H 2 S as a Physiologic Vasorelaxant: Hypertension in Mice with Deletion of Cystathionine γ-Lyase

Hypertension in mice lacking the gene for endothelial nitric oxide synthase

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The vasorelaxant effect of H2S as a novel endogenous gaseous KATP channel opener

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Two's company, three's a crowd: can H 2 S be the third endogenous gaseous transmitter?

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N OVEL N EURAL M ODULATORS

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Elevated blood pressures in mice lacking endothelial nitric oxide synthase

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Homocysteine and vascular disease

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H2S-induced vasorelaxation and underlying cellular and molecular mechanisms

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Hydrogen sulfide-induced relaxation of resistance mesenteric artery beds of rats

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Hydrogen Sulfide as a Neuromodulator

Kimura, H. (2002) · Molecular Neurobiology · doi:10.1385/mn:26:1:013 · Cited by 427

Inhibition of Hydrogen Sulfide Generation Contributes to Gastric Injury Caused by Anti-Inflammatory Nonsteroidal Drugs

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Hydrogen sulfide in cell survival: a double-edged sword

Yang, G. (2010) · Expert Review of Clinical Pharmacology · doi:10.1586/ecp.10.131 · Cited by 54

A Dual‐Response Fluorescent Probe Reveals the H 2 O 2 ‐Induced H 2 S Biogenesis through a Cystathionine β‐Synthase Pathway

Yi, L., Wei, L., Wang, R., Zhang, C., Zhang, J., Tan, T., & Xi, Z. (2015) · Chemistry - A European Journal · doi:10.1002/chem.201502832 · Cited by 54

A near-infrared fluorescent probe for monitoring fluvastatin-stimulated endogenous H 2 S production

Zhang, L., Zhu, H., Zhao, C., & Gu, X. (2016) · Chinese Chemical Letters · doi:10.1016/j.cclet.2016.07.008 · Cited by 54

Hydrogen Sulfide Improves Endothelial Dysfunction via Downregulating BMP4/COX‐2 Pathway in Rats with Hypertension

Xiao, L., Dong, J., Jin, S., Xue, H., Guo, Q., Teng, X., & Wu, Y. (2016) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2016/8128957 · Cited by 54

Genetics and pathophysiology of mammalian sulfate biology

Langford, R., Hurrion, E. M., & Dawson, P. A. (2016) · Journal of genetics and genomics/Journal of Genetics and Genomics · doi:10.1016/j.jgg.2016.08.001 · Cited by 55

Role of dietary amino acid balance in diet restriction‐mediated lifespan extension, renoprotection, and muscle weakness in aged mice

Yoshida, S., Yamahara, K., Kume, S., Koya, D., Yasuda‒Yamahara, M., Takeda, N., Osawa, N., Chin‒Kanasaki, M., Adachi, Y., Nagao, K., et al. (2018) · Aging Cell · doi:10.1111/acel.12796 · Cited by 54

Rationally designed pure-inorganic upconversion nanoprobes for ultra-highly selective hydrogen sulfide imaging and elimination in vivo

Liu, Y. L., Jia, Q., Zhai, X., Mao, F., Jiang, A., & Zhou, J. (2018) · Chemical Science · doi:10.1039/c8sc04464c · Cited by 54

MPST but not CSE is the primary regulator of hydrogen sulfide production and function in the coronary artery

Kuo, M. M., Kim, D. H., Jandu, S., Bergman, Y., Tan, S., Wang, H., Pandey, D., Abraham, T. P., Shoukas, A. A., Berkowitz, D. E., et al. (2015) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00574.2014 · Cited by 53

Redox regulation of endothelial cell fate

Song, P., & Zou, M. (2014) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-014-1598-z · Cited by 53

Modulation of thiol homeostasis induced by H2S-releasing aspirin

Giustarini, D., Soldato, P. D., Sparatore, A., & Rossi, R. (2010) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2010.02.014 · Cited by 54

Protein modifications involved in neurotransmitter and gasotransmitter signaling

Sen, N., & Snyder, S. H. (2010) · Trends in Neurosciences · doi:10.1016/j.tins.2010.07.004 · Cited by 54

Disassembly mediated fluorescence recovery of gold nanodots for selective sulfide sensing

Yuan, Z., Peng, M., Shi, L., Du, Y. P., Cai, N., He, Y., Chang, H., & Yeung, E. S. (2012) · Nanoscale · doi:10.1039/c2nr33202g · Cited by 53

The CBS/CSE system: a potential therapeutic target in NAFLD?

Sarna, L. K., Siow, Y. L., & Karmin, O. (2014) · Canadian Journal of Physiology and Pharmacology · doi:10.1139/cjpp-2014-0394 · Cited by 54

Exogenous H2S contributes to recovery of ischemic post-conditioning-induced cardioprotection by decrease of ROS level via down-regulation of NF-κB and JAK2-STAT3 pathways in the aging cardiomyocytes

Li, L., Li, M., Li, Y., Sun, W., Wang, Y., Bai, S., Li, H., Wu, B., Wang, R., Wang, R., et al. (2016) · Cell & Bioscience · doi:10.1186/s13578-016-0090-x · Cited by 53

Hydrogen sulfide-producing cystathionine γ-lyase is critical in the progression of kidney fibrosis

Han, S. J., Noh, M. R., Jung, J.-M., Ishii, I., Yoo, J., Kim, J. I., & Park, K. M. (2017) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2017.08.017 · Cited by 53

GYY4137, an H2S Slow-Releasing Donor, Prevents Nitrative Stress and α-Synuclein Nitration in an MPTP Mouse Model of Parkinson’s Disease

Hou, X., Yuan, Y., Sheng, Y., Yuan, B., Wang, Y., Zheng, J., Liu, C., Zhang, X., & Hu, L. (2017) · Frontiers in Pharmacology · doi:10.3389/fphar.2017.00741 · Cited by 53

H2S protects lipopolysaccharide-induced inflammation by blocking NFκB transactivation in endothelial cells

Bourque, C., Zhang, Y., Fu, M., Racine, M., Greasley, A., Pei, Y., Wu, L., Wang, R., & Yang, G. (2017) · Toxicology and Applied Pharmacology · doi:10.1016/j.taap.2017.11.004 · Cited by 53

The interaction of IGF-1/IGF-1R and hydrogen sulfide on the proliferation of mouse primary vascular smooth muscle cells

Shuang, T., Fu, M., Yang, G., Wu, L., & Wang, R. (2017) · Biochemical Pharmacology · doi:10.1016/j.bcp.2017.12.009 · Cited by 53

Sodium sulfide selectively induces oxidative stress, DNA damage, and mitochondrial dysfunction and radiosensitizes glioblastoma (GBM) cells.

Xiao, A. Y., Maynard, M. R., Piett, C. G., Nagel, Z. D., Alexander, J. S., Kevil, C. G., Berridge, M. V., Pattillo, C. B., Rosen, L., Miriyala, S., et al. (2019) · Redox Biology · doi:10.1016/j.redox.2019.101220 · Cited by 53

Role of hydrogen sulfide in health and disease

Jin, Y., Yuan, H., Liu, Y., Zhu, Y., Wang, Y., Liang, X., Gao, W., Ren, Z., Ji, X., & Wu, D. (2024) · MedComm · doi:10.1002/mco2.661 · Cited by 54

Postsynthetic modification of metal–organic framework for hydrogen sulfide detection

Zhang, X., Zhang, J., Hu, Q., Cui, Y., Yang, Y. Z., & Qian, G. (2015) · Applied Surface Science · doi:10.1016/j.apsusc.2015.07.166 · Cited by 52

Homocysteine and Hypertension in Diabetes: Does PPAR γ Have a Regulatory Role?

Sen, U., & Tyagi, S. C. (2010) · PPAR Research · doi:10.1155/2010/806538 · Cited by 52

Generation of DNA-Damaging Reactive Oxygen Species via the Autoxidation of Hydrogen Sulfide under Physiologically Relevant Conditions: Chemistry Relevant to Both the Genotoxic and Cell Signaling Properties of H 2 S

Hoffman, M. A., Rajapakse, A., Shen, X., & Gates, K. S. (2012) · Chemical Research in Toxicology · doi:10.1021/tx300066z · Cited by 51

Effects of AP39, a novel triphenylphosphonium derivatised anethole dithiolethione hydrogen sulfide donor, on rat haemodynamic parameters and chloride and calcium Cav3 and RyR2 channels

Tomášová, L., Pavlovičová, M., Máleková, Ľ., Mišák, A., Kristek, F., Grman, M., Čačányiová, S., Tomasek, M., Tomaskova, Z. S., Perry, A., et al. (2014) · Nitric Oxide · doi:10.1016/j.niox.2014.12.012 · Cited by 52

Hydrogen sulfide as a vasculoprotective factor

Streeter, E., Ng, H. H., & Hart, J. L. (2013) · Medical Gas Research · doi:10.1186/2045-9912-3-9 · Cited by 50

Fast‐Response Turn‐on Fluorescent Probes Based on Thiolysis of NBD Amine for H2S Bioimaging

Wang, R., Li, Z., Zhang, C., Li, Y., Xu, G., Zhang, Q., Li, L., Yi, L., & Xi, Z. (2016) · ChemBioChem · doi:10.1002/cbic.201600060 · Cited by 52

Hydrogen Sulfide Protects Against High-glucose–induced Apoptosis in Endothelial Cells

Guan, Q., Zhang, Y., Yu, C., Liu, Y., Gao, L., & Zhao, J. (2011) · Journal of Cardiovascular Pharmacology · doi:10.1097/fjc.0b013e31823b4915 · Cited by 52

Ratiometric QD-FRET Sensing of Aqueous H2S in Vitro

Shamirian, A., Afsari, H. S., Wu, D., Miller, L. W., & Snee, P. T. (2016) · Analytical Chemistry · doi:10.1021/acs.analchem.6b01310 · Cited by 52

The H2S-generating enzymes cystathionine β-synthase and cystathionine γ-lyase play a role in vascular development during normal lung alveolarization

Madurga, A., Golec, A., Pozarska, A., Ishii, I., Mižíková, I., Nardiello, C., Vadász, I., Herold, S., Mayer, K., Reichenberger, F., et al. (2015) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.00134.2015 · Cited by 52

Comparative proteomic analysis reveals the role of hydrogen sulfide in the adaptation of the alpine plant Lamiophlomis rotata to altitude gradient in the Northern Tibetan Plateau

Ma, L., Yang, L., Zhao, J., Wei, J., Kong, X., Wang, C., Zhang, X., Yang, Y., & Hu, X. (2014) · Planta · doi:10.1007/s00425-014-2209-9 · Cited by 52

Adipose-Vascular Coupling and Potential Therapeutics

Gollasch, M. (2016) · The Annual Review of Pharmacology and Toxicology · doi:10.1146/annurev-pharmtox-010716-104542 · Cited by 51

Comparisons between perivascular adipose tissue and the endothelium in their modulation of vascular tone

Zaborska, K. E., Wareing, M., & Austin, C. E. (2016) · British Journal of Pharmacology · doi:10.1111/bph.13648 · Cited by 51

The interaction of estrogen and CSE/H2S pathway in the development of atherosclerosis

Li, H., Mani, S., Wu, L., Fu, M., Shuang, T., Xu, C., & Wang, R. (2016) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00245.2016 · Cited by 52

Hydrogen sulfide inhibits high glucose-induced NADPH oxidase 4 expression and matrix increase by recruiting inducible nitric oxide synthase in kidney proximal tubular epithelial cells

Lee, H. J., Lee, D. Y., Mariappan, M. M., Féliers, D., Ghosh-Choudhury, G., Abboud, H. E., Gorin, Y. C., & Kasinath, B. S. (2017) · Journal of Biological Chemistry · doi:10.1074/jbc.m116.766758 · Cited by 51

Rapid Antidepressant Effect of Hydrogen Sulfide: Evidence for Activation of mTORC1-TrkB-AMPA Receptor Pathways

Hou, X.-Y., Hu, Z., Zhang, D.-Z., Lu, W., Zhou, J., Wu, P.-F., Guan, X., Han, Q.-Q., Deng, S., Zhang, H., et al. (2017) · Antioxidants and Redox Signaling · doi:10.1089/ars.2016.6737 · Cited by 51

Hydrogen Sulfide Attenuates Atherosclerosis in a Partially Ligated Carotid Artery Mouse model via Regulating Angiotensin Converting Enzyme 2 Expression

Lin, Y., Zeng, H., Gao, L., Gu, T., Wang, C., & Zhang, H. (2017) · Frontiers in Physiology · doi:10.3389/fphys.2017.00782 · Cited by 52

Fatty-acid receptor CD36 functions as a hydrogen sulfide-targeted receptor with its Cys333-Cys272 disulfide bond serving as a specific molecular switch to accelerate gastric cancer metastasis

Wang, R., Tao, B., Fan, Q., Wang, S., Chen, L., Zhang, J., Hao, Y., Dong, S., Wang, Z., Wang, W., et al. (2019) · EBioMedicine · doi:10.1016/j.ebiom.2019.06.037 · Cited by 52

Design strategy of multifunctional and high efficient hydrogen sulfide NIR fluorescent probe and its application in vivo

Zhou, K., Yang, Y.-T., Zhou, T., Jin, M., & Yin, C. (2020) · Dyes and Pigments · doi:10.1016/j.dyepig.2020.108901 · Cited by 52

Platelet‐derived growth factor‐BB induces cystathionine γ‐lyase expression in rat mesangial cells via a redox‐dependent mechanism

Hassan, M. I., Boosen, M., Schaefer, L., Kozlowska, J., Eisel, F., von Knethen, A., Beck, M., Hemeida, R. A. M., El‐Moselhy, M. A., Hamada, F. M. A., et al. (2012) · British Journal of Pharmacology · doi:10.1111/j.1476-5381.2012.01949.x · Cited by 52

New insights into RhoA/Rho-kinase signaling: a key regulator of vascular contraction

Nunes, K. P., & Webb, R. C. (2020) · Small GTPases · doi:10.1080/21541248.2020.1822721 · Cited by 51

Endogenous hydrogen sulfide in perivascular adipose tissue: role in the regulation of vascular tone in physiology and pathology

Bełtowski, J. (2013) · Canadian Journal of Physiology and Pharmacology · doi:10.1139/cjpp-2013-0001 · Cited by 51

Hydrogen sulfide and erectile function: a novel therapeutic target

Bianca, R. D. D. V., Sorrentino, R., Mirone, V. G., & Cirino, G. (2011) · Nature Reviews Urology · doi:10.1038/nrurol.2011.45 · Cited by 51

H2S signaling in redox regulation of cellular functions

Ju, Y., Zhang, W., Pei, Y., & Yang, G. (2013) · Canadian Journal of Physiology and Pharmacology · doi:10.1139/cjpp-2012-0293 · Cited by 51

Inhibition of hydrogen sulfide restores normal breathing stability and improves autonomic control during experimental heart failure

Río, R. D., Marcus, N. J., & Schultz, H. D. (2013) · Journal of Applied Physiology · doi:10.1152/japplphysiol.01503.2012 · Cited by 51

Hydrogen Sulfide–Releasing Aspirin Derivative ACS14 Exerts Strong Antithrombotic Effects In Vitro and In Vivo

Pircher, J., Fochler, F., Czermak, T., Mannell, H., Kraemer, B. F., Wörnle, M., Sparatore, A., Soldato, P. D., Pohl, U., & Krötz, F. (2012) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.112.300627 · Cited by 52

Hydrogen sulfide in the pathogenesis of atherosclerosis and its therapeutic potential

Lynn, E. G., & Austin, R. C. (2010) · Expert Review of Clinical Pharmacology · doi:10.1586/ecp.10.130 · Cited by 51

Sulfurous Gases As Biological Messengers and Toxins: Comparative Genetics of Their Metabolism in Model Organisms

Mathew, N. D., Schlipalius, D. I., & Ebert, P. R. (2011) · Journal of Toxicology · doi:10.1155/2011/394970 · Cited by 51

“Zipped Synthesis” by Cross-Metathesis Provides a Cystathionine β-Synthase Inhibitor that Attenuates Cellular H2S Levels and Reduces Neuronal Infarction in a Rat Ischemic Stroke Model

McCune, C. D., Chan, S. J., Beio, M. L., Shen, W., Chung, W. J., Szczesniak, L. M., Chai, C., Koh, S. Q., Wong, P. T. ‐., & Berkowitz, D. B. (2016) · ACS Central Science · doi:10.1021/acscentsci.6b00019 · Cited by 51

Two-Input Fluorescent Probe for Thiols and Hydrogen Sulfide Chemosensing and Live Cell Imaging

Dai, C.-G., Liu, X., Du, X., Zhang, Y., & Song, Q. (2016) · ACS Sensors · doi:10.1021/acssensors.6b00291 · Cited by 51

A long-lived phosphorescence iridium(III) complex as a switch on-off-on probe for live zebrafish monitoring of endogenous sulfide generation

Ko, C.-N., Yang, C., Lin, S., Li, S., Dong, Z., Liu, J., Lee, S. M., Leung, C., & Ma, D. (2017) · Biosensors and Bioelectronics · doi:10.1016/j.bios.2017.03.050 · Cited by 51

Endpoint or Kinetic Measurement of Hydrogen Sulfide Production Capacity in Tissue Extracts

Hine, C., & Mitchell, J. R. (2017) · BIO-PROTOCOL · doi:10.21769/bioprotoc.2382 · Cited by 53

Cystathionine γ-Lyase Modulates Flow-Dependent Vascular Remodeling

Yuan, S. S., Yurdagul, A., Peretik, J. M., Alfaidi, M., Al‐Yafeai, Z., Pardue, S., Pearson, B. H., Kevil, C. G., & Orr, A. W. (2018) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.118.311402 · Cited by 51

A highly sensitive fluorescent probe for hydrogen sulfide based on dicyanoisophorone and its imaging in living cells

Wang, J., Wen, Y., Huo, F., & Yin, C. (2019) · Sensors and Actuators B Chemical · doi:10.1016/j.snb.2019.05.038 · Cited by 51

Methionine restriction delays senescence and suppresses the senescence-associated secretory phenotype in the kidney through endogenous hydrogen sulfide

Wang, S., Wang, W., Liu, J., Song, Y.-H., Li, P., Sun, X., Cai, G., & Chen, X. (2019) · Cell Cycle · doi:10.1080/15384101.2019.1618124 · Cited by 52

Hydrogen Sulfide and Endoplasmic Reticulum Stress: A Potential Therapeutic Target for Central Nervous System Degeneration Diseases

Zhong, H., Yu, H., Chen, J., Sun, J. Y., Guo, L., Huang, P., & Zhong, Y. (2020) · Frontiers in Pharmacology · doi:10.3389/fphar.2020.00702 · Cited by 51

A colorimetric and ratiometric fluorescent probe with a large stokes shift for detection of hydrogen sulfide

Xiang, K., Liu, Y., Li, C., Tian, B., Tong, T., & Zhang, J. (2015) · Dyes and Pigments · doi:10.1016/j.dyepig.2015.06.037 · Cited by 50

Role of Hydrogen Sulfide in Early Blood-Brain Barrier Disruption following Transient Focal Cerebral Ischemia

Jiang, Z., Li, C., Manuel, M. L., Yuan, S. S., Kevil, C. G., McCarter, K. D., Lu, W., & Sun, H. (2015) · PLoS ONE · doi:10.1371/journal.pone.0117982 · Cited by 50

Fluorescent probes for hydrogen sulfide (H2S) and sulfane sulfur and their applications to biological studies

Shimamoto, K., & Hanaoka, K. (2014) · Nitric Oxide · doi:10.1016/j.niox.2014.11.008 · Cited by 50

Cardioprotective Effects of a Novel Hydrogen Sulfide Agent–Controlled Release Formulation of S-Propargyl-Cysteine on Heart Failure Rats and Molecular Mechanisms

Huang, C., Kan, J., Liu, X., Ma, F., Tran, B. H., Zou, Y., Wang, S., & Zhu, Y. Z. (2013) · PLoS ONE · doi:10.1371/journal.pone.0069205 · Cited by 50

Involvement of Potassium Channels and Calcium-Independent Mechanisms in Hydrogen Sulfide–Induced Relaxation of Rat Mesenteric Small Arteries

Hedegaard, E. R., Gouliaev, A., Winther, A. K., Arcanjo, D. D. R., Aalling, M., Renaltan, N. S., Wood, M. E., Whiteman, M., Skovgaard, N., & Simonsen, U. (2015) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.115.227017 · Cited by 50

Communication Is Key: Mechanisms of Intercellular Signaling in Vasodilation

Freed, J. K., & Gutterman, D. D. (2017) · Journal of Cardiovascular Pharmacology · doi:10.1097/fjc.0000000000000463 · Cited by 50

Hydrogen Sulfide Metabolism and Signaling in the Tumor Microenvironment

Giuffrè, A., Tomé, C. S., Fernandes, D., Zuhra, K., & Vicente, J. B. (2020) · Advances in experimental medicine and biology · doi:10.1007/978-3-030-34025-4_17 · Cited by 50

Hydrogen sulfide rescues high glucose-induced migration dysfunction in HUVECs by upregulating miR-126-3p

Xue, W., Chen, R.-Q., Zhang, Q., Li, X., Cao, L., Li, M.-Y., Li, Y., Lin, G., Chen, Y., Wang, M.-J., et al. (2020) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00406.2019 · Cited by 50

Hydrogen sulfide signaling in regulation of cell behaviors

Wang, Y., Yu, R., Wu, L., & Yang, G. (2020) · Nitric Oxide · doi:10.1016/j.niox.2020.07.002 · Cited by 50

Interaction of Methylglyoxal and Hydrogen Sulfide in Rat Vascular Smooth Muscle Cells

Chang, T., Untereiner, A. A., Liu, J., & Wu, L. (2009) · Antioxidants and Redox Signaling · doi:10.1089/ars.2009.2918 · Cited by 50

Hydrogen Sulfide Modulates Endothelial–Mesenchymal Transition in Heart Failure

Li, Z., Xia, H., Sharp, T. E., LaPenna, K. B., Katsouda, A., Elrod, J. W., Pfeilschifter, J. M., Beck, K., Xu, S. J., Xian, M., et al. (2022) · Circulation Research · doi:10.1161/circresaha.122.321326 · Cited by 49

Protein Persulfidation: Recent Progress and Future Directions

Luo, S., Kong, C., Ye, D., Liu, X., Wang, Y., Meng, G., Han, Y., Xie, L., & Ji, Y. H. (2023) · Antioxidants and Redox Signaling · doi:10.1089/ars.2022.0064 · Cited by 49

Synthesis of Sulfides and Persulfides Is Not Impeded by Disruption of Three Canonical Enzymes in Sulfur Metabolism

Abidin, Q. H. Z., Ida, T., Morita, M., Matsunaga, T., Nishimura, A., Jung, M., Hassan, N., Takata, T., Ishii, I., Kruger, W. D., et al. (2023) · Antioxidants · doi:10.3390/antiox12040868 · Cited by 49

Mesoporous silica nanoparticles for glutathione-triggered long-range and stable release of hydrogen sulfide

Sun, X., Kong, B., Wang, W., Chandran, P., Selomulya, C., Zhang, H., Zhu, K., Liu, Y., Yang, W., Guo, C., et al. (2015) · Journal of Materials Chemistry B · doi:10.1039/c5tb00354g · Cited by 49

Redox Biology: Computational Approaches to the Investigation of Functional Cysteine Residues

Marino, S. M., & Gladyshev, V. N. (2010) · Antioxidants and Redox Signaling · doi:10.1089/ars.2010.3561 · Cited by 50

Dysregulation of hydrogen sulphide metabolism impairs oviductal transport of embryos

Ning, N., Zhu, J., Du, Y., Gao, X., Liu, C., & Li, J. (2014) · Nature Communications · doi:10.1038/ncomms5107 · Cited by 49

Hydrogen sulfide promotes nitric oxide production in corpus cavernosum by enhancing expression of endothelial nitric oxide synthase

Meng, J., Adaikan, P. G., & Srilatha, B. (2012) · International Journal of Impotence Research · doi:10.1038/ijir.2012.39 · Cited by 49

Effects of hydrogen sulphide in smooth muscle

Dunn, W. R., Alexander, S. P. H., Ralevic, V., & Roberts, R. E. (2015) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2015.12.007 · Cited by 49

Remote sensing and in situ measurements of methane and ammonia emissions from a megacity dairy complex: Chino, CA

Leifer, I., Melton, C., Tratt, D. M., Buckland, K. N., Clarisse, L., Coheur, P., Frash, J., Gupta, M. X., Johnson, P. D., Leen, J. B., et al. (2016) · Environmental Pollution · doi:10.1016/j.envpol.2016.09.083 · Cited by 49

A luminogenic lanthanide-based probe for the highly selective detection of nanomolar sulfide levels in aqueous samples

Aulsebrook, M. L., Biswas, S., Leaver, F. M., Grace, M., Graham, B., Barrios, A. M., & Tuck, K. L. (2017) · Chemical Communications · doi:10.1039/c7cc01764b · Cited by 49

Exogenous H2S facilitating ubiquitin aggregates clearance via autophagy attenuates type 2 diabetes-induced cardiomyopathy

Wu, J., Tian, Z., Sun, Y., Lu, C., Liu, N., Gao, Z., Zhang, L., Dong, S., Yang, F., Zhong, X., et al. (2017) · Cell Death and Disease · doi:10.1038/cddis.2017.380 · Cited by 49

Hydrogen sulfide negatively regulates cd-induced cell death in cucumber (Cucumis sativus L) root tip cells

Luo, S., Tang, Z., Yu, J., Liao, W., Xie, J., Lv, J. C., Feng, Z., & Dawuda, M. M. (2020) · BMC Plant Biology · doi:10.1186/s12870-020-02687-8 · Cited by 49

Hydrogen sulphide as a signalling molecule regulating physiopathological processes in gastrointestinal motility

Jimenez, M., Gil, V, Martinez‐Cutillas, M., Mañé, N., & Gallego, D. (2017) · British Journal of Pharmacology · doi:10.1111/bph.13918 · Cited by 48

A β-diketonate–europium( iii ) complex-based fluorescent probe for highly sensitive time-gated luminescence detection of copper and sulfide ions in living cells

Wang, Y., Wang, H., Zhao, X., Jin, Y., Xiong, H.-Q., Yuan, J., & Wu, J. (2017) · New Journal of Chemistry · doi:10.1039/c7nj00802c · Cited by 48

Cystathionine γ lyase S-sulfhydrates Drp1 to ameliorate heart dysfunction

Wu, D., Tan, B., Sun, Y., & Hu, Q. (2022) · Redox Biology · doi:10.1016/j.redox.2022.102519 · Cited by 48

Imaging of living cells and zebrafish in vivo using a ratiometric fluorescent probe for hydrogen sulfide

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