Codon Concept

subject area of

• O⁶-Ethylguanine and O⁶-benzylguanine incorporated site-specifically in codon 12 of the rat H-ras gene induce semi-targeted as well as targeted mutations in Rat4 cells  Academic Article
• A Non-Long Terminal Repeat Retrotransposon Family Is Restricted to the Germ Line Micronucleus of the Ciliated Protozoan Tetrahymena thermophila  Academic Article
• A Thermodynamic Basis for Prebiotic Amino Acid Synthesis and the Nature of the First Genetic Code  Academic Article
• A Unified Model of Codon Reassignment in Alternative Genetic Codes  Academic Article
• A four-column theory for the origin of the genetic code: tracing the evolutionary pathways that gave rise to an optimized code  Academic Article
• A new frameshift β°-thalassemia mutation (codons 27–28 +C) found in a Chinese family  Academic Article
• A novel and de novo spontaneous point mutation (Glu271STOP) of the antithrombin gene results in a type I deficiency and thrombophilia  Academic Article
• A novel candidate region for ALS on chromosome 14q11.2  Academic Article
• A phylogenetic analysis based on the gene encoding phosphoglycerate kinase  Academic Article
• Absence of germline and somatic p53 alterations in children with sporadic brain tumors.  Academic Article
• Accuracy of p53 Codon 72 Polymorphism Status Determined by Multiple Laboratory Methods: A Latent Class Model Analysis  Academic Article
• Amber, ochre and opal suppressor tRNA genes derived from a human serine tRNA gene.  Academic Article
• Amino acid substitutions of the P2 residue of human antithrombin that either enhance or impair function  Academic Article
• An inducible mammalian amber suppressor: Propagation of a poliovirus mutant  Academic Article
• Antithrombin-III-Hamilton: a gene with a point mutation (guanine to adenine) in codon 382 causing impaired serine protease reactivity  Academic Article
• Antithrombin-III-Stockholm: a codon 392 (Gly----Asp) mutation with normal heparin binding and impaired serine protease reactivity  Academic Article
• Assay of HIV gp41 amino acid sequence to identify baseline variation and mutation development in patients with virologic failure on enfuvirtide☆  Academic Article
• Codon 24 (TAT>TAG) and Codon 32 (ATG>AGG) (Hb Rotterdam): Two Novel α2 Gene Mutations Associated with Mild α-Thalassemia Found in the Same Family After Newborn Screening  Academic Article
• Codon Bias and Base Composition Are Poor Indicators of Horizontally Transferred Genes  Academic Article
• Codon Usage and Selection on Proteins  Academic Article
• Codon Usage in Mitochondrial Genomes: Distinguishing Context-Dependent Mutation from Translational Selection  Academic Article
• Codon bias and frequency-dependent selection on the hemagglutinin epitopes of influenza A virus  Academic Article
• Coevolution of Codon Usage and tRNA Genes Leads to Alternative Stable States of Biased Codon Usage  Academic Article
• Contributions of Speed and Accuracy to Translational Selection in Bacteria  Academic Article
• DOMINANT β-THALASSEMIA DUE TO A NEWLY IDENTIFIED FRAMESHIFT MUTATION IN EXON 3 (CODON 113, GTG → TG)  Academic Article
• Detecting selection using a single genome sequence of M. tuberculosis and P. falciparum  Academic Article
• Estimating Selection Pressures from Limited Comparative Data  Academic Article
• Evolution of genes and genomes on the Drosophila phylogeny  Academic Article
• Evolution of mitochondrial-encoded cytochrome oxidase subunits in endothermic fish: The importance of taxon-sampling in codon-based models  Academic Article
• Expected frequencies of codon use as a function of mutation rates and codon fitnesses  Academic Article
• Frameshift Mutation in the α2-Globin Gene Causing α⁺-Thalassemia: Codon 49 (−GC)  Academic Article
• Ganglioside GM1 induces phosphorylation of mutant huntingtin and restores normal motor behavior in Huntington disease mice  Academic Article
• Gene amelioration demonstrated: the journey of nascent genes in bacteria  Academic Article
• Hb A₂Hong Kong – A Novel δ-Globin Variant in a Chinese Family Masks the Diagnosis of β-Thalassemia Trait  Academic Article
• Hb Adana (HBA2 or HBA1: c.179G > A) and alpha thalassemia: Genotype-phenotype correlation  Academic Article
• Hb H hydrops foetalis syndrome: a case report and review of literature  Academic Article
• Hb Presbyterian (HBB: c.327C>G) in a Nicaraguan Family  Academic Article
• IDENTIFICATION OF TWO NEW β-THALASSEMIA SPLICE MUTATIONS: IVS-I-1 (G → C) AND IVS-I (−2) (A → C)  Academic Article
• Identifican of A New High Oxygen Affinity Hemoglobin Variant: Hb Aurora [β139(H17)Asn→Tyr]  Academic Article
• Identification of a novel termination codon mutation (TAA-->TAT, Term-- >Tyr) in the alpha 2 globin gene of a Laotian girl with hemoglobin H disease [letter]  Academic Article
• Identification of two novel β°-thalassemia mutations in a filipino family: Frameshift codon 67 (− TG) and a β-globin gene deletion  Academic Article
• Introduction of UAG, UAA, and UGA nonsense mutations at a specific site in the Escherichia coli chloramphenicol acetyltransferase gene: use in measurement of amber, ochre, and opal suppression in mammalian cells.  Academic Article
• Mild β⁺-Thalassemia Associated With Two Linked Sequence Variants: IVS-II-839 (T>C) and IVS-II-844 (C>A)  Academic Article
• Multiple Mechanisms Promote the Retained Expression of Gene Duplicates in the Tetraploid Frog Xenopus laevis  Academic Article
• Neurological Proteins Are Not Enriched For Repetitive Sequences  Academic Article
• Novel Mutation of the α2-Globin Gene Initiation Codon (Atg→A-G) in a Vietnamese Girl with Hb H Disease  Academic Article
• Novel dominant β-thalassemia: Hb Boston-Kuwait [Codon 139/140(+T)]  Academic Article
• OGRe: a relational database for comparative analysis of mitochondrial genomes  Academic Article
• Pathways of Genetic Code Evolution in Ancient and Modern Organisms  Academic Article
• Positional effects on the structure and stability of abbreviated H-ras DNA sequences containing O6-methylguanine residues at codon 12  Academic Article
• Prenatal exclusion of β thalassaemia major by examination of maternal plasma  Academic Article
• Rapid Evolution Through Gene Duplication and Subfunctionalization of the Testes-Specific α4 Proteasome Subunits in DrosophilaSequence data from this article have been deposited with the EMBL/GenBank Data Libraries under accession nos. AY542377, AY542378, AY542379, AY542380, AY542381, AY542382, AY542383, AY542384, AY542385, AY542386, AY542387, AY542388, AY542389, AY542390, AY542391, AY542392, AY542393, AY542394, AY542395, AY542396, AY542397, AY542398, AY542399, AY542400, AY542401, AY542402, AY542403, AY542404, AY542405, AY542406, AY542407, AY542408, AY542409, AY542410, AY542411, AY542412, AY542413, AY542414, AY542415, AY542416, AY542417, AY542418, AY542419, AY542420, AY542421, AY542422, AY542423, AY542424, AY542425, AY542426, AY542427, AY542428, AY542429, AY542430, AY542431, AY542432.  Academic Article
• Sequencing of heat shock protein 70 (DnaK) homologs from Deinococcus proteolyticus and Thermomicrobium roseum and their integration in a protein-based phylogeny of prokaryotes  Academic Article
• Structure and function of tryptophan tRNA from wheat germ  Academic Article
• The First Report of a Homozygous Codons 9/10 (+T) β-Thalassemia Mutation in a Turkish Patient  Academic Article
• The Influence of Anticodon-Codon Interactions and Modified Bases on Codon Usage Bias in Bacteria  Academic Article
• The Italian AICE-Genetics hemophilia A database: results and correlation with clinical phenotype  Academic Article
• The Mechanisms of Codon Reassignments in Mitochondrial Genetic Codes  Academic Article
• The Transcriptional Repressor ZEB Regulates p73 Expression at the Crossroad between Proliferation and Differentiation  Academic Article
• The role of O⁶-alkylguanine-DNA alkyltransferase in protecting Rat4 cells against the mutagenic effects of O⁶-substituted guanine residues incorporated in codon 12 of the H-ras gene  Academic Article
• The sequences of heat shock protein 40 (DnaJ) homologs provide evidence for a close evolutionary relationship between the Deinococcus- Thermus group and cyanobacteria  Academic Article
• Three New α-Thalassemia Point Mutations Ascertained Through Newborn Screening  Academic Article
• Two novel beta-thalassemia mutations in the 5' and 3' noncoding regions of the beta-globin gene [see comments]  Academic Article
• α⁺-Thalassemia Due to a Frameshift Mutation of theα2-Globin Gene [codons 55/56 (+T) orHBA2: c.168dup]  Academic Article
• α⁺-Thalassemia Trait Caused by a Frameshift Mutation in Exon 2 of the α2-Globin Gene [HBA2 c.244delT]  Academic Article
• β-Thalassemia intermedia in a lebanese child due to homozygosity for the -88 (C→T) Mutation  Academic Article
• δβ-Thalassemia in an African-American: Identification of the deletion endpoints and PCR-Based diagnosis  Academic Article