Export by red blood cells of nitric oxide bioactivity

S-nitrosohaemoglobin: a dynamic activity of blood involved in vascular control

Jia, L., Bonaventura, C., Bonaventura, J., & Stamler, J. S. (1996) · Nature · doi:10.1038/380221a0 · Cited by 1,592

Blood Flow Regulation by S -Nitrosohemoglobin in the Physiological Oxygen Gradient

Stamler, J. S., Jia, L., Eu, J. P., McMahon, T. J., Demchenko, I. T., Bonaventura, J., Gernert, K., & Piantadosi, C. A. (1997) · Science · doi:10.1126/science.276.5321.2034 · Cited by 1,050

(S)NO Signals: Translocation, Regulation, and a Consensus Motif

Stamler, J. S., Toone, E. J., Lipton, S. A., & Sucher, N. J. (1997) · Neuron · doi:10.1016/s0896-6273(00)80310-4 · Cited by 679

Reactions between nitric oxide and haemoglobin under physiological conditions

Gow, A. J., & Stamler, J. S. (1998) · Nature · doi:10.1038/34402 · Cited by 562

Diffusion-limited reaction of free nitric oxide with erythrocytes

Liu, X., Miller, M. J. S., Joshi, M. S., Sadowska-Krowicka, H., Clark, D. A., & Lancaster, J. R. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.30.18709 · Cited by 512

The oxyhemoglobin reaction of nitric oxide

Gow, A. J., Luchsinger, B. P., Pawloski, J. R., Singel, D. J., & Stamler, J. S. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.16.9027 · Cited by 418

Structure and function of the cytoplasmic domain of band 3: center of erythrocyte membrane—peripheral protein interactions

Low, P. S. (1986) · Biochimica et Biophysica Acta (BBA) - Reviews on Biomembranes · doi:10.1016/0304-4157(86)90009-2 · Cited by 407

The interaction of hemoglobin with the cytoplasmic domain of band 3 of the human erythrocyte membrane.

Walder, J. A., Chatterjee, R., Steck, T. L., Low, P. S., Musso, G. F., Kaiser, E. T., Rogers, P. H., & Arnone, A. (1984) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)90956-7 · Cited by 302

Erythrocytes Possess an Intrinsic Barrier to Nitric Oxide Consumption

Vaughn, M. W., Huang, K., Kuo, L., & Liao, J. C. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.275.4.2342 · Cited by 220

Light-scattering measurements of hemoglobin binding to the erythrocyte membrane. Evidence for transmembrane effects related to a disulfonic stilbene binding to band 3

Salhany, J. M., Cordes, K. A., & Gaines, E. D. (1980) · Biochemistry · doi:10.1021/bi00548a028 · Cited by 144

Evidence that the degree of band 3 phosphorylation modulates human erythrocytes nitric oxide efflux – in vitro model of hyperfibrinogenemia

Almeida, J. P., Freitas-Santos, T., & Saldanha, C. (2011) · Clinical Hemorheology and Microcirculation · doi:10.3233/ch-2011-1490 · Cited by 14

Assessment of microvascular function in vivo using flow mediated skin fluorescence (FMSF) in patients with obstructive lung diseases: A preliminary study.

Majewski, S., Szewczyk, K., Białas, A., Miłkowska-Dymanowska, J., Kurmanowska, Z., & Górski, P. (2020) · Microvascular Research · doi:10.1016/j.mvr.2019.103914 · Cited by 15

Critical Redox and Allosteric Aspects of Nitric Oxide Interactions with Hemoglobin

Bonaventura, C., Fago, A., Henkens, R. W., & Crumbliss, A. L. (2004) · Antioxidants and Redox Signaling · doi:10.1089/ars.2004.6.979 · Cited by 14

Erythrocytes with T-State–Stabilized Hemoglobin as a Therapeutic Tool for Postischemic Liver Dysfunction

Suganuma, K., Tsukada, K., Kashiba, M., Tsuneshige, A., Furukawa, T., Kubota, T., Goda, N., Kitajima, M., Yonetani, T., & Suematsu, M. (2006) · Antioxidants and Redox Signaling · doi:10.1089/ars.2006.8.1847 · Cited by 14

Assessing NO‐Dependent Vasodilatation Using Vessel Bioassays at Defined Oxygen Tensions

Isbell, T. S., Koenitzer, J. R., Crawford, J. H., White, C. R., Kraus, D. W., & Patel, R. P. (2005) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/s0076-6879(05)96047-3 · Cited by 14

Chemical regulation of nitric oxide: a role for intracellular myoglobin?

Andriambeloson, E., & Witting, P. K. (2002) · Redox Report · doi:10.1179/135100002125000361 · Cited by 14

Preservation of endothelium nitric oxide release during beating heart surgery with respect to continuous flow cardiopulmonary bypass

Lanzarone, E., Gelmini, F., Fumero, R., Carini, M., Costantino, M. L., Fumero, R., & Alfieri, O. (2010) · Perfusion · doi:10.1177/0267659110364442 · Cited by 13

Inhibitory effects of nitrite on the reactions of bovine carbonic anhydrase II with CO2 and bicarbonate consistent with zinc-bound nitrite

Nielsen, P. M., & Fago, A. (2015) · Journal of Inorganic Biochemistry · doi:10.1016/j.jinorgbio.2015.04.013 · Cited by 12

Red cell physiology and signaling relevant to the critical care setting

Said, A. S., Rogers, S. C., & Doctor, A. (2015) · Current Opinion in Pediatrics · doi:10.1097/mop.0000000000000225 · Cited by 14

S-Nitrosylation and PEGylation of hemoglobin: Toward a blood substitute that recapitulates blood

Diesen, D. L., & Stamler, J. S. (2007) · Journal of Molecular and Cellular Cardiology · doi:10.1016/j.yjmcc.2007.03.739 · Cited by 13

S-Nitrosation and Ubiquitin-Proteasome System Interplay in Neuromuscular Disorders

Rizza, S., Montagna, C., Giacomo, G. D., Cirotti, C., & Filomeni, G. (2014) · International Journal of Cell Biology · doi:10.1155/2014/428764 · Cited by 13

Impaired Hemorheology in Exacerbations of COPD

Uğurlu, E., Kılıç-Toprak, E., Can, I., Kılıç-Erkek, Ö., Altınışık, G., & Bor-Küçükatay, M. (2017) · Canadian Respiratory Journal · doi:10.1155/2017/1286263 · Cited by 12

Down-Regulation of Hepatic Transporters for BSP in Rats with Indomethacin-Induced Intestinal Injury

Fujiyama, N., Shitara, Y., Ito, K., Masubuchi, Y., & Horie, T. (2007) · Biological and Pharmaceutical Bulletin · doi:10.1248/bpb.30.556 · Cited by 12

Real-time monitoring of nitric oxide in ischemic myocardium using an NO-selective electrode calibrated by electron spin resonance

Takahashi, S., Omori, Y., Miyazaki, H., Yoshino, F., Shoji, H., Lee, M., Todoki, K., Kamibayashi, M., & Murakami, E. (2003) · Life Sciences · doi:10.1016/j.lfs.2003.06.027 · Cited by 13

Reinvestigation of Drugs and Chemicals as Aquaporin-1 Inhibitors Using Pressure-Induced Hemolysis in Human Erythrocytes

Yamaguchi, T., Iwata, Y., Miura, S., & Kawada, K. (2012) · Biological and Pharmaceutical Bulletin · doi:10.1248/bpb.b12-00581 · Cited by 11

Control of tissue oxygenation by S-nitrosohemoglobin in human subjects

Reynolds, J. D. H., Posina, K., Zhu, L., Jenkins, T. L., Matto, F., Hausladen, A., Kashyap, V. S., Schilz, R. J., Zhang, R., Mannick, J. B., et al. (2023) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2220769120 · Cited by 11

Stimulation of Erythrocyte Soluble Guanylyl Cyclase Induces cGMP Export and Cardioprotection in Type 2 Diabetes

Jiao, T., Collado, A., Mahdi, A., Tengbom, J., Tratsiakovich, Y., Milne, G. T., Alvarsson, M., Lundberg, J. O., Zhou, Z., Yang, J., et al. (2023) · JACC Basic to Translational Science · doi:10.1016/j.jacbts.2023.02.017 · Cited by 12

Antagonists of the system L neutral amino acid transporter (LAT) promote endothelial adhesivity of human red blood cells

Dosier, L. B. M., Premkumar, V. J., Zhu, H., Akosman, I., Wempe, M. F., & McMahon, T. (2017) · Thrombosis and Haemostasis · doi:10.1160/th16-05-0373 · Cited by 11

Computational prediction of NO-dependent posttranslational modifications in plants: Current status and perspectives

Kolbert, Z., & Lindermayr, C. (2021) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2021.09.011 · Cited by 11

Redox-Regulated Plant Transcription Factors

Li, Y., & Loake, G. J. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-800854-6.00024-5 · Cited by 11

Role of N-acetyl-N-nitroso-tryptophan as nitric oxide donor in the modulation of HIF-1-dependent signaling

Berchner‐Pfannschmidt, U., Tug, S., Hu, J. J., Reyes, B. D., Fandrey, J., & Kirsch, M. (2010) · Biological Chemistry · doi:10.1515/bc.2010.054 · Cited by 11

Red blood cells carry out T cell growth and survival bioactivities that are sensitive to cyclosporine A

Antunes, R. D. S., Brandão, C., Carvalho, G., Girão, C., & Arosa, F. A. (2009) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-009-0119-y · Cited by 11

Microcirculation dysfunction in endotoxic shock rabbits is associated with impaired S-nitrosohemoglobin-mediated nitric oxide release from red blood cells: a preliminary study

Yao, B., Liu, D., Chai, W., Wang, X.-T., & Zhang, H. (2019) · Intensive Care Medicine Experimental · doi:10.1186/s40635-018-0215-0 · Cited by 11

Detection of N‐nitrosomelatonin and other N‐nitrosotryptophan derivatives by transnitrosation of APF and DAF‐2

Kirsch, M., & de GROOT, H. (2005) · Journal of Pineal Research · doi:10.1111/j.1600-079x.2005.00277.x · Cited by 11

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

Screening systems for the identification of S-nitrosylated proteins

Uehara, T., & Nishiya, T. (2010) · Nitric Oxide · doi:10.1016/j.niox.2010.11.002 · Cited by 10

Oxygen-Linked S-Nitrosation in Fish Myoglobins: A Cysteine-Specific Tertiary Allosteric Effect

Helbo, S., Gow, A. J., Jamil, A., Howes, B. D., Smulevich, G., & Fago, A. (2014) · PLoS ONE · doi:10.1371/journal.pone.0097012 · Cited by 10

Adverse Drug Reactions in the Intensive Care Unit

Moore, P. W., & Burkhart, K. (2017) · Springer eBooks · doi:10.1007/978-3-319-17900-1_33 · Cited by 10

Rapid remote conditioning mediates modulation of blood cell paracrine activity and leads to the production of a secretome with neuroprotective features

Bonová, P., Jachova, J., Némethová, M., Macakova, L., Bona, M., & Gottlieb, M. (2019) · Journal of Neurochemistry · doi:10.1111/jnc.14889 · Cited by 10

Superoxide determines nitric oxide uptake rate by vascular smooth muscle cells

Huang, K., Yin, C., Wu, J.-H., & Huang, H.-H. (2005) · FEBS Letters · doi:10.1016/j.febslet.2005.06.071 · Cited by 10

Reply to "NO adducts in mammalian red blood cells: too much or too little?"

Stamler, J. S., Hess, D. T., & Singel, D. J. (2003) · Nature Medicine · doi:10.1038/nm0503-482 · Cited by 10

Haemoglobin Saturation Controls The Red Blood Cell Mediated Hypoxic Vasorelaxation

Pinder, A. G., Rogers, S. C., Morris, K., & James, P. E. (2008) · Advances in experimental medicine and biology · doi:10.1007/978-0-387-85998-9_3 · Cited by 9

Influence of erythrocyte oxygenation and intravascular ATP on resting and exercising skeletal muscle blood flow in humans with mitochondrial myopathy

Jeppesen, T. D., Vissing, J., & González‐Alonso, J. (2011) · Mitochondrion · doi:10.1016/j.mito.2011.11.003 · Cited by 9

The SLC4 Anion Exchanger Gene Family

Stewart, A. K., & Alper, S. L. (2012) · Elsevier eBooks · doi:10.1016/b978-0-12-381462-3.00054-9 · Cited by 9

Controlling the Direction of S-Nitrosation versus Denitrosation: Reversible Cleavage and Formation of an S–N Bond within a Dicopper Center

Tao, W., Yerbulekova, A., Moore, C. E., Shafaat, H. S., & Zhang, S. (2022) · Journal of the American Chemical Society · doi:10.1021/jacs.1c12799 · Cited by 9

Is It Go or NO Go for S-Nitrosylation Modification-Based Therapies of Cystic Fibrosis Transmembrane Regulator Trafficking?

Zeitlin, P. L. (2006) · Molecular Pharmacology · doi:10.1124/mol.106.029207 · Cited by 9

α‐cardiac actin (ACTC) binds to the band 3 (AE1) cardiac isoform

Lima, P. R. M., Salles, T. S. I., Costa, F. F., & Saad, S. T. O. (2003) · Journal of Cellular Biochemistry · doi:10.1002/jcb.10561 · Cited by 9

S-nitrosohemoglobin is distinguished from other nitrosovasodilators by unique oxygen-dependent responses that support an allosteric mechanism of action

McMahon, T., Pawloski, J. R., Hess, D. T., Piantadosi, C. A., Luchsinger, B. P., Singel, D. J., & Stamler, J. S. (2003) · Blood · doi:10.1182/blood-2003-04-1058 · Cited by 9

Drugs Highly Associated with Infusion Reactions Reported using Two Different Data-mining Methodologies

Burkhart, P. W. M. K. K. (2014) · Journal of Blood Disorders & Transfusion · doi:10.4172/2155-9864.1000195 · Cited by 8

Deciphering Subtype-Selective Modulations in TRPA1 Biosensor Channels

Kozai, D., Sakaguchi, R., Ohwada, T., & Mori, Y. (2015) · Current Neuropharmacology · doi:10.2174/1570159x1302150525122020 · Cited by 8

A Comparative ESR Study on Blood and Tissue Nitric Oxide Concentration during Renal Ischemia-Reperfusion Injury

Ren, J., Fung, P. C. W., Chang, C., Shen, G., Lu, G., Chan, F. H. Y., Liu, K. J., & Shen, J. (2007) · Applied Magnetic Resonance · doi:10.1007/s00723-007-0024-1 · Cited by 8

Optimized S-nitrosohemoglobin Synthesis in Red Blood Cells to Preserve Hypoxic Vasodilation Via β Cys93

Hausladen, A., Qian, Z., Zhang, R., Premont, R. T., & Stamler, J. S. (2022) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.122.001194 · Cited by 7

Whole genome sequencing of the fast-swimming Southern bluefin tuna (Thunnus maccoyii)

Zhao, X., Huang, Y., Bian, C., You, X.-X., Zhang, X.-H., Chen, J.-M., Wang, M., Hu, C., Xu, Y.-L., Xu, J.-M., et al. (2022) · Frontiers in Genetics · doi:10.3389/fgene.2022.1020017 · Cited by 8

Hemoglobin S-nitrosation on oxygenation of nitrite/deoxyhemoglobin incubations is attenuated by methemoglobin

Laterreur, J., & English, A. M. (2007) · Journal of Inorganic Biochemistry · doi:10.1016/j.jinorgbio.2007.07.021 · Cited by 7

S‐Nitrosohemoglobin Levels and Patient Outcome After Transfusion During Pediatric Bypass Surgery

Matto, F., Kouretas, P. C., Smith, R., Ostrowsky, J., Cina, A. J., Hess, D. T., Stamler, J. S., & Reynolds, J. D. H. (2017) · Clinical and Translational Science · doi:10.1111/cts.12530 · Cited by 7

Nitric Oxide Damage to Colonocytes in Colitis-by-Association: Remote Transfer of Nitric Oxide to the Colon

Roediger, W. E. W. (2002) · Digestion · doi:10.1159/000063819 · Cited by 7

Regulation of Respiration and Endothelial Gene Expression by S-Nitrosothiols in Health and Disease

Palmer, L. A. (2006) · Proceedings of the American Thoracic Society · doi:10.1513/pats.200506-063bg · Cited by 7

Shear Stress and RBC-NOS Serine1177 Phosphorylation in Humans: A Dose Response

Horobin, J. T., Sabapathy, S., Kuck, L., & Simmonds, M. J. (2021) · Life · doi:10.3390/life11010036 · Cited by 6

Intravenous whole blood transfusion results in faster recovery of vascular integrity and increased survival in experimental cerebral malaria

Gul, S., Ackerman, H. C., Daniel‐Ribeiro, C. T., & Carvalho, L. J. M. (2022) · Memórias do Instituto Oswaldo Cruz · doi:10.1590/0074-02760220184 · Cited by 6

New Methods to Evaluate Endothelial Function: Evaluation of Endothelial Function by Hemoglobin-Nitric Oxide Complex Using Electron Paramagnetic Resonance Spectroscopy

Tsuchiya, K., Kirima, K., Yoshizumi, M., & Tamaki, T. (2003) · Journal of Pharmacological Sciences · doi:10.1254/jphs.93.417 · Cited by 6

Multiple Active Site Conformers in the Carbon Monoxide Complexes of Trematode Hemoglobins

Das, T. K., Dewilde, S., Friedman, J. M., Moens, L. J., & Rousseau, D. L. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m512054200 · Cited by 6

Oxygen

Lumb, A. B. (2016) · Elsevier eBooks · doi:10.1016/b978-0-7020-6294-0.00010-1 · Cited by 6

Comodulation of NO-Dependent Vasodilation by Erythroid Band 3 and Hemoglobin: A GP.Mur Athlete Study

Hsu, K., Liu, Y., Tseng, W., Huang, K., Liu, C., Chen, L., Lee, H.-L., Lin, H., Tseng, K., & Yeh, H. (2021) · Frontiers in Cardiovascular Medicine · doi:10.3389/fcvm.2021.740100 · Cited by 6

Systemic Disorders

Maxwell, L. G., Goodwin, S. R., Mancuso, T. J., Baum, V. C., Zuckerberg, A. L., Morgan, P. G., Motoyama, E. K., Davis, P. J., & Sullivan, K. (2011) · Elsevier eBooks · doi:10.1016/b978-0-323-06612-9.00036-5 · Cited by 6

Oxygen Delivery by Allosteric Effectors of Hemoglobin, Blood Substitutes, and Plasma Expanders

Campanini, B., Bruno, S., Raboni, S., & Mozzarelli, A. (2003) · Wiley eBooks · doi:10.1002/0471266949.bmc048 · Cited by 6

Transnitrosation Signals Oxyhemoglobin Desaturation

Marozkina, N. V., Gaston, B. M., & Doctor, A. (2008) · Circulation Research · doi:10.1161/circresaha.108.183442 · Cited by 6

The Risks of Blood Transfusion in Patients with Subarachnoid Hemorrhage

Marik, P. E. (2011) · Neurocritical Care · doi:10.1007/s12028-011-9654-0 · Cited by 6

Prevalence and Awareness of Hypertension in Seven Distinct Geographic Regions of Turkey: The SEMT HT Study

Bayram, F., Demir, Ö., Sabuncu, T., Eren, M. A., GEDİK, A. V., Çorapçıoğlu, D., & Kaya, A. (2021) · Endocrinology research and practice. · doi:10.25179/tjem.2020-78532 · Cited by 5

The role of blood nitrite in the control of hypoxic vasodilation

Fago, A., & Jensen, F. B. (2007) · Advances in experimental biology · doi:10.1016/s1872-2423(07)01009-5 · Cited by 5

Heme Protein Metabolism of NO and Nitrite

Kim‐Shapiro, D. B., & Gladwin, M. T. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-804273-1.00006-5 · Cited by 5

NOS, NO, and the Red Cell

Cortese-Krott, M. M., Kramer, C. M., & Kelm, M. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-804273-1.00014-4 · Cited by 5

Can endothelial hemoglobin-α regulate nitric oxide vasodilatory signaling?

Parikh, J., Kapela, A., & Tsoukias, N. M. (2017) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00315.2016 · Cited by 5

How Do Red Blood Cells Dilate Blood Vessels?

Allen, B. W., & Piantadosi, C. A. (2004) · Circulation Research · doi:10.1161/res.94.12.e105 · Cited by 5

S-Nitrosylation: Mechanistic Links between Nitric Oxide Signaling and Atherosclerosis

Xu, W., Chen, D., & Zhou, H. (2025) · Current Atherosclerosis Reports · doi:10.1007/s11883-025-01321-y · Cited by 4

Nitric oxide production and blood corpuscle dynamics in response to the endocrine status of female rats

Uematsu, K., Katayama, T., Katayama, H., 平塚, 美., Kiyomura, M., & Ito, M. (2010) · Thrombosis Research · doi:10.1016/j.thromres.2010.09.013 · Cited by 4

Influence of hemoglobin on blood pressure among people with GP.Mur blood type☆

Chen, Y., Hsu, K.-N., Lai, J. C., Chen, L., Kuo, M., Liao, C., & Hsu, K. (2022) · Journal of the Formosan Medical Association · doi:10.1016/j.jfma.2021.12.014 · Cited by 4

Extrapulmonary Effects of Inhaled Nitric Oxide

McMahon, T., & Doctor, A. (2012) · Proceedings of the American Thoracic Society · Cited by 4

Article Myoglobin: a pseudo‐enzymatic scavenger of nitric oxide

Ascenzi, P., & Brunori, M. (2001) · Biochemistry and Molecular Biology Education · doi:10.1111/j.1539-3429.2001.tb00116.x · Cited by 13

L-arginine erythrocyte transport increases during pregnancy and immediately postpartum

Galão, A. O., da Costa, B. E. P., d'Avila, D. O. L., & Poli‐de‐Figueiredo, C. E. (2004) · American Journal of Obstetrics and Gynecology · doi:10.1016/j.ajog.2004.01.008 · Cited by 4

Oxygen Delivery via Allosteric Effectors of Hemoglobin and Blood Substitutes

Bruno, S., Ronda, L., Faggiano, S., Bettati, S., & Mozzarelli, A. (2010) · Wiley eBooks · doi:10.1002/0471266949.bmc048.pub2 · Cited by 4

Intra‐carotid body inter‐cellular communication

Argent, L. P., Bose, A., & Paton, J. F. R. (2022) · Journal of the Royal Society of New Zealand · doi:10.1080/03036758.2022.2079681 · Cited by 3

Nitric Oxide and Hemoglobin: Physiological Implications

Shen, X., Kaye, A. D., Cornett, E. M., & Kevil, C. G. (2022) · Springer eBooks · doi:10.1007/978-3-030-95975-3_9 · Cited by 3

Physiology of Nitric Oxide in the Developing Lung

Kinsella, J. P., & Shaul, P. W. (2004) · Elsevier eBooks · doi:10.1016/b978-0-7216-9654-6.50073-4 · Cited by 3

S‐Nitroso‐ l ‐cysteine and ventilatory drive: A pediatric perspective

Hubbard, D., Tutrow, K. D., & Gaston, B. M. (2022) · Pediatric Pulmonology · doi:10.1002/ppul.26036 · Cited by 2

Ozone therapy: underestimated opportunities in the treatment of large joint diseases

Torgashin, A. N., Rodionova, S. S., & Torgashina, A. V. (2019) · Modern Rheumatology Journal · doi:10.14412/1996-7012-2019-3-126-129 · Cited by 3

The SLC4 Anion Exchanger Gene Family

Stewart, A. K., Kurschat, C. E., & Alper, S. L. (2008) · Elsevier eBooks · doi:10.1016/b978-012088488-9.50056-5 · Cited by 3

Crosstalk between Nitric Oxide and Bioinorganic Centers: Implications for Cellular Signaling

Oszajca, M., Polaczek, J., Rutkowska‐Zbik, D., Gurgul, I., Mazuryk, O., & Stochel, G. (2025) · The Chemical Record · doi:10.1002/tcr.202500128 · Cited by 2

Disrupted erythrocyte S1P-eNOS axis promotes hypoxia, hypertension and fibrosis in obstructive sleep apnoea-hypopnoea syndrome

Fan, Y., Chen, C., Luo, C., Zhou, S., Lu, H., Yu, F., He, Z., Wang, Y., Chou, Y., Li, Y., et al. (2026) · European Heart Journal · doi:10.1093/eurheartj/ehag405 · Cited by 2

L-Arginine-Dependent Nitric Oxide Production in the Blood of Patients with Type 2 Diabetes: A Pilot, Five-Year Prospective Study

Stoian, I. A.-M., Iosif, L., Gîlcă, M., Vlad, A., Tivig, I. C., Bradescu, O. M., & Savu, O. (2024) · Life · doi:10.3390/life14050556 · Cited by 2

Nitric Oxide Ameliorates the Effects of Hypoxia in Mice by Regulating Oxygen Transport by Hemoglobin

Zhou, X., Su, W.-T., Bao, Q., Cui, Y., Li, X.-X., Yang, Y.-D., Yang, C., Wang, C.-Y., Jiao, L., Chen, D.-W., et al. (2024) · High Altitude Medicine & Biology · doi:10.1089/ham.2023.0044 · Cited by 3

The hunt for transnitrosylase

Chakraborty, S., Choudhuri, A., Mishra, A., & Sengupta, R. (2024) · Nitric Oxide · doi:10.1016/j.niox.2024.09.004 · Cited by 2

Increased Anion Exchanger-1 (Band 3) on the Red Blood Cell Membrane Accelerates Scavenging of Nitric Oxide Metabolites and Predisposes Hypertension Risks

Chen, L., Chen, P.-L., Jiang, S., Lee, H.-L., Liu, Y., Chueh, A., Lin, J.-H., Chen, C. G., Hung, C., & Hsu, K. (2024) · Function · doi:10.1093/function/zqae052 · Cited by 2

Divergent roles of endothelial and red blood cell nitric oxide synthase in regulating cardiovascular function during anemia

Yogathasan, V., Wischmann, P., Solga, I., Jäger, L., Becher, S., Cortese-Krott, M. M., Gerdes, N., Kelm, M., Jung, C., & Chennupati, R. (2025) · Nitric Oxide · doi:10.1016/j.niox.2025.08.004 · Cited by 2

NO, SNO and low O2

Mato, J. M., Avila, M. A., & Corrales, F. J. (2001) · Nature Medicine · doi:10.1038/nm1001-1107 · Cited by 2

Regulation and Function of Protein S-Nitrosylation in Plant Stress

Kuruthukulangarakoola, G. T., & Lindermayr, C. (2013) · Springer eBooks · doi:10.1007/978-1-4614-6372-6_7 · Cited by 2

Adverse Drug Reactions in the ICU

Moore, P. W., & Burkhart, K. (2016) · Springer eBooks · doi:10.1007/978-3-319-20790-2_33-1 · Cited by 2

Biochemistry and detection of S-nitrosothiols

Möller, M. N., & Denicola, A. (2022) · Elsevier eBooks · doi:10.1016/b978-0-323-90219-9.00022-4 · Cited by 2

Mechanisms of Physiological and Neurotoxic Action of Hyperbaric Oxygen

It, D., Zhilyaev, S. Y., Платонова, Т. Ф., & Alekseeva, O. S. (2022) · Journal of Evolutionary Biochemistry and Physiology · doi:10.1134/s0022093022050246 · Cited by 2

Towards the crux of sex-dependent variability in red cell concentrates

William, N., Osmani, R., & Acker, J. P. (2023) · Transfusion and Apheresis Science · doi:10.1016/j.transci.2023.103827 · Cited by 2

Electrochemical assay of human haemoglobin S-nitrosylation by nitrosocysteine

Palmerini, C. A., Palombari, R., & Arienti, G. (2003) · Amino Acids · doi:10.1007/s00726-002-0355-z · Cited by 2

Biochemistry of Storage of Red Blood Cells

Stapley, R. D., Vitturi, D. A., & Patel, R. P. (2011) · Wiley eBooks · doi:10.1002/9781119975427.ch17 · Cited by 2

Functions of Blood Group Antigens

Stamler, J. S., & Telen, M. J. (2010) · doi:10.1002/9781444318531.ch22 · Cited by 2

The ventilatory response to hypoxia

Gozal, D., Gaston, B. M., Lipton, A. S., Johnson, M. A., Macdonald, T. L., & Lieberman, M. W. (2002) · Nature · doi:10.1038/419686b · Cited by 2

Assessment of the nitrosylation process

Borderie, D., & Ekindjian, O. G. (2008) · Current Opinion in Clinical Nutrition & Metabolic Care · doi:10.1097/mco.0b013e328309ec50 · Cited by 3

A Thousand Times NO

Bishopric, N. H. (2002) · Journal of Molecular and Cellular Cardiology · doi:10.1006/jmcc.2002.2009 · Cited by 2

Nitric Oxide and the Heme Oxygenase/Carbon Monoxide System

Foresti, R., Green, C. J., & Motterlini, R. (2001) · CRC Press eBooks · doi:10.1201/9781420041019.ch6 · Cited by 2

ERYTHROCYTES

Ingley, E., & Klinken, S. P. (2006) · Elsevier eBooks · doi:10.1016/b0-12-370879-6/00141-1 · Cited by 2

Hydrogen Sulfide, Reactive Nitrogen Species, and “The Joy of the Experimental Play*”

Cortese-Krott, M. M. (2022) · Wiley eBooks · doi:10.1002/9781119799900.ch4 · Cited by 2

SIRPα extracellular domain shed from neutrophils by ADAM10 aggravates sepsis via initiating nitric oxide release from erythrocyte

Liang, H., Lu, G., Bian, Z., Qu, S., Shi, L., Wang, J., Zen, K., & Liu, Y. (2025) · Journal of Advanced Research · doi:10.1016/j.jare.2025.08.019 · Cited by 1

Blood Oxygen Transport and Prooxidant-Antioxidant Balance in Rats under Hypothermia and Rewarming Combined with a Modification of L-arginine-NO Pathway

Зинчук, В. В., & Hlutkin, S. V. (2015) · Asian Journal of Pharmacy Nursing and Medical Sciences · doi:10.24203/ajpnms.v3i2.2253.g1388 · Cited by 1

Transport and Peripheral Bioactivities of Nitrogen Oxides Carried by Red Blood Cell Hemoglobin: Role in Oxygen Delivery

Sonveaux, P., Lobysheva, I. I., Féron, O., & McMahon, T. J. (2007) · Physiology · doi:10.1152/physiol.00042.2006 · Cited by 71

Hypoxic Vasodilation by Red Blood Cells and Impairment in Vascular Disorders.

Pawloski, J. R., McMahon, T., Ahearne, G., Piantadosi, C. A., Singel, D. J., & Stamler, J. S. (2004) · Blood · doi:10.1182/blood.v104.11.1585.1585 · Cited by 2

Hemoglobin β93 Cysteine Is Not Required for Export of Nitric Oxide Bioactivity From the Red Blood Cell

Sun, C., Yang, J., Kleschyov, A. L., Zhuge, Z., Carlström, M., Pernow, J., Wajih, N., Isbell, T. S., Oh, J., Cabrales, P., et al. (2019) · Circulation · doi:10.1161/circulationaha.118.039284 · Cited by 47

S-nitrosohaemoglobin: a dynamic activity of blood involved in vascular control

Jia, L., Bonaventura, C., Bonaventura, J., & Stamler, J. S. (1996) · Nature · doi:10.1038/380221a0 · Cited by 1,592

Hemoglobin as a chariot for NO bioactivity

Lane, P. B., & Gross, S. S. (2002) · Nature Medicine · doi:10.1038/nm0702-657 · Cited by 39