Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Merel V. Baks"'
Autor:
Daphne E. Boer, Mina Mirzaian, Maria J. Ferraz, Kimberley C. Zwiers, Merel V. Baks, Marc D. Hazeu, Roelof Ottenhoff, André R.A. Marques, Rianne Meijer, Jonathan C.P. Roos, Timothy M. Cox, Rolf G. Boot, Navraj Pannu, Herman S. Overkleeft, Marta Artola, Johannes M. Aerts
Publikováno v:
Journal of Lipid Research, Vol 62, Iss , Pp 100018- (2021)
Abstract: Deficiency of glucocerebrosidase (GBA), a lysosomal β-glucosidase, causes Gaucher disease. The enzyme hydrolyzes β-glucosidic substrates and transglucosylates cholesterol to cholesterol-β-glucoside. Here we show that recombinant human GB
Externí odkaz:
https://doaj.org/article/bde0e1b5189144b6972b5caa64f21aff
Autor:
Daphne E.C. Boer, Maria J. Ferraz, Rianne Meijer, Kimberley C. Zwiers, Mina Mirzaian, Jonathan C. P. Roos, Johannes M. F. G. Aerts, Navraj S. Pannu, Marc D. Hazeu, Herman S. Overkleeft, Rolf G. Boot, André R. A. Marques, Marta Artola, Roelof Ottenhoff, Merel V. Baks, Timothy M. Cox
Publikováno v:
Journal of Lipid Research, 62. ELSEVIER
Journal of Lipid Research
Journal of Lipid Research, Vol 62, Iss, Pp 100018-(2021)
Journal of lipid research, 62:RA120001043. American Society for Biochemistry and Molecular Biology Inc.
Journal of Lipid Research
Journal of Lipid Research, Vol 62, Iss, Pp 100018-(2021)
Journal of lipid research, 62:RA120001043. American Society for Biochemistry and Molecular Biology Inc.
Deficiency of glucocerebrosidase (GBA), a lysosomal beta-glucosidase, causes Gaucher disease. The enzyme hydrolyzes beta-glucosidic substrates and transglucosylates cholesterol to cholesterol-p-glucoside. Here we show that recombinant human GBA also
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f2f8307fc9146a377776a47bc11811f
https://hdl.handle.net/1887/3214386
https://hdl.handle.net/1887/3214386
