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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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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: 10 jun. 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 jun. 10 ] 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 jun. 10 ] Available from: https://doi.org/10.1038/s41598-022-09386-4
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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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: 10 jun. 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 jun. 10 ] 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 jun. 10 ] Available from: https://doi.org/10.1016/j.rbmo.2021.01.024
Artigo de periodico
CeTF: an R/Bioconductor package for transcription factor co-expression networks using regulatory impact factors (RIF) and partial correlation and information (PCIT) analysis (2021)
Biagi Junior, Carlos Alberto Oliveira de ; Nociti, Ricardo Perecin; Brotto, Danielle Barbosa; Funicheli, Breno Osvaldo; Ruy, Patrícia de Cássia; Ximenez, João Paulo Bianchi; Figueiredo, David Livingstone Alves; Silva Junior, Wilson Araújo da
Source: BMC Genomics. Unidades: FMRP, ICMC, FZEA, FCFRP
Subjects: BIOINFORMÁTICA, FATORES DE TRANSCRIÇÃO, EXPRESSÃO GÊNICA
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BIAGI JUNIOR, Carlos Alberto Oliveira de et al. CeTF: an R/Bioconductor package for transcription factor co-expression networks using regulatory impact factors (RIF) and partial correlation and information (PCIT) analysis. BMC Genomics, v. 22, n. 1, p. 1-8, 2021Tradução . . Disponível em: https://doi.org/10.1186/s12864-021-07918-2. Acesso em: 10 jun. 2024.
APA
Biagi Junior, C. A. O. de, Nociti, R. P., Brotto, D. B., Funicheli, B. O., Ruy, P. de C., Ximenez, J. P. B., et al. (2021). CeTF: an R/Bioconductor package for transcription factor co-expression networks using regulatory impact factors (RIF) and partial correlation and information (PCIT) analysis. BMC Genomics, 22( 1), 1-8. doi:10.1186/s12864-021-07918-2
NLM
Biagi Junior CAO de, Nociti RP, Brotto DB, Funicheli BO, Ruy P de C, Ximenez JPB, Figueiredo DLA, Silva Junior WA da. CeTF: an R/Bioconductor package for transcription factor co-expression networks using regulatory impact factors (RIF) and partial correlation and information (PCIT) analysis [Internet]. BMC Genomics. 2021 ; 22( 1): 1-8.[citado 2024 jun. 10 ] Available from: https://doi.org/10.1186/s12864-021-07918-2
Vancouver
Biagi Junior CAO de, Nociti RP, Brotto DB, Funicheli BO, Ruy P de C, Ximenez JPB, Figueiredo DLA, Silva Junior WA da. CeTF: an R/Bioconductor package for transcription factor co-expression networks using regulatory impact factors (RIF) and partial correlation and information (PCIT) analysis [Internet]. BMC Genomics. 2021 ; 22( 1): 1-8.[citado 2024 jun. 10 ] Available from: https://doi.org/10.1186/s12864-021-07918-2
Artigo de periodico
Molecular basis of various forms of maple syrup urine disease in Chilean patients (2021)
Campanholi, Diana Ruffato Resende; Margutti, Ana Vitoria Barban; Silva Junior, Wilson Araújo da ; Garcia, Daniel Fantozzi; Molfetta, Greice Andreotti de ; Marques, Adriana A.; Schwartz, Ida Vanessa Doederlein; Cornejo, V.; Hamilton, Valerie; Castro, Gabriela; Sperb-ludwig, Fernanda; Borges, Ester S.; Camelo Júnior, José Simon
Source: Molecular Genetics & Genomic Medicine. Unidade: FMRP
Subjects: AMINOÁCIDOS, ERROS INATOS DO METABOLISMO, LEUCENA, DOENÇA DA URINA DE XAROPE DE BORDO
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CAMPANHOLI, Diana Ruffato Resende et al. Molecular basis of various forms of maple syrup urine disease in Chilean patients. Molecular Genetics & Genomic Medicine, v. 9, n. 5, 2021Tradução . . Disponível em: https://doi.org/10.1002/mgg3.1616. Acesso em: 10 jun. 2024.
APA
Campanholi, D. R. R., Margutti, A. V. B., Silva Junior, W. A. da, Garcia, D. F., Molfetta, G. A. de, Marques, A. A., et al. (2021). Molecular basis of various forms of maple syrup urine disease in Chilean patients. Molecular Genetics & Genomic Medicine, 9( 5). doi:10.1002/mgg3.1616
NLM
Campanholi DRR, Margutti AVB, Silva Junior WA da, Garcia DF, Molfetta GA de, Marques AA, Schwartz IVD, Cornejo V, Hamilton V, Castro G, Sperb-ludwig F, Borges ES, Camelo Júnior JS. Molecular basis of various forms of maple syrup urine disease in Chilean patients [Internet]. Molecular Genetics & Genomic Medicine. 2021 ; 9( 5):[citado 2024 jun. 10 ] Available from: https://doi.org/10.1002/mgg3.1616
Vancouver
Campanholi DRR, Margutti AVB, Silva Junior WA da, Garcia DF, Molfetta GA de, Marques AA, Schwartz IVD, Cornejo V, Hamilton V, Castro G, Sperb-ludwig F, Borges ES, Camelo Júnior JS. Molecular basis of various forms of maple syrup urine disease in Chilean patients [Internet]. Molecular Genetics & Genomic Medicine. 2021 ; 9( 5):[citado 2024 jun. 10 ] Available from: https://doi.org/10.1002/mgg3.1616
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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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: 10 jun. 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 jun. 10 ] 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 jun. 10 ] Available from: https://doi.org/10.1186/s12885-021-07857-x
Artigo de periodico
Contribution of genetic ancestry and polygenic risk score in meeting vitamin B12 needs in healthy Brazilian children and adolescents (2021)
Fuzo, Carlos Alessandro; Ued, Fábio da Veiga ; Moco, Sofia; Cominetti, Ornella; Métairon, Sylviane; Pruvost, Solenn; Charpagne, Aline; Carayol, Jerome; Torrieri, Raul; Silva Junior, Wilson Araújo da ; Descombes, Patrick; Kaput, Jim; Monteiro, Jacqueline Pontes
Source: Scientific Reports. Unidades: FMRP, FCFRP
Subjects: GENEALOGIA, VITAMINA B12, POLIMORFISMO, ESTUDOS TRANSVERSAIS
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FUZO, Carlos Alessandro et al. Contribution of genetic ancestry and polygenic risk score in meeting vitamin B12 needs in healthy Brazilian children and adolescents. Scientific Reports, v. 11, n. 1, 2021Tradução . . Disponível em: https://doi.org/10.1038/s41598-021-91530-7. Acesso em: 10 jun. 2024.
APA
Fuzo, C. A., Ued, F. da V., Moco, S., Cominetti, O., Métairon, S., Pruvost, S., et al. (2021). Contribution of genetic ancestry and polygenic risk score in meeting vitamin B12 needs in healthy Brazilian children and adolescents. Scientific Reports, 11( 1). doi:10.1038/s41598-021-91530-7
NLM
Fuzo CA, Ued F da V, Moco S, Cominetti O, Métairon S, Pruvost S, Charpagne A, Carayol J, Torrieri R, Silva Junior WA da, Descombes P, Kaput J, Monteiro JP. Contribution of genetic ancestry and polygenic risk score in meeting vitamin B12 needs in healthy Brazilian children and adolescents [Internet]. Scientific Reports. 2021 ; 11( 1):[citado 2024 jun. 10 ] Available from: https://doi.org/10.1038/s41598-021-91530-7
Vancouver
Fuzo CA, Ued F da V, Moco S, Cominetti O, Métairon S, Pruvost S, Charpagne A, Carayol J, Torrieri R, Silva Junior WA da, Descombes P, Kaput J, Monteiro JP. Contribution of genetic ancestry and polygenic risk score in meeting vitamin B12 needs in healthy Brazilian children and adolescents [Internet]. Scientific Reports. 2021 ; 11( 1):[citado 2024 jun. 10 ] Available from: https://doi.org/10.1038/s41598-021-91530-7
Artigo de periodico
Mesenchymal stromal cells-based therapy in a murine model of elastase-induced emphysema: simvastatin as a potential adjuvant in cellular homing (2021)
Faria, Carolina Arruda de; Silva Junior, Wilson Araújo da ; Coelho, Karoline Brito Caetano Andrade; Bassi, Mirian; Colombari, Eduardo; Zanette, Dalila Luciola; Paes, Joao Tadeu Ribeiro
Source: Pulmonary Pharmacology & Therapeutics. Unidade: FMRP
Subjects: DOENÇA PULMONAR OBSTRUTIVA CRÔNICA, CÉLULAS ESTROMAIS, ENFISEMA PULMONAR, CÉLULAS-TRONCO
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FARIA, Carolina Arruda de et al. Mesenchymal stromal cells-based therapy in a murine model of elastase-induced emphysema: simvastatin as a potential adjuvant in cellular homing. Pulmonary Pharmacology & Therapeutics, v. 70, p. 1-10, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.pupt.2021.102075. Acesso em: 10 jun. 2024.
APA
Faria, C. A. de, Silva Junior, W. A. da, Coelho, K. B. C. A., Bassi, M., Colombari, E., Zanette, D. L., & Paes, J. T. R. (2021). Mesenchymal stromal cells-based therapy in a murine model of elastase-induced emphysema: simvastatin as a potential adjuvant in cellular homing. Pulmonary Pharmacology & Therapeutics, 70, 1-10. doi:10.1016/j.pupt.2021.102075
NLM
Faria CA de, Silva Junior WA da, Coelho KBCA, Bassi M, Colombari E, Zanette DL, Paes JTR. Mesenchymal stromal cells-based therapy in a murine model of elastase-induced emphysema: simvastatin as a potential adjuvant in cellular homing [Internet]. Pulmonary Pharmacology & Therapeutics. 2021 ; 70 1-10.[citado 2024 jun. 10 ] Available from: https://doi.org/10.1016/j.pupt.2021.102075
Vancouver
Faria CA de, Silva Junior WA da, Coelho KBCA, Bassi M, Colombari E, Zanette DL, Paes JTR. Mesenchymal stromal cells-based therapy in a murine model of elastase-induced emphysema: simvastatin as a potential adjuvant in cellular homing [Internet]. Pulmonary Pharmacology & Therapeutics. 2021 ; 70 1-10.[citado 2024 jun. 10 ] Available from: https://doi.org/10.1016/j.pupt.2021.102075
Artigo de periodico
GDAP1 mutations are frequent among Brazilian patients with autosomal recessive axonal Charcot-Marie-Tooth disease (2021)
Figueiredo, Fernanda Barbosa ; Silva Junior, Wilson Araújo da ; Giuliatti, Silvana ; Tomaselli, Pedro José; Lourenço, Charles Marques; Gouvêa, Silmara Paula; Covaleski, Anna Paula Paranhos Miranda; Hallak, Jaime Eduardo Cecilio ; Marques Júnior, Wilson
Source: Neuromuscular Disorders. Unidade: FMRP
Subjects: DOENÇAS DO SISTEMA NERVOSO, DOENÇAS DEGENERATIVAS, MUTAÇÃO GENÉTICA
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FIGUEIREDO, Fernanda Barbosa et al. GDAP1 mutations are frequent among Brazilian patients with autosomal recessive axonal Charcot-Marie-Tooth disease. Neuromuscular Disorders, v. 31, n. 6, p. 505-511, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.nmd.2021.03.005. Acesso em: 10 jun. 2024.
APA
Figueiredo, F. B., Silva Junior, W. A. da, Giuliatti, S., Tomaselli, P. J., Lourenço, C. M., Gouvêa, S. P., et al. (2021). GDAP1 mutations are frequent among Brazilian patients with autosomal recessive axonal Charcot-Marie-Tooth disease. Neuromuscular Disorders, 31( 6), 505-511. doi:10.1016/j.nmd.2021.03.005
NLM
Figueiredo FB, Silva Junior WA da, Giuliatti S, Tomaselli PJ, Lourenço CM, Gouvêa SP, Covaleski APPM, Hallak JEC, Marques Júnior W. GDAP1 mutations are frequent among Brazilian patients with autosomal recessive axonal Charcot-Marie-Tooth disease [Internet]. Neuromuscular Disorders. 2021 ; 31( 6): 505-511.[citado 2024 jun. 10 ] Available from: https://doi.org/10.1016/j.nmd.2021.03.005
Vancouver
Figueiredo FB, Silva Junior WA da, Giuliatti S, Tomaselli PJ, Lourenço CM, Gouvêa SP, Covaleski APPM, Hallak JEC, Marques Júnior W. GDAP1 mutations are frequent among Brazilian patients with autosomal recessive axonal Charcot-Marie-Tooth disease [Internet]. Neuromuscular Disorders. 2021 ; 31( 6): 505-511.[citado 2024 jun. 10 ] Available from: https://doi.org/10.1016/j.nmd.2021.03.005
Artigo de periodico
HJURP knockdown disrupts clonogenic capacity and increasesradiation-induced cell death of glioblastoma cells (2020)
Serafim, Rodolfo Bortolozo ; Cardoso, Cibele ; Di Cristofaro, Luis Fernando Macedo ; Soares, Christiane Pienna; Silva Junior, Wilson Araújo da ; Espreáfico, Enilza Maria ; Paço-Larson, Maria Luísa ; Price, Brendan D.; Valente, Valéria
Source: Cancer Gene Therapy. Unidade: FMRP
Subjects: NEOPLASIAS CEREBRAIS, GLIOMA
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SERAFIM, Rodolfo Bortolozo et al. HJURP knockdown disrupts clonogenic capacity and increasesradiation-induced cell death of glioblastoma cells. Cancer Gene Therapy, v. 27, n. 5, p. 319-329, 2020Tradução . . Disponível em: https://doi.org/10.1038/s41417-019-0103-0. Acesso em: 10 jun. 2024.
APA
Serafim, R. B., Cardoso, C., Di Cristofaro, L. F. M., Soares, C. P., Silva Junior, W. A. da, Espreáfico, E. M., et al. (2020). HJURP knockdown disrupts clonogenic capacity and increasesradiation-induced cell death of glioblastoma cells. Cancer Gene Therapy, 27( 5), 319-329. doi:10.1038/s41417-019-0103-0
NLM
Serafim RB, Cardoso C, Di Cristofaro LFM, Soares CP, Silva Junior WA da, Espreáfico EM, Paço-Larson ML, Price BD, Valente V. HJURP knockdown disrupts clonogenic capacity and increasesradiation-induced cell death of glioblastoma cells [Internet]. Cancer Gene Therapy. 2020 ; 27( 5): 319-329.[citado 2024 jun. 10 ] Available from: https://doi.org/10.1038/s41417-019-0103-0
Vancouver
Serafim RB, Cardoso C, Di Cristofaro LFM, Soares CP, Silva Junior WA da, Espreáfico EM, Paço-Larson ML, Price BD, Valente V. HJURP knockdown disrupts clonogenic capacity and increasesradiation-induced cell death of glioblastoma cells [Internet]. Cancer Gene Therapy. 2020 ; 27( 5): 319-329.[citado 2024 jun. 10 ] Available from: https://doi.org/10.1038/s41417-019-0103-0
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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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: 10 jun. 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 jun. 10 ] 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 jun. 10 ] Available from: https://doi.org/10.1186/s12920-019-0652-y
Artigo de periodico
Phylogenomic assessment of drug-resistant Mycobacterium tuberculosis strains from Beira, Mozambique (2020)
Namburete, Evangelina Inacio ; Dippenaar, Anzaan ; Conceição, Emilyn Costa ; Feliciano, Cinara Silva ; Nascimento, Margarida Maria Passeri do; Peronni, Kamila Chagas; Silva Junior, Wilson Araújo da ; Ferro, Josefo João; Harrison, Lee H.; Warren, Robin Mark; Bollela, Valdes Roberto
Source: Tuberculosis. Unidade: FMRP
Subjects: MEDICAMENTO, MYCOBACTERIUM TUBERCULOSIS, FILOGENIA, SEQUENCIAMENTO GENÉTICO, GENOMAS
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ABNT
NAMBURETE, Evangelina Inacio et al. Phylogenomic assessment of drug-resistant Mycobacterium tuberculosis strains from Beira, Mozambique. Tuberculosis, v. 121, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.tube.2020.101905. Acesso em: 10 jun. 2024.
APA
Namburete, E. I., Dippenaar, A., Conceição, E. C., Feliciano, C. S., Nascimento, M. M. P. do, Peronni, K. C., et al. (2020). Phylogenomic assessment of drug-resistant Mycobacterium tuberculosis strains from Beira, Mozambique. Tuberculosis, 121. doi:10.1016/j.tube.2020.101905
NLM
Namburete EI, Dippenaar A, Conceição EC, Feliciano CS, Nascimento MMP do, Peronni KC, Silva Junior WA da, Ferro JJ, Harrison LH, Warren RM, Bollela VR. Phylogenomic assessment of drug-resistant Mycobacterium tuberculosis strains from Beira, Mozambique [Internet]. Tuberculosis. 2020 ; 121[citado 2024 jun. 10 ] Available from: https://doi.org/10.1016/j.tube.2020.101905
Vancouver
Namburete EI, Dippenaar A, Conceição EC, Feliciano CS, Nascimento MMP do, Peronni KC, Silva Junior WA da, Ferro JJ, Harrison LH, Warren RM, Bollela VR. Phylogenomic assessment of drug-resistant Mycobacterium tuberculosis strains from Beira, Mozambique [Internet]. Tuberculosis. 2020 ; 121[citado 2024 jun. 10 ] Available from: https://doi.org/10.1016/j.tube.2020.101905
Artigo de periodico
Maple syrup urine disease in Brazilian patients: variants and clinical phenotype heterogeneity (2020)
Margutti, Ana Vitoria Barban; Silva Junior, Wilson Araújo da ; Garcia, Daniel Fantozzi; Molfetta, Greice Andreotti de ; Marques, Adriana Aparecida; Amorim, Tatiana; Prazeres, Vânia Mesquita Gadelha; Silva, Raquel Tavares Boy da; Miura, Irene Kazue; Seda Neto, Joao; Santos, Emerson de Santana; Santos, Mara Lúcia Schmitz Ferreira; Lourenço, Charles Marques; Tonon, Tássia; Sperb-ludwig, Fernanda; Souza, Carolina Fischinger Moura de; Schwartz, Ida Vanessa Döederlein; Camelo Júnior, José Simon
Source: Orphanet Journal of Rare Diseases. Unidade: FMRP
Subjects: AMINOÁCIDOS, ERROS INATOS DO METABOLISMO, DOENÇA DA URINA DE XAROPE DE BORDO
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ABNT
MARGUTTI, Ana Vitoria Barban et al. Maple syrup urine disease in Brazilian patients: variants and clinical phenotype heterogeneity. Orphanet Journal of Rare Diseases, v. 15, 2020Tradução . . Disponível em: https://doi.org/10.1186/s13023-020-01590-7. Acesso em: 10 jun. 2024.
APA
Margutti, A. V. B., Silva Junior, W. A. da, Garcia, D. F., Molfetta, G. A. de, Marques, A. A., Amorim, T., et al. (2020). Maple syrup urine disease in Brazilian patients: variants and clinical phenotype heterogeneity. Orphanet Journal of Rare Diseases, 15. doi:10.1186/s13023-020-01590-7
NLM
Margutti AVB, Silva Junior WA da, Garcia DF, Molfetta GA de, Marques AA, Amorim T, Prazeres VMG, Silva RTB da, Miura IK, Seda Neto J, Santos E de S, Santos MLSF, Lourenço CM, Tonon T, Sperb-ludwig F, Souza CFM de, Schwartz IVD, Camelo Júnior JS. Maple syrup urine disease in Brazilian patients: variants and clinical phenotype heterogeneity [Internet]. Orphanet Journal of Rare Diseases. 2020 ; 15[citado 2024 jun. 10 ] Available from: https://doi.org/10.1186/s13023-020-01590-7
Vancouver
Margutti AVB, Silva Junior WA da, Garcia DF, Molfetta GA de, Marques AA, Amorim T, Prazeres VMG, Silva RTB da, Miura IK, Seda Neto J, Santos E de S, Santos MLSF, Lourenço CM, Tonon T, Sperb-ludwig F, Souza CFM de, Schwartz IVD, Camelo Júnior JS. Maple syrup urine disease in Brazilian patients: variants and clinical phenotype heterogeneity [Internet]. Orphanet Journal of Rare Diseases. 2020 ; 15[citado 2024 jun. 10 ] Available from: https://doi.org/10.1186/s13023-020-01590-7
Artigo de periodico
Appetite effects of prefrontal stimulation depend on COMT Val158Met polymorphism: a randomized clinical trial (2019)
Fassini, Priscila Giacomo ; Das, Sai Krupa; Suen, Vivian Marques Miguel; Magerowski, Greta; Marchini, Julio Sergio ; Silva Junior, Wilson Araújo da ; Changyu, Shen; Alonso-Alonso, Miguel
Source: Appetite. Unidade: FMRP
Subjects: POLIMORFISMO, NEUROTRANSMISSORES, APETITE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FASSINI, Priscila Giacomo et al. Appetite effects of prefrontal stimulation depend on COMT Val158Met polymorphism: a randomized clinical trial. Appetite, v. 140, p. 142-150, 2019Tradução . . Disponível em: https://doi.org/10.1016/j.appet.2019.05.015. Acesso em: 10 jun. 2024.
APA
Fassini, P. G., Das, S. K., Suen, V. M. M., Magerowski, G., Marchini, J. S., Silva Junior, W. A. da, et al. (2019). Appetite effects of prefrontal stimulation depend on COMT Val158Met polymorphism: a randomized clinical trial. Appetite, 140, 142-150. doi:10.1016/j.appet.2019.05.015
NLM
Fassini PG, Das SK, Suen VMM, Magerowski G, Marchini JS, Silva Junior WA da, Changyu S, Alonso-Alonso M. Appetite effects of prefrontal stimulation depend on COMT Val158Met polymorphism: a randomized clinical trial [Internet]. Appetite. 2019 ; 140 142-150.[citado 2024 jun. 10 ] Available from: https://doi.org/10.1016/j.appet.2019.05.015
Vancouver
Fassini PG, Das SK, Suen VMM, Magerowski G, Marchini JS, Silva Junior WA da, Changyu S, Alonso-Alonso M. Appetite effects of prefrontal stimulation depend on COMT Val158Met polymorphism: a randomized clinical trial [Internet]. Appetite. 2019 ; 140 142-150.[citado 2024 jun. 10 ] Available from: https://doi.org/10.1016/j.appet.2019.05.015
Trabalho de evento-resumo periodico
An algorith for diagnosis of hereditary angiodema with normal C1-inhibitor: Applying molecular approach to clinical practice (2019)
Dias, Marina Mendonça; Moreno, Adriana Santos ; Maia, L. S. M.; Nunes, Fernanda Leonel; Campos, W. N.; Ferriani, Mariana Paes Leme; Silva Junior, Wilson Araújo da ; Arruda, Luisa Karla de Paula
Source: Allergy : European Journal of Allergy and Clinical Immunology. Conference titles: European Academy of Allergy and Clinical Immunology Congress - EAACI. Unidade: FMRP
Subjects: DOENÇAS VASCULARES, ANGIOEDEMA, DIAGNÓSTICO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
DIAS, Marina Mendonça et al. An algorith for diagnosis of hereditary angiodema with normal C1-inhibitor: Applying molecular approach to clinical practice. Allergy : European Journal of Allergy and Clinical Immunology. West Sussex: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. Disponível em: https://doi.org/10.1111/all.13998. Acesso em: 10 jun. 2024. , 2019
APA
Dias, M. M., Moreno, A. S., Maia, L. S. M., Nunes, F. L., Campos, W. N., Ferriani, M. P. L., et al. (2019). An algorith for diagnosis of hereditary angiodema with normal C1-inhibitor: Applying molecular approach to clinical practice. Allergy : European Journal of Allergy and Clinical Immunology. West Sussex: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. doi:10.1111/all.13998
NLM
Dias MM, Moreno AS, Maia LSM, Nunes FL, Campos WN, Ferriani MPL, Silva Junior WA da, Arruda LK de P. An algorith for diagnosis of hereditary angiodema with normal C1-inhibitor: Applying molecular approach to clinical practice [Internet]. Allergy : European Journal of Allergy and Clinical Immunology. 2019 ; 74( S106): 756.[citado 2024 jun. 10 ] Available from: https://doi.org/10.1111/all.13998
Vancouver
Dias MM, Moreno AS, Maia LSM, Nunes FL, Campos WN, Ferriani MPL, Silva Junior WA da, Arruda LK de P. An algorith for diagnosis of hereditary angiodema with normal C1-inhibitor: Applying molecular approach to clinical practice [Internet]. Allergy : European Journal of Allergy and Clinical Immunology. 2019 ; 74( S106): 756.[citado 2024 jun. 10 ] Available from: https://doi.org/10.1111/all.13998
Artigo de periodico
Serotonin synthesis protects the mouse colonic crypt from DNA damage and colorectal tumorigenesis (2019)
Sakita, Juliana Yumi; Bader, Michael ; Santos, Emerson Soares dos ; Garcia, Sérgio Britto ; Minto, Stefânia Bovo ; Alenina, Natalia; Brunaldi, Mariângela Ottoboni ; Carvalho, Milene Cristina de; Vidotto, Thiago ; Gasparotto, Bianca; Martins, Ronaldo Bragança ; Silva Junior, Wilson Araújo da ; Brandão, Marcus Lira ; Leite, Caio A; Cunha, Fernando de Queiroz ; Karsenty, Gerard; Squire, Jeremy Andrew ; Uyemura, Sérgio Akira ; Kannen, Vinicius
Source: The Journal of Pathology. Unidades: FMRP, FFCLRP, FCFRP, FFLCH
Subjects: NEOPLASIAS COLORRETAIS, CARCINOGÊNESE, SEROTONINA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SAKITA, Juliana Yumi et al. Serotonin synthesis protects the mouse colonic crypt from DNA damage and colorectal tumorigenesis. The Journal of Pathology, v. 249, n. 1, p. 102-113, 2019Tradução . . Disponível em: https://doi.org/10.1002/path.5285. Acesso em: 10 jun. 2024.
APA
Sakita, J. Y., Bader, M., Santos, E. S. dos, Garcia, S. B., Minto, S. B., Alenina, N., et al. (2019). Serotonin synthesis protects the mouse colonic crypt from DNA damage and colorectal tumorigenesis. The Journal of Pathology, 249( 1), 102-113. doi:10.1002/path.5285
NLM
Sakita JY, Bader M, Santos ES dos, Garcia SB, Minto SB, Alenina N, Brunaldi MO, Carvalho MC de, Vidotto T, Gasparotto B, Martins RB, Silva Junior WA da, Brandão ML, Leite CA, Cunha F de Q, Karsenty G, Squire JA, Uyemura SA, Kannen V. Serotonin synthesis protects the mouse colonic crypt from DNA damage and colorectal tumorigenesis [Internet]. The Journal of Pathology. 2019 ; 249( 1): 102-113.[citado 2024 jun. 10 ] Available from: https://doi.org/10.1002/path.5285
Vancouver
Sakita JY, Bader M, Santos ES dos, Garcia SB, Minto SB, Alenina N, Brunaldi MO, Carvalho MC de, Vidotto T, Gasparotto B, Martins RB, Silva Junior WA da, Brandão ML, Leite CA, Cunha F de Q, Karsenty G, Squire JA, Uyemura SA, Kannen V. Serotonin synthesis protects the mouse colonic crypt from DNA damage and colorectal tumorigenesis [Internet]. The Journal of Pathology. 2019 ; 249( 1): 102-113.[citado 2024 jun. 10 ] Available from: https://doi.org/10.1002/path.5285
Artigo de periodico
Molecular basis of familial adenomatous polyposis in the southeast of Brazil: identification of six novel mutations (2019)
Araujo, Luiza Ferreira de ; Molfetta, Greice Andreotti de ; Vincenzi, Otávio Costa; Huber, Jair ; Teixeira, Lorena Alves; Ferraz, Victor Evangelista de Faria ; Silva Junior, Wilson Araújo da
Source: The International Journal of Biological Markers. Unidade: FMRP
Subjects: POPULAÇÃO, BIOMARCADORES, NEOPLASIAS, PREDISPOSIÇÃO GENÉTICA PARA DOENÇA, MUTAÇÃO GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ARAUJO, Luiza Ferreira de et al. Molecular basis of familial adenomatous polyposis in the southeast of Brazil: identification of six novel mutations. The International Journal of Biological Markers, v. 34, n. 1, p. 80–89, 2019Tradução . . Disponível em: https://doi.org/10.1177/1724600818814462. Acesso em: 10 jun. 2024.
APA
Araujo, L. F. de, Molfetta, G. A. de, Vincenzi, O. C., Huber, J., Teixeira, L. A., Ferraz, V. E. de F., & Silva Junior, W. A. da. (2019). Molecular basis of familial adenomatous polyposis in the southeast of Brazil: identification of six novel mutations. The International Journal of Biological Markers, 34( 1), 80–89. doi:10.1177/1724600818814462
NLM
Araujo LF de, Molfetta GA de, Vincenzi OC, Huber J, Teixeira LA, Ferraz VE de F, Silva Junior WA da. Molecular basis of familial adenomatous polyposis in the southeast of Brazil: identification of six novel mutations [Internet]. The International Journal of Biological Markers. 2019 ; 34( 1): 80–89.[citado 2024 jun. 10 ] Available from: https://doi.org/10.1177/1724600818814462
Vancouver
Araujo LF de, Molfetta GA de, Vincenzi OC, Huber J, Teixeira LA, Ferraz VE de F, Silva Junior WA da. Molecular basis of familial adenomatous polyposis in the southeast of Brazil: identification of six novel mutations [Internet]. The International Journal of Biological Markers. 2019 ; 34( 1): 80–89.[citado 2024 jun. 10 ] Available from: https://doi.org/10.1177/1724600818814462
Artigo de periodico
A global functional analysis of missense mutations reveals two major hotspots in the PALB2 tumor suppressor (2019)
Rodrigue, Amélie; Margaillan, Guillaume; Gomes, Thiago Torres; Coulombe, Yan; Montalban, Gemma; Carvalho, Simone da Costa e Silva; Milano, Larissa; Ducy, Mandy; De-Gregoriis, Giuliana; Dellaire, Graham ; Silva Junior, Wilson Araújo da ; Monteiro, Alvaro N.; Carvalho, Marcelo A.; Simard, Jacques ; Masson, Jean-Yves
Source: Nucleic Acids Research. Unidade: FMRP
Subjects: CARCINOGÊNESE, MUTAÇÃO GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RODRIGUE, Amélie et al. A global functional analysis of missense mutations reveals two major hotspots in the PALB2 tumor suppressor. Nucleic Acids Research, v. 47, n. 20, p. 10662–10677, 2019Tradução . . Disponível em: https://doi.org/10.1093/nar/gkz780. Acesso em: 10 jun. 2024.
APA
Rodrigue, A., Margaillan, G., Gomes, T. T., Coulombe, Y., Montalban, G., Carvalho, S. da C. e S., et al. (2019). A global functional analysis of missense mutations reveals two major hotspots in the PALB2 tumor suppressor. Nucleic Acids Research, 47( 20), 10662–10677. doi:10.1093/nar/gkz780
NLM
Rodrigue A, Margaillan G, Gomes TT, Coulombe Y, Montalban G, Carvalho S da C e S, Milano L, Ducy M, De-Gregoriis G, Dellaire G, Silva Junior WA da, Monteiro AN, Carvalho MA, Simard J, Masson J-Y. A global functional analysis of missense mutations reveals two major hotspots in the PALB2 tumor suppressor [Internet]. Nucleic Acids Research. 2019 ; 47( 20): 10662–10677.[citado 2024 jun. 10 ] Available from: https://doi.org/10.1093/nar/gkz780
Vancouver
Rodrigue A, Margaillan G, Gomes TT, Coulombe Y, Montalban G, Carvalho S da C e S, Milano L, Ducy M, De-Gregoriis G, Dellaire G, Silva Junior WA da, Monteiro AN, Carvalho MA, Simard J, Masson J-Y. A global functional analysis of missense mutations reveals two major hotspots in the PALB2 tumor suppressor [Internet]. Nucleic Acids Research. 2019 ; 47( 20): 10662–10677.[citado 2024 jun. 10 ] Available from: https://doi.org/10.1093/nar/gkz780
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
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 10 jun. 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 jun. 10 ] 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 jun. 10 ] Available from: https://doi.org/10.1093/humrep/dez225
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
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 10 jun. 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 jun. 10 ] 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 jun. 10 ] Available from: https://doi.org/10.1038/s41598-019-47363-6
Artigo de periodico
Xpert MTB/RIF performance to diagnose tuberculosis and rifampicin resistance in a reference centre in southern Brazil (2019)
Feliciano, Cinara Silva ; Menon, Lucas José Bazzo; Anselmo, Livia Maria Pala ; Dippenaar, Anzaan ; Warren, Robin Mark; Silva Junior, Wilson Araújo da ; Bollela, Valdes Roberto
Source: ERJ Open Research. Unidade: FMRP
Subjects: TUBERCULOSE, DIAGNÓSTICO CLÍNICO, TESTES DE SENSIBILIDADE MICROBIANA, ANTIBIÓTICOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FELICIANO, Cinara Silva et al. Xpert MTB/RIF performance to diagnose tuberculosis and rifampicin resistance in a reference centre in southern Brazil. ERJ Open Research, v. 5, n. 3, 2019Tradução . . Disponível em: https://doi.org/10.1183/23120541.00043-2019. Acesso em: 10 jun. 2024.
APA
Feliciano, C. S., Menon, L. J. B., Anselmo, L. M. P., Dippenaar, A., Warren, R. M., Silva Junior, W. A. da, & Bollela, V. R. (2019). Xpert MTB/RIF performance to diagnose tuberculosis and rifampicin resistance in a reference centre in southern Brazil. ERJ Open Research, 5( 3). doi:10.1183/23120541.00043-2019
NLM
Feliciano CS, Menon LJB, Anselmo LMP, Dippenaar A, Warren RM, Silva Junior WA da, Bollela VR. Xpert MTB/RIF performance to diagnose tuberculosis and rifampicin resistance in a reference centre in southern Brazil [Internet]. ERJ Open Research. 2019 ; 5( 3):[citado 2024 jun. 10 ] Available from: https://doi.org/10.1183/23120541.00043-2019
Vancouver
Feliciano CS, Menon LJB, Anselmo LMP, Dippenaar A, Warren RM, Silva Junior WA da, Bollela VR. Xpert MTB/RIF performance to diagnose tuberculosis and rifampicin resistance in a reference centre in southern Brazil [Internet]. ERJ Open Research. 2019 ; 5( 3):[citado 2024 jun. 10 ] Available from: https://doi.org/10.1183/23120541.00043-2019

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