SFX by Ex Libris Inc.

Title:	UDP-GlcNAc 2-epimerase: a regulator of cell surface sialylation
Source:	Science [0036-8075] Keppler, O T yr:1999

Basic

Sorry, no full text available...

Please use the document delivery service (see below)

Holding information

Holdings in library search engine ALBERT

Document delivery

Request document via Library/Bibliothek

Users interested in this article also expressed an interest in the following:
description	1.	Eisenberg, I. "The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathy." Nature Genetics 29.1 (2001): 83-7.
description	2.	Murkin, A. "Identification and mechanism of a bacterial hydrolyzing UDP-N-acetylglucosamine 2-epimerase." Biochemistry 43.44 (2004): 14290-14298.
description	3.	Hinderlich, S. "A bifunctional enzyme catalyzes the first two steps in N-acetylneuraminic acid biosynthesis of rat liver - Purification and characterization of UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase." The Journal of biological chemistry 272.39 (1997): 24313-24318.
description	4.	Eisenberg, I. "Mutations spectrum of GNE in hereditary inclusion body myopathy sparing the quadriceps." Human mutation 21.1 (2003): 99-99.
description	5.	Kamiya, K. "Substrate-mediated proton relay mechanism for the religation reaction in topoisomerase II." Journal of biomolecular structure & dynamics 32.11 (2014): 1759-1765.
description	6.	Mirabella, M. "An Italian family with autosomal recessive quadriceps-sparing inclusion-body myopathy (ARQS-IBM) linked to chromosome 9p1." Neurological sciences 21.2 (2000): 99-102.
description	7.	Sala, R. "Properties and kinetic analysis of UDP-glucose dehydrogenase from group a streptococci - Irreversible inhibition by UDP-chloroacetol." Journal of biological chemistry 272.6 (1997): 3416-3422.
description	8.	Huizing, M. "Hypoglycosylation of alpha-dystroglycan in patients with hereditary IBM due to GNE mutations." Molecular genetics and metabolism (2004): 196-202.
description	9.	Chou, Wayne K. "Sialic acid biosynthesis: stereochemistry and mechanism of the reaction catalyzed by the mammalian UDP-N-acetylglucosamine 2-epimerase." Journal of the American Chemical Society 125.9 (2003): 2455-2461.
description	10.	Weihofen, Wilhelm A. "Structures of Human N-Acetylglucosamine Kinase in Two Complexes with N-Acetylglucosamine and with ADP/Glucose: Insights into Substrate Specificity and Regulation." Journal of molecular biology 364.3 (2006): 388-399.
description	11.	KROLL, J. "THE BEX LOCUS IN ENCAPSULATED HAEMOPHILUS-INFLUENZAE - A CHROMOSOMAL REGION INVOLVED IN CAPSULE POLYSACCHARIDE EXPORT." Molecular microbiology 4.11 (1990): 1853-1862.
description	12.	Liu, J. "Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy." Nature genetics 20.1 (1998): 31-6.
description	13.	Vann, W F F. "Purification and characterization of the Escherichia coli K1 neuB gene product N-acetylneuraminic acid synthetase." Glycobiology 7.5: 697-701.
description	14.	Hackenberger, Christian R. "Chemoselective labeling of engineered fucosylated glycoproteins." Chembiochem 8.15 (2007): 1763-1765.
description	15.	Hsu, T. "Alkynyl sugar analogs for the labeling and visualization of glycoconjugates in cells." Proceedings of the National Academy of Sciences of the United States of America 104.8 (2007): 2614-2619.
description	16.	Kayashima, T. "Nonaka myopathy is caused by mutations in the UDP-N-acetylglucosamine-2-epimerase/N-acetylmannosamine kinase gene (GNE)." Journal of human genetics 47.2 (2002): 77-79.
description	17.	Weihl, C. "Novel GNE mutations in two phenotypically distinct HIBM2 patients." Neuromuscular disorders 21.2 (2010): 102-105.
description	18.	Bansal, D. "Defective membrane repair in dysferlin-deficient muscular dystrophy." Nature 423.6936 (2003): 168-72.
description	19.	Needham, M. "Genetics of inclusion-body myositis." Muscle & nerve 35.5 (2007): 549-61.
description	20.	Palumbo, M. "Metal ion and inter-domain interactions as functional networks in E. coli topoisomerase I." Gene (Amsterdam) 524.2 (2013): 253-260.