Frederico Alisson da Silva

Instituição:

Universidade Federal do Rio de Janeiro

Centro:

Centro de Ciências da Saúde

Unidade:

Instituto de Microbiologia

Departamento:

Departamento de Imunologia/IM

School of Medicine - University of California San Diego
Glicobiologia | Doutorado | 2012 - 2012

Universidade Federal do Rio de Janeiro
Ciências Biológicas (Biofísica) | Doutorado | 2009 - 2013

Universidade Federal do Rio de Janeiro
Ciências Biológicas (Biofísica) | Mestrado | 2007 - 2009

Universidade Federal do Rio de Janeiro
Ciências Biológicas: Microbiologia e Imunologia | Graduação | 2003 - 2006

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Titulo	DOI	Ano
CD43 sialoglycoprotein modulates cardiac inflammation and murine susceptibility to Trypanosoma cruzi infection	10.1038/s41598-019-45138-7	2019
Cellular glycosylation senses metabolic changes and modulates cell plasticity during EMT	10.1002/dvdy.24553	2018
Emerging role of glycosylation in the polarization of tumor-associated macrophages	10.1016/j.phrs.2019.104285	2019
Evidences for the involvement of cell surface glycans in stem cell pluripotency and differentiation	10.1093/glycob/cwu012	2014
GM2/GM3 controls the organizational status of CD82/Met microdomains: further studies in GM2/GM3 complexation	10.1007/s10719-022-10061-z	2022
Gut bacteria responding to dietary change encode sialidases that exhibit preference for red meat-associated carbohydrates	10.1038/s41564-019-0564-9	2019
Human evolutionary loss of epithelial Neu5Gc expression and species-specific susceptibility to cholera	10.1371/journal.ppat.1007133	2018
Human risk of diseases associated with red meat intake: Analysis of current theories and proposed role for metabolic incorporation of a non-human sialic acid	10.1016/j.mam.2016.07.002	2016
Hyperglycemia alters N-glycans on colon cancer cells through increased production of activated monosaccharides	10.1007/s10719-022-10057-9	2022
Increase of O-Glycosylated Oncofetal Fibronectin in High Glucose-Induced Epithelial-Mesenchymal Transition of Cultured Human Epithelial Cells	10.1371/journal.pone.0060471	2013

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Titulo	DOI	Ano
A incorporação do ácido siálico exógeno Neu5Gc modula a via de sinalização de EGF/EGFR em células de carcinoma de cólon humano		2021
Absence of CD43 modulates immune response and compromise T cells homing to heart during Trypanosoma cruzi infection		2008
Alteration of CD8+ cell surface sialylation by trans-sialidase activity during Trypanosoma cruzi infection		2008
CD43 interaction with actin regulatory proteins regulates T cell trafficking to cardiac tissue during Trypanosoma cruzi infection		2011
Dietary intake of non-human sialic acid Neu5Gc promotes tumor growth in human-like mouse models of colorectal cancer.		2014
Effects of the active and inactive trans-sialidase of Trypanosoma cruzi on the coestimulation and traffic of t cells in vivo		2006
Effects of trans-sialidase on the stimulation and traffic of T cells during Trypanosoma cruzi infection		2006
Glycophotype analysis of induced pluripotent stem cells generated from menstrual blood-derived mesenchymal cells		2011
HIPERGLICEMIA E PROGRESSÃO TUMORAL NO CÂNCER DE CÓLON		2021
Inactive trans-sialidase from Trypanosoma cruzi binds to CD43 and activates humam neutrophils trough ERK pathway		2005

Exibindo 1 a 10 de 29 resultados