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Artigo de periodico
iPSC-derived cells for whole liver bioengineering (2024)
Silva, Kayque Alves Telles ; Pacheco, Lara ; Chianca, Fernanda; Komatsu, Sabrina ; Chiovatto, Caroline; Zatz, Mayana ; Goulart, Ernesto
Source: Frontiers in Bioengineering and Biotechnology. Unidades: IB, BIOTECNOLOGIA
Subjects: FÍGADO, BIOENGENHARIA, CÉLULAS-TRONCO
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ABNT
SILVA, Kayque Alves Telles et al. iPSC-derived cells for whole liver bioengineering. Frontiers in Bioengineering and Biotechnology, v. 12, 2024Tradução . . Disponível em: https://doi.org/10.3389/fbioe.2024.1338762. Acesso em: 15 jul. 2024.
APA
Silva, K. A. T., Pacheco, L., Chianca, F., Komatsu, S., Chiovatto, C., Zatz, M., & Goulart, E. (2024). iPSC-derived cells for whole liver bioengineering. Frontiers in Bioengineering and Biotechnology, 12. doi:10.3389/fbioe.2024.1338762
NLM
Silva KAT, Pacheco L, Chianca F, Komatsu S, Chiovatto C, Zatz M, Goulart E. iPSC-derived cells for whole liver bioengineering [Internet]. Frontiers in Bioengineering and Biotechnology. 2024 ; 12[citado 2024 jul. 15 ] Available from: https://doi.org/10.3389/fbioe.2024.1338762
Vancouver
Silva KAT, Pacheco L, Chianca F, Komatsu S, Chiovatto C, Zatz M, Goulart E. iPSC-derived cells for whole liver bioengineering [Internet]. Frontiers in Bioengineering and Biotechnology. 2024 ; 12[citado 2024 jul. 15 ] Available from: https://doi.org/10.3389/fbioe.2024.1338762
Artigo de periodico
Genetically modified ZIKA virus as a microRNA-sensitive oncolytic virus against central nervous system tumors (2024)
Novaes, Gabriela Machado; Lima, Caroline; Longo, Carla; Machado, Pedro Henrique; Silva, Thais Peron; Olberg, Giovanna Gonçalves de Oliveira; Módolo, Diego Grando; Pereira, Márcia Cristina Leite; Santos , Tiago Goss; Zatz, Mayana ; Lagares, David; Franco, Marcelo de; Ho, Paulo Lee; Bulstrode, Harry; Okamoto, Oswaldo Keith ; Kaid, Carolini
Source: Molecular Therapy. Unidade: IB
Subjects: CÉLULAS-TRONCO, IMUNOTERAPIA, ZIKA VÍRUS, GENÉTICA
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NOVAES, Gabriela Machado et al. Genetically modified ZIKA virus as a microRNA-sensitive oncolytic virus against central nervous system tumors. Molecular Therapy, v. 32, n. 2, p. 440-456, 2024Tradução . . Disponível em: https://doi.org/10.1016/j.ymthe.2024.01.006. Acesso em: 15 jul. 2024.
APA
Novaes, G. M., Lima, C., Longo, C., Machado, P. H., Silva, T. P., Olberg, G. G. de O., et al. (2024). Genetically modified ZIKA virus as a microRNA-sensitive oncolytic virus against central nervous system tumors. Molecular Therapy, 32( 2), 440-456. doi:10.1016/j.ymthe.2024.01.006
NLM
Novaes GM, Lima C, Longo C, Machado PH, Silva TP, Olberg GG de O, Módolo DG, Pereira MCL, Santos TG, Zatz M, Lagares D, Franco M de, Ho PL, Bulstrode H, Okamoto OK, Kaid C. Genetically modified ZIKA virus as a microRNA-sensitive oncolytic virus against central nervous system tumors [Internet]. Molecular Therapy. 2024 ; 32( 2): 440-456.[citado 2024 jul. 15 ] Available from: https://doi.org/10.1016/j.ymthe.2024.01.006
Vancouver
Novaes GM, Lima C, Longo C, Machado PH, Silva TP, Olberg GG de O, Módolo DG, Pereira MCL, Santos TG, Zatz M, Lagares D, Franco M de, Ho PL, Bulstrode H, Okamoto OK, Kaid C. Genetically modified ZIKA virus as a microRNA-sensitive oncolytic virus against central nervous system tumors [Internet]. Molecular Therapy. 2024 ; 32( 2): 440-456.[citado 2024 jul. 15 ] Available from: https://doi.org/10.1016/j.ymthe.2024.01.006
Artigo de periodico
Correction: Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19 (2024)
Matuozzo, Daniela ; Talouarn, Estelle ; Marchal, Astrid; Manry, Jeremy; Seeleuthner, Yoann; Zhang, Yu; Bolze, Alexandre ; Chaldebas, Matthieu; Condino Neto, Antonio ; Zatz, Mayana
Source: Genome Medicine. Unidades: IB, ICB
Subjects: IMUNOLOGIA, COVID-19
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MATUOZZO, Daniela et al. Correction: Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19. Genome Medicine, v. 16, 2024Tradução . . Disponível em: https://doi.org/10.1186/s13073-023-01173-8. Acesso em: 15 jul. 2024.
APA
Matuozzo, D., Talouarn, E., Marchal, A., Manry, J., Seeleuthner, Y., Zhang, Y., et al. (2024). Correction: Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19. Genome Medicine, 16. Recuperado de https://doi.org/10.1186/s13073-023-01173-8
NLM
Matuozzo D, Talouarn E, Marchal A, Manry J, Seeleuthner Y, Zhang Y, Bolze A, Chaldebas M, Condino Neto A, Zatz M. Correction: Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19 [Internet]. Genome Medicine. 2024 ; 16[citado 2024 jul. 15 ] Available from: https://doi.org/10.1186/s13073-023-01173-8
Vancouver
Matuozzo D, Talouarn E, Marchal A, Manry J, Seeleuthner Y, Zhang Y, Bolze A, Chaldebas M, Condino Neto A, Zatz M. Correction: Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19 [Internet]. Genome Medicine. 2024 ; 16[citado 2024 jul. 15 ] Available from: https://doi.org/10.1186/s13073-023-01173-8
Artigo de periodico
Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19 (2023)
Matuozzo, Daniela ; Talouarn, Estelle ; Marchal, Astrid; Manry, Jeremy; Seeleuthner, Yoann; Zhang, Yu; Bolze, Alexandre ; Chaldebas, Matthieu; Condino Neto, Antonio ; Zatz, Mayana
Source: Genome Medicine. Unidades: IB, ICB
Subjects: IMUNOLOGIA, COVID-19
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ABNT
MATUOZZO, Daniela et al. Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19. Genome Medicine, v. 15, p. 1-25, 2023Tradução . . Disponível em: https://doi.org/10.1186/s13073-023-01173-8. Acesso em: 15 jul. 2024.
APA
Matuozzo, D., Talouarn, E., Marchal, A., Manry, J., Seeleuthner, Y., Zhang, Y., et al. (2023). Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19. Genome Medicine, 15, 1-25. doi:10.1186/s13073-023-01173-8
NLM
Matuozzo D, Talouarn E, Marchal A, Manry J, Seeleuthner Y, Zhang Y, Bolze A, Chaldebas M, Condino Neto A, Zatz M. Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19 [Internet]. Genome Medicine. 2023 ; 15 1-25.[citado 2024 jul. 15 ] Available from: https://doi.org/10.1186/s13073-023-01173-8
Vancouver
Matuozzo D, Talouarn E, Marchal A, Manry J, Seeleuthner Y, Zhang Y, Bolze A, Chaldebas M, Condino Neto A, Zatz M. Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19 [Internet]. Genome Medicine. 2023 ; 15 1-25.[citado 2024 jul. 15 ] Available from: https://doi.org/10.1186/s13073-023-01173-8
Artigo de periodico
Association between APOE-ε4 allele and cognitive function is mediated by Alzheimer’s disease pathology: a population-based autopsy study in an admixed sample (2023)
Paradela, Regina Silva ; Justo, Alberto Fernando Oliveira ; Paes, Vítor Ribeiro; Leite, Renata E. P ; Pasqualucci, Carlos A ; Grinberg, Lea T. ; Naslavsky, Michel Satya ; Zatz, Mayana ; Nitrini, Ricardo ; Jacob Filho, Wilson ; Suemoto, Claudia Kimie
Source: Acta Neuropathologica Communications. Unidades: FM, IB
Subjects: APOLIPOPROTEÍNAS, DOENÇAS DO SISTEMA NERVOSO, COGNIÇÃO, DEMÊNCIA
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ABNT
PARADELA, Regina Silva et al. Association between APOE-ε4 allele and cognitive function is mediated by Alzheimer’s disease pathology: a population-based autopsy study in an admixed sample. Acta Neuropathologica Communications, v. 11, 2023Tradução . . Disponível em: https://doi.org/10.1186/s40478-023-01681-z. Acesso em: 15 jul. 2024.
APA
Paradela, R. S., Justo, A. F. O., Paes, V. R., Leite, R. E. P., Pasqualucci, C. A., Grinberg, L. T., et al. (2023). Association between APOE-ε4 allele and cognitive function is mediated by Alzheimer’s disease pathology: a population-based autopsy study in an admixed sample. Acta Neuropathologica Communications, 11. doi:10.1186/s40478-023-01681-z
NLM
Paradela RS, Justo AFO, Paes VR, Leite REP, Pasqualucci CA, Grinberg LT, Naslavsky MS, Zatz M, Nitrini R, Jacob Filho W, Suemoto CK. Association between APOE-ε4 allele and cognitive function is mediated by Alzheimer’s disease pathology: a population-based autopsy study in an admixed sample [Internet]. Acta Neuropathologica Communications. 2023 ; 11[citado 2024 jul. 15 ] Available from: https://doi.org/10.1186/s40478-023-01681-z
Vancouver
Paradela RS, Justo AFO, Paes VR, Leite REP, Pasqualucci CA, Grinberg LT, Naslavsky MS, Zatz M, Nitrini R, Jacob Filho W, Suemoto CK. Association between APOE-ε4 allele and cognitive function is mediated by Alzheimer’s disease pathology: a population-based autopsy study in an admixed sample [Internet]. Acta Neuropathologica Communications. 2023 ; 11[citado 2024 jul. 15 ] Available from: https://doi.org/10.1186/s40478-023-01681-z
Artigo de periodico
Neurodegeneration‐associated protein VAPB regulates proliferation in medulloblastoma (2023)
Assoni, Amanda Faria ; Mitsugi, Thiago Giove ; Wardenaar, René; Ferreira, Raiane Oliveira ; Jandrey, Elisa Helena Farias ; Novaes, Gabriela Machado ; Granha, Isabela Fonseca de Oliveira ; Bakker, Petra ; Kaid, Carolini ; Zatz, Mayana ; Foijer, Floris ; Okamoto, Oswaldo Keith
Source: Scientific Reports. Unidade: IB
Subjects: MEDULOBLASTOMA, DEGENERAÇÃO NEURAL
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ABNT
ASSONI, Amanda Faria et al. Neurodegeneration‐associated protein VAPB regulates proliferation in medulloblastoma. Scientific Reports, v. 13, n. art. 19481, 2023Tradução . . Disponível em: https://doi.org/10.1038/s41598-023-45319-5. Acesso em: 15 jul. 2024.
APA
Assoni, A. F., Mitsugi, T. G., Wardenaar, R., Ferreira, R. O., Jandrey, E. H. F., Novaes, G. M., et al. (2023). Neurodegeneration‐associated protein VAPB regulates proliferation in medulloblastoma. Scientific Reports, 13( art. 19481). doi:10.1038/s41598-023-45319-5
NLM
Assoni AF, Mitsugi TG, Wardenaar R, Ferreira RO, Jandrey EHF, Novaes GM, Granha IF de O, Bakker P, Kaid C, Zatz M, Foijer F, Okamoto OK. Neurodegeneration‐associated protein VAPB regulates proliferation in medulloblastoma [Internet]. Scientific Reports. 2023 ; 13( art. 19481):[citado 2024 jul. 15 ] Available from: https://doi.org/10.1038/s41598-023-45319-5
Vancouver
Assoni AF, Mitsugi TG, Wardenaar R, Ferreira RO, Jandrey EHF, Novaes GM, Granha IF de O, Bakker P, Kaid C, Zatz M, Foijer F, Okamoto OK. Neurodegeneration‐associated protein VAPB regulates proliferation in medulloblastoma [Internet]. Scientific Reports. 2023 ; 13( art. 19481):[citado 2024 jul. 15 ] Available from: https://doi.org/10.1038/s41598-023-45319-5
Artigo de periodico
Report of a young patient with brain calcifications with a novel homozygous MYORG variant (2023)
Sadok, Sara H; Borges-Medeiros, Rayssa L; Oliveira, Danyllo F. de; Zatz, Mayana ; Oliveira, João Ricardo Mendes de
Source: Gene. Unidade: IB
Subjects: MUTAÇÃO GENÉTICA, SEQUENCIAMENTO GENÉTICO, GENÉTICA MÉDICA
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ABNT
SADOK, Sara H et al. Report of a young patient with brain calcifications with a novel homozygous MYORG variant. Gene, v. 859, 2023Tradução . . Disponível em: https://doi.org/10.1016/j.gene.2023.147213. Acesso em: 15 jul. 2024.
APA
Sadok, S. H., Borges-Medeiros, R. L., Oliveira, D. F. de, Zatz, M., & Oliveira, J. R. M. de. (2023). Report of a young patient with brain calcifications with a novel homozygous MYORG variant. Gene, 859. doi:10.1016/j.gene.2023.147213
NLM
Sadok SH, Borges-Medeiros RL, Oliveira DF de, Zatz M, Oliveira JRM de. Report of a young patient with brain calcifications with a novel homozygous MYORG variant [Internet]. Gene. 2023 ; 859[citado 2024 jul. 15 ] Available from: https://doi.org/10.1016/j.gene.2023.147213
Vancouver
Sadok SH, Borges-Medeiros RL, Oliveira DF de, Zatz M, Oliveira JRM de. Report of a young patient with brain calcifications with a novel homozygous MYORG variant [Internet]. Gene. 2023 ; 859[citado 2024 jul. 15 ] Available from: https://doi.org/10.1016/j.gene.2023.147213
Artigo de periodico
Apolipoprotein E ε2 allele is associated with lower risk of carotid artery obstruction in a population-based autopsy study (2023)
Paradela, Regina Silva ; Itáo, Daniela Souza Farias ; Leite, Renata E.P; Pasqualucci, Carlos A; Grinberg, Lea T ; Naslavsky, Michel ; Zatz, Mayana ; Nitrini, Ricardo ; Jacob Filho, Wilson ; Suemoto, Claudia Kimie
Source: ournal of Stroke & Cerebrovascular Diseases. Unidades: IB, FM
Subjects: APOLIPOPROTEÍNAS, POLIMORFISMO, ARTERIOSCLEROSE, EPIDEMIOLOGIA
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ABNT
PARADELA, Regina Silva et al. Apolipoprotein E ε2 allele is associated with lower risk of carotid artery obstruction in a population-based autopsy study. ournal of Stroke & Cerebrovascular Diseases, v. 32, n. art. 107229, 2023Tradução . . Disponível em: https://doi.org/10.1016/j.jstrokecerebrovasdis.2023.107229. Acesso em: 15 jul. 2024.
APA
Paradela, R. S., Itáo, D. S. F., Leite, R. E. P., Pasqualucci, C. A., Grinberg, L. T., Naslavsky, M., et al. (2023). Apolipoprotein E ε2 allele is associated with lower risk of carotid artery obstruction in a population-based autopsy study. ournal of Stroke & Cerebrovascular Diseases, 32( art. 107229). doi:10.1016/j.jstrokecerebrovasdis.2023.107229
NLM
Paradela RS, Itáo DSF, Leite REP, Pasqualucci CA, Grinberg LT, Naslavsky M, Zatz M, Nitrini R, Jacob Filho W, Suemoto CK. Apolipoprotein E ε2 allele is associated with lower risk of carotid artery obstruction in a population-based autopsy study [Internet]. ournal of Stroke & Cerebrovascular Diseases. 2023 ; 32( art. 107229):[citado 2024 jul. 15 ] Available from: https://doi.org/10.1016/j.jstrokecerebrovasdis.2023.107229
Vancouver
Paradela RS, Itáo DSF, Leite REP, Pasqualucci CA, Grinberg LT, Naslavsky M, Zatz M, Nitrini R, Jacob Filho W, Suemoto CK. Apolipoprotein E ε2 allele is associated with lower risk of carotid artery obstruction in a population-based autopsy study [Internet]. ournal of Stroke & Cerebrovascular Diseases. 2023 ; 32( art. 107229):[citado 2024 jul. 15 ] Available from: https://doi.org/10.1016/j.jstrokecerebrovasdis.2023.107229
Artigo de periodico
Apolipoprotein e genotypes were not associated with intracranial atherosclerosis: a population-based autopsy study (2023)
Paradela, Regina Silva; Farias-Itao, Daniela Souza; Pasqualucci, Carlos A; Grinberg, Lea T; Naslavsky, Michel ; Zatz, Mayana ; Nitrini, Ricardo ; Jacob Filho, Wilson ; Suemoto, Claudia Kimie ; Leite, Renata E. P
Source: Cardiovascular Pathology. Unidades: FM, IB
Subjects: ESTUDOS TRANSVERSAIS, ARTÉRIAS CARÓTIDAS, AUTÓPSIA
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ABNT
PARADELA, Regina Silva et al. Apolipoprotein e genotypes were not associated with intracranial atherosclerosis: a population-based autopsy study. Cardiovascular Pathology, v. Jan./Fe, 2023Tradução . . Disponível em: https://doi.org/10.1016/j.carpath.2022.107479. Acesso em: 15 jul. 2024.
APA
Paradela, R. S., Farias-Itao, D. S., Pasqualucci, C. A., Grinberg, L. T., Naslavsky, M., Zatz, M., et al. (2023). Apolipoprotein e genotypes were not associated with intracranial atherosclerosis: a population-based autopsy study. Cardiovascular Pathology, Jan./Fe. doi:10.1016/j.carpath.2022.107479
NLM
Paradela RS, Farias-Itao DS, Pasqualucci CA, Grinberg LT, Naslavsky M, Zatz M, Nitrini R, Jacob Filho W, Suemoto CK, Leite REP. Apolipoprotein e genotypes were not associated with intracranial atherosclerosis: a population-based autopsy study [Internet]. Cardiovascular Pathology. 2023 ; Jan./Fe[citado 2024 jul. 15 ] Available from: https://doi.org/10.1016/j.carpath.2022.107479
Vancouver
Paradela RS, Farias-Itao DS, Pasqualucci CA, Grinberg LT, Naslavsky M, Zatz M, Nitrini R, Jacob Filho W, Suemoto CK, Leite REP. Apolipoprotein e genotypes were not associated with intracranial atherosclerosis: a population-based autopsy study [Internet]. Cardiovascular Pathology. 2023 ; Jan./Fe[citado 2024 jul. 15 ] Available from: https://doi.org/10.1016/j.carpath.2022.107479
Artigo de periodico
IFNγ protects motor neurons from oxidative stress via enhanced global protein synthesis in FUS-associated amyotrophic lateral sclerosis (2023)
Assoni, Amanda Faria; Guerrero, Erika N; Wardenaar, René; Oliveira, Danyllo; Bakker, Petra L; Alves, Luciana M; Carvalho, Valdemir M ; Okamoto, Oswaldo Keith ; Zatz, Mayana ; Foijer, Floris
Source: Brain Pathology. Unidade: IB
Subjects: ESCLEROSE AMIOTRÓFICA LATERAL, MEDULOBLASTOMA, DEGENERAÇÃO NEURAL
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ABNT
ASSONI, Amanda Faria et al. IFNγ protects motor neurons from oxidative stress via enhanced global protein synthesis in FUS-associated amyotrophic lateral sclerosis. Brain Pathology, 2023Tradução . . Disponível em: https://doi.org/10.1111/bpa.13206. Acesso em: 15 jul. 2024.
APA
Assoni, A. F., Guerrero, E. N., Wardenaar, R., Oliveira, D., Bakker, P. L., Alves, L. M., et al. (2023). IFNγ protects motor neurons from oxidative stress via enhanced global protein synthesis in FUS-associated amyotrophic lateral sclerosis. Brain Pathology. doi:10.1111/bpa.13206
NLM
Assoni AF, Guerrero EN, Wardenaar R, Oliveira D, Bakker PL, Alves LM, Carvalho VM, Okamoto OK, Zatz M, Foijer F. IFNγ protects motor neurons from oxidative stress via enhanced global protein synthesis in FUS-associated amyotrophic lateral sclerosis [Internet]. Brain Pathology. 2023 ;[citado 2024 jul. 15 ] Available from: https://doi.org/10.1111/bpa.13206
Vancouver
Assoni AF, Guerrero EN, Wardenaar R, Oliveira D, Bakker PL, Alves LM, Carvalho VM, Okamoto OK, Zatz M, Foijer F. IFNγ protects motor neurons from oxidative stress via enhanced global protein synthesis in FUS-associated amyotrophic lateral sclerosis [Internet]. Brain Pathology. 2023 ;[citado 2024 jul. 15 ] Available from: https://doi.org/10.1111/bpa.13206
Artigo de periodico
Inherited and acquired errors of type I interferon immunity govern susceptibility to COVID-19 and multisystem inflammatory syndrome in children (2023)
Bucciol, Giorgia; Zatz, Mayana
Source: Journal of Allergy and Clinical Immunology. Unidade: IB
Subjects: IMUNIDADE, PANDEMIAS, COVID-19
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ABNT
BUCCIOL, Giorgia e ZATZ, Mayana. Inherited and acquired errors of type I interferon immunity govern susceptibility to COVID-19 and multisystem inflammatory syndrome in children. Journal of Allergy and Clinical Immunology, v. 151, n. 4, p. 832-840, 2023Tradução . . Disponível em: https://doi.org/10.1016/j.jaci.2023.02.003. Acesso em: 15 jul. 2024.
APA
Bucciol, G., & Zatz, M. (2023). Inherited and acquired errors of type I interferon immunity govern susceptibility to COVID-19 and multisystem inflammatory syndrome in children. Journal of Allergy and Clinical Immunology, 151( 4), 832-840. doi:10.1016/j.jaci.2023.02.003
NLM
Bucciol G, Zatz M. Inherited and acquired errors of type I interferon immunity govern susceptibility to COVID-19 and multisystem inflammatory syndrome in children [Internet]. Journal of Allergy and Clinical Immunology. 2023 ; 151( 4): 832-840.[citado 2024 jul. 15 ] Available from: https://doi.org/10.1016/j.jaci.2023.02.003
Vancouver
Bucciol G, Zatz M. Inherited and acquired errors of type I interferon immunity govern susceptibility to COVID-19 and multisystem inflammatory syndrome in children [Internet]. Journal of Allergy and Clinical Immunology. 2023 ; 151( 4): 832-840.[citado 2024 jul. 15 ] Available from: https://doi.org/10.1016/j.jaci.2023.02.003
Artigo de periodico
Amyotrophic Lateral Sclerosis, FUS and Protein Synthesis Defects (2023)
Assoni, Amanda Faria ; Foijer, Floris; Zatz, Mayana
Source: Stem Cell Reviews and Reports. Unidade: IB
Subjects: ESCLEROSE AMIOTRÓFICA LATERAL, MEDULOBLASTOMA, DEGENERAÇÃO NEURAL
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ABNT
ASSONI, Amanda Faria e FOIJER, Floris e ZATZ, Mayana. Amyotrophic Lateral Sclerosis, FUS and Protein Synthesis Defects. Stem Cell Reviews and Reports, v. 19, p. 625–638, 2023Tradução . . Disponível em: https://doi.org/10.1007/s12015-022-10489-8. Acesso em: 15 jul. 2024.
APA
Assoni, A. F., Foijer, F., & Zatz, M. (2023). Amyotrophic Lateral Sclerosis, FUS and Protein Synthesis Defects. Stem Cell Reviews and Reports, 19, 625–638. doi:10.1007/s12015-022-10489-8
NLM
Assoni AF, Foijer F, Zatz M. Amyotrophic Lateral Sclerosis, FUS and Protein Synthesis Defects [Internet]. Stem Cell Reviews and Reports. 2023 ; 19 625–638.[citado 2024 jul. 15 ] Available from: https://doi.org/10.1007/s12015-022-10489-8
Vancouver
Assoni AF, Foijer F, Zatz M. Amyotrophic Lateral Sclerosis, FUS and Protein Synthesis Defects [Internet]. Stem Cell Reviews and Reports. 2023 ; 19 625–638.[citado 2024 jul. 15 ] Available from: https://doi.org/10.1007/s12015-022-10489-8
Artigo de periodico
Characterization of pharmacogenomic variants in a Brazilian admixed cohort of elderly individuals based on whole-genome sequencing data (2023)
Bertholim-Nasciben, Luciana; Scliar, Marilia O ; Deborto, Guilherme; Thiruvahindrapuram, Bhooma; Scherer, Stephen W; Duarte, Yeda Aparecida de Oliveira ; Zatz, Mayana ; Suarez-Kurtz, Guilherme; Parra, Esteban J; Naslavsky, Michel
Source: Frontiers in Pharmacology. Unidades: EE, IB, FSP, FMRP
Subjects: SEQUENCIAMENTO GENÉTICO, IDOSOS, GENOMAS
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ABNT
BERTHOLIM-NASCIBEN, Luciana et al. Characterization of pharmacogenomic variants in a Brazilian admixed cohort of elderly individuals based on whole-genome sequencing data. Frontiers in Pharmacology, v. 11, 2023Tradução . . Disponível em: https://doi.org/10.3389/fphar.2023.1178715. Acesso em: 15 jul. 2024.
APA
Bertholim-Nasciben, L., Scliar, M. O., Deborto, G., Thiruvahindrapuram, B., Scherer, S. W., Duarte, Y. A. de O., et al. (2023). Characterization of pharmacogenomic variants in a Brazilian admixed cohort of elderly individuals based on whole-genome sequencing data. Frontiers in Pharmacology, 11. doi:10.3389/fphar.2023.1178715
NLM
Bertholim-Nasciben L, Scliar MO, Deborto G, Thiruvahindrapuram B, Scherer SW, Duarte YA de O, Zatz M, Suarez-Kurtz G, Parra EJ, Naslavsky M. Characterization of pharmacogenomic variants in a Brazilian admixed cohort of elderly individuals based on whole-genome sequencing data [Internet]. Frontiers in Pharmacology. 2023 ; 11[citado 2024 jul. 15 ] Available from: https://doi.org/10.3389/fphar.2023.1178715
Vancouver
Bertholim-Nasciben L, Scliar MO, Deborto G, Thiruvahindrapuram B, Scherer SW, Duarte YA de O, Zatz M, Suarez-Kurtz G, Parra EJ, Naslavsky M. Characterization of pharmacogenomic variants in a Brazilian admixed cohort of elderly individuals based on whole-genome sequencing data [Internet]. Frontiers in Pharmacology. 2023 ; 11[citado 2024 jul. 15 ] Available from: https://doi.org/10.3389/fphar.2023.1178715
Artigo de periodico
Immunogenetics of HLA-B: SNP, allele, and haplotype diversity in populations from different continents and ancestry backgrounds (2023)
Silva, Nayane Dos Santos Brito ; Souza, Andreia Da Silva ; Andrade, Heloisa De Souza ; Pereira, Raphaela Neto; Castro, Camila Ferreira Bannwart ; Vince, Nicolas ; Limou, Sophie ; Naslavsky, Michel ; Zatz, Mayana ; Duarte, Yeda Aparecida de Oliveira ; Mendes Junior, Celso Teixeira ; Castelli, Erick Da Cruz
Source: HLA: immune response genetics. Unidades: IB, EE, FFCLRP, FMRP
Subjects: GENOMAS, GENES, GENEALOGIA
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ABNT
SILVA, Nayane Dos Santos Brito et al. Immunogenetics of HLA-B: SNP, allele, and haplotype diversity in populations from different continents and ancestry backgrounds. HLA: immune response genetics, v. 101, n. 6, p. 634-646, 2023Tradução . . Disponível em: https://doi.org/10.1111/tan.15043. Acesso em: 15 jul. 2024.
APA
Silva, N. D. S. B., Souza, A. D. S., Andrade, H. D. S., Pereira, R. N., Castro, C. F. B., Vince, N., et al. (2023). Immunogenetics of HLA-B: SNP, allele, and haplotype diversity in populations from different continents and ancestry backgrounds. HLA: immune response genetics, 101( 6), 634-646. doi:10.1111/tan.15043
NLM
Silva NDSB, Souza ADS, Andrade HDS, Pereira RN, Castro CFB, Vince N, Limou S, Naslavsky M, Zatz M, Duarte YA de O, Mendes Junior CT, Castelli EDC. Immunogenetics of HLA-B: SNP, allele, and haplotype diversity in populations from different continents and ancestry backgrounds [Internet]. HLA: immune response genetics. 2023 ; 101( 6): 634-646.[citado 2024 jul. 15 ] Available from: https://doi.org/10.1111/tan.15043
Vancouver
Silva NDSB, Souza ADS, Andrade HDS, Pereira RN, Castro CFB, Vince N, Limou S, Naslavsky M, Zatz M, Duarte YA de O, Mendes Junior CT, Castelli EDC. Immunogenetics of HLA-B: SNP, allele, and haplotype diversity in populations from different continents and ancestry backgrounds [Internet]. HLA: immune response genetics. 2023 ; 101( 6): 634-646.[citado 2024 jul. 15 ] Available from: https://doi.org/10.1111/tan.15043
Artigo de periodico
Challenges and recommendations to increasing the use of exome sequencing and whole genome sequencing for diagnosing rare diseases in Brazil: an expert perspective (2023)
Félix, Têmis Maria ; Souza, Carolina Fischinger Moura de ; Oliveira, João Bosco; Rico-Restrepo, Mariana; Zanoteli, Edmar ; Zatz, Mayana ; Giugliani, Roberto
Source: International Journal for Equity in Health. Unidades: IB, FM
Subjects: GENOMAS, SEQUENCIAMENTO GENÉTICO, DOENÇAS RARAS
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ABNT
FÉLIX, Têmis Maria et al. Challenges and recommendations to increasing the use of exome sequencing and whole genome sequencing for diagnosing rare diseases in Brazil: an expert perspective. International Journal for Equity in Health, v. 22, n. 11, 2023Tradução . . Disponível em: https://doi.org/10.1186/s12939-022-01809-y. Acesso em: 15 jul. 2024.
APA
Félix, T. M., Souza, C. F. M. de, Oliveira, J. B., Rico-Restrepo, M., Zanoteli, E., Zatz, M., & Giugliani, R. (2023). Challenges and recommendations to increasing the use of exome sequencing and whole genome sequencing for diagnosing rare diseases in Brazil: an expert perspective. International Journal for Equity in Health, 22( 11). doi:10.1186/s12939-022-01809-y
NLM
Félix TM, Souza CFM de, Oliveira JB, Rico-Restrepo M, Zanoteli E, Zatz M, Giugliani R. Challenges and recommendations to increasing the use of exome sequencing and whole genome sequencing for diagnosing rare diseases in Brazil: an expert perspective [Internet]. International Journal for Equity in Health. 2023 ;22( 11):[citado 2024 jul. 15 ] Available from: https://doi.org/10.1186/s12939-022-01809-y
Vancouver
Félix TM, Souza CFM de, Oliveira JB, Rico-Restrepo M, Zanoteli E, Zatz M, Giugliani R. Challenges and recommendations to increasing the use of exome sequencing and whole genome sequencing for diagnosing rare diseases in Brazil: an expert perspective [Internet]. International Journal for Equity in Health. 2023 ;22( 11):[citado 2024 jul. 15 ] Available from: https://doi.org/10.1186/s12939-022-01809-y
Artigo de periodico
Challenges in selecting admixture models and marker sets to infer genetic ancestry in a Brazilian admixed population (2022)
Escher, Luciana Maia; Naslavsky, Michel ; Scliar, Marília O; Duarte, Yeda Aparecida de Oliveira ; Zatz, Mayana ; Nunes, Kelly
Source: Scientific Reports. Unidades: IB, EE
Subjects: MISCIGENAÇÃO, GENEALOGIA, GENOMAS
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ABNT
ESCHER, Luciana Maia et al. Challenges in selecting admixture models and marker sets to infer genetic ancestry in a Brazilian admixed population. Scientific Reports, v. 12, 2022Tradução . . Disponível em: https://doi.org/10.1038/s41598-022-25521-7. Acesso em: 15 jul. 2024.
APA
Escher, L. M., Naslavsky, M., Scliar, M. O., Duarte, Y. A. de O., Zatz, M., & Nunes, K. (2022). Challenges in selecting admixture models and marker sets to infer genetic ancestry in a Brazilian admixed population. Scientific Reports, 12. doi:10.1038/s41598-022-25521-7
NLM
Escher LM, Naslavsky M, Scliar MO, Duarte YA de O, Zatz M, Nunes K. Challenges in selecting admixture models and marker sets to infer genetic ancestry in a Brazilian admixed population [Internet]. Scientific Reports. 2022 ; 12[citado 2024 jul. 15 ] Available from: https://doi.org/10.1038/s41598-022-25521-7
Vancouver
Escher LM, Naslavsky M, Scliar MO, Duarte YA de O, Zatz M, Nunes K. Challenges in selecting admixture models and marker sets to infer genetic ancestry in a Brazilian admixed population [Internet]. Scientific Reports. 2022 ; 12[citado 2024 jul. 15 ] Available from: https://doi.org/10.1038/s41598-022-25521-7
Artigo de periodico
Author Correction: whole-genome sequencing of 1,171 elderly admixed individuals from Brazil (2022)
Naslavsky, Michel ; Scliar, Marilia O ; Yamamoto, Guilherme L ; Wang, Jaqueline Yu Ting; Zverinova, Stepanka; Karp, Tatiana; Nunes, Kelly ; Ceroni, José Ricardo Magliocco; Carvalho, Diego Lima de; Simões, Carlos Eduardo da Silva; Bozoklian, Daniel; Nonaka, Ricardo; Silva, Nayane dos Santos Brito; Souza, Andreia da Silva; Andrade, Heloísa de Souza; Passos, Marília Rodrigues Silva; Castro, Camila Ferreira Bannwart; Mendes-Junior, Celso T; Mercuri, Rafael L. V; Miller, Thiago L. A; Buzzo, Jose Leonel; Rego, Fernanda O; Araújo, Nathalia M; Magalhães, Wagner C. S; Mingroni Netto, Regina Celia ; Borda, Victor; Guio, Heinner; Rojas, Carlos P; Sanchez, Cesar; Caceres, Omar; Dean, Michael; Barreto, Mauricio L; Lima-Costa, Maria Fernanda; Horta, Bernardo L; Tarazona-Santos, Eduardo; Meyer, Diogo ; Galante, Pedro A. F; Guryev, Victor; Castelli, Erick C; Duarte, Yeda Aparecida de Oliveira ; Passos-Bueno, Maria Rita ; Zatz, Mayana
Source: Nature. Unidades: IB, FFCLRP, EE, FM, BIOINFORMÁTICA, IQ
Subjects: GENOMAS, SEQUENCIAMENTO GENÉTICO, IDOSOS, MISCIGENAÇÃO
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ABNT
NASLAVSKY, Michel et al. Author Correction: whole-genome sequencing of 1,171 elderly admixed individuals from Brazil. Nature, v. 13, n. 1831, 2022Tradução . . Disponível em: https://doi.org/10.1038/s41467-022-29575-z. Acesso em: 15 jul. 2024.
APA
Naslavsky, M., Scliar, M. O., Yamamoto, G. L., Wang, J. Y. T., Zverinova, S., Karp, T., et al. (2022). Author Correction: whole-genome sequencing of 1,171 elderly admixed individuals from Brazil. Nature, 13( 1831). doi:10.1038/s41467-022-29575-z
NLM
Naslavsky M, Scliar MO, Yamamoto GL, Wang JYT, Zverinova S, Karp T, Nunes K, Ceroni JRM, Carvalho DL de, Simões CE da S, Bozoklian D, Nonaka R, Silva N dos SB, Souza A da S, Andrade H de S, Passos MRS, Castro CFB, Mendes-Junior CT, Mercuri RLV, Miller TLA, Buzzo JL, Rego FO, Araújo NM, Magalhães WCS, Mingroni Netto RC, Borda V, Guio H, Rojas CP, Sanchez C, Caceres O, Dean M, Barreto ML, Lima-Costa MF, Horta BL, Tarazona-Santos E, Meyer D, Galante PAF, Guryev V, Castelli EC, Duarte YA de O, Passos-Bueno MR, Zatz M. Author Correction: whole-genome sequencing of 1,171 elderly admixed individuals from Brazil [Internet]. Nature. 2022 ; 13( 1831):[citado 2024 jul. 15 ] Available from: https://doi.org/10.1038/s41467-022-29575-z
Vancouver
Naslavsky M, Scliar MO, Yamamoto GL, Wang JYT, Zverinova S, Karp T, Nunes K, Ceroni JRM, Carvalho DL de, Simões CE da S, Bozoklian D, Nonaka R, Silva N dos SB, Souza A da S, Andrade H de S, Passos MRS, Castro CFB, Mendes-Junior CT, Mercuri RLV, Miller TLA, Buzzo JL, Rego FO, Araújo NM, Magalhães WCS, Mingroni Netto RC, Borda V, Guio H, Rojas CP, Sanchez C, Caceres O, Dean M, Barreto ML, Lima-Costa MF, Horta BL, Tarazona-Santos E, Meyer D, Galante PAF, Guryev V, Castelli EC, Duarte YA de O, Passos-Bueno MR, Zatz M. Author Correction: whole-genome sequencing of 1,171 elderly admixed individuals from Brazil [Internet]. Nature. 2022 ; 13( 1831):[citado 2024 jul. 15 ] Available from: https://doi.org/10.1038/s41467-022-29575-z
Artigo de periodico
MS-driven metabolic alterations are recapitulated in iPSC-Derived astrocytes (2022)
Nunes, Bruno Ghirotto ; Oliveira, Danyllo Felipe de ; Cipelli, Marcella ; Basso, Paulo José ; Lima, Jean De ; Breda, Cristiane Naffah de Souza ; Ribeiro, Henrique Caldeira da ; Silva, Camille Cristine Caldeira da ; Sertié, Andréa L ; Oliveira, Antonio Edson Rocha ; Hiyane, Meire Ioshie ; Galdini, Elia G. ; Sussulini, Alessandra ; Oliveira, Enedina Maria Lobato de ; Zatz, Mayana ; Câmara, Niels Olsen Saraiva ; Nakaya, Helder Takashi Imoto ; Kowaltowski, Alicia Juliana
Source: Annals of Neurology. Unidades: ICB, IB, FCF, IQ
Subjects: IMUNOLOGIA, ASTRÓCITOS, CÉLULAS-TRONCO, ÁCIDO GLUTÂMICO, MITOCÔNDRIAS, ESCLEROSE MÚLTIPLA, MICROSCOPIA ELETRÔNICA, CITOMETRIA DE FLUXO, CITOCINAS, EXPRESSÃO GÊNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
NUNES, Bruno Ghirotto et al. MS-driven metabolic alterations are recapitulated in iPSC-Derived astrocytes. Annals of Neurology, v. 91, n. 5, p. 652-659, 2022Tradução . . Disponível em: https://doi.org/10.1002/ana.26336. Acesso em: 15 jul. 2024.
APA
Nunes, B. G., Oliveira, D. F. de, Cipelli, M., Basso, P. J., Lima, J. D., Breda, C. N. de S., et al. (2022). MS-driven metabolic alterations are recapitulated in iPSC-Derived astrocytes. Annals of Neurology, 91( 5), 652-659. doi:10.1002/ana.26336
NLM
Nunes BG, Oliveira DF de, Cipelli M, Basso PJ, Lima JD, Breda CN de S, Ribeiro HC da, Silva CCC da, Sertié AL, Oliveira AER, Hiyane MI, Galdini EG, Sussulini A, Oliveira EML de, Zatz M, Câmara NOS, Nakaya HTI, Kowaltowski AJ. MS-driven metabolic alterations are recapitulated in iPSC-Derived astrocytes [Internet]. Annals of Neurology. 2022 ; 91( 5): 652-659.[citado 2024 jul. 15 ] Available from: https://doi.org/10.1002/ana.26336
Vancouver
Nunes BG, Oliveira DF de, Cipelli M, Basso PJ, Lima JD, Breda CN de S, Ribeiro HC da, Silva CCC da, Sertié AL, Oliveira AER, Hiyane MI, Galdini EG, Sussulini A, Oliveira EML de, Zatz M, Câmara NOS, Nakaya HTI, Kowaltowski AJ. MS-driven metabolic alterations are recapitulated in iPSC-Derived astrocytes [Internet]. Annals of Neurology. 2022 ; 91( 5): 652-659.[citado 2024 jul. 15 ] Available from: https://doi.org/10.1002/ana.26336
Trabalho de evento-resumo
Genomics and the Future of Medicine (2022)
Zatz, Mayana
Conference titles: International Conference on Environmental Mutagens.
Subjects: GENÔMICA, MEDICINA, COVID-19
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ZATZ, Mayana. Genomics and the Future of Medicine. 2022, Anais.. Ottawa: [s.n.], 2022. . Acesso em: 15 jul. 2024.
APA
Zatz, M. (2022). Genomics and the Future of Medicine. In . Ottawa.
NLM
Zatz M. Genomics and the Future of Medicine. 2022 ;[citado 2024 jul. 15 ]
Vancouver
Zatz M. Genomics and the Future of Medicine. 2022 ;[citado 2024 jul. 15 ]
Artigo de periodico
Tandem duplication within the DMD gene in Labrador retrievers with a mild clinical phenotype (2022)
Shelton, G. Diane ; Minor, Katie M; Vieira, Natassia M; Kunkel, Louis M; Friedenberg, Steven G; Cullen, Jonah N; Guo, Ling T; Zatz, Mayana ; Mickelson, James R
Source: Neuromuscular Disorders. Unidade: IB
Subjects: DISTROFIA MUSCULAR, SEQUENCIAMENTO GENÉTICO, MIOPATIAS CONGÊNITAS ESTRUTURAIS, CÃO GOLDEN RETRIEVER
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SHELTON, G. Diane et al. Tandem duplication within the DMD gene in Labrador retrievers with a mild clinical phenotype. Neuromuscular Disorders, v. 32, n. 10, p. 836-841, 2022Tradução . . Disponível em: https://doi.org/10.1016/j.nmd.2022.08.001. Acesso em: 15 jul. 2024.
APA
Shelton, G. D., Minor, K. M., Vieira, N. M., Kunkel, L. M., Friedenberg, S. G., Cullen, J. N., et al. (2022). Tandem duplication within the DMD gene in Labrador retrievers with a mild clinical phenotype. Neuromuscular Disorders, 32( 10), 836-841. doi:10.1016/j.nmd.2022.08.001
NLM
Shelton GD, Minor KM, Vieira NM, Kunkel LM, Friedenberg SG, Cullen JN, Guo LT, Zatz M, Mickelson JR. Tandem duplication within the DMD gene in Labrador retrievers with a mild clinical phenotype [Internet]. Neuromuscular Disorders. 2022 ; 32( 10): 836-841.[citado 2024 jul. 15 ] Available from: https://doi.org/10.1016/j.nmd.2022.08.001
Vancouver
Shelton GD, Minor KM, Vieira NM, Kunkel LM, Friedenberg SG, Cullen JN, Guo LT, Zatz M, Mickelson JR. Tandem duplication within the DMD gene in Labrador retrievers with a mild clinical phenotype [Internet]. Neuromuscular Disorders. 2022 ; 32( 10): 836-841.[citado 2024 jul. 15 ] Available from: https://doi.org/10.1016/j.nmd.2022.08.001

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