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Artigo de periodico
Comprehensive germline mutation analysis and clinical profile in a large cohort of Brazilian xeroderma pigmentosum patients (2020)
Santiago, Karina Miranda ; Castro, Ligia Pereira ; Duprat Neto, José Pedreira ; Nóbrega, Amanda Aparecida França de ; Pinto, C. A. L.; Prolla, Patrícia Ashton ; Vairo, Filippo Pinto e ; Medeiros, Paula F. V. de ; Ribeiro, Erlane M. ; Ribeiro, Bethania de Freitas Rodrigues ; Valle, Fabio Francesconi do ; Doriqui, M. J. R.; Leite, Carlos Heli Bezerra ; Rocha, Rafael M. ; Moura, Livia Maria Silva ; Munford, Veridiana ; Galante, Pedro Alexandre Favoretto ; Menck, Carlos Frederico Martins ; Rogatto, Silvia R. ; Achatz, Maria Isabel
Source: Journal European Academy of Dermatology and Venereology. Unidades: ICB, BIOINFORMÁTICA
Subjects: MICROBIOLOGIA, ESTUDOS DE COORTES, MUTAÇÃO GENÉTICA, MELANOMA, NEOPLASIAS CUTÂNEAS
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ABNT
SANTIAGO, Karina Miranda et al. Comprehensive germline mutation analysis and clinical profile in a large cohort of Brazilian xeroderma pigmentosum patients. Journal European Academy of Dermatology and Venereology, v. 34, n. 10, p. 2392-2401, 2020Tradução . . Disponível em: https://doi.org/10.1111/jdv.16405. Acesso em: 07 nov. 2024.
APA
Santiago, K. M., Castro, L. P., Duprat Neto, J. P., Nóbrega, A. A. F. de, Pinto, C. A. L., Prolla, P. A., et al. (2020). Comprehensive germline mutation analysis and clinical profile in a large cohort of Brazilian xeroderma pigmentosum patients. Journal European Academy of Dermatology and Venereology, 34( 10), 2392-2401. doi:10.1111/jdv.16405
NLM
Santiago KM, Castro LP, Duprat Neto JP, Nóbrega AAF de, Pinto CAL, Prolla PA, Vairo FP e, Medeiros PFV de, Ribeiro EM, Ribeiro B de FR, Valle FF do, Doriqui MJR, Leite CHB, Rocha RM, Moura LMS, Munford V, Galante PAF, Menck CFM, Rogatto SR, Achatz MI. Comprehensive germline mutation analysis and clinical profile in a large cohort of Brazilian xeroderma pigmentosum patients [Internet]. Journal European Academy of Dermatology and Venereology. 2020 ; 34( 10): 2392-2401.[citado 2024 nov. 07 ] Available from: https://doi.org/10.1111/jdv.16405
Vancouver
Santiago KM, Castro LP, Duprat Neto JP, Nóbrega AAF de, Pinto CAL, Prolla PA, Vairo FP e, Medeiros PFV de, Ribeiro EM, Ribeiro B de FR, Valle FF do, Doriqui MJR, Leite CHB, Rocha RM, Moura LMS, Munford V, Galante PAF, Menck CFM, Rogatto SR, Achatz MI. Comprehensive germline mutation analysis and clinical profile in a large cohort of Brazilian xeroderma pigmentosum patients [Internet]. Journal European Academy of Dermatology and Venereology. 2020 ; 34( 10): 2392-2401.[citado 2024 nov. 07 ] Available from: https://doi.org/10.1111/jdv.16405
Artigo de periodico
Germline mutation in MUS81 resulting in impaired protein stability is associated with Familial Breast and Thyroid Cancer (2020)
Pinheiro, Maisa ; Lupinacci, Fernanda Cristina Sulla; Santiago, Karina Miranda ; Drigo, Sandra Aparecida ; Marchi, Fabio Albuquerque; Fonseca-Alves, Carlos Eduardo; Andrade, Sónia C. S ; Aagaard, Mads Malik ; Basso, Tatiane Ramos; Reis, Mariana Bisarro dos; Villacis, Rolando André Rios; Roffé, Martin ; Achatz, Maria Isabel ; Rogatto, Silvia Regina
Source: Cancers. Unidade: IB
Subjects: NEOPLASIAS MAMÁRIAS, NEOPLASIAS DA TIREOIDE, MUTAÇÃO GENÉTICA, MELANOMA
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ABNT
PINHEIRO, Maisa et al. Germline mutation in MUS81 resulting in impaired protein stability is associated with Familial Breast and Thyroid Cancer. Cancers, v. 12, n. 5, 2020Tradução . . Disponível em: https://doi.org/10.3390/cancers12051289. Acesso em: 07 nov. 2024.
APA
Pinheiro, M., Lupinacci, F. C. S., Santiago, K. M., Drigo, S. A., Marchi, F. A., Fonseca-Alves, C. E., et al. (2020). Germline mutation in MUS81 resulting in impaired protein stability is associated with Familial Breast and Thyroid Cancer. Cancers, 12( 5). doi:10.3390/cancers12051289
NLM
Pinheiro M, Lupinacci FCS, Santiago KM, Drigo SA, Marchi FA, Fonseca-Alves CE, Andrade SCS, Aagaard MM, Basso TR, Reis MB dos, Villacis RAR, Roffé M, Achatz MI, Rogatto SR. Germline mutation in MUS81 resulting in impaired protein stability is associated with Familial Breast and Thyroid Cancer [Internet]. Cancers. 2020 ; 12( 5):[citado 2024 nov. 07 ] Available from: https://doi.org/10.3390/cancers12051289
Vancouver
Pinheiro M, Lupinacci FCS, Santiago KM, Drigo SA, Marchi FA, Fonseca-Alves CE, Andrade SCS, Aagaard MM, Basso TR, Reis MB dos, Villacis RAR, Roffé M, Achatz MI, Rogatto SR. Germline mutation in MUS81 resulting in impaired protein stability is associated with Familial Breast and Thyroid Cancer [Internet]. Cancers. 2020 ; 12( 5):[citado 2024 nov. 07 ] Available from: https://doi.org/10.3390/cancers12051289
Artigo de periodico
The breast cancer immunophenotype of TP53-p.R337H carriers is different from that observed among other pathogenic TP53 mutation carriers (2015)
Fitarelli-Kiehl, Mariana; Giacomazzi, Juliana; Santos-Silva, Patricia; Graudenz, Marcia Silveira; Palmero, Edenir Inez; Michelli, Rodrigo Augusto Depieri; Achatz, Maria Isabel; Osório, Cynthia Aparecida Bueno de Toledo; Ferraz, Victor Evangelista de Faria; Picanço, Clarissa Gondim; Ashton-Prolla, Patricia
Source: Familial Cancer. Unidade: FMRP
Subjects: NEOPLASIAS MAMÁRIAS (GENÉTICA), MUTAÇÃO GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FITARELLI-KIEHL, Mariana et al. The breast cancer immunophenotype of TP53-p.R337H carriers is different from that observed among other pathogenic TP53 mutation carriers. Familial Cancer, v. 14, n. 2, p. 333–336, 2015Tradução . . Disponível em: https://doi.org/10.1007/s10689-015-9779-y. Acesso em: 07 nov. 2024.
APA
Fitarelli-Kiehl, M., Giacomazzi, J., Santos-Silva, P., Graudenz, M. S., Palmero, E. I., Michelli, R. A. D., et al. (2015). The breast cancer immunophenotype of TP53-p.R337H carriers is different from that observed among other pathogenic TP53 mutation carriers. Familial Cancer, 14( 2), 333–336. doi:10.1007/s10689-015-9779-y
NLM
Fitarelli-Kiehl M, Giacomazzi J, Santos-Silva P, Graudenz MS, Palmero EI, Michelli RAD, Achatz MI, Osório CAB de T, Ferraz VE de F, Picanço CG, Ashton-Prolla P. The breast cancer immunophenotype of TP53-p.R337H carriers is different from that observed among other pathogenic TP53 mutation carriers [Internet]. Familial Cancer. 2015 ; 14( 2): 333–336.[citado 2024 nov. 07 ] Available from: https://doi.org/10.1007/s10689-015-9779-y
Vancouver
Fitarelli-Kiehl M, Giacomazzi J, Santos-Silva P, Graudenz MS, Palmero EI, Michelli RAD, Achatz MI, Osório CAB de T, Ferraz VE de F, Picanço CG, Ashton-Prolla P. The breast cancer immunophenotype of TP53-p.R337H carriers is different from that observed among other pathogenic TP53 mutation carriers [Internet]. Familial Cancer. 2015 ; 14( 2): 333–336.[citado 2024 nov. 07 ] Available from: https://doi.org/10.1007/s10689-015-9779-y
Trabalho de evento-resumo
Rare germline copy number variations in hereditary cutaneous melanoma (2014)
Fidalgo, Felipe; Rodrigues, Tatiane; Silva, Amanda Gonçalves; Facure, Luciana; Nóbrega, Amanda; Sá, Bianca; Duprat, João Pereira; Achatz, Maria Isabel; Rosenberg, Carla ; Carraro, Dirce Maria; Krepischi, Ana Cristina Victorino
Conference titles: Annual Meeting of American Association for Cancer Research. Unidade: IB
Subjects: MELANOMA, NEOPLASIAS (GENÉTICA), MUTAÇÃO GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FIDALGO, Felipe et al. Rare germline copy number variations in hereditary cutaneous melanoma. 2014, Anais.. San Diego: AACR, 2014. Disponível em: http://www.abstractsonline.com/Plan/ViewAbstract.aspx?sKey=32d6f306-9518-4b16-a390-31bd497ca997&cKey=0cb8274c-fa8e-4165-afc3-34265a033482&mKey=6ffe1446-a164-476a-92e7-c26446874d93. Acesso em: 07 nov. 2024.
APA
Fidalgo, F., Rodrigues, T., Silva, A. G., Facure, L., Nóbrega, A., Sá, B., et al. (2014). Rare germline copy number variations in hereditary cutaneous melanoma. In . San Diego: AACR. Recuperado de http://www.abstractsonline.com/Plan/ViewAbstract.aspx?sKey=32d6f306-9518-4b16-a390-31bd497ca997&cKey=0cb8274c-fa8e-4165-afc3-34265a033482&mKey=6ffe1446-a164-476a-92e7-c26446874d93
NLM
Fidalgo F, Rodrigues T, Silva AG, Facure L, Nóbrega A, Sá B, Duprat JP, Achatz MI, Rosenberg C, Carraro DM, Krepischi ACV. Rare germline copy number variations in hereditary cutaneous melanoma [Internet]. 2014 ;[citado 2024 nov. 07 ] Available from: http://www.abstractsonline.com/Plan/ViewAbstract.aspx?sKey=32d6f306-9518-4b16-a390-31bd497ca997&cKey=0cb8274c-fa8e-4165-afc3-34265a033482&mKey=6ffe1446-a164-476a-92e7-c26446874d93
Vancouver
Fidalgo F, Rodrigues T, Silva AG, Facure L, Nóbrega A, Sá B, Duprat JP, Achatz MI, Rosenberg C, Carraro DM, Krepischi ACV. Rare germline copy number variations in hereditary cutaneous melanoma [Internet]. 2014 ;[citado 2024 nov. 07 ] Available from: http://www.abstractsonline.com/Plan/ViewAbstract.aspx?sKey=32d6f306-9518-4b16-a390-31bd497ca997&cKey=0cb8274c-fa8e-4165-afc3-34265a033482&mKey=6ffe1446-a164-476a-92e7-c26446874d93

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