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For: Miyamoto R, Otsuguro K, Yamaguchi S, Ito S. Contribution of cysteine aminotransferase and mercaptopyruvate sulfurtransferase to hydrogen sulfide production in peripheral neurons. J Neurochem 2014;130:29-40. [DOI: 10.1111/jnc.12698] [Cited by in Crossref: 38] [Cited by in F6Publishing: 38] [Article Influence: 4.8] [Reference Citation Analysis]
Number Citing Articles
1 Pilkington LI, Deed RC, Parish-virtue K, Huang C, Walker ME, Jiranek V, Barker D, Fedrizzi B. Iterative synthetic strategies and gene deletant experiments enable the first identification of polysulfides in Saccharomyces cerevisiae. Chem Commun 2019;55:8868-71. [DOI: 10.1039/c9cc03020d] [Cited by in Crossref: 4] [Article Influence: 1.3] [Reference Citation Analysis]
2 Lignelli E, Palumbo F, Bayindir SG, Nagahara N, Vadász I, Herold S, Seeger W, Morty RE. The H2S-generating enzyme 3-mercaptopyruvate sulfurtransferase regulates pulmonary vascular smooth muscle cell migration and proliferation but does not impact normal or aberrant lung development. Nitric Oxide 2021;107:31-45. [PMID: 33338600 DOI: 10.1016/j.niox.2020.12.002] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
3 Coletta C, Módis K, Szczesny B, Brunyánszki A, Oláh G, Rios EC, Yanagi K, Ahmad A, Papapetropoulos A, Szabo C. Regulation of Vascular Tone, Angiogenesis and Cellular Bioenergetics by the 3-Mercaptopyruvate Sulfurtransferase/H2S Pathway: Functional Impairment by Hyperglycemia and Restoration by DL-α-Lipoic Acid. Mol Med 2015;21:1-14. [PMID: 25715337 DOI: 10.2119/molmed.2015.00035] [Cited by in Crossref: 76] [Cited by in F6Publishing: 76] [Article Influence: 10.9] [Reference Citation Analysis]
4 Pedre B, Barayeu U, Ezeriņa D, Dick TP. The mechanism of action of N-acetylcysteine (NAC): The emerging role of H2S and sulfane sulfur species. Pharmacol Ther 2021;228:107916. [PMID: 34171332 DOI: 10.1016/j.pharmthera.2021.107916] [Reference Citation Analysis]
5 Luo H, Wu PF, Han QQ, Cao Y, Deng SL, Wang J, Deng Q, Wang F, Chen JG. Reactive Sulfur Species Emerge as Gliotransmitters to Support Memory via Sulfuration-Dependent Gating of NR2A-Containing N-Methyl-d-Aspartate Subtype Glutamate Receptor Function. Antioxid Redox Signal 2019;30:1880-99. [PMID: 30187770 DOI: 10.1089/ars.2018.7503] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 1.5] [Reference Citation Analysis]
6 Ahmad A, Druzhyna N, Szabo C. Effect of 3-mercaptopyruvate Sulfurtransferase Deficiency on the Development of Multiorgan Failure, Inflammation, and Wound Healing in Mice Subjected to Burn Injury. J Burn Care Res 2019;40:148-56. [PMID: 30649358 DOI: 10.1093/jbcr/irz007] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]
7 Thirumalaivasan N, Venkatesan P, Wu S. Highly selective turn-on probe for H 2 S with imaging applications in vitro and in vivo. New J Chem 2017;41:13510-5. [DOI: 10.1039/c7nj02869e] [Cited by in Crossref: 13] [Article Influence: 2.6] [Reference Citation Analysis]
8 Eleftheriadis T, Pissas G, Nikolaou E, Liakopoulos V, Stefanidis I. The H2S-Nrf2-Antioxidant Proteins Axis Protects Renal Tubular Epithelial Cells of the Native Hibernator Syrian Hamster from Reoxygenation-Induced Cell Death. Biology (Basel) 2019;8:E74. [PMID: 31574983 DOI: 10.3390/biology8040074] [Cited by in Crossref: 4] [Cited by in F6Publishing: 5] [Article Influence: 1.3] [Reference Citation Analysis]
9 Fräsdorf B, Radon C, Leimkühler S. Characterization and interaction studies of two isoforms of the dual localized 3-mercaptopyruvate sulfurtransferase TUM1 from humans. J Biol Chem 2014;289:34543-56. [PMID: 25336638 DOI: 10.1074/jbc.M114.605733] [Cited by in Crossref: 36] [Cited by in F6Publishing: 19] [Article Influence: 4.5] [Reference Citation Analysis]
10 Hartle MD, Tillotson MR, Prell JS, Pluth MD. Spectroscopic investigation of the reaction of metallo-protoporphyrins with hydrogen sulfide. J Inorg Biochem 2017;173:152-7. [PMID: 28551529 DOI: 10.1016/j.jinorgbio.2017.04.021] [Cited by in Crossref: 12] [Cited by in F6Publishing: 8] [Article Influence: 2.4] [Reference Citation Analysis]
11 Olson KR, Gao Y, DeLeon ER, Arif M, Arif F, Arora N, Straub KD. Catalase as a sulfide-sulfur oxido-reductase: An ancient (and modern?) regulator of reactive sulfur species (RSS). Redox Biol 2017;12:325-39. [PMID: 28285261 DOI: 10.1016/j.redox.2017.02.021] [Cited by in Crossref: 77] [Cited by in F6Publishing: 72] [Article Influence: 15.4] [Reference Citation Analysis]
12 Zhang Y, Yang J, Wang T, Wang S, Liu J, Yin C, Ye Z. Decreased Endogenous Hydrogen Sulfide Generation in Penile Tissues of Diabetic Rats With Erectile Dysfunction. The Journal of Sexual Medicine 2016;13:350-60. [DOI: 10.1016/j.jsxm.2016.01.002] [Cited by in Crossref: 18] [Cited by in F6Publishing: 17] [Article Influence: 3.0] [Reference Citation Analysis]
13 Tomita M, Nagahara N, Ito T. Expression of 3-Mercaptopyruvate Sulfurtransferase in the Mouse. Molecules 2016;21:E1707. [PMID: 27973427 DOI: 10.3390/molecules21121707] [Cited by in Crossref: 20] [Cited by in F6Publishing: 17] [Article Influence: 3.3] [Reference Citation Analysis]
14 Shan H, Chu Y, Chang P, Yang L, Wang Y, Zhu S, Zhang M, Tao L. Neuroprotective effects of hydrogen sulfide on sodium azide‑induced autophagic cell death in PC12 cells. Mol Med Rep 2017;16:5938-46. [PMID: 28849152 DOI: 10.3892/mmr.2017.7363] [Cited by in Crossref: 17] [Cited by in F6Publishing: 14] [Article Influence: 3.4] [Reference Citation Analysis]
15 Cupp-Sutton KA, Ashby MT. Biological Chemistry of Hydrogen Selenide. Antioxidants (Basel) 2016;5:E42. [PMID: 27879667 DOI: 10.3390/antiox5040042] [Cited by in Crossref: 29] [Cited by in F6Publishing: 24] [Article Influence: 4.8] [Reference Citation Analysis]
16 Tsubota M, Okawa Y, Irie Y, Maeda M, Ozaki T, Sekiguchi F, Ishikura H, Kawabata A. Involvement of the cystathionine-γ-lyase/Cav3.2 pathway in substance P-induced bladder pain in the mouse, a model for nonulcerative bladder pain syndrome. Neuropharmacology 2018;133:254-63. [PMID: 29407215 DOI: 10.1016/j.neuropharm.2018.01.037] [Cited by in Crossref: 7] [Cited by in F6Publishing: 6] [Article Influence: 1.8] [Reference Citation Analysis]
17 Walsh BJC, Giedroc DP. H2S and reactive sulfur signaling at the host-bacterial pathogen interface. J Biol Chem 2020;295:13150-68. [PMID: 32699012 DOI: 10.1074/jbc.REV120.011304] [Cited by in Crossref: 9] [Cited by in F6Publishing: 5] [Article Influence: 4.5] [Reference Citation Analysis]
18 Miyamoto R, Otsuguro K, Yamaguchi S, Ito S. Neuronal regulation of expression of hydrogen sulfide-producing enzyme cystathionine β-synthase in rat spinal cord astrocytes. Neurosci Res 2015;97:52-9. [PMID: 25797494 DOI: 10.1016/j.neures.2015.03.003] [Cited by in Crossref: 14] [Cited by in F6Publishing: 14] [Article Influence: 2.0] [Reference Citation Analysis]
19 Citi V, Corvino A, Fiorino F, Frecentese F, Magli E, Perissutti E, Santagada V, Brogi S, Flori L, Gorica E, Testai L, Martelli A, Calderone V, Caliendo G, Severino B. Structure-activity relationships study of isothiocyanates for H2S releasing properties: 3-Pyridyl-isothiocyanate as a new promising cardioprotective agent. J Adv Res 2021;27:41-53. [PMID: 33318865 DOI: 10.1016/j.jare.2020.02.017] [Cited by in Crossref: 9] [Cited by in F6Publishing: 6] [Article Influence: 4.5] [Reference Citation Analysis]
20 Zuhra K, Augsburger F, Majtan T, Szabo C. Cystathionine-β-Synthase: Molecular Regulation and Pharmacological Inhibition. Biomolecules 2020;10:E697. [PMID: 32365821 DOI: 10.3390/biom10050697] [Cited by in Crossref: 27] [Cited by in F6Publishing: 25] [Article Influence: 13.5] [Reference Citation Analysis]
21 Jiang X, MacArthur MR, Treviño-Villarreal JH, Kip P, Ozaki CK, Mitchell SJ, Mitchell JR. Intracellular H2S production is an autophagy-dependent adaptive response to DNA damage. Cell Chem Biol 2021:S2451-9456(21)00261-0. [PMID: 34166610 DOI: 10.1016/j.chembiol.2021.05.016] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
22 Frankowska M, Wiliński B, Somogyi E, Piotrowska J, Filip M, Opoka W. Cocaine exposure alters H2S tissue concentrations in peripheral mouse organs. Pharmacol Rep 2015;67:421-5. [PMID: 25933948 DOI: 10.1016/j.pharep.2014.11.001] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.3] [Reference Citation Analysis]
23 Zhang J, Shi C, Wang H, Gao C, Chang P, Chen X, Shan H, Zhang M, Tao L. Hydrogen sulfide protects against cell damage through modulation of PI3K/Akt/Nrf2 signaling. Int J Biochem Cell Biol 2019;117:105636. [PMID: 31654751 DOI: 10.1016/j.biocel.2019.105636] [Cited by in Crossref: 13] [Cited by in F6Publishing: 12] [Article Influence: 4.3] [Reference Citation Analysis]
24 Stipanuk MH. Metabolism of Sulfur-Containing Amino Acids: How the Body Copes with Excess Methionine, Cysteine, and Sulfide. The Journal of Nutrition 2020;150:2494S-505S. [DOI: 10.1093/jn/nxaa094] [Cited by in Crossref: 6] [Cited by in F6Publishing: 5] [Article Influence: 3.0] [Reference Citation Analysis]
25 Yang B, Zhao W, Yin C, Bai Y, Wang S, Xing G, Li F, Bian J, Aschner M, Cai J, Shi H, Lu R. Acute acrylonitrile exposure inhibits endogenous H2S biosynthesis in rat brain and liver: The role of CBS/3-MPST-H2S pathway in its astrocytic toxicity. Toxicology 2021;451:152685. [PMID: 33486070 DOI: 10.1016/j.tox.2021.152685] [Reference Citation Analysis]
26 Peng SY, Wu X, Lu T, Cui G, Chen G. Research progress of hydrogen sulfide in Alzheimer's disease from laboratory to hospital: a narrative review. Med Gas Res 2020;10:125-9. [PMID: 33004710 DOI: 10.4103/2045-9912.296043] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
27 Yuan C, Hou HT, Chen HX, Wang J, Wang ZQ, Chen TN, Novakovic A, Marinko M, Yang Q, Liu ZG, He GW. Hydrogen sulfide-mediated endothelial function and the interaction with eNOS and PDE5A activity in human internal mammary arteries. J Int Med Res 2019;47:3778-91. [PMID: 31155983 DOI: 10.1177/0300060519847386] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
28 Lachén-Montes M, González-Morales A, de Morentin XM, Pérez-Valderrama E, Ausín K, Zelaya MV, Serna A, Aso E, Ferrer I, Fernández-Irigoyen J, Santamaría E. An early dysregulation of FAK and MEK/ERK signaling pathways precedes the β-amyloid deposition in the olfactory bulb of APP/PS1 mouse model of Alzheimer's disease. J Proteomics 2016;148:149-58. [PMID: 27498392 DOI: 10.1016/j.jprot.2016.07.032] [Cited by in Crossref: 37] [Cited by in F6Publishing: 33] [Article Influence: 6.2] [Reference Citation Analysis]
29 Yuan S, Patel RP, Kevil CG. Working with nitric oxide and hydrogen sulfide in biological systems. Am J Physiol Lung Cell Mol Physiol 2015;308:L403-15. [PMID: 25550314 DOI: 10.1152/ajplung.00327.2014] [Cited by in Crossref: 47] [Cited by in F6Publishing: 44] [Article Influence: 5.9] [Reference Citation Analysis]
30 Toohey JI. Possible Involvement of Hydrosulfide in B12-Dependent Methyl Group Transfer. Molecules 2017;22:E582. [PMID: 28379205 DOI: 10.3390/molecules22040582] [Cited by in Crossref: 11] [Cited by in F6Publishing: 12] [Article Influence: 2.2] [Reference Citation Analysis]
31 Adams JC, Bell PD, Bodine SC, Brooks HL, Bunnett N, Joe B, Keehan KH, Kleyman TR, Marette A, Morty RE, Ramírez JM, Thomsen MB, Yates BJ, Zucker IH. An American Physiological Society cross-journal Call for Papers on "Deconstructing Organs: Single-Cell Analyses, Decellularized Organs, Organoids, and Organ-on-a-Chip Models". Am J Physiol Lung Cell Mol Physiol 2020;319:L266-72. [PMID: 32609556 DOI: 10.1152/ajplung.00311.2020] [Cited by in Crossref: 6] [Cited by in F6Publishing: 5] [Article Influence: 3.0] [Reference Citation Analysis]
32 Scrivner O, Kumar MR, Sorokolet K, Wong A, Kebaara B, Farmer PJ. Characterization of Endogenous and Extruded H2S and Small Oxoacids of Sulfur (SOS) in Cell Cultures. ACS Chem Biol 2021. [PMID: 34374506 DOI: 10.1021/acschembio.1c00257] [Reference Citation Analysis]
33 Pedre B, Dick TP. 3-Mercaptopyruvate sulfurtransferase: an enzyme at the crossroads of sulfane sulfur trafficking. Biol Chem 2021;402:223-37. [PMID: 33055309 DOI: 10.1515/hsz-2020-0249] [Cited by in Crossref: 5] [Cited by in F6Publishing: 6] [Article Influence: 2.5] [Reference Citation Analysis]
34 Zhao FL, Fang F, Qiao PF, Yan N, Gao D, Yan Y. AP39, a Mitochondria-Targeted Hydrogen Sulfide Donor, Supports Cellular Bioenergetics and Protects against Alzheimer's Disease by Preserving Mitochondrial Function in APP/PS1 Mice and Neurons. Oxid Med Cell Longev 2016;2016:8360738. [PMID: 27057285 DOI: 10.1155/2016/8360738] [Cited by in Crossref: 26] [Cited by in F6Publishing: 26] [Article Influence: 4.3] [Reference Citation Analysis]
35 Malard E, Valable S, Bernaudin M, Pérès E, Chatre L. The Reactive Species Interactome in the Brain. Antioxid Redox Signal 2021;35:1176-206. [PMID: 34498917 DOI: 10.1089/ars.2020.8238] [Reference Citation Analysis]
36 Eleftheriadis T, Pissas G, Nikolaou E, Filippidis G, Liakopoulos V, Stefanidis I. Mistimed H2S upregulation, Nrf2 activation and antioxidant proteins levels in renal tubular epithelial cells subjected to anoxia and reoxygenation. Biomed Rep 2020;13:3. [PMID: 32509306 DOI: 10.3892/br.2020.1309] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
37 Gonzalez-Carter DA, Leo BF, Ruenraroengsak P, Chen S, Goode AE, Theodorou IG, Chung KF, Carzaniga R, Shaffer MS, Dexter DT, Ryan MP, Porter AE. Silver nanoparticles reduce brain inflammation and related neurotoxicity through induction of H2S-synthesizing enzymes. Sci Rep 2017;7:42871. [PMID: 28251989 DOI: 10.1038/srep42871] [Cited by in Crossref: 59] [Cited by in F6Publishing: 50] [Article Influence: 11.8] [Reference Citation Analysis]
38 Ujike A, Kuraishi T, Yamaguchi S, Eguchi R, Kitano T, Kamise J, Ito S, Otsuguro K. IL-1β augments H2S-induced increase in intracellular Ca2+ through polysulfides generated from H2S/NO interaction. Eur J Pharmacol 2018;821:88-96. [PMID: 29337193 DOI: 10.1016/j.ejphar.2018.01.006] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 0.8] [Reference Citation Analysis]