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Nitric oxide inhibits FTO demethylase activity to regulate N6-methyladenosine mRNA methylation

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Mono- and binuclear dinitrosyl iron complexes with thiol-containing ligands in various biosystems

Vanin, A. F., Mikoyan, V. D., Kubrina, L. N., Borodulin, R. R., & Burgova, E. N. (2015) · BIOPHYSICS · doi:10.1134/s0006350915040247 · Cited by 16

Structural and Electronic Responses to the Three Redox Levels of Fe(NO)N2S2‐Fe(NO)2

Ghosh, P., Ding, S., Quiroz, M., Bhuvanesh, N. S. P., Hsieh, C., Palacios, P. M., Pierce, B. S., Darensbourg, M. Y., & Hall, M. B. (2018) · Chemistry - A European Journal · doi:10.1002/chem.201804168 · Cited by 17

Monomeric Dinitrosyl Iron Complexes: Synthesis and Reactivity

Tran, C. T., Skodje, K. M., & Kim, E. (2014) · Progress in inorganic chemistry · doi:10.1002/9781118869994.ch05 · Cited by 15

Vorinostat exhibits anticancer effects in triple-negative breast cancer cells by preventing nitric oxide-driven histone deacetylation

Palczewski, M. B., Kuschman, H. P., Bovee, R. C., Hickok, J. R., & Thomas, D. D. (2021) · Biological Chemistry · doi:10.1515/hsz-2020-0323 · Cited by 14

The Chemical Biology of NO that Regulates Oncogenic Signaling and Metabolism: NOS2 and Its Role in Inflammatory Disease

Miranda, K. M., Ridnour, L. A., Cheng, R. Y. S., Wink, D. A., & Thomas, D. D. (2023) · Critical Reviews™ in Oncogenesis · doi:10.1615/critrevoncog.2023047302 · Cited by 13

The role of nitric oxide (NO) in the body growth rate of birds

Titov, V. Y., Михайловна, Д. А., Fisinin, V. I., Borkhunova, E. N., Kondratov, G. V., Slesarenko, N. A., & Kochish, I. I. (2018) · World s Poultry Science Journal · doi:10.1017/s0043933918000661 · Cited by 14

Redox activities of mono- and binuclear forms of low-molecular and protein-bound dinitrosyl iron complexes with thiol-containing ligands

Borodulin, R. R., Dereven’kov, I. А., Burbaev, D. S., Makarov, S. V., Mikoyan, V. D., Сереженков, В. А., Kubrina, L. N., Ivanović‐Burmazović, I., & Vanin, A. F. (2014) · Nitric Oxide · doi:10.1016/j.niox.2014.06.005 · Cited by 14

Hammett correlations as test of mechanism of CO-induced disulfide elimination from dinitrosyl iron complexes

Pulukkody, R., Kyran, S. J., Drummond, M. J., Hsieh, C., Darensbourg, D. J., & Darensbourg, M. Y. (2014) · Chemical Science · doi:10.1039/c4sc01523a · Cited by 13

Ascorbate attenuates red light mediated vasodilation: Potential role of S-nitrosothiols

Keszler, Á., Lindemer, B. J., Hogg, N., & Lohr, N. L. (2018) · Redox Biology · doi:10.1016/j.redox.2018.09.008 · Cited by 13

The Fe2(NO)2 Diamond Core: A Unique Structural Motif In Non‐Heme Iron–NO Chemistry

Dong, H. T., Speelman, A. L., Kozemchak, C. E., Sil, D., Krebs, C., & Lehnert, N. (2019) · Angewandte Chemie · doi:10.1002/ange.201911968 · Cited by 13

Enzymatic Sensor Detects Some Forms of Nitric Oxide Donors Undetectable by Other Methods in Living Tissues

Titov, V. Y., Kosenko, O. V., Starkova, E. S., Kondratov, G. V., Borkhunova, E. N., Petrov, V. A., & Osipov, A. N. (2016) · Bulletin of Experimental Biology and Medicine · doi:10.1007/s10517-016-3557-1 · Cited by 12

A Conspectus of Cellular Mechanisms of Nitrosothiol Formation from Nitric Oxide

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The Peroxidatic Thiol of Peroxiredoxin 1 is Nitrosated by Nitrosoglutathione but Coordinates to the Dinitrosyl Iron Complex of Glutathione

Truzzi, D. R., Alves, S. V., Netto, L. E. S., & Augusto, O. (2020) · Antioxidants · doi:10.3390/antiox9040276 · Cited by 15

Development of (NO)Fe(N2S2) as a Metallodithiolate Spin Probe Ligand: A Case Study Approach

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Unraveling signatures of chicken genetic diversity and divergent selection in breed-specific patterns of early myogenesis, nitric oxide metabolism and post-hatch growth

Kochish, I. I., Titov, V. Y., Nikonov, I. N., Brazhnik, E. A., Vorobyov, N. I., Korenyuga, M. V., Myasnikova, O. V., Михайловна, Д. А., Griffin, D. K., & Romanov, M. N. (2023) · Frontiers in Genetics · doi:10.3389/fgene.2022.1092242 · Cited by 10

Nitric oxide and thiols: Chemical biology, signalling paradigms and vascular therapeutic potential

Dent, M. R., & DeMartino, A. W. (2023) · British Journal of Pharmacology · doi:10.1111/bph.16274 · Cited by 11

Nitric oxide is an epigenetic regulator of histone post-translational modifications in cancer

Palczewski, M. B., Kuschman, H. P., & Thomas, D. D. (2019) · Current Opinion in Physiology · doi:10.1016/j.cophys.2019.05.006 · Cited by 10

Effects of Glutathione and Histidine on NO Release from a Dimeric Dinitrosyl Iron Complex (DNIC)

Pectol, D. C., Khan, S. A., Elsabahy, M., Wooley, K. L., Lim, S., & Darensbourg, M. Y. (2020) · Inorganic Chemistry · doi:10.1021/acs.inorgchem.0c02196 · Cited by 10

Nitric Oxide-induced Conversion of Cellular Chelatable Iron into Macromolecule-bound Paramagnetic Dinitrosyliron Complexes

Toledo, J. C., Bosworth, C. A., Hennon, S. W., Mahtani, H., Bergonia, H. A., & Lancaster, J. R. (2008) · Journal of Biological Chemistry · doi:10.1074/jbc.m707862200 · Cited by 119

Nitrosothiol Formation and Protection against Fenton Chemistry by Nitric Oxide-induced Dinitrosyliron Complex Formation from Anoxia-initiated Cellular Chelatable Iron Increase

Li, Q., Li, C., Mahtani, H. K., Du, J., Patel, A. R., & Lancaster, J. R. (2014) · Journal of Biological Chemistry · doi:10.1074/jbc.m114.569764 · Cited by 52

Dinitrosyl Iron Complexes (DNICs). From Spontaneous Assembly to Biological Roles

Truzzi, D. R., Medeiros, N. M., Augusto, O., & Ford, P. C. (2021) · Inorganic Chemistry · doi:10.1021/acs.inorgchem.1c00823 · Cited by 52

Crucial role of lysosomal iron in the formation of dinitrosyl iron complexes in vivo

Lewandowska, H., Męczyńska‐Wielgosz, S., Sochanowicz, B., Sadło, J., & Kruszewski, M. K. (2006) · JBIC Journal of Biological Inorganic Chemistry · doi:10.1007/s00775-006-0192-8 · Cited by 29

The source of non-heme iron that binds nitric oxide in cultivated macrophages

Vanin, A. F., Gb, M., Moroz, I. A., Mordvintcev, P. I., Сереженков, В. А., & Burbaev, D. S. (1992) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/0167-4889(92)90231-y · Cited by 58