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Cited by in CrossRef
For: Munaron L. Shuffling the cards in signal transduction: Calcium, arachidonic acid and mechanosensitivity. World J Biol Chem 2011; 2(4): 59-66 [PMID: 21537474 DOI: 10.4331/wjbc.v2.i4.59]
URL: https://www.wjgnet.com/1949-8454/full/v2/i4/59.htm
Number Citing Articles
1
C. Jansen, L. M.N. Shimoda, J. Starkus, I. Lange, N. Rysavy, K. Maaetoft-Udsen, C. Tobita, A.J. Stokes, H Turner. In vitroexposure toHymenopteravenom and constituents activates discrete ionotropic pathways in mast cellsChannels 2019; 13(1): 264 doi: 10.1080/19336950.2019.1629225
2
Roberto Berra-Romani, Pawan Faris, Sharon Negri, Laura Botta, Tullio Genova, Francesco Moccia. Arachidonic Acid Evokes an Increase in Intracellular Ca2+ Concentration and Nitric Oxide Production in Endothelial Cells from Human Brain MicrocirculationCells 2019; 8(7): 689 doi: 10.3390/cells8070689
3
Takatoshi Uchida, Shota Shimizu, Reiko Yamagishi, Suzumi M. Tokuoka, Yoshihiro Kita, Rei Sakata, Megumi Honjo, Makoto Aihara, Alexander G Obukhov. TRPV4 is activated by mechanical stimulation to induce prostaglandins release in trabecular meshwork, lowering intraocular pressurePLOS ONE 2021; 16(10): e0258911 doi: 10.1371/journal.pone.0258911
4
Cherubino Di Lorenzo, Gianluca Coppola, Valeria La Salvia, Francesco Pierelli. Nasal decongestant and chronic headache: a case of naphazoline overuse headache?F1000Research 2013; 2: 237 doi: 10.12688/f1000research.2-237.v1
5
Skopec* Robert. Naphazoline nitrate treat the Frey effect of microwave and other sonic weapon’s damages in Human’s Internal, Endogenous OrgansAnnals of Biomedical Science and Engineering 2019; 3(1): 001 doi: 10.29328/journal.abse.1001004
6
Borys Kuzminov, Vira Turkina, Yuriy Кuzminov. Rationale for naphazoline effects in-depth studyCurrent Issues in Pharmacy and Medical Sciences 2018; 31(1): 29 doi: 10.1515/cipms-2018-0007
7
Takatoshi Uchida, Shota Shimizu, Reiko Yamagishi, Suzumi M. Tokuoka, Yoshihiro Kita, Megumi Honjo, Makoto Aihara. Mechanical stretch induces Ca2+ influx and extracellular release of PGE2 through Piezo1 activation in trabecular meshwork cellsScientific Reports 2021; 11(1) doi: 10.1038/s41598-021-83713-z
8
Peter W. Reeh, Michael J. M. Fischer. Nobel somatosensations and painPflügers Archiv - European Journal of Physiology 2022; 474(4): 405 doi: 10.1007/s00424-022-02667-x
9
Binnaz Leblebicioglu, John Connors, Angelo Mariotti. Principles of endocrinologyPeriodontology 2000 2013; 61(1): 54 doi: 10.1111/j.1600-0757.2011.00440.x
10
L. Munaron. Systems biology of ion channels and transporters in tumor angiogenesis: An omics viewBiochimica et Biophysica Acta (BBA) - Biomembranes 2015; 1848(10): 2647 doi: 10.1016/j.bbamem.2014.10.031
11
Xuan Luo, Valentine Seveau de Noray, Laurene Aoun, Martine Biarnes-Pelicot, Pierre-Olivier Strale, Vincent Studer, Marie-Pierre Valignat, Olivier Theodoly. Lymphocytes perform reverse adhesive haptotaxis mediated by LFA-1 integrinsJournal of Cell Science 2020; 133(16) doi: 10.1242/jcs.242883
12
Yulia Artemenko, Lucas Axiotakis, Jane Borleis, Pablo A. Iglesias, Peter N. Devreotes. Chemical and mechanical stimuli act on common signal transduction and cytoskeletal networksProceedings of the National Academy of Sciences 2016; 113(47) doi: 10.1073/pnas.1608767113
13
Estella Zuccolo, Silvia Dragoni, Valentina Poletto, Paolo Catarsi, Daniele Guido, Alessandra Rappa, Marta Reforgiato, Francesco Lodola, Dmitry Lim, Vittorio Rosti, Germano Guerra, Francesco Moccia. Arachidonic acid-evoked Ca2+ signals promote nitric oxide release and proliferation in human endothelial colony forming cellsVascular Pharmacology 2016; 87: 159 doi: 10.1016/j.vph.2016.09.005
14
Francesco Moccia. Endothelial Ca2+ Signaling and the Resistance to Anticancer Treatments: Partners in CrimeInternational Journal of Molecular Sciences 2018; 19(1): 217 doi: 10.3390/ijms19010217
15
György Csaba. Biocommunication of Ciliates2016; : 121 doi: 10.1007/978-3-319-32211-7_8
16
Sonja M. Mueller-Tribbensee, Manoj Karna, Mohammad Khalil, Markus F. Neurath, Peter W. Reeh, Matthias A. Engel, David D McKemy. Differential Contribution of TRPA1, TRPV4 and TRPM8 to Colonic Nociception in MicePLOS ONE 2015; 10(7): e0128242 doi: 10.1371/journal.pone.0128242
17
Yidan Chen, Ying Su, Feng Wang. The Piezo1 ion channel in glaucoma: a new perspective on mechanical stressHuman Cell 2022; 35(5): 1307 doi: 10.1007/s13577-022-00738-w
18
Francesco Moccia, Germano Guerra. Ca2+ Signalling in Endothelial Progenitor Cells: Friend or Foe?Journal of Cellular Physiology 2016; 231(2): 314 doi: 10.1002/jcp.25126
19
Yanxia Zhao, Qun Wang, Shi Wang, Xiaoman Liu, Jae-HyuK Yu, Weifa Zheng, Xiuguo Zhang. Disturbance in biosynthesis of arachidonic acid impairs the sexual development of the onion blight pathogen Stemphylium eturmiunumCurrent Genetics 2019; 65(3): 759 doi: 10.1007/s00294-019-00930-w
20
Pedro Martín, Melisa Moncada, Nicolás Enrique, Agustín Asuaje, Juan Manuel Valdez Capuccino, Carlos Gonzalez, Verónica Milesi. Arachidonic acid activation of BKCa (Slo1) channels associated to the β1-subunit in human vascular smooth muscle cellsPflügers Archiv - European Journal of Physiology 2014; 466(9): 1779 doi: 10.1007/s00424-013-1422-x
21
Alessandra Gilardino, Federico Catalano, Federico Alessandro Ruffinatti, Gabriele Alberto, Bernd Nilius, Susanna Antoniotti, Gianmario Martra, Davide Lovisolo. Interaction of SiO2 nanoparticles with neuronal cells: Ionic mechanisms involved in the perturbation of calcium homeostasisThe International Journal of Biochemistry & Cell Biology 2015; 66: 101 doi: 10.1016/j.biocel.2015.07.012
22
Wenning Yang, Xiaoquan Jiang, Jingtong Liu, Dongying Qi, Zhiqiang Luo, Guohua Yu, Xueyan Li, Muli Sen, Hongjiao Chen, Wei Liu, Yang Liu, Guopeng Wang. Integrated Strategy From In Vitro, In Situ, In Vivo to In Silico for Predicting Active Constituents and Exploring Molecular Mechanisms of Tongfengding Capsule for Treating Gout by Inhibiting Inflammatory ResponsesFrontiers in Pharmacology 2021; 12 doi: 10.3389/fphar.2021.759157