Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Justin Furcich"'
Autor:
Miles C. Smith, Lalitha R. Belur, Andrea D. Karlen, Olivia Erlanson, Justin Furcich, Troy C. Lund, Davis Seelig, Kelley F. Kitto, Carolyn A. Fairbanks, Kwi Hye Kim, Nick Buss, R. Scott McIvor
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 32, Iss 1, Pp 101201- (2024)
Mucopolysaccharidosis type II (MPS II) is an X-linked recessive lysosomal disease caused by iduronate-2-sulfatase (IDS) deficiency, leading to accumulation of glycosaminoglycans (GAGs) and the emergence of progressive disease. Enzyme replacement ther
Externí odkaz:
https://doaj.org/article/a2a8c79881364444bb7633c2c34e66ec
Autor:
Miles C. Smith, Lalitha R. Belur, Andrea D. Karlen, Olivia Erlanson, Kelly M. Podetz-Pedersen, Jessica McKenzie, Jenn Detellis, Khatuna Gagnidze, Geoffrey Parsons, Nicholas Robinson, Shelby Labarre, Saumil Shah, Justin Furcich, Troy C. Lund, Hsing-Chen Tsai, R. Scott McIvor, Melissa Bonner
Publikováno v:
Human Gene Therapy. 33:1279-1292
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cdfc4a893a7f592726a497c6e2ab15bd
https://doi.org/10.1089/hum.2022.141
https://doi.org/10.1089/hum.2022.141
Autor:
Miles C. Smith, Lalitha R. Belur, Andrea D. Karlen, Kelly Podetz-Pedersen, Olivia Erlanson, Kanut Laoharawee, Justin Furcich, Troy C. Lund, Yun You, Davis Seelig, Beau R. Webber, R. Scott McIvor
Publikováno v:
Molecular Genetics and Metabolism. 138:107539
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cb82b16f4e5d018e083f00ba27699721
https://doi.org/10.1016/j.ymgme.2023.107539
https://doi.org/10.1016/j.ymgme.2023.107539