Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Nedel Sant'Ana A"'
Autor:
Vitória Brum da Silva Nunes, Camila Kehl Dias, Juliete Nathali Scholl, Alexia Nedel Sant’Ana, Amanda de Fraga Dias, Mariela Granero Farias, Ana Paula Alegretti, Monalisa Sosnoski, Liane Esteves Daudt, Mariana Bohns Michalowski, Ana Maria Oliveira Battastini, Alessandra Aparecida Paz, Fabrício Figueiró
Publikováno v:
Discover Oncology, Vol 13, Iss 1, Pp 1-15 (2022)
Abstract Purpose Although risk-stratified chemotherapy regimens improve B-cell acute lymphoblastic leukemia (B-ALL) clinical outcome, relapse occurs in a significant number of cases. The identification of new therapeutic targets as well as prognostic
Externí odkaz:
https://doaj.org/article/3a581ca919d8488aa265a987c716ea9d
Autor:
Alexia Nedel Sant'Ana, Anelise Bergmann Araújo, Ana Helena da Rosa Paz, Fabiany da Costa Gonçalves
Publikováno v:
Repositório Institucional da UFRGS
Universidade Federal do Rio Grande do Sul (UFRGS)
instacron:UFRGS
World Journal of Stem Cells, 13(9), 1160-1176. Baishideng Publishing Group
World Journal of Stem Cells
Universidade Federal do Rio Grande do Sul (UFRGS)
instacron:UFRGS
World Journal of Stem Cells, 13(9), 1160-1176. Baishideng Publishing Group
World Journal of Stem Cells
Mesenchymal stromal cells (MSCs) are multipotent and self-renewing stem cells that have great potential as cell therapy for autoimmune and inflammatory disorders, as well as for other clinical conditions, due to their immunoregulatory and regenerativ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c39ebb305d1caddce655fe4c79a07ae
Autor:
Fernanda Sales Luiz Vianna, Alexia Nedel Sant'Ana, Ana Paula Pizzio Becker, Fernanda Hendges de Bitencourt, Carmen Regla Vargas, Dévora N Randon, Fernanda Sperb-Ludwig, Angela Sitta, Ida Vanessa Doederlein Schwartz
Publikováno v:
Genetics and Molecular Biology, Vol 43, Iss 3 (2020)
Genetics and Molecular Biology
Genetics and Molecular Biology
Citrullinemia type 1 (CTLNI), long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency (LCHADD), and mut0 methylmalonic acidemia (mut0 MMA) are inborn errors of metabolism (IEMs) associated with sudden unexpected death in infancy (SUDI). Its most common
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