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Artigo de periodico
The p.P56S mutation in the VAPB gene is not due to a single founder: first European case. [Letter to the editor] (2010)
Funke, A. D.; Esser, M.; Krüttgen, A.; Weis, J.; Mitne Neto, Miguel; Lazar, M.; Nishimura, A. L.; Sperfela, A. D.; Trillenberg, P.; Senderek, Jan; Krasnianski, M.; Zatz, Mayana ; Zierz, S.; Deschauer, M.
Source: Clinical Genetics. Unidade: IB
Assunto: MUTAÇÃO GENÉTICA
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ABNT
FUNKE, A. D. et al. The p.P56S mutation in the VAPB gene is not due to a single founder: first European case. [Letter to the editor]. Clinical Genetics, v. 77, n. 3, p. 302-303, 2010Tradução . . Acesso em: 19 nov. 2024.
APA
Funke, A. D., Esser, M., Krüttgen, A., Weis, J., Mitne Neto, M., Lazar, M., et al. (2010). The p.P56S mutation in the VAPB gene is not due to a single founder: first European case. [Letter to the editor]. Clinical Genetics, 77( 3), 302-303.
NLM
Funke AD, Esser M, Krüttgen A, Weis J, Mitne Neto M, Lazar M, Nishimura AL, Sperfela AD, Trillenberg P, Senderek J, Krasnianski M, Zatz M, Zierz S, Deschauer M. The p.P56S mutation in the VAPB gene is not due to a single founder: first European case. [Letter to the editor]. Clinical Genetics. 2010 ; 77( 3): 302-303.[citado 2024 nov. 19 ]
Vancouver
Funke AD, Esser M, Krüttgen A, Weis J, Mitne Neto M, Lazar M, Nishimura AL, Sperfela AD, Trillenberg P, Senderek J, Krasnianski M, Zatz M, Zierz S, Deschauer M. The p.P56S mutation in the VAPB gene is not due to a single founder: first European case. [Letter to the editor]. Clinical Genetics. 2010 ; 77( 3): 302-303.[citado 2024 nov. 19 ]
Artigo de periodico
Transcriptional regulation differs in affected facioscapulohumeral muscular dystrophy patients compared to asymptomatic related carriers (2009)
Arashiro, Patrícia; Eisenberg, Iris; Kho, Alvin T.; Cerqueira, Antonia Maria Pereira; Canovas, Marta; Silva, Helga C. A.; Pavanello, Rita de Cássia M.; Verjovski-Almeida, Sergio ; Kunkel, Louis M.; Zatz, Mayana
Source: PNAS. Unidades: IB, IQ
Assunto: DISTROFIA MUSCULAR
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ABNT
ARASHIRO, Patrícia et al. Transcriptional regulation differs in affected facioscapulohumeral muscular dystrophy patients compared to asymptomatic related carriers. PNAS, v. 106, n. 15, p. 6220-6225, 2009Tradução . . Disponível em: https://doi.org/10.1073/pnas.0901573106. Acesso em: 19 nov. 2024.
APA
Arashiro, P., Eisenberg, I., Kho, A. T., Cerqueira, A. M. P., Canovas, M., Silva, H. C. A., et al. (2009). Transcriptional regulation differs in affected facioscapulohumeral muscular dystrophy patients compared to asymptomatic related carriers. PNAS, 106( 15), 6220-6225. doi:10.1073/pnas.0901573106
NLM
Arashiro P, Eisenberg I, Kho AT, Cerqueira AMP, Canovas M, Silva HCA, Pavanello R de CM, Verjovski-Almeida S, Kunkel LM, Zatz M. Transcriptional regulation differs in affected facioscapulohumeral muscular dystrophy patients compared to asymptomatic related carriers [Internet]. PNAS. 2009 ; 106( 15): 6220-6225.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1073/pnas.0901573106
Vancouver
Arashiro P, Eisenberg I, Kho AT, Cerqueira AMP, Canovas M, Silva HCA, Pavanello R de CM, Verjovski-Almeida S, Kunkel LM, Zatz M. Transcriptional regulation differs in affected facioscapulohumeral muscular dystrophy patients compared to asymptomatic related carriers [Internet]. PNAS. 2009 ; 106( 15): 6220-6225.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1073/pnas.0901573106
Artigo de periodico
Multipotent stem cells from umbilical cord: Cord is richer than blood! (2008)
Secco, Mariane; Zucconi, Eder; Vieira, Natássia M.; Fogaça, Luciana Luchesi Quintanilha; Cerqueira, Antonia; Carvalho, Maria Denise F.; Jazedje, Tatiana; Okamoto, Oswaldo Keith ; Muotri, Alysson Renato; Zatz, Mayana
Source: Stem Cells. Unidade: IB
Assunto: CORDÃO UMBILICAL
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ABNT
SECCO, Mariane et al. Multipotent stem cells from umbilical cord: Cord is richer than blood!. Stem Cells, v. 26, n. 1, p. 246-150, 2008Tradução . . Acesso em: 19 nov. 2024.
APA
Secco, M., Zucconi, E., Vieira, N. M., Fogaça, L. L. Q., Cerqueira, A., Carvalho, M. D. F., et al. (2008). Multipotent stem cells from umbilical cord: Cord is richer than blood!. Stem Cells, 26( 1), 246-150.
NLM
Secco M, Zucconi E, Vieira NM, Fogaça LLQ, Cerqueira A, Carvalho MDF, Jazedje T, Okamoto OK, Muotri AR, Zatz M. Multipotent stem cells from umbilical cord: Cord is richer than blood!. Stem Cells. 2008 ; 26( 1): 246-150.[citado 2024 nov. 19 ]
Vancouver
Secco M, Zucconi E, Vieira NM, Fogaça LLQ, Cerqueira A, Carvalho MDF, Jazedje T, Okamoto OK, Muotri AR, Zatz M. Multipotent stem cells from umbilical cord: Cord is richer than blood!. Stem Cells. 2008 ; 26( 1): 246-150.[citado 2024 nov. 19 ]
Artigo de periodico
Human multipotent adipose-derived stem cells restore dystrophin expression of Duchenne skeletal-muscle cells in vitro (2008)
Vieira, Natássia M.; Brandalise, Vanessa; Zucconi, Eder; Jazedje, Tatiana; Secco, Mariane; Nunes, Viviane Abreu; Strauss, Bryan Eric; Vainzof, Mariz ; Zatz, Mayana
Source: Biology of the Cell. Unidade: IB
Assunto: DISTROFIA MUSCULAR
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ABNT
VIEIRA, Natássia M. et al. Human multipotent adipose-derived stem cells restore dystrophin expression of Duchenne skeletal-muscle cells in vitro. Biology of the Cell, v. 100, p. 231-241, 2008Tradução . . Disponível em: https://doi.org/10.1042/bc20070102. Acesso em: 19 nov. 2024.
APA
Vieira, N. M., Brandalise, V., Zucconi, E., Jazedje, T., Secco, M., Nunes, V. A., et al. (2008). Human multipotent adipose-derived stem cells restore dystrophin expression of Duchenne skeletal-muscle cells in vitro. Biology of the Cell, 100, 231-241. doi:10.1042/bc20070102
NLM
Vieira NM, Brandalise V, Zucconi E, Jazedje T, Secco M, Nunes VA, Strauss BE, Vainzof M, Zatz M. Human multipotent adipose-derived stem cells restore dystrophin expression of Duchenne skeletal-muscle cells in vitro [Internet]. Biology of the Cell. 2008 ; 100 231-241.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1042/bc20070102
Vancouver
Vieira NM, Brandalise V, Zucconi E, Jazedje T, Secco M, Nunes VA, Strauss BE, Vainzof M, Zatz M. Human multipotent adipose-derived stem cells restore dystrophin expression of Duchenne skeletal-muscle cells in vitro [Internet]. Biology of the Cell. 2008 ; 100 231-241.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1042/bc20070102
Artigo de periodico
Mutations in the KIAA0196 gene at the SPG8 locus cause hereditary spastic paraplegia (2007)
Valdmanis, Paul N.; Meijer, Inge A.; Reynolds, Annie; Lei, Adrienne; MacLeod, Patrick; Schlesinger, David; Zatz, Mayana ; Reid, Evan; Dion, Patrick A.; Drapeau, Pierre; Rouleau, Guy A.
Source: American Journal of Human Genetics. Unidade: IB
Subjects: DOENÇAS NEURODEGENERATIVAS, DOENÇAS HEREDITÁRIAS
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ABNT
VALDMANIS, Paul N. et al. Mutations in the KIAA0196 gene at the SPG8 locus cause hereditary spastic paraplegia. American Journal of Human Genetics, v. 80, n. 1, p. 152-161, 2007Tradução . . Acesso em: 19 nov. 2024.
APA
Valdmanis, P. N., Meijer, I. A., Reynolds, A., Lei, A., MacLeod, P., Schlesinger, D., et al. (2007). Mutations in the KIAA0196 gene at the SPG8 locus cause hereditary spastic paraplegia. American Journal of Human Genetics, 80( 1), 152-161.
NLM
Valdmanis PN, Meijer IA, Reynolds A, Lei A, MacLeod P, Schlesinger D, Zatz M, Reid E, Dion PA, Drapeau P, Rouleau GA. Mutations in the KIAA0196 gene at the SPG8 locus cause hereditary spastic paraplegia. American Journal of Human Genetics. 2007 ; 80( 1): 152-161.[citado 2024 nov. 19 ]
Vancouver
Valdmanis PN, Meijer IA, Reynolds A, Lei A, MacLeod P, Schlesinger D, Zatz M, Reid E, Dion PA, Drapeau P, Rouleau GA. Mutations in the KIAA0196 gene at the SPG8 locus cause hereditary spastic paraplegia. American Journal of Human Genetics. 2007 ; 80( 1): 152-161.[citado 2024 nov. 19 ]
Artigo de periodico
A mutation in human VAP-B-MSP domain, present in ALS patients, affects the interaction with other cellular proteins (2007)
Mitne Neto, Miguel; Ramos, Celso Raúl Romero; Pimenta, Daniel Carvalho; Luz, Juliana Silva da; Nishimura, Agnes Lumi; Gonzales, Fernando Alexis; Oliveira, Carla Columbano de ; Zatz, Mayana
Source: Protein Expression and Purification. Unidades: IQ, IB
Subjects: BIOQUÍMICA, PROTEÍNAS
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ABNT
MITNE NETO, Miguel et al. A mutation in human VAP-B-MSP domain, present in ALS patients, affects the interaction with other cellular proteins. Protein Expression and Purification, v. 55, n. 1, p. 139-146, 2007Tradução . . Disponível em: https://doi.org/10.1016/j.pep.2007.04.007. Acesso em: 19 nov. 2024.
APA
Mitne Neto, M., Ramos, C. R. R., Pimenta, D. C., Luz, J. S. da, Nishimura, A. L., Gonzales, F. A., et al. (2007). A mutation in human VAP-B-MSP domain, present in ALS patients, affects the interaction with other cellular proteins. Protein Expression and Purification, 55( 1), 139-146. doi:10.1016/j.pep.2007.04.007
NLM
Mitne Neto M, Ramos CRR, Pimenta DC, Luz JS da, Nishimura AL, Gonzales FA, Oliveira CC de, Zatz M. A mutation in human VAP-B-MSP domain, present in ALS patients, affects the interaction with other cellular proteins [Internet]. Protein Expression and Purification. 2007 ; 55( 1): 139-146.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1016/j.pep.2007.04.007
Vancouver
Mitne Neto M, Ramos CRR, Pimenta DC, Luz JS da, Nishimura AL, Gonzales FA, Oliveira CC de, Zatz M. A mutation in human VAP-B-MSP domain, present in ALS patients, affects the interaction with other cellular proteins [Internet]. Protein Expression and Purification. 2007 ; 55( 1): 139-146.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1016/j.pep.2007.04.007
Artigo de periodico
Central core disease due to recessive mutations in RYR1 gene: is it more common than described? (2007)
Kossugue, Patricia Mayumi; Paim, Julia F.; Navarro, Monica M.; Silva, Helga Cristina Almeida da; Pavanello, Rita de Cássia M.; Gurgel-Giannetti, Juliana; Zatz, Mayana ; Vainzof, Mariz
Source: Muscle & Nerve. Unidade: IB
Subjects: MIOPATIAS CONGÊNITAS ESTRUTURAIS, MUTAÇÃO GENÉTICA
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ABNT
KOSSUGUE, Patricia Mayumi et al. Central core disease due to recessive mutations in RYR1 gene: is it more common than described?. Muscle & Nerve, v. 35, n. 5, p. 670-674, 2007Tradução . . Disponível em: https://doi.org/10.1002/mus.20715. Acesso em: 19 nov. 2024.
APA
Kossugue, P. M., Paim, J. F., Navarro, M. M., Silva, H. C. A. da, Pavanello, R. de C. M., Gurgel-Giannetti, J., et al. (2007). Central core disease due to recessive mutations in RYR1 gene: is it more common than described? Muscle & Nerve, 35( 5), 670-674. doi:10.1002/mus.20715
NLM
Kossugue PM, Paim JF, Navarro MM, Silva HCA da, Pavanello R de CM, Gurgel-Giannetti J, Zatz M, Vainzof M. Central core disease due to recessive mutations in RYR1 gene: is it more common than described? [Internet]. Muscle & Nerve. 2007 ; 35( 5): 670-674.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1002/mus.20715
Vancouver
Kossugue PM, Paim JF, Navarro MM, Silva HCA da, Pavanello R de CM, Gurgel-Giannetti J, Zatz M, Vainzof M. Central core disease due to recessive mutations in RYR1 gene: is it more common than described? [Internet]. Muscle & Nerve. 2007 ; 35( 5): 670-674.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1002/mus.20715
Artigo de periodico
Stem cells from umbilical cord blood differentiate into myotubes and express dystrophin in vitro only after exposure to in vivo muscle environment (2007)
Nunes, Viviane Abreu; Cavaçana, Natale; Canovas, Marta; Strauss, Bryan Eric; Zatz, Mayana
Source: Biology of the Cell. Unidade: IB
Subjects: DISTROFIA MUSCULAR, DIFERENCIAÇÃO CELULAR
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ABNT
NUNES, Viviane Abreu et al. Stem cells from umbilical cord blood differentiate into myotubes and express dystrophin in vitro only after exposure to in vivo muscle environment. Biology of the Cell, v. 99, p. 185-196, 2007Tradução . . Disponível em: https://doi.org/10.1042/bc20060075. Acesso em: 19 nov. 2024.
APA
Nunes, V. A., Cavaçana, N., Canovas, M., Strauss, B. E., & Zatz, M. (2007). Stem cells from umbilical cord blood differentiate into myotubes and express dystrophin in vitro only after exposure to in vivo muscle environment. Biology of the Cell, 99, 185-196. doi:10.1042/bc20060075
NLM
Nunes VA, Cavaçana N, Canovas M, Strauss BE, Zatz M. Stem cells from umbilical cord blood differentiate into myotubes and express dystrophin in vitro only after exposure to in vivo muscle environment [Internet]. Biology of the Cell. 2007 ; 99 185-196.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1042/bc20060075
Vancouver
Nunes VA, Cavaçana N, Canovas M, Strauss BE, Zatz M. Stem cells from umbilical cord blood differentiate into myotubes and express dystrophin in vitro only after exposure to in vivo muscle environment [Internet]. Biology of the Cell. 2007 ; 99 185-196.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1042/bc20060075
Artigo de periodico
A new evidence for the maintenance of the sarcoglycan complex in muscle sarcolemma in spite of the primary absence of 'delta'-SG protein (2007)
Gouveia, Telma Luciana Furtado; Kossugue, Patricia Mayumi; Paim, Julia F.; Zatz, Mayana ; Anderson, Louise V. B.; Nigro, Vicenzo; Vainzof, Mariz
Source: Journal of Molecular Medicine. Unidade: IB
Subjects: DISTROFIA MUSCULAR, MUTAÇÃO GENÉTICA, PROTEÍNAS MUSCULARES
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ABNT
GOUVEIA, Telma Luciana Furtado et al. A new evidence for the maintenance of the sarcoglycan complex in muscle sarcolemma in spite of the primary absence of 'delta'-SG protein. Journal of Molecular Medicine, v. 85, n. 4, p. 415-420, 2007Tradução . . Disponível em: https://doi.org/10.1007/s00109-007-0163-8. Acesso em: 19 nov. 2024.
APA
Gouveia, T. L. F., Kossugue, P. M., Paim, J. F., Zatz, M., Anderson, L. V. B., Nigro, V., & Vainzof, M. (2007). A new evidence for the maintenance of the sarcoglycan complex in muscle sarcolemma in spite of the primary absence of 'delta'-SG protein. Journal of Molecular Medicine, 85( 4), 415-420. doi:10.1007/s00109-007-0163-8
NLM
Gouveia TLF, Kossugue PM, Paim JF, Zatz M, Anderson LVB, Nigro V, Vainzof M. A new evidence for the maintenance of the sarcoglycan complex in muscle sarcolemma in spite of the primary absence of 'delta'-SG protein [Internet]. Journal of Molecular Medicine. 2007 ; 85( 4): 415-420.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1007/s00109-007-0163-8
Vancouver
Gouveia TLF, Kossugue PM, Paim JF, Zatz M, Anderson LVB, Nigro V, Vainzof M. A new evidence for the maintenance of the sarcoglycan complex in muscle sarcolemma in spite of the primary absence of 'delta'-SG protein [Internet]. Journal of Molecular Medicine. 2007 ; 85( 4): 415-420.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1007/s00109-007-0163-8
Artigo de periodico
Mutation in the Scyl1 gene encoding amino-terminal kinase-like protein causes a recessive form of spinocerebellar neurodegeneration (2007)
Schmidt, Wolfgang M.; Kraus, Cornelia; Höger, Harald; Oberndorfer, Felicitas; Branka, Manuela; Bingemann, Sonja; Lassmann, Hans; Müller, Markus; Macedo-Souza, Lúcia Inês; Vainzof, Mariz ; Zatz, Mayana ; Reis, André; Bittner, Reginald E.
Source: EMBO reports. Unidade: IB
Subjects: DOENÇAS NEURODEGENERATIVAS, MUTAÇÃO GENÉTICA
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ABNT
SCHMIDT, Wolfgang M. et al. Mutation in the Scyl1 gene encoding amino-terminal kinase-like protein causes a recessive form of spinocerebellar neurodegeneration. EMBO reports, v. 8, n. 7, p. 691-697, 2007Tradução . . Disponível em: https://doi.org/10.1038/sj.embor.7401001. Acesso em: 19 nov. 2024.
APA
Schmidt, W. M., Kraus, C., Höger, H., Oberndorfer, F., Branka, M., Bingemann, S., et al. (2007). Mutation in the Scyl1 gene encoding amino-terminal kinase-like protein causes a recessive form of spinocerebellar neurodegeneration. EMBO reports, 8( 7), 691-697. doi:10.1038/sj.embor.7401001
NLM
Schmidt WM, Kraus C, Höger H, Oberndorfer F, Branka M, Bingemann S, Lassmann H, Müller M, Macedo-Souza LI, Vainzof M, Zatz M, Reis A, Bittner RE. Mutation in the Scyl1 gene encoding amino-terminal kinase-like protein causes a recessive form of spinocerebellar neurodegeneration [Internet]. EMBO reports. 2007 ; 8( 7): 691-697.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1038/sj.embor.7401001
Vancouver
Schmidt WM, Kraus C, Höger H, Oberndorfer F, Branka M, Bingemann S, Lassmann H, Müller M, Macedo-Souza LI, Vainzof M, Zatz M, Reis A, Bittner RE. Mutation in the Scyl1 gene encoding amino-terminal kinase-like protein causes a recessive form of spinocerebellar neurodegeneration [Internet]. EMBO reports. 2007 ; 8( 7): 691-697.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1038/sj.embor.7401001
Artigo de periodico
Red-green color vision impairment in Duchenne Muscular Dystrophy (2007)
Costa, Marcelo Fernandes da ; Oliveira, André Gustavo Fernandes; Feitosa-Santana, Claudia; Zatz, Mayana ; Ventura, Dora Selma Fix
Source: American Journal of Human Genetics. Unidades: IB, IP
Subjects: DISTROFIA MUSCULAR, MUTAÇÃO GENÉTICA
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ABNT
COSTA, Marcelo Fernandes da et al. Red-green color vision impairment in Duchenne Muscular Dystrophy. American Journal of Human Genetics, v. 80, n. 6, p. 1064-1075, 2007Tradução . . Acesso em: 19 nov. 2024.
APA
Costa, M. F. da, Oliveira, A. G. F., Feitosa-Santana, C., Zatz, M., & Ventura, D. S. F. (2007). Red-green color vision impairment in Duchenne Muscular Dystrophy. American Journal of Human Genetics, 80( 6), 1064-1075.
NLM
Costa MF da, Oliveira AGF, Feitosa-Santana C, Zatz M, Ventura DSF. Red-green color vision impairment in Duchenne Muscular Dystrophy. American Journal of Human Genetics. 2007 ; 80( 6): 1064-1075.[citado 2024 nov. 19 ]
Vancouver
Costa MF da, Oliveira AGF, Feitosa-Santana C, Zatz M, Ventura DSF. Red-green color vision impairment in Duchenne Muscular Dystrophy. American Journal of Human Genetics. 2007 ; 80( 6): 1064-1075.[citado 2024 nov. 19 ]
Artigo de periodico
Sarcoglycanopathies: a multiplex molecular analysis for the most common mutations (2006)
Gouveia, Telma Luciana Furtado; Paim, Julia F. O.; Pavanello, Rita de Cássia M.; Zatz, Mayana ; Vainzof, Mariz
Source: Diagnostic Molecular Pathology. Unidade: IB
Subjects: DISTROFIA MUSCULAR, MUTAÇÃO GENÉTICA, GENÉTICA MÉDICA
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ABNT
GOUVEIA, Telma Luciana Furtado et al. Sarcoglycanopathies: a multiplex molecular analysis for the most common mutations. Diagnostic Molecular Pathology, v. 15, n. ju 2006, p. 95-100, 2006Tradução . . Acesso em: 19 nov. 2024.
APA
Gouveia, T. L. F., Paim, J. F. O., Pavanello, R. de C. M., Zatz, M., & Vainzof, M. (2006). Sarcoglycanopathies: a multiplex molecular analysis for the most common mutations. Diagnostic Molecular Pathology, 15( ju 2006), 95-100.
NLM
Gouveia TLF, Paim JFO, Pavanello R de CM, Zatz M, Vainzof M. Sarcoglycanopathies: a multiplex molecular analysis for the most common mutations. Diagnostic Molecular Pathology. 2006 ; 15( ju 2006): 95-100.[citado 2024 nov. 19 ]
Vancouver
Gouveia TLF, Paim JFO, Pavanello R de CM, Zatz M, Vainzof M. Sarcoglycanopathies: a multiplex molecular analysis for the most common mutations. Diagnostic Molecular Pathology. 2006 ; 15( ju 2006): 95-100.[citado 2024 nov. 19 ]
Artigo de periodico
Association of MAO A polymorphism and alcoholism in Brazilian females (2005)
Guindalini, Camila; Scivoletto, Sandra; Ferreira, Ricardo G. M.; Nishimura, Agnes Lumi; Zilberman, Mônica Levit; Peluso, Marco Aurélio Monteiro; Zatz, Mayana
Source: Psychiatric Genetics. Unidade: IB
Subjects: POLIMORFISMO, ALCOOLISMO
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ABNT
GUINDALINI, Camila et al. Association of MAO A polymorphism and alcoholism in Brazilian females. Psychiatric Genetics, v. 15, n. 2, p. 141-144, 2005Tradução . . Disponível em: https://doi.org/10.1097/00041444-200506000-00011. Acesso em: 19 nov. 2024.
APA
Guindalini, C., Scivoletto, S., Ferreira, R. G. M., Nishimura, A. L., Zilberman, M. L., Peluso, M. A. M., & Zatz, M. (2005). Association of MAO A polymorphism and alcoholism in Brazilian females. Psychiatric Genetics, 15( 2), 141-144. doi:10.1097/00041444-200506000-00011
NLM
Guindalini C, Scivoletto S, Ferreira RGM, Nishimura AL, Zilberman ML, Peluso MAM, Zatz M. Association of MAO A polymorphism and alcoholism in Brazilian females [Internet]. Psychiatric Genetics. 2005 ; 15( 2): 141-144.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1097/00041444-200506000-00011
Vancouver
Guindalini C, Scivoletto S, Ferreira RGM, Nishimura AL, Zilberman ML, Peluso MAM, Zatz M. Association of MAO A polymorphism and alcoholism in Brazilian females [Internet]. Psychiatric Genetics. 2005 ; 15( 2): 141-144.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1097/00041444-200506000-00011
Artigo de periodico
Monoamine oxidase a polymorphism in brazilian patients (2005)
Nishimura, Agnes Lumi; Guindalini, Camila; Oliveira, João Ricardo Mendes de; Nitrini, Ricardo; Bahia, Valéria Santoro; Brito-Marques, Paulo Roberto; Otto, Paulo A ; Zatz, Mayana
Source: Journal of Molecular Neuroscience. Unidades: FM, IB
Subjects: DEMÊNCIA, NEUROLOGIA, POLIMORFISMO
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ABNT
NISHIMURA, Agnes Lumi et al. Monoamine oxidase a polymorphism in brazilian patients. Journal of Molecular Neuroscience, v. 27, p. 213-217, 2005Tradução . . Acesso em: 19 nov. 2024.
APA
Nishimura, A. L., Guindalini, C., Oliveira, J. R. M. de, Nitrini, R., Bahia, V. S., Brito-Marques, P. R., et al. (2005). Monoamine oxidase a polymorphism in brazilian patients. Journal of Molecular Neuroscience, 27, 213-217.
NLM
Nishimura AL, Guindalini C, Oliveira JRM de, Nitrini R, Bahia VS, Brito-Marques PR, Otto PA, Zatz M. Monoamine oxidase a polymorphism in brazilian patients. Journal of Molecular Neuroscience. 2005 ; 27 213-217.[citado 2024 nov. 19 ]
Vancouver
Nishimura AL, Guindalini C, Oliveira JRM de, Nitrini R, Bahia VS, Brito-Marques PR, Otto PA, Zatz M. Monoamine oxidase a polymorphism in brazilian patients. Journal of Molecular Neuroscience. 2005 ; 27 213-217.[citado 2024 nov. 19 ]
Artigo de periodico
The most common mutation in FKRP causing limb girdle muscular dystrophy type 2I (LGMD2I) may have occurred only once and is present in Hutterites and other populations (2005)
Frosk, Patrick; Greenberg, Cheryl R.; Tennese, Alysa A. P.; Lamont, Ryan; Nylen, Edward; Hirst, Cheryl; Frappier, Danielle; Rolsin, Micole M.; Zaik, Michaela; Bushby, Kate; Straub, Volker; Zatz, Mayana ; Paula, Flavia de; Morgan, Kenneth; Fujiwara, T. Mary; Wrogemann, Klaus
Source: Human Mutation. Unidade: IB
Subjects: DISTROFIA MUSCULAR, GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FROSK, Patrick et al. The most common mutation in FKRP causing limb girdle muscular dystrophy type 2I (LGMD2I) may have occurred only once and is present in Hutterites and other populations. Human Mutation, v. 25, n. 1, p. 38-44, 2005Tradução . . Disponível em: https://doi.org/10.1002/humu.20110. Acesso em: 19 nov. 2024.
APA
Frosk, P., Greenberg, C. R., Tennese, A. A. P., Lamont, R., Nylen, E., Hirst, C., et al. (2005). The most common mutation in FKRP causing limb girdle muscular dystrophy type 2I (LGMD2I) may have occurred only once and is present in Hutterites and other populations. Human Mutation, 25( 1), 38-44. doi:10.1002/humu.20110
NLM
Frosk P, Greenberg CR, Tennese AAP, Lamont R, Nylen E, Hirst C, Frappier D, Rolsin MM, Zaik M, Bushby K, Straub V, Zatz M, Paula F de, Morgan K, Fujiwara TM, Wrogemann K. The most common mutation in FKRP causing limb girdle muscular dystrophy type 2I (LGMD2I) may have occurred only once and is present in Hutterites and other populations [Internet]. Human Mutation. 2005 ; 25( 1): 38-44.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1002/humu.20110
Vancouver
Frosk P, Greenberg CR, Tennese AAP, Lamont R, Nylen E, Hirst C, Frappier D, Rolsin MM, Zaik M, Bushby K, Straub V, Zatz M, Paula F de, Morgan K, Fujiwara TM, Wrogemann K. The most common mutation in FKRP causing limb girdle muscular dystrophy type 2I (LGMD2I) may have occurred only once and is present in Hutterites and other populations [Internet]. Human Mutation. 2005 ; 25( 1): 38-44.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1002/humu.20110
Artigo de periodico
Association of genetic variants in alcohol dehydrogenase 4 with alcohol dependence in brazilian patients (2005)
Guindalini, Camila; Scivoletto, Sandra; Ferreira, Ricardo G. M.; Breen, Gerome; Zilberman, Monica L.; Peluso, Marco Aurélio; Zatz, Mayana
Source: American Journal of Psychiatry. Unidade: IB
Subjects: ALCOÓLATRAS, VARIAÇÃO GENÉTICA, DEPENDENTES QUÍMICOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GUINDALINI, Camila et al. Association of genetic variants in alcohol dehydrogenase 4 with alcohol dependence in brazilian patients. American Journal of Psychiatry, v. 162, n. 5, p. 1005-1007, 2005Tradução . . Acesso em: 19 nov. 2024.
APA
Guindalini, C., Scivoletto, S., Ferreira, R. G. M., Breen, G., Zilberman, M. L., Peluso, M. A., & Zatz, M. (2005). Association of genetic variants in alcohol dehydrogenase 4 with alcohol dependence in brazilian patients. American Journal of Psychiatry, 162( 5), 1005-1007.
NLM
Guindalini C, Scivoletto S, Ferreira RGM, Breen G, Zilberman ML, Peluso MA, Zatz M. Association of genetic variants in alcohol dehydrogenase 4 with alcohol dependence in brazilian patients. American Journal of Psychiatry. 2005 ; 162( 5): 1005-1007.[citado 2024 nov. 19 ]
Vancouver
Guindalini C, Scivoletto S, Ferreira RGM, Breen G, Zilberman ML, Peluso MA, Zatz M. Association of genetic variants in alcohol dehydrogenase 4 with alcohol dependence in brazilian patients. American Journal of Psychiatry. 2005 ; 162( 5): 1005-1007.[citado 2024 nov. 19 ]
Artigo de periodico
Analysis of IL-1'alfa', IL-1'beta', and IL-RA polymorphisms in dysthymia (2004)
Fertuzinhos, Sofia M. M.; Oliveira, João R. Mendes de; Nishimura, Agnes Lumi; Pontual, Deyse; Carvalho, Daniel Resende; Sougey, Everton Botelho; Otto, Paulo A ; Zatz, Mayana
Source: Journal of Molecular Neuroscience. Unidade: IB
Subjects: TRANSTORNOS MENTAIS, TRANSTORNO DISTÍMICO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FERTUZINHOS, Sofia M. M. et al. Analysis of IL-1'alfa', IL-1'beta', and IL-RA polymorphisms in dysthymia. Journal of Molecular Neuroscience, v. 22, n. 3, p. 251-255, 2004Tradução . . Acesso em: 19 nov. 2024.
APA
Fertuzinhos, S. M. M., Oliveira, J. R. M. de, Nishimura, A. L., Pontual, D., Carvalho, D. R., Sougey, E. B., et al. (2004). Analysis of IL-1'alfa', IL-1'beta', and IL-RA polymorphisms in dysthymia. Journal of Molecular Neuroscience, 22( 3), 251-255.
NLM
Fertuzinhos SMM, Oliveira JRM de, Nishimura AL, Pontual D, Carvalho DR, Sougey EB, Otto PA, Zatz M. Analysis of IL-1'alfa', IL-1'beta', and IL-RA polymorphisms in dysthymia. Journal of Molecular Neuroscience. 2004 ; 22( 3): 251-255.[citado 2024 nov. 19 ]
Vancouver
Fertuzinhos SMM, Oliveira JRM de, Nishimura AL, Pontual D, Carvalho DR, Sougey EB, Otto PA, Zatz M. Analysis of IL-1'alfa', IL-1'beta', and IL-RA polymorphisms in dysthymia. Journal of Molecular Neuroscience. 2004 ; 22( 3): 251-255.[citado 2024 nov. 19 ]
Artigo de periodico
Lack of association between the brain-derived neurotrophin factor (C-270T) polymorphism and late-onset Alzheimers disease (LOAD) in Brazilian patients (2004)
Nishimura, Agnes Lumi; Oliveira, João Ricardo Mendes de; Nitrini, Ricardo; Bahia, Valéria Santoro; Brito-Marques, Paulo Roberto; Otto, Paulo A ; Zatz, Mayana
Source: Journal of Molecular Neuroscience. Unidades: FM, IB
Subjects: DOENÇA DE ALZHEIMER, POLIMORFISMO, APOLIPOPROTEÍNAS, BRASIL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
NISHIMURA, Agnes Lumi et al. Lack of association between the brain-derived neurotrophin factor (C-270T) polymorphism and late-onset Alzheimers disease (LOAD) in Brazilian patients. Journal of Molecular Neuroscience, v. 22, p. 257-260, 2004Tradução . . Acesso em: 19 nov. 2024.
APA
Nishimura, A. L., Oliveira, J. R. M. de, Nitrini, R., Bahia, V. S., Brito-Marques, P. R., Otto, P. A., & Zatz, M. (2004). Lack of association between the brain-derived neurotrophin factor (C-270T) polymorphism and late-onset Alzheimers disease (LOAD) in Brazilian patients. Journal of Molecular Neuroscience, 22, 257-260.
NLM
Nishimura AL, Oliveira JRM de, Nitrini R, Bahia VS, Brito-Marques PR, Otto PA, Zatz M. Lack of association between the brain-derived neurotrophin factor (C-270T) polymorphism and late-onset Alzheimers disease (LOAD) in Brazilian patients. Journal of Molecular Neuroscience. 2004 ; 22 257-260.[citado 2024 nov. 19 ]
Vancouver
Nishimura AL, Oliveira JRM de, Nitrini R, Bahia VS, Brito-Marques PR, Otto PA, Zatz M. Lack of association between the brain-derived neurotrophin factor (C-270T) polymorphism and late-onset Alzheimers disease (LOAD) in Brazilian patients. Journal of Molecular Neuroscience. 2004 ; 22 257-260.[citado 2024 nov. 19 ]
Artigo de periodico
A new form of autosomal dominant limb-girdle muscular dystrophy (LGMD1G) with progressive fingers and toes flexion limitation maps to chromosome 4p21 (2004)
Starling, Alessandra; Kok, Fernando; Passos-Bueno, Maria Rita ; Vainzof, Mariz ; Zatz, Mayana
Source: European Journal of Human Genetics. Unidade: IB
Assunto: DISTROFIA MUSCULAR
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
STARLING, Alessandra et al. A new form of autosomal dominant limb-girdle muscular dystrophy (LGMD1G) with progressive fingers and toes flexion limitation maps to chromosome 4p21. European Journal of Human Genetics, v. 12, n. 12, p. 1033-1040, 2004Tradução . . Disponível em: https://doi.org/10.1038/sj.ejhg.5201289. Acesso em: 19 nov. 2024.
APA
Starling, A., Kok, F., Passos-Bueno, M. R., Vainzof, M., & Zatz, M. (2004). A new form of autosomal dominant limb-girdle muscular dystrophy (LGMD1G) with progressive fingers and toes flexion limitation maps to chromosome 4p21. European Journal of Human Genetics, 12( 12), 1033-1040. doi:10.1038/sj.ejhg.5201289
NLM
Starling A, Kok F, Passos-Bueno MR, Vainzof M, Zatz M. A new form of autosomal dominant limb-girdle muscular dystrophy (LGMD1G) with progressive fingers and toes flexion limitation maps to chromosome 4p21 [Internet]. European Journal of Human Genetics. 2004 ; 12( 12): 1033-1040.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1038/sj.ejhg.5201289
Vancouver
Starling A, Kok F, Passos-Bueno MR, Vainzof M, Zatz M. A new form of autosomal dominant limb-girdle muscular dystrophy (LGMD1G) with progressive fingers and toes flexion limitation maps to chromosome 4p21 [Internet]. European Journal of Human Genetics. 2004 ; 12( 12): 1033-1040.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1038/sj.ejhg.5201289
Artigo de periodico
Protein and DNA Analysis for the prenatal diagnosis of 'alpha'2-Laminin-Deficient congenital muscular dystrophy (2004)
Yamamoto, Lydia Uraco; Gallop, Thomas R.; Naccache, Nadyr Fernandes; Pavanello, Rita de Cássia M.; Zanoteli, Edmar; Zatz, Mayana ; Vainzof, Mariz
Source: Diagnostic Molecular Pathology. Unidade: IB
Subjects: DISTROFIA MUSCULAR, DIAGNÓSTICO PRÉ-NATAL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
YAMAMOTO, Lydia Uraco et al. Protein and DNA Analysis for the prenatal diagnosis of 'alpha'2-Laminin-Deficient congenital muscular dystrophy. Diagnostic Molecular Pathology, v. 13, n. 3, p. 167-171, 2004Tradução . . Acesso em: 19 nov. 2024.
APA
Yamamoto, L. U., Gallop, T. R., Naccache, N. F., Pavanello, R. de C. M., Zanoteli, E., Zatz, M., & Vainzof, M. (2004). Protein and DNA Analysis for the prenatal diagnosis of 'alpha'2-Laminin-Deficient congenital muscular dystrophy. Diagnostic Molecular Pathology, 13( 3), 167-171.
NLM
Yamamoto LU, Gallop TR, Naccache NF, Pavanello R de CM, Zanoteli E, Zatz M, Vainzof M. Protein and DNA Analysis for the prenatal diagnosis of 'alpha'2-Laminin-Deficient congenital muscular dystrophy. Diagnostic Molecular Pathology. 2004 ; 13( 3): 167-171.[citado 2024 nov. 19 ]
Vancouver
Yamamoto LU, Gallop TR, Naccache NF, Pavanello R de CM, Zanoteli E, Zatz M, Vainzof M. Protein and DNA Analysis for the prenatal diagnosis of 'alpha'2-Laminin-Deficient congenital muscular dystrophy. Diagnostic Molecular Pathology. 2004 ; 13( 3): 167-171.[citado 2024 nov. 19 ]

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