Zobrazeno 1 - 10
of 112
pro vyhledávání: '"E. A. Gregorio"'
'Prion-like' seeding and propagation of oligomeric protein assemblies in neurodegenerative disorders
Publikováno v:
Frontiers in Neuroscience, Vol 18 (2024)
Intra- or extracellular aggregates of proteins are central pathogenic features in most neurodegenerative disorders. The accumulation of such proteins in diseased brains is believed to be the end-stage of a stepwise aggregation of misfolded monomers t
Externí odkaz:
https://doaj.org/article/c1e48e850d5b47848ab565dc12d52b9e
Publikováno v:
Memorias do Instituto Oswaldo Cruz, Vol 87, Iss 3, Pp 375-380 (1992)
We studied the ultrastructural aspects of pre-pupae and pupae ovaries of Dermatobia hominis. Physiological degeneration of gonial cells was observed: (a) after the ovarioles differentiation, in the oogonia residing in the apical region of the ovary;
Externí odkaz:
https://doaj.org/article/96284cdd6beb40348cf36a658747ca87
Publikováno v:
Memorias do Instituto Oswaldo Cruz, Vol 85, Iss 3, Pp 305-313 (1990)
The ultrastructure and distribution of gonial and somatic cells in the ovary of Dermatobia hominis was studied during the 3rd larval instar. In larvae weighing between 400 and 500 mg, the ovary is partially divided into basal and apical regions by ob
Externí odkaz:
https://doaj.org/article/350bbafe867a45cb8f38b12ab7c600af
Autor:
S. E. Burruel-Ibarra, R. A. Esquer-Osuna, R. G. Valdez-Melchor, D. A. Cuevas-Acu馻, L. QuihuiCota, J. Ju醨ez, J. C. Campos-Garc韆, E. Valbuena-Gregorio, M. A. L髉ez-Mata
Publikováno v:
Journal of Renewable Materials. 11:2647-2663
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ab2083940388a99c80cb9077741d0fd6
https://doi.org/10.32604/jrm.2023.027372
https://doi.org/10.32604/jrm.2023.027372
Autor:
Maria Chiara De Santis, L. Gozzelino, E. Ratto, J. Margaria, A. Costamagna, F. Gulluni, E. Di Gregorio, E. Mina, N. Lorito, M. Bacci, R. Lattanzio, G. Sala, P. Cappello, F. Novelli, C. Vicentini, E. Giovannetti, V. Corbo, A. Scarpa, P. Porporato, A. Morandi, E. Hirsch, M. Martini
Publikováno v:
Pancreatology. 22:e76-e77
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0ce66035e1fc0e9011032e4cecffb513
https://doi.org/10.1016/j.pan.2022.06.198
https://doi.org/10.1016/j.pan.2022.06.198
Autor:
O. Beltrán, M. Luna, E. Valbuena-Gregorio, R. G. Valdez-Melchor, S. E. Burruel-Ibarra, L. Quihui-Cota, S. Ruiz-Cruz, J. Juárez, M. A. López-Mata
Publikováno v:
Materials Research v.25 2022
Materials research (São Carlos. Online)
Universidade Federal de São Carlos (UFSCAR)
instacron:ABM ABC ABPOL
Materials Research, Volume: 25, Article number: e20210534, Published: 04 APR 2022
Materials research (São Carlos. Online)
Universidade Federal de São Carlos (UFSCAR)
instacron:ABM ABC ABPOL
Materials Research, Volume: 25, Article number: e20210534, Published: 04 APR 2022
Interest in developing novel wound dressings with antibacterial properties elaborated from natural sources continues to grow. In this study, a Tween-80 (T80)-stabilized carvacrol (CAR) emulsion was incorporated into pectin (PEC) membranes at 0 (contr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b622704fde013c748ef283578bae6040
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1516-14392022000100304
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1516-14392022000100304
The MATR3 gene encoding the protein Matrin3 is implicated in the pathogenesis of the neurodegenerative disease amyotrophic lateral sclerosis (ALS). Matrin3 forms neuronal cytoplasmic and nuclear inclusions in ALS-affected neurons. Additionally, 13 he
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e46c2a5c8dd41fbbe530b9c366a51d3d
https://doi.org/10.1101/2021.08.24.457481
https://doi.org/10.1101/2021.08.24.457481
Autor:
Marilene H. Lopes, Lilian Tsai-Wei Lin, Marco A. M. Prado, Abdul Razzaq, Soojie Hong, Martin L. Duennwald, Brendan Charles, Flavio H. Beraldo, Sonja E. Di Gregorio, Vania F. Prado
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
Protein misfolding is a central feature of most neurodegenerative diseases. Molecular chaperones can modulate the toxicity associated with protein misfolding, but it remains elusive which molecular chaperones and co-chaperones interact with specific
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1cc91e78995ebfef9eb2e05f878979c0
Autor:
A. Esposito, A. Migliaccio, C. Tupini, D. D’Alonzo, I. Lampronti, A. Bragonzi, M.C. Dechecchi, E. De Gregorio, A. Guaragna
Publikováno v:
Journal of Cystic Fibrosis. 21:S51
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::967ca330029f9ca32bc21a76cd1c0eb5
https://doi.org/10.1016/s1569-1993(22)00305-8
https://doi.org/10.1016/s1569-1993(22)00305-8