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Results 1 - 10 of 25 for Codon
  1. How do genes direct the production of proteins?: MedlinePlus Genetics 
    ... nucleotides. Each sequence of three nucleotides, called a codon, usually codes for one particular amino acid. (Amino ... assembly continues until the ribosome encounters a “stop” codon (a sequence of three nucleotides that does not ...
    https://medlineplus.gov/.../understanding/howgeneswork/makingprotein - Genetics
  2. PRNP gene 
    ... O, Hefter H, Korth C. Prion protein gene codon 129 modulates clinical course of neurological Wilson disease. ... Gessner R. Influence of homozygosity for methionine at codon 129 of the human prion gene on the ...
    https://medlineplus.gov/genetics/gene/prnp - Genetics
  3. SLC22A5 gene 
    ... HR. A mutation creating an upstream translation initiation codon in SLC22A5 5'UTR is a frequent cause ...
    https://medlineplus.gov/genetics/gene/slc22a5 - Genetics
  4. SMAD4 gene 
    ... A, Cormier-Daire V. Mutations at a single codon in Mad homology 2 domain of SMAD4 cause ...
    https://medlineplus.gov/genetics/gene/smad4 - Genetics
  5. Roberts syndrome 
    ... cases of ESCO2 mutations, including novel missense and codon deletion in the acetyltransferase domain, correlates with ESCO2 ...
    https://medlineplus.gov/genetics/condition/roberts-syndrome - Genetics
  6. Anonychia congenita 
    ... congenital hyponychia and evidence for a polymorphic initiation codon (p.M1I). BMC Med Genet. 2012 Dec 13; ...
    https://medlineplus.gov/genetics/condition/anonychia-congenita - Genetics
  7. Gyrate atrophy of the choroid and retina 
    ... V, Kaiser-Kupfer M, Valle D. An initiator codon mutation in ornithine-delta-aminotransferase causing gyrate atrophy ...
    https://medlineplus.gov/.../gyrate-atrophy-of-the-choroid-and-retina - Genetics
  8. HSD3B2 gene 
    ... JI. A novel nonstop mutation in the stop codon and a novel missense mutation in the type ...
    https://medlineplus.gov/genetics/gene/hsd3b2 - Genetics
  9. APP gene 
    ... Madrid I, Levy E, Marder K, Frangione B. Codon 618 variant of Alzheimer amyloid gene associated with ...
    https://medlineplus.gov/genetics/gene/app - Genetics
  10. 3-beta-hydroxysteroid dehydrogenase deficiency 
    ... JI. A novel nonstop mutation in the stop codon and a novel missense mutation in the type ...
    https://medlineplus.gov/...a-hydroxysteroid-dehydrogenase-deficiency - Genetics
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