Zobrazeno 1 - 10
of 10
pro vyhledávání: '"João Kleber Novais Pereira"'
Autor:
João Kleber Novais Pereira, Marília Berlofa Visacri, Nicolás Saavedra, Kathleen Saavedra, Nadine de Godoy Torso, Pedro Eduardo Nascimento Silva Vasconcelos, Luis A. Salazar, Pía Loren, Patricia Moriel
Publikováno v:
International Journal of Molecular Sciences
International Journal of Molecular Sciences, Vol 22, Iss 12765, p 12765 (2021)
International Journal of Molecular Sciences, Vol 22, Iss 12765, p 12765 (2021)
The purpose of this systematic review was to map out and summarize scientific evidence on dysregulated microRNAs (miRNAs) that can be possible biomarkers or therapeutic targets for cisplatin nephrotoxicity and have already been tested in humans, anim
Autor:
Fabiola Traina, João Kleber Novais Pereira, Fernando Ferreira Costa, Matheus Rodrigues Lopes, João Agostinho Machado-Neto, Sara Teresinha Olalla Saad, Beatriz Corey Morini, Patricia Favaro
Publikováno v:
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Universidade de São Paulo (USP)
instacron:USP
Background Constitutive activation of the PI3K pathway in T cell acute lymphoblastic leukaemia (T-ALL) has been reported and in a mouse model, PI3K activation, together with MYC, cooperates in Burkitt lymphoma (BL) pathogenesis. We investigated the e
Autor:
Sara Teresinha Olalla Saad, Paula de Melo Campos, Patricia Favaro, João Agostinho Machado-Neto, Matheus Rodrigues Lopes, João Kleber Novais Pereira, Fabiola Traina
Publikováno v:
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Applied Cancer Research, Vol 37, Iss 1, Pp 1-6 (2017)
Universidade de São Paulo (USP)
instacron:USP
Applied Cancer Research, Vol 37, Iss 1, Pp 1-6 (2017)
Myelodysplastic syndromes (MDS) are a heterogeneous group of disorders characterized by ineffective hematopoiesis and risk of leukemia transformation. There is evidence to suggest the participation of immune system deregulation in MDS pathogenesis. I
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d4102a6321994c1ed87c4cdc79642f9b
Autor:
João Kleber Novais Pereira
Publikováno v:
Biblioteca Digital de Teses e Dissertações da Universidade Estadual de Campinas (UNICAMP)
Universidade Estadual de Campinas (UNICAMP)
instacron:UNICAMP
Universidade Estadual de Campinas (UNICAMP)
instacron:UNICAMP
Orientadores: Patrícia Maria Bergamo Favaro, Sara Teresinha Olalla Saad Dissertação (mestrado) - Universidade Estadual de Campinas, Faculdade de Ciências Médicas Resumo: As neoplasias linfoides constituem um grupo heterogêneo de doenças origin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0563b828aa42e4511a899f3cf587020f
Autor:
João Kleber Novais Pereira, Anne J. Ridley, Sara Teresinha Olalla Saad, Elvira Infante, Fernando Ferreira Costa, João Agostinho Machado-Neto, Matheus Rodrigues Lopes, Patricia Favaro, Mariana Lazarini, Fabiola Traina
Publikováno v:
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Universidade de São Paulo (USP)
instacron:USP
The human FMNL1 is expressed predominantly in hematopoietic cells and has been described previously as overexpressed in hematopoietic malignancies. However, it is not known whether FMNL1 contributes to leukemogenesis. Here, we investigate the FMNL1 f
Autor:
Simone Cristina Olenscki Gilli, João Kleber Novais Pereira, Sara Teresinha Olalla Saad, João Agostinho Machado-Neto, Paula de Melo Campos, Fabiola Traina, Matheus Rodrigues Lopes, Helymar da Costa Machado, Patricia Favaro
Publikováno v:
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Universidade de São Paulo (USP)
instacron:USP
The role of the immune system in myelodysplastic syndrome (MDS) progression has been widely accepted, although mechanisms underlying this immune dysfunction are not clear. CD4+ and CD8+ lymphocyte profiles in the peripheral blood of MDS patients were
Autor:
Patricia Favaro, João Agostinho Machado-Neto, João Kleber Novais Pereira, Fabiola Traina, Adriana S. S. Duarte, Sara Teresinha Olalla Saad, Matheus Rodrigues Lopes
Publikováno v:
Leukemia research. 36(10)
a b s t r a c t Recent studies have indicated the Musashi2/NUMB pathway as the key regulator of differentiation in chronic myeloid leukemia; however, a comparison of both gene expressions has not yet been made in myelodysplastic syndrome (MDS) and in
Autor:
S. Olalla Saad, J.A. Machado-Neto, João Kleber Novais Pereira, P. De Melo Campos, I. Lorand-Metze, Matheus Rodrigues Lopes, Patricia Favaro, F. Traina
Publikováno v:
Leukemia Research. 37:S132-S133
Autor:
Matheus Rodrigues Lopes, João Agostinho Machado-Neto, Fabiola Traina, João Kleber Novais Pereira, Irene Lorand-Metze, Fernando Ferreira Costa, Sara Teresinha Olalla Saad, Patricia Favaro
Publikováno v:
Blood. 122:1519-1519
Background Myelodysplastic syndromes (MDS) are disorders characterized by morphological dysplasia, impaired differentiation and defective cellular functions, resulting in peripheral cytopenias. FMNL1 belongs to a family of formin-related proteins, in
Autor:
João Agostinho Machado-Neto, Fabiola Traina, Sara Teresinha Olalla Saad, Paula de Melo Campos, João Kleber Novais Pereira, Patricia Favaro, Matheus Rodrigues Lopes
Publikováno v:
Blood. 120:3836-3836
Abstract 3836 Low-risk MDS is characterized by increased apoptosis in the bone marrow and autoimmune disease-like profile, whereas advanced MDS is distinguished by immune evasion, lower apoptosis and secondary DNA damage, facilitating progress into a