Codon Concept

subject area of

• A Non-Long Terminal Repeat Retrotransposon Family Is Restricted to the Germ Line Micronucleus of the Ciliated Protozoan Tetrahymena thermophila  Journal Articles
• A Thermodynamic Basis for Prebiotic Amino Acid Synthesis and the Nature of the First Genetic Code  Journal Articles
• A Unified Model of Codon Reassignment in Alternative Genetic Codes  Journal Articles
• A four-column theory for the origin of the genetic code: tracing the evolutionary pathways that gave rise to an optimized code  Journal Articles
• A new frameshift β°‐thalassemia mutation (codons 27–28 +C) found in a Chinese family  Journal Articles
• A novel and de novo spontaneous point mutation (Glu271STOP) of the antithrombin gene results in a type I deficiency and thrombophilia  Journal Articles
• A novel candidate region for ALS on chromosome 14q11.2  Journal Articles
• A phylogenetic analysis based on the gene encoding phosphoglycerate kinase  Journal Articles
• Accuracy of p53 Codon 72 Polymorphism Status Determined by Multiple Laboratory Methods: A Latent Class Model Analysis  Journal Articles
• Amber, ochre and opal suppressor tRNA genes derived from a human serine tRNA gene.  Journal Articles
• Amino acid substitutions of the P2 residue of human antithrombin that either enhance or impair function  Journal Articles
• An inducible mammalian amber suppressor: Propagation of a poliovirus mutant  Journal Articles
• Antithrombin-III-Hamilton: a gene with a point mutation (guanine to adenine) in codon 382 causing impaired serine protease reactivity  Journal Articles
• Antithrombin-III-Stockholm: a codon 392 (Gly----Asp) mutation with normal heparin binding and impaired serine protease reactivity  Journal Articles
• Assay of HIV gp41 amino acid sequence to identify baseline variation and mutation development in patients with virologic failure on enfuvirtide☆  Journal Articles
• 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  Journal Articles
• Codon Bias and Base Composition Are Poor Indicators of Horizontally Transferred Genes  Journal Articles
• Codon Usage and Selection on Proteins  Journal Articles
• Codon Usage in Mitochondrial Genomes: Distinguishing Context-Dependent Mutation from Translational Selection  Journal Articles
• Codon bias and frequency-dependent selection on the hemagglutinin epitopes of influenza A virus  Journal Articles
• Coevolution of Codon Usage and tRNA Genes Leads to Alternative Stable States of Biased Codon Usage  Journal Articles
• Contributions of Speed and Accuracy to Translational Selection in Bacteria  Journal Articles
• DOMINANT β-THALASSEMIA DUE TO A NEWLY IDENTIFIED FRAMESHIFT MUTATION IN EXON 3 (CODON 113, GTG → TG)  Journal Articles
• Detecting selection using a single genome sequence of M. tuberculosis and P. falciparum  Journal Articles
• Estimating Selection Pressures from Limited Comparative Data  Journal Articles
• Evolution of genes and genomes on the Drosophila phylogeny  Journal Articles
• Evolution of mitochondrial-encoded cytochrome oxidase subunits in endothermic fish: The importance of taxon-sampling in codon-based models  Journal Articles
• Expected frequencies of codon use as a function of mutation rates and codon fitnesses  Journal Articles
• Frameshift Mutation in the α2-Globin Gene Causing α⁺-Thalassemia: Codon 49 (−GC)  Journal Articles
• Ganglioside GM1 induces phosphorylation of mutant huntingtin and restores normal motor behavior in Huntington disease mice  Journal Articles
• Gene amelioration demonstrated: the journey of nascent genes in bacteria  Journal Articles
• Hb A₂Hong Kong – A Novel δ-Globin Variant in a Chinese Family Masks the Diagnosis of β-Thalassemia Trait  Journal Articles
• Hb Adana (HBA2 or HBA1: c.179G > A) and alpha thalassemia: Genotype–phenotype correlation  Journal Articles
• Hb H hydrops foetalis syndrome: a case report and review of literature  Journal Articles
• Hb Presbyterian (HBB: c.327C>G) in a Nicaraguan Family  Journal Articles
• IDENTIFICATION OF TWO NEW β-THALASSEMIA SPLICE MUTATIONS: IVS-I-1 (G → C) AND IVS-I (−2) (A → C)  Journal Articles
• Identifican of A New High Oxygen Affinity Hemoglobin Variant: Hb Aurora [β139(H17)Asn→Tyr]  Journal Articles
• 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]  Journal Articles
• Identification of two novel β°-thalassemia mutations in a filipino family: Frameshift codon 67 (− TG) and a β-globin gene deletion  Journal Articles
• 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.  Journal Articles
• Mild β⁺-Thalassemia Associated With Two Linked Sequence Variants: IVS-II-839 (T>C) and IVS-II-844 (C>A)  Journal Articles
• Multiple Mechanisms Promote the Retained Expression of Gene Duplicates in the Tetraploid Frog Xenopus laevis  Journal Articles
• Neurological Proteins Are Not Enriched For Repetitive Sequences  Journal Articles
• Novel Mutation of the α2-Globin Gene Initiation Codon (Atg→A-G) in a Vietnamese Girl with Hb H Disease  Journal Articles
• Novel dominant β‐thalassemia: Hb Boston‐Kuwait [Codon 139/140(+T)]  Journal Articles
• OGRe: a relational database for comparative analysis of mitochondrial genomes  Journal Articles
• Pathways of Genetic Code Evolution in Ancient and Modern Organisms  Journal Articles
• Prenatal exclusion of β thalassaemia major by examination of maternal plasma  Journal Articles
• 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.  Journal Articles
• Sequencing of heat shock protein 70 (DnaK) homologs from Deinococcus proteolyticus and Thermomicrobium roseum and their integration in a protein-based phylogeny of prokaryotes  Journal Articles
• The First Report of a Homozygous Codons 9/10 (+T) β-Thalassemia Mutation in a Turkish Patient  Journal Articles
• The Influence of Anticodon-Codon Interactions and Modified Bases on Codon Usage Bias in Bacteria  Journal Articles
• The Mechanisms of Codon Reassignments in Mitochondrial Genetic Codes  Journal Articles
• The Transcriptional Repressor ZEB Regulates p73 Expression at the Crossroad between Proliferation and Differentiation  Journal Articles
• The sequences of heat shock protein 40 (DnaJ) homologs provide evidence for a close evolutionary relationship between the Deinococcus- Thermus group and cyanobacteria  Journal Articles
• Three New α-Thalassemia Point Mutations Ascertained Through Newborn Screening  Journal Articles
• Two novel beta-thalassemia mutations in the 5' and 3' noncoding regions of the beta-globin gene [see comments]  Journal Articles
• α⁺-Thalassemia Due to a Frameshift Mutation of theα2-Globin Gene [codons 55/56 (+T) orHBA2: c.168dup]  Journal Articles
• α⁺-Thalassemia Trait Caused by a Frameshift Mutation in Exon 2 of the α2-Globin Gene [HBA2 c.244delT]  Journal Articles
• β-Thalassemia intermedia in a lebanese child due to homozygosity for the -88 (C→T) Mutation  Journal Articles
• δβ-Thalassemia in an African-American: Identification of the deletion endpoints and PCR-Based diagnosis  Journal Articles