ReP USP - Resultado da busca

Artigo de periodico
Cochlea cell-specific marker expression upon in vitro Hes1 knockdown (2021)
Batissoco, A.C ; Lezirovitz, K ; Zanatta, D. B ; Hemza, C. R. M. L ; Vasques, L. R ; Strauss, B. E ; Mingroni Netto, Regina Celia ; Haddad, Luciana Amaral ; Bento, R. F ; Oiticica, J
Source: Brazilian Journal of Medical and Biological Research. Unidades: IB, FM, BIOTECNOLOGIA
Subjects: PERDA AUDITIVA, MUTAÇÃO GENÉTICA, EXPRESSÃO GÊNICA, DOENÇAS GENÉTICAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BATISSOCO, A.C et al. Cochlea cell-specific marker expression upon in vitro Hes1 knockdown. Brazilian Journal of Medical and Biological Research, v. 54, n. 7, 2021Tradução . . Disponível em: https://doi.org/10.1590/1414-431X2020e10579. Acesso em: 16 out. 2024.
APA
Batissoco, A. C., Lezirovitz, K., Zanatta, D. B., Hemza, C. R. M. L., Vasques, L. R., Strauss, B. E., et al. (2021). Cochlea cell-specific marker expression upon in vitro Hes1 knockdown. Brazilian Journal of Medical and Biological Research, 54( 7). doi:10.1590/1414-431X2020e10579
NLM
Batissoco AC, Lezirovitz K, Zanatta DB, Hemza CRML, Vasques LR, Strauss BE, Mingroni Netto RC, Haddad LA, Bento RF, Oiticica J. Cochlea cell-specific marker expression upon in vitro Hes1 knockdown [Internet]. Brazilian Journal of Medical and Biological Research. 2021 ; 54( 7):[citado 2024 out. 16 ] Available from: https://doi.org/10.1590/1414-431X2020e10579
Vancouver
Batissoco AC, Lezirovitz K, Zanatta DB, Hemza CRML, Vasques LR, Strauss BE, Mingroni Netto RC, Haddad LA, Bento RF, Oiticica J. Cochlea cell-specific marker expression upon in vitro Hes1 knockdown [Internet]. Brazilian Journal of Medical and Biological Research. 2021 ; 54( 7):[citado 2024 out. 16 ] Available from: https://doi.org/10.1590/1414-431X2020e10579
Artigo de periodico
Transplantation and survival of mouse inner ear progenitor/stem cells in the organ of Corti after cochleostomy of hearing-impaired guinea pigs: preliminary results (2016)
Barboza Jr., L.C.M.; Lezirovitz, K.; Zanatta, D.B.; Strauss, B E; Mingroni Netto, Regina Celia ; Oiticica, J.; Haddad, Luciana Amaral ; Bento, Ricardo Ferreira
Source: Brazilian Journal of Medical and Biological Research. Unidades: IB, FM
Subjects: PERDA AUDITIVA COCLEAR, CÓCLEA, CÉLULAS-TRONCO, TRANSPLANTES, IMUNOHISTOQUÍMICA, COBAIAS, PROCEDIMENTOS CIRÚRGICOS OTOLÓGICOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BARBOZA JR., L.C.M. et al. Transplantation and survival of mouse inner ear progenitor/stem cells in the organ of Corti after cochleostomy of hearing-impaired guinea pigs: preliminary results. Brazilian Journal of Medical and Biological Research, v. 49, n. 4, 2016Tradução . . Disponível em: https://doi.org/10.1590/1414-431x20155064. Acesso em: 16 out. 2024.
APA
Barboza Jr., L. C. M., Lezirovitz, K., Zanatta, D. B., Strauss, B. E., Mingroni Netto, R. C., Oiticica, J., et al. (2016). Transplantation and survival of mouse inner ear progenitor/stem cells in the organ of Corti after cochleostomy of hearing-impaired guinea pigs: preliminary results. Brazilian Journal of Medical and Biological Research, 49( 4). doi:10.1590/1414-431x20155064
NLM
Barboza Jr. LCM, Lezirovitz K, Zanatta DB, Strauss BE, Mingroni Netto RC, Oiticica J, Haddad LA, Bento RF. Transplantation and survival of mouse inner ear progenitor/stem cells in the organ of Corti after cochleostomy of hearing-impaired guinea pigs: preliminary results [Internet]. Brazilian Journal of Medical and Biological Research. 2016 ;49( 4):[citado 2024 out. 16 ] Available from: https://doi.org/10.1590/1414-431x20155064
Vancouver
Barboza Jr. LCM, Lezirovitz K, Zanatta DB, Strauss BE, Mingroni Netto RC, Oiticica J, Haddad LA, Bento RF. Transplantation and survival of mouse inner ear progenitor/stem cells in the organ of Corti after cochleostomy of hearing-impaired guinea pigs: preliminary results [Internet]. Brazilian Journal of Medical and Biological Research. 2016 ;49( 4):[citado 2024 out. 16 ] Available from: https://doi.org/10.1590/1414-431x20155064
Artigo de periodico
Stability of XIST repression in relation to genomic imprinting following global genome demethylation in a human cell line (2014)
Araújo, E.S.S. de; Vasques, L.R.; Stabellini, R.; Krepischi, Ana Cristina Victorino ; Pereira, Lygia da Veiga
Source: Brazilian Journal of Medical and Biological Research. Unidade: IB
Subjects: CROMOSSOMOS HUMANOS, CROMOSSOMO X, NEOPLASIAS, GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ARAÚJO, E.S.S. de et al. Stability of XIST repression in relation to genomic imprinting following global genome demethylation in a human cell line. Brazilian Journal of Medical and Biological Research, p. on-line, 2014Tradução . . Disponível em: https://doi.org/10.1590/1414-431X20144058. Acesso em: 16 out. 2024.
APA
Araújo, E. S. S. de, Vasques, L. R., Stabellini, R., Krepischi, A. C. V., & Pereira, L. da V. (2014). Stability of XIST repression in relation to genomic imprinting following global genome demethylation in a human cell line. Brazilian Journal of Medical and Biological Research, on-line. doi:10.1590/1414-431X20144058
NLM
Araújo ESS de, Vasques LR, Stabellini R, Krepischi ACV, Pereira L da V. Stability of XIST repression in relation to genomic imprinting following global genome demethylation in a human cell line [Internet]. Brazilian Journal of Medical and Biological Research. 2014 ; on-line.[citado 2024 out. 16 ] Available from: https://doi.org/10.1590/1414-431X20144058
Vancouver
Araújo ESS de, Vasques LR, Stabellini R, Krepischi ACV, Pereira L da V. Stability of XIST repression in relation to genomic imprinting following global genome demethylation in a human cell line [Internet]. Brazilian Journal of Medical and Biological Research. 2014 ; on-line.[citado 2024 out. 16 ] Available from: https://doi.org/10.1590/1414-431X20144058
Artigo de periodico
Behavioral meaningful opioidergic stimulation activates kappa receptor gene expression (2012)
Teodorov, Elizabeth; Ferrari, Merari de Fátima Ramires ; Fior-Chadi, Débora Rejane ; Camarini, Rosana ; Felício, Luciano Freitas
Source: Brazilian Journal of Medical and Biological Research. Unidades: IB, ICB, FMVZ
Subjects: REAÇÃO EM CADEIA POR POLIMERASE, EXPRESSÃO GÊNICA, FARMACOECONOMIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
TEODOROV, Elizabeth et al. Behavioral meaningful opioidergic stimulation activates kappa receptor gene expression. Brazilian Journal of Medical and Biological Research, v. 45, n. 10, p. 982-987, 2012Tradução . . Disponível em: https://doi.org/10.1590/S0100-879X2012007500091. Acesso em: 16 out. 2024.
APA
Teodorov, E., Ferrari, M. de F. R., Fior-Chadi, D. R., Camarini, R., & Felício, L. F. (2012). Behavioral meaningful opioidergic stimulation activates kappa receptor gene expression. Brazilian Journal of Medical and Biological Research, 45( 10), 982-987. doi:10.1590/S0100-879X2012007500091
NLM
Teodorov E, Ferrari M de FR, Fior-Chadi DR, Camarini R, Felício LF. Behavioral meaningful opioidergic stimulation activates kappa receptor gene expression [Internet]. Brazilian Journal of Medical and Biological Research. 2012 ; 45( 10): 982-987.[citado 2024 out. 16 ] Available from: https://doi.org/10.1590/S0100-879X2012007500091
Vancouver
Teodorov E, Ferrari M de FR, Fior-Chadi DR, Camarini R, Felício LF. Behavioral meaningful opioidergic stimulation activates kappa receptor gene expression [Internet]. Brazilian Journal of Medical and Biological Research. 2012 ; 45( 10): 982-987.[citado 2024 out. 16 ] Available from: https://doi.org/10.1590/S0100-879X2012007500091
Artigo de periodico
A Brazilian family with hereditary inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia (2011)
Fanganiello, R. D.; Kimonis, V. E.; Nitrini, R.; Côrte, C. C.; Passos-Bueno, Maria Rita
Source: Brazilian Journal of Medical and Biological Research. Unidades: FM, IB
Subjects: DEMÊNCIA (GENÉTICA), DOENÇAS HEREDITÁRIAS, MUTAÇÃO GENÉTICA, DOENÇAS ÓSSEAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FANGANIELLO, R. D. et al. A Brazilian family with hereditary inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia. Brazilian Journal of Medical and Biological Research, v. 44, n. 4, p. 374-380, 2011Tradução . . Disponível em: https://doi.org/10.1590/S0100-879X2011007500028. Acesso em: 16 out. 2024.
APA
Fanganiello, R. D., Kimonis, V. E., Nitrini, R., Côrte, C. C., & Passos-Bueno, M. R. (2011). A Brazilian family with hereditary inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia. Brazilian Journal of Medical and Biological Research, 44( 4), 374-380. doi:10.1590/S0100-879X2011007500028
NLM
Fanganiello RD, Kimonis VE, Nitrini R, Côrte CC, Passos-Bueno MR. A Brazilian family with hereditary inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia [Internet]. Brazilian Journal of Medical and Biological Research. 2011 ; 44( 4): 374-380.[citado 2024 out. 16 ] Available from: https://doi.org/10.1590/S0100-879X2011007500028
Vancouver
Fanganiello RD, Kimonis VE, Nitrini R, Côrte CC, Passos-Bueno MR. A Brazilian family with hereditary inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia [Internet]. Brazilian Journal of Medical and Biological Research. 2011 ; 44( 4): 374-380.[citado 2024 out. 16 ] Available from: https://doi.org/10.1590/S0100-879X2011007500028
Artigo de periodico
Candidate gene linkage analysis indicates genetic heterogeneity in Marfan syndrome (2011)
Teixeira, L. V. S.; Mandelbaum, K. L.; Pereira, Lygia da Veiga ; Perez, A B A
Source: Brazilian Journal of Medical and Biological Research. Unidade: IB
Subjects: MUTAÇÃO GENÉTICA, DOENÇAS GENÉTICAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
TEIXEIRA, L. V. S. et al. Candidate gene linkage analysis indicates genetic heterogeneity in Marfan syndrome. Brazilian Journal of Medical and Biological Research, v. 44, n. 8, p. 793-800, 2011Tradução . . Disponível em: https://doi.org/10.1590/S0100-879X2011007500095. Acesso em: 16 out. 2024.
APA
Teixeira, L. V. S., Mandelbaum, K. L., Pereira, L. da V., & Perez, A. B. A. (2011). Candidate gene linkage analysis indicates genetic heterogeneity in Marfan syndrome. Brazilian Journal of Medical and Biological Research, 44( 8), 793-800. doi:10.1590/S0100-879X2011007500095
NLM
Teixeira LVS, Mandelbaum KL, Pereira L da V, Perez ABA. Candidate gene linkage analysis indicates genetic heterogeneity in Marfan syndrome [Internet]. Brazilian Journal of Medical and Biological Research. 2011 ; 44( 8): 793-800.[citado 2024 out. 16 ] Available from: https://doi.org/10.1590/S0100-879X2011007500095
Vancouver
Teixeira LVS, Mandelbaum KL, Pereira L da V, Perez ABA. Candidate gene linkage analysis indicates genetic heterogeneity in Marfan syndrome [Internet]. Brazilian Journal of Medical and Biological Research. 2011 ; 44( 8): 793-800.[citado 2024 out. 16 ] Available from: https://doi.org/10.1590/S0100-879X2011007500095
Artigo de periodico
A novel missense mutation p.L76P in the GJB2 gene causing nonsyndromic recessive deafness in a Brazilian family (2009)
Batissoco, Ana Carla; Auricchio, Maria Teresa Ballester de Melo; Kimura, L.; Tabith Junior, Alfredo; Mingroni Netto, Regina Celia
Source: Brazilian Journal of Medical and Biological Research. Unidade: IB
Assunto: MUTAÇÃO GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BATISSOCO, Ana Carla et al. A novel missense mutation p.L76P in the GJB2 gene causing nonsyndromic recessive deafness in a Brazilian family. Brazilian Journal of Medical and Biological Research, v. 42, n. 2, p. 168-171, 2009Tradução . . Disponível em: https://doi.org/10.1590/s0100-879x2009000200004. Acesso em: 16 out. 2024.
APA
Batissoco, A. C., Auricchio, M. T. B. de M., Kimura, L., Tabith Junior, A., & Mingroni Netto, R. C. (2009). A novel missense mutation p.L76P in the GJB2 gene causing nonsyndromic recessive deafness in a Brazilian family. Brazilian Journal of Medical and Biological Research, 42( 2), 168-171. doi:10.1590/s0100-879x2009000200004
NLM
Batissoco AC, Auricchio MTB de M, Kimura L, Tabith Junior A, Mingroni Netto RC. A novel missense mutation p.L76P in the GJB2 gene causing nonsyndromic recessive deafness in a Brazilian family [Internet]. Brazilian Journal of Medical and Biological Research. 2009 ; 42( 2): 168-171.[citado 2024 out. 16 ] Available from: https://doi.org/10.1590/s0100-879x2009000200004
Vancouver
Batissoco AC, Auricchio MTB de M, Kimura L, Tabith Junior A, Mingroni Netto RC. A novel missense mutation p.L76P in the GJB2 gene causing nonsyndromic recessive deafness in a Brazilian family [Internet]. Brazilian Journal of Medical and Biological Research. 2009 ; 42( 2): 168-171.[citado 2024 out. 16 ] Available from: https://doi.org/10.1590/s0100-879x2009000200004
Artigo de periodico
Association of polymorphisms at the ADIPOR1 regulatory region with type 2 diabetes and body mass index in a Brazilian population with European or African ancestry (2008)
Yeh, E.; Kimura, L.; Errera, Flávia Imbroisi Valle; Angeli, Claudia Blanes; Mingroni Netto, Regina Celia ; Silva, M. E. R.; Canani, L. H. S.; Passos-Bueno, Maria Rita
Source: Brazilian Journal of Medical and Biological Research. Unidade: IB
Subjects: DIABETES MELLITUS, POLIMORFISMO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
YEH, E. et al. Association of polymorphisms at the ADIPOR1 regulatory region with type 2 diabetes and body mass index in a Brazilian population with European or African ancestry. Brazilian Journal of Medical and Biological Research, v. 41, n. 6, p. 468-472, 2008Tradução . . Disponível em: https://doi.org/10.1590/s0100-879x2008000600005. Acesso em: 16 out. 2024.
APA
Yeh, E., Kimura, L., Errera, F. I. V., Angeli, C. B., Mingroni Netto, R. C., Silva, M. E. R., et al. (2008). Association of polymorphisms at the ADIPOR1 regulatory region with type 2 diabetes and body mass index in a Brazilian population with European or African ancestry. Brazilian Journal of Medical and Biological Research, 41( 6), 468-472. doi:10.1590/s0100-879x2008000600005
NLM
Yeh E, Kimura L, Errera FIV, Angeli CB, Mingroni Netto RC, Silva MER, Canani LHS, Passos-Bueno MR. Association of polymorphisms at the ADIPOR1 regulatory region with type 2 diabetes and body mass index in a Brazilian population with European or African ancestry [Internet]. Brazilian Journal of Medical and Biological Research. 2008 ; 41( 6): 468-472.[citado 2024 out. 16 ] Available from: https://doi.org/10.1590/s0100-879x2008000600005
Vancouver
Yeh E, Kimura L, Errera FIV, Angeli CB, Mingroni Netto RC, Silva MER, Canani LHS, Passos-Bueno MR. Association of polymorphisms at the ADIPOR1 regulatory region with type 2 diabetes and body mass index in a Brazilian population with European or African ancestry [Internet]. Brazilian Journal of Medical and Biological Research. 2008 ; 41( 6): 468-472.[citado 2024 out. 16 ] Available from: https://doi.org/10.1590/s0100-879x2008000600005
Artigo de periodico
Prevalence of the A1555G (12S rRNA) and tRNASer(UCN) mitochondrial mutations in hearing-impaired Brazilian patients (2006)
Abreu-Silva, Ronaldo Serafim; Lezirovitz, Karina; Braga, M. C. C.; Spinelli, M.; Pirana, Sulene; Della-Rosa, Valter Augusto; Otto, Paulo A ; Mingroni Netto, Regina Celia
Source: Brazilian Journal of Medical and Biological Research. Unidade: IB
Subjects: DNA MITOCONDRIAL, MUTAÇÃO GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ABREU-SILVA, Ronaldo Serafim et al. Prevalence of the A1555G (12S rRNA) and tRNASer(UCN) mitochondrial mutations in hearing-impaired Brazilian patients. Brazilian Journal of Medical and Biological Research, v. 39, n. 2, p. 219-226, 2006Tradução . . Disponível em: http://www.scielo.br/pdf/bjmbr/v39n2/v39n2a08.pdf. Acesso em: 16 out. 2024.
APA
Abreu-Silva, R. S., Lezirovitz, K., Braga, M. C. C., Spinelli, M., Pirana, S., Della-Rosa, V. A., et al. (2006). Prevalence of the A1555G (12S rRNA) and tRNASer(UCN) mitochondrial mutations in hearing-impaired Brazilian patients. Brazilian Journal of Medical and Biological Research, 39( 2), 219-226. Recuperado de http://www.scielo.br/pdf/bjmbr/v39n2/v39n2a08.pdf
NLM
Abreu-Silva RS, Lezirovitz K, Braga MCC, Spinelli M, Pirana S, Della-Rosa VA, Otto PA, Mingroni Netto RC. Prevalence of the A1555G (12S rRNA) and tRNASer(UCN) mitochondrial mutations in hearing-impaired Brazilian patients [Internet]. Brazilian Journal of Medical and Biological Research. 2006 ; 39( 2): 219-226.[citado 2024 out. 16 ] Available from: http://www.scielo.br/pdf/bjmbr/v39n2/v39n2a08.pdf
Vancouver
Abreu-Silva RS, Lezirovitz K, Braga MCC, Spinelli M, Pirana S, Della-Rosa VA, Otto PA, Mingroni Netto RC. Prevalence of the A1555G (12S rRNA) and tRNASer(UCN) mitochondrial mutations in hearing-impaired Brazilian patients [Internet]. Brazilian Journal of Medical and Biological Research. 2006 ; 39( 2): 219-226.[citado 2024 out. 16 ] Available from: http://www.scielo.br/pdf/bjmbr/v39n2/v39n2a08.pdf
Artigo de periodico
Protein defects in neuromuscular diseases (2003)
Vainzof, Mariz ; Zatz, Mayana
Source: Brazilian Journal of Medical and Biological Research. Unidade: IB
Subjects: DISTROFIA MUSCULAR, DOENÇAS NEUROMUSCULARES, MUTAÇÃO GENÉTICA, PROTEÍNAS MUSCULARES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VAINZOF, Mariz e ZATZ, Mayana. Protein defects in neuromuscular diseases. Brazilian Journal of Medical and Biological Research, v. 36, p. 543-555, 2003Tradução . . Disponível em: https://doi.org/10.1590/S0100-879X2003000500001. Acesso em: 16 out. 2024.
APA
Vainzof, M., & Zatz, M. (2003). Protein defects in neuromuscular diseases. Brazilian Journal of Medical and Biological Research, 36, 543-555. doi:10.1590/S0100-879X2003000500001
NLM
Vainzof M, Zatz M. Protein defects in neuromuscular diseases [Internet]. Brazilian Journal of Medical and Biological Research. 2003 ; 36 543-555.[citado 2024 out. 16 ] Available from: https://doi.org/10.1590/S0100-879X2003000500001
Vancouver
Vainzof M, Zatz M. Protein defects in neuromuscular diseases [Internet]. Brazilian Journal of Medical and Biological Research. 2003 ; 36 543-555.[citado 2024 out. 16 ] Available from: https://doi.org/10.1590/S0100-879X2003000500001
Artigo de periodico
The study of genetic polymorphisms related to serotonin in Alzheimer's disease: a new perspective in a heterogenic disorder (1999)
Oliveira, J. R. M.; Zatz, Mayana
Source: Brazilian Journal of Medical and Biological Research. Unidade: IB
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
OLIVEIRA, J. R. M. e ZATZ, Mayana. The study of genetic polymorphisms related to serotonin in Alzheimer's disease: a new perspective in a heterogenic disorder. Brazilian Journal of Medical and Biological Research, v. 32, n. 4, p. 463-467, 1999Tradução . . Disponível em: https://doi.org/10.1590/s0100-879x1999000400014. Acesso em: 16 out. 2024.
APA
Oliveira, J. R. M., & Zatz, M. (1999). The study of genetic polymorphisms related to serotonin in Alzheimer's disease: a new perspective in a heterogenic disorder. Brazilian Journal of Medical and Biological Research, 32( 4), 463-467. doi:10.1590/s0100-879x1999000400014
NLM
Oliveira JRM, Zatz M. The study of genetic polymorphisms related to serotonin in Alzheimer's disease: a new perspective in a heterogenic disorder [Internet]. Brazilian Journal of Medical and Biological Research. 1999 ; 32( 4): 463-467.[citado 2024 out. 16 ] Available from: https://doi.org/10.1590/s0100-879x1999000400014
Vancouver
Oliveira JRM, Zatz M. The study of genetic polymorphisms related to serotonin in Alzheimer's disease: a new perspective in a heterogenic disorder [Internet]. Brazilian Journal of Medical and Biological Research. 1999 ; 32( 4): 463-467.[citado 2024 out. 16 ] Available from: https://doi.org/10.1590/s0100-879x1999000400014
Artigo de periodico
Study of a region on yeast chromosome XIII that complements pet G199 mutants (COX7) and carries a new non-essential gene (1998)
Nobrega, Marina Pasetto; Graminha, M A S; Troitskaya, E N; Nobrega, Francisco Gorgonio da
Source: Brazilian Journal of Medical and Biological Research. Unidades: IB, ICB
Assunto: MICROBIOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
NOBREGA, Marina Pasetto et al. Study of a region on yeast chromosome XIII that complements pet G199 mutants (COX7) and carries a new non-essential gene. Brazilian Journal of Medical and Biological Research, v. 31, p. 355-363, 1998Tradução . . Disponível em: https://doi.org/10.1590/s0100-879x1998000300004. Acesso em: 16 out. 2024.
APA
Nobrega, M. P., Graminha, M. A. S., Troitskaya, E. N., & Nobrega, F. G. da. (1998). Study of a region on yeast chromosome XIII that complements pet G199 mutants (COX7) and carries a new non-essential gene. Brazilian Journal of Medical and Biological Research, 31, 355-363. doi:10.1590/s0100-879x1998000300004
NLM
Nobrega MP, Graminha MAS, Troitskaya EN, Nobrega FG da. Study of a region on yeast chromosome XIII that complements pet G199 mutants (COX7) and carries a new non-essential gene [Internet]. Brazilian Journal of Medical and Biological Research. 1998 ; 31 355-363.[citado 2024 out. 16 ] Available from: https://doi.org/10.1590/s0100-879x1998000300004
Vancouver
Nobrega MP, Graminha MAS, Troitskaya EN, Nobrega FG da. Study of a region on yeast chromosome XIII that complements pet G199 mutants (COX7) and carries a new non-essential gene [Internet]. Brazilian Journal of Medical and Biological Research. 1998 ; 31 355-363.[citado 2024 out. 16 ] Available from: https://doi.org/10.1590/s0100-879x1998000300004
Artigo de periodico
Clastogenic effects of different ureaplasma urealyticum serovars on human chromosomes (1997)
Cunha, Regina Ayr Florio da; Koiffmann, Celia Priszkulnik ; Souza, D. H.; Takei, K
Source: Brazilian Journal of Medical and Biological Research. Unidades: FCF, IB
Subjects: BIOQUÍMICA, BIOLOGIA MOLECULAR
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CUNHA, Regina Ayr Florio da et al. Clastogenic effects of different ureaplasma urealyticum serovars on human chromosomes. Brazilian Journal of Medical and Biological Research, v. 30, n. ju 1997, p. 749-757, 1997Tradução . . Disponível em: https://doi.org/10.1590/s0100-879x1997000600008. Acesso em: 16 out. 2024.
APA
Cunha, R. A. F. da, Koiffmann, C. P., Souza, D. H., & Takei, K. (1997). Clastogenic effects of different ureaplasma urealyticum serovars on human chromosomes. Brazilian Journal of Medical and Biological Research, 30( ju 1997), 749-757. doi:10.1590/s0100-879x1997000600008
NLM
Cunha RAF da, Koiffmann CP, Souza DH, Takei K. Clastogenic effects of different ureaplasma urealyticum serovars on human chromosomes [Internet]. Brazilian Journal of Medical and Biological Research. 1997 ; 30( ju 1997): 749-757.[citado 2024 out. 16 ] Available from: https://doi.org/10.1590/s0100-879x1997000600008
Vancouver
Cunha RAF da, Koiffmann CP, Souza DH, Takei K. Clastogenic effects of different ureaplasma urealyticum serovars on human chromosomes [Internet]. Brazilian Journal of Medical and Biological Research. 1997 ; 30( ju 1997): 749-757.[citado 2024 out. 16 ] Available from: https://doi.org/10.1590/s0100-879x1997000600008
Artigo de periodico
Use of chromosome 5q markers for confirming the diagnosis of proximal spinal muscular atrophy (1993)
Whittle, M R; Zatz, Mayana ; Reinach, Fernando de Castro
Source: Brazilian Journal of Medical and Biological Research. Unidade: IB
Subjects: BIOQUÍMICA, TÉCNICAS E PROCEDIMENTOS DE LABORATÓRIO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
WHITTLE, M R e ZATZ, Mayana e REINACH, Fernando de Castro. Use of chromosome 5q markers for confirming the diagnosis of proximal spinal muscular atrophy. Brazilian Journal of Medical and Biological Research, v. 26, p. 1157-73, 1993Tradução . . Acesso em: 16 out. 2024.
APA
Whittle, M. R., Zatz, M., & Reinach, F. de C. (1993). Use of chromosome 5q markers for confirming the diagnosis of proximal spinal muscular atrophy. Brazilian Journal of Medical and Biological Research, 26, 1157-73.
NLM
Whittle MR, Zatz M, Reinach F de C. Use of chromosome 5q markers for confirming the diagnosis of proximal spinal muscular atrophy. Brazilian Journal of Medical and Biological Research. 1993 ;26 1157-73.[citado 2024 out. 16 ]
Vancouver
Whittle MR, Zatz M, Reinach F de C. Use of chromosome 5q markers for confirming the diagnosis of proximal spinal muscular atrophy. Brazilian Journal of Medical and Biological Research. 1993 ;26 1157-73.[citado 2024 out. 16 ]
Artigo de periodico
Dna sequence amplification in sciarid flies: results and perspectives (1991)
Lara, F J S; Stocker, A J; Amabis, José Mariano
Source: Brazilian Journal of Medical and Biological Research. Unidade: IB
Assunto: GENÉTICA MOLECULAR
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LARA, F J S e STOCKER, A J e AMABIS, José Mariano. Dna sequence amplification in sciarid flies: results and perspectives. Brazilian Journal of Medical and Biological Research, v. 24, n. 3 , p. 233-48, 1991Tradução . . Acesso em: 16 out. 2024.
APA
Lara, F. J. S., Stocker, A. J., & Amabis, J. M. (1991). Dna sequence amplification in sciarid flies: results and perspectives. Brazilian Journal of Medical and Biological Research, 24( 3 ), 233-48.
NLM
Lara FJS, Stocker AJ, Amabis JM. Dna sequence amplification in sciarid flies: results and perspectives. Brazilian Journal of Medical and Biological Research. 1991 ;24( 3 ): 233-48.[citado 2024 out. 16 ]
Vancouver
Lara FJS, Stocker AJ, Amabis JM. Dna sequence amplification in sciarid flies: results and perspectives. Brazilian Journal of Medical and Biological Research. 1991 ;24( 3 ): 233-48.[citado 2024 out. 16 ]
Artigo de periodico
In vivo effects of ecdysterone on puff formation, and rna and protein synthesis in the salivary glands of rhynchosciara americana (1991)
Alvarenga, C A S; Winter, Carlos Eduardo ; Stocker, A J; Pueyo, M T; Lara, F J S
Source: Brazilian Journal of Medical and Biological Research. Unidades: IB, IQ, ICB
Subjects: GENÉTICA MOLECULAR, PARASITOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ALVARENGA, C A S et al. In vivo effects of ecdysterone on puff formation, and rna and protein synthesis in the salivary glands of rhynchosciara americana. Brazilian Journal of Medical and Biological Research, v. 24, n. 10, p. 985-1002, 1991Tradução . . Acesso em: 16 out. 2024.
APA
Alvarenga, C. A. S., Winter, C. E., Stocker, A. J., Pueyo, M. T., & Lara, F. J. S. (1991). In vivo effects of ecdysterone on puff formation, and rna and protein synthesis in the salivary glands of rhynchosciara americana. Brazilian Journal of Medical and Biological Research, 24( 10), 985-1002.
NLM
Alvarenga CAS, Winter CE, Stocker AJ, Pueyo MT, Lara FJS. In vivo effects of ecdysterone on puff formation, and rna and protein synthesis in the salivary glands of rhynchosciara americana. Brazilian Journal of Medical and Biological Research. 1991 ;24( 10): 985-1002.[citado 2024 out. 16 ]
Vancouver
Alvarenga CAS, Winter CE, Stocker AJ, Pueyo MT, Lara FJS. In vivo effects of ecdysterone on puff formation, and rna and protein synthesis in the salivary glands of rhynchosciara americana. Brazilian Journal of Medical and Biological Research. 1991 ;24( 10): 985-1002.[citado 2024 out. 16 ]
Artigo de periodico
Influence on rp4 plasmid on extracellular protease excretion by proteus mirabilis (1985)
Costa, S. O. P; Bonato, M C M; Bianco, M
Source: Brazilian Journal of Medical and Biological Research. Unidade: IB
Subjects: GENÉTICA MOLECULAR, MICROBIOLOGIA, PLASMÍDEOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
COSTA, S. O. P e BONATO, M C M e BIANCO, M. Influence on rp4 plasmid on extracellular protease excretion by proteus mirabilis. Brazilian Journal of Medical and Biological Research, v. 18, p. 378-97, 1985Tradução . . Acesso em: 16 out. 2024.
APA
Costa, S. O. P., Bonato, M. C. M., & Bianco, M. (1985). Influence on rp4 plasmid on extracellular protease excretion by proteus mirabilis. Brazilian Journal of Medical and Biological Research, 18, 378-97.
NLM
Costa SOP, Bonato MCM, Bianco M. Influence on rp4 plasmid on extracellular protease excretion by proteus mirabilis. Brazilian Journal of Medical and Biological Research. 1985 ;18 378-97.[citado 2024 out. 16 ]
Vancouver
Costa SOP, Bonato MCM, Bianco M. Influence on rp4 plasmid on extracellular protease excretion by proteus mirabilis. Brazilian Journal of Medical and Biological Research. 1985 ;18 378-97.[citado 2024 out. 16 ]

USP Schools

ReP

Filtros

USP Schools

Departament

Authors

USP affiliated authors

Date published

Subjects

Indexado em