Zobrazeno 1 - 10
of 21
pro vyhledávání: '"N-sulfoglucosamine sulfohydrolase"'
Autor:
Joaquin Seras‐Franzoso, Zamira V. Díaz‐Riascos, José Luis Corchero, Patricia González, Natalia García‐Aranda, Mònica Mandaña, Roger Riera, Ana Boullosa, Sandra Mancilla, Alba Grayston, Marc Moltó‐Abad, Elena Garcia‐Fruitós, Rosa Mendoza, Guillem Pintos‐Morell, Lorenzo Albertazzi, Anna Rosell, Josefina Casas, Antonio Villaverde, Simó Schwartz Jr, Ibane Abasolo
Publikováno v:
Journal of Extracellular Vesicles, Vol 10, Iss 5, Pp n/a-n/a (2021)
Abstract In the present study the use of extracellular vesicles (EVs) as vehicles for therapeutic enzymes in lysosomal storage disorders was explored. EVs were isolated from mammalian cells overexpressing alpha‐galactosidase A (GLA) or N‐sulfoglu
Externí odkaz:
https://doaj.org/article/017c9b6b0e7544dbad5fbbce1391a4b6
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 5, Iss C, Pp 60-62 (2015)
Deficient N-sulfoglucosamine sulfohydrolase (SGSH) enzyme activity causes mucopolysaccharidosis (MPS) type IIIA. A fluorimetric SGSH activity assay is commonly used to examine patient cells. Here, we modified this method for brain homogenates and def
Externí odkaz:
https://doaj.org/article/e35af6316e95450f90480b5c0a4939dd
Autor:
Rosa Mendoza, Zamira V. Díaz-Riascos, Sandra Mancilla, Lorenzo Albertazzi, Natalia García-Aranda, Ana Boullosa, Antonio Villaverde, Monica Mandaña, Patricia González, Ibane Abasolo, Anna Rosell, Guillem Pintos-Morell, José Luis Corchero, Josefina Casas, Simó Schwartz, Alba Grayston, Joaquin Seras-Franzoso, Roger Riera, Elena García-Fruitós, Marc Moltó-Abad
Publikováno v:
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
Journal of Extracellular Vesicles, Vol 10, Iss 5, Pp n/a-n/a (2021)
Scientia
Journal of Extracellular Vesicles
Digital.CSIC. Repositorio Institucional del CSIC
instname
Universitat Autònoma de Barcelona
Journal of Extracellular Vesicles, Vol 10, Iss 5, Pp n/a-n/a (2021)
Scientia
Journal of Extracellular Vesicles
Digital.CSIC. Repositorio Institucional del CSIC
instname
In the present study the use of extracellular vesicles (EVs) as vehicles for therapeutic enzymes in lysosomal storage disorders was explored. EVs were isolated from mammalian cells overexpressing alpha‐galactosidase A (GLA) or N‐sulfoglucosamine
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::702cb6a58bfe0e56afbde20b3d5154b2
http://hdl.handle.net/10261/234882
http://hdl.handle.net/10261/234882
Autor:
Nicole Muschol, Marcel du Moulin, Luise Ammer, Anja Köhn, Cornelia Rudolph, Sarah Kabisch, Lorenz Grigull
Publikováno v:
Molecular Genetics and Metabolism Reports
Molecular Genetics and Metabolism Reports, Vol 23, Iss, Pp-(2020)
Molecular Genetics and Metabolism Reports, Vol 23, Iss, Pp-(2020)
Background Mucopolysaccharidosis type IIIA (MPS IIIA, Sanfilippo A syndrome) is a chronic progressive neurodegenerative storage disorder caused by a deficiency of lysosomal sulfamidase. The clinical hallmarks are sleep disturbances, behavioral abnorm
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a778c89879896cc236478fb88a53708d
http://europepmc.org/articles/PMC7093801
http://europepmc.org/articles/PMC7093801
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 22, Iss, Pp-(2020)
Molecular Genetics and Metabolism Reports
Molecular Genetics and Metabolism Reports
Mucopolysaccharidosis III A (MPS IIIA) is an autosomal recessive lysosomal storage disorder caused by deficiency of the enzyme sulfamidase. The disorder results in accumulation of heparan sulfate, lysosomal enlargement and cellular and organ dysfunct
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ea5926859a8eba56927ab317fa4978ed
http://www.sciencedirect.com/science/article/pii/S221442691930196X
http://www.sciencedirect.com/science/article/pii/S221442691930196X
Autor:
Hideto Morimoto, Kazuki Miyauchi, Atsushi Imakiire, Satowa Tanaka, Jun Ito, Kohtaro Minami, Shinji Kakimoto, Hiroyuki Sonoda, Sachiho Kida, Tohru Hirato, Yuri Koshimura
Publikováno v:
Molecular Genetics and Metabolism. 132:S105-S106
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::12111ad8b3ec69a33bd12e2d47d426eb
https://doi.org/10.1016/j.ymgme.2020.12.258
https://doi.org/10.1016/j.ymgme.2020.12.258
Akademický článek
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Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 5, Iss C, Pp 60-62 (2015)
Deficient N-sulfoglucosamine sulfohydrolase (SGSH) enzyme activity causes mucopolysaccharidosis (MPS) type IIIA. A fluorimetric SGSH activity assay is commonly used to examine patient cells. Here, we modified this method for brain homogenates and def
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b149468e3d565d7ed16f840bc0e7f375
Publikováno v:
Molecular Genetics and Metabolism Reports
Deficient N-sulfoglucosamine sulfohydrolase (SGSH) enzyme activity causes mucopolysaccharidosis (MPS) type IIIA. A fluorimetric SGSH activity assay is commonly used to examine patient cells. Here, we modified this method for brain homogenates and def
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6ded4dcc975fb4ff590704494f166dcc
https://pubmed.ncbi.nlm.nih.gov/28652977
https://pubmed.ncbi.nlm.nih.gov/28652977