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Artigo de periodico
Genomics and epidemiology for gastric adenocarcinomas (GE4GAC): a Brazilian initiative to study gastric cancer (2019)
Bartelli, Thais F; Abrantes, Lais L. Senda de; Freitas, Helano C; Thomas, Andrew Maltez ; Moda, Bruno Spinetti; Valieris, Renan; Coelho, Luiz G. V; Khayat, André; Demachki, Sâmia; Santiago, Karina M; Burbano, Rommel ; Barbosa, Monica S; Brito, Alexandre M; Santana, Vilma ; Andrade, Hanna B; Mello, Celso A. L; Claro, Laura C. L; Carraro, Dirce M; Martins, Vilma R; Setubal, Joao Carlos
Source: Applied Cancer Research. Unidade: IQ
Subjects: GENÔMICA, NEOPLASIAS GÁSTRICAS, EPIDEMIOLOGIA
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ABNT
BARTELLI, Thais F et al. Genomics and epidemiology for gastric adenocarcinomas (GE4GAC): a Brazilian initiative to study gastric cancer. Applied Cancer Research, v. 39, n. 12, p. 1-4, 2019Tradução . . Disponível em: https://doi.org/10.1186/s41241-019-0081-4. Acesso em: 03 nov. 2024.
APA
Bartelli, T. F., Abrantes, L. L. S. de, Freitas, H. C., Thomas, A. M., Moda, B. S., Valieris, R., et al. (2019). Genomics and epidemiology for gastric adenocarcinomas (GE4GAC): a Brazilian initiative to study gastric cancer. Applied Cancer Research, 39( 12), 1-4. doi:10.1186/s41241-019-0081-4
NLM
Bartelli TF, Abrantes LLS de, Freitas HC, Thomas AM, Moda BS, Valieris R, Coelho LGV, Khayat A, Demachki S, Santiago KM, Burbano R, Barbosa MS, Brito AM, Santana V, Andrade HB, Mello CAL, Claro LCL, Carraro DM, Martins VR, Setubal JC. Genomics and epidemiology for gastric adenocarcinomas (GE4GAC): a Brazilian initiative to study gastric cancer [Internet]. Applied Cancer Research. 2019 ; 39( 12): 1-4.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1186/s41241-019-0081-4
Vancouver
Bartelli TF, Abrantes LLS de, Freitas HC, Thomas AM, Moda BS, Valieris R, Coelho LGV, Khayat A, Demachki S, Santiago KM, Burbano R, Barbosa MS, Brito AM, Santana V, Andrade HB, Mello CAL, Claro LCL, Carraro DM, Martins VR, Setubal JC. Genomics and epidemiology for gastric adenocarcinomas (GE4GAC): a Brazilian initiative to study gastric cancer [Internet]. Applied Cancer Research. 2019 ; 39( 12): 1-4.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1186/s41241-019-0081-4
Artigo de periodico
A non-functional galanin receptor-2 in a multiple sclerosis patient (2019)
Garcia-Rosa, Sheila; Trivella, Daniela Barretto Barbosa; Marques, Vanessa Daccach; Serafim, Rodolfo Bortolozo; Pereira, José Geraldo de Carvalho; Lorenzi, Julio Cesar Cetrulo; Molfetta, Greice Andreotti de ; Christo, Paulo Pereira; Olival, Guilherme Sciascia do; Marchitto, Vania Balardin Toller; Brum, Doralina Guimarães; Sabedot, Thais Sarraf; Noushmehr, Houtan ; Farias, Alessandro dos Santos; Santos, Leonilda Maria Barbosa dos; Machado, José Augusto Nogueira; Souza, Jorge E. S.; Romano, Camila Malta; Conde, Rodrigo Melo; Santos, Antonio Carlos dos ; Guerreiro, Carlos Tostes; Schreuder, Willem H.; Gleber-Netto, Frederico Omar; Amorim, Maria; Valieris, Renan; Silva, Israel Tojal da; Silva Junior, Wilson Araújo da ; Nunes, Diana Noronha; Oliveira, Paulo Sérgio Lopes de; Valente, Valéria; Arruda, Maria Augusta; Hill, Stephen J.; Barreira, Amilton Antunes; Dias Neto, Emmanuel
Source: The Pharmacogenomics Journal. Unidades: FMRP, BIOINFORMÁTICA
Subjects: ESCLEROSE MÚLTIPLA, RECEPTORES, DNA, RNA
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ABNT
GARCIA-ROSA, Sheila et al. A non-functional galanin receptor-2 in a multiple sclerosis patient. The Pharmacogenomics Journal, v. 19, n. 1, p. 72-82, 2019Tradução . . Disponível em: https://doi.org/10.1038/s41397-018-0032-6. Acesso em: 03 nov. 2024.
APA
Garcia-Rosa, S., Trivella, D. B. B., Marques, V. D., Serafim, R. B., Pereira, J. G. de C., Lorenzi, J. C. C., et al. (2019). A non-functional galanin receptor-2 in a multiple sclerosis patient. The Pharmacogenomics Journal, 19( 1), 72-82. doi:10.1038/s41397-018-0032-6
NLM
Garcia-Rosa S, Trivella DBB, Marques VD, Serafim RB, Pereira JG de C, Lorenzi JCC, Molfetta GA de, Christo PP, Olival GS do, Marchitto VBT, Brum DG, Sabedot TS, Noushmehr H, Farias A dos S, Santos LMB dos, Machado JAN, Souza JES, Romano CM, Conde RM, Santos AC dos, Guerreiro CT, Schreuder WH, Gleber-Netto FO, Amorim M, Valieris R, Silva IT da, Silva Junior WA da, Nunes DN, Oliveira PSL de, Valente V, Arruda MA, Hill SJ, Barreira AA, Dias Neto E. A non-functional galanin receptor-2 in a multiple sclerosis patient [Internet]. The Pharmacogenomics Journal. 2019 ; 19( 1): 72-82.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1038/s41397-018-0032-6
Vancouver
Garcia-Rosa S, Trivella DBB, Marques VD, Serafim RB, Pereira JG de C, Lorenzi JCC, Molfetta GA de, Christo PP, Olival GS do, Marchitto VBT, Brum DG, Sabedot TS, Noushmehr H, Farias A dos S, Santos LMB dos, Machado JAN, Souza JES, Romano CM, Conde RM, Santos AC dos, Guerreiro CT, Schreuder WH, Gleber-Netto FO, Amorim M, Valieris R, Silva IT da, Silva Junior WA da, Nunes DN, Oliveira PSL de, Valente V, Arruda MA, Hill SJ, Barreira AA, Dias Neto E. A non-functional galanin receptor-2 in a multiple sclerosis patient [Internet]. The Pharmacogenomics Journal. 2019 ; 19( 1): 72-82.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1038/s41397-018-0032-6
Artigo de periodico
miRNAs 144-3p, 34a-5p, and 206 are a useful signature for distinguishing uterine leiomyosarcoma from other smooth muscle tumors (2019)
Schiavon, Beatriz Nunes; Carvalho, Katia Candido; Camillo, Cláudia Malheiros Coutinho; Baiocchi, Glauco; Valieris, Renan; Drummond, Rodrigo; Silva, Israel Tojal da; Brot, Louise De; Soares, Fernando Augusto; Cunha, Isabela Werneck da
Source: Surgical and Experimental Pathology. Unidade: FO
Subjects: AMELOBLASTOMA, PROGNÓSTICO
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ABNT
SCHIAVON, Beatriz Nunes et al. miRNAs 144-3p, 34a-5p, and 206 are a useful signature for distinguishing uterine leiomyosarcoma from other smooth muscle tumors. Surgical and Experimental Pathology, 2019Tradução . . Disponível em: https://doi.org/10.1186/s42047-019-0032-0. Acesso em: 03 nov. 2024.
APA
Schiavon, B. N., Carvalho, K. C., Camillo, C. M. C., Baiocchi, G., Valieris, R., Drummond, R., et al. (2019). miRNAs 144-3p, 34a-5p, and 206 are a useful signature for distinguishing uterine leiomyosarcoma from other smooth muscle tumors. Surgical and Experimental Pathology. doi:10.1186/s42047-019-0032-0
NLM
Schiavon BN, Carvalho KC, Camillo CMC, Baiocchi G, Valieris R, Drummond R, Silva IT da, Brot LD, Soares FA, Cunha IW da. miRNAs 144-3p, 34a-5p, and 206 are a useful signature for distinguishing uterine leiomyosarcoma from other smooth muscle tumors [Internet]. Surgical and Experimental Pathology. 2019 ;[citado 2024 nov. 03 ] Available from: https://doi.org/10.1186/s42047-019-0032-0
Vancouver
Schiavon BN, Carvalho KC, Camillo CMC, Baiocchi G, Valieris R, Drummond R, Silva IT da, Brot LD, Soares FA, Cunha IW da. miRNAs 144-3p, 34a-5p, and 206 are a useful signature for distinguishing uterine leiomyosarcoma from other smooth muscle tumors [Internet]. Surgical and Experimental Pathology. 2019 ;[citado 2024 nov. 03 ] Available from: https://doi.org/10.1186/s42047-019-0032-0
Trabalho de evento-resumo periodico
Identification of new promising germline variants in melanoma-prone patients (2018)
Fidalgo, Felipe; Facure, Luciana; Barros, Bruna; Valieris, Renan; Torrezan, Giovana; Sá, Bianca de; Nóbrega, Amanda; Achatz, Maria Isabel; Duprat, João; Rosenberg, Carla ; Souza, Sandro; Krepischi, Ana Cristina Victorino ; Carraro, Dirce Maria
Source: Clinical Cancer Research. Conference titles: AACR International Conference on Translational Cancer Medicine. Unidade: IB
Subjects: MELANOMA, PREDISPOSIÇÃO GENÉTICA PARA DOENÇA, MUTAÇÃO GENÉTICA, BIOLOGIA MOLECULAR, GENÉTICA MÉDICA
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ABNT
FIDALGO, Felipe et al. Identification of new promising germline variants in melanoma-prone patients. Clinical Cancer Research. Philadelphia: Instituto de Biociências, Universidade de São Paulo. Disponível em: http://clincancerres.aacrjournals.org/content/24/1_Supplement/A20. Acesso em: 03 nov. 2024. , 2018
APA
Fidalgo, F., Facure, L., Barros, B., Valieris, R., Torrezan, G., Sá, B. de, et al. (2018). Identification of new promising germline variants in melanoma-prone patients. Clinical Cancer Research. Philadelphia: Instituto de Biociências, Universidade de São Paulo. Recuperado de http://clincancerres.aacrjournals.org/content/24/1_Supplement/A20
NLM
Fidalgo F, Facure L, Barros B, Valieris R, Torrezan G, Sá B de, Nóbrega A, Achatz MI, Duprat J, Rosenberg C, Souza S, Krepischi ACV, Carraro DM. Identification of new promising germline variants in melanoma-prone patients [Internet]. Clinical Cancer Research. 2018 ; 24( 1):[citado 2024 nov. 03 ] Available from: http://clincancerres.aacrjournals.org/content/24/1_Supplement/A20
Vancouver
Fidalgo F, Facure L, Barros B, Valieris R, Torrezan G, Sá B de, Nóbrega A, Achatz MI, Duprat J, Rosenberg C, Souza S, Krepischi ACV, Carraro DM. Identification of new promising germline variants in melanoma-prone patients [Internet]. Clinical Cancer Research. 2018 ; 24( 1):[citado 2024 nov. 03 ] Available from: http://clincancerres.aacrjournals.org/content/24/1_Supplement/A20
Artigo de periodico
Utility of trio-based exome sequencing in the elucidation of the genetic basis of isolated syndromic intellectual disability: illustrative cases (2018)
Carneiro, Thaise NR; Krepischi, Ana Cristina Victorino ; Costa, Sílvia S; Silva, Israel Tojal da; Vianna-Morgante, Angela M ; Valieris, Renan; Ezquina, Suzana AM; Bertola, Débora R; Otto, Paulo A ; Rosenberg, Carla
Source: The Application of Clinical Genetics. Unidade: IB
Subjects: GENOMAS, SEQUENCIAMENTO GENÉTICO, DOENÇAS GENÉTICAS, DEFICIÊNCIA MENTAL, EXONS, DIAGNÓSTICO
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ABNT
CARNEIRO, Thaise NR et al. Utility of trio-based exome sequencing in the elucidation of the genetic basis of isolated syndromic intellectual disability: illustrative cases. The Application of Clinical Genetics, v. 11, p. 93-98, 2018Tradução . . Disponível em: https://doi.org/10.2147/TACG.S165799. Acesso em: 03 nov. 2024.
APA
Carneiro, T. N. R., Krepischi, A. C. V., Costa, S. S., Silva, I. T. da, Vianna-Morgante, A. M., Valieris, R., et al. (2018). Utility of trio-based exome sequencing in the elucidation of the genetic basis of isolated syndromic intellectual disability: illustrative cases. The Application of Clinical Genetics, 11, 93-98. doi:10.2147/TACG.S165799
NLM
Carneiro TNR, Krepischi ACV, Costa SS, Silva IT da, Vianna-Morgante AM, Valieris R, Ezquina SAM, Bertola DR, Otto PA, Rosenberg C. Utility of trio-based exome sequencing in the elucidation of the genetic basis of isolated syndromic intellectual disability: illustrative cases [Internet]. The Application of Clinical Genetics. 2018 ; 11 93-98.[citado 2024 nov. 03 ] Available from: https://doi.org/10.2147/TACG.S165799
Vancouver
Carneiro TNR, Krepischi ACV, Costa SS, Silva IT da, Vianna-Morgante AM, Valieris R, Ezquina SAM, Bertola DR, Otto PA, Rosenberg C. Utility of trio-based exome sequencing in the elucidation of the genetic basis of isolated syndromic intellectual disability: illustrative cases [Internet]. The Application of Clinical Genetics. 2018 ; 11 93-98.[citado 2024 nov. 03 ] Available from: https://doi.org/10.2147/TACG.S165799
Artigo de periodico
Exome sequencing of multiple-sclerosis patients and their unaffected first-degree relatives (2017)
Garcia-Rosa, Sheila; Amorim, Maria Galli de; Valieris, Renan; Marques, Vanessa Daccach; Lorenzi, Júlio César Cetrulo; Toller, Vania Balardin; Olival, Guilherme Sciascia do; Silva Júnior, Wilson Araújo da; Silva, Israel Tojal da; Barreira, Amilton Antunes; Nunes, Diana Noronha; Dias-Neto, Emmanuel
Source: BMC Research Notes. Unidade: FMRP
Subjects: ESCLEROSE MÚLTIPLA, SEQUENCIAMENTO GENÉTICO
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ABNT
GARCIA-ROSA, Sheila et al. Exome sequencing of multiple-sclerosis patients and their unaffected first-degree relatives. BMC Research Notes, v. 10, n. 1, 2017Tradução . . Disponível em: https://doi.org/10.1186/s13104-017-3072-0. Acesso em: 03 nov. 2024.
APA
Garcia-Rosa, S., Amorim, M. G. de, Valieris, R., Marques, V. D., Lorenzi, J. C. C., Toller, V. B., et al. (2017). Exome sequencing of multiple-sclerosis patients and their unaffected first-degree relatives. BMC Research Notes, 10( 1). doi:10.1186/s13104-017-3072-0
NLM
Garcia-Rosa S, Amorim MG de, Valieris R, Marques VD, Lorenzi JCC, Toller VB, Olival GS do, Silva Júnior WA da, Silva IT da, Barreira AA, Nunes DN, Dias-Neto E. Exome sequencing of multiple-sclerosis patients and their unaffected first-degree relatives [Internet]. BMC Research Notes. 2017 ; 10( 1):[citado 2024 nov. 03 ] Available from: https://doi.org/10.1186/s13104-017-3072-0
Vancouver
Garcia-Rosa S, Amorim MG de, Valieris R, Marques VD, Lorenzi JCC, Toller VB, Olival GS do, Silva Júnior WA da, Silva IT da, Barreira AA, Nunes DN, Dias-Neto E. Exome sequencing of multiple-sclerosis patients and their unaffected first-degree relatives [Internet]. BMC Research Notes. 2017 ; 10( 1):[citado 2024 nov. 03 ] Available from: https://doi.org/10.1186/s13104-017-3072-0
Artigo de periodico
A total transcriptome profiling method for plasma-derived extracellular vesicles: applications for liquid biopsies (2017)
Amorim, Maria G.; Valieris, Renan; Drummond, Rodrigo D.; Pizzi, Melissa P.; Freitas, Vanessa Morais ; Sinigaglia-Coimbra, Rita; Calin, George A.; Pasqualini, Renata; Arap, Wadih; Silva, Israel T.; Dias-Neto, Emmanuel; Nunes, Diana N.
Source: Scientific Reports. Unidade: ICB
Assunto: HISTOLOGIA
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ABNT
AMORIM, Maria G. et al. A total transcriptome profiling method for plasma-derived extracellular vesicles: applications for liquid biopsies. Scientific Reports, v. 7, n. 1, p. 1-11, 2017Tradução . . Disponível em: https://doi.org/10.1038/s41598-017-14264-5. Acesso em: 03 nov. 2024.
APA
Amorim, M. G., Valieris, R., Drummond, R. D., Pizzi, M. P., Freitas, V. M., Sinigaglia-Coimbra, R., et al. (2017). A total transcriptome profiling method for plasma-derived extracellular vesicles: applications for liquid biopsies. Scientific Reports, 7( 1), 1-11. doi:10.1038/s41598-017-14264-5
NLM
Amorim MG, Valieris R, Drummond RD, Pizzi MP, Freitas VM, Sinigaglia-Coimbra R, Calin GA, Pasqualini R, Arap W, Silva IT, Dias-Neto E, Nunes DN. A total transcriptome profiling method for plasma-derived extracellular vesicles: applications for liquid biopsies [Internet]. Scientific Reports. 2017 ; 7( 1): 1-11.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1038/s41598-017-14264-5
Vancouver
Amorim MG, Valieris R, Drummond RD, Pizzi MP, Freitas VM, Sinigaglia-Coimbra R, Calin GA, Pasqualini R, Arap W, Silva IT, Dias-Neto E, Nunes DN. A total transcriptome profiling method for plasma-derived extracellular vesicles: applications for liquid biopsies [Internet]. Scientific Reports. 2017 ; 7( 1): 1-11.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1038/s41598-017-14264-5

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