Codon
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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
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A Non-Long Terminal Repeat Retrotransposon Family Is Restricted to the Germ Line Micronucleus of the Ciliated Protozoan
Tetrahymena thermophila Academic Article
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A Thermodynamic Basis for Prebiotic Amino Acid Synthesis and the Nature of the First Genetic Code Academic Article
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A Unified Model of Codon Reassignment in Alternative Genetic Codes Academic Article
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A four-column theory for the origin of the genetic code: tracing the evolutionary pathways that gave rise to an optimized code Academic Article
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A new frameshift β°-thalassemia mutation (codons 27–28 +C) found in a Chinese family Academic Article
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A novel and de novo spontaneous point mutation (Glu271STOP) of the antithrombin gene results in a type I deficiency and thrombophilia Academic Article
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A novel candidate region for ALS on chromosome 14q11.2 Academic Article
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A phylogenetic analysis based on the gene encoding phosphoglycerate kinase Academic Article
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Absence of germline and somatic p53 alterations in children with sporadic brain tumors. Academic Article
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Accuracy of p53 Codon 72 Polymorphism Status Determined by Multiple Laboratory Methods: A Latent Class Model Analysis Academic Article
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Amber, ochre and opal suppressor tRNA genes derived from a human serine tRNA gene. Academic Article
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Amino acid substitutions of the P2 residue of human antithrombin that either enhance or impair function Academic Article
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An inducible mammalian amber suppressor: Propagation of a poliovirus mutant Academic Article
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Antithrombin-III-Hamilton: a gene with a point mutation (guanine to adenine) in codon 382 causing impaired serine protease reactivity Academic Article
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Antithrombin-III-Stockholm: a codon 392 (Gly----Asp) mutation with normal heparin binding and impaired serine protease reactivity Academic Article
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Assay of HIV gp41 amino acid sequence to identify baseline variation and mutation development in patients with virologic failure on enfuvirtide☆ Academic Article
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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
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Codon Bias and Base Composition Are Poor Indicators of Horizontally Transferred Genes Academic Article
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Codon Usage and Selection on Proteins Academic Article
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Codon Usage in Mitochondrial Genomes: Distinguishing Context-Dependent Mutation from Translational Selection Academic Article
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Codon bias and frequency-dependent selection on the hemagglutinin epitopes of influenza A virus Academic Article
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Coevolution of Codon Usage and tRNA Genes Leads to Alternative Stable States of Biased Codon Usage Academic Article
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Contributions of Speed and Accuracy to Translational Selection in Bacteria Academic Article
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DOMINANT β-THALASSEMIA DUE TO A NEWLY IDENTIFIED FRAMESHIFT MUTATION IN EXON 3 (CODON 113, GTG → TG) Academic Article
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Detecting selection using a single genome sequence of M. tuberculosis and P. falciparum Academic Article
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Estimating Selection Pressures from Limited Comparative Data Academic Article
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Evolution of genes and genomes on the Drosophila phylogeny Academic Article
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Evolution of mitochondrial-encoded cytochrome oxidase subunits in endothermic fish: The importance of taxon-sampling in codon-based models Academic Article
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Expected frequencies of codon use as a function of mutation rates and codon fitnesses Academic Article
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Frameshift Mutation in the α2-Globin Gene Causing α+-Thalassemia: Codon 49 (−GC) Academic Article
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Ganglioside GM1 induces phosphorylation of mutant huntingtin and restores normal motor behavior in Huntington disease mice Academic Article
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Gene amelioration demonstrated: the journey of nascent genes in bacteria Academic Article
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Hb A2Hong Kong – A Novel δ-Globin Variant in a Chinese Family Masks the Diagnosis of β-Thalassemia Trait Academic Article
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Hb Adana (HBA2 or HBA1: c.179G > A) and alpha thalassemia: Genotype-phenotype correlation Academic Article
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Hb H hydrops foetalis syndrome: a case report and review of literature Academic Article
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Hb Presbyterian (HBB: c.327C>G) in a Nicaraguan Family Academic Article
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IDENTIFICATION OF TWO NEW β-THALASSEMIA SPLICE MUTATIONS: IVS-I-1 (G → C) AND IVS-I (−2) (A → C) Academic Article
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Identifican of A New High Oxygen Affinity Hemoglobin Variant: Hb Aurora [β139(H17)Asn→Tyr] Academic Article
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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
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Identification of two novel β°-thalassemia mutations in a filipino family: Frameshift codon 67 (− TG) and a β-globin gene deletion Academic Article
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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
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Mild β+-Thalassemia Associated With Two Linked Sequence Variants: IVS-II-839 (T>C) and IVS-II-844 (C>A) Academic Article
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Multiple Mechanisms Promote the Retained Expression of Gene Duplicates in the Tetraploid Frog Xenopus laevis Academic Article
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Neurological Proteins Are Not Enriched For Repetitive Sequences Academic Article
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Novel Mutation of the α2-Globin Gene Initiation Codon (Atg→A-G) in a Vietnamese Girl with Hb H Disease Academic Article
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Novel dominant β-thalassemia: Hb Boston-Kuwait [Codon 139/140(+T)] Academic Article
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OGRe: a relational database for comparative analysis of mitochondrial genomes Academic Article
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Pathways of Genetic Code Evolution in Ancient and Modern Organisms Academic Article
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Positional effects on the structure and stability of abbreviated H-ras DNA sequences containing O6-methylguanine residues at codon 12 Academic Article
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Prenatal exclusion of β thalassaemia major by examination of maternal plasma Academic Article
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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
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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
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Structure and function of tryptophan tRNA from wheat germ Academic Article
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The First Report of a Homozygous Codons 9/10 (+T) β-Thalassemia Mutation in a Turkish Patient Academic Article
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The Influence of Anticodon-Codon Interactions and Modified Bases on Codon Usage Bias in Bacteria Academic Article
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The Italian AICE-Genetics hemophilia A database: results and correlation with clinical phenotype Academic Article
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The Mechanisms of Codon Reassignments in Mitochondrial Genetic Codes Academic Article
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The Transcriptional Repressor ZEB Regulates p73 Expression at the Crossroad between Proliferation and Differentiation Academic Article
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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
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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
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Three New α-Thalassemia Point Mutations Ascertained Through Newborn Screening Academic Article
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Two novel beta-thalassemia mutations in the 5' and 3' noncoding regions of the beta-globin gene [see comments] Academic Article
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α+-Thalassemia Due to a Frameshift Mutation of theα2-Globin Gene [codons 55/56 (+T) orHBA2: c.168dup] Academic Article
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α+-Thalassemia Trait Caused by a Frameshift Mutation in Exon 2 of the α2-Globin Gene [HBA2 c.244delT] Academic Article
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β-Thalassemia intermedia in a lebanese child due to homozygosity for the -88 (C→T) Mutation Academic Article
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δβ-Thalassemia in an African-American: Identification of the deletion endpoints and PCR-Based diagnosis Academic Article