Skip to search formSkip to main contentSkip to account menu

Codon, Nonsense

Known as: Codon, Premature Stop, Codon, Premature Termination, Premature Stop Codons 
An amino acid-specifying codon that has been converted to a stop codon (CODON, TERMINATOR) by mutation. Its occurance is abnormal causing premature… 
National Institutes of Health

Related topics

Related topics

15 relations
Amber Nonsense MutationCodon, UnassignedIn BloodNonsense mutation

Narrower (2)

Ochre Nonsense CodonOpal Nonsense Codon

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2002
Highly Cited
2002
A basolateral sorting motif in the MICA cytoplasmic tail
The MHC class I chain-related MICA molecule is a stress-induced, highly polymorphic, epithelia-specific, membrane-bound… 
Highly Cited
1996
Highly Cited
1996
A high incidence of BRCA1 mutations in 20 breast-ovarian cancer families.
We have analyzed 20 breast-ovarian cancer families, the majority of which show positive evidence of linkage to chromosome 17q12… 
Highly Cited
1993
Highly Cited
1993
Genomic structure of growth hormone genes in chinook salmon (Oncorhynchus tshawytscha): presence of two functional genes, GH-I and GH-II, and a male-specific pseudogene, GH-psi.
Two chinook salmon (Oncorhynchus tshawytscha) growth hormone genes (a functional GH-I gene and a pseudogene, GH-psi) were… 
Review
1993
Review
1993
A second mutation in the type II procollagen gene (COL2AI) causing stickler syndrome (arthro-ophthalmopathy) is also a premature termination codon.
Genetic linkage analyses suggest that mutations in type II collagen may be responsible for Stickler syndrome, or arthro… 
Highly Cited
1991
Highly Cited
1991
Biosynthetic method for introducing unnatural amino acids site-specifically into proteins.
Highly Cited
1991
Highly Cited
1991
Functional analysis of human cardiac gap junction channel mutants.
The connexins form a family of membrane spanning proteins that assemble into gap junction channels. The biophysical properties of… 
Highly Cited
1991
Highly Cited
1991
Point mutations in the beta-subunit of cytochrome b558 leading to X-linked chronic granulomatous disease.
The NADPH:O2 oxidoreductase of phagocytic leukocytes is an important enzyme for the bactericidal activity of these cells… 
Highly Cited
1989
Highly Cited
1989
Mutations in the catalytic domain of human coagulation factor IX: rapid characterization by direct genomic sequencing of DNA fragments displaying an altered melting behavior.
Highly Cited
1974
Highly Cited
1974
Altered reading of genetic signals fused to the N operon of bacteriophage lambda: genetic evidence for modification of polymerase by the protein product of the N gene.
Highly Cited
1965
Highly Cited
1965
Suppressor genes for nonsense mutations. I. The Su-1, Su-2 and Su-3 genes of Escherichia coli.
By clicking accept or continuing to use the site, you agree to the terms outlined in our Privacy Policy (opens in a new tab), Terms of Service (opens in a new tab), and Dataset License (opens in a new tab)