Hydrophobic Man-1-P derivatives correct abnormal glycosylation in Type I congenital disorder of glycosylation fibroblasts

By Eklund Erik A.   Merbouh Nabyl   Ichikawa Mie   Nishikawa Atsushi   Clima Jessica M.   Dorman James A.   Norberg Thomas   Freeze Hudson H.  

Glycobiology, Vol. 15, Iss. 11, 2005-11 ,pp. : 1084-1093

Oxford University Press

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Modeling human congenital disorder of glycosylation type IIa in the mouse: conservation of asparagine-linked glycan-dependent functions in mammalian physiology and insights into disease pathogenesis

By Levinson S.  

Glycobiology, Vol. 11, Iss. 12, 2001-12 ,pp. : 1051-1070

Oxford University Press

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Defect in N-glycosylation of proteins is tissue-dependent in Congenital Disorders of Glycosylation Ia

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Glycobiology, Vol. 10, Iss. 12, 2000-11 ,pp. : 1277-1281

Oxford University Press

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A Genome-Wide Screen for Hyposmia Susceptibility Loci

By Pinto Jayant M.   Thanaviratananich Sanguansak   Hayes M. Geoffrey   Naclerio Robert M.   Ober Carole  

Chemical Senses, Vol. 33, Iss. 4, 2008-04 ,pp. : 319-329

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Increased fucosylation and reduced branching of serum glycoprotein N-glycans in all known subtypes of congenital disorder of glycosylation I

By Callewaert N.  

Glycobiology, Vol. 13, Iss. 5, 2003-05 ,pp. : 367-375

Oxford University Press

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