Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Ivy Zortéa S Parise"'
Autor:
Eric Baudin, Enzo Lalli, Pascal Finetti, Letizia Canu, Michaela Luconi, François Bertucci, Nelly Durand, Angelo Paci, Giulia Cantini, Silviu Sbiera, Abir Al Ghuzlan, Martin Fassnacht, Ivy Zortéa S Parise, Iuliu Sbiera, Ségolène Hescot, Mirna M O Figueiredo, Heloisa Komechen, Bonald C. Figueiredo, Daniel Birnbaum, Mabrouka Doghman-Bouguerra, Gabriella Nesi
Publikováno v:
Cancers
Cancers, MDPI, 2020, 12, ⟨10.3390/cancers12030689⟩
Volume 12
Issue 3
Cancers, Vol 12, Iss 3, p 689 (2020)
Cancers, 2020, 12, ⟨10.3390/cancers12030689⟩
Cancers, MDPI, 2020, 12, ⟨10.3390/cancers12030689⟩
Volume 12
Issue 3
Cancers, Vol 12, Iss 3, p 689 (2020)
Cancers, 2020, 12, ⟨10.3390/cancers12030689⟩
The SF-1 transcription factor target gene FATE1 encodes a cancer-testis antigen that has an important role in regulating apoptosis and response to chemotherapy in adrenocortical carcinoma (ACC) cells. Autoantibodies directed against FATE1 were previo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3fcfcffdb64cc8066c904137ca3d5565
https://www.hal.inserm.fr/inserm-02508381/document
https://www.hal.inserm.fr/inserm-02508381/document
Autor:
Patricia Ashton-Prolla, Tatiana Ei-Jaick B Costa, Madson Q. Almeida, Maria Nirvana Formiga, Berenice B. Mendonca, Kara N. Maxwell, Geoffrey Neale, Mariana M Paraizo, Andrew J. Murphy, Enzo Lalli, Meredith Yeager, Jinghui Zhang, Laurence Brugières, Ana Claudia Latronico, Jinling Wang, Wenan Chen, Carolina Mathias, Evadnie Rampersaud, Gang Wu, Dominique Vaur, Sharon A. Savage, Sahlua Volc, Vania Balderrama Brondani, Gabriela E. S. Felix, Camila Matzenbacher Bittar, Elena M. Stoffel, Enilze Maria de Souza Fonseca Ribeiro, Hector Salvador, Vicente Odone-Filho, Kristine Jones, Tobias Else, Kayla V. Hamilton, Alberto S. Pappo, Edenir Inêz Palmero, Guillermo L. Chantada, Karina Miranda Santiago, Emerson Wander Silva Soares, Moara Machado, Kim E. Nichols, Maria Isabel Achatz, Payal P. Klincha, Cintia Regina Niederauer Ramos, Kelvin C. de Andrade, Luis Kowalski, Raul C. Ribeiro, Heloisa Komechen, Aurelie Vogt, Jon P. Connelly, Yoan Diekmann, Márta Korbonits, Eric Letouzé, Maria Candida Barisson Villares Fragoso, Bonald C. Figueiredo, Carlos Rodriguez-Galindo, Ivy Zortéa S Parise, Cinzia Lavarino, Gerard P. Zambetti, Henrique de Campos Reis Galvão, Weiyin Zhou, Shondra M. Pruett-Miller, Michael R. Clay, Emilia M. Pinto, Mark G. Thomas, Jose Luis Fuster-Soler
Publikováno v:
Science Advances
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
instname
r-FSJD: Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
instname
r-FSJD: Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
The XAF1-E134* variant increases the cancer risk for carriers of the TP53-R337H allele.
Cancer risk is highly variable in carriers of the common TP53-R337H founder allele, possibly due to the influence of modifier genes. Whole-genome sequencing
Cancer risk is highly variable in carriers of the common TP53-R337H founder allele, possibly due to the influence of modifier genes. Whole-genome sequencing
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8bb9b87a026bef839378660581a1f6cc
http://fundanet.fsjd.org/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=17947
http://fundanet.fsjd.org/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=17947
Autor:
Ivy Zortéa S, Parise, Guilherme A, Parise, Lúcia, Noronha, Mirvat, Surakhy, Thiago Demetrius, Woiski, Denise B, Silva, Tatiana Ei-Jaick B, Costa, Maria Helena C P, Del-Valle, Heloisa, Komechen, Roberto, Rosati, Melyssa Grignet, Ribeiro, Marilza Leal, Nascimento, José Antônio de, Souza, Diancarlos P, Andrade, Mariana M, Paraizo, Marjorana Martini R, Galvão, José Renato S, Barbosa, Miriam Lacerda, Barbosa, Gislaine C, Custódio, Mirna M O, Figueiredo, Ana Luiza M R, Fabro, Gareth, Bond, Marco, Volante, Enzo, Lalli, Bonald C, Figueiredo
Publikováno v:
Cancers
Adrenocortical carcinoma (ACC) is a rare disease among children. Our goal was to identify prognostic biomarkers in 48 primary ACCs from children (2.83 ± 2.3 y; mean age ± SD) by evaluating the tumor stage and outcome for an age of diagnosis before
Autor:
Mariana M Paraizo, Enzo Lalli, Gareth L. Bond, Ivy Zortéa S Parise, Emilia M. Pinto, Hannah Carter, Meghana Pagadala, Gerard P. Zambetti, Marsha D. Wallace, Heloisa Komechen, Mirvat Surakhy, Bonald C. Figueiredo, Elisabeth E. Bond, Husein Perez, Matteo Di Giovannantonio, Ping Zhang, David Malkin, Lukasz Filip Grochola
Publikováno v:
British Journal of Cancer
Background Genome-wide association studies (GWASs) have enriched the fields of genomics and drug development. Adrenocortical carcinoma (ACC) is a rare cancer with a bimodal age distribution and inadequate treatment options. Paediatric ACC is frequent
Autor:
Mariana M Paraizo, Diancarlos P. Andrade, Ivy Zortéa S Parise, Enzo Lalli, Marco Volante, Heloisa Komechen, Mirvat Surakhy, Bonald C. Figueiredo, Marjorana Martini R Galvão, Marilza Leal Nascimento, Miriam L. Barbosa, Tatiana Ei-Jaick B Costa, Thiago Demetrius Woiski, Ana Luiza M. R. Fabro, Denise B Silva, José Antônio de Souza, Maria Helena C P Del-Valle, José Renato S. Barbosa, Mirna M O Figueiredo, Gislaine Custódio, Roberto Rosati, Melyssa Grignet Ribeiro, Lucia de Noronha, Gareth L. Bond, Guilherme A Parise
Publikováno v:
Cancers
Cancers, MDPI, 2019, 11 (11), pp.1730. ⟨10.3390/cancers11111730⟩
Cancers, 2019, 11 (11), pp.1730. ⟨10.3390/cancers11111730⟩
Cancers, Vol 11, Iss 11, p 1730 (2019)
Volume 11
Issue 11
Cancers, MDPI, 2019, 11 (11), pp.1730. ⟨10.3390/cancers11111730⟩
Cancers, 2019, 11 (11), pp.1730. ⟨10.3390/cancers11111730⟩
Cancers, Vol 11, Iss 11, p 1730 (2019)
Volume 11
Issue 11
Adrenocortical carcinoma (ACC) is a rare disease among children. Our goal was to identify prognostic biomarkers in 48 primary ACCs from children (2.83 ±
2.3 y
mean age ±
SD) by evaluating the tumor stage and outcome for an
2.3 y
mean age ±
SD) by evaluating the tumor stage and outcome for an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3356c3e7c8163df88cd589ec427fb338
https://www.hal.inserm.fr/inserm-02437545/document
https://www.hal.inserm.fr/inserm-02437545/document
Autor:
Mara Albonei Dudeque Pianovski, Guilherme A Parise, Jorge Alberto Ledesma, Mirna M O Figueiredo, Humberto C. Ibañez, Cesar Cavalli Sabbaga, Danilo C. Carvalho, Sohaila B.I. Arram, Sylvio Gilberto Andrade Avilla, Yinmei Zhou, Luciano R. Mengarelli, José Renato S. Barbosa, Lisiane de Castro Poncio, Geneci F.R. Lima, Roberto Rosati, Carmem M.C.M. Fiori, Raul C. Ribeiro, Thiago Demetrius Woiski, Francisco R.O. Figueiredo, Ivy Zortéa S Parise, Elis R. Sade, Sérvio Túlio Stinghen, Roberto Pontarolo, Nilton Kiesel Filho, Heloisa Komechen, Bonald C. Figueiredo, Enzo Lalli, Gislaine Custódio, Gerard P. Zambetti, Leila Grisa
Publikováno v:
Journal of Clinical Oncology. 31:2619-2626
Purpose The incidence of pediatric adrenocortical tumors (ACTs) is remarkably high in southern Brazil, where more than 90% of patients carry the germline TP53 mutation R337H. We assessed the impact of early detection of this mutation and of surveilla
Autor:
Flora M Watanabe, Luciane R. Cavalli, Vicente Odone Filho, Guilherme A Parise, Ivy Zortéa S Parise, Bassem R. Haddad, Luiz Gonzaga Caleffe, Janice D. Rone, Bonald C. Figueiredo, Mara Albonei Dudeque Pianovski, Sérgio Ossamu Ioshii, Ewerton M Maggio
Publikováno v:
Journal of Pediatric Hematology/Oncology. 28:82-87
Summary: The authors report on the incidence and clinical characteristics of neuroblastoma in southern Brazil. The aims of the study were to evaluate the age at diagnosis, tumor stage, MYCN status, and tumor histopathology, and to relate these factor