Zobrazeno 1 - 10
of 111
pro vyhledávání: '"Ronald Feitosa Pinheiro"'
Autor:
Daniela de Paula Borges, Rinna Maria Arruda Rodrigues dos Santos, Elvira Rodrigues Pereira Velloso, Howard Lopes Ribeiro Junior, Irene Beatriz Larripa, Maria Fernanda Camacho, Jacqueline González, Leandro Daniel Burgos Pratx, Sílvia Maria Meira Magalhães, Carolina Bárbara Belli, Ronald Feitosa Pinheiro
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 45, Iss 2, Pp 147-153 (2023)
Nucleotide excision repair pathway (NER) is an essential mechanism for single-strand breaks (SSB) repair while xeroderma pigmentosum family (XPA to XPG) is the most important system to NER. Myelodysplastic syndrome (MDS) is a heterogeneous hematologi
Externí odkaz:
https://doaj.org/article/7e7f59c9a5db4e1a8a945e60719cb5a3
Autor:
Lara de Holanda Jucá Silveira, Cleto Dantas Nogueira, Carolina Teixeira Costa, Priscila Timbó de Azevedo, Silvia Maria Meira Magalhães, Ronald Feitosa Pinheiro
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 45, Iss 1, Pp 90-94 (2023)
Externí odkaz:
https://doaj.org/article/c14ef13d359c41ea9226ff6a46a7d5eb
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 45, Iss 1, Pp 124-126 (2023)
Externí odkaz:
https://doaj.org/article/d6aad85671554a75818f377cdd9d4297
Autor:
Renan da Silva Santos, Daniel Pascoalino Pinheiro, Louhanna Pinheiro Rodrigues Teixeira, Sarah Leyenne Alves Sales, Maria Claudia dos Santos Luciano, Mayara Magna de Lima Melo, Ronald Feitosa Pinheiro, Kaio César Simiano Tavares, Gilvan Pessoa Furtado, Claudia Pessoa, Cristiana Libardi Miranda Furtado
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-10 (2021)
Abstract The imprinted H19 long non-coding RNA, a knowing oncofetal gene, presents a controversial role during the carcinogenesis process since its tumor suppressor or oncogenic activity is not completely elucidated. Since H19 lncRNA is involved in m
Externí odkaz:
https://doaj.org/article/fa96d963cb0e487eafea13981072274b
Autor:
Luiz Gustavo Almeida de Carvalho, Tatiana Takahasi Komoto, Daniel Antunes Moreno, João Vitor Caetano Goes, Roberta Taiane Germano de Oliveira, Mayara Magna de Lima Melo, Mariela Estefany Gislene Vera Roa, Paola Gyuliane Gonçalves, Carlos Victor Montefusco-Pereira, Ronald Feitosa Pinheiro, Howard Lopes Ribeiro Junior
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 12, p 10058 (2023)
The aim of this study was to evaluate the expression of USP7, USP15, UBE2O, and UBE2T genes in Myelodysplastic neoplasm (MDS) to identify possible targets of ubiquitination and deubiquitination in MDS pathobiology. To achieve this, eight datasets fro
Externí odkaz:
https://doaj.org/article/1bd3a841a2bf48568b066f9e86312e88
Autor:
Abdullah Mahmood Ali, Yumin Huang, Ronald Feitosa Pinheiro, Fumin Xue, Jingping Hu, Nicholas Iverson, Daniela Hoehn, Diego Coutinho, Jehanzeb Kayani, Brian Chernak, Joseph Lane, Christopher Hillyer, Naomi Galili, Joseph Jurcic, Narla Mohandas, Xiuli An, Azra Raza
Publikováno v:
Blood Advances, Vol 2, Iss 12, Pp 1393-1402 (2018)
Abstract: Anemia is the defining feature in most patients with myelodysplastic syndromes (MDS), yet defects in erythropoiesis have not been well characterized. We examined freshly obtained bone marrow (BM) samples for stage-specific abnormalities dur
Externí odkaz:
https://doaj.org/article/53545c28418145669201fd7942148022
Autor:
Bruno Memória Okubo, Anacélia Gomes de Matos, Howard Lopes Ribeiro Junior, Daniela de Paula Borges, Roberta Taiane Germano de Oliveira, Marilena Facundo de Castro, Manoel Ricardo Alves Martins, Romélia Pinheiro Gonçalves, Pedro Felipe Carvalhedo Bruin, Ronald Feitosa Pinheiro, Silvia Maria Meira Magalhães
Publikováno v:
PLoS ONE, Vol 12, Iss 9, p e0184079 (2017)
BACKGROUND/OBJECTIVES:The ageing process is associated with gradual decline in respiratory system performance. Anemia is highly prevalent among older adults and usually associated with adverse outcomes. Myelodysplastic syndromes (MDS) are a heterogen
Externí odkaz:
https://doaj.org/article/69e77ed526a24084b52fe6547a5ce7b4
Publikováno v:
Revista Brasileira de Cancerologia, Vol 62, Iss 2 (2016)
Introdução: A síndrome mielodisplástica (SMD) é uma doença clonal da célula progenitora hematopoiética apresentando um processo patogênico associado a um evento genético inicial nas células-tronco (lesão no DNA) que leva ao aparecimento d
Externí odkaz:
https://doaj.org/article/a4c484d6aa8941949dc923110776bc86
Publikováno v:
Revista Brasileira de Cancerologia, Vol 60, Iss 1 (2014)
Introdução: Estudos mostram que alterações na expressão de genes relacionados ao fuso mitótico (AURKA e AURKB) e ponto de checagem mitótico (CDC20 e MAD2L1) estão envolvidas na instabilidade cromossômica e progressão da doença em tumores s
Externí odkaz:
https://doaj.org/article/ba0f6285cffd4120a72ca31fc7edec6a
Publikováno v:
Revista Brasileira de Cancerologia, Vol 59, Iss 4 (2013)
Introdução: A síndrome mielodisplásica (SMD) e um grupo de doenças clonais das células tronco hematopoiéticas (HSC) caracterizadas por citopenia periférica, displasia em linhagens mieloides e aumento do risco de desenvolvimento para leucemia
Externí odkaz:
https://doaj.org/article/bbe618e5edde4be5ba5fd5cfff50adab