Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Matheus Carvalho Bürger"'
Autor:
Rodrigo Guarischi-Sousa, José Eduardo Kroll, Adriano Bonaldi, Paulo Marques Pierry, Darine Villela, Camila Alves Souza, Juliana Santos Silva, Matheus Carvalho Bürger, Felipe Azevedo Oliveira, Marcelo Gomes de Paula, Fabiana Marcelino Meliso, Luiz Gustavo de Almeida, Priscilla Morais Monfredini, Ana Gabriela de Oliveira, Fernanda Milanezi, Cristovam Scapulatempo-Neto, Guilherme Lopes Yamamoto
Publikováno v:
Diagnostics, Vol 13, Iss 21, p 3293 (2023)
Homologous recombination deficiency (HRD) has become an important prognostic and predictive biomarker for patients with high-grade serous ovarian cancer who may benefit from poly-ADP ribose polymerase inhibitors (PARPi) and platinum-based therapies.
Externí odkaz:
https://doaj.org/article/4c4d7f2f44b64e2682d2576a31490d4d
Autor:
Aline Simoneti Fonseca, Anelisa Ramão, Matheus Carvalho Bürger, Jorge Estefano Santana de Souza, Dalila Lucíola Zanette, Greice Andreotti de Molfetta, Luiza Ferreira de Araújo, Rafaela de Barros e Lima Bueno, Graziela Moura Aguiar, Jessica Rodrigues Plaça, Cleidson de Pádua Alves, Anemari Ramos Dinarte dos Santos, Daniel Onofre Vidal, Gyl Eanes Barros Silva, Rodrigo Alexandre Panepucci, Fernanda Maris Peria, Omar Feres, José Joaquim Ribeiro da Rocha, Marco Antonio Zago, Wilson Araújo Silva
Publikováno v:
BMC Cancer, Vol 21, Iss 1, Pp 1-14 (2021)
Abstract Background Colorectal cancer (CRC) is one of the most common cancers worldwide; it is the fourth leading cause of death in the world and the third in Brazil. Mutations in the APC, DCC, KRAS and TP53 genes have been associated with the progre
Externí odkaz:
https://doaj.org/article/714a3d32697943ac85805bff473fd4b1
Autor:
Cláudia Regina Santos Silva, Joice Matos Biselli-Périco, Bruna Lancia Zampieri, Wilson Araujo Silva, Jorge Estefano Santana de Souza, Matheus Carvalho Bürger, Eny Maria Goloni-Bertollo, Érika Cristina Pavarino
Publikováno v:
Mediators of Inflammation, Vol 2016 (2016)
Objective. The aim of the study was to investigate the expression patterns of a specific set of genes involved in the inflammation process in children with Down Syndrome (DS) and children without the syndrome (control group) to identify differences t
Externí odkaz:
https://doaj.org/article/b9b1193180394c56899a9da62f1f89a9
Autor:
Bruna Lancia Zampieri, Joice Matos Biselli-Périco, Jorge Estefano Santana de Souza, Matheus Carvalho Bürger, Wilson Araújo Silva Júnior, Eny Maria Goloni-Bertollo, Erika Cristina Pavarino
Publikováno v:
PLoS ONE, Vol 9, Iss 9, p e107218 (2014)
Individuals with Down syndrome (DS) have a high incidence of immunological alterations with increased susceptibility to bacterial and viral infections and high frequency of different types of hematologic malignancies and autoimmune disorders. In the
Externí odkaz:
https://doaj.org/article/413fcb5bff8e4236b942847e99d8ac92
Autor:
Matheus Carvalho Bürger
Publikováno v:
Biblioteca Digital de Teses e Dissertações da USPUniversidade de São PauloUSP.
A dengue é uma infecção viral sistêmica que pode se manifestar clinicamente de diversas formas, desde febres leves a hemorragia e síndrome do choque, condições potencialmente fatais. Diversos estudos já foram publicados investigando as mudan
Autor:
Joice Matos Biselli, Bruna Lancia Zampieri, Patrícia Matos Biselli-Chicote, Jorge Estefano Santana de Souza, Matheus Carvalho Bürger, Wilson Araújo da Silva Jr, Eny Maria Goloni-Bertollo, Érika Cristina Pavarino
Publikováno v:
Human Cell
Down syndrome (DS), caused by trisomy of chromosome 21 (HSA21), results in a broad range of phenotypes. However, the determinants contributing to the complex and variable phenotypic expression of DS are still not fully known. Changes in microRNAs (mi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::649266f1214c5209140469b34a297d02
https://doi.org/10.1007/s13577-022-00672-x
https://doi.org/10.1007/s13577-022-00672-x
Autor:
Matheus Carvalho Bürger, Patricia Rossi Sacramento-Bobotis, Sandro Félix Perazzio, Monize Nakamoto Provisor Santos, Rafaela Rogerio Floriano de Souza, Vivian Pedigone Cintra, Chong Ae Kim, Gustavo Marquezani Spolador, Michele Groenner Penna, Miguel Mitne-Neto, Maria Carolina Pintao, Rodrigo Fernandes Ramalho, Gil Monteiro Novo Filho, Wagner A.R. Baratela, Christine Hsiaoyun Chung, Caroline Monaco Moreira, Otavio Jose Eulalio Pereira, Aurelio Pimenta Dutra, Alexandre Ricardo dos Santos Fornari, Rafael Alves da Silva, Daniele Paixão, Caroline Olivati, Caio Robledo D'Angioli Costa Quaio, Elisa Napolitano Ferreira, Juliana Emilia Prior Carnavalli
Publikováno v:
American Journal of Medical Genetics Part C: Seminars in Medical Genetics. 187:364-372
Several Mendelian disorders follow an autosomal recessive inheritance pattern. Epidemiological information on many inherited disorders may be useful to guide health policies for rare diseases, but it is often inadequate, particularly in developing co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3fd32bc40c0e902546254bf724a82a06
https://doi.org/10.1002/ajmg.c.31932
https://doi.org/10.1002/ajmg.c.31932
Autor:
Fonseca, Aline Simoneti, Anelisa Ramão, Matheus Carvalho Bürger, Souza, Jorge Estefano Santana De, Zanette, Dalila Lucíola, Greice Andreotti De Molfetta, Araújo, Luiza Ferreira De, Bueno, Rafaela De Barros E Lima, Aguiar, Graziela Moura, Plaça, Jessica Rodrigues, Cleidson De Pádua Alves, Anemari Ramos Dinarte Dos Santos, Vidal, Daniel Onofre, Gyl Eanes Barros Silva, Panepucci, Rodrigo Alexandre, Peria, Fernanda Maris, Feres, Omar, Rocha, José Joaquim Ribeiro Da, Zago, Marco Antonio, Silva, Wilson Araújo
Additional file 2 Table S2. Observed mutations in APC,TP53 and KRAS genes.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::442d93d433eefacf97fac980e43ed276
Autor:
Fonseca, Aline Simoneti, Anelisa Ramão, Matheus Carvalho Bürger, Souza, Jorge Estefano Santana De, Zanette, Dalila Lucíola, Greice Andreotti De Molfetta, Araújo, Luiza Ferreira De, Bueno, Rafaela De Barros E Lima, Aguiar, Graziela Moura, Plaça, Jessica Rodrigues, Cleidson De Pádua Alves, Anemari Ramos Dinarte Dos Santos, Vidal, Daniel Onofre, Gyl Eanes Barros Silva, Panepucci, Rodrigo Alexandre, Peria, Fernanda Maris, Feres, Omar, Rocha, José Joaquim Ribeiro Da, Zago, Marco Antonio, Silva, Wilson Araújo
Additional file 4 Figure S2. Apoptosis assay. The HT29 and SW480 cell lines did not show any changes in the apoptosis’ rates (A) and cell viability (B).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1fda206821e93c423ff56045e2b06702
Autor:
Fonseca, Aline Simoneti, Anelisa Ramão, Matheus Carvalho Bürger, Souza, Jorge Estefano Santana De, Zanette, Dalila Lucíola, Greice Andreotti De Molfetta, Araújo, Luiza Ferreira De, Bueno, Rafaela De Barros E Lima, Aguiar, Graziela Moura, Plaça, Jessica Rodrigues, Cleidson De Pádua Alves, Anemari Ramos Dinarte Dos Santos, Vidal, Daniel Onofre, Gyl Eanes Barros Silva, Panepucci, Rodrigo Alexandre, Peria, Fernanda Maris, Feres, Omar, Rocha, José Joaquim Ribeiro Da, Zago, Marco Antonio, Silva, Wilson Araújo
Additional file 5 Table S3. Enrichment of signaling pathways analysis.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0dafb6079749d3d96ab235ca58a40cf3