Health / Medical Topics

    Guanosine to Cytosine Transversion Abnormality

    A point mutation involving the substitution of Cytosine (a pyrimidine base) for Guanosine (a purine base) in a DNA sequence from eukaryotic or prokaryotic organisms. This abnormality can be either heritable or occur somatically. (NCI Thesaurus)




    YOU MAY ALSO LIKE

    A point mutation involving the substitution of Adenosine (a purine base) for Guanosine (a purine base) in a DNA sequence from eukaryotic…
    A purine nucleoside formed from a beta-N9-glycosidic bond between guanine and a ribose ring and is essential for metabolism.
    Encoded by human GNA12 Gene (G-Alpha 4 (G(12)) Family), 380-aa 44-kDa membrane-bound Guanine Nucleotide Binding Protein Alpha 12 is a G protein…
    Guanine nucleotide-binding protein subunit alpha-11 (359 aa, ~42 kDa) is encoded by the human GNA11 gene. This protein is involved in the…
    Guanine nucleotide binding protein is a member of a G protein subfamily that mediates signal transduction; component of pertussis toxin-insensitive (PTX) heterotrimeric…
    Guanine Nucleotide-Binding Protein G(q) Subunit Alpha (353 aa, ~41 kDa) is encoded by the human GNAQ gene. This protein may play a…

    © 1991-2023 The Titi Tudorancea Bulletin | Titi Tudorancea® is a Registered Trademark | Terms of use and privacy policy
    Contact