Literatura académica sobre el tema "Fura-2"
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Artículos de revistas sobre el tema "Fura-2"
Tran, N. N. P., P. Leroy, L. Bellucci, A. Robert, A. Nicolas, J. Atkinson y C. Capdeville-Atkinson. "Intracellular concentrations of Fura-2 and Fura-2/AM in vascular smooth muscle cells following perfusion loading of Fura-2/AM". Pharmacological Research 31 (enero de 1995): 206. http://dx.doi.org/10.1016/1043-6618(95)87082-2.
Texto completoHurley, T. W., M. P. Ryan y R. W. Brinck. "Changes of cytosolic Ca2+ interfere with measurements of cytosolic Mg2+ using mag-fura-2". American Journal of Physiology-Cell Physiology 263, n.º 2 (1 de agosto de 1992): C300—C307. http://dx.doi.org/10.1152/ajpcell.1992.263.2.c300.
Texto completoKass, G. E., D. L. Webb, S. C. Chow, J. Llopis y P. O. Berggren. "Receptor-mediated Mn2+ influx in rat hepatocytes: comparison of cells loaded with Fura-2 ester and cells microinjected with Fura-2 salt". Biochemical Journal 302, n.º 1 (15 de agosto de 1994): 5–9. http://dx.doi.org/10.1042/bj3020005.
Texto completoOwen, C. S. "Spectra of intracellular Fura-2". Cell Calcium 12, n.º 6 (junio de 1991): 385–93. http://dx.doi.org/10.1016/0143-4160(91)90064-l.
Texto completoBecker, P. L. y F. S. Fay. "Photobleaching of fura-2 and its effect on determination of calcium concentrations". American Journal of Physiology-Cell Physiology 253, n.º 4 (1 de octubre de 1987): C613—C618. http://dx.doi.org/10.1152/ajpcell.1987.253.4.c613.
Texto completoJensen, P. E., M. J. Mulvany, C. Aalkjaer, H. Nilsson y H. Yamaguchi. "Free cytosolic Ca2+ measured with Ca(2+)-selective electrodes and fura 2 in rat mesenteric resistance arteries". American Journal of Physiology-Heart and Circulatory Physiology 265, n.º 2 (1 de agosto de 1993): H741—H746. http://dx.doi.org/10.1152/ajpheart.1993.265.2.h741.
Texto completoScaduto, Russell C. y Lee W. Grotyohann. "Hydrolysis of Ca2+-sensitive fluorescent probes by perfused rat heart". American Journal of Physiology-Heart and Circulatory Physiology 285, n.º 5 (noviembre de 2003): H2118—H2124. http://dx.doi.org/10.1152/ajpheart.00881.2001.
Texto completoCarroll, S. L., M. G. Klein y M. F. Schneider. "Calcium transients in intact rat skeletal muscle fibers in agarose gel". American Journal of Physiology-Cell Physiology 269, n.º 1 (1 de julio de 1995): C28—C34. http://dx.doi.org/10.1152/ajpcell.1995.269.1.c28.
Texto completoSteinberg, S. F., J. P. Bilezikian y Q. Al-Awqati. "Fura-2 fluorescence is localized to mitochondria in endothelial cells". American Journal of Physiology-Cell Physiology 253, n.º 5 (1 de noviembre de 1987): C744—C747. http://dx.doi.org/10.1152/ajpcell.1987.253.5.c744.
Texto completoTram, N. N. P., P. Leroy, L. Bellucci, A. Robert, A. Nicolas, J. Atkinson y C. Capdeville-Atkinson. "Intracellular concentrations of Fura-2 and Fura-2/AM in vascular smooth muscle cells following perfusion loading of Fura-2/AM in arterial segments". Cell Calcium 18, n.º 5 (noviembre de 1995): 420–28. http://dx.doi.org/10.1016/0143-4160(95)90057-8.
Texto completoTesis sobre el tema "Fura-2"
Silva, Orivaldo Lopes da. "Incorporação de cálcio iônico em células ósseas induzida por campo elétrico". Universidade de São Paulo, 1995. http://www.teses.usp.br/teses/disponiveis/76/76132/tde-10062014-163725/.
Texto completoEndogenous electrical signals have been thought to affect bone remodeling, metabolism, healing and growth. Much literature exists concerning the effect of external electrical signals on synthetic, mitogenic, and proliferative responses of osteoblasts or osteoblast-like cells in vitro. Physiological responses to electrical stimulation are thought to be due to cellular mechanisms involving cytosolic calcium concentration changes. In this study this cellular effect was observed by directly stimulating primary culture bone cells from Sprague-Dawley rat calvaria at physiological significant field strength of 10 mV/cm and frequency 1,5 MHz. Electric field transduction mechanisms are investigated by measuring the real-time electric field effect on cytosolic Ca+2 concentrations using Fura-2 fluorescence technology in a system capable of measurement on a cell-by-cell basis. The electrical stimulations resulted in significant changes in cytosolic calcium concentration. More specifically, an increase was noted in calcium oscillation amplitude and duration, and a variable response latency period for the cells studied.
Hadrovic, Banina. "A study of TRPV1 and TRPV4 ion channels in the beta cells by using fura-2 based microfluorometry". Thesis, Mälardalen University, School of Sustainable Development of Society and Technology, 2009. http://urn.kb.se/resolve?urn=urn:nbn:se:mdh:diva-7350.
Texto completoThe calcium ion (Ca2+) is an important ion that regulates many cellular functions including exocytosis, contraction of muscles, neural functions, fertilization and cell division. In the plasma membrane of cells there are different Ca2+ channels, including the transient receptor potential (TRP) family of cation channels. The TRP channels are activated by physical stimuli like temperature, stretch, osmolality, and also various ligands. These channels are divided into seven subfamilies, namely TRPC, TRPV, TRPM, TRPML, TRPA, TRPP, and TRPN.
TRP channels can regulate the cytoplasmic free Ca2+ concentration ([Ca2+]i) and are therefore important for research of insulin secretion from beta (β) cells. With TRP research new and more effective treatment methods for people with diabetes can be developed. People with type 2 diabetes have a decreased insulin secretion from beta (β) cells, in response to glucose. Cytoplasmic free Ca2+ concentration ([Ca2+]i) is important for insulin secretion. It is therefore desirable to find compounds that can increase [Ca2+]i in pancreatic β cells and thereby increase insulin secretion.
The aim of this project was to investigate whether pancreatic β cells express TRPV1 and TRPV4 ion channels. If the channels are expressed in β cells the [Ca2+]i can be increased by identifying substances that stimulate TRPV1 and TRPV4 channels. The results can then be used for providing better treatment for patients with diabetes type 2. Insulinoma cells from rat (S5 cells) were used as a model for β cells. [Ca2+]i was measured from single fura-2 loaded S5 cells by ratiometric microfluorometry. To test whether TRPV1 is expressed,
N-(4-hydroxyphenyl)-Arachidonoylamide (AM404) and [5-hydroxyl-1-(4-hydroxy-3-methoxyphenyl)decan-3-one] ([6]-gingerol) were used. To test whether TRPV4 was expressed, a TRPV4-selective agonist 4alpha-Phorbol 12,13-Didecanoate namely 4α–PDD was used.
The two agonist of TRPV1, AM404 and [6]-gingerol increased [Ca2+]i . Capsaicin a classical activator of TRPV1 used as a control also increased [Ca2+]i . These increases were inhibited by capsazepine, a specific blocker of TRPV1. 4α–PDD, a specific agonist of TRPV4 also increased [Ca2+]i. These results suggest that S5 cells express both TRPV1 and TRPV4 channels and that AM404, [6]-gingerol and 4α–PDD are potential substances for increasing the insulin secretion from β cells.
Kalciumjonen (Ca2+) är en viktig jon och förmedlar signaler i processer som cellutsöndring, muskelkontraktion, nervfunktion, fertilisering och celldelning. I cellers plasmamembran finns det olika sorters Ca2+ -kanaler, inklusive transient receptor potential (TRP) jonkanalerna. TRP kanalerna aktiveras av fysisk stimulans, så som temperatur, utsträckning, osmolalitet men också av olika ligander. TRP kanalerna är indelade i sju underfamiljer, TRPC, TRPV, TRPM, TRPML, TRPA, TRPP,och TRPN.
TRP kanalerna reglerar den fria Ca2+ koncentrationen ([Ca2+]i) i cytoplasman och är därmed viktiga för forskning inom insulinutsöndringen från beta (β) celler. Med denna forskning kan nya och effektivare behandlingsmetoder för personer med diabetes utvecklas. Personer med typ 2 diabetes har bl.a. en minskad insulinfrisättning i beta (β) celler som orsakar en glukosökning i blodet. Den fria Ca2+ -koncentrationen ([Ca2+]i) i cytoplasman är viktig för insulinfrisättningen. Det är därför önskvärt att hitta kemiska föreningar som kan bidra till en ökning av [Ca2+]i i bukspottkörtelns β celler och därmed också ge en ökad insulinfrisättning.
Målet med detta projekt har varit att undersöka om β celler från bukspottkörtel uttrycker jonkanalerna TRPV1 och TRPV4. Om β celler uttrycker dessa kanaler kan [Ca2+]i i cytoplasman ökas genom att identifiera substanser som stimulerar just TRPV1 och TRPV4 kanaler. Resultaten kan användas för att bidra med bättre behandling till diabetespatienter med typ 2 diabetes. Tumoriserade celler från råtta (S5) användes som modell för β celler. [Ca2+]i mättes från enskilda fura-2 laddade S5 celler med hjälp av ett ratiometriskt mikrofluorometriskt system. För att undersöka om TRPV1 finns testades ämnena N-(4-hydroxyphenyl)-Arachidonoylamide (AM404) och [5-hydroxyl-1-(4-hydroxy-3-methoxyphenyl)decan-3-one] ([6]-gingerol). För att undersöka om TRPV4 finns användes det TRPV4-specifika ämnet (4alpha-Phorbol 12,13-Didecanoate)
4α–PDD.
De båda TRPV1 agonisterna AM404 och [6]-gingerol inducerade en ökning i [Ca2+]i. Capsaicin som är en klassisk TRPV1 agonist ökade också [Ca2+]i och användes som kontroll. Alla dessa koncentrationsökningar inhiberades av capsazepine, som är en TRPV1- antagonist. 4α–PDD som är en specifik TRPV4 agonist ökade också [Ca2+]i.
Resultaten tyder på att S5 cellerna uttrycker både TRPV1 och TRPV4 kanaler samt att AM404, [6]-gingerol och 4α–PDD är alla substanser med potential att öka insulinfrisättningen från bukspottkörtelns β celler.
Beurg, Maryline. "Couplage excitation-contraction des cellules musculaires striées : étude des variations transitoires de calcium par imagerie de fura-2". Bordeaux 1, 1995. http://www.theses.fr/1995BOR10530.
Texto completoLascombe, Marie-Laure. "Le couplage excitation-contraction dans les cellules musculaires striées normales et dysgéniques : étude par imagerie de fluorescence de fura-2". Bordeaux 1, 1992. http://www.theses.fr/1992BOR10519.
Texto completoCastro, Kraftchenko Joel y kraf0005@flinders edu au. "STORE OPERATED Ca2+ CHANNELS IN LIVER CELLS: REGULATION BY BILE ACIDS AND A SUB-REGION OF THE ENDOPLASMIC RETICULUM". Flinders University. Medicine, 2008. http://catalogue.flinders.edu.au./local/adt/public/adt-SFU20080826.135311.
Texto completoScanlon, Mary. "Cellular mechanism of neutrophil chemotaxis: the role of CA+2, as viewed with the fluorescent dye, FURA-2, in the polarization of human polymorphonuclear leukocytes following stimulation with the chemoattractant, F-Methionyl-Leucyl-Phenylalanine: a thesis". eScholarship@UMMS, 1987. https://escholarship.umassmed.edu/gsbs_diss/320.
Texto completoWesterlund, Johanna. "Pulsatile insulin release from single islets of Langerhans". Doctoral thesis, Uppsala University, Department of Medical Cell Biology, 2000. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-494.
Texto completoInsulin release from single islets of Langerhans is pulsatile. The secretory activities of the islets in the pancreas are coordinated resulting in plasma insulin oscillations. Nutrients amplitude-regulate the insulin pulses without influencing their frequency. Diabetic patients show an abnormal plasma insulin pattern, but the cause of the disturbance remains to be elucidated. Ithe present thesis the influence of the cytoplasmic calcium concentratio([Ca2+]i) and cell metabolism on pulsatile insulin release was examined in single islets of Langerhans from ob/ob-mice. Glucose stimulation of insulin release involves closure of ATP-sensitive K+ channels (KATP channels), depolarization, and Ca2+ influx in β-cells. In the presence of 11 mM glucose, pulsatile insulin secretion occurs in synchrony with oscillations i[Ca2+]i. When [Ca2+]i is low and stable, e.g. under basal conditions, low amplitude insulin pulses are still observed. When [Ca2+]i is elevated and non-oscillating, e.g. when the β-cells are depolarized by potassium, high amplitude insulin pulses are observed. The frequency of the insulin pulses under these conditions is similar to that observed when [Ca2+]i oscillations are present. By permanently opening or closing the KATP channels with diazoxide or tolbutamide, respectively, it was investigated if glucose can modulate pulsatile insulin secretion when it does not influence the channel activity. Under these conditions, [Ca2+]i remained stable whereas the amplitude of the insulin pulses increased with sugar stimulation without change in the frequency. Metabolic inhibition blunted but did not prevent the insulin pulses. The results indicate that oscillations in metabolism can generate pulsatile insulin release when [Ca2+]i is stable. However, under physiological conditions, pulsatile secretion is driven by oscillations in metabolism and [Ca2+]i, acting in synergy.
Egunlusi, Ayodeji Olatunde. "Novel tricycloundecane derivatives as potential N-methyl-Daspartate receptor and calcium channel inhibitors for neuroprotection". Thesis, University of the Western Cape, 2014. http://hdl.handle.net/11394/3904.
Texto completoThis study focused on the synthesis of a series of novel tricycloundecane derivatives and evaluation of these compounds for neuroprotection using the fluorescent ratiometric calcium assay that indicates the ability of the test compounds to inhibit NMDA receptors and VGCC. The cycloaddition reaction between p-benzoquinone and monomerised dicyclopentadiene yielded tricycloundeca- 4,9-diene-3,6-dione which was used as the base structure and further derivatised. These derivatives were conjugated with benzylamine to form a series of imines and amines. A total of 10 compounds were synthesised for evaluation of inhibition of calcium influx through NMDA receptor channels and voltage-gated calcium channels. The structures were confirmed using NMR, IR and MS. On the proton NMR, the characteristic AB-quartet system was observed in the region of 1-2 ppm for all the compounds and the aromatic moiety was observed between 6.5-7.5 ppm for the novel polycyclic amines. These, with other functional groups, were used to confirm the individual structures
Liu, Li. "Roles of PMCA Isoforms in Ca2+-Homeostasis and Contractility of Bladder Smooth Muscle: Evidence from PMCA Gene-Ablated Mice". Cincinnati, Ohio : University of Cincinnati, 2007. http://rave.ohiolink.edu/etdc/view.cgi?acc_num=ucin1178307168.
Texto completoAdvisor: Richard J. Paul. Title from electronic thesis title page (viewed Apr. 4, 2009). Keywords: PMCA (human gene symbols; ATP2B); SERCA2 (human gene symbols; ATP2A2); NCX; bladder smooth muscle; Ca²⁺ homeostasis; gene-altered mice. Ca²⁺ waves; Ca²⁺ sparks; Fura-PE3; Fluo-4; Indo-1; multi-photon microscopy. Includes abstract. Includes bibliographical references.
Ahmed, Meftun. "Oscillatory Ca2+ signaling in glucose-stimulated murine pancreatic β-cells : Modulation by amino acids, glucagon, caffeine and ryanodine". Doctoral thesis, Uppsala University, Department of Medical Cell Biology, 2001. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-1408.
Texto completoOscillations in cytoplasmic Ca2+ concentration ([Ca2+]i) is the key signal in glucose-stimulated β-cells governing pulsatile insulin release. The glucose response of mouse β-cells is often manifested as slow oscillations and rapid transients of [Ca2+] i. In the present study, microfluorometric technique was used to evaluate the role of amino acids, glucagon, ryanodine and caffeine on the generation and maintenance of [Ca2+] i oscillations and transients in individual murine β-cells and isolated mouse pancreatic islets. The amino acids glycine, alanine and arginine, at around their physiological concentrations, transformed the glucose-induced slow oscillations of [Ca2+] i in isolated mouse β-cells into sustained elevation. Increased Ca2+ entry promoted the reappearance of the slow [Ca2+] i oscillations. The [Ca2+] i oscillations were more resistant to amino acid transformation in intact islets, supporting the idea that cellular interactions are important for maintaining the oscillatory activity. Individual rat β-cells responded to glucose stimulation with slow [Ca2+] i oscillations due to periodic entry of Ca2+ as well as with transients evoked by mobilization of intracellular stores. The [Ca2+] i oscillations in rat β-cells had a slightly lower frequency than those in mouse β-cells and were more easily transformed into sustained elevation in the presence of glucagon or caffeine. The transients of [Ca2+] i were more common in rat than in mouse β-cells and often appeared in synchrony also in cells lacking physical contact. Depolarization enhanced the generation of [Ca2+] i transients. In accordance with the idea that β-cells have functionally active ryanodine receptors, it was found that ryanodine sometimes restored oscillatory activity abolished by caffeine. However, the IP3 receptors are the major Ca2+ release channels both in β-cells from rats and mice. Single β-cells from ob/ob mice did not differ from those of lean controls with regard to frequency, amplitudes and half-widths of the slow [Ca2+] i oscillations. Nevertheless, there was an excessive firing of [Ca2+] i transients in the β-cells from the ob/ob mice, which was suppressed by leptin at close to physiological concentrations. The enhanced firing of [Ca2+] i transients in ob/ob mouse β-cells may be due to the absence of leptin and mediated by activation of the phospholipase C signaling pathway.
Libros sobre el tema "Fura-2"
Furī na 2-ri. Tōkyō: Sonī Magajinzu, 2006.
Buscar texto completoSpells of fury: Building Windows 95 games using DirectX 2. Corte Madera, CA: Waite Group Press, 1996.
Buscar texto completoNara-ken Tenri-shi Furu iseki Jōmon jidai sōki no chōsa: 1984 12--1985 2 chōsa. [Tenri-shi]: Maizō Bunkazai Tenrikyō Chōsadan, 1988.
Buscar texto completoOperation Urgent Fury: The planning and execution of joint operations in Grenada, 12 October-2 November 1983. Washington, DC: Joint History Office, Office of the Chairman of the Joint Chiefs of Staff, 1997.
Buscar texto completoPerry, Philip J. Synthesis and biological evaluation of novel cytotoxic heterocyclic compounds: Furo (2,3-b) naphthoquinones and 2-aryl-4H-3,1-benzoxazin-4-ones. Leicester: De Montfort University, 1996.
Buscar texto completoMoore, URS Dames &. Inventory of dioxin and furan emissions to air, land and water in Ireland for 2000 and 2010 (2000-DS-2-M1): Synthesis report. Johnstown Castle, Co. Wexford: Environmental Protection Agency, 2002.
Buscar texto completoMarkaz Dirāsāt al-Khalīj wa-al-Jazīrah al-ʻArabīyah, ed. Nadwat Duwal Majlis al-Taʻāwun al-Khalījī wa-Juhūd Taḥqīq al-Amn wa-al-Istiqrār khilāla al-ʻAqd al-Qādim, al-Furaṣ wa-al-Quyūd: 1-2 Māyū 2001, al-Kuwayt. [Kuwait]: Markaz Dirāsāt al-Khalīj wa-al-Jazīrah al-ʻArabīyah, Jāmiʻat al-Kuwayt, 2001.
Buscar texto completoSuzuki, Hidetaku. Jugyō-zukuri o chūshin ni kamaeta kyōdō kenkyū no soshikika: Kyōshoku daigakuin de mananda koto o furu ni ikashi, kenkyū kadai "manabiyasui kankyō no sōzō, yorokobi ga kanjirareru jugyō o mezashite" no moto kenkyū o susumeta, kenkyū shunin to shite no 2-nenkan o furikaette. Fukui-shi: Fukui Daigaku Daigakuin Kyōikugaku Kenkyūka Kyōshoku Kaihatsu Senkō, 2009.
Buscar texto completoArnold, J. Douglas y Zach Meston. Awesome Sega Genesis Secrets 3. Lahaina, HI: Sandwich Islands Publishing, 1993.
Buscar texto completoPrima. Official Sega Genesis: Power Tips Book, Volume 3. Rocklin, CA: Prima Publishing, 1994.
Buscar texto completoCapítulos de libros sobre el tema "Fura-2"
Grouselle, M. y D. Georgescauld. "Fura-2 Imaging of Intracellular Free Calcium Dynamics in Excitable Cells". En Water and Ions in Biomolecular Systems, 229–40. Basel: Birkhäuser Basel, 1990. http://dx.doi.org/10.1007/978-3-0348-7253-9_23.
Texto completoPatel, Anish, Robert A. Hirst, Charlotte Harrison, Kazuyoshi Hirota y David G. Lambert. "Measurement of [Ca2+]i in Whole Cell Suspensions Using Fura-2". En Methods in Molecular Biology, 37–47. Totowa, NJ: Humana Press, 2012. http://dx.doi.org/10.1007/978-1-62703-086-1_2.
Texto completoXu, Yan-Jun, Qiming Shao y Naranjan S. Dhalla. "Fura-2 fluorescent technique for the assessment of Ca2+ homeostasis in cardiomyocytes". En Novel Methods in Molecular and Cellular Biochemistry of Muscle, 149–57. Boston, MA: Springer US, 1997. http://dx.doi.org/10.1007/978-1-4615-6353-2_16.
Texto completoSmith, Stephen J., Luis R. Osses y George J. Augustine. "Fura-2 Imaging of Localized Calcium Accumulation Within Squid ‘Giant’ Presynaptic Terminal". En Calcium and Ion Channel Modulation, 147–55. Boston, MA: Springer US, 1988. http://dx.doi.org/10.1007/978-1-4613-0975-8_12.
Texto completoJohnson, Martin. "Calcium Imaging of Store-Operated Calcium (Ca2+) Entry (SOCE) in HEK293 Cells Using Fura-2". En Calcium Signalling, 163–72. New York, NY: Springer New York, 2019. http://dx.doi.org/10.1007/978-1-4939-9018-4_15.
Texto completoWiltink, Anneke, Arnoud van der Laarse, Nel P. M. Herrmann-Erlee, Joke M. van der Meer y Dirk L. Ypey. "The Use of the Fluorescent Probe Fura-2 For Intracellular Free Calcium Measurements: Some Methodological Aspects". En Biotechnology Applications of Microinjection, Microscopic Imaging, and Fluorescence, 133–42. Boston, MA: Springer US, 1993. http://dx.doi.org/10.1007/978-1-4615-2828-9_16.
Texto completoHayes, Brendan A., P. V. Avdonin y U. S. Ryan. "MAG-FURA-2 Elicited Fluorescent Response of Subcellular Magnesium in Endothelial Cells: A Sharp Contrast with Calcium". En Vascular Endothelium, 256–57. Boston, MA: Springer US, 1991. http://dx.doi.org/10.1007/978-1-4615-3736-6_35.
Texto completoDe Nadai, Andrea, Nicola Vajente, Diana Pendin y Andrea Mattarei. "Mt-fura-2, a Ratiometric Mitochondria-Targeted Ca2+ Sensor. Determination of Spectroscopic Properties and Ca2+ Imaging Assays". En Methods in Molecular Biology, 187–215. New York, NY: Springer US, 2021. http://dx.doi.org/10.1007/978-1-0716-1262-0_12.
Texto completoHayashi, H., N. Noda, H. Miyata, S. Suzuki, A. Kobayashi, M. Hirano, T. Kawai, T. Hayashi y N. Yamazaki. "Changes in Cell Morphology, [Ca2+]i and pHi During Metabolic Inhibition in Isolated Myocytes of Diabetic Rats Using Dual-Loading of Fura-2 and BCECF". En Developments in Cardiovascular Medicine, 183–98. Boston, MA: Springer US, 1992. http://dx.doi.org/10.1007/978-1-4615-3512-6_18.
Texto completoWinkelmann, J. "Diffusion of air (1); 2-methyl-furan (2)". En Gases in Gases, Liquids and their Mixtures, 1816. Berlin, Heidelberg: Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-49718-9_1374.
Texto completoActas de conferencias sobre el tema "Fura-2"
Poll, C. T. y J. Westwick. "THE ROLE OF IONISED INTRACELLULAR FREE CALCIUM ([Ca++]i) IN THROMBIN-INDUCED DENSE GRANULE SECRETION". En XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644475.
Texto completoKoyama, M., F. Katabami, K. Matsuno, H. Matsumiya, K. Abe, K. Sakurada, S. Ozasa, I. Maekawa y T. Miyazaki. "THROMBIN-INDUCED BIPHASIC Ca2+TRANSIENT DETECTED BY FURA-2 FLUORESCENCE WAS COUPLED WITH BIPHASIC Ca2+ UPTAKE IN PLATELETS". En XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644476.
Texto completoLanza, F., A. Beretz, M. Kubina y J.-P. Cazenave. "INCREASED AGGREGATION AND SECRETION RESPONSES OF HUMAN PLATELETS WHEN LOADED WITH THE CALCIUM FLUORESCENT PROBES QUIN2 AND FURA-2". En XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643760.
Texto completoVan den Bergh, Viviane, Katrien Meuwis, Noel Boens, Frans C. De Schryver, Michel Vincent, Jacques Gallay y Marcel Ameloot. "Photophysical study of the Ca2+ indicator Fura-2 and the K+ indicator PBFI". En OE/LASE '94, editado por Joseph R. Lakowicz. SPIE, 1994. http://dx.doi.org/10.1117/12.182705.
Texto completoRao, Gundu H. R. y James G. White. "INFLUENCE OF CALCIUM FLUX ON STABILITY OF PLATELET MICROTUBULE COILS". En XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643904.
Texto completoWatts, I. S., R. J. Keery y P. Lumlev. "EFFECT OF EXTRACELLULAR Ca2+ UPON AGONIST-INDUCED Ca2+ TRANSIENTS IN HUMAN PLATELETS: COMPARISON OF QUIN 2 AND FURA 2". En XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644525.
Texto completoAswani, Kavita. "LED illumination for fluorescence from Fura-2 to Cy7.5 and beyond: A true lamp replacement". En Light-Emitting Devices, Materials, and Applications XXV, editado por Martin Strassburg, Jong Kyu Kim y Michael R. Krames. SPIE, 2021. http://dx.doi.org/10.1117/12.2576651.
Texto completoMatsuno, K., F. Katabami, M. Koyama, K. Abe, K. Sakurada, T. Miyazaki, S. Ozasa, H. Saitoh, I. Maekawa y H. Matsumiya. "PLATELET-ACTIVATING FACTOR (PAF)-INDUCED INTRACELLULAR Ca MOBILIZATION IN HUMAN PLATELETS." En XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643483.
Texto completoLascombe, M. L., M. Grouselle, J. P. Desmazès, D. Georgescauld, J. Koenig y J. Chapron. "FURA-2 imaging of intracellular free Ca2+ dynamics and distribution induced by acetylcholine and caffeine in embryonic skeletal muscle cells". En The living cell in four dimensions. AIP, 1991. http://dx.doi.org/10.1063/1.40602.
Texto completoOraevsky, Alexander A., Olga A. Cabello, Qin Shan, Frank K. Tittel y Philip D. Henry. "Detection of calcium activity in human monocytes by the fura-2 fluorescence method: in vitro differentiation sensitizes cells to dihydropyridine calcium channel modulators". En OE/LASE '94, editado por George S. Abela. SPIE, 1994. http://dx.doi.org/10.1117/12.179909.
Texto completoInformes sobre el tema "Fura-2"
Philosoph-Hadas, Sonia, Richard Crain, Shimon Meir, Nehemia Aharoni y Susan Lurie. Calcium-Mediated Signal Transduction during Leaf Senescence. United States Department of Agriculture, noviembre de 1995. http://dx.doi.org/10.32747/1995.7604925.bard.
Texto completoRouseff, Russell L. y Michael Naim. Characterization of Unidentified Potent Flavor Changes during Processing and Storage of Orange and Grapefruit Juices. United States Department of Agriculture, septiembre de 2002. http://dx.doi.org/10.32747/2002.7585191.bard.
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