Zobrazeno 1 - 10
of 37
pro vyhledávání: '"Hebert Fabricio Culler"'
Autor:
Luís Alberto de Pádua Covas Lage, Hebert Fabricio Culler, Cadiele Oliana Reichert, Sheila Aparecida Coelho da Siqueira, Juliana Pereira
Publikováno v:
Frontiers in Oncology, Vol 13 (2023)
Angioimmunoblastic T-cell lymphoma (AITL) is the second most frequent subtype of mature T-cell lymphoma (MTCL) in the Western world. It derives from the monoclonal proliferation of T-follicular helper (TFH) cells and is characterized by an exacerbate
Externí odkaz:
https://doaj.org/article/46199a247b5d4a1a9ac13ec74565b8d8
Autor:
Hebert Fabricio Culler
Publikováno v:
Biblioteca Digital de Teses e Dissertações da USPUniversidade de São PauloUSP.
As Escherichia coli enteropatogênica atípicas (EPECa) são capazes de causar a lesão A/E e não transportam o pEAF. Biofilmes microbianos são definidos como comunidades complexas formadas por microrganismos aderidos a superfícies envoltas por um
Autor:
Luís Alberto de Pádua Covas Lage, Guilherme Carneiro Barreto, Hebert Fabricio Culler, Jéssica Billar Cavalcante, Lucas Bassolli de Oliveira Alves, Luciana Nardinelli, Israel Bendit, Maria Cláudia Nogueira Zerbini, Vanderson Rocha, Juliana Pereira
Publikováno v:
Cancer Biomarkers. 35:179-191
INTRODUCTION: Nodal peripheral T-cell lymphomas [nPTCL] constitute a heterogeneous group of rare malignancies with aggressive biological behavior and poor prognosis. Epigenetic phenomena involving genes that control DNA-methylation and histone deacet
Autor:
Luis Alberto de Padua Covas Lage, Rita Novello de Vita, Lucas Bassolli de Oliveira Alves, Mayara D'Auria Jacomassi, Hebert Fabricio Culler, Cadiele Oliana Reichert, Renata Oliveira Costa, Sheila Aparecida Coelho de Siqueira, Vanderson Rocha, Juliana Pereira
Publikováno v:
Blood. 140:9533-9535
Autor:
Luis Alberto de Padua Covas Lage, Vinícius Araújo Soares, Thales Dalessandro Meneguin, Hebert Fabricio Culler, Cadiele Oliana Reichert, Mayara D'Auria Jacomassi, Diego Gomes Cândido Reis, Maria Cláudia Nogueira Zerbini, Renata Oliveira Costa, Vanderson Rocha, Juliana Pereira
Publikováno v:
Blood. 140:6699-6701
Autor:
Luis Alberto de Padua Covas Lage, Pedro Paulo Faust Machado, Cadiele Oliana Reichert, Eliana C M Cristina Martins Miranda, Hebert Fabricio Culler, Sheila Aparecida Coelho de Siqueira, Renata Oliveira Costa, Denis Miyashiro, Jose Sanches, Vanderson Rocha, Carlos S. Chiattone, Juliana Pereira
Publikováno v:
Blood. 140:3701-3703
Autor:
Luis Alberto de Padua Covas Lage, Guilherme Carneiro Barreto, Hebert Fabricio Culler, Jéssica Billar Cavalcanti, Cadiele Oliana Reichert, Renata Oliveira Costa, Debora Levy, Maria Cláudia Nogueira Zerbini, Vanderson Rocha, Juliana Pereira
Publikováno v:
Blood. 140:11903-11904
Autor:
Debora Levy, Juliana Pereira, Karolliny Silva de Oliveira, Lis Vilela de Almeida, Lapc Lage, Youko Nukui, Hebert Fabricio Culler, Daniel Silva Nogueira, José Roberto Assis Filho, Vanderson Rocha
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 43, Iss, Pp S72-(2021)
Introduction ATLL is a rare and aggressive neoplasm caused by the human T-lymphotropic virus type 1 (HTLV-1). It is estimated that at least 5-10 million people carry HTLV-1 and 2-5% out of them will develop ATLL. Our group demonstrated an increase of
Autor:
Debora Levy, Vanderson Rocha, Juliana Pereira, GC Barreto, Claudio Vinicius Brito, Cadiele Oliana Reichert, Lapc Lage, Maria Claudia Nogueira Zerbini, Hebert Fabricio Culler
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 43, Iss, Pp S71-S72 (2021)
Introduction: Nodal-PTCL constitute a heterogeneous group of rare malignancies derived from mature T-lymphocytes. It presents aggressive clinical-biological behavior and distinct outcomes. These tumors have significant geographic variation, making im
Autor:
Vanderson Rocha, Lbo Alves, Luciana Nardinelli, Israel Bendit, GC Barreto, JB Cavalcanti, Hebert Fabricio Culler, Lapc Lage, Juliana Pereira
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 43, Iss, Pp S101-S102 (2021)
Introduction: Nodal-PTCL constitute a rare group of aggressive malignancies with heterogeneous clinical-biological presentation and outcomes. Recently its pathophysiological knowledge has been highly improved, with descriptions of gene mutations asso