| Year |
Citation |
Score |
| 2024 |
Jiang Y, Mingard C, Huber SM, Takhaveev V, McKeague M, Kizaki S, Schneider M, Ziegler N, Hürlimann V, Hoeng J, Sierro N, Ivanov NV, Sturla SJ. Correction to "Quantification and Mapping of Alkylation in the Human Genome Reveal Single Nucleotide Resolution Precursors of Mutational Signatures". Acs Central Science. 10: 487. PMID 38435521 DOI: 10.1021/acscentsci.3c01597 |
0.641 |
|
| 2024 |
Son K, Takhaveev V, Mor V, Yu H, Dillier E, Zilio N, Püllen NJL, Ivanov D, Ulrich HD, Sturla SJ, Schärer OD. Trabectedin derails transcription-coupled nucleotide excision repair to induce DNA breaks in highly transcribed genes. Nature Communications. 15: 1388. PMID 38360910 DOI: 10.1038/s41467-024-45664-7 |
0.365 |
|
| 2023 |
Maritz C, Khaleghi R, Yancoskie MN, Diethelm S, Brülisauer S, Ferreira NS, Jiang Y, Sturla SJ, Naegeli H. ASH1L-MRG15 methyltransferase deposits H3K4me3 and FACT for damage verification in nucleotide excision repair. Nature Communications. 14: 3892. PMID 37393406 DOI: 10.1038/s41467-023-39635-7 |
0.338 |
|
| 2023 |
Jiang Y, Mingard C, Huber SM, Takhaveev V, McKeague M, Kizaki S, Schneider M, Ziegler N, Hürlimann V, Hoeng J, Sierro N, Ivanov NV, Sturla SJ. Quantification and Mapping of Alkylation in the Human Genome Reveal Single Nucleotide Resolution Precursors of Mutational Signatures. Acs Central Science. 9: 362-372. PMID 36968528 DOI: 10.1021/acscentsci.2c01100 |
0.722 |
|
| 2022 |
Ramirez Garcia A, Hurley K, Marastoni G, Diard M, Hofer S, Greppi A, Hardt WD, Lacroix C, Sturla SJ, Schwab C. Pathogenic and Commensal Gut Bacteria Harboring Glycerol/Diol Dehydratase Metabolize Glycerol and Produce DNA-Reactive Acrolein. Chemical Research in Toxicology. PMID 36116084 DOI: 10.1021/acs.chemrestox.2c00137 |
0.326 |
|
| 2022 |
Kellum AH, Pallan PS, Nilforoushan A, Sturla SJ, Stone MP, Egli M. Conformation and Pairing Properties of an -Methyl-2'-deoxyguanosine-Directed Benzimidazole Nucleoside Analog in Duplex DNA. Chemical Research in Toxicology. PMID 35973057 DOI: 10.1021/acs.chemrestox.2c00165 |
0.386 |
|
| 2022 |
Sun J, Antczak NM, Gahlon HL, Sturla SJ. Molecular beacons with oxidized bases report on substrate specificity of DNA oxoguanine glycosylases. Chemical Science. 13: 4295-4302. PMID 35509469 DOI: 10.1039/d1sc05648d |
0.351 |
|
| 2021 |
Aloisi CMN, Escher NA, Kim HS, Geisen SM, Fontana GA, Yeo JE, Schärer OD, Sturla SJ. A combination of direct reversion and nucleotide excision repair counters the mutagenic effects of DNA carboxymethylation. Dna Repair. 110: 103262. PMID 35030424 DOI: 10.1016/j.dnarep.2021.103262 |
0.417 |
|
| 2021 |
Kostka T, Empl MT, Seiwert N, Geisen SM, Hoffmann P, Adam J, Seeger B, Shay JW, Christmann M, Sturla SJ, Fahrer J, Steinberg P. Repair of O6-carboxymethylguanine adducts by O6-methylguanine-DNA methyltransferase in human colon epithelial cells. Carcinogenesis. PMID 34115837 DOI: 10.1093/carcin/bgab049 |
0.358 |
|
| 2021 |
Ramirez Garcia A, Zhang J, Greppi A, Constancias F, Wortmann E, Wandres M, Hurley K, Pascual-García A, Ruscheweyh HJ, Sturla SJ, Lacroix C, Schwab C. Impact of manipulation of glycerol/diol dehydratase activity on intestinal microbiota ecology and metabolism. Environmental Microbiology. PMID 33587772 DOI: 10.1111/1462-2920.15431 |
0.4 |
|
| 2021 |
Aloisi CMN, Sandell ES, Sturla SJ. A Chemical Link between Meat Consumption and Colorectal Cancer Development? Chemical Research in Toxicology. PMID 33417435 DOI: 10.1021/acs.chemrestox.0c00395 |
0.373 |
|
| 2020 |
Mingard C, Wu J, McKeague M, Sturla SJ. Next-generation DNA damage sequencing. Chemical Society Reviews. PMID 32968744 DOI: 10.1039/d0cs00647e |
0.741 |
|
| 2020 |
Aloisi CMN, Nilforoushan A, Ziegler N, Sturla SJ. Sequence-Specific Quantitation of Mutagenic DNA Damage via Polymerase Amplification with an Artificial Nucleotide. Journal of the American Chemical Society. PMID 32196326 DOI: 10.1021/Jacs.9B11746 |
0.531 |
|
| 2020 |
Passow KT, Antczak NM, Sturla SJ, Harki DA. Synthesis of 4-Cyanoindole Nucleosides, 4-Cyanoindole-2'-Deoxyribonucleoside-5'-Triphosphate (4CIN-TP), and Enzymatic Incorporation of 4CIN-TP into DNA. Current Protocols in Nucleic Acid Chemistry. 80: e101. PMID 31909864 DOI: 10.1002/Cpnc.101 |
0.49 |
|
| 2019 |
Zhang J, Lacroix C, Wortmann E, Ruscheweyh HJ, Sunagawa S, Sturla SJ, Schwab C. Gut microbial beta-glucuronidase and glycerol/diol dehydratase activity contribute to dietary heterocyclic amine biotransformation. Bmc Microbiology. 19: 99. PMID 31096909 DOI: 10.1186/S12866-019-1483-X |
0.487 |
|
| 2019 |
Gahlon HL, Sturla SJ. Determining Steady-State Kinetics of DNA Polymerase Nucleotide Incorporation. Methods in Molecular Biology (Clifton, N.J.). 1973: 299-311. PMID 31016710 DOI: 10.1007/978-1-4939-9216-4_19 |
0.502 |
|
| 2019 |
Räz MH, Aloisi CMN, Gahlon HL, Sturla SJ. DNA Adduct-Directed Synthetic Nucleosides. Accounts of Chemical Research. PMID 30964643 DOI: 10.1021/Acs.Accounts.9B00054 |
0.829 |
|
| 2019 |
Zhang J, Empl MT, Schneider M, Schröder B, Stadnicka-Michalak J, Breves G, Steinberg P, Sturla SJ. Gut microbial transformation of the dietary mutagen MeIQx may reduce exposure levels without altering intestinal transport. Toxicology in Vitro : An International Journal Published in Association With Bibra. PMID 30954653 DOI: 10.1016/J.Tiv.2019.04.004 |
0.461 |
|
| 2019 |
Aloisi CMN, Sturla SJ, Gahlon HL. A gene-targeted polymerase-mediated strategy to identify O-methylguanine damage. Chemical Communications (Cambridge, England). 55: 3895-3898. PMID 30860216 DOI: 10.1039/C9Cc00278B |
0.432 |
|
| 2019 |
Wu J, Sturla SJ, Burrows CJ, Fleming AM. Impact of DNA Oxidation on Toxicology: From Quantification to Genomics. Chemical Research in Toxicology. PMID 30807111 DOI: 10.1021/Acs.Chemrestox.9B00046 |
0.402 |
|
| 2019 |
Berger FD, Manderville RA, Sturla SJ. Adduct Fluorescence as a Tool to Decipher Sequence Impact on Frameshift Mutations Mediated by a C-Linked C8-Biphenyl-Guanine Lesion. Chemical Research in Toxicology. PMID 30785283 DOI: 10.1021/Acs.Chemrestox.9B00016 |
0.412 |
|
| 2019 |
Räz MH, Sandell E, Patil K, Gillingham DG, Sturla SJ. High Sensitivity of Human Translesion DNA Synthesis Polymerase κ to Variation in O-carboxymethylguanine Structures. Acs Chemical Biology. PMID 30645109 DOI: 10.1021/Acschembio.8B00802 |
0.821 |
|
| 2018 |
Kraus A, McKeague M, Seiwert N, Nagel G, Geisen SM, Ziegler N, Trantakis IA, Kaina B, Thomas AD, Sturla SJ, Fahrer J. Immunological and mass spectrometry-based approaches to determine thresholds of the mutagenic DNA adduct O-methylguanine in vivo. Archives of Toxicology. PMID 30446773 DOI: 10.1007/S00204-018-2355-0 |
0.718 |
|
| 2018 |
Räz MH, Sturla SJ, Gahlon HL. Hydrogen bonding interactions at DNA terminus promote extension from methylguanine lesions by human extender DNA polymerase ζ. Biochemistry. PMID 30222325 DOI: 10.1021/Acs.Biochem.8B00861 |
0.816 |
|
| 2018 |
McKeague M, Otto C, Räz MH, Angelov T, Sturla SJ. Base-pairing partner modulates alkylguanine alkyltransferase. Acs Chemical Biology. PMID 30040894 DOI: 10.1021/Acschembio.8B00446 |
0.796 |
|
| 2018 |
Wu J, Mckeague M, Sturla SJ. Nucleotide-resolution genome-wide mapping of oxidative DNA damage by click-code-seq. Journal of the American Chemical Society. PMID 29944356 DOI: 10.1021/Jacs.8B03715 |
0.736 |
|
| 2018 |
Stornetta A, Kieren Deng KC, Danielli S, Liyanage HDS, Sturla SJ, Wilson WR, Gu Y. Drug-DNA adducts as biomarkers for metabolic activation of the nitro-aromatic nitrogen mustard prodrug PR-104A. Biochemical Pharmacology. PMID 29630868 DOI: 10.1016/J.Bcp.2018.04.004 |
0.397 |
|
| 2018 |
Zhang J, Sturla S, Lacroix C, Schwab C. Gut Microbial Glycerol Metabolism as an Endogenous Acrolein Source. Mbio. 9. PMID 29339426 DOI: 10.1128/Mbio.01947-17 |
0.496 |
|
| 2018 |
Dahlmann HA, Berger FD, Kung RW, Wyss LA, Gubler I, McKeague M, Wetmore SD, Sturla SJ. Fluorescent Nucleobase Analogues with Extended Pi Surfaces Stabilize DNA Duplexes Containing O
6
-Alkylguanine Adducts Helvetica Chimica Acta. 101: e1800066. DOI: 10.1002/Hlca.201800066 |
0.742 |
|
| 2017 |
Berger FD, Sturla SJ, Kung RW, Montina T, Wetmore SD, Manderville RA. Conformational Preference and Fluorescence Response of a C-Linked C8-Biphenyl-Guanine Lesion in the NarI Mutational Hotspot: Evidence for Enhanced Syn Adduct Formation. Chemical Research in Toxicology. PMID 29186656 DOI: 10.1021/Acs.Chemrestox.7B00266 |
0.373 |
|
| 2017 |
Betz K, Nilforoushan A, Wyss LA, Diederichs K, Sturla SJ, Marx A. Structural basis for the selective incorporation of an artificial nucleotide opposite a DNA adduct by a DNA polymerase Chemical Communications. 53: 12704-12707. PMID 29136072 DOI: 10.1039/C7Cc07173F |
0.535 |
|
| 2017 |
Malvezzi S, Farnung L, Aloisi CMN, Angelov T, Cramer P, Sturla SJ. Mechanism of RNA polymerase II stalling by DNA alkylation. Proceedings of the National Academy of Sciences of the United States of America. PMID 29087308 DOI: 10.1073/Pnas.1706592114 |
0.419 |
|
| 2017 |
Zhang J, Empl MT, Schwab C, Fekry MI, Engels C, Schneider M, Lacroix C, Steinberg P, Sturla SJ. Gut microbial transformation of the dietary imidazoquinoxaline mutagen MeIQx reduces its cytotoxic and mutagenic potency. Toxicological Sciences : An Official Journal of the Society of Toxicology. PMID 28666384 DOI: 10.1093/Toxsci/Kfx132 |
0.479 |
|
| 2017 |
Geigle SN, Wyss LA, Sturla SJ, Gillingham DG. Copper carbenes alkylate guanine chemoselectively through a substrate directed reaction. Chemical Science. 8: 499-506. PMID 28451197 DOI: 10.1039/C6Sc03502G |
0.35 |
|
| 2017 |
Stornetta A, Villalta PW, Gossner F, Wilson WR, Balbo S, Sturla SJ. DNA Adduct Profiles Predict in Vitro Cell Viability after Treatment with the Experimental Anticancer Prodrug PR104A. Chemical Research in Toxicology. PMID 28140568 DOI: 10.1021/Acs.Chemrestox.6B00412 |
0.516 |
|
| 2017 |
Otto C, Spivak G, Aloisi CM, Menigatti M, Nägeli H, Hanawalt PC, Tanasova M, Sturla SJ. Modulation of cytotoxicity by transcription-coupled nucleotide excision repair is independent of the requirement for bioactivation of acylfulvene. Chemical Research in Toxicology. PMID 28076683 DOI: 10.1021/Acs.Chemrestox.6B00240 |
0.77 |
|
| 2016 |
Mentegari E, Crespan E, Bavagnoli L, Kissova M, Bertoletti F, Sabbioneda S, Imhof R, Sturla SJ, Nilforoushan A, Hübscher U, van Loon B, Maga G. Ribonucleotide incorporation by human DNA polymerase η impacts translesion synthesis and RNase H2 activity. Nucleic Acids Research. PMID 27994034 DOI: 10.1093/Nar/Gkw1275 |
0.457 |
|
| 2016 |
Stornetta A, Zimmermann M, Cimino GD, Henderson PT, Sturla SJ. DNA Adducts from Anticancer Drugs as Candidate Predictive Markers for Precision Medicine. Chemical Research in Toxicology. PMID 27936622 DOI: 10.1021/Acs.Chemrestox.6B00380 |
0.382 |
|
| 2016 |
Malvezzi S, Angelov T, Sturla SJ. Minor Groove 3-Deaza-Adenosine Analogues: Synthesis and Bypass in Translesion DNA Synthesis. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 27862447 DOI: 10.1002/Chem.201604289 |
0.536 |
|
| 2016 |
Engels C, Schwab C, Zhang J, Stevens MJ, Bieri C, Ebert MO, McNeill K, Sturla SJ, Lacroix C. Acrolein contributes strongly to antimicrobial and heterocyclic amine transformation activities of reuterin. Scientific Reports. 6: 36246. PMID 27819285 DOI: 10.1038/Srep36246 |
0.499 |
|
| 2016 |
Räz MH, Hidaka K, Sturla SJ, Sugiyama H, Endo M. Torsional Constraints of DNA Substrates Impact Cas9 Cleavage. Journal of the American Chemical Society. PMID 27709924 DOI: 10.1021/Jacs.6B08915 |
0.808 |
|
| 2016 |
Räz MH, Dexter HR, Millington CL, Van Loon B, Williams DM, Sturla SJ. Bypass of mutagenic O(6)-Carboxymethylguanine DNA Adducts by Human Y- and B-Family Polymerases. Chemical Research in Toxicology. PMID 27404553 DOI: 10.1021/Acs.Chemrestox.6B00168 |
0.815 |
|
| 2016 |
Wyss LA, Nilforoushan A, Williams DM, Marx A, Sturla SJ. The use of an artificial nucleotide for polymerase-based recognition of carcinogenic O6-alkylguanine DNA adducts. Nucleic Acids Research. PMID 27378785 DOI: 10.1093/Nar/Gkw589 |
0.534 |
|
| 2016 |
Trantakis IA, Nilforoushan A, Dahlmann HA, Stäuble CK, Sturla SJ. In-gene Quantification of O(6)-Methylguanine with Elongated Nucleoside Analogues on Gold Nanoprobes. Journal of the American Chemical Society. PMID 27314828 DOI: 10.1021/Jacs.6B03599 |
0.501 |
|
| 2016 |
Crespan E, Furrer A, Rösinger M, Bertoletti F, Mentegari E, Chiapparini G, Imhof R, Ziegler N, Sturla SJ, Hübscher U, van Loon B, Maga G. Impact of ribonucleotide incorporation by DNA polymerases β and λ on oxidative base excision repair. Nature Communications. 7: 10805. PMID 26917111 DOI: 10.1038/Ncomms10805 |
0.449 |
|
| 2016 |
Malvezzi S, Angelov T, Farnung L, Aloisi C, Cramer P, Sturla SJ. Inhibition of DNA replication and miscoding potential of minor groove alkylation: Structure-function insight from 3-deazaadenosines. Toxicology Letters. 258. DOI: 10.1016/J.Toxlet.2016.06.1504 |
0.46 |
|
| 2015 |
Fekry MI, Engels C, Zhang J, Schwab C, Lacroix C, Sturla SJ, Chassard C. The strict anaerobic gut microbe Eubacterium hallii transforms the carcinogenic dietary heterocyclic amine 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine (PhIP). Environmental Microbiology Reports. PMID 26711372 DOI: 10.1111/1758-2229.12369 |
0.466 |
|
| 2015 |
Stornetta A, Villalta PW, Hecht SS, Sturla SJ, Balbo S. Screening for DNA Alkylation Mono and Crosslinked Adducts with a Comprehensive LC-MS(3) Adductomic Approach. Analytical Chemistry. PMID 26509677 DOI: 10.1021/Acs.Analchem.5B02759 |
0.601 |
|
| 2015 |
Malvezzi S, Sturla SJ, Tanasova M. Data in support of quantification of pyrophosphate as a universal approach to determine polymerase activity and assay polymerase inhibitors. Data in Brief. 4: 14-8. PMID 26217754 DOI: 10.1016/J.Dib.2015.04.006 |
0.459 |
|
| 2015 |
Tanasova M, Goeldi S, Meyer F, Hanawalt PC, Spivak G, Sturla SJ. Altered minor-groove hydrogen bonds in DNA block transcription elongation by T7 RNA polymerase. Chembiochem : a European Journal of Chemical Biology. 16: 1212-8. PMID 25881991 DOI: 10.1002/Cbic.201500077 |
0.418 |
|
| 2015 |
Nilforoushan A, Furrer A, Wyss LA, van Loon B, Sturla SJ. Nucleotides with altered hydrogen bonding capacities impede human DNA polymerase η by reducing synthesis in the presence of the major cisplatin DNA adduct. Journal of the American Chemical Society. 137: 4728-34. PMID 25786104 DOI: 10.1021/Ja512547G |
0.525 |
|
| 2015 |
Malvezzi S, Sturla SJ, Tanasova M. Quantification of pyrophosphate as a universal approach to determine polymerase activity and assay polymerase inhibitors. Analytical Biochemistry. 478: 1-7. PMID 25772306 DOI: 10.1016/J.Ab.2015.03.002 |
0.501 |
|
| 2015 |
Wyss LA, Nilforoushan A, Eichenseher F, Suter U, Blatter N, Marx A, Sturla SJ. Specific incorporation of an artificial nucleotide opposite a mutagenic DNA adduct by a DNA polymerase. Journal of the American Chemical Society. 137: 30-3. PMID 25490521 DOI: 10.1021/Ja5100542 |
0.553 |
|
| 2014 |
Sproviero M, Verwey AM, Rankin KM, Witham AA, Soldatov DV, Manderville RA, Fekry MI, Sturla SJ, Sharma P, Wetmore SD. Structural and biochemical impact of C8-aryl-guanine adducts within the NarI recognition DNA sequence: influence of aryl ring size on targeted and semi-targeted mutagenicity. Nucleic Acids Research. 42: 13405-21. PMID 25361967 DOI: 10.1093/Nar/Gku1093 |
0.453 |
|
| 2014 |
Trantakis IA, Sturla SJ. Gold nanoprobes for detecting DNA adducts. Chemical Communications (Cambridge, England). 50: 15517-20. PMID 25354716 DOI: 10.1039/C4Cc07184K |
0.46 |
|
| 2014 |
Gahlon HL, Boby ML, Sturla SJ. O6-alkylguanine postlesion DNA synthesis is correct with the right complement of hydrogen bonding. Acs Chemical Biology. 9: 2807-14. PMID 25259614 DOI: 10.1021/Cb500415Q |
0.451 |
|
| 2014 |
Madureira DJ, Weiss FT, Van Midwoud P, Helbling DE, Sturla SJ, Schirmer K. Systems toxicology approach to understand the kinetics of benzo(a)pyrene uptake, biotransformation, and DNA adduct formation in a liver cell model. Chemical Research in Toxicology. 27: 443-53. PMID 24446834 DOI: 10.1021/Tx400446Q |
0.349 |
|
| 2014 |
Glatt H, Pietsch KE, Sturla SJ, Meinl W. Sulfotransferase-independent genotoxicity of illudin S and its acylfulvene derivatives in bacterial and mammalian cells. Archives of Toxicology. 88: 161-9. PMID 23881331 DOI: 10.1007/S00204-013-1097-2 |
0.316 |
|
| 2014 |
Wyss LA, Sturla SJ. DNA polymerase-mediated incorporation of benzimidazolederived nucleotides in O 6 -benzylguanine adduct bypass Collection of Czechoslovak Chemical Communications. 14: 411-412. DOI: 10.1135/Css201414411 |
0.517 |
|
| 2014 |
Dahlmann HA, Sturla SJ. Synthetic nucleosides for probing stability and polymerase processing of DNA adducts Collection of Czechoslovak Chemical Communications. 14: 93-96. DOI: 10.1135/Css201414093 |
0.472 |
|
| 2013 |
van Midwoud PM, Sturla SJ. Improved efficacy of acylfulvene in colon cancer cells when combined with a nuclear excision repair inhibitor. Chemical Research in Toxicology. 26: 1674-82. PMID 24099590 DOI: 10.1021/Tx400255F |
0.494 |
|
| 2013 |
Angelov T, Dahlmann HA, Sturla SJ. Oligonucleotide probes containing pyrimidine analogs reveal diminished hydrogen bonding capacity of the DNA adduct O⁶-methyl-G in DNA duplexes. Bioorganic & Medicinal Chemistry. 21: 6212-6. PMID 23969036 DOI: 10.1016/J.Bmc.2013.07.036 |
0.416 |
|
| 2013 |
Stornetta A, Angelov T, Guengerich FP, Sturla SJ. Incorporation of nucleoside probes opposite O⁶-methylguanine by Sulfolobus solfataricus DNA polymerase Dpo4: importance of hydrogen bonding. Chembiochem : a European Journal of Chemical Biology. 14: 1634-9. PMID 23959784 DOI: 10.1002/Cbic.201300296 |
0.519 |
|
| 2013 |
Trantakis IA, Bolisetty S, Mezzenga R, Sturla SJ. Reversible aggregation of DNA-decorated gold nanoparticles controlled by molecular recognition. Langmuir : the Acs Journal of Surfaces and Colloids. 29: 10824-30. PMID 23883185 DOI: 10.1021/La401211U |
0.335 |
|
| 2013 |
Kuska MS, Majdi Yazdi M, Witham AA, Dahlmann HA, Sturla SJ, Wetmore SD, Manderville RA. Influence of chlorine substitution on the hydrolytic stability of biaryl ether nucleoside adducts produced by phenolic toxins. The Journal of Organic Chemistry. 78: 7176-85. PMID 23819526 DOI: 10.1021/Jo401122J |
0.333 |
|
| 2013 |
Gahlon HL, Sturla SJ. Hydrogen bonding or stacking interactions in differentiating duplex stability in oligonucleotides containing synthetic nucleoside probes for alkylated DNA. Chemistry (Weinheim An Der Bergstrasse, Germany). 19: 11062-7. PMID 23801518 DOI: 10.1002/Chem.201204593 |
0.517 |
|
| 2013 |
Kowal EA, Lad RR, Pallan PS, Dhummakupt E, Wawrzak Z, Egli M, Sturla SJ, Stone MP. Recognition of O6-benzyl-2'-deoxyguanosine by a perimidinone-derived synthetic nucleoside: a DNA interstrand stacking interaction. Nucleic Acids Research. 41: 7566-76. PMID 23748954 DOI: 10.1093/Nar/Gkt488 |
0.755 |
|
| 2013 |
Gahlon HL, Schweizer WB, Sturla SJ. Tolerance of base pair size and shape in postlesion DNA synthesis. Journal of the American Chemical Society. 135: 6384-7. PMID 23560524 DOI: 10.1021/Ja311434S |
0.48 |
|
| 2013 |
Pietsch KE, van Midwoud PM, Villalta PW, Sturla SJ. Quantification of acylfulvene- and illudin S-DNA adducts in cells with variable bioactivation capacities. Chemical Research in Toxicology. 26: 146-55. PMID 23227857 DOI: 10.1021/Tx300430R |
0.456 |
|
| 2013 |
Stornetta A, Angelov T, Guengerich FP, Sturla SJ. Corrigendum to Incorporation of nucleoside probes opposite O6-methylguanine by sulfolobus solfataricus DNA polymerase Dpo4: Importance of hydrogen bonding [ChemBioChem, 14, (2013), 1634-1639], DOI 10.1002/cbic.201300296 Chembiochem. 14: 1918. DOI: 10.1002/cbic.201300564 |
0.338 |
|
| 2011 |
Dahlmann HA, Sturla SJ. Synthesis of oxygen-linked 8-phenoxyl-deoxyguanosine nucleoside analogues. European Journal of Organic Chemistry. 2011. PMID 24273446 DOI: 10.1002/Ejoc.201100013 |
0.36 |
|
| 2011 |
Pietsch KE, Neels JF, Yu X, Gong J, Sturla SJ. Chemical and enzymatic reductive activation of acylfulvene to isomeric cytotoxic reactive intermediates. Chemical Research in Toxicology. 24: 2044-54. PMID 21939268 DOI: 10.1021/Tx200401U |
0.389 |
|
| 2011 |
Guza R, Kotandeniya D, Murphy K, Dissanayake T, Lin C, Giambasu GM, Lad RR, Wojciechowski F, Amin S, Sturla SJ, Hudson RH, York DM, Jankowiak R, Jones R, Tretyakova NY. Influence of C-5 substituted cytosine and related nucleoside analogs on the formation of benzo[a]pyrene diol epoxide-dG adducts at CG base pairs of DNA. Nucleic Acids Research. 39: 3988-4006. PMID 21245046 DOI: 10.1093/Nar/Gkq1341 |
0.766 |
|
| 2010 |
Sturla SJ, Buchwald SL. ChemInform Abstract: Monocyclopentadienyltitanium Aryloxide Complexes: Preparation, Characterization, and Application in Cyclization Reactions. Cheminform. 33: no-no. DOI: 10.1002/chin.200229058 |
0.347 |
|
| 2010 |
Sturla SJ, Kablaoui NM, Buchwald SL. ChemInform Abstract: A Titanocene-Catalyzed Intramolecular Ene Reaction: Cycloisomerization of Enynes and Dienynes. Cheminform. 30: no-no. DOI: 10.1002/chin.199929044 |
0.708 |
|
| 2009 |
Dahlmann HA, Vaidyanathan VG, Sturla SJ. Investigating the biochemical impact of DNA damage with structure-based probes: abasic sites, photodimers, alkylation adducts, and oxidative lesions. Biochemistry. 48: 9347-59. PMID 19757831 DOI: 10.1021/Bi901059K |
0.433 |
|
| 2008 |
Liu X, Moody EC, Hecht SS, Sturla SJ. Deoxygenated phosphorothioate inositol phosphate analogs: synthesis, phosphatase stability, and binding affinity. Bioorganic & Medicinal Chemistry. 16: 3419-27. PMID 17981044 DOI: 10.1016/J.Bmc.2007.10.032 |
0.395 |
|
| 2007 |
Neels JF, Gong J, Yu X, Sturla SJ. Quantitative correlation of drug bioactivation and deoxyadenosine alkylation by acylfulvene. Chemical Research in Toxicology. 20: 1513-9. PMID 17900171 DOI: 10.1021/Tx7001756 |
0.416 |
|
| 2007 |
Sturla SJ. DNA adduct profiles: chemical approaches to addressing the biological impact of DNA damage from small molecules. Current Opinion in Chemical Biology. 11: 293-9. PMID 17574899 DOI: 10.1016/J.Cbpa.2007.05.021 |
0.508 |
|
| 2007 |
Vaidyanathan VG, Villalta PW, Sturla SJ. Nucleobase-dependent reactivity of a quinone metabolite of pentachlorophenol. Chemical Research in Toxicology. 20: 913-9. PMID 17497895 DOI: 10.1021/Tx600359D |
0.532 |
|
| 2007 |
Gong J, Sturla SJ. A synthetic nucleoside probe that discerns a DNA adduct from unmodified DNA. Journal of the American Chemical Society. 129: 4882-3. PMID 17402738 DOI: 10.1021/Ja070688G |
0.545 |
|
| 2007 |
Gong J, Vaidyanathan VG, Yu X, Kensler TW, Peterson LA, Sturla SJ. Depurinating acylfulvene-DNA adducts: characterizing cellular chemical reactions of a selective antitumor agent. Journal of the American Chemical Society. 129: 2101-11. PMID 17256933 DOI: 10.1021/Ja0665951 |
0.531 |
|
| 2006 |
Lao Y, Villalta PW, Sturla SJ, Wang M, Hecht SS. Quantitation of pyridyloxobutyl DNA adducts of tobacco-specific nitrosamines in rat tissue DNA by high-performance liquid chromatography-electrospray ionization-tandem mass spectrometry. Chemical Research in Toxicology. 19: 674-82. PMID 16696570 DOI: 10.1021/Tx050351X |
0.711 |
|
| 2006 |
Gong J, Neels JF, Yu X, Kensler TW, Peterson LA, Sturla SJ. Investigating the role of stereochemistry in the activity of anticancer acylfulvenes: synthesis, reductase-mediated bioactivation, and cellular toxicity. Journal of Medicinal Chemistry. 49: 2593-9. PMID 16610802 DOI: 10.1021/Jm051104T |
0.359 |
|
| 2006 |
Hecht SS, Huang C, Stoner GD, Li J, Kenney PM, Sturla SJ, Carmella SG. Identification of cyanidin glycosides as constituents of freeze-dried black raspberries which inhibit anti-benzo[a]pyrene-7,8-diol-9,10-epoxide induced NFkappaB and AP-1 activity. Carcinogenesis. 27: 1617-26. PMID 16522666 DOI: 10.1093/Carcin/Bgi366 |
0.448 |
|
| 2005 |
Nguyen TN, Bertagnolli AD, Villalta PW, Bühlmann P, Sturla SJ. Characterization of a deoxyguanosine adduct of tetrachlorobenzoquinone: dichlorobenzoquinone-1,N2-etheno-2'-deoxyguanosine. Chemical Research in Toxicology. 18: 1770-6. PMID 16300387 DOI: 10.1021/Tx050204Z |
0.413 |
|
| 2005 |
Sturla SJ, Scott J, Lao Y, Hecht SS, Villalta PW. Mass spectrometric analysis of relative levels of pyridyloxobutylation adducts formed in the reaction of DNA with a chemically activated form of the tobacco-specific carcinogen 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone. Chemical Research in Toxicology. 18: 1048-55. PMID 15962940 DOI: 10.1021/Tx050028U |
0.722 |
|
| 2004 |
Hecht SS, Villalta PW, Sturla SJ, Cheng G, Yu N, Upadhyaya P, Wang M. Identification of O2-substituted pyrimidine adducts formed in reactions of 4-(acetoxymethylnitrosamino)- 1-(3-pyridyl)-1-butanone and 4-(acetoxymethylnitros- amino)-1-(3-pyridyl)-1-butanol with DNA. Chemical Research in Toxicology. 17: 588-97. PMID 15144215 DOI: 10.1021/Tx034263T |
0.62 |
|
| 2003 |
Wang M, Cheng G, Sturla SJ, Shi Y, McIntee EJ, Villalta PW, Upadhyaya P, Hecht SS. Identification of adducts formed by pyridyloxobutylation of deoxyguanosine and DNA by 4-(acetoxymethylnitrosamino)-1-(3-pyridyl)-1-butanone, a chemically activated form of tobacco specific carcinogens. Chemical Research in Toxicology. 16: 616-26. PMID 12755591 DOI: 10.1021/Tx034003B |
0.6 |
|
| 2003 |
Upadhyaya P, Sturla SJ, Tretyakova N, Ziegel R, Villalta PW, Wang M, Hecht SS. Identification of adducts produced by the reaction of 4-(acetoxymethylnitrosamino)-1-(3-pyridyl)-1-butanol with deoxyguanosine and DNA. Chemical Research in Toxicology. 16: 180-90. PMID 12588189 DOI: 10.1021/Tx0256376 |
0.535 |
|
| 2003 |
Cheng G, Shi Y, Sturla SJ, Jalas JR, McIntee EJ, Villalta PW, Wang M, Hecht SS. Reactions of formaldehyde plus acetaldehyde with deoxyguanosine and DNA: formation of cyclic deoxyguanosine adducts and formaldehyde cross-links. Chemical Research in Toxicology. 16: 145-52. PMID 12588185 DOI: 10.1021/Tx025614R |
0.51 |
|
| 2002 |
Sturla SJ, Buchwald SL. Cobalt-phosphite-catalyzed asymmetric Pauson-Khand reaction. The Journal of Organic Chemistry. 67: 3398-403. PMID 12003551 DOI: 10.1021/Jo016038R |
0.439 |
|
| 2002 |
Sturla SJ, Buchwald SL. Monocyclopentadienyltitanium aryloxide complexes: Preparation, characterization, and application in cyclization reactions Organometallics. 21: 739-748. DOI: 10.1021/Om010755U |
0.442 |
|
| 1999 |
Sturla SJ, Buchwald SL. Catalytic Asymmetric Cyclocarbonylation of Nitrogen-Containing Enynes. The Journal of Organic Chemistry. 64: 5547-5550. PMID 11674619 DOI: 10.1021/Jo990384F |
0.415 |
|
| 1999 |
Sturla SJ, Kablaoui NM, Buchwald SL. A titanocene-catalyzed intramolecular ene reaction: Cycloisomerization of enynes and dienynes [12] Journal of the American Chemical Society. 121: 1976-1977. DOI: 10.1021/Ja9839567 |
0.72 |
|
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