Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Viviane, Freiberger"'
Autor:
Clarissa M. Comim, Jaime A. Soares, Adriano Alberti, Viviane Freiberger, Letícia Ventura, Paula Dias, Aryadnne L. Schactae, Leoberto R. Grigollo, Amanda V. Steckert, Daniel F. Martins, Rudy J. Nodari Junior, Mariz Vainzof, João Quevedo
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
Autor:
Lilian Leite Fausto, Adriano Alberti, Gabriela Kades, Risoní Pereira Dias de Carvalho, Viviane Freiberger, Leticia Ventura, Paula Dias, Eliton Marcio Zanoni, Ben Hur Soares, Matheus Luchini Dutra, Daniel Fernandes Martins, Clarissa Martinelli Comim
Duchenne muscular dystrophy (DMD) is one of the X-linked recessive progressive muscular dystrophies, characterized by progressive degeneration of skeletal muscle and multisystemic involvement, including the central nervous system (CNS). To investigat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::abbe15a4d5190fcdd535e545371f1583
https://doi.org/10.21203/rs.3.rs-1965435/v1
https://doi.org/10.21203/rs.3.rs-1965435/v1
Autor:
Daniel Martins, Andreza Hoepers, Bruna Becker da Silva, Rudy José Nodari Júnior, Leoberto Ricardo Grigollo, Letícia Ventura, Clarissa M. Comim, Emilio L. Streck, Adriano Alberti, Cristina Salar Andreu, Viviane Freiberger
Publikováno v:
Journal of Molecular Neuroscience. 70:1552-1564
Duchenne muscular dystrophy (DMD) is a condition caused by an amendment to the X chromosome, inherited as a recessive trait, and affects 1:3500 live births, especially males. Low-intensity exercise is known to decrease certain parameters associated w
Autor:
Clarissa M. Comim, Jaime A. Soares, Adriano Alberti, Viviane Freiberger, Letícia Ventura, Paula Dias, Aryadnne L. Schactae, Leoberto R. Grigollo, Amanda V. Steckert, Daniel F. Martins, Rudy J. Nodari Junior, Mariz Vainzof, João Quevedo
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c8a45cf40d1bbd8071aa23ee79214db7
Autor:
Matheus Luchini Dutra, Paula Dias, Viviane Freiberger, Leticia Ventura, Clarissa Martinelli Comim, Daniel Fernandes Martins, Franciane Bobinski
Publikováno v:
Neuroscience Letters. 793:136974
Prenatal factors such as viral or bacterial infections occurring mainly during the first trimesters of pregnancy can increase the incidence of autism spectrum disorder (ASD) in children. In an animal model, it is already known that maternal immune ac
Autor:
Letícia Ventura, Matheus L Dutra, Viviane Freiberger, Daiane Bragagnolo, Verônica V. Horewicz, Clarissa M. Comim, Paula Dias
Publikováno v:
BioMed Research International
BioMed Research International, Vol 2019 (2019)
BioMed Research International, Vol 2019 (2019)
The neonatal immune system is still immature, which makes it more susceptible to the infectious agents. Neonatal immune activation is associated with increased permeability of the blood-brain barrier, causing an inflammatory cascade in the CNS and al
Autor:
Adriano Alberti, Leoberto Ricardo Grigollo, Priscila Mantovani Nocetti, Daniel Martins, Viviane Freiberger, Cristina Salar Andreau, Letícia Ventura, Clarissa M. Comim, Rudy José Nodari Júnior
Duchenne muscular dystrophy (DMD) is a genetic disease, which is associated to progressive skeletal muscle degeneration. In humans, DMD has early onset, causes developmental delays, and is a devastating disease that drastically diminishes the quality
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::613f1c4595fe965a32bec0f56467dae0
https://doi.org/10.21203/rs.3.rs-496821/v1
https://doi.org/10.21203/rs.3.rs-496821/v1
Autor:
Clarissa M, Comim, Jaime A, Soares, Adriano, Alberti, Viviane, Freiberger, Letícia, Ventura, Paula, Dias, Aryadnne L, Schactae, Leoberto R, Grigollo, Amanda V, Steckert, Daniel F, Martins, Rudy J Nodari, Junior, Mariz, Vainzof, João, Quevedo
Publikováno v:
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical NeurophysiologyReferences. 43(7)
Congenital Muscular Dystrophy type 1D (MDC1D) is characterized by a hypoglycosylation of α-dystroglycan protein (α-DG), and this may be strongly implicated in increased skeletal muscle tissue degeneration and abnormal brain development, leading to
Autor:
Gracielle Fin, Letícia Ventura, Leoberto Ricardo Grigollo, Ben Hur Soares, Paula Dias, Adriano Alberti, Fabiana Schuelter-Trevisol, Gislaine T. Rezin, Josiane Aparecida de Jesus, Carina Rossoni, Fabiane Pertille, Clarissa M. Comim, Fabiana Meneghetti Dallacosta, Eliane Traebert, Betine Pinto Moehlecke Iser, Rudy José Nodari Júnior, Viviane Freiberger, Bruna Becker da Silva
Publikováno v:
World Journal of Clinical Cases
At the end of 2019, a new disease with pandemic potential appeared in China. It was a novel coronavirus called coronavirus disease 2019 (COVID-19). Later, in the first quarter of 2020, the World Health Organization declared the outbreak of this disea
Autor:
Bruna Becker da Silva, Matheus L Dutra, Aline D Schlindwein, Letícia Ventura, Paula Dias, Viviane Freiberger, Clarissa M. Comim, Vinicius B Thiesen
Publikováno v:
Acta neuropsychiatrica. 32(6)
Objective:To evaluate the involvement of nod-like receptor pyrin domain-containing protein 3 (NLRP3) inflammasome in schizophrenia-like behaviour in young animals exposed to maternal immune activation (MIA).Methods:To this aim, on the 15th gestationa