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Artigo de periodico
Transcriptomic analysis of cumulus cells shows altered pathways in patients with minimal and mild endometriosis (2022)
Luz, Caroline Mantovani da; Da Broi, Michele Gomes; Koopman, Larissa de Oliveira; Plaça, Jessica Rodrigues; Silva Júnior, Wilson Araújo; Ferriani, Rui Alberto; Meola, Juliana; Navarro, Paula Andrea de Albuquerque Salles
Source: Scientific Reports. Unidade: FMRP
Subjects: ENDOMETRIOSE, CÉLULAS
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ABNT
LUZ, Caroline Mantovani da et al. Transcriptomic analysis of cumulus cells shows altered pathways in patients with minimal and mild endometriosis. Scientific Reports, v. 12, n. 1, 2022Tradução . . Disponível em: https://doi.org/10.1038/s41598-022-09386-4. Acesso em: 16 nov. 2024.
APA
Luz, C. M. da, Da Broi, M. G., Koopman, L. de O., Plaça, J. R., Silva Júnior, W. A., Ferriani, R. A., et al. (2022). Transcriptomic analysis of cumulus cells shows altered pathways in patients with minimal and mild endometriosis. Scientific Reports, 12( 1). doi:10.1038/s41598-022-09386-4
NLM
Luz CM da, Da Broi MG, Koopman L de O, Plaça JR, Silva Júnior WA, Ferriani RA, Meola J, Navarro PA de AS. Transcriptomic analysis of cumulus cells shows altered pathways in patients with minimal and mild endometriosis [Internet]. Scientific Reports. 2022 ; 12( 1):[citado 2024 nov. 16 ] Available from: https://doi.org/10.1038/s41598-022-09386-4
Vancouver
Luz CM da, Da Broi MG, Koopman L de O, Plaça JR, Silva Júnior WA, Ferriani RA, Meola J, Navarro PA de AS. Transcriptomic analysis of cumulus cells shows altered pathways in patients with minimal and mild endometriosis [Internet]. Scientific Reports. 2022 ; 12( 1):[citado 2024 nov. 16 ] Available from: https://doi.org/10.1038/s41598-022-09386-4
Tese (Doutorado)
Evaluation of molecular profiles and microenvironments in B-cell lymphomas (2022)
Plaça, Jessica Rodrigues; Silva Junior, Wilson Araújo da (Orientador)
Unidade: FMRP
Subjects: BIOINFORMÁTICA, LINFOMA, LINFÓCITOS B, EXPRESSÃO GÊNICA
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ABNT
PLAÇA, Jessica Rodrigues. Evaluation of molecular profiles and microenvironments in B-cell lymphomas. 2022. Tese (Doutorado) – Universidade de São Paulo, Ribeirão Preto, 2022. Disponível em: https://www.teses.usp.br/teses/disponiveis/17/17154/tde-08092022-163315/. Acesso em: 16 nov. 2024.
APA
Plaça, J. R. (2022). Evaluation of molecular profiles and microenvironments in B-cell lymphomas (Tese (Doutorado). Universidade de São Paulo, Ribeirão Preto. Recuperado de https://www.teses.usp.br/teses/disponiveis/17/17154/tde-08092022-163315/
NLM
Plaça JR. Evaluation of molecular profiles and microenvironments in B-cell lymphomas [Internet]. 2022 ;[citado 2024 nov. 16 ] Available from: https://www.teses.usp.br/teses/disponiveis/17/17154/tde-08092022-163315/
Vancouver
Plaça JR. Evaluation of molecular profiles and microenvironments in B-cell lymphomas [Internet]. 2022 ;[citado 2024 nov. 16 ] Available from: https://www.teses.usp.br/teses/disponiveis/17/17154/tde-08092022-163315/
Artigo de periodico
Altered transcriptome in cumulus cells of infertile women with advanced endometriosis with and without endometrioma (2021)
Luz, Caroline Mantovani da; Da Broi, Michele Gomes ; Plaça, Jessica Rodrigues; Silva Junior, Wilson Araújo da ; Meola, Juliana ; Navarro, Paula Andrea de Albuquerque Salles
Source: Reproductive BioMedicine Online. Unidade: FMRP
Subjects: ENDOMETRIOSE, INFERTILIDADE FEMININA, OÓCITOS, EXPRESSÃO GÊNICA
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ABNT
LUZ, Caroline Mantovani da et al. Altered transcriptome in cumulus cells of infertile women with advanced endometriosis with and without endometrioma. Reproductive BioMedicine Online, v. 42, n. 5, p. 952-962, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.rbmo.2021.01.024. Acesso em: 16 nov. 2024.
APA
Luz, C. M. da, Da Broi, M. G., Plaça, J. R., Silva Junior, W. A. da, Meola, J., & Navarro, P. A. de A. S. (2021). Altered transcriptome in cumulus cells of infertile women with advanced endometriosis with and without endometrioma. Reproductive BioMedicine Online, 42( 5), 952-962. doi:10.1016/j.rbmo.2021.01.024
NLM
Luz CM da, Da Broi MG, Plaça JR, Silva Junior WA da, Meola J, Navarro PA de AS. Altered transcriptome in cumulus cells of infertile women with advanced endometriosis with and without endometrioma [Internet]. Reproductive BioMedicine Online. 2021 ; 42( 5): 952-962.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1016/j.rbmo.2021.01.024
Vancouver
Luz CM da, Da Broi MG, Plaça JR, Silva Junior WA da, Meola J, Navarro PA de AS. Altered transcriptome in cumulus cells of infertile women with advanced endometriosis with and without endometrioma [Internet]. Reproductive BioMedicine Online. 2021 ; 42( 5): 952-962.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1016/j.rbmo.2021.01.024
Artigo de periodico
Upregulation of HOX genes promotes cell migration and proliferation in head and neck squamous cell carcinoma (2021)
Aguiar, Graziela de Moura; Ramão, Anelisa; Plaça, Jessica Rodrigues; Simões, Sarah Capelupe; Scaraboto, Natália Volgarine; Freitas-Castro, Felipe; Cardoso, Cibele; Sousa, Josane de Freitas; Silva Junior, Wilson Araújo da
Source: Tumor Biology. Unidade: FMRP
Subjects: NEOPLASIAS DE CABEÇA E PESCOÇO, BIOMARCADORES, CARCINOGÊNESE, PROLIFERAÇÃO CELULAR, BIOINFORMÁTICA, CARCINOMA DE CÉLULAS ESCAMOSAS
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ABNT
AGUIAR, Graziela de Moura et al. Upregulation of HOX genes promotes cell migration and proliferation in head and neck squamous cell carcinoma. Tumor Biology, v. 43, p. 263-278, 2021Tradução . . Disponível em: https://doi.org/10.3233/TUB-211525. Acesso em: 16 nov. 2024.
APA
Aguiar, G. de M., Ramão, A., Plaça, J. R., Simões, S. C., Scaraboto, N. V., Freitas-Castro, F., et al. (2021). Upregulation of HOX genes promotes cell migration and proliferation in head and neck squamous cell carcinoma. Tumor Biology, 43, 263-278. doi:10.3233/TUB-211525
NLM
Aguiar G de M, Ramão A, Plaça JR, Simões SC, Scaraboto NV, Freitas-Castro F, Cardoso C, Sousa J de F, Silva Junior WA da. Upregulation of HOX genes promotes cell migration and proliferation in head and neck squamous cell carcinoma [Internet]. Tumor Biology. 2021 ; 43 263-278.[citado 2024 nov. 16 ] Available from: https://doi.org/10.3233/TUB-211525
Vancouver
Aguiar G de M, Ramão A, Plaça JR, Simões SC, Scaraboto NV, Freitas-Castro F, Cardoso C, Sousa J de F, Silva Junior WA da. Upregulation of HOX genes promotes cell migration and proliferation in head and neck squamous cell carcinoma [Internet]. Tumor Biology. 2021 ; 43 263-278.[citado 2024 nov. 16 ] Available from: https://doi.org/10.3233/TUB-211525
Artigo de periodico
ETV4 plays a role on the primary events during the adenoma-adenocarcinoma progression in colorectal cancer (2021)
Fonseca, Aline Simoneti; Ramão, Anelisa; Bürger, Matheus Carvalho; Souza, Jorge Estefano Santana de; Zanette, Dalila Luciola; Molfetta, Greice Andreotti de ; Araujo, Luiza Ferreira de ; Bueno, Rafaela de Barros e Lima; Aguiar, Graziela de Moura; Plaça, Jessica Rodrigues; Alves, Cleidson de Pádua; Santos, Anemari Ramos Dinarte dos; Vidal, Daniel Onofre; Silva, Gyl Eanes Barros; Panepucci, Rodrigo Alexandre; Peria, Fernanda Maris ; Féres, Omar; Rocha, José Joaquim Ribeiro da ; Zago, Marco Antonio; Silva Junior, Wilson Araújo da
Source: BMC Cancer. Unidade: FMRP
Subjects: ADENOCARCINOMA, ADENOMA, BIOMARCADORES, LINHAGEM CELULAR, TRANSFORMAÇÃO CELULAR NEOPLÁSICA, NEOPLASIAS COLORRETAIS, REGULAÇÃO GÊNICA, PROTEÍNAS PROTO-ONCOGÊNICAS
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ABNT
FONSECA, Aline Simoneti et al. ETV4 plays a role on the primary events during the adenoma-adenocarcinoma progression in colorectal cancer. BMC Cancer, v. 21, n. 1, 2021Tradução . . Disponível em: https://doi.org/10.1186/s12885-021-07857-x. Acesso em: 16 nov. 2024.
APA
Fonseca, A. S., Ramão, A., Bürger, M. C., Souza, J. E. S. de, Zanette, D. L., Molfetta, G. A. de, et al. (2021). ETV4 plays a role on the primary events during the adenoma-adenocarcinoma progression in colorectal cancer. BMC Cancer, 21( 1). doi:10.1186/s12885-021-07857-x
NLM
Fonseca AS, Ramão A, Bürger MC, Souza JES de, Zanette DL, Molfetta GA de, Araujo LF de, Bueno R de B e L, Aguiar G de M, Plaça JR, Alves C de P, Santos ARD dos, Vidal DO, Silva GEB, Panepucci RA, Peria FM, Féres O, Rocha JJR da, Zago MA, Silva Junior WA da. ETV4 plays a role on the primary events during the adenoma-adenocarcinoma progression in colorectal cancer [Internet]. BMC Cancer. 2021 ; 21( 1):[citado 2024 nov. 16 ] Available from: https://doi.org/10.1186/s12885-021-07857-x
Vancouver
Fonseca AS, Ramão A, Bürger MC, Souza JES de, Zanette DL, Molfetta GA de, Araujo LF de, Bueno R de B e L, Aguiar G de M, Plaça JR, Alves C de P, Santos ARD dos, Vidal DO, Silva GEB, Panepucci RA, Peria FM, Féres O, Rocha JJR da, Zago MA, Silva Junior WA da. ETV4 plays a role on the primary events during the adenoma-adenocarcinoma progression in colorectal cancer [Internet]. BMC Cancer. 2021 ; 21( 1):[citado 2024 nov. 16 ] Available from: https://doi.org/10.1186/s12885-021-07857-x
Artigo de periodico
Gene expression profile in immortalized human periodontal ligament fibroblasts through hTERT ectopic expression:: transcriptome and bioinformatic analysis (2021)
Nogueira, Lygia S; Vasconcelos, Carolina P; Mitre, Geovanni Pereira; Bittencourt, Leonardo Oliveira ; Plaça, Jessica Rodrigues ; Kataoka, Maria Sueli da Silva; Pinheiro, João de Jesus Viana ; Garlet, Gustavo Pompermaier ; Oliveira, Edivaldo Herculano Correa de ; Lima, Rafael Rodrigues
Source: Frontiers in Molecular Biosciences. Unidades: FOB, FMRP
Subjects: CULTURA DE CÉLULAS, PERIODONTO DE PROTEÇÃO, EXPRESSÃO GÊNICA, REGENERAÇÃO TECIDUAL GUIADA, PROTEÍNAS DE LIGAÇÃO DO CÁLCIO
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ABNT
NOGUEIRA, Lygia S et al. Gene expression profile in immortalized human periodontal ligament fibroblasts through hTERT ectopic expression:: transcriptome and bioinformatic analysis. Frontiers in Molecular Biosciences, v. 8, p. 9 , 2021Tradução . . Disponível em: https://doi.org/10.3389/fmolb.2021.679548. Acesso em: 16 nov. 2024.
APA
Nogueira, L. S., Vasconcelos, C. P., Mitre, G. P., Bittencourt, L. O., Plaça, J. R., Kataoka, M. S. da S., et al. (2021). Gene expression profile in immortalized human periodontal ligament fibroblasts through hTERT ectopic expression:: transcriptome and bioinformatic analysis. Frontiers in Molecular Biosciences, 8, 9 . doi:10.3389/fmolb.2021.679548
NLM
Nogueira LS, Vasconcelos CP, Mitre GP, Bittencourt LO, Plaça JR, Kataoka MS da S, Pinheiro J de JV, Garlet GP, Oliveira EHC de, Lima RR. Gene expression profile in immortalized human periodontal ligament fibroblasts through hTERT ectopic expression:: transcriptome and bioinformatic analysis [Internet]. Frontiers in Molecular Biosciences. 2021 ; 8 9 .[citado 2024 nov. 16 ] Available from: https://doi.org/10.3389/fmolb.2021.679548
Vancouver
Nogueira LS, Vasconcelos CP, Mitre GP, Bittencourt LO, Plaça JR, Kataoka MS da S, Pinheiro J de JV, Garlet GP, Oliveira EHC de, Lima RR. Gene expression profile in immortalized human periodontal ligament fibroblasts through hTERT ectopic expression:: transcriptome and bioinformatic analysis [Internet]. Frontiers in Molecular Biosciences. 2021 ; 8 9 .[citado 2024 nov. 16 ] Available from: https://doi.org/10.3389/fmolb.2021.679548
Artigo de periodico
Screening of variants in the transcript profile of eutopic endometrium from infertile women with endometriosis during the implantation window (2021)
Da Broi, Michele Gomes ; Plaça, Jessica Rodrigues; Silva Junior, Wilson Araújo da ; Ferriani, Rui Alberto; Navarro, Paula Andrea de Albuquerque Salles
Source: Revista Brasileira de Ginecologia e Obstetrícia / RBGO Gynecology and Obstetrics. Unidade: FMRP
Subjects: ENDOMETRIOSE, INFERTILIDADE FEMININA, SEQUENCIAMENTO GENÉTICO, RNA, MUTAÇÃO GENÉTICA
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ABNT
DA BROI, Michele Gomes et al. Screening of variants in the transcript profile of eutopic endometrium from infertile women with endometriosis during the implantation window. Revista Brasileira de Ginecologia e Obstetrícia / RBGO Gynecology and Obstetrics, v. 43, n. 6, p. 457-466, 2021Tradução . . Disponível em: https://doi.org/10.1055/s-0041-1730287. Acesso em: 16 nov. 2024.
APA
Da Broi, M. G., Plaça, J. R., Silva Junior, W. A. da, Ferriani, R. A., & Navarro, P. A. de A. S. (2021). Screening of variants in the transcript profile of eutopic endometrium from infertile women with endometriosis during the implantation window. Revista Brasileira de Ginecologia e Obstetrícia / RBGO Gynecology and Obstetrics, 43( 6), 457-466. doi:10.1055/s-0041-1730287
NLM
Da Broi MG, Plaça JR, Silva Junior WA da, Ferriani RA, Navarro PA de AS. Screening of variants in the transcript profile of eutopic endometrium from infertile women with endometriosis during the implantation window [Internet]. Revista Brasileira de Ginecologia e Obstetrícia / RBGO Gynecology and Obstetrics. 2021 ; 43( 6): 457-466.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1055/s-0041-1730287
Vancouver
Da Broi MG, Plaça JR, Silva Junior WA da, Ferriani RA, Navarro PA de AS. Screening of variants in the transcript profile of eutopic endometrium from infertile women with endometriosis during the implantation window [Internet]. Revista Brasileira de Ginecologia e Obstetrícia / RBGO Gynecology and Obstetrics. 2021 ; 43( 6): 457-466.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1055/s-0041-1730287
Artigo de periodico
Non-lethal concentration of meHg causes marked responses in the DNA repair, integrity, and replication pathways in the exposed human salivary gland cell line (2021)
Nogueira, Lygia Sega; Vasconcelos, Carolina P.; Plaça, Jessica Rodrigues ; Mitre, Geovanni Pereira; Bittencourt, Leonardo Oliveira; Kataoka, Maria Sueli da Silva ; Oliveira, Edivaldo H. C. de; Lima, Rafael Rodrigues
Source: Frontiers in Pharmacology. Unidade: FMRP
Subjects: BIOMARCADORES, GLÂNDULAS SALIVARES, TOXICOLOGIA, LINHAGEM CELULAR
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ABNT
NOGUEIRA, Lygia Sega et al. Non-lethal concentration of meHg causes marked responses in the DNA repair, integrity, and replication pathways in the exposed human salivary gland cell line. Frontiers in Pharmacology, v. 12, p. 1-8, 2021Tradução . . Disponível em: https://doi.org/10.3389/fphar.2021.698671. Acesso em: 16 nov. 2024.
APA
Nogueira, L. S., Vasconcelos, C. P., Plaça, J. R., Mitre, G. P., Bittencourt, L. O., Kataoka, M. S. da S., et al. (2021). Non-lethal concentration of meHg causes marked responses in the DNA repair, integrity, and replication pathways in the exposed human salivary gland cell line. Frontiers in Pharmacology, 12, 1-8. doi:10.3389/fphar.2021.698671
NLM
Nogueira LS, Vasconcelos CP, Plaça JR, Mitre GP, Bittencourt LO, Kataoka MS da S, Oliveira EHC de, Lima RR. Non-lethal concentration of meHg causes marked responses in the DNA repair, integrity, and replication pathways in the exposed human salivary gland cell line [Internet]. Frontiers in Pharmacology. 2021 ; 12 1-8.[citado 2024 nov. 16 ] Available from: https://doi.org/10.3389/fphar.2021.698671
Vancouver
Nogueira LS, Vasconcelos CP, Plaça JR, Mitre GP, Bittencourt LO, Kataoka MS da S, Oliveira EHC de, Lima RR. Non-lethal concentration of meHg causes marked responses in the DNA repair, integrity, and replication pathways in the exposed human salivary gland cell line [Internet]. Frontiers in Pharmacology. 2021 ; 12 1-8.[citado 2024 nov. 16 ] Available from: https://doi.org/10.3389/fphar.2021.698671
Artigo de periodico
Contributions of HOX genes to cancer hallmarks: enrichment pathway analysis and review (2020)
Brotto, Danielle Barbosa; Siena, Ádamo Davi Diógenes; Barros, Isabela Ichihara de ; Carvalho, Simone da Costa e Silva; Muys, Bruna Rodrigues; Goedert, Lucas; Cardoso, Cibele ; Plaça, Jessica Rodrigues ; Ramão, Anelisa; Squire, Jeremy Andrew ; Araujo, Luiza Ferreira de; Silva Junior, Wilson Araújo da
Source: Tumor Biology. Unidades: FMRP, ESALQ
Subjects: CARCINOGÊNESE, EMBRIOGÊNESE, EXPRESSÃO GÊNICA, FATORES DE TRANSCRIÇÃO, GENES HOMEOBOX, NEOPLASIAS, REGULAÇÃO GÊNICA
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ABNT
BROTTO, Danielle Barbosa et al. Contributions of HOX genes to cancer hallmarks: enrichment pathway analysis and review. Tumor Biology, v. 42, n. 5, 2020Tradução . . Disponível em: https://doi.org/10.1177/1010428320918050. Acesso em: 16 nov. 2024.
APA
Brotto, D. B., Siena, Á. D. D., Barros, I. I. de, Carvalho, S. da C. e S., Muys, B. R., Goedert, L., et al. (2020). Contributions of HOX genes to cancer hallmarks: enrichment pathway analysis and review. Tumor Biology, 42( 5). doi:10.1177/1010428320918050
NLM
Brotto DB, Siena ÁDD, Barros II de, Carvalho S da C e S, Muys BR, Goedert L, Cardoso C, Plaça JR, Ramão A, Squire JA, Araujo LF de, Silva Junior WA da. Contributions of HOX genes to cancer hallmarks: enrichment pathway analysis and review [Internet]. Tumor Biology. 2020 ; 42( 5):[citado 2024 nov. 16 ] Available from: https://doi.org/10.1177/1010428320918050
Vancouver
Brotto DB, Siena ÁDD, Barros II de, Carvalho S da C e S, Muys BR, Goedert L, Cardoso C, Plaça JR, Ramão A, Squire JA, Araujo LF de, Silva Junior WA da. Contributions of HOX genes to cancer hallmarks: enrichment pathway analysis and review [Internet]. Tumor Biology. 2020 ; 42( 5):[citado 2024 nov. 16 ] Available from: https://doi.org/10.1177/1010428320918050
Artigo de periodico
Germline variants in DNA repair genes associated with hereditary breast and ovarian cancer syndrome: analysis of a 21 gene panel in the Brazilian population (2020)
Carvalho, Simone da Costa e Silva; Cury, Nathalia Moreno; Brotto, Danielle Barbosa; Araujo, Luiza Ferreira de; Rosa, Reginaldo Cruz Alves ; Texeira, Lorena Alves; Plaça, Jessica Rodrigues ; Marques, Adriana Aparecida; Peronni, Kamila Chagas; Ruy, Patrícia de Cássia; Molfetta, Greice Andreotti de ; Moriguti, Júlio César ; Carraro, Dirce Maria ; Palmero, Edenir Inêz; Ashton-Prolla, Patricia; Ferraz, Victor Evangelista de Faria ; Silva Junior, Wilson Araújo da
Source: BMC Medical Genomics. Unidades: FMRP, IB
Subjects: GENES, REPARAÇÃO DE DNA, NEOPLASIAS MAMÁRIAS, NEOPLASIAS OVARIANAS, HERANÇA GENÉTICA
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ABNT
CARVALHO, Simone da Costa e Silva et al. Germline variants in DNA repair genes associated with hereditary breast and ovarian cancer syndrome: analysis of a 21 gene panel in the Brazilian population. BMC Medical Genomics, v. 13, n. 1, 2020Tradução . . Disponível em: https://doi.org/10.1186/s12920-019-0652-y. Acesso em: 16 nov. 2024.
APA
Carvalho, S. da C. e S., Cury, N. M., Brotto, D. B., Araujo, L. F. de, Rosa, R. C. A., Texeira, L. A., et al. (2020). Germline variants in DNA repair genes associated with hereditary breast and ovarian cancer syndrome: analysis of a 21 gene panel in the Brazilian population. BMC Medical Genomics, 13( 1). doi:10.1186/s12920-019-0652-y
NLM
Carvalho S da C e S, Cury NM, Brotto DB, Araujo LF de, Rosa RCA, Texeira LA, Plaça JR, Marques AA, Peronni KC, Ruy P de C, Molfetta GA de, Moriguti JC, Carraro DM, Palmero EI, Ashton-Prolla P, Ferraz VE de F, Silva Junior WA da. Germline variants in DNA repair genes associated with hereditary breast and ovarian cancer syndrome: analysis of a 21 gene panel in the Brazilian population [Internet]. BMC Medical Genomics. 2020 ; 13( 1):[citado 2024 nov. 16 ] Available from: https://doi.org/10.1186/s12920-019-0652-y
Vancouver
Carvalho S da C e S, Cury NM, Brotto DB, Araujo LF de, Rosa RCA, Texeira LA, Plaça JR, Marques AA, Peronni KC, Ruy P de C, Molfetta GA de, Moriguti JC, Carraro DM, Palmero EI, Ashton-Prolla P, Ferraz VE de F, Silva Junior WA da. Germline variants in DNA repair genes associated with hereditary breast and ovarian cancer syndrome: analysis of a 21 gene panel in the Brazilian population [Internet]. BMC Medical Genomics. 2020 ; 13( 1):[citado 2024 nov. 16 ] Available from: https://doi.org/10.1186/s12920-019-0652-y
Trabalho de evento-resumo
Landscape of HOX driven regulation in cancer (2019)
Plaça, Jessica Rodrigues ; Sousa, Josane de Freitas ; Silva, Israel Tojal da; Silva Junior, Wilson Araújo da
Source: Resumos. Conference titles: Brazilian Congress of Genetics. Unidade: FMRP
Subjects: NEOPLASIAS, REGULAÇÃO GÊNICA
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ABNT
PLAÇA, Jessica Rodrigues et al. Landscape of HOX driven regulation in cancer. 2019, Anais.. Águas de Lindóia: Sociedade Brasileira de Genética, 2019. Disponível em: https://www.sbg.org.br/sites/default/files/e_book_genetica2019_online_0.pdf. Acesso em: 16 nov. 2024.
APA
Plaça, J. R., Sousa, J. de F., Silva, I. T. da, & Silva Junior, W. A. da. (2019). Landscape of HOX driven regulation in cancer. In Resumos. Águas de Lindóia: Sociedade Brasileira de Genética. Recuperado de https://www.sbg.org.br/sites/default/files/e_book_genetica2019_online_0.pdf
NLM
Plaça JR, Sousa J de F, Silva IT da, Silva Junior WA da. Landscape of HOX driven regulation in cancer [Internet]. Resumos. 2019 ;[citado 2024 nov. 16 ] Available from: https://www.sbg.org.br/sites/default/files/e_book_genetica2019_online_0.pdf
Vancouver
Plaça JR, Sousa J de F, Silva IT da, Silva Junior WA da. Landscape of HOX driven regulation in cancer [Internet]. Resumos. 2019 ;[citado 2024 nov. 16 ] Available from: https://www.sbg.org.br/sites/default/files/e_book_genetica2019_online_0.pdf
Trabalho de evento-resumo
Upregulation of HOX genes promotes cell migration and proliferation in head and neck squamous cell carcinoma (2019)
Aguiar, Graziela de Moura ; Ramão, Anelisa ; Plaça, Jessica Rodrigues ; Simões, Sarah Capelupe; Scaraboto, Natália Volgarine; Cardoso, Cibele ; Sousa, Josane de Freitas ; Silva Junior, Wilson Araújo da
Source: Resumos. Conference titles: Brazilian Congress of Genetics. Unidade: FMRP
Subjects: PROLIFERAÇÃO CELULAR, CABEÇA, CARCINOMA, PESCOÇO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
AGUIAR, Graziela de Moura et al. Upregulation of HOX genes promotes cell migration and proliferation in head and neck squamous cell carcinoma. 2019, Anais.. Águas de Lindóia: Sociedade Brasileira de Genética, 2019. Disponível em: https://www.sbg.org.br/sites/default/files/e_book_genetica2019_online_0.pdf. Acesso em: 16 nov. 2024.
APA
Aguiar, G. de M., Ramão, A., Plaça, J. R., Simões, S. C., Scaraboto, N. V., Cardoso, C., et al. (2019). Upregulation of HOX genes promotes cell migration and proliferation in head and neck squamous cell carcinoma. In Resumos. Águas de Lindóia: Sociedade Brasileira de Genética. Recuperado de https://www.sbg.org.br/sites/default/files/e_book_genetica2019_online_0.pdf
NLM
Aguiar G de M, Ramão A, Plaça JR, Simões SC, Scaraboto NV, Cardoso C, Sousa J de F, Silva Junior WA da. Upregulation of HOX genes promotes cell migration and proliferation in head and neck squamous cell carcinoma [Internet]. Resumos. 2019 ;[citado 2024 nov. 16 ] Available from: https://www.sbg.org.br/sites/default/files/e_book_genetica2019_online_0.pdf
Vancouver
Aguiar G de M, Ramão A, Plaça JR, Simões SC, Scaraboto NV, Cardoso C, Sousa J de F, Silva Junior WA da. Upregulation of HOX genes promotes cell migration and proliferation in head and neck squamous cell carcinoma [Internet]. Resumos. 2019 ;[citado 2024 nov. 16 ] Available from: https://www.sbg.org.br/sites/default/files/e_book_genetica2019_online_0.pdf
Trabalho de evento-resumo
Molecular and functional characterization of variants found in DNA repair genes in a brazilian cohort with hereditary breast and ovarian cancer (2019)
Carvalho, Simone da Costa e Silva; Brotto, Danielle Barbosa ; Araújo, Luiza Ferreira de; Teixeira, Lorena Alves; Plaça, Jessica Rodrigues ; Peronni, Kamila Chagas; Molfetta, Greice Andreotti de ; Ferraz, Victor Evangelista de Faria ; Silva Junior, Wilson Araújo da
Source: Resumos. Conference titles: Brazilian Congress of Genetics. Unidade: FMRP
Subjects: NEOPLASIAS OVARIANAS, DNA, HEREDITARIEDADE
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ABNT
CARVALHO, Simone da Costa e Silva et al. Molecular and functional characterization of variants found in DNA repair genes in a brazilian cohort with hereditary breast and ovarian cancer. 2019, Anais.. Águas de Lindóia: Sociedade Brasileira de Genética, 2019. Disponível em: https://www.sbg.org.br/sites/default/files/e_book_genetica2019_online_0.pdf. Acesso em: 16 nov. 2024.
APA
Carvalho, S. da C. e S., Brotto, D. B., Araújo, L. F. de, Teixeira, L. A., Plaça, J. R., Peronni, K. C., et al. (2019). Molecular and functional characterization of variants found in DNA repair genes in a brazilian cohort with hereditary breast and ovarian cancer. In Resumos. Águas de Lindóia: Sociedade Brasileira de Genética. Recuperado de https://www.sbg.org.br/sites/default/files/e_book_genetica2019_online_0.pdf
NLM
Carvalho S da C e S, Brotto DB, Araújo LF de, Teixeira LA, Plaça JR, Peronni KC, Molfetta GA de, Ferraz VE de F, Silva Junior WA da. Molecular and functional characterization of variants found in DNA repair genes in a brazilian cohort with hereditary breast and ovarian cancer [Internet]. Resumos. 2019 ;[citado 2024 nov. 16 ] Available from: https://www.sbg.org.br/sites/default/files/e_book_genetica2019_online_0.pdf
Vancouver
Carvalho S da C e S, Brotto DB, Araújo LF de, Teixeira LA, Plaça JR, Peronni KC, Molfetta GA de, Ferraz VE de F, Silva Junior WA da. Molecular and functional characterization of variants found in DNA repair genes in a brazilian cohort with hereditary breast and ovarian cancer [Internet]. Resumos. 2019 ;[citado 2024 nov. 16 ] Available from: https://www.sbg.org.br/sites/default/files/e_book_genetica2019_online_0.pdf
Trabalho de evento-resumo
Functional characterization of the HOXB2 gene in glioblastoma cell lines (2019)
Scaraboto, Natália Volgarine; Cardoso, Cibele ; Serafim, Rodolfo Bortolozo ; Plaça, Jessica Rodrigues ; Valente, Valéria; Silva Junior, Wilson Araújo da
Source: Resumos. Conference titles: Brazilian Congress of Genetics. Unidade: FMRP
Subjects: LINHAGEM CELULAR, NEOPLASIAS CEREBRAIS
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ABNT
SCARABOTO, Natália Volgarine et al. Functional characterization of the HOXB2 gene in glioblastoma cell lines. 2019, Anais.. Águas de Lindóia: Sociedade Brasileira de Genética, 2019. Disponível em: https://www.sbg.org.br/sites/default/files/e_book_genetica2019_online_0.pdf. Acesso em: 16 nov. 2024.
APA
Scaraboto, N. V., Cardoso, C., Serafim, R. B., Plaça, J. R., Valente, V., & Silva Junior, W. A. da. (2019). Functional characterization of the HOXB2 gene in glioblastoma cell lines. In Resumos. Águas de Lindóia: Sociedade Brasileira de Genética. Recuperado de https://www.sbg.org.br/sites/default/files/e_book_genetica2019_online_0.pdf
NLM
Scaraboto NV, Cardoso C, Serafim RB, Plaça JR, Valente V, Silva Junior WA da. Functional characterization of the HOXB2 gene in glioblastoma cell lines [Internet]. Resumos. 2019 ;[citado 2024 nov. 16 ] Available from: https://www.sbg.org.br/sites/default/files/e_book_genetica2019_online_0.pdf
Vancouver
Scaraboto NV, Cardoso C, Serafim RB, Plaça JR, Valente V, Silva Junior WA da. Functional characterization of the HOXB2 gene in glioblastoma cell lines [Internet]. Resumos. 2019 ;[citado 2024 nov. 16 ] Available from: https://www.sbg.org.br/sites/default/files/e_book_genetica2019_online_0.pdf
Trabalho de evento-resumo
Analysis of potential disease-causing variants in a patient with intellectual disability via whole-exome sequencing (2019)
Ruy, Patricia de Cássia; Barros, Isabela Ichihara ; Rosa, Reginaldo Cruz Alves ; Plaça, Jessica Rodrigues ; Corveloni, Amanda Cristina; Cardoso, Cibele ; Souza, Aline Fernanda de ; Biagi Junior, Carlos Alberto Oliveira de ; Siena, Ádamo Davi Diogenes; Zueli, Kamila Peronni; Tellechea, Maria Florencia ; Carvalho, Simone da Costa e Silva; Molfetta, Greice Andreotti de ; Pina Neto, João Monteiro de ; Silva Junior, Wilson Araújo da
Source: Proceedings. Conference titles: X-Meeting International Conference of the AB3C. Unidades: FMRP, FZEA
Subjects: SEQUENCIAMENTO GENÉTICO, PESSOAS COM DEFICIÊNCIA INTELECTUAL
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ABNT
RUY, Patricia de Cássia et al. Analysis of potential disease-causing variants in a patient with intellectual disability via whole-exome sequencing. 2019, Anais.. Campos do Jordão: Associação Brasileira de Bioinformática e Biologia Computacional, 2019. Disponível em: http://drive.ab3c.org.br/index.php/s/WDdbkSCMs5onm49. Acesso em: 16 nov. 2024.
APA
Ruy, P. de C., Barros, I. I., Rosa, R. C. A., Plaça, J. R., Corveloni, A. C., Cardoso, C., et al. (2019). Analysis of potential disease-causing variants in a patient with intellectual disability via whole-exome sequencing. In Proceedings. Campos do Jordão: Associação Brasileira de Bioinformática e Biologia Computacional. Recuperado de http://drive.ab3c.org.br/index.php/s/WDdbkSCMs5onm49
NLM
Ruy P de C, Barros II, Rosa RCA, Plaça JR, Corveloni AC, Cardoso C, Souza AF de, Biagi Junior CAO de, Siena ÁDD, Zueli KP, Tellechea MF, Carvalho S da C e S, Molfetta GA de, Pina Neto JM de, Silva Junior WA da. Analysis of potential disease-causing variants in a patient with intellectual disability via whole-exome sequencing [Internet]. Proceedings. 2019 ;[citado 2024 nov. 16 ] Available from: http://drive.ab3c.org.br/index.php/s/WDdbkSCMs5onm49
Vancouver
Ruy P de C, Barros II, Rosa RCA, Plaça JR, Corveloni AC, Cardoso C, Souza AF de, Biagi Junior CAO de, Siena ÁDD, Zueli KP, Tellechea MF, Carvalho S da C e S, Molfetta GA de, Pina Neto JM de, Silva Junior WA da. Analysis of potential disease-causing variants in a patient with intellectual disability via whole-exome sequencing [Internet]. Proceedings. 2019 ;[citado 2024 nov. 16 ] Available from: http://drive.ab3c.org.br/index.php/s/WDdbkSCMs5onm49
Trabalho de evento-resumo
Integrative transcriptomic and epigenomic analysis reveals long noncoding RNAs with both altered gene expression and methylation pattern during melanomagenesis (2019)
Siena, Ádamo Davi Diogenes; Plaça, Jessica Rodrigues ; Barros, Isabela Ichihara; Biagi Junior, Carlos Alberto Oliveira de ; Silva Junior, Wilson Araújo da
Source: Resumos. Conference titles: Brazilian Congress of Genetics. Unidade: FMRP
Subjects: RNA, MELANOMA, EXPRESSÃO GÊNICA
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ABNT
SIENA, Ádamo Davi Diogenes et al. Integrative transcriptomic and epigenomic analysis reveals long noncoding RNAs with both altered gene expression and methylation pattern during melanomagenesis. 2019, Anais.. Águas de Lindóia: Sociedade Brasileira de Genética, 2019. Disponível em: https://www.sbg.org.br/sites/default/files/e_book_genetica2019_online_0.pdf. Acesso em: 16 nov. 2024.
APA
Siena, Á. D. D., Plaça, J. R., Barros, I. I., Biagi Junior, C. A. O. de, & Silva Junior, W. A. da. (2019). Integrative transcriptomic and epigenomic analysis reveals long noncoding RNAs with both altered gene expression and methylation pattern during melanomagenesis. In Resumos. Águas de Lindóia: Sociedade Brasileira de Genética. Recuperado de https://www.sbg.org.br/sites/default/files/e_book_genetica2019_online_0.pdf
NLM
Siena ÁDD, Plaça JR, Barros II, Biagi Junior CAO de, Silva Junior WA da. Integrative transcriptomic and epigenomic analysis reveals long noncoding RNAs with both altered gene expression and methylation pattern during melanomagenesis [Internet]. Resumos. 2019 ;[citado 2024 nov. 16 ] Available from: https://www.sbg.org.br/sites/default/files/e_book_genetica2019_online_0.pdf
Vancouver
Siena ÁDD, Plaça JR, Barros II, Biagi Junior CAO de, Silva Junior WA da. Integrative transcriptomic and epigenomic analysis reveals long noncoding RNAs with both altered gene expression and methylation pattern during melanomagenesis [Internet]. Resumos. 2019 ;[citado 2024 nov. 16 ] Available from: https://www.sbg.org.br/sites/default/files/e_book_genetica2019_online_0.pdf
Trabalho de evento-resumo
The loss of a long noncoding RNA can lead to delayed neural development (2019)
Silva Junior, Wilson Araújo da ; Pina Neto, João Monteiro de ; Molfetta, Greice Andreotti de ; Carvalho, Simone da Costa e Silva; Tellechea, Maria Florencia ; Peronni, Kamila Chagas; Siena, Ádamo Davi Diogenes; Biagi Junior, Carlos Alberto Oliveira de ; Souza, Aline Fernanda de ; Cardoso, Cibele ; Corveloni, Amanda Cristina; Plaça, Jessica Rodrigues ; Rosa, Reginaldo Cruz Alves ; Ruy, Patrícia de Cássia; Barros, Isabela Ichihara de
Source: Resumos. Conference titles: Brazilian Congress of Genetics. Unidades: FMRP, FZEA
Subjects: RNA, PESSOAS COM DEFICIÊNCIA INTELECTUAL, DOENÇAS CEREBRAIS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SILVA JUNIOR, Wilson Araújo da et al. The loss of a long noncoding RNA can lead to delayed neural development. 2019, Anais.. Águas de Lindóia: Sociedade Brasileira de Genética, 2019. Disponível em: https://www.sbg.org.br/sites/default/files/e_book_genetica2019_online_0.pdf. Acesso em: 16 nov. 2024.
APA
Silva Junior, W. A. da, Pina Neto, J. M. de, Molfetta, G. A. de, Carvalho, S. da C. e S., Tellechea, M. F., Peronni, K. C., et al. (2019). The loss of a long noncoding RNA can lead to delayed neural development. In Resumos. Águas de Lindóia: Sociedade Brasileira de Genética. Recuperado de https://www.sbg.org.br/sites/default/files/e_book_genetica2019_online_0.pdf
NLM
Silva Junior WA da, Pina Neto JM de, Molfetta GA de, Carvalho S da C e S, Tellechea MF, Peronni KC, Siena ÁDD, Biagi Junior CAO de, Souza AF de, Cardoso C, Corveloni AC, Plaça JR, Rosa RCA, Ruy P de C, Barros II de. The loss of a long noncoding RNA can lead to delayed neural development [Internet]. Resumos. 2019 ;[citado 2024 nov. 16 ] Available from: https://www.sbg.org.br/sites/default/files/e_book_genetica2019_online_0.pdf
Vancouver
Silva Junior WA da, Pina Neto JM de, Molfetta GA de, Carvalho S da C e S, Tellechea MF, Peronni KC, Siena ÁDD, Biagi Junior CAO de, Souza AF de, Cardoso C, Corveloni AC, Plaça JR, Rosa RCA, Ruy P de C, Barros II de. The loss of a long noncoding RNA can lead to delayed neural development [Internet]. Resumos. 2019 ;[citado 2024 nov. 16 ] Available from: https://www.sbg.org.br/sites/default/files/e_book_genetica2019_online_0.pdf
Artigo de periodico
Whole transcriptome analysis reveals correlation of long noncoding RNA ZEB1-AS1 with invasive profile in melanoma (2019)
Siena, Ádamo Davi Diógenes; Plaça, Jéssica Rodrigues ; Araújo, Luiza Ferreira; Barros, Isabela Ichihara ; Peronni, Kamila Chagas; Molfetta, Greice Andreotti de ; Biagi Junior, Carlos Alberto Oliveira de ; Espreáfico, Enilza Maria ; Sousa, Josane de Freitas; Silva Júnior, Wilson Araújo da
Source: Scientific Reports. Unidade: FMRP
Subjects: RNA, MELANOMA
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ABNT
SIENA, Ádamo Davi Diógenes et al. Whole transcriptome analysis reveals correlation of long noncoding RNA ZEB1-AS1 with invasive profile in melanoma. Scientific Reports, v. 9, 2019Tradução . . Disponível em: https://doi.org/10.1038/s41598-019-47363-6. Acesso em: 16 nov. 2024.
APA
Siena, Á. D. D., Plaça, J. R., Araújo, L. F., Barros, I. I., Peronni, K. C., Molfetta, G. A. de, et al. (2019). Whole transcriptome analysis reveals correlation of long noncoding RNA ZEB1-AS1 with invasive profile in melanoma. Scientific Reports, 9. doi:10.1038/s41598-019-47363-6
NLM
Siena ÁDD, Plaça JR, Araújo LF, Barros II, Peronni KC, Molfetta GA de, Biagi Junior CAO de, Espreáfico EM, Sousa J de F, Silva Júnior WA da. Whole transcriptome analysis reveals correlation of long noncoding RNA ZEB1-AS1 with invasive profile in melanoma [Internet]. Scientific Reports. 2019 ; 9[citado 2024 nov. 16 ] Available from: https://doi.org/10.1038/s41598-019-47363-6
Vancouver
Siena ÁDD, Plaça JR, Araújo LF, Barros II, Peronni KC, Molfetta GA de, Biagi Junior CAO de, Espreáfico EM, Sousa J de F, Silva Júnior WA da. Whole transcriptome analysis reveals correlation of long noncoding RNA ZEB1-AS1 with invasive profile in melanoma [Internet]. Scientific Reports. 2019 ; 9[citado 2024 nov. 16 ] Available from: https://doi.org/10.1038/s41598-019-47363-6
Artigo de periodico
Is the profile of transcripts altered in the eutopic endometrium of infertile women with endometriosis during the implantation window? (2019)
Da Broi, Michele Gomes ; Meola, Juliana ; Plaça, Jessica Rodrigues ; Peronni, Kamila Chagas; Rocha Júnior, Carlos Valério da; Silva Junior, Wilson Araújo da ; Ferriani, Rui Alberto ; Navarro, Paula Andrea de Albuquerque Salles
Source: Human Reproduction. Unidade: FMRP
Subjects: ENDOMÉTRIO, ENDOMETRIOSE, INFERTILIDADE FEMININA
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ABNT
DA BROI, Michele Gomes et al. Is the profile of transcripts altered in the eutopic endometrium of infertile women with endometriosis during the implantation window?. Human Reproduction, v. 34, n. 12, p. 2381-2390, 2019Tradução . . Disponível em: https://doi.org/10.1093/humrep/dez225. Acesso em: 16 nov. 2024.
APA
Da Broi, M. G., Meola, J., Plaça, J. R., Peronni, K. C., Rocha Júnior, C. V. da, Silva Junior, W. A. da, et al. (2019). Is the profile of transcripts altered in the eutopic endometrium of infertile women with endometriosis during the implantation window? Human Reproduction, 34( 12), 2381-2390. doi:10.1093/humrep/dez225
NLM
Da Broi MG, Meola J, Plaça JR, Peronni KC, Rocha Júnior CV da, Silva Junior WA da, Ferriani RA, Navarro PA de AS. Is the profile of transcripts altered in the eutopic endometrium of infertile women with endometriosis during the implantation window? [Internet]. Human Reproduction. 2019 ; 34( 12): 2381-2390.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1093/humrep/dez225
Vancouver
Da Broi MG, Meola J, Plaça JR, Peronni KC, Rocha Júnior CV da, Silva Junior WA da, Ferriani RA, Navarro PA de AS. Is the profile of transcripts altered in the eutopic endometrium of infertile women with endometriosis during the implantation window? [Internet]. Human Reproduction. 2019 ; 34( 12): 2381-2390.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1093/humrep/dez225
Artigo de periodico
Accuracy of whole genome sequencing versus phenotypic (MGIT) and commercial molecular tests for detection of drug-resistant Mycobacterium tuberculosis isolated from patients in Brazil and Mozambique (2018)
Feliciano, Cinara Silva ; Namburete, Evangelina Inacio ; Plaça, Jéssica Rodrigues; Peronni, Kamila; Dippenaar, Anzaan ; Warren, Robin Mark; Silva Júnior, Wilson Araújo da ; Bollela, Valdes Roberto
Source: Tuberculosis. Unidade: FMRP
Subjects: TUBERCULOSE, SEQUENCIAMENTO GENÉTICO, TESTES DE SENSIBILIDADE MICROBIANA, MUTAÇÃO, MYCOBACTERIUM TUBERCULOSIS
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ABNT
FELICIANO, Cinara Silva et al. Accuracy of whole genome sequencing versus phenotypic (MGIT) and commercial molecular tests for detection of drug-resistant Mycobacterium tuberculosis isolated from patients in Brazil and Mozambique. Tuberculosis, v. 110, p. 59-67, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.tube.2018.04.003. Acesso em: 16 nov. 2024.
APA
Feliciano, C. S., Namburete, E. I., Plaça, J. R., Peronni, K., Dippenaar, A., Warren, R. M., et al. (2018). Accuracy of whole genome sequencing versus phenotypic (MGIT) and commercial molecular tests for detection of drug-resistant Mycobacterium tuberculosis isolated from patients in Brazil and Mozambique. Tuberculosis, 110, 59-67. doi:10.1016/j.tube.2018.04.003
NLM
Feliciano CS, Namburete EI, Plaça JR, Peronni K, Dippenaar A, Warren RM, Silva Júnior WA da, Bollela VR. Accuracy of whole genome sequencing versus phenotypic (MGIT) and commercial molecular tests for detection of drug-resistant Mycobacterium tuberculosis isolated from patients in Brazil and Mozambique [Internet]. Tuberculosis. 2018 ; 110 59-67.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1016/j.tube.2018.04.003
Vancouver
Feliciano CS, Namburete EI, Plaça JR, Peronni K, Dippenaar A, Warren RM, Silva Júnior WA da, Bollela VR. Accuracy of whole genome sequencing versus phenotypic (MGIT) and commercial molecular tests for detection of drug-resistant Mycobacterium tuberculosis isolated from patients in Brazil and Mozambique [Internet]. Tuberculosis. 2018 ; 110 59-67.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1016/j.tube.2018.04.003

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