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Traffic (Copenhagen, Denmark)|October 10, 2013
Dissecting functions of the conserved oligomeric Golgi tethering complex using a cell-free assayNathanael P Cottam, Katherine M Wilson, Bobby G Ng, et al.
Biochemical and Biophysical Research Communications|October 9, 2022
Comparative proteomics reveals elevated CCN2 in NGLY1-deficient cellsRebecca Hetz, Carlo Magaway, Jaylene Everett, et al.
Human Molecular Genetics|March 5, 2002
A frequent mild mutation in ALG6 may exacerbate the clinical severity of patients with congenital disorder of glycosylation Ia (CDG-Ia) caused by phosphomannomutase deficiencyVibeke Westphal, Susanne Kjaergaard, Els Schollen, et al.
Journal of Immunology (Baltimore, Md. : 1950)|December 21, 2000
A novel anionic modification of N-glycans on mammalian endothelial cells is recognized by activated neutrophils and modulates acute inflammatory responsesG Srikrishna, D K Toomre, A Manzi, et al.
Journal of the Formosan Medical Association = Taiwan Yi Zhi|September 14, 2004
Carbohydrate deficient glycoprotein syndrome type IaKai-Lin Chu, Yin-Hsiu Chien, Chen-En Tsai, et al.
Journal of Microbiology & Biology Education|June 16, 2018
The Art of Science Communication-A Novel Approach to Science Communication TrainingSusanna Greer, Hannah Alexander, Thomas O Baldwin, et al.
Molecular Genetics and Metabolism|July 12, 2003
Congenital disorder of glycosylation Ic in patients of Indian originJ W Newell, N-S Seo, G M Enns, et al.
Biochemical and Biophysical Research Communications|December 3, 2005
Congenital disorder of glycosylation Ic due to a de novo deletion and an hALG-6 mutationErik A Eklund, Liangwu Sun, Samuel P Yang, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|April 24, 2010
Molecular imaging of N-linked glycosylation suggests glycan biosynthesis is a novel target for cancer therapyJoseph N Contessa, Mahaveer S Bhojani, Hudson H Freeze, et al.
The Journal of Clinical Investigation|November 1, 1994
Carbohydrate-deficient glycoprotein syndrome: not an N-linked oligosaccharide processing defect, but an abnormality in lipid-linked oligosaccharide biosynthesis?L D Powell, K Paneerselvam, R Vij, et al.
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