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Endostatin T48 variant has an impaired affinity to basement membrane components (2005)
Suzuki, Oscar T.; Tu, H.; Pihlajaniemi, T.; Godoi, P. H.; Oliva, Glaucius; Olsen, Bjørn Reino; Passos-Bueno, Maria Rita
Fonte: Poster. Nome do evento: Annual Meeting of the American Society of Human Genetics. Unidades: IFSC, IB
Assuntos: FÁRMACOS, GENÉTICA MÉDICA, ANORMALIDADES CROMOSSÔMICAS
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ABNT
SUZUKI, Oscar T. et al. Endostatin T48 variant has an impaired affinity to basement membrane components. 2005, Anais.. Salt Lake City: Instituto de Física de São Carlos, Universidade de São Paulo, 2005. . Acesso em: 21 maio 2024.
APA
Suzuki, O. T., Tu, H., Pihlajaniemi, T., Godoi, P. H., Oliva, G., Olsen, B. R., & Passos-Bueno, M. R. (2005). Endostatin T48 variant has an impaired affinity to basement membrane components. In Poster. Salt Lake City: Instituto de Física de São Carlos, Universidade de São Paulo.
NLM
Suzuki OT, Tu H, Pihlajaniemi T, Godoi PH, Oliva G, Olsen BR, Passos-Bueno MR. Endostatin T48 variant has an impaired affinity to basement membrane components. Poster. 2005 ;[citado 2024 maio 21 ]
Vancouver
Suzuki OT, Tu H, Pihlajaniemi T, Godoi PH, Oliva G, Olsen BR, Passos-Bueno MR. Endostatin T48 variant has an impaired affinity to basement membrane components. Poster. 2005 ;[citado 2024 maio 21 ]
Artigo de periodico
Evidence of neuronal migration disorders in knobloch syndrome: clinical and molecular analysis of two novel families (2003)
Kliemann, Susana; Waetge, Ricardo T. L.; Suzuki, Oscar T.; Passos-Bueno, Maria Rita ; Rosemberg, Sergio
Fonte: American Journal of Medical Genetics. Unidades: FM, IB
Assuntos: OFTALMOPATIAS (IMUNOLOGIA), OFTALMOPATIAS (GENÉTICA), ANTICORPOS, BIOLOGIA MOLECULAR
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ABNT
KLIEMANN, Susana et al. Evidence of neuronal migration disorders in knobloch syndrome: clinical and molecular analysis of two novel families. American Journal of Medical Genetics, v. 119 A, n. 1, p. 15-19, 2003Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.20070. Acesso em: 21 maio 2024.
APA
Kliemann, S., Waetge, R. T. L., Suzuki, O. T., Passos-Bueno, M. R., & Rosemberg, S. (2003). Evidence of neuronal migration disorders in knobloch syndrome: clinical and molecular analysis of two novel families. American Journal of Medical Genetics, 119 A( 1), 15-19. doi:10.1002/ajmg.a.20070
NLM
Kliemann S, Waetge RTL, Suzuki OT, Passos-Bueno MR, Rosemberg S. Evidence of neuronal migration disorders in knobloch syndrome: clinical and molecular analysis of two novel families [Internet]. American Journal of Medical Genetics. 2003 ; 119 A( 1): 15-19.[citado 2024 maio 21 ] Available from: https://doi.org/10.1002/ajmg.a.20070
Vancouver
Kliemann S, Waetge RTL, Suzuki OT, Passos-Bueno MR, Rosemberg S. Evidence of neuronal migration disorders in knobloch syndrome: clinical and molecular analysis of two novel families [Internet]. American Journal of Medical Genetics. 2003 ; 119 A( 1): 15-19.[citado 2024 maio 21 ] Available from: https://doi.org/10.1002/ajmg.a.20070
Artigo de periodico
Genotype-phenotype correlations in 35 Brazilian families with sarcoglycanopathies including the description of three novel mutations. [http://www.jmedgenet.com/cgi/content/full/40/2/e12] (2003)
Moreira, E. S.; Vainzof, Mariz ; Suzuki, Oscar T.; Pavanello, Rita de Cássia M.; Zatz, Mayana ; Passos-Bueno, Maria Rita
Fonte: Journal of Medical Genetics. Unidade: IB
Assuntos: DISTROFIA MUSCULAR, MUTAÇÃO GENÉTICA
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ABNT
MOREIRA, E. S. et al. Genotype-phenotype correlations in 35 Brazilian families with sarcoglycanopathies including the description of three novel mutations. [http://www.jmedgenet.com/cgi/content/full/40/2/e12]. Journal of Medical Genetics, v. 40, p. e12, 2003Tradução . . Acesso em: 21 maio 2024.
APA
Moreira, E. S., Vainzof, M., Suzuki, O. T., Pavanello, R. de C. M., Zatz, M., & Passos-Bueno, M. R. (2003). Genotype-phenotype correlations in 35 Brazilian families with sarcoglycanopathies including the description of three novel mutations. [http://www.jmedgenet.com/cgi/content/full/40/2/e12]. Journal of Medical Genetics, 40, e12.
NLM
Moreira ES, Vainzof M, Suzuki OT, Pavanello R de CM, Zatz M, Passos-Bueno MR. Genotype-phenotype correlations in 35 Brazilian families with sarcoglycanopathies including the description of three novel mutations. [http://www.jmedgenet.com/cgi/content/full/40/2/e12]. Journal of Medical Genetics. 2003 ; 40 e12.[citado 2024 maio 21 ]
Vancouver
Moreira ES, Vainzof M, Suzuki OT, Pavanello R de CM, Zatz M, Passos-Bueno MR. Genotype-phenotype correlations in 35 Brazilian families with sarcoglycanopathies including the description of three novel mutations. [http://www.jmedgenet.com/cgi/content/full/40/2/e12]. Journal of Medical Genetics. 2003 ; 40 e12.[citado 2024 maio 21 ]
Artigo de periodico
Telethonin protein expression in neuromuscular disorders (2002)
Vainzof, Mariz ; Moreira, Eloisa S.; Suzuki, Oscar T.; Faulkner, Georgine; Valle, Georgio; Beggs, Alan H.; Carpen, Olli; Ribeiro, Alberto de Freitas ; Zanoteli, Edmar; Gurgel-Gianneti, Juliana; Tsanaclis, Ana Maria Crous; Silva, Helga Cristina Almeida da; Passos-Bueno, Maria Rita ; Zatz, Mayana
Fonte: Biochimica et Biophysica Acta. Unidades: IB, FM
Assuntos: DISTROFIA MUSCULAR, DOENÇAS NEUROMUSCULARES
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ABNT
VAINZOF, Mariz et al. Telethonin protein expression in neuromuscular disorders. Biochimica et Biophysica Acta, v. 1588, n. 1, p. 33-40, 2002Tradução . . Disponível em: https://doi.org/10.1016/s0925-4439(02)00113-8. Acesso em: 21 maio 2024.
APA
Vainzof, M., Moreira, E. S., Suzuki, O. T., Faulkner, G., Valle, G., Beggs, A. H., et al. (2002). Telethonin protein expression in neuromuscular disorders. Biochimica et Biophysica Acta, 1588( 1), 33-40. doi:10.1016/s0925-4439(02)00113-8
NLM
Vainzof M, Moreira ES, Suzuki OT, Faulkner G, Valle G, Beggs AH, Carpen O, Ribeiro A de F, Zanoteli E, Gurgel-Gianneti J, Tsanaclis AMC, Silva HCA da, Passos-Bueno MR, Zatz M. Telethonin protein expression in neuromuscular disorders [Internet]. Biochimica et Biophysica Acta. 2002 ; 1588( 1): 33-40.[citado 2024 maio 21 ] Available from: https://doi.org/10.1016/s0925-4439(02)00113-8
Vancouver
Vainzof M, Moreira ES, Suzuki OT, Faulkner G, Valle G, Beggs AH, Carpen O, Ribeiro A de F, Zanoteli E, Gurgel-Gianneti J, Tsanaclis AMC, Silva HCA da, Passos-Bueno MR, Zatz M. Telethonin protein expression in neuromuscular disorders [Internet]. Biochimica et Biophysica Acta. 2002 ; 1588( 1): 33-40.[citado 2024 maio 21 ] Available from: https://doi.org/10.1016/s0925-4439(02)00113-8
Artigo de periodico
Molecular analysis of collagen XVIII reveals novel mutations, presence of a third isoform, and possible genetic heterogeneity in Knobloch syndrome (2002)
Suzuki, Oscar T.; Sertié, Andréa Laurato; Der Kaloustian, Vazken M.; Kok, Fernando; Carpenter, M.; Murray, J; Czeizel, A E; Kliemann, Susana E.; Rosemberg, Sérgio; Monteiro, M.; Olsen, Bjorn Reino; Passos-Bueno, Maria Rita
Fonte: American Journal of Human Genetics. Unidades: IB, FM
Assuntos: DEGENERAÇÃO RETINIANA, DOENÇAS RETINIANAS, CEGUEIRA
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ABNT
SUZUKI, Oscar T. et al. Molecular analysis of collagen XVIII reveals novel mutations, presence of a third isoform, and possible genetic heterogeneity in Knobloch syndrome. American Journal of Human Genetics, v. 71, p. 1320-1329, 2002Tradução . . Acesso em: 21 maio 2024.
APA
Suzuki, O. T., Sertié, A. L., Der Kaloustian, V. M., Kok, F., Carpenter, M., Murray, J., et al. (2002). Molecular analysis of collagen XVIII reveals novel mutations, presence of a third isoform, and possible genetic heterogeneity in Knobloch syndrome. American Journal of Human Genetics, 71, 1320-1329.
NLM
Suzuki OT, Sertié AL, Der Kaloustian VM, Kok F, Carpenter M, Murray J, Czeizel AE, Kliemann SE, Rosemberg S, Monteiro M, Olsen BR, Passos-Bueno MR. Molecular analysis of collagen XVIII reveals novel mutations, presence of a third isoform, and possible genetic heterogeneity in Knobloch syndrome. American Journal of Human Genetics. 2002 ; 71 1320-1329.[citado 2024 maio 21 ]
Vancouver
Suzuki OT, Sertié AL, Der Kaloustian VM, Kok F, Carpenter M, Murray J, Czeizel AE, Kliemann SE, Rosemberg S, Monteiro M, Olsen BR, Passos-Bueno MR. Molecular analysis of collagen XVIII reveals novel mutations, presence of a third isoform, and possible genetic heterogeneity in Knobloch syndrome. American Journal of Human Genetics. 2002 ; 71 1320-1329.[citado 2024 maio 21 ]
Artigo de periodico-carta/editorial
Limb-girdle muscular dystrophy type 2G is caudes by mutations in the gene encoding the sarcomeric protein telethonin. [Carta] (2000)
Moreira, Eloisa S.; Wiltshire, Tim J.; Faulkner, Georgine; Nilforoushan, Antje; Vainzof, Mariz ; Suzuki, Oscar T.; Valle, Giorgio; Reeves, Roger; Zatz, Mayana ; Passos-Bueno, Maria Rita ; Jenne, Dieter E.
Fonte: Nature Genetics. Unidade: IB
Assunto: GENÉTICA MÉDICA
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ABNT
MOREIRA, Eloisa S. et al. Limb-girdle muscular dystrophy type 2G is caudes by mutations in the gene encoding the sarcomeric protein telethonin. [Carta]. Nature Genetics. New York: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 21 maio 2024. , 2000
APA
Moreira, E. S., Wiltshire, T. J., Faulkner, G., Nilforoushan, A., Vainzof, M., Suzuki, O. T., et al. (2000). Limb-girdle muscular dystrophy type 2G is caudes by mutations in the gene encoding the sarcomeric protein telethonin. [Carta]. Nature Genetics. New York: Instituto de Biociências, Universidade de São Paulo.
NLM
Moreira ES, Wiltshire TJ, Faulkner G, Nilforoushan A, Vainzof M, Suzuki OT, Valle G, Reeves R, Zatz M, Passos-Bueno MR, Jenne DE. Limb-girdle muscular dystrophy type 2G is caudes by mutations in the gene encoding the sarcomeric protein telethonin. [Carta]. Nature Genetics. 2000 ; 24 163-166.[citado 2024 maio 21 ]
Vancouver
Moreira ES, Wiltshire TJ, Faulkner G, Nilforoushan A, Vainzof M, Suzuki OT, Valle G, Reeves R, Zatz M, Passos-Bueno MR, Jenne DE. Limb-girdle muscular dystrophy type 2G is caudes by mutations in the gene encoding the sarcomeric protein telethonin. [Carta]. Nature Genetics. 2000 ; 24 163-166.[citado 2024 maio 21 ]

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