Bibliographies thématiques / Soluble guanylyl cyclase stimulator

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Littérature scientifique sur le sujet « Soluble guanylyl cyclase stimulator »

Auteur : Grafiati
Publié le 2 juin 2025
Mis à jour le 31 juillet 2025

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Articles de revues sur le sujet "Soluble guanylyl cyclase stimulator"

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Zuo, Zhiyi, and Roger A. Johns. "Halothane, Enflurane, and Isoflurane Do Not Affect the Basal or Agonist-stimulated Activity of Partially Isolated Soluble and Particulate Guanylyl Cyclases of Rat Brain." Anesthesiology 83, no. 2 (1995): 395–404. http://dx.doi.org/10.1097/00000542-199508000-00020.

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Background Evidence suggests that inhalational anesthetics interact with the nitric oxide-guanylyl cyclase signaling pathway in the central nervous system and that the inhibitation of this pathway in brain may result in an anesthetic, analgesic, or sedative effect. The mechanism of the effects inhalational anesthetics on this signaling pathway is not clear. This study attempted to determine whether inhalational anesthetics directly affect soluble or particulate guanylyl cyclase activity in a partially isolated enzyme system. Methods The effects of halothane (0.44-4.4%), enflurane (1.34-6.7%),
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Grześk, Grzegorz, Adrianna Witczyńska, Magdalena Węglarz, et al. "Soluble Guanylyl Cyclase Activators—Promising Therapeutic Option in the Pharmacotherapy of Heart Failure and Pulmonary Hypertension." Molecules 28, no. 2 (2023): 861. http://dx.doi.org/10.3390/molecules28020861.

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Endogenous nitric oxide (NO)-dependent vascular relaxation plays a leading role in the homeostasis of the cardiovascular, pulmonary, and vascular systems and organs, such as the kidneys, brain, and liver. The mechanism of the intracellular action of NO in blood vessels involves the stimulation of the activity of the soluble cytosolic form of guanylyl cyclase (soluble guanylyl cyclase, sGC), increasing the level of cyclic 3′-5′—guanosine monophosphate (cGMP) in smooth muscle and subsequent vasodilation. In recent years, a new group of drugs, soluble guanylyl cyclase stimulators, has found its w
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Krizhanovsky, Valery, Orly Agamy, and Michael Naim. "Sucrose-stimulated subsecond transient increase in cGMP level in rat intact circumvallate taste bud cells." American Journal of Physiology-Cell Physiology 279, no. 1 (2000): C120—C125. http://dx.doi.org/10.1152/ajpcell.2000.279.1.c120.

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Initial sweet taste transduction is expected to occur in the subsecond time range. We demonstrate a rapid and transient (75–250 ms) increase of cGMP (but not cAMP) level in rat intact circumvallate taste cells after stimulation by sucrose. This rapid increase does not occur in nonsensory epithelial cells. Pretreatment with a nonspecific phosphodiesterase (PDE) inhibitor (IBMX), a specific cAMP-PDE4 inhibitor (denbufylline), or an adenylyl cyclase activator (forskolin) all increased basal cAMP and abolished the sucrose-stimulated cGMP increase at 150 ms. Pretreatment with a soluble guanylyl cyc
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Johns, Roger A., Alexandra Tichotsky, Michael Muro, James P. Spaeth, Timothy D. Le Cras, and Appavoo Rengasamy. "Halothane and Isoflurane Inhibit Endothelium-derived Relaxing Factor-dependent Cyclic Guanosine Monophosphate Accumulation in Endothelial Cell-Vascular Smooth Muscle Co-cultures Independent of an Effect on Guanylyl Cyclase Activation." Anesthesiology 83, no. 4 (1995): 823–34. http://dx.doi.org/10.1097/00000542-199510000-00023.

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Background Interaction of inhalational anesthetics with the nitric oxide signaling pathway and the mechanism of such effects are controversial. The aim of this study was to clarify the sites and mechanism of inhalational anesthetic interaction with the vascular nitric oxide and guanylyl cyclase signaling pathway. Methods To specifically study the mechanism of anesthetic interaction with the nitric oxide-guanylyl cyclase pathway, cultured vascular smooth muscle and endothelial cell-vascular smooth muscle (EC-VSM) co-culture models were chosen. Monolayer cultures of VSM with or without cultured
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Liu, Zhenguo, Kanji Nakatsu, James F. Brien, E. Danielle Beaton, Gerald S. Marks, and Donald H. Maurice. "Selective sequestration of nitric oxide by subcellular components of vascular smooth muscle and platelets: relationship to nitric oxide stimulation of the soluble guanylyl cyclase." Canadian Journal of Physiology and Pharmacology 71, no. 12 (1993): 938–45. http://dx.doi.org/10.1139/y93-142.

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Sequestration of nitric oxide (NO) by subcellular fractions isolated from bovine pulmonary arterial medial layer (BPA) and rabbit platelets (RP) was studied utilizing a novel chemiluminescence – headspace gas technique. Sequestration in all fractions was similarly rapid (5 min) and remained constant for at least 30 min. When incubated with 108 pmol of NO, the BPA mitochondrial, microsomal, and nuclear fractions sequestered 22.8 ± 1.9, 20.5 ± 2.2 and 15.2 ± 3.6% of the NO, respectively (n = 14). However, significantly more of the 108 pmol of NO, 36.8 ± 2.8 and 32.9 ± 3.6%, respectively, was seq
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Mace, Eric H., Melissa J. Kimlinger, Frederic T. Billings, and Marcos G. Lopez. "Targeting Soluble Guanylyl Cyclase during Ischemia and Reperfusion." Cells 12, no. 14 (2023): 1903. http://dx.doi.org/10.3390/cells12141903.

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Ischemia and reperfusion (IR) damage organs and contribute to many disease states. Few effective treatments exist that attenuate IR injury. The augmentation of nitric oxide (NO) signaling remains a promising therapeutic target for IR injury. NO binds to soluble guanylyl cyclase (sGC) to regulate vasodilation, maintain endothelial barrier integrity, and modulate inflammation through the production of cyclic-GMP in vascular smooth muscle. Pharmacologic sGC stimulators and activators have recently been developed. In preclinical studies, sGC stimulators, which augment the reduced form of sGC, and
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Hempel, A., T. Noll, A. Muhs, and H. M. Piper. "Functional antagonism between cAMP and cGMP on permeability of coronary endothelial monolayers." American Journal of Physiology-Heart and Circulatory Physiology 270, no. 4 (1996): H1264—H1271. http://dx.doi.org/10.1152/ajpheart.1996.270.4.h1264.

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The role of the intracellular second messengers guanosine 3', 5'-cyclic monophosphate (cGMP) and adenosine 3', 5'-cyclic monophosphate (cAMP) in the control of macromolecule permeability was studied in cultured monolayers of microvascular coronary endothelial cells from rat. Macromolecule permeability was determined as passage of fluorescein isothiocyanate (FITC)-labeled albumin across the monolayers. Activation of adenylyl cyclase by the beta-adrenoceptor agonist isoproterenol (Iso; 10(-5) M) and the A2-adenosine receptor agonist 5'-(N-ethylcarboxamido)-adenosine (NECA; 10(-7) M) induced an i
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Veltman, Douwe M., Jeroen Roelofs, Ruchira Engel, Antonie J. W. G. Visser, and Peter J. M. Van Haastert. "Activation of Soluble Guanylyl Cyclase at the Leading Edge during Dictyostelium Chemotaxis." Molecular Biology of the Cell 16, no. 2 (2005): 976–83. http://dx.doi.org/10.1091/mbc.e04-08-0701.

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Dictyostelium contains two guanylyl cyclases, GCA, a 12-transmembrane enzyme, and sGC, a homologue of mammalian soluble adenylyl cyclase. sGC provides nearly all chemoattractant-stimulated cGMP formation and is essential for efficient chemotaxis toward cAMP. We show that in resting cells the major fraction of the sGC-GFP fusion protein localizes to the cytosol, and a small fraction is associated to the cell cortex. With the artificial substrate Mn2+/GTP, sGC activity and protein exhibit a similar distribution between soluble and particulate fraction of cell lysates. However, with the physiolog
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Ben Aissa, Manel, Alycia F. Tipton, Zachariah Bertels, et al. "Soluble guanylyl cyclase is a critical regulator of migraine-associated pain." Cephalalgia 38, no. 8 (2017): 1471–84. http://dx.doi.org/10.1177/0333102417737778.

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Background Nitric oxide (NO) has been heavily implicated in migraine. Nitroglycerin is a prototypic NO-donor, and triggers migraine in humans. However, nitroglycerin also induces oxidative/nitrosative stress and is a source of peroxynitrite – factors previously linked with migraine etiology. Soluble guanylyl cyclase (sGC) is the high affinity NO receptor in the body, and the aim of this study was to identify the precise role of sGC in acute and chronic migraine. Methods We developed a novel brain-bioavailable sGC stimulator (VL-102), and tested its hyperalgesic properties in mice. We also dete
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Piggott, Leslie A., Kathryn A. Hassell, Zuzana Berkova, Andrew P. Morris, Michael Silberbach, and Thomas C. Rich. "Natriuretic Peptides and Nitric Oxide Stimulate cGMP Synthesis in Different Cellular Compartments." Journal of General Physiology 128, no. 1 (2006): 3–14. http://dx.doi.org/10.1085/jgp.200509403.

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Cyclic nucleotide-gated (CNG) channels are a family of ion channels activated by the binding of cyclic nucleotides. Endogenous channels have been used to measure cyclic nucleotide signals in photoreceptor outer segments and olfactory cilia for decades. Here we have investigated the subcellular localization of cGMP signals by monitoring CNG channel activity in response to agonists that activate either particulate or soluble guanylyl cyclase. CNG channels were heterologously expressed in either human embryonic kidney (HEK)-293 cells that stably overexpress a particulate guanylyl cyclase (HEK-NPR
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Thèses sur le sujet "Soluble guanylyl cyclase stimulator"

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Wales, Jessica A., Cheng-Yu Chen, Linda Breci, et al. "Discovery of stimulator binding to a conserved pocket in the heme domain of soluble guanylyl cyclase." AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC, 2018. http://hdl.handle.net/10150/627055.

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Soluble guanylyl cyclase (sGC) is the receptor for nitric oxide and a highly sought-after therapeutic target for the management of cardiovascular diseases. New compounds that stimulate sGC show clinical promise, but where these stimulator compounds bind and how they function remains unknown. Here, using a photolyzable diazirine derivative of a novel stimulator compound, IWP-051, and MS analysis, we localized drug binding to the 1 heme domain of sGC proteins from the hawkmoth Manduca sexta and from human. Covalent attachments to the stimulator were also identified in bacterial homologs of the s
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Nedvetsky, Pavel I. "Regulation of the nitric oxide receptor, soluble guanylyl cyclase." Doctoral thesis, [S.l. : s.n.], 2003. http://deposit.ddb.de/cgi-bin/dokserv?idn=969682026.

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Delago, Antonia. "Functional analysis of soluble guanylyl cyclase expression in insects." Thesis, Queen Mary, University of London, 2004. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.407766.

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MA, Xiaolei. "Structural Studies of Soluble Guanylyl Cyclase and Its Bacterial Homologs." Case Western Reserve University School of Graduate Studies / OhioLINK, 2008. http://rave.ohiolink.edu/etdc/view?acc_num=case1208379599.

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Ogley, Scott Carson. "Structure and Function of Manduca Sexta Soluble Guanylyl Cyclase PASα Domain". Thesis, The University of Arizona, 2011. http://hdl.handle.net/10150/144916.

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Fritz, Bradley. "MOLECULAR MODEL OF SOLUBLE GUANYLYL CYCLASE: INSIGHT INTO ALLOSTERY IN NITRIC OXIDE SIGNALING." Diss., The University of Arizona, 2011. http://hdl.handle.net/10150/205214.

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Soluble guanylyl cyclase (sGC), the nitric oxide (NO) receptor, is a 150 kDa heterodimeric multi-domain protein that contains heme in the β subunit. Binding of NO to heme leads to rupture of the proximal histidine bond, increased catalytic conversion of GTP to cGMP at a distant guanylyl cyclase catalytic domain, and vasodilation through cGMP signaling. The structure of sGC has not been determined, and little is known about the mechanism by which NO binding to heme leads to increased catalysis. The small molecule YC-1 is known to stimulate sGC activity, but the exact YC-1 binding site and mecha
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Purohit, Rahul. "The Mechanism of Allosteric Regulation in Soluble Guanylate Cyclase." Diss., The University of Arizona, 2014. http://hdl.handle.net/10150/333219.

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Nitric oxide (NO), a reactive diatomic gas and a potent signaling molecule, is required for proper cardiovascular functioning. Soluble guanylate cyclase (sGC), a heterodimeric heme protein, is the key intracellular NO receptor protein which, upon NO binding, undergoes conformational changes leading to catalysis and the cGMP signaling cascade. Several small molecules that allosterically stimulate sGC have been developed for treatment of pulmonary hypertension, but little is known about their binding site or how they stimulate activity. This dissertation describes experiments designed to uncover
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Chia, Karin Kim Mae. "Soluble guanylyl cyclase modulates redox-dependent regulation of the cardiac sodium potassium pump." Thesis, The University of Sydney, 2013. http://hdl.handle.net/2123/9464.

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Modulation of redox-dependent regulation of the Na+-K+ pump is a potential therapeutic strategy in heart failure. This Thesis examined if stimulation of soluble guanylyl cyclase (sGC) can modulate oxidative signalling to the Na+-K+ pump in rabbit cardiomyocytes and the mechanisms by which this may occur. sGC stimulation with 3-(5’-hydroxymethyl-2’-furyl)-1-benzylindazole (YC-1) attenuated the Angiotensin (Ang) II-induced 1) inhibition of the electrogenic Na+-K+ pump current (Ip), 2) O2•-sensitive fluorescence, 3) serine phosphorylation of p47phox (necessary for NADPH oxidase activation) and
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Yamamoto, Takehiro, Yuki Moriya, Norio Suzuki та Chikako Morinaga. "Identification of tandem organization of soluble guanylyl cyclase α_1 and β_1 subunit genes in the Japanese pufferfish (Fugu rubripes) genome: comparison with their human homologues". Laboratory of Freshwater Fish Stocks Bioscience and Biotechnology Center Nagoya University, 2007. http://hdl.handle.net/2237/13831.

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Gao, Shuai. "The Pro-Survival Functions of Soluble Guanylyl Cyclase Alpha-1 (sGCa1) and Zinc Finger Protein 280B (ZNF280B) in Prostate Cancer." University of Toledo / OhioLINK, 2013. http://rave.ohiolink.edu/etdc/view?acc_num=toledo1373307941.

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Chapitres de livres sur le sujet "Soluble guanylyl cyclase stimulator"

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Koesling, D., and A. Friebe. "Enzymology of Soluble Guanylyl Cyclase." In Nitric Oxide. Springer Berlin Heidelberg, 2000. http://dx.doi.org/10.1007/978-3-642-57077-3_5.

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Koesling, Doris, and Ari Sitaramayya. "Soluble Guanylyl Cyclase: The Nitric Oxide Receptor." In Signal Transduction: Pathways, Mechanisms and Diseases. Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-642-02112-1_18.

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Bellamy, Tomas C., and John Garthwaite. "The receptor-like properties of Nitric oxide-activated soluble guanylyl cyclase in intact cells." In Guanylate Cyclase. Springer US, 2002. http://dx.doi.org/10.1007/978-1-4615-0927-1_15.

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Pino, María Teresa, and Jimena Paula Cabilla. "Soluble Guanylyl Cyclase Alpha1 Subunit as a Biomarker of Toxicity: Applications to Investigate Endocrine-Disrupting Chemicals." In Biomarkers in Toxicology. Springer International Publishing, 2023. http://dx.doi.org/10.1007/978-3-031-07392-2_1.

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Pino, María Teresa, and Jimena Paula Cabilla. "Soluble Guanylyl Cyclase Alpha1 Subunit as a Biomarker of Toxicity: Applications to Investigate Endocrine-Disrupting Chemicals." In Biomarkers in Toxicology. Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-030-87225-0_1-1.

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Follmann, Markus, Corina Becker, Lothar Roessig, Peter Sandner, and Johannes-Peter Stasch. "CASE HISTORY: DISCOVERY AND DEVELOPMENT OF VERQUVO® (VERICIGUAT), A SOLUBLE GUANYLATE CYCLASE (SGC) STIMULATOR FOR THE TREATMENT OF CHRONIC HEART FAILURE." In Medicinal Chemistry Reviews. MEDI, Inc. Published by American Chemical Society., 2023. http://dx.doi.org/10.1021/mc-2023-vol58.ch21.

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Hancock, John T. "Cyclic nucleotides, cyclases and G proteins." In Cell Signalling. Oxford University Press, 2016. http://dx.doi.org/10.1093/hesc/9780199658480.003.0007.

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This chapter demonstrates the alteration of a class of molecules called cyclic nucleotides. Cyclic nucleotides, in particular cAMP and cGMP, are central signalling molecules in many transduction pathways. The chapter emphasizes that alteration of the concentration of other molecules is one of the most common ways for the signal to be propagated in a cell. It then explores the mechanisms involved in control of the cyclic nucleotides production. The chapter also investigates how cAMP is produced from ATP by enzymes known as adenylyl cyclases. It defines adenylyl cyclase as a single polypeptide i
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Friebe, Andreas, and Doris Koesling. "Guanylyl Cyclase, Soluble." In xPharm: The Comprehensive Pharmacology Reference. Elsevier, 2007. http://dx.doi.org/10.1016/b978-008055232-3.60607-5.

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Waldman, Scott A., Dale C. Leitman, and Ferid Murad. "[36] Immunoaffinity purification of soluble guanylyl cyclase." In Methods in Enzymology. Elsevier, 1991. http://dx.doi.org/10.1016/0076-6879(91)95185-m.

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Martin, Emil, Vladimir Berka, Ah‐Lim Tsai, and Ferid Murad. "Soluble Guanylyl Cyclase: The Nitric Oxide Receptor." In Methods in Enzymology. Elsevier, 2005. http://dx.doi.org/10.1016/s0076-6879(05)96040-0.

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Actes de conférences sur le sujet "Soluble guanylyl cyclase stimulator"

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Egemnazarov, Bakytbek, Varazik Amirjanians, Baktybek Kojonazarov, et al. "Inhalative Application Of Soluble Guanylyl Cyclase Stimulator BAY 41-8543 For Treatement Of Pulmonary Arterial Hypertension." In American Thoracic Society 2010 International Conference, May 14-19, 2010 • New Orleans. American Thoracic Society, 2010. http://dx.doi.org/10.1164/ajrccm-conference.2010.181.1_meetingabstracts.a6307.

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Roos, B., J. J. Teske, J. Ravix, C. M. Pabelick, R. D. Britt, and Y. S. Prakash. "Targeting Soluble Guanylyl Cyclase Dysfunction in Hyperoxia-Exposed Developing Airways." In American Thoracic Society 2020 International Conference, May 15-20, 2020 - Philadelphia, PA. American Thoracic Society, 2020. http://dx.doi.org/10.1164/ajrccm-conference.2020.201.1_meetingabstracts.a1238.

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Kollau, Alexander, Michael Russwurm, Doris Koesling, Astrid Schrammel, and Bernd Mayer. "Natural compounds from cured tobacco are reversible inhibitors of soluble guanylyl cyclase." In cGMP: Generators, Effectors and Therapeutic Implications. ScienceOpen, 2024. http://dx.doi.org/10.14293/cgmp.000010.v1.

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Kollau, Alexander, Michael Russwurm, Doris Koesling, Astrid Schrammel, and Bernd Mayer. "Natural compounds from cured tobacco are reversible inhibitors of soluble guanylyl cyclase." In cGMP: Generators, Effectors and Therapeutic Implications. ScienceOpen, 2024. http://dx.doi.org/10.14293/cgmp.24000065.v1.

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Kovaleva, V. D., and A. B. Uzdensky. "Soluble guanylyl cyclase is involved in PDT-induced injury of crayfish glial cells." In Saratov Fall Meeting 2015, edited by Elina A. Genina, Valery V. Tuchin, Vladimir L. Derbov, et al. SPIE, 2016. http://dx.doi.org/10.1117/12.2229826.

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Gandy, A., J. Ravix, R. D. Britt, et al. "Hyperoxia-Induced Soluble Guanylyl Cyclase (sGC) Dysfunction in Developing Airway Causes Remodeling and Fibrosis." In American Thoracic Society 2020 International Conference, May 15-20, 2020 - Philadelphia, PA. American Thoracic Society, 2020. http://dx.doi.org/10.1164/ajrccm-conference.2020.201.1_meetingabstracts.a4408.

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Anidi, Ifeanyi U., Laura E. Servinsky, Otgonchimeg Rentsendorj, Jeremy Gao, Alan L. Scott, and David B. Pearse. "Lung Endothelial Barrier Dysfunction In Murine Malaria: Role Of CD36 And Soluble Guanylyl Cyclase (sGC)." In American Thoracic Society 2011 International Conference, May 13-18, 2011 • Denver Colorado. American Thoracic Society, 2011. http://dx.doi.org/10.1164/ajrccm-conference.2011.183.1_meetingabstracts.a3755.

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Ravix, J., R. D. Britt, A. M. Roesler, et al. "Hyperoxia-Induced Soluble Guanylyl Cyclase (sGC) Dysfunction in Developing Airway Involves the Calcium Sensing Receptor (CaSR)." In American Thoracic Society 2019 International Conference, May 17-22, 2019 - Dallas, TX. American Thoracic Society, 2019. http://dx.doi.org/10.1164/ajrccm-conference.2019.199.1_meetingabstracts.a2180.

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Seimetz, Michael, Nirmal Parajuli, Alexandra Pichl, et al. "Prevention Of Cigarette Smoke-Induced Pulmonary Hypertension By The Soluble Guanylate Cyclase Stimulator Riociguat." In American Thoracic Society 2012 International Conference, May 18-23, 2012 • San Francisco, California. American Thoracic Society, 2012. http://dx.doi.org/10.1164/ajrccm-conference.2012.185.1_meetingabstracts.a3416.

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Antunes, Edson, and Priscila Kakuda. "Soluble Guanylyl Cyclase Expression (sGC) in Platelets in Experimental Sepsis: Effect of the sGC Activator BAY 60-2770." In XXIII Congresso de Iniciação Científica da Unicamp. Galoá, 2015. http://dx.doi.org/10.19146/pibic-2015-37741.

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