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Artigo de periodico
The impact of leptin and its receptor polymorphisms on type 1 diabetes in a population of northwest Iran (2022)
Sorkhabi, Parviz Azimnasab ; Asl, Maryam Soltani ; Kfoury Junior, José Roberto ; Algenstaedt, Petra; Mehmetzade, Hakan Farzin; Aghdam, Yashar Hashemi
Source: Annals of Human Biology. Unidade: FMVZ
Subjects: LEPTINA, DIABETES MELLITUS INSULINO-DEPENDENTE, POLIMORFISMO, IRÃ
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SORKHABI, Parviz Azimnasab et al. The impact of leptin and its receptor polymorphisms on type 1 diabetes in a population of northwest Iran. Annals of Human Biology, v. 49, n. 7-8, p. 317-32, 2022Tradução . . Disponível em: https://doi.org/10.1080/03014460.2022.2134453. Acesso em: 09 nov. 2024.
APA
Sorkhabi, P. A., Asl, M. S., Kfoury Junior, J. R., Algenstaedt, P., Mehmetzade, H. F., & Aghdam, Y. H. (2022). The impact of leptin and its receptor polymorphisms on type 1 diabetes in a population of northwest Iran. Annals of Human Biology, 49( 7-8), 317-32. doi:10.1080/03014460.2022.2134453
NLM
Sorkhabi PA, Asl MS, Kfoury Junior JR, Algenstaedt P, Mehmetzade HF, Aghdam YH. The impact of leptin and its receptor polymorphisms on type 1 diabetes in a population of northwest Iran [Internet]. Annals of Human Biology. 2022 ; 49( 7-8): 317-32.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1080/03014460.2022.2134453
Vancouver
Sorkhabi PA, Asl MS, Kfoury Junior JR, Algenstaedt P, Mehmetzade HF, Aghdam YH. The impact of leptin and its receptor polymorphisms on type 1 diabetes in a population of northwest Iran [Internet]. Annals of Human Biology. 2022 ; 49( 7-8): 317-32.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1080/03014460.2022.2134453
Artigo de periodico
FONA-7, a novel extended-spectrum β-lactamase variant of the FONA family identified in Serratia fonticola (2021)
Fuentes-Castillo, Danny ; Power, Pablo ; Cerdeira, Louise ; Cardenas-Arias, Adriana ; Moura, Quézia ; Oliveira, Flavio A.; Levy, Carlos Emilio ; Gutkind, Gabriel ; Catão-Dias, José Luiz ; Lincopan, Nilton
Source: Microbial Drug Resistance. Unidades: FMVZ, ICB
Subjects: AVES SELVAGENS, MICROBIOLOGIA, AGENTES ANTIMICROBIANOS, BACTÉRIAS ANAERÓBICAS GRAM-NEGATIVAS, ENTEROBACTERIACEAE, RESISTÊNCIA MICROBIANA ÀS DROGAS, POLIMORFISMO, ANTIBIÓTICOS, GENÔMICA, AMÉRICA DO SUL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FUENTES-CASTILLO, Danny et al. FONA-7, a novel extended-spectrum β-lactamase variant of the FONA family identified in Serratia fonticola. Microbial Drug Resistance, v. 27, n. 5, p. 585-589, 2021Tradução . . Disponível em: https://doi.org/10.1089/mdr.2020.0061. Acesso em: 09 nov. 2024.
APA
Fuentes-Castillo, D., Power, P., Cerdeira, L., Cardenas-Arias, A., Moura, Q., Oliveira, F. A., et al. (2021). FONA-7, a novel extended-spectrum β-lactamase variant of the FONA family identified in Serratia fonticola. Microbial Drug Resistance, 27( 5), 585-589. doi:10.1089/mdr.2020.0061
NLM
Fuentes-Castillo D, Power P, Cerdeira L, Cardenas-Arias A, Moura Q, Oliveira FA, Levy CE, Gutkind G, Catão-Dias JL, Lincopan N. FONA-7, a novel extended-spectrum β-lactamase variant of the FONA family identified in Serratia fonticola [Internet]. Microbial Drug Resistance. 2021 ; 27( 5): 585-589.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1089/mdr.2020.0061
Vancouver
Fuentes-Castillo D, Power P, Cerdeira L, Cardenas-Arias A, Moura Q, Oliveira FA, Levy CE, Gutkind G, Catão-Dias JL, Lincopan N. FONA-7, a novel extended-spectrum β-lactamase variant of the FONA family identified in Serratia fonticola [Internet]. Microbial Drug Resistance. 2021 ; 27( 5): 585-589.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1089/mdr.2020.0061
Artigo de periodico
An ancient founder mutation in PROKR2 impairs human reproduction (2012)
Stefanija, Magdalena Avbelj; Jeanpierre, Marc; Sykiotis, Gerasimos P.; Young, Jacques; Quinton, Richard; Abreu, Ana Paula; Plummer, Lacey; Au, Margaret G.; Balasubramanian, Ravikumar; Dwyer, Andrew A.; Florez, Jose C.; Cheetham, Timothy; Pearce, Simon H.; Purushothaman, Radhika; Schinzel, Albert; Pugeat, Michel; Jacobson-Dickman, Elka E.; Ten, Svetlana; Latronico, Ana Claudia; Gusella, James F.; Dode, Catherine; Crowley Jr, William F.; Pitteloud, Nelly
Source: Human Molecular Genetics. Unidade: FM
Subjects: FENÓTIPOS, GENÓTIPOS, INFLAMAÇÃO, MUTAÇÃO GENÉTICA, POLIMORFISMO, HIPOGANADISMO (DIAGNÓSTICO), GONADOTROFINAS HIPOFISÁRIAS (DEFICIÊNCIA)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
STEFANIJA, Magdalena Avbelj et al. An ancient founder mutation in PROKR2 impairs human reproduction. Human Molecular Genetics, v. 21, n. 19, p. 4314-4324, 2012Tradução . . Disponível em: https://doi.org/10.1093/hmg/dds264. Acesso em: 09 nov. 2024.
APA
Stefanija, M. A., Jeanpierre, M., Sykiotis, G. P., Young, J., Quinton, R., Abreu, A. P., et al. (2012). An ancient founder mutation in PROKR2 impairs human reproduction. Human Molecular Genetics, 21( 19), 4314-4324. doi:10.1093/hmg/dds264
NLM
Stefanija MA, Jeanpierre M, Sykiotis GP, Young J, Quinton R, Abreu AP, Plummer L, Au MG, Balasubramanian R, Dwyer AA, Florez JC, Cheetham T, Pearce SH, Purushothaman R, Schinzel A, Pugeat M, Jacobson-Dickman EE, Ten S, Latronico AC, Gusella JF, Dode C, Crowley Jr WF, Pitteloud N. An ancient founder mutation in PROKR2 impairs human reproduction [Internet]. Human Molecular Genetics. 2012 ; 21( 19): 4314-4324.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1093/hmg/dds264
Vancouver
Stefanija MA, Jeanpierre M, Sykiotis GP, Young J, Quinton R, Abreu AP, Plummer L, Au MG, Balasubramanian R, Dwyer AA, Florez JC, Cheetham T, Pearce SH, Purushothaman R, Schinzel A, Pugeat M, Jacobson-Dickman EE, Ten S, Latronico AC, Gusella JF, Dode C, Crowley Jr WF, Pitteloud N. An ancient founder mutation in PROKR2 impairs human reproduction [Internet]. Human Molecular Genetics. 2012 ; 21( 19): 4314-4324.[citado 2024 nov. 09 ] Available from: https://doi.org/10.1093/hmg/dds264

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