Results 31 to 40 of about 1,400 (108)
9-Deaza-2′-deoxyguanosine (CdG) is a C-nucleoside and an analogue of the abundant promutagen 8-oxo-2′-deoxyguanosine (OdG). Like 2′-deoxyguanosine (dG), CdG should form a stable base pair with dC, but similar to OdG, CdG contains an N7-hydrogen that ...
Carol A. Parish (669279) +4 more
core +1 more source
Multi-Log Cytotoxicity of Carbocyclic 2′-Deoxyguanosine in HSV-TK-Expressing Human Tumor Cells [PDF]
Ganciclovir (GCV) is widely used as a prodrug for selective activation in tumor cells expressing herpes simplex virus thymidine kinase (HSV-TK) because of its ability to induce multi-log cytotoxicity to HSV-TK-expressing as well as nonexpressing ...
Boucher, Paul D. +8 more
core +1 more source
8,5′-Cyclopurines, making up an important class of ionizing radiation-induced tandem DNA damage, are repaired only by nucleotide excision repair (NER).
Vijay P. Jasti +11 more
core +1 more source
RFT1 deficiency in three novel CDG patients [PDF]
The medical significance of N-glycosylation is underlined by a group of inherited human disorders called Congenital Disorders of Glycosylation (CDG). One key step in the biosynthesis of the Glc(3)Man(9)GlcNAc(2)-PP-dolichol precursor, essential for N ...
Ludman, M D +11 more
core +1 more source
8,5′-Cyclopurines, making up an important class of ionizing radiation-induced tandem DNA damage, are repaired only by nucleotide excision repair (NER).
Ashis K. Basu (630373) +5 more
core +1 more source
UEG Week 2014 Poster Presentations
United European Gastroenterology Journal, Volume 2, Issue S1, Page A132-A605, October 2014.
wiley +1 more source
Dietary mannose supplementation in phosphomannomutase 2 deficiency (PMM2-CDG)
Background!#!PMM2-CDG (CDG-Ia) is the most frequent N-glycosylation disorder. While supplying mannose to PMM2-deficient fibroblasts corrects the altered N-glycosylation in vitro, short term therapeutic approaches with mannose supplementation in PMM2-CDG ...
DuChesne, Ingrid +4 more
core +1 more source
Reactive oxygen species generate many lesions in DNA, including R and S diastereomers of 8,5′-cyclo-2′-deoxyadenosine (cdA) and 8,5′-cyclo-2′-deoxyguanosine (cdG).
Ashis K. Basu (630373) +3 more
core +1 more source
DataSheet4_SRD5A3-CDG: Emerging Phenotypic Features of an Ultrarare CDG Subtype.pdf
Background: SRD5A3-CDG is a rare N-glycosylation defect caused by steroid 5 alpha reductase type 3 deficiency. Its key feature is an early severe visual impairment with variable ocular anomalies often leading to diagnosis.
Kshitij Mankad (6749432) +5 more
core +1 more source
COG5-CDG with a Mild Neurohepatic Presentation
The conserved oligomeric Golgi (COG) complex is an eight subunit protein involved in the retrograde transport of Golgi components. It affects the localization of several Golgi glycosyltransferases and hence is involved in N- and O-glycosylation.
Wong, K.Y. +23 more
core +1 more source

