Stop codon (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Stop codon" in English language version.

Last modified: 18:30:08, 7 February 2026 (UTC)

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4846nih.gov

5^th place

3029doi.org

2^nd place

88semanticscholar.org

15^th place

8^th place

66adsabs.harvard.edu

14^th place

9^th place

33worldcat.org

4^th place

31books.google.com

3^rd place

22nature.com

207^th place

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11hdl.handle.net

66^th place

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11sciencedirect.com

137^th place

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11oup.com

292^nd place

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11science.org

1,007^th place

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11bookrags.com

5,823^rd place

4,904^th place

11archives-ouvertes.fr

1,143^rd place

973^rd place

11ted.com

2,839^th place

2,020^th place

adsabs.harvard.edu (Global: 14^th place; English: 9^th place)

ui.adsabs.harvard.edu

Barrell, B. G.; Bankier, A. T.; Drouin, J. (1979-11-08). "A different genetic code in human mitochondria". Nature. 282 (5735): 189–194. Bibcode:1979Natur.282..189B. doi:10.1038/282189a0. ISSN 0028-0836. PMID 226894. S2CID 4335828.
Zinoni, F; Birkmann, A; Stadtman, T; Böck, A (1986). "Nucleotide sequence and expression of the selenocysteine-containing polypeptide of formate dehydrogenase (formate-hydrogen-lyase-linked) from Escherichia coli". Proceedings of the National Academy of Sciences. 83 (13): 4650–4. Bibcode:1986PNAS...83.4650Z. doi:10.1073/pnas.83.13.4650. PMC 323799. PMID 2941757.
Kryukov, G; Gladyshev, V (2003). "Characterization of mammalian selenoproteomes". Science. 300 (5624): 1439–43. Bibcode:2003Sci...300.1439K. doi:10.1126/science.1083516. PMID 12775843. S2CID 10363908.
Brenner, S.; Stretton, A. O. W.; Kaplan, S. (1965). "Genetic Code: The 'Nonsense' Triplets for Chain Termination and their Suppression". Nature. 206 (4988): 994–8. Bibcode:1965Natur.206..994B. doi:10.1038/206994a0. PMID 5320272. S2CID 28502898.
Brenner, S.; Barnett, L.; Katz, E. R.; Crick, F. H. C. (1967). "UGA: A Third Nonsense Triplet in the Genetic Code". Nature. 213 (5075): 449–50. Bibcode:1967Natur.213..449B. doi:10.1038/213449a0. PMID 6032223. S2CID 4211867.
Wong, Tit-Yee; Schwartzbach, Steve (2015). "Protein mis-termination initiates genetic diseases, cancers, and restricts bacterial genome expansion". Journal of Environmental Science and Health, Part C. 33 (3): 255–85. Bibcode:2015JESHC..33..255W. doi:10.1080/10590501.2015.1053461. PMID 26087060. S2CID 20380447.

archives-ouvertes.fr (Global: 1,143^rd place; English: 973^rd place)

hal.archives-ouvertes.fr

Torres-Torronteras, J.; Rodriguez-Palmero, A.; et al. (2011). "A novel nonstop mutation in TYMP does not induce nonstop mRNA decay in a MNGIE patient with severe neuropathy" (PDF). Hum. Mutat. 32 (4): E2061–E2068. doi:10.1002/humu.21447. PMID 21412940. S2CID 24446773.

bookrags.com (Global: 5,823^rd place; English: 4,904^th place)

Robin Cook. "Amber, Ocher, and Opal Mutations Summary". World of Genetics. Gale.

books.google.com (Global: 3^rd place; English: 3^rd place)

Lewin, Benjamin; Krebs, Jocelyn E.; Goldstein, Elliott S.; Kilpatrick, Stephen T. (2011-04-18). Lewin's Essential GENES. Jones & Bartlett. ISBN 978-1-4496-4380-5.

doi.org (Global: 2^nd place; English: 2^nd place)

Barrell, B. G.; Bankier, A. T.; Drouin, J. (1979-11-08). "A different genetic code in human mitochondria". Nature. 282 (5735): 189–194. Bibcode:1979Natur.282..189B. doi:10.1038/282189a0. ISSN 0028-0836. PMID 226894. S2CID 4335828.
Nedelcu, A.M.; Lee, R.W.; Lemieux, G.; Gray, M.W.; Burger, G. (June 2000). "The complete mitochondrial DNA sequence of Scenedesmus obliquus reflects an intermediate stage in the evolution of the green algal mitochondrial genome". Genome Research. 10 (6): 819–831. doi:10.1101/gr.10.6.819. PMC 310893. PMID 10854413.
Wideman, Jeremy G.; Monier, Adam; Rodríguez-Martínez, Raquel; Leonard, Guy; Cook, Emily; Poirier, Camille; Maguire, Finlay; Milner, David S.; Irwin, Nicholas A. T.; Moore, Karen; Santoro, Alyson E. (2019-11-25). "Unexpected mitochondrial genome diversity revealed by targeted single-cell genomics of heterotrophic flagellated protists". Nature Microbiology. 5 (1): 154–165. doi:10.1038/s41564-019-0605-4. hdl:10871/39819. ISSN 2058-5276. PMID 31768028. S2CID 208279678.
Swart, Estienne Carl; Serra, Valentina; Petroni, Giulio; Nowacki, Mariusz (2016). "Genetic Codes with No Dedicated Stop Codon: Context-Dependent Translation Termination". Cell. 166 (3): 691–702. doi:10.1016/j.cell.2016.06.020. PMC 4967479. PMID 27426948.
Zinoni, F; Birkmann, A; Stadtman, T; Böck, A (1986). "Nucleotide sequence and expression of the selenocysteine-containing polypeptide of formate dehydrogenase (formate-hydrogen-lyase-linked) from Escherichia coli". Proceedings of the National Academy of Sciences. 83 (13): 4650–4. Bibcode:1986PNAS...83.4650Z. doi:10.1073/pnas.83.13.4650. PMC 323799. PMID 2941757.
Böck, A (2013). "Selenoprotein Synthesis". Encyclopedia of Biological Chemistry. pp. 210–3. doi:10.1016/B978-0-12-378630-2.00025-6. ISBN 978-0-12-378631-9. Retrieved 23 August 2021.
Mix, H; Lobanov, A; Gladyshev, V (2007). "SECIS elements in the coding regions of selenoprotein transcripts are functional in higher eukaryotes". Nucleic Acids Research. 35 (2): 414–423. doi:10.1093/nar/gkl1060. PMC 1802603. PMID 17169995.
Kryukov, G; Gladyshev, V (2003). "Characterization of mammalian selenoproteomes". Science. 300 (5624): 1439–43. Bibcode:2003Sci...300.1439K. doi:10.1126/science.1083516. PMID 12775843. S2CID 10363908.
Povolotskaya IS, Kondrashov FA, Ledda A, Vlasov PK (2012). "Stop codons in bacteria are not selectively equivalent". Biology Direct. 7 30. doi:10.1186/1745-6150-7-30. PMC 3549826. PMID 22974057.
Korkmaz, Gürkan; Holm, Mikael; Wiens, Tobias; Sanyal, Suparna (2014). "Comprehensive Analysis of Stop Codon Usage in Bacteria and Its Correlation with Release Factor Abundance". The Journal of Biological Chemistry. 289 (44): 775–806. doi:10.1074/jbc.M114.606632. PMC 4215218. PMID 25217634.
Wong, Tit-Yee; Fernandes, Sanjit; Sankhon, Naby; Leong, Patrick P; Kuo, Jimmy; Liu, Jong-Kang (2008). "Role of Premature Stop Codons in Bacterial Evolution". Journal of Bacteriology. 190 (20): 6718–25. doi:10.1128/JB.00682-08. PMC 2566208. PMID 18708500.
Ito, Koichi; Uno, Makiko; Nakamura, Yoshikazu (1999). "A tripeptide 'anticodon' deciphers stop codons in messenger RNA". Nature. 403 (6770): 680–4. doi:10.1038/35001115. PMID 10688208. S2CID 4331695.
Korkmaz, Gürkan; Sanyal, Suparna (2017). "R213I mutation in release factor 2 (RF2) is one step forward for engineering an omnipotent release factor in bacteria Escherichia coli". Journal of Biological Chemistry. 292 (36): 15134–42. doi:10.1074/jbc.M117.785238. PMC 5592688. PMID 28743745.
Stahl FW (1995). "The amber mutants of phage T4". Genetics. 141 (2): 439–442. doi:10.1093/genetics/141.2.439. PMC 1206745. PMID 8647382.
Edgar B (October 2004). "The genome of bacteriophage T4: an archeological dig". Genetics. 168 (2): 575–82. doi:10.1093/genetics/168.2.575. PMC 1448817. PMID 15514035.
Brenner, S.; Stretton, A. O. W.; Kaplan, S. (1965). "Genetic Code: The 'Nonsense' Triplets for Chain Termination and their Suppression". Nature. 206 (4988): 994–8. Bibcode:1965Natur.206..994B. doi:10.1038/206994a0. PMID 5320272. S2CID 28502898.
Brenner, S.; Barnett, L.; Katz, E. R.; Crick, F. H. C. (1967). "UGA: A Third Nonsense Triplet in the Genetic Code". Nature. 213 (5075): 449–50. Bibcode:1967Natur.213..449B. doi:10.1038/213449a0. PMID 6032223. S2CID 4211867.
Pang S.; Wang W.; et al. (2002). "A novel nonstop mutation in the stop codon and a novel missense mutation in the type II 3beta-hydroxysteroid dehydrogenase (3beta-HSD) gene causing, respectively, nonclassic and classic 3beta-HSD deficiency congenital adrenal hyperplasia". J Clin Endocrinol Metab. 87 (6): 2556–63. doi:10.1210/jcem.87.6.8559. PMID 12050213.
Doucette, L.; et al. (2011). "A novel, non-stop mutation in FOXE3 causes an autosomal dominant form of variable anterior segment dysgenesis including Peters anomaly". European Journal of Human Genetics. 19 (3): 293–9. doi:10.1038/ejhg.2010.210. PMC 3062009. PMID 21150893.
Torres-Torronteras, J.; Rodriguez-Palmero, A.; et al. (2011). "A novel nonstop mutation in TYMP does not induce nonstop mRNA decay in a MNGIE patient with severe neuropathy" (PDF). Hum. Mutat. 32 (4): E2061–E2068. doi:10.1002/humu.21447. PMID 21412940. S2CID 24446773.
Spaull, R; Steel, D; Barwick, K; Prabhakar, P; Wakeling, E; Kurian, MA (2022-07-23). "STXBP1 Stop-Loss Mutation Associated with Complex Early Onset Movement Disorder without Epilepsy". Movement Disorders Clinical Practice. 9 (6): 837–840. doi:10.1002/mdc3.13509. PMC 9346254. PMID 35937496.
Seligmann, Hervé; Pollock, David D. (2004). "The Ambush Hypothesis: Hidden Stop Codons Prevent Off-Frame Gene Reading". DNA and Cell Biology. 23 (10): 701–5. doi:10.1089/1044549042476910. PMID 15585128.
Cavalcanti, Andre; Chang, Charlotte H.; Morgens, David W. (2013). "Ambushing the ambush hypothesis: predicting and evaluating off-frame codon frequencies in Prokaryotic Genomes". BMC Genomics. 14 (418): 1–8. doi:10.1186/1471-2164-14-418. PMC 3700767. PMID 23799949.
Wong, Tit-Yee; Schwartzbach, Steve (2015). "Protein mis-termination initiates genetic diseases, cancers, and restricts bacterial genome expansion". Journal of Environmental Science and Health, Part C. 33 (3): 255–85. Bibcode:2015JESHC..33..255W. doi:10.1080/10590501.2015.1053461. PMID 26087060. S2CID 20380447.
Namy O, Rousset JP, Napthine S, Brierley I (2004). "Reprogrammed genetic decoding in cellular gene expression". Molecular Cell. 13 (2): 157–68. doi:10.1016/S1097-2765(04)00031-0. PMID 14759362.
Schueren F, Lingner T, George R, Hofhuis J, Gartner J, Thoms S (2014). "Peroxisomal lactate dehydrogenase is generated by translational readthrough in mammals". eLife. 3 e03640. doi:10.7554/eLife.03640. PMC 4359377. PMID 25247702.
Hofhuis J, Schueren F, Nötzel C, Lingner T, Gärtner J, Jahn O, Thoms S (2016). "The functional readthrough extension of malate dehydrogenase reveals a modification of the genetic code". Open Biol. 6 (11) 160246. doi:10.1098/rsob.160246. PMC 5133446. PMID 27881739.
Blanchet S, Cornu D, Argentini M, Namy O (2014). "New insights into the incorporation of natural suppressor tRNAs at stop codons in Saccharomyces cerevisiae". Nucleic Acids Res. 42 (15): 10061–72. doi:10.1093/nar/gku663. PMC 4150775. PMID 25056309.
Ghosh, Souvik; Guimaraes, Joao C; Lanzafame, Manuela; Schmidt, Alexander; Syed, Afzal Pasha; Dimitriades, Beatrice; Börsch, Anastasiya; Ghosh, Shreemoyee; Mittal, Nitish; Montavon, Thomas; Correia, Ana Luisa; Danner, Johannes; Meister, Gunter; Terracciano, Luigi M; Pfeffer, Sébastien; Piscuoglio, Salvatore; Zavolan, Mihaela (15 September 2020). "Prevention of dsRNA-induced interferon signaling by AGO1x is linked to breast cancer cell proliferation". The EMBO Journal. 39 (18) e103922. doi:10.15252/embj.2019103922. PMC 7507497. PMID 32812257.

hdl.handle.net (Global: 66^th place; English: 34^th place)

Wideman, Jeremy G.; Monier, Adam; Rodríguez-Martínez, Raquel; Leonard, Guy; Cook, Emily; Poirier, Camille; Maguire, Finlay; Milner, David S.; Irwin, Nicholas A. T.; Moore, Karen; Santoro, Alyson E. (2019-11-25). "Unexpected mitochondrial genome diversity revealed by targeted single-cell genomics of heterotrophic flagellated protists". Nature Microbiology. 5 (1): 154–165. doi:10.1038/s41564-019-0605-4. hdl:10871/39819. ISSN 2058-5276. PMID 31768028. S2CID 208279678.

nature.com (Global: 207^th place; English: 347^th place)

Barrell, B. G.; Bankier, A. T.; Drouin, J. (1979-11-08). "A different genetic code in human mitochondria". Nature. 282 (5735): 189–194. Bibcode:1979Natur.282..189B. doi:10.1038/282189a0. ISSN 0028-0836. PMID 226894. S2CID 4335828.
Wideman, Jeremy G.; Monier, Adam; Rodríguez-Martínez, Raquel; Leonard, Guy; Cook, Emily; Poirier, Camille; Maguire, Finlay; Milner, David S.; Irwin, Nicholas A. T.; Moore, Karen; Santoro, Alyson E. (2019-11-25). "Unexpected mitochondrial genome diversity revealed by targeted single-cell genomics of heterotrophic flagellated protists". Nature Microbiology. 5 (1): 154–165. doi:10.1038/s41564-019-0605-4. hdl:10871/39819. ISSN 2058-5276. PMID 31768028. S2CID 208279678.

nih.gov (Global: 5^th place; English: 5^th place)

pubmed.ncbi.nlm.nih.gov

Barrell, B. G.; Bankier, A. T.; Drouin, J. (1979-11-08). "A different genetic code in human mitochondria". Nature. 282 (5735): 189–194. Bibcode:1979Natur.282..189B. doi:10.1038/282189a0. ISSN 0028-0836. PMID 226894. S2CID 4335828.
Nedelcu, A.M.; Lee, R.W.; Lemieux, G.; Gray, M.W.; Burger, G. (June 2000). "The complete mitochondrial DNA sequence of Scenedesmus obliquus reflects an intermediate stage in the evolution of the green algal mitochondrial genome". Genome Research. 10 (6): 819–831. doi:10.1101/gr.10.6.819. PMC 310893. PMID 10854413.
Wideman, Jeremy G.; Monier, Adam; Rodríguez-Martínez, Raquel; Leonard, Guy; Cook, Emily; Poirier, Camille; Maguire, Finlay; Milner, David S.; Irwin, Nicholas A. T.; Moore, Karen; Santoro, Alyson E. (2019-11-25). "Unexpected mitochondrial genome diversity revealed by targeted single-cell genomics of heterotrophic flagellated protists". Nature Microbiology. 5 (1): 154–165. doi:10.1038/s41564-019-0605-4. hdl:10871/39819. ISSN 2058-5276. PMID 31768028. S2CID 208279678.
Swart, Estienne Carl; Serra, Valentina; Petroni, Giulio; Nowacki, Mariusz (2016). "Genetic Codes with No Dedicated Stop Codon: Context-Dependent Translation Termination". Cell. 166 (3): 691–702. doi:10.1016/j.cell.2016.06.020. PMC 4967479. PMID 27426948.
Zinoni, F; Birkmann, A; Stadtman, T; Böck, A (1986). "Nucleotide sequence and expression of the selenocysteine-containing polypeptide of formate dehydrogenase (formate-hydrogen-lyase-linked) from Escherichia coli". Proceedings of the National Academy of Sciences. 83 (13): 4650–4. Bibcode:1986PNAS...83.4650Z. doi:10.1073/pnas.83.13.4650. PMC 323799. PMID 2941757.
Mix, H; Lobanov, A; Gladyshev, V (2007). "SECIS elements in the coding regions of selenoprotein transcripts are functional in higher eukaryotes". Nucleic Acids Research. 35 (2): 414–423. doi:10.1093/nar/gkl1060. PMC 1802603. PMID 17169995.
Kryukov, G; Gladyshev, V (2003). "Characterization of mammalian selenoproteomes". Science. 300 (5624): 1439–43. Bibcode:2003Sci...300.1439K. doi:10.1126/science.1083516. PMID 12775843. S2CID 10363908.
Povolotskaya IS, Kondrashov FA, Ledda A, Vlasov PK (2012). "Stop codons in bacteria are not selectively equivalent". Biology Direct. 7 30. doi:10.1186/1745-6150-7-30. PMC 3549826. PMID 22974057.
Korkmaz, Gürkan; Holm, Mikael; Wiens, Tobias; Sanyal, Suparna (2014). "Comprehensive Analysis of Stop Codon Usage in Bacteria and Its Correlation with Release Factor Abundance". The Journal of Biological Chemistry. 289 (44): 775–806. doi:10.1074/jbc.M114.606632. PMC 4215218. PMID 25217634.
Wong, Tit-Yee; Fernandes, Sanjit; Sankhon, Naby; Leong, Patrick P; Kuo, Jimmy; Liu, Jong-Kang (2008). "Role of Premature Stop Codons in Bacterial Evolution". Journal of Bacteriology. 190 (20): 6718–25. doi:10.1128/JB.00682-08. PMC 2566208. PMID 18708500.
Ito, Koichi; Uno, Makiko; Nakamura, Yoshikazu (1999). "A tripeptide 'anticodon' deciphers stop codons in messenger RNA". Nature. 403 (6770): 680–4. doi:10.1038/35001115. PMID 10688208. S2CID 4331695.
Korkmaz, Gürkan; Sanyal, Suparna (2017). "R213I mutation in release factor 2 (RF2) is one step forward for engineering an omnipotent release factor in bacteria Escherichia coli". Journal of Biological Chemistry. 292 (36): 15134–42. doi:10.1074/jbc.M117.785238. PMC 5592688. PMID 28743745.
Stahl FW (1995). "The amber mutants of phage T4". Genetics. 141 (2): 439–442. doi:10.1093/genetics/141.2.439. PMC 1206745. PMID 8647382.
Edgar B (October 2004). "The genome of bacteriophage T4: an archeological dig". Genetics. 168 (2): 575–82. doi:10.1093/genetics/168.2.575. PMC 1448817. PMID 15514035.
Brenner, S.; Stretton, A. O. W.; Kaplan, S. (1965). "Genetic Code: The 'Nonsense' Triplets for Chain Termination and their Suppression". Nature. 206 (4988): 994–8. Bibcode:1965Natur.206..994B. doi:10.1038/206994a0. PMID 5320272. S2CID 28502898.
Brenner, S.; Barnett, L.; Katz, E. R.; Crick, F. H. C. (1967). "UGA: A Third Nonsense Triplet in the Genetic Code". Nature. 213 (5075): 449–50. Bibcode:1967Natur.213..449B. doi:10.1038/213449a0. PMID 6032223. S2CID 4211867.
Pang S.; Wang W.; et al. (2002). "A novel nonstop mutation in the stop codon and a novel missense mutation in the type II 3beta-hydroxysteroid dehydrogenase (3beta-HSD) gene causing, respectively, nonclassic and classic 3beta-HSD deficiency congenital adrenal hyperplasia". J Clin Endocrinol Metab. 87 (6): 2556–63. doi:10.1210/jcem.87.6.8559. PMID 12050213.
Doucette, L.; et al. (2011). "A novel, non-stop mutation in FOXE3 causes an autosomal dominant form of variable anterior segment dysgenesis including Peters anomaly". European Journal of Human Genetics. 19 (3): 293–9. doi:10.1038/ejhg.2010.210. PMC 3062009. PMID 21150893.
Torres-Torronteras, J.; Rodriguez-Palmero, A.; et al. (2011). "A novel nonstop mutation in TYMP does not induce nonstop mRNA decay in a MNGIE patient with severe neuropathy" (PDF). Hum. Mutat. 32 (4): E2061–E2068. doi:10.1002/humu.21447. PMID 21412940. S2CID 24446773.
Spaull, R; Steel, D; Barwick, K; Prabhakar, P; Wakeling, E; Kurian, MA (2022-07-23). "STXBP1 Stop-Loss Mutation Associated with Complex Early Onset Movement Disorder without Epilepsy". Movement Disorders Clinical Practice. 9 (6): 837–840. doi:10.1002/mdc3.13509. PMC 9346254. PMID 35937496.
Seligmann, Hervé; Pollock, David D. (2004). "The Ambush Hypothesis: Hidden Stop Codons Prevent Off-Frame Gene Reading". DNA and Cell Biology. 23 (10): 701–5. doi:10.1089/1044549042476910. PMID 15585128.
Cavalcanti, Andre; Chang, Charlotte H.; Morgens, David W. (2013). "Ambushing the ambush hypothesis: predicting and evaluating off-frame codon frequencies in Prokaryotic Genomes". BMC Genomics. 14 (418): 1–8. doi:10.1186/1471-2164-14-418. PMC 3700767. PMID 23799949.
Wong, Tit-Yee; Schwartzbach, Steve (2015). "Protein mis-termination initiates genetic diseases, cancers, and restricts bacterial genome expansion". Journal of Environmental Science and Health, Part C. 33 (3): 255–85. Bibcode:2015JESHC..33..255W. doi:10.1080/10590501.2015.1053461. PMID 26087060. S2CID 20380447.
Namy O, Rousset JP, Napthine S, Brierley I (2004). "Reprogrammed genetic decoding in cellular gene expression". Molecular Cell. 13 (2): 157–68. doi:10.1016/S1097-2765(04)00031-0. PMID 14759362.
Schueren F, Lingner T, George R, Hofhuis J, Gartner J, Thoms S (2014). "Peroxisomal lactate dehydrogenase is generated by translational readthrough in mammals". eLife. 3 e03640. doi:10.7554/eLife.03640. PMC 4359377. PMID 25247702.
Hofhuis J, Schueren F, Nötzel C, Lingner T, Gärtner J, Jahn O, Thoms S (2016). "The functional readthrough extension of malate dehydrogenase reveals a modification of the genetic code". Open Biol. 6 (11) 160246. doi:10.1098/rsob.160246. PMC 5133446. PMID 27881739.
Blanchet S, Cornu D, Argentini M, Namy O (2014). "New insights into the incorporation of natural suppressor tRNAs at stop codons in Saccharomyces cerevisiae". Nucleic Acids Res. 42 (15): 10061–72. doi:10.1093/nar/gku663. PMC 4150775. PMID 25056309.
Ghosh, Souvik; Guimaraes, Joao C; Lanzafame, Manuela; Schmidt, Alexander; Syed, Afzal Pasha; Dimitriades, Beatrice; Börsch, Anastasiya; Ghosh, Shreemoyee; Mittal, Nitish; Montavon, Thomas; Correia, Ana Luisa; Danner, Johannes; Meister, Gunter; Terracciano, Luigi M; Pfeffer, Sébastien; Piscuoglio, Salvatore; Zavolan, Mihaela (15 September 2020). "Prevention of dsRNA-induced interferon signaling by AGO1x is linked to breast cancer cell proliferation". The EMBO Journal. 39 (18) e103922. doi:10.15252/embj.2019103922. PMC 7507497. PMID 32812257.

ncbi.nlm.nih.gov

Nedelcu, A.M.; Lee, R.W.; Lemieux, G.; Gray, M.W.; Burger, G. (June 2000). "The complete mitochondrial DNA sequence of Scenedesmus obliquus reflects an intermediate stage in the evolution of the green algal mitochondrial genome". Genome Research. 10 (6): 819–831. doi:10.1101/gr.10.6.819. PMC 310893. PMID 10854413.
Swart, Estienne Carl; Serra, Valentina; Petroni, Giulio; Nowacki, Mariusz (2016). "Genetic Codes with No Dedicated Stop Codon: Context-Dependent Translation Termination". Cell. 166 (3): 691–702. doi:10.1016/j.cell.2016.06.020. PMC 4967479. PMID 27426948.
Zinoni, F; Birkmann, A; Stadtman, T; Böck, A (1986). "Nucleotide sequence and expression of the selenocysteine-containing polypeptide of formate dehydrogenase (formate-hydrogen-lyase-linked) from Escherichia coli". Proceedings of the National Academy of Sciences. 83 (13): 4650–4. Bibcode:1986PNAS...83.4650Z. doi:10.1073/pnas.83.13.4650. PMC 323799. PMID 2941757.
Mix, H; Lobanov, A; Gladyshev, V (2007). "SECIS elements in the coding regions of selenoprotein transcripts are functional in higher eukaryotes". Nucleic Acids Research. 35 (2): 414–423. doi:10.1093/nar/gkl1060. PMC 1802603. PMID 17169995.
Povolotskaya IS, Kondrashov FA, Ledda A, Vlasov PK (2012). "Stop codons in bacteria are not selectively equivalent". Biology Direct. 7 30. doi:10.1186/1745-6150-7-30. PMC 3549826. PMID 22974057.
Korkmaz, Gürkan; Holm, Mikael; Wiens, Tobias; Sanyal, Suparna (2014). "Comprehensive Analysis of Stop Codon Usage in Bacteria and Its Correlation with Release Factor Abundance". The Journal of Biological Chemistry. 289 (44): 775–806. doi:10.1074/jbc.M114.606632. PMC 4215218. PMID 25217634.
"Escherichia coli str. K-12 substr. MG1655, complete genome [Genbank Accession Number: U00096]". GenBank. NCBI. Retrieved 2013-01-27.
Wong, Tit-Yee; Fernandes, Sanjit; Sankhon, Naby; Leong, Patrick P; Kuo, Jimmy; Liu, Jong-Kang (2008). "Role of Premature Stop Codons in Bacterial Evolution". Journal of Bacteriology. 190 (20): 6718–25. doi:10.1128/JB.00682-08. PMC 2566208. PMID 18708500.
Korkmaz, Gürkan; Sanyal, Suparna (2017). "R213I mutation in release factor 2 (RF2) is one step forward for engineering an omnipotent release factor in bacteria Escherichia coli". Journal of Biological Chemistry. 292 (36): 15134–42. doi:10.1074/jbc.M117.785238. PMC 5592688. PMID 28743745.
Stahl FW (1995). "The amber mutants of phage T4". Genetics. 141 (2): 439–442. doi:10.1093/genetics/141.2.439. PMC 1206745. PMID 8647382.
Edgar B (October 2004). "The genome of bacteriophage T4: an archeological dig". Genetics. 168 (2): 575–82. doi:10.1093/genetics/168.2.575. PMC 1448817. PMID 15514035.
Doucette, L.; et al. (2011). "A novel, non-stop mutation in FOXE3 causes an autosomal dominant form of variable anterior segment dysgenesis including Peters anomaly". European Journal of Human Genetics. 19 (3): 293–9. doi:10.1038/ejhg.2010.210. PMC 3062009. PMID 21150893.
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Stop codon (English Wikipedia)

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