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Frontiers in Cell and Developmental Biology|October 1, 2021
A Dominant Heterozygous Mutation in COG4 Causes Saul-Wilson Syndrome, a Primordial Dwarfism, and Disrupts Zebrafish Development via Wnt SignalingZhi-Jie Xia, Xin-Xin I Zeng, Mitali Tambe, et al.Pediatrics International : Official Journal of the Japan Pediatric Society|June 22, 2016
Congenital nephrotic syndrome in an infant with ALG1-congenital disorder of glycosylationLyndsay A Harshman, Bobby G Ng, Hudson H Freeze, et al.Human Mutation|July 23, 2003
Deficiency of UDP-GlcNAc:Dolichol Phosphate N-Acetylglucosamine-1 Phosphate Transferase (DPAGT1) causes a novel congenital disorder of Glycosylation Type IjXiaohua Wu, Jeffrey S Rush, Denise Karaoglu, et al.Nature Medicine|April 27, 2004
Mutation of the COG complex subunit gene COG7 causes a lethal congenital disorderXiaohua Wu, Richard A Steet, Ognian Bohorov, et al.Glycobiology|August 5, 2005
Hydrophobic Man-1-P derivatives correct abnormal glycosylation in Type I congenital disorder of glycosylation fibroblastsErik A Eklund, Nabyl Merbouh, Mie Ichikawa, et al.The Journal of Clinical Investigation|December 8, 2007
Heparan sulfate and syndecan-1 are essential in maintaining murine and human intestinal epithelial barrier functionLars Bode, Camilla Salvestrini, Pyong Woo Park, et al.Disease Models & Mechanisms|May 19, 2019
Selective inhibition of N-linked glycosylation impairs receptor tyrosine kinase processingElsenoor Klaver, Peng Zhao, Melanie May, et al.Traffic (Copenhagen, Denmark)|June 25, 2010
Spatial regulation of Golgi phosphatidylinositol-4-phosphate is required for enzyme localization and glycosylation fidelityFei Ying Cheong, Vandana Sharma, Anastasia Blagoveshchenskaya, et al.Pediatric Neurology|February 17, 2019
Arrest of Fetal Brain Development in ALG11-Congenital Disorder of GlycosylationSarah B Mulkey, Bobby G Ng, Gilbert L Vezina, et al.Journal of Cellular Biochemistry|June 1, 2010
Carboxylated N-glycans on RAGE promote S100A12 binding and signalingGeetha Srikrishna, Jonamani Nayak, Bernd Weigle, et al.Pageof 31