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Thymidine to Adenosine Transversion Abnormality
A point mutation involving the substitution of Adenosine (a purine base) for Thymidine (a pyrimidine base) in a DNA sequence from eukaryotic or prokaryotic organisms. This abnormality can be either heritable or occur somatically. (NCI Thesaurus)
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Thymidine phosphorylase (482 aa, ~50 kDa) is encoded by the human TYMP gene. This protein plays a role in pyrimidine metabolism, DNA…
Expressed (as long 266-aa 31-kDa precursor and short 235-aa alternative isoforms) predominantly in liver, pancreas, muscle, and brain by human TK2 Gene…
Thymidine kinase, cytosolic (234 aa, ~25 kDa) is encoded by the human TK1 gene. This protein plays a role in pyrimidine…
Human Thymidine Kinases (Thymidine Kinase Family) catalyze thymidine phosphorylation via ATP to deoxythymidine monophosphate.
A chemical compound found in DNA. Also used as treatment for mucositis.
The veins that drain blood from the thymus into the left brachiocephalic vein.
