Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Hallana Souza Santos"'
Autor:
Fabiano de Oliveira Poswar, Hallana Souza Santos, Angela Barreto Santiago Santos, Solano Vinicius Berger, Carolina Fischinger Moura de Souza, Roberto Giugliani, Guilherme Baldo
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 8 (2022)
Background: Cardiovascular involvement is among the main features of MPS disorders and it is also a significant cause of morbidity and mortality. The range of manifestations includes cardiac valve disease, conduction abnormalities, left ventricular h
Externí odkaz:
https://doaj.org/article/353071d14208452c8583cc3bafdb241e
Autor:
Edina Poletto, Roselena Silvestri Schuh, Eduardo C. Filippi-Chiela, Luiza Rodrigues, Luisa Natalia Pimentel Vera, Hallana Souza Santos, Guilherme Baldo, Lia Bruschi
Publikováno v:
Current Gene Therapy. 21:406-430
Gene therapy is a technique that aims at the delivery of nucleic acids to cells, to obtain a therapeutic effect. In situ gene therapy consists of the administration of the gene product to a specific site. It possesses several advantages, such as the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f26dee9827d621a32348a0d3c14f3599
https://doi.org/10.2174/1566523221666210504103323
https://doi.org/10.2174/1566523221666210504103323
Publikováno v:
Progress in molecular biology and translational science. 182
Mucopolysaccharidoses (MPS) and mucolipidoses (ML) are disorders that alter lysosome function. While MPS are caused by mutation in enzymes that degrade glycosaminoglycans, the ML are disorders characterized by reduced function in the phosphotransfera
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2f05e03866eba52a623b4df616ca64c8
https://pubmed.ncbi.nlm.nih.gov/34175047
https://pubmed.ncbi.nlm.nih.gov/34175047
Autor:
Roselena Silvestri Schuh, Edina Poletto, Hallana Souza Santos, Ursula da Silveira Matte, Guilherme Baldo
Publikováno v:
Progress in Molecular Biology and Translational Science ISBN: 9780323853019
Mucopolysaccharidoses (MPS) and mucolipidoses (ML) are disorders that alter lysosome function. While MPS are caused by mutation in enzymes that degrade glycosaminoglycans, the ML are disorders characterized by reduced function in the phosphotransfera
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d0f98e6985b0ef7fd3a135511fc48eb2
https://doi.org/10.1016/bs.pmbts.2021.01.026
https://doi.org/10.1016/bs.pmbts.2021.01.026
