- Why has nature invented three stop codons of DNA and only one start codon?2012 | First Faculty of Medicine
- Nuclear genetic codes with a different meaning of the UAG and the UAA codon2017 | Faculty of Science
- Low mutational rate of K-ras codon 12 in singular bronchoscopy specimens in suspected lung cancer2005 | First Faculty of Medicine, Third Faculty of Medicine
- Ambiguous decoding of the CUG codon alters the functionality of the Candida albicans translation initiation factor 4E2010 | Faculty of Science
- Short tRNA anticodon stem and mutant eRF1 allow stop codon reassignment2023 | Faculty of Science
- Translation initiation factor elF3 promotes programmed stop codon readthrough2015 | Faculty of Science
- uS3/Rps3 controls fidelity of translation termination and programmed stop codon readthrough in co-operation with eIF32019 | Faculty of Science
- Development and Characterization of a Chronic Hepatitis B Murine Model With a Mutation in the START Codon of an HBV Polymerase2023 | Faculty of Science, Faculty of Physical Education and Sport, Central Library of Charles University
- Hepatitis C virus internal ribosome entry site initiates protein synthesis at the authentic initiation codon in yeast2007 | Faculty of Science
- The occurence of point mutations in codon 13 of the K-ras gene by colorectal tumours2002 | Faculty of Medicine in Hradec Králové
- Patient with deletion of STOP codon in ATP6 gene mtDNA: the gene expression analysisPublication without faculty affiliation
- GUG is an efficient initiation codon to translate the human mitochondrial ATP6 gene2004 | First Faculty of Medicine
- Development of codon-optimized pH-sensitive GFP probes for in vivo organellar measurements.Publication without faculty affiliation
- p53 codon 72 polymorphism in pancreatic juice of patients with hepatobiliary diseasesPublication without faculty affiliation
- GUG is an efficient initiation codon to translate the human mitochondrial ATP6 gene2004 | Faculty of Physical Education and Sport
- No association between the TP53 codon 72 polymorphism and risk or prognosis of Hodgkin and non-Hodgkin lymphoma2011 | First Faculty of Medicine, Central Library of Charles University, Second Faculty of Medicine, Third Faculty of Medicine
- Rules of UGA-N decoding by near-cognate tRNAs and analysis of readthrough on short uORFs in yeast2016 | Faculty of Science
- A novel HLA-A null allele (A*02:395N ) with stop codon in exon 2 generated by single nucleotide exchange2013 | Faculty of Medicine in Pilsen
- Mapping 3 ' transcript ends in the bank vole (Clethrionomys glareolus) mitochondrial genome with RNA-Seq2015 | Faculty of Science
- A severe connatal form of Pelizaeus Merzbacher disease in a Czech boy caused by a novel mutation (725C > A, Ala242Glu) at the 'Jimpy(msd) codon' in the PLP gene2002 | Second Faculty of Medicine
- Molecular studies in 10 cases of Rubinstein-Taybi syndrome, including a mild variant showing a missense in codon 1175 of CREBBP2002 | Second Faculty of Medicine
- Yeast applied readthrough inducing system (YARIS): an invivo assay for the comprehensive study of translational readthrough2019 | Faculty of Science
- Evidence for an Independent Hydrogenosome-to-Mitosome Transition in the CL3 Lineage of Fornicates2022 | Faculty of Science
- Cystic fibrosis patients bearing both the common missense mutation GlyRIGHTWARDS ARROWAsp at codon 551 and the ΔF508 mutation are clinically indistinguishable from ΔF508 homozygotes, except for decreased risk of meconium ileus1992 | Second Faculty of Medicine
- A reappraisal of Aspergillus section Nidulantes with descriptions of two new sterigmatocystin-producing species2016 | Faculty of Science
- Why does DNA have three terminal triplets and only one initial triplet?2011 | First Faculty of Medicine
- Dominant beta-thalassaemic Alleles in the Czech and Slovak Population [beta-thalassaemic mutations in the codons 112 (T-A) and 121 (G-T) and unstable haemoglobin variant Hradec Králové or alfa2 beta2 115 (G17) Ala-Asp]1994 | First Faculty of Medicine
- β-tubulin paralogue tubC is frequently misidentified as the benA gene in Aspergillus section Nigri taxonomy: primer specifity testing and taxonomical consequences2012 | Faculty of Science, Faculty of Physical Education and Sport, First Faculty of Medicine
- A Rare Truncating BRCA2 Variant and Genetic Susceptibility to Upper Aerodigestive Tract Cancer2015 | First Faculty of Medicine
- Rare variants of large effect in BRCA2 and CHEK2 affect risk of lung cancer (Reprinted from Nature Genetics vol 46, pg 736, 2014 10.1038/ng.3002)2014 | First Faculty of Medicine