Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
5R01CA020421-19
Application #
2086841
Study Section
Physiological Chemistry Study Section (PC)
Project Start
1976-12-01
Project End
1999-01-31
Budget Start
1996-02-01
Budget End
1997-01-31
Support Year
19
Fiscal Year
1996
Total Cost
Indirect Cost
Name
Johns Hopkins University
Department
Biochemistry
Type
Schools of Public Health
DUNS #
045911138
City
Baltimore
State
MD
Country
United States
Zip Code
21218
Acosta-Serrano, Alvaro; O'Rear, Jessica; Quellhorst, George et al. (2004) Defects in the N-linked oligosaccharide biosynthetic pathway in a Trypanosoma brucei glycosylation mutant. Eukaryot Cell 3:255-63
Pu, Lixia; Scocca, Jane R; Walker, Brian K et al. (2003) A single point mutation resulting in an adversely reduced expression of DPM2 in the Lec15.1 cells. Biochem Biophys Res Commun 312:555-61
Pu, Lixia; Scocca, Jane R; Walker, Brian K et al. (2003) The divergent 5' ends of DPM2 mRNAs originate from the alternative splicing of two adjacent introns: characterization of the hamster DPM2 gene. Biochem Biophys Res Commun 312:817-24
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Walker, B K; Lei, H; Krag, S S (1998) A functional link between N-linked glycosylation and apoptosis in Chinese hamster ovary cells. Biochem Biophys Res Commun 250:264-70
Kaiden, A; Rosenwald, A G; Cacan, R et al. (1998) Transfer of two oligosaccharides to protein in a Chinese hamster ovary cell B211 which utilizes polyprenol for its N-linked glycosylation intermediates. Arch Biochem Biophys 358:303-12
Duvet, S; Labiau, O; Mir, A M et al. (1998) Cytosolic deglycosylation process of newly synthesized glycoproteins generates oligomannosides possessing one GlcNAc residue at the reducing end. Biochem J 335 ( Pt 2):389-96

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