. Caryologia, v. 55, n. 1, p. 73-79, 2002Tradução . . Disponível em: https://doi.org/10.1080/00087114.2002.10589260. Acesso em: 17 nov. 2024.
APA
Santos, V. H. dos, Foresti, F., Oliveira, C., Almeida-Toledo, L. F. de, Toledo Filho, S. de A., & Bernardino, G. (2002). Synaptonemal complex analysis in the fish species Piaractus mesopotamicus and Colossoma macropomum, and in their interspecific hybrid. Caryologia, 55( 1), 73-79. doi:10.1080/00087114.2002.10589260
NLM
Santos VH dos, Foresti F, Oliveira C, Almeida-Toledo LF de, Toledo Filho S de A, Bernardino G. Synaptonemal complex analysis in the fish species Piaractus mesopotamicus and Colossoma macropomum, and in their interspecific hybrid [Internet]. Caryologia. 2002 ; 55( 1): 73-79.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1080/00087114.2002.10589260
Vancouver
Santos VH dos, Foresti F, Oliveira C, Almeida-Toledo LF de, Toledo Filho S de A, Bernardino G. Synaptonemal complex analysis in the fish species Piaractus mesopotamicus and Colossoma macropomum, and in their interspecific hybrid [Internet]. Caryologia. 2002 ; 55( 1): 73-79.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1080/00087114.2002.10589260
Artigo de periodico
New approaches in epidemiology in neuromuscular disease (2002)
Poortman, Y.; Zatz, Mayana ; Mackenzie, A.; Zerres, Klaus
Source: Acta Myologica. Unidade: IB
Subjects: DOENÇAS NEUROMUSCULARES, EPIDEMIOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
POORTMAN, Y. et al. New approaches in epidemiology in neuromuscular disease. Acta Myologica, v. 21, p. 151-153, 2002Tradução . . Acesso em: 17 nov. 2024.
APA
Poortman, Y., Zatz, M., Mackenzie, A., & Zerres, K. (2002). New approaches in epidemiology in neuromuscular disease. Acta Myologica, 21, 151-153.
NLM
Poortman Y, Zatz M, Mackenzie A, Zerres K. New approaches in epidemiology in neuromuscular disease. Acta Myologica. 2002 ; 21 151-153.[citado 2024 nov. 17 ]
Vancouver
Poortman Y, Zatz M, Mackenzie A, Zerres K. New approaches in epidemiology in neuromuscular disease. Acta Myologica. 2002 ; 21 151-153.[citado 2024 nov. 17 ]
Artigo de periodico
A molecular phylogenetic analysis in Gymnotus species (Pisces: Gymnotiformes) with inferences on chromosome evolution (2001)
Fernandes-Matioli, Flora Maria de Campos; Almeida-Toledo, Lurdes Foresti de
Source: Caryologia. Unidade: IB
Subjects: PEIXES, CROMOSSOMOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FERNANDES-MATIOLI, Flora Maria de Campos e ALMEIDA-TOLEDO, Lurdes Foresti de. A molecular phylogenetic analysis in Gymnotus species (Pisces: Gymnotiformes) with inferences on chromosome evolution. Caryologia, v. 54, n. 1, p. 23-30, 2001Tradução . . Disponível em: https://doi.org/10.1080/00087114.2001.10589210. Acesso em: 17 nov. 2024.
APA
Fernandes-Matioli, F. M. de C., & Almeida-Toledo, L. F. de. (2001). A molecular phylogenetic analysis in Gymnotus species (Pisces: Gymnotiformes) with inferences on chromosome evolution. Caryologia, 54( 1), 23-30. doi:10.1080/00087114.2001.10589210
NLM
Fernandes-Matioli FM de C, Almeida-Toledo LF de. A molecular phylogenetic analysis in Gymnotus species (Pisces: Gymnotiformes) with inferences on chromosome evolution [Internet]. Caryologia. 2001 ; 54( 1): 23-30.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1080/00087114.2001.10589210
Vancouver
Fernandes-Matioli FM de C, Almeida-Toledo LF de. A molecular phylogenetic analysis in Gymnotus species (Pisces: Gymnotiformes) with inferences on chromosome evolution [Internet]. Caryologia. 2001 ; 54( 1): 23-30.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1080/00087114.2001.10589210
Trabalho de evento-resumo
X-inactivation in carriers of the fragile X full mutation: comparison between blood and skin cells (2001)
Vianna-Morgante, Angela M ; Costa, Silvia Souza da
Source: Abstracts. Conference titles: International Workshop on Fragile X and X-Linked Mental Retardation. Unidade: IB
Subjects: MUTAÇÃO (BIOLOGIA), RETARDO MENTAL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VIANNA-MORGANTE, Angela M e COSTA, Silvia Souza da. X-inactivation in carriers of the fragile X full mutation: comparison between blood and skin cells. 2001, Anais.. Frascati: Instituto de Biociências, Universidade de São Paulo, 2001. . Acesso em: 17 nov. 2024.
APA
Vianna-Morgante, A. M., & Costa, S. S. da. (2001). X-inactivation in carriers of the fragile X full mutation: comparison between blood and skin cells. In Abstracts. Frascati: Instituto de Biociências, Universidade de São Paulo.
NLM
Vianna-Morgante AM, Costa SS da. X-inactivation in carriers of the fragile X full mutation: comparison between blood and skin cells. Abstracts. 2001 ;[citado 2024 nov. 17 ]
Vancouver
Vianna-Morgante AM, Costa SS da. X-inactivation in carriers of the fragile X full mutation: comparison between blood and skin cells. Abstracts. 2001 ;[citado 2024 nov. 17 ]
Trabalho de evento-resumo
Genetic diversity of FMR1 CGC and linked microsatellites in South American populations (2001)
Mingroni Netto, Regina Celia ; Angeli, Claudia Blanes; Auricchio, Maria Teresa B. M.; Capelli, Leonardo Pires; Leal Mesquita, Emygdia Rosa do Rego Pires; Ribeiro-dos-Santos, Andrea K. C.; Ferrari, Irany; Hutz, Mara H; Salzano, Francisco Mauro; Hill, K.; Hurtado, A. M.; Vianna-Morgante, Angela M
Source: Resumo. Conference titles: International Workshop on Fragile X and X-Linked Mental Retardation. Unidade: IB
Subjects: GENES, GENÉTICA DE POPULAÇÕES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MINGRONI NETTO, Regina Celia et al. Genetic diversity of FMR1 CGC and linked microsatellites in South American populations. 2001, Anais.. Frascati: Instituto de Biociências, Universidade de São Paulo, 2001. . Acesso em: 17 nov. 2024.
APA
Mingroni Netto, R. C., Angeli, C. B., Auricchio, M. T. B. M., Capelli, L. P., Leal Mesquita, E. R. do R. P., Ribeiro-dos-Santos, A. K. C., et al. (2001). Genetic diversity of FMR1 CGC and linked microsatellites in South American populations. In Resumo. Frascati: Instituto de Biociências, Universidade de São Paulo.
NLM
Mingroni Netto RC, Angeli CB, Auricchio MTBM, Capelli LP, Leal Mesquita ER do RP, Ribeiro-dos-Santos AKC, Ferrari I, Hutz MH, Salzano FM, Hill K, Hurtado AM, Vianna-Morgante AM. Genetic diversity of FMR1 CGC and linked microsatellites in South American populations. Resumo. 2001 ;[citado 2024 nov. 17 ]
Vancouver
Mingroni Netto RC, Angeli CB, Auricchio MTBM, Capelli LP, Leal Mesquita ER do RP, Ribeiro-dos-Santos AKC, Ferrari I, Hutz MH, Salzano FM, Hill K, Hurtado AM, Vianna-Morgante AM. Genetic diversity of FMR1 CGC and linked microsatellites in South American populations. Resumo. 2001 ;[citado 2024 nov. 17 ]
Artigo de periodico
Chromosome R-banding pattern and conservaion of a marker chromosome in four species, genus Astyanax (Characidae, Tetragonopterinae) (2001)
Daniel-Silva, Maria de Fátima Zambelli; Almeida-Toledo, Lurdes Foresti de
Source: Caryologia. Unidade: IB
Subjects: PEIXES, CROMOSSOMOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
DANIEL-SILVA, Maria de Fátima Zambelli e ALMEIDA-TOLEDO, Lurdes Foresti de. Chromosome R-banding pattern and conservaion of a marker chromosome in four species, genus Astyanax (Characidae, Tetragonopterinae). Caryologia, v. 54, n. 3, p. 209-215, 2001Tradução . . Disponível em: https://doi.org/10.1080/00087114.2001.10589228. Acesso em: 17 nov. 2024.
APA
Daniel-Silva, M. de F. Z., & Almeida-Toledo, L. F. de. (2001). Chromosome R-banding pattern and conservaion of a marker chromosome in four species, genus Astyanax (Characidae, Tetragonopterinae). Caryologia, 54( 3), 209-215. doi:10.1080/00087114.2001.10589228
NLM
Daniel-Silva M de FZ, Almeida-Toledo LF de. Chromosome R-banding pattern and conservaion of a marker chromosome in four species, genus Astyanax (Characidae, Tetragonopterinae) [Internet]. Caryologia. 2001 ; 54( 3): 209-215.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1080/00087114.2001.10589228
Vancouver
Daniel-Silva M de FZ, Almeida-Toledo LF de. Chromosome R-banding pattern and conservaion of a marker chromosome in four species, genus Astyanax (Characidae, Tetragonopterinae) [Internet]. Caryologia. 2001 ; 54( 3): 209-215.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1080/00087114.2001.10589228
Trabalho de evento
Palaeopathology as one of the tools to unravel the way of life of a brazilian shellmound population (2000)
Okumura, Mercedes ; Eggers, Sabine
Source: Proceedings. Conference titles: European Meeting of the Palaeopathology Association. Unidade: IB
Subjects: PALEOPATOLOGIA HUMANA, ESQUELETO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
OKUMURA, Mercedes e EGGERS, Sabine. Palaeopathology as one of the tools to unravel the way of life of a brazilian shellmound population. 2000, Anais.. Chieti: Instituto de Biociências, Universidade de São Paulo, 2000. . Acesso em: 17 nov. 2024.
APA
Okumura, M., & Eggers, S. (2000). Palaeopathology as one of the tools to unravel the way of life of a brazilian shellmound population. In Proceedings. Chieti: Instituto de Biociências, Universidade de São Paulo.
NLM
Okumura M, Eggers S. Palaeopathology as one of the tools to unravel the way of life of a brazilian shellmound population. Proceedings. 2000 ;[citado 2024 nov. 17 ]
Vancouver
Okumura M, Eggers S. Palaeopathology as one of the tools to unravel the way of life of a brazilian shellmound population. Proceedings. 2000 ;[citado 2024 nov. 17 ]

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