Author:
Harzer K.,Paton B. C.,Poulos A.,Kustermann-Kuhn B.,Roggendorf W.,Grisar T.,Popp M.
Publisher
Springer Science and Business Media LLC
Subject
Pediatrics, Perinatology and Child Health
Reference41 articles.
1. Berent SL, Radin NS (1981) β-Glucosidase activator protein from bovine spleen (“coglucosidase”). Arch Biochem Biophys 208: 248–260
2. Berent SL, Radin NS (1981) Mechanism of action of glucocerebrosidase by co-β-glucosidase (glucosidase activator protein). Biochim Biophys Acta 664:572–582
3. Brady RO (1978) Glucosyl ceramide lipidosis: Gaucher disease. In: Stanbury JB, Wyngaarden JB, Fredrickson DS (eds) The metabolic basis of inherited disease, 4th edn. McGraw-Hill, New York, pp 731–746
4. Christomanou H, Kleinschmidt T (1985). Isolation of two forms of an activator protein for the enzymic sphingomyelin degradation from human Gaucher spleen. Biol Chem. Hoppe Seyler 366:245–256
5. Christomanou H, Aignesberger A, Linke RP (1986) Immunochemical characterization of two activator proteins stimulating enzymic sphingomyelin degradation in vitro. Absence of one of them in a human Gaucher disease variant. Biol Chem. Hoppe Seyler 367:879–890
Cited by
201 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献