Results 21 to 30 of about 1,400 (108)
Synthesis of [1,3, NH2‐15N3] (5′S)‐8,5′‐cyclo‐2′‐deoxyguanosine [PDF]
Rajat S Das, Ashis K Basu
exaly +2 more sources
Data of ESI-QTOF mass spectrum of PMM2-CDG
Text data of Fig. 5. ESI-QTOF mass spectrum of PMM2-CDG. (A) The multiply-charged ions of three transferrin isoforms are completely overlapped at m/z 2,211.
Yoshinao Wada (12201750) +1 more
core +1 more source
Stability of N‑Glycosidic Bond of (5′S)‑8,5′-Cyclo-2′-deoxyguanosine
8,5′-Cyclopurine deoxynucleosides are unique tandem lesions containing an additional covalent bond between the base and the sugar. These mutagenic and genotoxic lesions are repaired only by nucleotide excision repair. The N-glycosidic (or C1′-N9) bond of
Ashis K. Basu (630373) +4 more
core +1 more source
Autosomal Recessive Dilated Cardiomyopathy due to DOLK Mutations Results from Abnormal Dystroglycan O-Mannosylation [PDF]
Genetic causes for autosomal recessive forms of dilated cardiomyopathy (DCM) are only rarely identified, although they are thought to contribute considerably to sudden cardiac death and heart failure, especially in young children.
van Reeuwijk, Jeroen +100 more
core +1 more source
Exposure of aqueous solutions of DNA to X- or γ-rays, which induces the hydroxyl radical as one of the major reactive oxygen species (ROS), can result in the generation of a battery of single-nucleobase and bulky DNA lesions. These include the (5′R) and (
Candace R. Guerrero (1331547) +2 more
core +1 more source
SRD5A3 is required for converting polyprenol to dolichol and is mutated in a congenital glycosylation disorder. [PDF]
N-linked glycosylation is the most frequent modification of secreted and membrane-bound proteins in eukaryotic cells, disruption of which is the basis of the congenital disorders of glycosylation (CDGs).
Hudson H. Freeze +74 more
core +1 more source
Structures of (5′S)-8,5′-Cyclo-2′-deoxyguanosine Mismatched with dA or dT
Diastereomeric 8,5′-cyclopurine 2′-deoxynucleosides, containing a covalent bond between the deoxyribose and the purine base, are induced in DNA by ionizing radiation.
Ashis K. Basu (630373) +3 more
core +1 more source
Structure of (5′S)-8,5′-Cyclo-2′-deoxyguanosine in DNA
Diastereomeric 8,5′-cyclopurine 2′-deoxynucleosides, containing a covalent bond between the deoxyribose and the purine base, represent an important class of DNA damage induced by ionizing radiation.
Ashis K. Basu (630373) +3 more
core +1 more source
The (5′S)-8,5′-cyclo-2′-deoxyguanosine (S-cdG) lesion is produced from reactions of DNA with hydroxyl radicals generated from ionizing radiation or endogenous oxidative metabolisms.
Wenyan Xu (1453525) +5 more
core +1 more source
Chemistry and Biology of 8,5\u27-Cyclo-2\u27-deoxyguanosine and Other DNA Lesions
8,5’-Cyclopurine deoxynucleosides are unique tandem lesions containing an additional covalent bond between the base and the sugar. These mutagenic and genotoxic lesions are repaired only by nucleotide excision repair (NER). It was shown that the R-cdA is
Das, Rajat S
core +1 more source

