Zobrazeno 1 - 10
of 26
pro vyhledávání: '"P.C.G. Onofre-Oliveira"'
Autor:
Jonathan R. Volpatti, James J. Dowling, Hernan Gonorazky, Alper Celik, P.C.G. Onofre-Oliveira, Nika Maani, Ege Sarikaya, Nesrin Sabha
X-linked myotubular myopathy is a severe monogenetic disorder of the skeletal muscle caused by loss of expression/function mutations in theMTM1(myotubularin) gene. There is a growing understanding of the pathologic and molecular abnormalities associa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::826c4e64e7315864f888fdec189c5899
https://doi.org/10.1101/2021.10.11.463940
https://doi.org/10.1101/2021.10.11.463940
Autor:
Mariz Vainzof, P.C.G. Onofre-Oliveira
Publikováno v:
Methods in Molecular Biology ISBN: 9781071601372
The study of the population of muscle satellite cells (SC) is important to understand muscle regeneration and its involvement in the different dystrophic processes. We studied two dystrophic mouse models, Largemyd and Lama2dy2j/J, that show an intens
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2422ec333a326d36a59479e94c236ac4
https://doi.org/10.1007/978-1-0716-0138-9_13
https://doi.org/10.1007/978-1-0716-0138-9_13
Autor:
Antonio Fernando Ribeiro, Stephanie A. Fernandes, Mariz Vainzof, A.L.F. Santos, Lucas Santos Souza, Camila F. Almeida, P.C.G. Onofre-Oliveira, Danielle A. Guerrieri, Renata Ishiba
Publikováno v:
Scientific Reports
Scientific Reports, Vol 9, Iss 1, Pp 1-11 (2019)
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Scientific Reports, Vol 9, Iss 1, Pp 1-11 (2019)
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Satellite cells (SCs) are the main muscle stem cells responsible for its regenerative capacity. In muscular dystrophies, however, a failure of the regenerative process results in muscle degeneration and weakness. To analyze the effect of different de
Autor:
P.C.G. Onofre-Oliveira, M. Garcia-Castaneda, Jonathan R. Volpatti, Robert T. Dirksen, Stephanie Brennan, James J. Dowling, Nesrin Sabha, A. Michelucci, Linda Groom
Publikováno v:
Neuromuscular Disorders. 29:S136
Autor:
Antonio Fernando Ribeiro, Camila F. Almeida, D. Ayub-Guerrieri, P.C.G. Onofre-Oliveira, A.L.F. Santos, Stephanie A. Fernandes, Mariz Vainzof, Renata Ishiba, P. Calyjur
Publikováno v:
PLoS ONE, Vol 11, Iss 3, p e0150748 (2016)
PLoS ONE
PLoS ONE
The mdx mouse is a good genetic and molecular murine model for Duchenne Muscular Dystrophy (DMD), a progressive and devastating muscle disease. However, this model is inappropriate for testing new therapies due to its mild phenotype. Here, we transfe
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 genetically determined muscular dystrophies are caused by mutations in genes coding for muscle proteins. Differences in the phenotypes are mainly the age of onset and velocity of progression. Muscle weakness is the consequence of myofiber degener
Autor:
Mariz Vainzof, P.C.G. Onofre-Oliveira, Stephanie A. Fernandes, Camila F. Almeida, Vincent Mouly, Anne Bigot
Publikováno v:
Neuromuscular Disorders. 26:S194
Autor:
V.F. Lopes, D. Ayub-Guerrieri, Lygia da Veiga Pereira, Camila F Almeida, Poliana C. M. Martins-Machado, Mariz Vainzof, P.C.G. Onofre-Oliveira
Danielle Ayub-Guerrieri1, Poliana C. M. Martins-Machado1, Paula C.G. Onofre-Oliveira1, Lygia V. Pereira2, Camila F. Almeida1, Vanessa F. Lopes1 and Mariz Vainzof1 1Laboratory of Muscle Proteins and Comparative Histopathology, Human Genome Research Ce
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f24d8b1850f5a436f2a075c5533879aa
https://doi.org/10.5772/24598
https://doi.org/10.5772/24598
Autor:
Camila F. Almeida, Monize Lazar, L.U. Yamamoto, Guilherme L. Yamamoto, P.C.G. Onofre-Oliveira, Helga Cristina Almeida da Silva, Mayana Zatz, L. Nogueira, Mariz Vainzof
Publikováno v:
Neuromuscular Disorders. 24:834-835
X-linked myopathy with excessive autophagy (XMEA) is an inherited, slowly progressive myopathy, characterized by membrane-bound sarcoplasmic vacuoles in muscle fibers. Proximal muscle weakness in early childhood is observed, but with no cardiac, nor
Autor:
Antonio Carlos dos Santos, P.C.G. Onofre-Oliveira, P. Calyjur, Camila F. Almeida, Mariz Vainzof
Publikováno v:
Neuromuscular Disorders. 25:S291