Examples of using Codon in English and their translations into Polish
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Colloquial
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Computer
At least one codon encodes the information for each of the 20 amino acids used in the synthesis of proteins during translation.
three base pairs, this is called a codon, because it codes for amino acids.
the article could be used when addressing the topics of codon usage and degeneracy;
Estimated from 16,403 melanomas with annotated BRAF codon 600 mutations in the public COSMIC database, release 71 November 2014.
looking for the AUG start codon nucleic acid triplet.
Resistance: HIV-1 resistance to emtricitabine develops as the result of changes at codon 184 causing the methionine to be changed to a valine(an isoleucine intermediate has also been observed) of the HIV reverse transcriptase.
Tests for mutations in codon 918 are generally performed on the basis of information about the phenotype,
stop codons of mRNA, and tRNA, which provides the amino acid once bound with a complimentary mRNA codon.
with adenine(A) in the codon AAG makes no change to the protein:
Each group of three nucleotides in the sequence, called a codon, corresponds either to one of the twenty possible amino acids in a protein or an instruction to end the amino acid sequence; this correspondence is called the genetic code.
A nonsense mutation is a point mutation in a sequence of DNA that results in a premature stop codon, or a nonsense codon in the transcribed mRNA, and possibly a truncated, and often nonfunctional protein product.
which constitute 30% of mutations, the Stop codon arises at the mutation site,
Rarely not tested Classic MEN 2A is most likely if a mutation within codon 634 occurs, while other mutations are connected with a significantly lower probability of the development of a pheochromocytoma- as a result of the mutation the familial MTC usually develops without other endocrinopathies tab.
It is assumed that codon 159 is the boundary between AAPC
if the mutation occurs within codon 634(the full syndrome with parathyroid hyperactivity occurs especially often when cysteine is replaced with arginine),
their transformational potential is rather small- apart from the mutation in codon 790 which was demonstrated in both FMTC
Fixed a problem when translating codons with N.
Mutations which occur between codons 1403 and 1587 lead to the intensification of extra-colonic symptoms.
The occurrence of desmoid tumours is associated with mutations in the region between codons 1445 and 1578.
The typical course of polyposis with numerous polyps takes place when the Stop signal occurs between codons 169 and 1600.