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The effects of bromodeoxyuridine and bromouracil on regeneration inHydra.

Wilhelm Roux' Archiv fur Entwicklungsmechanik der Organismen

Goyns MH, Stanisstreet M.
PMID: 28304714
Wilhelm Roux Arch Entwickl Mech Org. 1974 Jun;175(2):87-90. doi: 10.1007/BF00574294.

The effects on tentacle regeneration inHydra of two DNA-antimetabolites, bromouracil and bromodeoxyuridine, have been studied. Bromouracil inhibits tentacle regeneration inH. vulgaris andH. viridis; bromodeoxynridine inhibits tentacle regeneration inH. vulgaris but notH. viridis over the range of concentrations studied. Thus...

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Goyns MH, Stanisstreet M. The effects of bromodeoxyuridine and bromouracil on regeneration inHydra. Wilhelm Roux Arch Entwickl Mech Org. 1974;175(2):87-90doi: 10.1007/BF00574294.
Goyns, M. H., & Stanisstreet, M. (1974). The effects of bromodeoxyuridine and bromouracil on regeneration inHydra. Wilhelm Roux' Archiv fur Entwicklungsmechanik der Organismen, 175(2), 87-90. https://doi.org/10.1007/BF00574294
Goyns, M H, and Stanisstreet, M. "The effects of bromodeoxyuridine and bromouracil on regeneration inHydra." Wilhelm Roux' Archiv fur Entwicklungsmechanik der Organismen vol. 175,2 (1974): 87-90. doi: https://doi.org/10.1007/BF00574294
Goyns MH, Stanisstreet M. The effects of bromodeoxyuridine and bromouracil on regeneration inHydra. Wilhelm Roux Arch Entwickl Mech Org. 1974 Jun;175(2):87-90. doi: 10.1007/BF00574294. PMID: 28304714.
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Photoreaction of DNA Containing 5-Halouracil and its Products.

Photochemistry and photobiology

Tashiro R, Sugiyama H.
PMID: 34543451
Photochem Photobiol. 2021 Sep 20; doi: 10.1111/php.13521. Epub 2021 Sep 20.

5-Halouracil, which is a DNA base analog in which the methyl group at the C5 position of thymine is replaced with a halogen atom, has been used in studies of DNA damage. In DNA strands, the uracil radical generated...

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Tashiro R, Sugiyama H. Photoreaction of DNA Containing 5-Halouracil and its Products. Photochem Photobiol. 2021;doi: 10.1111/php.13521.
Tashiro, R., & Sugiyama, H. (2021). Photoreaction of DNA Containing 5-Halouracil and its Products. Photochemistry and photobiology, . https://doi.org/10.1111/php.13521
Tashiro, Ryu, and Sugiyama, Hiroshi. "Photoreaction of DNA Containing 5-Halouracil and its Products." Photochemistry and photobiology vol. (2021). doi: https://doi.org/10.1111/php.13521
Tashiro R, Sugiyama H. Photoreaction of DNA Containing 5-Halouracil and its Products. Photochem Photobiol. 2021 Sep 20; doi: 10.1111/php.13521. Epub 2021 Sep 20. PMID: 34543451.
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Cytosine Iminyl Radical (cytN.

The journal of physical chemistry. A

Kumar A, Sevilla MD.
PMID: 28586202
J Phys Chem A. 2017 Jun 29;121(25):4825-4829. doi: 10.1021/acs.jpca.7b04034. Epub 2017 Jun 16.

Halogen-substituted pyrimidines, such as 5-bromouracil and 5-iodouracil, have been used as radio therapeutic (RT) agents in cancer treatment. The radiosensitizing activity of 5-bromouracil is attributed to its reaction with electron which produce the highly reactive uracil-5-yl radical by dissociating...

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Kumar A, Sevilla MD. Cytosine Iminyl Radical (cytN. J Phys Chem A. 2017;121(25):4825-4829doi: 10.1021/acs.jpca.7b04034.
Kumar, A., & Sevilla, M. D. (2017). Cytosine Iminyl Radical (cytN. The journal of physical chemistry. A, 121(25), 4825-4829. https://doi.org/10.1021/acs.jpca.7b04034
Kumar, Anil, and Sevilla, Michael D. "Cytosine Iminyl Radical (cytN." The journal of physical chemistry. A vol. 121,25 (2017): 4825-4829. doi: https://doi.org/10.1021/acs.jpca.7b04034
Kumar A, Sevilla MD. Cytosine Iminyl Radical (cytN. J Phys Chem A. 2017 Jun 29;121(25):4825-4829. doi: 10.1021/acs.jpca.7b04034. Epub 2017 Jun 16. PMID: 28586202; PMCID: PMC5521985.
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Fragmentation of pure and hydrated clusters of 5Br-uracil by low energy carbon ions: observation of hydrated fragments.

Physical chemistry chemical physics : PCCP

Castrovilli MC, Markush P, Bolognesi P, Rousseau P, Maclot S, Cartoni A, Delaunay R, Domaracka A, Kočišek J, Huber BA, Avaldi L, Lima N.
PMID: 28657102
Phys Chem Chem Phys. 2017 Aug 02;19(30):19807-19814. doi: 10.1039/c7cp02233f.

The fragmentation of the isolated 5-bromouracil (5BrU) molecule and pure and nano-hydrated 5BrU clusters induced by low energy

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Castrovilli MC, Markush P, Bolognesi P, et al. Fragmentation of pure and hydrated clusters of 5Br-uracil by low energy carbon ions: observation of hydrated fragments. Phys Chem Chem Phys. 2017;19(30):19807-19814doi: 10.1039/c7cp02233f.
Castrovilli, M. C., Markush, P., Bolognesi, P., Rousseau, P., Maclot, S., Cartoni, A., Delaunay, R., Domaracka, A., Kočišek, J., Huber, B. A., Avaldi, L., & Lima, N. (2017). Fragmentation of pure and hydrated clusters of 5Br-uracil by low energy carbon ions: observation of hydrated fragments. Physical chemistry chemical physics : PCCP, 19(30), 19807-19814. https://doi.org/10.1039/c7cp02233f
Castrovilli, M C, et al. "Fragmentation of pure and hydrated clusters of 5Br-uracil by low energy carbon ions: observation of hydrated fragments." Physical chemistry chemical physics : PCCP vol. 19,30 (2017): 19807-19814. doi: https://doi.org/10.1039/c7cp02233f
Castrovilli MC, Markush P, Bolognesi P, Rousseau P, Maclot S, Cartoni A, Delaunay R, Domaracka A, Kočišek J, Huber BA, Avaldi L, Lima N. Fragmentation of pure and hydrated clusters of 5Br-uracil by low energy carbon ions: observation of hydrated fragments. Phys Chem Chem Phys. 2017 Aug 02;19(30):19807-19814. doi: 10.1039/c7cp02233f. PMID: 28657102.
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Proton-coupled electron transfer is the dominant mechanism of reduction of haloacetates by the α-hydroxyethyl radical in aqueous media.

Physical chemistry chemical physics : PCCP

DŽeba I, Bonifačić M, Nikšić-Franjić I, Ljubić I.
PMID: 30033455
Phys Chem Chem Phys. 2018 Aug 01;20(30):19829-19840. doi: 10.1039/c8cp03544j.

The reaction systems of α-hydroxyalkyl radicals with halogenated organics in aqueous solutions are uniquely suited for studying the fundamentally important proton-coupled electron transfer (PCET) mechanism in competition with alternatives such as substitution, hydrogen abstraction, halogen atom abstraction etc. We...

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DŽeba I, Bonifačić M, Nikšić-Franjić I, et al. Proton-coupled electron transfer is the dominant mechanism of reduction of haloacetates by the α-hydroxyethyl radical in aqueous media. Phys Chem Chem Phys. 2018;20(30):19829-19840doi: 10.1039/c8cp03544j.
DŽeba, I., Bonifačić, M., Nikšić-Franjić, I., & Ljubić, I. (2018). Proton-coupled electron transfer is the dominant mechanism of reduction of haloacetates by the α-hydroxyethyl radical in aqueous media. Physical chemistry chemical physics : PCCP, 20(30), 19829-19840. https://doi.org/10.1039/c8cp03544j
DŽeba, Iva, et al. "Proton-coupled electron transfer is the dominant mechanism of reduction of haloacetates by the α-hydroxyethyl radical in aqueous media." Physical chemistry chemical physics : PCCP vol. 20,30 (2018): 19829-19840. doi: https://doi.org/10.1039/c8cp03544j
DŽeba I, Bonifačić M, Nikšić-Franjić I, Ljubić I. Proton-coupled electron transfer is the dominant mechanism of reduction of haloacetates by the α-hydroxyethyl radical in aqueous media. Phys Chem Chem Phys. 2018 Aug 01;20(30):19829-19840. doi: 10.1039/c8cp03544j. PMID: 30033455.
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[Effect of inhibitors of DNA-, RNA-, and protein synthesis on growth and antheridium formation in Anemia phyllitidis].

Planta

Schraudolf H.
PMID: 24549887
Planta. 1967 Jun;74(2):123-47. doi: 10.1007/BF00388325.

A number of inhibitors of DNA-, RNA-, and protein synthesis were applied to prothallia of Anemia phyllitidis, and their effects were investigated with regard to cell division and inhibition of antheridium formation (after induction by gibberellin A3). All compounds...

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Schraudolf H. Wirkung von hemmstoffen der DNS-, RNS- und proteinsynthese auf wachstum und antheridienbildung in prothallien von Anemia phyllitidis L. [Effect of inhibitors of DNA-, RNA-, and protein synthesis on growth and antheridium formation in Anemia phyllitidis]. Planta. 1967;74(2):123-47doi: 10.1007/BF00388325.
Schraudolf, H. (1967). Wirkung von hemmstoffen der DNS-, RNS- und proteinsynthese auf wachstum und antheridienbildung in prothallien von Anemia phyllitidis L. [Effect of inhibitors of DNA-, RNA-, and protein synthesis on growth and antheridium formation in Anemia phyllitidis]. Planta, 74(2), 123-47. https://doi.org/10.1007/BF00388325
Schraudolf, H. "Wirkung von hemmstoffen der DNS-, RNS- und proteinsynthese auf wachstum und antheridienbildung in prothallien von Anemia phyllitidis L." [Effect of inhibitors of DNA-, RNA-, and protein synthesis on growth and antheridium formation in Anemia phyllitidis]. Planta vol. 74,2 (1967): 123-47. doi: https://doi.org/10.1007/BF00388325
Schraudolf H. Wirkung von hemmstoffen der DNS-, RNS- und proteinsynthese auf wachstum und antheridienbildung in prothallien von Anemia phyllitidis L. [Effect of inhibitors of DNA-, RNA-, and protein synthesis on growth and antheridium formation in Anemia phyllitidis]. Planta. 1967 Jun;74(2):123-47. doi: 10.1007/BF00388325. German. PMID: 24549887.
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Fecundity of Panagrellus silusiae Treated with Ethyl methanesulphonate and 5-bromouracil.

Journal of nematology

Samoiloff MR, Smith AC.
PMID: 19322387
J Nematol. 1971 Jul;3(3):299-300.

No abstract available.

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Samoiloff MR, Smith AC. Fecundity of Panagrellus silusiae Treated with Ethyl methanesulphonate and 5-bromouracil. J Nematol. 1971;3(3):299-300
Samoiloff, M. R., & Smith, A. C. (1971). Fecundity of Panagrellus silusiae Treated with Ethyl methanesulphonate and 5-bromouracil. Journal of nematology, 3(3), 299-300.
Samoiloff, M R, and Smith, A C. "Fecundity of Panagrellus silusiae Treated with Ethyl methanesulphonate and 5-bromouracil." Journal of nematology vol. 3,3 (1971): 299-300.
Samoiloff MR, Smith AC. Fecundity of Panagrellus silusiae Treated with Ethyl methanesulphonate and 5-bromouracil. J Nematol. 1971 Jul;3(3):299-300. PMID: 19322387; PMCID: PMC2619876.
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Effect of Bromouracil-containing Deoxyribonucleic Acid on Bacillus subtilis.

Journal of bacteriology

Gimlin DM, Hardman SD, Kelley BN, Butler GC, Leach FR.
PMID: 16562122
J Bacteriol. 1966 Aug;92(2):366-74. doi: 10.1128/jb.92.2.366-374.1966.

Gimlin, Dixie M. (Oklahoma State University, Stillwater), Sue D. Hardman, Betty N. Kelley, Grace C. Butler, and Franklin R. Leach. Effect of bromouracil-containing deoxyribonucleic acid on Bacillus subtilis. J. Bacteriol. 92:366-374. 1966.-Replacement of one-half of the thymine with bromouracil...

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Gimlin DM, Hardman SD, Kelley BN, et al. Effect of Bromouracil-containing Deoxyribonucleic Acid on Bacillus subtilis. J Bacteriol. 1966;92(2):366-74doi: 10.1128/jb.92.2.366-374.1966.
Gimlin, D. M., Hardman, S. D., Kelley, B. N., Butler, G. C., & Leach, F. R. (1966). Effect of Bromouracil-containing Deoxyribonucleic Acid on Bacillus subtilis. Journal of bacteriology, 92(2), 366-74. https://doi.org/10.1128/jb.92.2.366-374.1966
Gimlin, D M, et al. "Effect of Bromouracil-containing Deoxyribonucleic Acid on Bacillus subtilis." Journal of bacteriology vol. 92,2 (1966): 366-74. doi: https://doi.org/10.1128/jb.92.2.366-374.1966
Gimlin DM, Hardman SD, Kelley BN, Butler GC, Leach FR. Effect of Bromouracil-containing Deoxyribonucleic Acid on Bacillus subtilis. J Bacteriol. 1966 Aug;92(2):366-74. doi: 10.1128/jb.92.2.366-374.1966. PMID: 16562122; PMCID: PMC276250.
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Reactions of 2-Propanol Radical with Halogenated Organics in Aqueous Solution: Theoretical Evidence for Proton-Coupled Electron Transfer and Competing Mechanisms.

The journal of physical chemistry. B

Ljubić I, Sabljić A, Bonifačić M.
PMID: 27766877
J Phys Chem B. 2016 Nov 17;120(45):11810-11820. doi: 10.1021/acs.jpcb.6b08765. Epub 2016 Nov 02.

The reactions of α-hydroxyalkyl radicals in aqueous medium are of interest because they exhibit a rich variety of fundamentally important competing mechanisms, such as proton-coupled electron transfer (PCET), hydrogen atom transfer, free radical substitutions, abstractions and additions, etc. We...

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Ljubić I, Sabljić A, Bonifačić M. Reactions of 2-Propanol Radical with Halogenated Organics in Aqueous Solution: Theoretical Evidence for Proton-Coupled Electron Transfer and Competing Mechanisms. J Phys Chem B. 2016;120(45):11810-11820doi: 10.1021/acs.jpcb.6b08765.
Ljubić, I., Sabljić, A., & Bonifačić, M. (2016). Reactions of 2-Propanol Radical with Halogenated Organics in Aqueous Solution: Theoretical Evidence for Proton-Coupled Electron Transfer and Competing Mechanisms. The journal of physical chemistry. B, 120(45), 11810-11820. https://doi.org/10.1021/acs.jpcb.6b08765
Ljubić, Ivan, et al. "Reactions of 2-Propanol Radical with Halogenated Organics in Aqueous Solution: Theoretical Evidence for Proton-Coupled Electron Transfer and Competing Mechanisms." The journal of physical chemistry. B vol. 120,45 (2016): 11810-11820. doi: https://doi.org/10.1021/acs.jpcb.6b08765
Ljubić I, Sabljić A, Bonifačić M. Reactions of 2-Propanol Radical with Halogenated Organics in Aqueous Solution: Theoretical Evidence for Proton-Coupled Electron Transfer and Competing Mechanisms. J Phys Chem B. 2016 Nov 17;120(45):11810-11820. doi: 10.1021/acs.jpcb.6b08765. Epub 2016 Nov 02. PMID: 27766877.
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Microfluorimetric analysis of spatial and temporal patterns of immobilized cell growth.

Biotechnology and bioengineering

Kuhn RH, Peretti SW, Ollis DF.
PMID: 18600770
Biotechnol Bioeng. 1991 Aug 05;38(4):340-52. doi: 10.1002/bit.260380404.

Pronounced spatial nonuniformities in cell density, physiology, and activity frequently arise within densely packed immobilized cell supports. For a more fundamental understanding of immobilized cell phenomena, we have developed high-resolution microfluorimetric procedures to analyze local variations in both immobilized...

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Kuhn RH, Peretti SW, Ollis DF. Microfluorimetric analysis of spatial and temporal patterns of immobilized cell growth. Biotechnol Bioeng. 1991;38(4):340-52doi: 10.1002/bit.260380404.
Kuhn, R. H., Peretti, S. W., & Ollis, D. F. (1991). Microfluorimetric analysis of spatial and temporal patterns of immobilized cell growth. Biotechnology and bioengineering, 38(4), 340-52. https://doi.org/10.1002/bit.260380404
Kuhn, R H, et al. "Microfluorimetric analysis of spatial and temporal patterns of immobilized cell growth." Biotechnology and bioengineering vol. 38,4 (1991): 340-52. doi: https://doi.org/10.1002/bit.260380404
Kuhn RH, Peretti SW, Ollis DF. Microfluorimetric analysis of spatial and temporal patterns of immobilized cell growth. Biotechnol Bioeng. 1991 Aug 05;38(4):340-52. doi: 10.1002/bit.260380404. PMID: 18600770.
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DNA synthesis in cytokinin-autotrophic tobacco cells : Effect of bromodeoxyuridine, fluorodeoxyuridine, and kinetin.

Planta

Bezděk M, Vyskot B.
PMID: 24302418
Planta. 1981 Jul;152(3):215-24. doi: 10.1007/BF00385147.

DNA isolated from various Nicotiana tabacum cell types, differing in their degree of hormone autotrophy and incubated in the presence of bromodeoxyuridine (BrdUrd), was analyzed by isopycnic CsCl gradient centrifugation. All cell types incorporate BrdUrd into DNA in such...

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Bezděk M, Vyskot B. DNA synthesis in cytokinin-autotrophic tobacco cells : Effect of bromodeoxyuridine, fluorodeoxyuridine, and kinetin. Planta. 1981;152(3):215-24doi: 10.1007/BF00385147.
Bezděk, M., & Vyskot, B. (1981). DNA synthesis in cytokinin-autotrophic tobacco cells : Effect of bromodeoxyuridine, fluorodeoxyuridine, and kinetin. Planta, 152(3), 215-24. https://doi.org/10.1007/BF00385147
Bezděk, M, and Vyskot, B. "DNA synthesis in cytokinin-autotrophic tobacco cells : Effect of bromodeoxyuridine, fluorodeoxyuridine, and kinetin." Planta vol. 152,3 (1981): 215-24. doi: https://doi.org/10.1007/BF00385147
Bezděk M, Vyskot B. DNA synthesis in cytokinin-autotrophic tobacco cells : Effect of bromodeoxyuridine, fluorodeoxyuridine, and kinetin. Planta. 1981 Jul;152(3):215-24. doi: 10.1007/BF00385147. PMID: 24302418.
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INDUCTION OF SPECIFIC MUTATIONS WITH 5-BROMOURACIL.

Proceedings of the National Academy of Sciences of the United States of America

Benzer S, Freese E.
PMID: 16590151
Proc Natl Acad Sci U S A. 1958 Feb;44(2):112-9. doi: 10.1073/pnas.44.2.112.

No abstract available.

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Benzer S, Freese E. INDUCTION OF SPECIFIC MUTATIONS WITH 5-BROMOURACIL. Proc Natl Acad Sci U S A. 1958;44(2):112-9doi: 10.1073/pnas.44.2.112.
Benzer, S., & Freese, E. (1958). INDUCTION OF SPECIFIC MUTATIONS WITH 5-BROMOURACIL. Proceedings of the National Academy of Sciences of the United States of America, 44(2), 112-9. https://doi.org/10.1073/pnas.44.2.112
Benzer, S, and Freese, E. "INDUCTION OF SPECIFIC MUTATIONS WITH 5-BROMOURACIL." Proceedings of the National Academy of Sciences of the United States of America vol. 44,2 (1958): 112-9. doi: https://doi.org/10.1073/pnas.44.2.112
Benzer S, Freese E. INDUCTION OF SPECIFIC MUTATIONS WITH 5-BROMOURACIL. Proc Natl Acad Sci U S A. 1958 Feb;44(2):112-9. doi: 10.1073/pnas.44.2.112. PMID: 16590151; PMCID: PMC335373.
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