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Trabalho de evento-resumo periodico
Heterochromatin hypomethylation in American marsupials (2001)
Svartman, Marta; Viégas-Pèquignot, E.; Niveleau, A
Source: Chromosome Research. Conference titles: International Chromosome Conference. Unidade: IB
Assunto: MARSUPIALIA
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ABNT
SVARTMAN, Marta e VIÉGAS-PÈQUIGNOT, E. e NIVELEAU, A. Heterochromatin hypomethylation in American marsupials. Chromosome Research. London: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 01 nov. 2024. , 2001
APA
Svartman, M., Viégas-Pèquignot, E., & Niveleau, A. (2001). Heterochromatin hypomethylation in American marsupials. Chromosome Research. London: Instituto de Biociências, Universidade de São Paulo.
NLM
Svartman M, Viégas-Pèquignot E, Niveleau A. Heterochromatin hypomethylation in American marsupials. Chromosome Research. 2001 ; 9 se 2001.[citado 2024 nov. 01 ]
Vancouver
Svartman M, Viégas-Pèquignot E, Niveleau A. Heterochromatin hypomethylation in American marsupials. Chromosome Research. 2001 ; 9 se 2001.[citado 2024 nov. 01 ]
Artigo de periodico
Morphologically differentiated sex chromosomes in neotropical freshwater fish (2001)
Almeida-Toledo, Lurdes Foresti de; Foresti, Fausto
Source: Genetica. Unidade: IB
Subjects: PEIXES, CITOGENÉTICA, CROMOSSOMOS SEXUAIS
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ALMEIDA-TOLEDO, Lurdes Foresti de e FORESTI, Fausto. Morphologically differentiated sex chromosomes in neotropical freshwater fish. Genetica, v. 111, p. 91-100, 2001Tradução . . Acesso em: 01 nov. 2024.
APA
Almeida-Toledo, L. F. de, & Foresti, F. (2001). Morphologically differentiated sex chromosomes in neotropical freshwater fish. Genetica, 111, 91-100.
NLM
Almeida-Toledo LF de, Foresti F. Morphologically differentiated sex chromosomes in neotropical freshwater fish. Genetica. 2001 ; 111 91-100.[citado 2024 nov. 01 ]
Vancouver
Almeida-Toledo LF de, Foresti F. Morphologically differentiated sex chromosomes in neotropical freshwater fish. Genetica. 2001 ; 111 91-100.[citado 2024 nov. 01 ]
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
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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: 01 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. 01 ] 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. 01 ] Available from: https://doi.org/10.1080/00087114.2001.10589210
Trabalho de evento-resumo periodico
Sporadic mutations in TCOF1 arise both in maternal and paternal chromosomes and are not related to advanced parental age (2001)
Splendore, Alessandra; Jabs, E. W.; Passos-Bueno, Maria Rita
Source: American Journal of Human Genetics. Conference titles: Annual Meeting of the American Society of Human Genetics. Unidade: IB
Assunto: MUTAÇÃO GENÉTICA
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ABNT
SPLENDORE, Alessandra e JABS, E. W. e PASSOS-BUENO, Maria Rita. Sporadic mutations in TCOF1 arise both in maternal and paternal chromosomes and are not related to advanced parental age. American Journal of Human Genetics. Chicago: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 01 nov. 2024. , 2001
APA
Splendore, A., Jabs, E. W., & Passos-Bueno, M. R. (2001). Sporadic mutations in TCOF1 arise both in maternal and paternal chromosomes and are not related to advanced parental age. American Journal of Human Genetics. Chicago: Instituto de Biociências, Universidade de São Paulo.
NLM
Splendore A, Jabs EW, Passos-Bueno MR. Sporadic mutations in TCOF1 arise both in maternal and paternal chromosomes and are not related to advanced parental age. American Journal of Human Genetics. 2001 ; 69( 4): 614.[citado 2024 nov. 01 ]
Vancouver
Splendore A, Jabs EW, Passos-Bueno MR. Sporadic mutations in TCOF1 arise both in maternal and paternal chromosomes and are not related to advanced parental age. American Journal of Human Genetics. 2001 ; 69( 4): 614.[citado 2024 nov. 01 ]
Trabalho de evento-resumo periodico
A new form of autosomal dominant late onset spinal muscular atrophy (2001)
Bernardino, Andréa L. F.; Richieri-Costa, Antonio; Passos-Bueno, Maria Rita ; Cerqueira, A M P
Source: American Journal of Human Genetics. Conference titles: Annual Meeting of the American Society of Human Genetics. Unidades: IB, HRAC
Assunto: ATROFIA MUSCULAR
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ABNT
BERNARDINO, Andréa L. F. et al. A new form of autosomal dominant late onset spinal muscular atrophy. American Journal of Human Genetics. Chicago: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 01 nov. 2024. , 2001
APA
Bernardino, A. L. F., Richieri-Costa, A., Passos-Bueno, M. R., & Cerqueira, A. M. P. (2001). A new form of autosomal dominant late onset spinal muscular atrophy. American Journal of Human Genetics. Chicago: Instituto de Biociências, Universidade de São Paulo.
NLM
Bernardino ALF, Richieri-Costa A, Passos-Bueno MR, Cerqueira AMP. A new form of autosomal dominant late onset spinal muscular atrophy. American Journal of Human Genetics. 2001 ; 69( 4): 524.[citado 2024 nov. 01 ]
Vancouver
Bernardino ALF, Richieri-Costa A, Passos-Bueno MR, Cerqueira AMP. A new form of autosomal dominant late onset spinal muscular atrophy. American Journal of Human Genetics. 2001 ; 69( 4): 524.[citado 2024 nov. 01 ]
Trabalho de evento-resumo periodico
Evidence for association of the BCL3 gene in 98 Brazilian nonsyndromic clefting patients using the transmission disequilibrium test (TDT) (2001)
Gaspar, D A; Pavanello, Rita de Cássia M.; Araujo, B C; André, Márcia; Steman, Silvio; Matioli, Sergio Russo ; Passos-Bueno, Maria Rita
Source: American Journal of Human Genetics. Conference titles: Annual Meeting of the American Society of Human Genetics. Unidades: IB, FO
Subjects: DOENÇAS GENÉTICAS, MALFORMAÇÕES
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ABNT
GASPAR, D A et al. Evidence for association of the BCL3 gene in 98 Brazilian nonsyndromic clefting patients using the transmission disequilibrium test (TDT). American Journal of Human Genetics. Chicago: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 01 nov. 2024. , 2001
APA
Gaspar, D. A., Pavanello, R. de C. M., Araujo, B. C., André, M., Steman, S., Matioli, S. R., & Passos-Bueno, M. R. (2001). Evidence for association of the BCL3 gene in 98 Brazilian nonsyndromic clefting patients using the transmission disequilibrium test (TDT). American Journal of Human Genetics. Chicago: Instituto de Biociências, Universidade de São Paulo.
NLM
Gaspar DA, Pavanello R de CM, Araujo BC, André M, Steman S, Matioli SR, Passos-Bueno MR. Evidence for association of the BCL3 gene in 98 Brazilian nonsyndromic clefting patients using the transmission disequilibrium test (TDT). American Journal of Human Genetics. 2001 ; 69( 4): 574.[citado 2024 nov. 01 ]
Vancouver
Gaspar DA, Pavanello R de CM, Araujo BC, André M, Steman S, Matioli SR, Passos-Bueno MR. Evidence for association of the BCL3 gene in 98 Brazilian nonsyndromic clefting patients using the transmission disequilibrium test (TDT). American Journal of Human Genetics. 2001 ; 69( 4): 574.[citado 2024 nov. 01 ]
Trabalho de evento-resumo
Genetic and morphological variability in booby species of the Brazilian coast (2001)
Miyaki, Cristina Yumi ; Baumgarten, Melina M
Source: Programa y resumenes. Conference titles: Reunión da Sociedad Caribeña de Ornitología. Unidade: IB
Assunto: AVES
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ABNT
MIYAKI, Cristina Yumi e BAUMGARTEN, Melina M. Genetic and morphological variability in booby species of the Brazilian coast. 2001, Anais.. Topes de Collante: Instituto de Biociências, Universidade de São Paulo, 2001. . Acesso em: 01 nov. 2024.
APA
Miyaki, C. Y., & Baumgarten, M. M. (2001). Genetic and morphological variability in booby species of the Brazilian coast. In Programa y resumenes. Topes de Collante: Instituto de Biociências, Universidade de São Paulo.
NLM
Miyaki CY, Baumgarten MM. Genetic and morphological variability in booby species of the Brazilian coast. Programa y resumenes. 2001 ;[citado 2024 nov. 01 ]
Vancouver
Miyaki CY, Baumgarten MM. Genetic and morphological variability in booby species of the Brazilian coast. Programa y resumenes. 2001 ;[citado 2024 nov. 01 ]
Artigo de periodico
Cytosolic thioredoxin peroxidase I is essential for the antioxidant defense of yeast with dysfunctional mitochondria (2001)
Demasi, Ana P. D.; Pereira, Gonçalo Amarante Guimarães; Netto, Luis Eduardo Soares
Source: FEBS Lettes. Unidade: IB
Subjects: EXPRESSÃO GÊNICA, RESPIRAÇÃO (DEFICIÊNCIA), OXIGÊNIO
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ABNT
DEMASI, Ana P. D. e PEREIRA, Gonçalo Amarante Guimarães e NETTO, Luis Eduardo Soares. Cytosolic thioredoxin peroxidase I is essential for the antioxidant defense of yeast with dysfunctional mitochondria. FEBS Lettes, v. 509, n. 3, p. 430-434, 2001Tradução . . Disponível em: https://doi.org/10.1016/s0014-5793(01)03215-x. Acesso em: 01 nov. 2024.
APA
Demasi, A. P. D., Pereira, G. A. G., & Netto, L. E. S. (2001). Cytosolic thioredoxin peroxidase I is essential for the antioxidant defense of yeast with dysfunctional mitochondria. FEBS Lettes, 509( 3), 430-434. doi:10.1016/s0014-5793(01)03215-x
NLM
Demasi APD, Pereira GAG, Netto LES. Cytosolic thioredoxin peroxidase I is essential for the antioxidant defense of yeast with dysfunctional mitochondria [Internet]. FEBS Lettes. 2001 ; 509( 3): 430-434.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/s0014-5793(01)03215-x
Vancouver
Demasi APD, Pereira GAG, Netto LES. Cytosolic thioredoxin peroxidase I is essential for the antioxidant defense of yeast with dysfunctional mitochondria [Internet]. FEBS Lettes. 2001 ; 509( 3): 430-434.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/s0014-5793(01)03215-x
Trabalho de evento-resumo
Genetic variability in body species of the Brazilian coast (2001)
Baumgarten, Melina M; Kohlrausch, Adriana B; Miyaki, Cristina Yumi
Source: Abstracts. Conference titles: Stated Meeting American Ornitologists' Union. Unidade: IB
Subjects: AVES, DNA
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ABNT
BAUMGARTEN, Melina M e KOHLRAUSCH, Adriana B e MIYAKI, Cristina Yumi. Genetic variability in body species of the Brazilian coast. 2001, Anais.. Seattle: Instituto de Biociências, Universidade de São Paulo, 2001. . Acesso em: 01 nov. 2024.
APA
Baumgarten, M. M., Kohlrausch, A. B., & Miyaki, C. Y. (2001). Genetic variability in body species of the Brazilian coast. In Abstracts. Seattle: Instituto de Biociências, Universidade de São Paulo.
NLM
Baumgarten MM, Kohlrausch AB, Miyaki CY. Genetic variability in body species of the Brazilian coast. Abstracts. 2001 ;[citado 2024 nov. 01 ]
Vancouver
Baumgarten MM, Kohlrausch AB, Miyaki CY. Genetic variability in body species of the Brazilian coast. Abstracts. 2001 ;[citado 2024 nov. 01 ]
Artigo de periodico
Selectively labeling the heterologous protein in Escherichia coli for NMR studies: a strategy to speed Up NMR spectroscopy (2001)
Almeida, F. C. L.; Amorim, G. C.; Moreau, V. H.; Sousa, V. O.; Creazola, A. T.; Creazola, A. T.; Américo, T. A.; Pais, A. P. N.; Leite, A; Netto, Luis Eduardo Soares ; Giordano, R J; Valente, A. P.
Source: Journal of Magnetic Resonance. Unidade: IB
Assunto: PROTEÍNAS
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ABNT
ALMEIDA, F. C. L. et al. Selectively labeling the heterologous protein in Escherichia coli for NMR studies: a strategy to speed Up NMR spectroscopy. Journal of Magnetic Resonance, v. 148, n. 1, p. 142-146, 2001Tradução . . Disponível em: https://doi.org/10.1006/jmre.2000.2213. Acesso em: 01 nov. 2024.
APA
Almeida, F. C. L., Amorim, G. C., Moreau, V. H., Sousa, V. O., Creazola, A. T., Creazola, A. T., et al. (2001). Selectively labeling the heterologous protein in Escherichia coli for NMR studies: a strategy to speed Up NMR spectroscopy. Journal of Magnetic Resonance, 148( 1), 142-146. doi:10.1006/jmre.2000.2213
NLM
Almeida FCL, Amorim GC, Moreau VH, Sousa VO, Creazola AT, Creazola AT, Américo TA, Pais APN, Leite A, Netto LES, Giordano RJ, Valente AP. Selectively labeling the heterologous protein in Escherichia coli for NMR studies: a strategy to speed Up NMR spectroscopy [Internet]. Journal of Magnetic Resonance. 2001 ; 148( 1): 142-146.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1006/jmre.2000.2213
Vancouver
Almeida FCL, Amorim GC, Moreau VH, Sousa VO, Creazola AT, Creazola AT, Américo TA, Pais APN, Leite A, Netto LES, Giordano RJ, Valente AP. Selectively labeling the heterologous protein in Escherichia coli for NMR studies: a strategy to speed Up NMR spectroscopy [Internet]. Journal of Magnetic Resonance. 2001 ; 148( 1): 142-146.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1006/jmre.2000.2213
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
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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: 01 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. 01 ]
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. 01 ]
Artigo de periodico
Allele frequency distribution of three STR Loci (CSF1PO, TPOX, and TH01) in a Brazilian population sample (2001)
Soares Vieira, José Arnaldo; Munoz, Daniel Romero; Iwamura, Edna Sadayo Miazato; Billerbeck, Ana Elisa Correia; Otto, Paulo A
Source: Journal of Forensic Sciences. Unidades: FM, IB
Assunto: MEDICINA LEGAL
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ABNT
SOARES VIEIRA, José Arnaldo et al. Allele frequency distribution of three STR Loci (CSF1PO, TPOX, and TH01) in a Brazilian population sample. Journal of Forensic Sciences, v. 46, n. 4, p. 996-997, 2001Tradução . . Disponível em: https://doi.org/10.1520/jfs15085j. Acesso em: 01 nov. 2024.
APA
Soares Vieira, J. A., Munoz, D. R., Iwamura, E. S. M., Billerbeck, A. E. C., & Otto, P. A. (2001). Allele frequency distribution of three STR Loci (CSF1PO, TPOX, and TH01) in a Brazilian population sample. Journal of Forensic Sciences, 46( 4), 996-997. doi:10.1520/jfs15085j
NLM
Soares Vieira JA, Munoz DR, Iwamura ESM, Billerbeck AEC, Otto PA. Allele frequency distribution of three STR Loci (CSF1PO, TPOX, and TH01) in a Brazilian population sample [Internet]. Journal of Forensic Sciences. 2001 ; 46( 4): 996-997.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1520/jfs15085j
Vancouver
Soares Vieira JA, Munoz DR, Iwamura ESM, Billerbeck AEC, Otto PA. Allele frequency distribution of three STR Loci (CSF1PO, TPOX, and TH01) in a Brazilian population sample [Internet]. Journal of Forensic Sciences. 2001 ; 46( 4): 996-997.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1520/jfs15085j
Trabalho de evento-resumo periodico
Six novel point mutations in the dystrophin gene identified in Brazilian Duchenne patients (2001)
Vagenas, Dulci do Nascimento Fonseca; Cerqueira, A.; Torres, A.; Pavanello, Rita de Cássia M.; Passos-Bueno, Maria Rita ; Zatz, Mayana
Source: American Journal of Human Genetics. Conference titles: Annual Meeting of the American Society of Human Genetics. Unidade: IB
Assunto: DISTROFIA MUSCULAR
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ABNT
VAGENAS, Dulci do Nascimento Fonseca et al. Six novel point mutations in the dystrophin gene identified in Brazilian Duchenne patients. American Journal of Human Genetics. Chicago: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 01 nov. 2024. , 2001
APA
Vagenas, D. do N. F., Cerqueira, A., Torres, A., Pavanello, R. de C. M., Passos-Bueno, M. R., & Zatz, M. (2001). Six novel point mutations in the dystrophin gene identified in Brazilian Duchenne patients. American Journal of Human Genetics. Chicago: Instituto de Biociências, Universidade de São Paulo.
NLM
Vagenas D do NF, Cerqueira A, Torres A, Pavanello R de CM, Passos-Bueno MR, Zatz M. Six novel point mutations in the dystrophin gene identified in Brazilian Duchenne patients. American Journal of Human Genetics. 2001 ; 69( 4): 442.[citado 2024 nov. 01 ]
Vancouver
Vagenas D do NF, Cerqueira A, Torres A, Pavanello R de CM, Passos-Bueno MR, Zatz M. Six novel point mutations in the dystrophin gene identified in Brazilian Duchenne patients. American Journal of Human Genetics. 2001 ; 69( 4): 442.[citado 2024 nov. 01 ]
Trabalho de evento-resumo periodico
Recurrent basque and brailian mutation in LGMD2A (Calpainopathy) brazilian families (2001)
Paula, Flavia de; Viegas, R.; Kai, A.; Moreira, E S; Passos-Bueno, Maria Rita ; Vainzof, Mariz ; Nigro, Vicenzo; Zatz, Mayana
Source: European Journal of Human Genetics. Conference titles: International Congress of Human Genetics. Unidade: IB
Assunto: GENÉTICA MÉDICA
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ABNT
PAULA, Flavia de et al. Recurrent basque and brailian mutation in LGMD2A (Calpainopathy) brazilian families. European Journal of Human Genetics. Basingstoke: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 01 nov. 2024. , 2001
APA
Paula, F. de, Viegas, R., Kai, A., Moreira, E. S., Passos-Bueno, M. R., Vainzof, M., et al. (2001). Recurrent basque and brailian mutation in LGMD2A (Calpainopathy) brazilian families. European Journal of Human Genetics. Basingstoke: Instituto de Biociências, Universidade de São Paulo.
NLM
Paula F de, Viegas R, Kai A, Moreira ES, Passos-Bueno MR, Vainzof M, Nigro V, Zatz M. Recurrent basque and brailian mutation in LGMD2A (Calpainopathy) brazilian families. European Journal of Human Genetics. 2001 ; 9 396.[citado 2024 nov. 01 ]
Vancouver
Paula F de, Viegas R, Kai A, Moreira ES, Passos-Bueno MR, Vainzof M, Nigro V, Zatz M. Recurrent basque and brailian mutation in LGMD2A (Calpainopathy) brazilian families. European Journal of Human Genetics. 2001 ; 9 396.[citado 2024 nov. 01 ]
Trabalho de evento-resumo periodico
Muscular dystrophies; same mutation but different clinical courses? The next challenge (2001)
Zatz, Mayana ; Vainzof, Mariz ; Passos-Bueno, Maria Rita
Source: European Journal of Human Genetics. Conference titles: International Congress of Human Genetics. Unidade: IB
Assunto: GENÉTICA MÉDICA
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ABNT
ZATZ, Mayana e VAINZOF, Mariz e PASSOS-BUENO, Maria Rita. Muscular dystrophies; same mutation but different clinical courses? The next challenge. European Journal of Human Genetics. Basingstoke: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 01 nov. 2024. , 2001
APA
Zatz, M., Vainzof, M., & Passos-Bueno, M. R. (2001). Muscular dystrophies; same mutation but different clinical courses? The next challenge. European Journal of Human Genetics. Basingstoke: Instituto de Biociências, Universidade de São Paulo.
NLM
Zatz M, Vainzof M, Passos-Bueno MR. Muscular dystrophies; same mutation but different clinical courses? The next challenge. European Journal of Human Genetics. 2001 ; 9 68-69.[citado 2024 nov. 01 ]
Vancouver
Zatz M, Vainzof M, Passos-Bueno MR. Muscular dystrophies; same mutation but different clinical courses? The next challenge. European Journal of Human Genetics. 2001 ; 9 68-69.[citado 2024 nov. 01 ]
Trabalho de evento-resumo
Phylogeographic study in wild populations of the blue-and-yellow macaw (Ara ararauna) by the analysis of mitochondrial DNA sequences (2001)
Miyaki, Cristina Yumi ; Caparroz, Renato ; Bianchi, C A; Morgante, João Stenghel
Source: Programa y resumenes. Conference titles: Reunión da Sociedad Caribeña de Ornitología. Unidade: IB
Assunto: AVES
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ABNT
MIYAKI, Cristina Yumi et al. Phylogeographic study in wild populations of the blue-and-yellow macaw (Ara ararauna) by the analysis of mitochondrial DNA sequences. 2001, Anais.. Topes de Collante: Instituto de Biociências, Universidade de São Paulo, 2001. . Acesso em: 01 nov. 2024.
APA
Miyaki, C. Y., Caparroz, R., Bianchi, C. A., & Morgante, J. S. (2001). Phylogeographic study in wild populations of the blue-and-yellow macaw (Ara ararauna) by the analysis of mitochondrial DNA sequences. In Programa y resumenes. Topes de Collante: Instituto de Biociências, Universidade de São Paulo.
NLM
Miyaki CY, Caparroz R, Bianchi CA, Morgante JS. Phylogeographic study in wild populations of the blue-and-yellow macaw (Ara ararauna) by the analysis of mitochondrial DNA sequences. Programa y resumenes. 2001 ;[citado 2024 nov. 01 ]
Vancouver
Miyaki CY, Caparroz R, Bianchi CA, Morgante JS. Phylogeographic study in wild populations of the blue-and-yellow macaw (Ara ararauna) by the analysis of mitochondrial DNA sequences. Programa y resumenes. 2001 ;[citado 2024 nov. 01 ]
Trabalho de evento-resumo
5S and 18S rDNA loclaization in four species of Serrasalminae (Pisces, Characiformes) by fluorescent in situ hybridization (2001)
Almeida-Toledo, Lurdes Foresti de; Daniel-Silva, Maria de Fátima Zambelli
Source: Abstracts. Conference titles: European Congress of Ichthyology. Unidade: IB
Subjects: PEIXES, CHARACIFORMES, DNA
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ABNT
ALMEIDA-TOLEDO, Lurdes Foresti de e DANIEL-SILVA, Maria de Fátima Zambelli. 5S and 18S rDNA loclaization in four species of Serrasalminae (Pisces, Characiformes) by fluorescent in situ hybridization. 2001, Anais.. Prague: Instituto de Biociências, Universidade de São Paulo, 2001. . Acesso em: 01 nov. 2024.
APA
Almeida-Toledo, L. F. de, & Daniel-Silva, M. de F. Z. (2001). 5S and 18S rDNA loclaization in four species of Serrasalminae (Pisces, Characiformes) by fluorescent in situ hybridization. In Abstracts. Prague: Instituto de Biociências, Universidade de São Paulo.
NLM
Almeida-Toledo LF de, Daniel-Silva M de FZ. 5S and 18S rDNA loclaization in four species of Serrasalminae (Pisces, Characiformes) by fluorescent in situ hybridization. Abstracts. 2001 ;[citado 2024 nov. 01 ]
Vancouver
Almeida-Toledo LF de, Daniel-Silva M de FZ. 5S and 18S rDNA loclaization in four species of Serrasalminae (Pisces, Characiformes) by fluorescent in situ hybridization. Abstracts. 2001 ;[citado 2024 nov. 01 ]
Artigo de periodico
Singlet molecular oxygen triggers the soxRS Regulon of Escherichia coli (2001)
Agnez-Lima, Lucymara F; Di Mascio, Paolo ; Demple, Bruce; Menck, Carlos Frederico Martins
Source: Biological Chemistry. Unidades: IQ, IB
Assunto: MICROBIOLOGIA
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ABNT
AGNEZ-LIMA, Lucymara F et al. Singlet molecular oxygen triggers the soxRS Regulon of Escherichia coli. Biological Chemistry, v. 382, p. 1071-1075, 2001Tradução . . Disponível em: https://doi.org/10.1515/bc.2001.134. Acesso em: 01 nov. 2024.
APA
Agnez-Lima, L. F., Di Mascio, P., Demple, B., & Menck, C. F. M. (2001). Singlet molecular oxygen triggers the soxRS Regulon of Escherichia coli. Biological Chemistry, 382, 1071-1075. doi:10.1515/bc.2001.134
NLM
Agnez-Lima LF, Di Mascio P, Demple B, Menck CFM. Singlet molecular oxygen triggers the soxRS Regulon of Escherichia coli [Internet]. Biological Chemistry. 2001 ;3821071-1075.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1515/bc.2001.134
Vancouver
Agnez-Lima LF, Di Mascio P, Demple B, Menck CFM. Singlet molecular oxygen triggers the soxRS Regulon of Escherichia coli [Internet]. Biological Chemistry. 2001 ;3821071-1075.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1515/bc.2001.134
Artigo de periodico
Allele-specific X-linked gene activity in normal human cells assayed by expressed single nucleotide polymorphisms (cSNPs) (2001)
Vasques, Luciana dos Reis; Pereira, Lygia da Veiga
Source: DNA Research. Unidade: IB
Subjects: CROMOSSOMOS, EXPRESSÃO GÊNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VASQUES, Luciana dos Reis e PEREIRA, Lygia da Veiga. Allele-specific X-linked gene activity in normal human cells assayed by expressed single nucleotide polymorphisms (cSNPs). DNA Research, v. 8, n. 4, p. 173-177, 2001Tradução . . Acesso em: 01 nov. 2024.
APA
Vasques, L. dos R., & Pereira, L. da V. (2001). Allele-specific X-linked gene activity in normal human cells assayed by expressed single nucleotide polymorphisms (cSNPs). DNA Research, 8( 4), 173-177.
NLM
Vasques L dos R, Pereira L da V. Allele-specific X-linked gene activity in normal human cells assayed by expressed single nucleotide polymorphisms (cSNPs). DNA Research. 2001 ; 8( 4): 173-177.[citado 2024 nov. 01 ]
Vancouver
Vasques L dos R, Pereira L da V. Allele-specific X-linked gene activity in normal human cells assayed by expressed single nucleotide polymorphisms (cSNPs). DNA Research. 2001 ; 8( 4): 173-177.[citado 2024 nov. 01 ]
Trabalho de evento-resumo periodico
Mitochondrial mutation A1555G (12rRNA) and connexion 2635delG mutation are frequent causes of deafness in Brazil (2001)
Mingroni Netto, Regina Celia ; Abreu-Silva, Ronaldo Serafim; Braga, M. C. C.; Lezirovitz, Karina; Della Rosa, Valter Augusto; Pirana, Sulene; Spinelli, M.; Otto, Paulo A
Source: American Journal of Human Genetics. Conference titles: Annual Meeting of the American Society of Human Genetics. Unidade: IB
Assunto: MUTAÇÃO GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MINGRONI NETTO, Regina Celia et al. Mitochondrial mutation A1555G (12rRNA) and connexion 2635delG mutation are frequent causes of deafness in Brazil. American Journal of Human Genetics. Chicago: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 01 nov. 2024. , 2001
APA
Mingroni Netto, R. C., Abreu-Silva, R. S., Braga, M. C. C., Lezirovitz, K., Della Rosa, V. A., Pirana, S., et al. (2001). Mitochondrial mutation A1555G (12rRNA) and connexion 2635delG mutation are frequent causes of deafness in Brazil. American Journal of Human Genetics. Chicago: Instituto de Biociências, Universidade de São Paulo.
NLM
Mingroni Netto RC, Abreu-Silva RS, Braga MCC, Lezirovitz K, Della Rosa VA, Pirana S, Spinelli M, Otto PA. Mitochondrial mutation A1555G (12rRNA) and connexion 2635delG mutation are frequent causes of deafness in Brazil. American Journal of Human Genetics. 2001 ; 69( 4): 543.[citado 2024 nov. 01 ]
Vancouver
Mingroni Netto RC, Abreu-Silva RS, Braga MCC, Lezirovitz K, Della Rosa VA, Pirana S, Spinelli M, Otto PA. Mitochondrial mutation A1555G (12rRNA) and connexion 2635delG mutation are frequent causes of deafness in Brazil. American Journal of Human Genetics. 2001 ; 69( 4): 543.[citado 2024 nov. 01 ]

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