Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Paige C. Amendum"'
Autor:
Paige C. Amendum, Shaukat Khan, Seiji Yamaguchi, Hironori Kobayashi, Yasuhiko Ago, Yasuyuki Suzuki, Betul Celik, Estera Rintz, Jobayer Hossain, Wendi Xiao, Shunji Tomatsu
Publikováno v:
Diagnostics, Vol 11, Iss 9, p 1563 (2021)
Glycosaminoglycans (GAGs) are present in proteoglycans, which play critical physiological roles in various tissues. They are known to be elevated in mucopolysaccharidoses (MPS), a group of rare inherited metabolic diseases in which the lysosomal enzy
Externí odkaz:
https://doaj.org/article/87569f724e1a49779bed1f799c7e0d32
Publikováno v:
Methods in Molecular Biology ISBN: 9781071629451
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a1ddbabcf0c9c1befb950409b10fde42
https://doi.org/10.1007/978-1-0716-2946-8_1
https://doi.org/10.1007/978-1-0716-2946-8_1
Autor:
Matthew Piechnik, Paige C. Amendum, Kazuki Sawamoto, Molly Stapleton, Shaukat Khan, Nidhi Fnu, Victor Álvarez, Angelica Maria Herreño Pachon, Olivier Danos, Joseph T. Bruder, Subha Karumuthil-Melethil, Shunji Tomatsu
Publikováno v:
International Journal of Molecular Sciences; Volume 23; Issue 20; Pages: 12693
Adeno-associated virus (AAV) vector-based therapies can effectively correct some disease pathology in murine models with mucopolysaccharidoses. However, immunogenicity can limit therapeutic effect as immune responses target capsid proteins, transduce
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::78c3b2d0ff5777290423eb717e88e027
Autor:
Jobayer Hossain, Shaukat Khan, Seiji Yamaguchi, Wendi Xiao, Betul Celik, Hironori Kobayashi, Paige C. Amendum, Yasuyuki Suzuki, Shunji Tomatsu, Estera Rintz, Yasuhiko Ago
Publikováno v:
Diagnostics
Volume 11
Issue 9
Diagnostics, Vol 11, Iss 1563, p 1563 (2021)
Volume 11
Issue 9
Diagnostics, Vol 11, Iss 1563, p 1563 (2021)
Glycosaminoglycans (GAGs) are present in proteoglycans, which play critical physiological roles in various tissues. They are known to be elevated in mucopolysaccharidoses (MPS), a group of rare inherited metabolic diseases in which the lysosomal enzy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1ba55f27ba6a3844e983308766712aa4