Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Maria Candida B. V. Fragoso"'
Autor:
Isabelle P. A. Magalhaes, Bibiana D. Boger, Nathalia L. Gomes, Guilherme L. P. Martins, Leomarques A. Bomfim, Gustavo F. C. Fagundes, Roberta S. Rocha, Fernando M. A. Coelho, Jose L. Chambo, Ana Claudia Latronico, Maria Candida B. V. Fragoso, Ana O. Hoff, Berenice B. Mendonca, Marcos R. Menezes, Madson Q. Almeida
Publikováno v:
Frontiers in Endocrinology, Vol 15 (2024)
For pheochromocytoma and paraganglioma (PPGL), the efficacy of percutaneous ablative therapies in achieving control of metastatic tumors measuring
Externí odkaz:
https://doaj.org/article/a05ac4f5952e47e791492ce49c6ba160
Autor:
Fernanda S. Bachega, Caio V. Suartz, Madson Q. Almeida, Vania B. Brondani, Helaine L. S. Charchar, Amanda M. F. Lacombe, Sebastião N. Martins-Filho, Iberê C. Soares, Maria Claudia N. Zerbini, Francisco T. Dénes, Berenice Mendonca, Roberto I. Lopes, Ana Claudia Latronico, Maria Candida B. V. Fragoso
Publikováno v:
Journal of Clinical Medicine, Vol 11, Iss 22, p 6641 (2022)
Pediatric adrenocortical tumors (PACTs) represent rare causes of malignancies. However, the south/southeast regions of Brazil are known to have a high incidence of PACTs because of the founder effect associated with a germline pathogenic variant of t
Externí odkaz:
https://doaj.org/article/406b91253b4c487babb1b7e0e0d38c28
Autor:
Ricardo V. Araujo, Claudia V. Chang, Valter A. S. Cescato, Maria Candida B. V. Fragoso, Marcello D. Bronstein, Berenice B. Mendonca, Ivo J. P. Arnhold, Luciani R. S. Carvalho
Publikováno v:
Clinics, Vol 68, Iss 6, Pp 887-891 (2013)
OBJECTIVE: The expression of transcription factors involved in early pituitary development, such as PROP1 and POU1F1, has been detected in pituitary adenoma tissues. In this study, we sought to characterize the transcriptional profiles of PROP1, POU1
Externí odkaz:
https://doaj.org/article/99138c18f16244c6a757b078d6a625c1
Autor:
Rodrigo A. Toledo, Berenice B. Mendonca, Maria Candida B. V. Fragoso, Iberê C. Soares, Madson Q. Almeida, Michelle B. Moraes, Delmar M. Lourenço-Jr, Venâncio A. F. Alves, Marcello D. Bronstein, Sergio P. A. Toledo
Publikováno v:
Clinics, Vol 65, Iss 4, Pp 407-415 (2010)
OBJECTIVE: Non-pituitary tumors have been reported in a subset of patients harboring germline mutations in the aryl hydrocarbon receptor-interacting protein (AIP) gene. However, no detailed investigations of non-pituitary tumors of AIP-mutated patien
Externí odkaz:
https://doaj.org/article/bd3acfd134e94c3fb447bd7d6ce60425
Autor:
Gary D. Hammer, Maria Candida B. V. Fragoso, Thomas J. Giordano, William E. Rainey, Suely K. N. Marie, Ana Claudia Latronico, Berenice B. Mendonca, Maria Claudia N. Zerbini, Beatriz M. P. Mariani, Juilee Rege, Michelle Vinco, Madson Q. Almeida, Bhramar Mukherjee, Tobias Else, Antonio Marcondes Lerario, Dipika R. Mohan
Complete clinical and molecular data of all samples used in this study.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3fea28a24e6750c6c4460d2f4cbdf020
https://doi.org/10.1158/1078-0432.22469486.v1
https://doi.org/10.1158/1078-0432.22469486.v1
Autor:
Gary D. Hammer, Maria Candida B. V. Fragoso, Thomas J. Giordano, William E. Rainey, Suely K. N. Marie, Ana Claudia Latronico, Berenice B. Mendonca, Maria Claudia N. Zerbini, Beatriz M. P. Mariani, Juilee Rege, Michelle Vinco, Madson Q. Almeida, Bhramar Mukherjee, Tobias Else, Antonio Marcondes Lerario, Dipika R. Mohan
Purpose:Adrenocortical carcinoma (ACC) is a rare, aggressive malignancy with few therapies; however, patients with locoregional disease have variable outcomes. The Cancer Genome Atlas project on ACC (ACC-TCGA) identified that cancers of patients with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::16a0b5d82af107db42066deedc47a0b9
https://doi.org/10.1158/1078-0432.c.6527273.v1
https://doi.org/10.1158/1078-0432.c.6527273.v1
Autor:
Gary D. Hammer, Maria Candida B. V. Fragoso, Thomas J. Giordano, William E. Rainey, Suely K. N. Marie, Ana Claudia Latronico, Berenice B. Mendonca, Maria Claudia N. Zerbini, Beatriz M. P. Mariani, Juilee Rege, Michelle Vinco, Madson Q. Almeida, Bhramar Mukherjee, Tobias Else, Antonio Marcondes Lerario, Dipika R. Mohan
This compiled PDF includes Supplementary Tables S3, S4, S6, S7, and S8, as follows: Supp. Table S3. G0S2 hypermethylation predicts CIMP-high. Supp. Table S4. Clinical characteristics of FMUSP+UM ACC and ACA Cohorts. Supp. Table S6. EpiTect accurately
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1dcc99679b3747a04c984747c14df6f7
https://doi.org/10.1158/1078-0432.22469483
https://doi.org/10.1158/1078-0432.22469483
Autor:
Gustavo F C Fagundes, Felipe Freitas-Castro, Lucas S Santana, Ana Caroline F Afonso, Janaina Petenuci, Mariana F A Funari, Augusto G Guimaraes, Felipe L Ledesma, Maria Adelaide A Pereira, Carolina R Victor, Marcela S M Ferrari, Fernando M A Coelho, Victor Srougi, Fabio Y Tanno, Jose L Chambo, Ana Claudia Latronico, Berenice B Mendonca, Maria Candida B V Fragoso, Ana O Hoff, Madson Q Almeida
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism.
ContextLimited information is available concerning the genetic spectrum of pheochromocytoma and paraganglioma (PPGL) patients in South America. Germline SDHB large deletions are very rare worldwide, but most of the individuals harboring the SDHB exon
Publikováno v:
Frontiers in Endocrinology. 13
β-catenin programs a tissue-specific epigenetic vulnerability in aggressive adrenocortical carcinoma
Autor:
Dipika R. Mohan, Kleiton S. Borges, Isabella Finco, Christopher R. LaPensee, Juilee Rege, April L. Solon, Donald W. Little, Tobias Else, Madson Q. Almeida, Derek Dang, James Haggerty-Skeans, April A. Apfelbaum, Michelle Vinco, Alda Wakamatsu, Beatriz MP Mariani, Larissa Amorin, Ana Claudia Latronico, Berenice B. Mendonca, Maria Claudia N. Zerbini, Elizabeth R. Lawlor, Ryoma Ohi, Richard J. Auchus, William E. Rainey, Suely K. N. Marie, Thomas J. Giordano, Sriram Venneti, Maria Candida B. V. Fragoso, David T. Breault, Antonio Marcondes Lerario, Gary D. Hammer
Adrenocortical carcinoma (ACC) is a rare cancer in which tissue-specific differentiation is paradoxically associated with dismal outcomes. The differentiated ACC subtype CIMP-high is prevalent, incurable, and routinely fatal. CIMP-high ACC possess ab
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9810854af32882553cc7a6cfe3b60b1e
https://doi.org/10.1101/2022.07.02.497654
https://doi.org/10.1101/2022.07.02.497654