Zobrazeno 1 - 10
of 19
pro vyhledávání: '"João C S, Bizario"'
Autor:
Flavia Ismael, Beatriz Zaramella, Tatiane Battagin, João C. S. Bizario, Júlia Gallego, Victoria Villela, Lilian Bezerra de Queiroz, Fabio E. Leal, Julio Torales, Antonio Ventriglio, Megan E. Marziali, Priscila D. Gonçalves, Silvia S. Martins, João M. Castaldelli-Maia
Publikováno v:
Frontiers in Public Health, Vol 9 (2021)
Externí odkaz:
https://doaj.org/article/c843f152f5ff461086d5d452aa0ed209
Autor:
Flavia Ismael, Beatriz Zaramella, Tatiane Battagin, João C. S. Bizario, Júlia Gallego, Victoria Villela, Lilian Bezerra de Queiroz, Fabio E. Leal, Julio Torales, Antonio Ventriglio, Megan E. Marziali, Priscila D. Gonçalves, Silvia S. Martins, João M. Castaldelli-Maia
Publikováno v:
Frontiers in Public Health, Vol 9 (2021)
Background: There is a need for prospective studies investigating substance use variations in mild COVID-19 patients. These individuals represent the majority of patients affected by the disease and are routinely treated at home, facing periods of qu
Externí odkaz:
https://doaj.org/article/35a6906813af4fe2a30af4dcbdd65d8a
Autor:
Marcelo Dias-Baruffi, Luis Garcia, Clementina Sitzia, Chiara Villa, Andrea Farini, João C. S. Bizario, Mirella Meregalli, P. Razini, Pamela Bella, Marzia Belicchi, Yvan Torrente, Letizia Cassinelli, L. Jardim, Daniele Parolini, Silvia Erratico
Publikováno v:
Molecular therapy : the journal of the American Society of Gene Therapy. 24(11)
Duchenne muscular dystrophy is the most common genetic muscular dystrophy. It is caused by mutations in the dystrophin gene, leading to absence of muscular dystrophin and to progressive degeneration of skeletal muscle. We have demonstrated that the e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::02033133fd9aa84a0ffb3589da6725b9
https://pubmed.ncbi.nlm.nih.gov/27506452
https://pubmed.ncbi.nlm.nih.gov/27506452
Autor:
João C. S. Bizario, Simon P. Quenneville, Pierre Chapdelaine, Jean-Christophe Dominique, Daniel Giuliano Cerri, Christophe Pichavant, Jacques P. Tremblay, Daniel Skuk, Joe N. Kornegay, Xiao Xiao
Publikováno v:
Molecular Therapy. 18:1002-1009
Duchenne muscular dystrophy (DMD) is characterized by the absence of dystrophin. Several previous studies demonstrated the feasibility of delivering microdystrophin complementary DNA (cDNA) into mouse and normal nonhuman primate muscles by ex vivo ge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::543dda6ff8455dc315efd0cffcfc68b1
https://doi.org/10.1038/mt.2010.23
https://doi.org/10.1038/mt.2010.23
Autor:
Juliana Caldas Ribeiro, Lilian Cataldi Rodrigues, M. C. R. Costa, Paula Sakemi Fukuhara, Fabíola Attié de Castro, Gislane Lelis Vilela de Oliveira, João C. S. Bizario, Daniel Giuliano Cerri, Auro Nomizo, Daniela Dover de Araújo
Publikováno v:
Journal of Neuroimmunology. 212:93-101
Myofiber degeneration, inflammation, and fibrosis are remarkable features of Duchenne muscular dystrophy. We hypothesized that the administration of imatinib mesylate, an inhibitor of tyrosine kinase and TGF-beta pro-fibrogenic activity, could improv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b1bec0274aabdd667fe381e1cc657d86
https://doi.org/10.1016/j.jneuroim.2009.05.006
https://doi.org/10.1016/j.jneuroim.2009.05.006
Autor:
M. C. R. Costa, Mariana C. Coelho, Sibere R. Oliveira, Daniel Giuliano Cerri, Sean R. Stowell, João C. S. Bizario, Richard D. Cummings, Daniela Dover de Araújo, Lilian Cataldi Rodrigues, Marcelo Dias-Baruffi
Publikováno v:
Glycobiology. 18:842-850
Muscle degenerative diseases such as Duchenne Muscular Dystrophy are incurable and treatment options are still restrained. Understanding the mechanisms and factors responsible for muscle degeneration and regeneration will facilitate the development o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b3a515db5eecd90b41d6192dcf7bf00c
https://doi.org/10.1093/glycob/cwn079
https://doi.org/10.1093/glycob/cwn079
Autor:
Erasmo Barbante Casella, Cristina Miuki Abe Jacob, Fabíola Attié de Castro, Gaël Ménasché, João C. S. Bizario, Lilian Maria Cristofani, Júlio César Voltarelli, Geneviève de Saint-Basile, Jérôme Feldmann, Enilza Maria Espreáfico
Publikováno v:
Journal of Clinical Immunology. 24:397-410
Griscelli syndrome (GS) is caused by mutations in the MYO5A (GS1), RAB27A (GS2), or MLPH (GS3) genes, all of which lead to a similar pigmentary dilution. In addition, GS1 patients show primary neurological impairment, whereas GS2 patients present imm
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aaa9829334338737052d0a0e20ce7da8
https://doi.org/10.1023/b:joci.0000029119.83799.cb
https://doi.org/10.1023/b:joci.0000029119.83799.cb
Autor:
Márika K. Oliveira, Alexandre D. Damião, Patricia Vianna Bonini Palma, Roy E. Larson, Enilza Maria Espreáfico, Júlio C. Voltarelli, Josane F. Sousa, Fabíola Attié de Castro, Rafael N. Fernandes, João C. S. Bizario
Publikováno v:
Journal of Leukocyte Biology. 71:195-204
Myosin-V is involved in organelle and vesicle trafficking inSaccharomyces cerevisiae and in other eukaryotic cells from yeast to human. In the present study, we determined by FACS that the major subpopulations of the peripheral blood mononuclear cell
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d873a33168a19f00d0d4d9a799d17587
https://doi.org/10.1189/jlb.71.2.195
https://doi.org/10.1189/jlb.71.2.195
Autor:
João C S, Bizario, Fabíola A, Castro, Josane F, Sousa, Rafael N, Fernandes, Alexandre D, Damião, Márika K, Oliveira, Patrícia V B, Palma, Roy E, Larson, Júlio C, Voltarelli, Enilza M, Espreafico
Publikováno v:
Journal of leukocyte biology. 71(2)
Myosin-V is involved in organelle and vesicle trafficking in Saccharomyces cerevisiae and in other eukaryotic cells from yeast to human. In the present study, we determined by FACS that the major subpopulations of the peripheral blood mononuclear cel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::df8832fc83fd10e236b0082ec8ad5332
https://pubmed.ncbi.nlm.nih.gov/11818439
https://pubmed.ncbi.nlm.nih.gov/11818439
Autor:
Karin Krogh, Joseph S. Wolenski, João C. S. Bizario, Vasiliki Tsakraklides, Enilza Maria Espreáfico, Lillian Wang, Roy E. Larson
Publikováno v:
Journal of cell science. 112
Class-V myosins are two-headed actin-based mechanoenzymes that function in the transport and subcellular localization of organelles and possibly in the outgrowth of cellular processes. To determine which domains of myosin-V are involved in intracellu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aefffb1ad667d06bcb7821914f5aacfc
https://pubmed.ncbi.nlm.nih.gov/10444380
https://pubmed.ncbi.nlm.nih.gov/10444380