Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Isabel Cristina Chagas Barbin"'
Autor:
Rafaela Benatti de Oliveira, Isabel Cristina Chagas Barbin, Henrique Salustiano Silva, Ana Carolina Castro Curado, Marcia Cristina Aparecida Thomaz
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::93b45f98cdd3d79faea2101d71f9b218
https://doi.org/10.22533/at.ed.63319110313
https://doi.org/10.22533/at.ed.63319110313
Autor:
Maria Julia Marques, Isabel Cristina Chagas Barbin, Humberto Santo Neto, Juliano Alves Pereira, Matheus Bersan Rovere, Drielen de Oliveira Moreira
Publikováno v:
Journal of Anatomy. 228:784-791
We examined the effects of exercise on diaphragm degeneration and cardiomyopathy in dystrophin-deficient mdx mice. Mdx mice (11 months of age) were exercised (swimming) for 2 months to worsen diaphragm degeneration. Control mdx mice were kept sedenta
Autor:
Maria Julia Marques, H. Santo Neto, Isabel Cristina Chagas Barbin, Daniela Silva Oggian, Ana Paula Tiemi Taniguti, Renato Ferretti
Publikováno v:
Acta Biologica Hungarica. 61:168-174
Cardiac failure secondary to myocardial fibrosis (MF) significantly contributes to death in Duchenne muscular dystrophy (DMD), a fatal form of muscle disease. In aging, the mdx mice, an animal model of DMD, MF is similar to that observed in humans. N
Autor:
Maria Julia Marques, Daniella Silva Oggiam, Humberto Santo Neto, Renato Ferretti, Isabel Cristina Chagas Barbin
Publikováno v:
Muscle & Nerve. 40:466-468
We evaluated the effects of long-term administration of deflazacort (DFZ) on the progression of myocardial fibrosis in mdx mice. Mdx mice (6 months old) were treated with DFZ for 15 months. Myocardial fibrosis (MF) was evaluated by histomorphometric
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
Orientador: Humberto Santo Neto Dissertação (mestrado) - Universidade Estadual de Campinas, Instituto de Biologia Resumo: A Distrofia Muscular de Duchenne (DMD) é uma miopatia caracterizada pela ausência de distrofina, uma proteína estrutural da
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::927d6c01cb28494cf4677551c43d37c3