Mutation of Nogo-B Receptor, a Subunit of cis-Prenyltransferase, Causes a Congenital Disorder of Glycosylation-Reference-Cited by-同舟云学术

Mutation of Nogo-B Receptor, a Subunit of cis-Prenyltransferase, Causes a Congenital Disorder of Glycosylation

Published:2014-09 Issue:3 Volume:20 Page:448-457
ISSN:1550-4131
Container-title:Cell Metabolism
language:en
Short-container-title:Cell Metabolism

Author:

Park Eon Joo,Grabińska Kariona A.,Guan Ziqiang,Stránecký Viktor,Hartmannová Hana,Hodaňová Kateřina,Barešová Veronika,Sovová Jana,Jozsef Levente,Ondrušková Nina,Hansíková Hana,Honzík Tomáš,Zeman Jiří,Hůlková Helena,Wen Rong,Kmoch Stanislav,Sessa William C.

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Physiology

Reference27 articles.

1. A noninvasive genetic/pharmacologic strategy for visualizing cell morphology and clonal relationships in the mouse;Badea;J. Neurosci.,2003

2. SRD5A3 is required for converting polyprenol to dolichol and is mutated in a congenital glycosylation disorder;Cantagrel;Cell,2010

3. Cholesterol synthesis inhibitor U18666A and the role of sterol metabolism and trafficking in numerous pathophysiological processes;Cenedella;Lipids,2009

4. Niemann-Pick type C disease: importance of N-glycosylation sites for function and cellular location of the NPC2 protein;Chikh;Mol. Genet. Metab.,2004

5. Crystal structure of cis-prenyl chain elongating enzyme, undecaprenyl diphosphate synthase;Fujihashi;Proc. Natl. Acad. Sci. USA,2001

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