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Defective glycosyltransferases are not good for your health.
Schachter H, Tan J, Sarkar M, Yip B, Chen S, Dunn J, Jaeken J. Schachter H, et al. Among authors: tan j. Adv Exp Med Biol. 1998;435:9-27. doi: 10.1007/978-1-4615-5383-0_2. Adv Exp Med Biol. 1998. PMID: 9498061 Review. No abstract available.
Carbohydrate-deficient glycoprotein syndrome type II. An autosomal recessive N-acetylglucosaminyltransferase II deficiency different from typical hereditary erythroblastic multinuclearity, with a positive acidified-serum lysis test (HEMPAS).
Charuk JH, Tan J, Bernardini M, Haddad S, Reithmeier RA, Jaeken J, Schachter H. Charuk JH, et al. Among authors: tan j. Eur J Biochem. 1995 Jun 1;230(2):797-805. doi: 10.1111/j.1432-1033.1995.0797h.x. Eur J Biochem. 1995. PMID: 7607254 Free article.
The human UDP-N-acetylglucosamine: alpha-6-D-mannoside-beta-1,2- N-acetylglucosaminyltransferase II gene (MGAT2). Cloning of genomic DNA, localization to chromosome 14q21, expression in insect cells and purification of the recombinant protein.
Tan J, D'Agostaro AF, Bendiak B, Reck F, Sarkar M, Squire JA, Leong P, Schachter H. Tan J, et al. Eur J Biochem. 1995 Jul 15;231(2):317-28. doi: 10.1111/j.1432-1033.1995.tb20703.x. Eur J Biochem. 1995. PMID: 7635144 Free article.
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.
Wang Y, Tan J, Sutton-Smith M, Ditto D, Panico M, Campbell RM, Varki NM, Long JM, Jaeken J, Levinson SR, Wynshaw-Boris A, Morris HR, Le D, Dell A, Schachter H, Marth JD. Wang Y, et al. Among authors: tan j. Glycobiology. 2001 Dec;11(12):1051-70. doi: 10.1093/glycob/11.12.1051. Glycobiology. 2001. PMID: 11805078
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