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Molecular Genetics and Metabolism|January 23, 2009
Exogenous mannose does not raise steady state mannose-6-phosphate pools of normal or N-glycosylation-deficient human fibroblastsAya Higashidani, Lars Bode, Atsushi Nishikawa, et al.
Current Drug Discovery Technologies|August 24, 2006
The Nuclear Overhauser Effect in the lead identification processMarilisa Leone, Hudson H Freeze, Chui Sien Chan, et al.
The Journal of Biological Chemistry|November 24, 2022
GLUT1 is a highly efficient L-fucose transporterBobby G Ng, Paulina Sosicka, Zhijie Xia, et al.
Human Mutation|October 1, 2003
Identification of a frequent variant in ALG6, the cause of Congenital Disorder of Glycosylation-IcVibeke Westphal, Ming Xiao, Pui-Yan Kwok, et al.
Biochemical and Molecular Medicine|August 1, 1997
Abnormal metabolism of mannose in families with carbohydrate-deficient glycoprotein syndrome type 1K Panneerselvam, J R Etchison, F Skovby, et al.
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