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Artigo de periodico
Protein Arginylation is regulated during SARS-CoV-2 infection (2023)
Silva, Janaina Macedo da ; Fernandes, Livia Rosa ; Gomes, Vinicius de Morais ; Santiago, Veronica Feijoli ; Santos, Deivid Martins ; Molnar Catarina Maria Stanischesk ; Barboza, Bruno Rafael ; Souza, Edmarcia Elisa de ; Marques, Rodolfo Ferreira ; Boscardin, Silvia Beatriz ; Durigon, Edison Luiz ; Marinho, Claudio Romero Farias ; Wrenger, Carsten ; Marie, Suely Kazue Nagahashi ; Palmisano, Giuseppe
Source: Viruses. Unidades: ICB, FM
Subjects: PARASITOLOGIA, MICROBIOLOGIA, ENZIMAS, METABOLISMO DE PROTEÍNA, COVID-19, PROTEÍNAS, LISOSSOMOS, MACRÓFAGOS, INFECÇÕES POR CORONAVIRUS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SILVA, Janaina Macedo da et al. Protein Arginylation is regulated during SARS-CoV-2 infection. Viruses, v. 15, n. 2, p. 1-25, 2023Tradução . . Disponível em: https://doi.org/10.3390/v15020290. Acesso em: 05 nov. 2024.
APA
Silva, J. M. da, Fernandes, L. R., Gomes, V. de M., Santiago, V. F., Santos, D. M., Molnar Catarina Maria Stanischesk,, et al. (2023). Protein Arginylation is regulated during SARS-CoV-2 infection. Viruses, 15( 2), 1-25. doi:10.3390/v15020290
NLM
Silva JM da, Fernandes LR, Gomes V de M, Santiago VF, Santos DM, Molnar Catarina Maria Stanischesk, Barboza BR, Souza EE de, Marques RF, Boscardin SB, Durigon EL, Marinho CRF, Wrenger C, Marie SKN, Palmisano G. Protein Arginylation is regulated during SARS-CoV-2 infection [Internet]. Viruses. 2023 ; 15( 2): 1-25.[citado 2024 nov. 05 ] Available from: https://doi.org/10.3390/v15020290
Vancouver
Silva JM da, Fernandes LR, Gomes V de M, Santiago VF, Santos DM, Molnar Catarina Maria Stanischesk, Barboza BR, Souza EE de, Marques RF, Boscardin SB, Durigon EL, Marinho CRF, Wrenger C, Marie SKN, Palmisano G. Protein Arginylation is regulated during SARS-CoV-2 infection [Internet]. Viruses. 2023 ; 15( 2): 1-25.[citado 2024 nov. 05 ] Available from: https://doi.org/10.3390/v15020290
Artigo de periodico
Biallelic UBE4A loss-of-function variants cause intellectual disability and global developmental delay (2021)
Melo, Uirá Souto ; Bonner, Devon ; Lloyd, Kevin C. Kent ; Moshiri, Ala ; Willis, Brandon ; Lanoue, Louise ; Bower, Lynette; Leonard, Brian C. ; Martins, Davi Jardim ; Gomes, Fernando ; Leite, Felipe de Souza ; Oliveira, Danyllo ; Kitajima, João Paulo; Monteiro, Fabiola P. ; Zatz, Mayana ; Menck, Carlos Frederico Martins ; Wheeler, Matthew T. ; Bernstein, Jonathan A. ; Dumas, Kevin; Spiteri, Elizabeth ; Di Donato, Nataliya ; Jahn, Arne ; Hashem, Mais; Alsaif, Hessa S. ; Chedrawi, Aziza; Alkuraya, Fowzan S. ; Kok, Fernando ; Byers, Heather M.
Source: Genetics in Medicine. Unidades: IB, ICB, FM
Subjects: MICROBIOLOGIA, EXONS, GENOMAS, PESSOAS COM DEFICIÊNCIA INTELECTUAL, DOENÇAS DO DESENVOLVIMENTO ÓSSEO, VARIAÇÃO GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MELO, Uirá Souto et al. Biallelic UBE4A loss-of-function variants cause intellectual disability and global developmental delay. Genetics in Medicine, v. 23, n. 4, p. 6611-668, 2021Tradução . . Disponível em: https://doi.org/10.1038/s41436-020-01047-z. Acesso em: 05 nov. 2024.
APA
Melo, U. S., Bonner, D., Lloyd, K. C. K., Moshiri, A., Willis, B., Lanoue, L., et al. (2021). Biallelic UBE4A loss-of-function variants cause intellectual disability and global developmental delay. Genetics in Medicine, 23( 4), 6611-668. doi:10.1038/s41436-020-01047-z
NLM
Melo US, Bonner D, Lloyd KCK, Moshiri A, Willis B, Lanoue L, Bower L, Leonard BC, Martins DJ, Gomes F, Leite F de S, Oliveira D, Kitajima JP, Monteiro FP, Zatz M, Menck CFM, Wheeler MT, Bernstein JA, Dumas K, Spiteri E, Di Donato N, Jahn A, Hashem M, Alsaif HS, Chedrawi A, Alkuraya FS, Kok F, Byers HM. Biallelic UBE4A loss-of-function variants cause intellectual disability and global developmental delay [Internet]. Genetics in Medicine. 2021 ; 23( 4): 6611-668.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1038/s41436-020-01047-z
Vancouver
Melo US, Bonner D, Lloyd KCK, Moshiri A, Willis B, Lanoue L, Bower L, Leonard BC, Martins DJ, Gomes F, Leite F de S, Oliveira D, Kitajima JP, Monteiro FP, Zatz M, Menck CFM, Wheeler MT, Bernstein JA, Dumas K, Spiteri E, Di Donato N, Jahn A, Hashem M, Alsaif HS, Chedrawi A, Alkuraya FS, Kok F, Byers HM. Biallelic UBE4A loss-of-function variants cause intellectual disability and global developmental delay [Internet]. Genetics in Medicine. 2021 ; 23( 4): 6611-668.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1038/s41436-020-01047-z
Artigo de periodico
Overexpression of KLC2 due to a homozygous deletion in the non-coding region causes SPOAN syndrome (2015)
Melo, Uira S; Macedo-Souza, Lucia I; Figueiredo, Thalita; Muotri, Alysson R; Gleeson, , Joseph G; Coux, Gabriela; Armas, Pablo; Calcaterra, Nora B; Kitajima, João P; Amorim, Simone; Olávio, Thiago R; Griesi-Oliveira, Karina; Coatti, Giuliana C; Rocha, Clarissa R. R; Martins-Pinheiro, Marinalva; Menck, Carlos Frederico Martins ; Zaki, Maha S; Kok, Fernando; Zatz, Mayana ; Santos, Silvana
Source: Human Molecular Genetics. Unidades: ICB, FM, IB
Subjects: DOENÇAS NEURODEGENERATIVAS, SEQUENCIAMENTO GENÉTICO, DOENÇAS GENÉTICAS, MAPEAMENTO GENÉTICO, NEUROGENÉTICA, HEREDITARIEDADE, REPARAÇÃO DE DNA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MELO, Uira S et al. Overexpression of KLC2 due to a homozygous deletion in the non-coding region causes SPOAN syndrome. Human Molecular Genetics, p. 1-9, 2015Tradução . . Disponível em: https://doi.org/10.1093/hmg/ddv388. Acesso em: 05 nov. 2024.
APA
Melo, U. S., Macedo-Souza, L. I., Figueiredo, T., Muotri, A. R., Gleeson,, Coux, G., et al. (2015). Overexpression of KLC2 due to a homozygous deletion in the non-coding region causes SPOAN syndrome. Human Molecular Genetics, 1-9. doi:10.1093/hmg/ddv388
NLM
Melo US, Macedo-Souza LI, Figueiredo T, Muotri AR, Gleeson, Coux G, Armas P, Calcaterra NB, Kitajima JP, Amorim S, Olávio TR, Griesi-Oliveira K, Coatti GC, Rocha CRR, Martins-Pinheiro M, Menck CFM, Zaki MS, Kok F, Zatz M, Santos S. Overexpression of KLC2 due to a homozygous deletion in the non-coding region causes SPOAN syndrome [Internet]. Human Molecular Genetics. 2015 ; 1-9.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1093/hmg/ddv388
Vancouver
Melo US, Macedo-Souza LI, Figueiredo T, Muotri AR, Gleeson, Coux G, Armas P, Calcaterra NB, Kitajima JP, Amorim S, Olávio TR, Griesi-Oliveira K, Coatti GC, Rocha CRR, Martins-Pinheiro M, Menck CFM, Zaki MS, Kok F, Zatz M, Santos S. Overexpression of KLC2 due to a homozygous deletion in the non-coding region causes SPOAN syndrome [Internet]. Human Molecular Genetics. 2015 ; 1-9.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1093/hmg/ddv388
Artigo de periodico
Mutation in PNKP presenting initially as axonal Charcot-Marie-Tooth disease (2015)
Pedroso, José Luiz; Rocha, Clarissa R. R.; Macedo-Souza, Lucia I.; Mario, Vitor de; Marques Junior, Wilson; Barsottini, Orlando G. P.; Oliveira, Acary S. Bulle; Menck, Carlos Frederico Martins ; Kok, Fernando
Source: Neurology: Genetics. Unidades: ICB, FM
Assunto: MICROBIOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PEDROSO, José Luiz et al. Mutation in PNKP presenting initially as axonal Charcot-Marie-Tooth disease. Neurology: Genetics, v. 1, n. 4, p. 1-3, 2015Tradução . . Disponível em: https://doi.org/10.1212/NXG.0000000000000030. Acesso em: 05 nov. 2024.
APA
Pedroso, J. L., Rocha, C. R. R., Macedo-Souza, L. I., Mario, V. de, Marques Junior, W., Barsottini, O. G. P., et al. (2015). Mutation in PNKP presenting initially as axonal Charcot-Marie-Tooth disease. Neurology: Genetics, 1( 4), 1-3. doi:10.1212/NXG.0000000000000030
NLM
Pedroso JL, Rocha CRR, Macedo-Souza LI, Mario V de, Marques Junior W, Barsottini OGP, Oliveira ASB, Menck CFM, Kok F. Mutation in PNKP presenting initially as axonal Charcot-Marie-Tooth disease [Internet]. Neurology: Genetics. 2015 ; 1( 4): 1-3.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1212/NXG.0000000000000030
Vancouver
Pedroso JL, Rocha CRR, Macedo-Souza LI, Mario V de, Marques Junior W, Barsottini OGP, Oliveira ASB, Menck CFM, Kok F. Mutation in PNKP presenting initially as axonal Charcot-Marie-Tooth disease [Internet]. Neurology: Genetics. 2015 ; 1( 4): 1-3.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1212/NXG.0000000000000030

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