화학공학소재연구정보센터
검색결과 : 8건
No. Article
1 Complementarity of electrophoretic, mass spectrometric, and gene sequencing techniques for the diagnosis and characterization of congenital disorders of glycosylation
Bruneel A, Cholet S, Drouin-Garraud V, Jacquemont ML, Cano A, Megarbane A, Ruel C, Cheillan D, Dupre T, Vuillaumier-Barrot S, Seta N, Fenaille F
Electrophoresis, 39(24), 3123, 2018
2 Mannose metabolism: More than meets the eye
Sharma V, Ichikawa M, Freeze HH
Biochemical and Biophysical Research Communications, 453(2), 220, 2014
3 Physiologic and pathophysiologic consequences of altered sialylation and glycosylation on ion channel function
Baycin-Hizal D, Gottschalk A, Jacobson E, Mai S, Wolozny D, Zhang H, Krag SS, Betenbaugh MJ
Biochemical and Biophysical Research Communications, 453(2), 243, 2014
4 Polyisoprenoids - Secondary metabolites or physiologically important superlipids?
Surmacz L, Swiezewska E
Biochemical and Biophysical Research Communications, 407(4), 627, 2011
5 Analysis and metabolic engineering of lipid-linked oligosaccharides in glycosylation-deficient CHO cells
Jones MB, Tomiya N, Betenbaugh MJ, Krag SS
Biochemical and Biophysical Research Communications, 395(1), 36, 2010
6 Congenital disorder of glycosylation Ia: New differentially expressed proteins identified by 2-DE
Richard E, Vega AI, Perez B, Roche C, Velazquez R, Ugarte M, Perez-Cerda C
Biochemical and Biophysical Research Communications, 379(2), 267, 2009
7 Screening for OST deficiencies in unsolved CDG-I patients
Vleugels W, Schollen E, Foulquier F, Matthijs G
Biochemical and Biophysical Research Communications, 390(3), 769, 2009
8 Characterization of transferrin glycoforms in human serum by CE-UV and CE-ESI-MS
Sanz-Nebot V, Balaguer E, Benavente F, Neususs C, Barbosa J
Electrophoresis, 28(12), 1949, 2007