825 research outputs found

    Torsade de pointes caused by polypharmacy and substance abuse in a patient with human immunodeficiency virus

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    Drug-induced QT prolongation is a potentially dangerous adverse effect of some medication combinations. When QT prolongation progresses to torsade de pointes, life-threatening or fatal outcomes may result. A 57-year-old man with a history of human immunodeficiency syndrome on abacavir, nevirapine, tenofovir, voriconazole, and methadone presented to the emergency department with a chief complaint of new-onset seizures. The physical exam was unremarkable. The electrocardiogram demonstrated sinus bradycardia and a prolonged QTc interval of 690 ms. In the emergency department, he had several episodes of torsade de pointes (TdP) and ventricular tachycardia that resolved spontaneously. These episodes were accompanied by an alteration in mentation and generalized twitching. Magnesium and amiodarone were effective in terminating the dysrhythmia. The patient had multiple risk factors for prolonged QT syndrome including human immunodeficiency virus infection, methadone therapy, and polypharmacy leading to potential drug interactions. Physicians must be aware of multidrug interactions potentiating QT prolongation and leading to torsade de pointes

    Direct comparison of methionine restriction with leucine restriction on the metabolic health of C57BL/6J mice

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    EKL was the recipient of a BBSRC postgraduate studentship. This work was funded by Tenovus Scotland project grant to MD and NM (G13/07) and BBSRC DTG. MD is also supported by the British Heart Foundation (PG/09/048/27675, PG/11/8/28703 and PG/14/43/30889) and Diabetes UK (14/0004853). NM is funded by British Heart Foundation (PG/16/90/32518).Peer reviewedPublisher PD

    Different fetal-neonatal outcomes in siblings born to a mother with Graves-Basedow disease after total thyroidectomy: a case series

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    ABSTRACT:INTRODUCTION: We describe three different fetal or neonatal outcomes in the offspring of a mother who had persistent circulating thyrotropin receptor antibodies despite having undergone a total thyroidectomy several years before. CASE PRESENTATION: The three different outcomes were an intrauterine death, a mild and transient fetal and neonatal hyperthyroidism and a severe fetal and neonatal hyperthyroidism that required specific therapy. CONCLUSIONS: The three cases are interesting because of the different outcomes, the absence of a direct correlation between thyrotropin receptor antibody levels and clinical signs, and the persistence of thyrotropin receptor antibodies several years after a total thyroidectomy

    Chemical tuning for potential antitumor fluoroquinolones

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    [EN] Phototoxic effects of 6,8 dihalogenated quinolones confers to this type of molecules a potential property as photochemotherapeutic agents. Two photodehalogenation processes seem to be involved in the remarkable photoinduced cellular damage. In this context, a new 6,8 dihalogenated quinolone 1 (1-methyl-6,8-difluoro-4-oxo-7-aminodimethy1-1,4-dihydroquinoline-3-carboxylic acid) was synthesized looking for improving the phototoxic properties of fluoroquinolones (FQ) and to determine the role of the photodegradation pathways in the FQ phototoxicity. With this purpose, fluorescence emissions, laser flash photolysis experiments and photodegradation studies were performed with compound 1 using 1-ethyl-6,8-difluoro-4-oxo-7-aminodimethy1-1,4-dihidroquinoline-3-carboxylic acid (2) and lomefloxacin (LFX) as reference compounds. The shortening of alkyl chain of the N(1) of the quinolone ring revealed a lifetime increase of the reactive aryl cation generated from photolysis of the three FQ and a significant reduction of the FQ photodegradation quantum yield. The fact that these differences were smaller when the same study was done using a hydrogen donor solvent (ethanol-aqueous buffer, 50/50 v/v) evidenced the highest ability of the reactive intermediate arising from 1 to produce intermolecular alkylations. These results were correlated with in vitro 3T3 NRU phototoxicity test. Thus, when PhotoIrritation-Factor (PIF) was determined for 1, 2 and LFX using cytotoxicity profiles of BALB/c 3T3 fibroblasts treated with each compound in the presence and absence of UVA light, a PIF more higher than 30 was obtained for 1 while the values for 2 and LFX were only higher than 8 and 10, respectively. Thereby, the present study illustrates an approach to modulate the photosensitizing properties of FQ with the purpose to improve the chemotherapeutic properties of antitumor quinolones. Moreover, the results obtained in this study also evidence that the key pathway responsible for the phototoxic properties associated with dihalogenated quinolones is the aryl cation generation.Financial support from Spanish government (MINECO grant CTQ2014-54729-C2-2-P and Severo Ochoa fellowship for C. A., Carlos III Institute of Health grant PI16/01877), and the Generalitat Valenciana (PROMETEO program, 2017-075). We thank M.P. Marin of IIS La Fe Microscopy Unit for confocal microscopy.Anaya-GonzĂĄlez, C.; Soldevila Serrano, S.; GarcĂ­a-LaĂ­nez, G.; Bosca Mayans, F.; Andreu Ros, MI. (2019). Chemical tuning for potential antitumor fluoroquinolones. Free Radical Biology and Medicine. 141:150-158. https://doi.org/10.1016/j.freeradbiomed.2019.06.010S150158141Domagala, J. M., Hanna, L. D., Heifetz, C. L., Hutt, M. P., Mich, T. F., Sanchez, J. P., & Solomon, M. (1986). New structure-activity relationships of the quinolone antibacterials using the target enzyme. The development and application of a DNA gyrase assay. Journal of Medicinal Chemistry, 29(3), 394-404. doi:10.1021/jm00153a015Kang, D.-H., Kim, J.-S., Jung, M.-J., Lee, E.-S., Jahng, Y., Kwon, Y., & Na, Y. (2008). New insight for fluoroquinophenoxazine derivatives as possibly new potent topoisomerase I inhibitor. Bioorganic & Medicinal Chemistry Letters, 18(4), 1520-1524. doi:10.1016/j.bmcl.2007.12.053AzĂ©ma, J., Guidetti, B., Dewelle, J., Le Calve, B., Mijatovic, T., Korolyov, A., 
 Kiss, R. (2009). 7-((4-Substituted)piperazin-1-yl) derivatives of ciprofloxacin: Synthesis and in vitro biological evaluation as potential antitumor agents. Bioorganic & Medicinal Chemistry, 17(15), 5396-5407. doi:10.1016/j.bmc.2009.06.053Cullen, M., & Baijal, S. (2009). Prevention of febrile neutropenia: use of prophylactic antibiotics. British Journal of Cancer, 101(S1), S11-S14. doi:10.1038/sj.bjc.6605270Kim, K., Pollard, J. M., Norris, A. J., McDonald, J. T., Sun, Y., Micewicz, E., 
 McBride, W. H. (2009). High-Throughput Screening Identifies Two Classes of Antibiotics as Radioprotectors: Tetracyclines and Fluoroquinolones. Clinical Cancer Research, 15(23), 7238-7245. doi:10.1158/1078-0432.ccr-09-1964Al-Trawneh, S. A., Zahra, J. A., Kamal, M. R., El-Abadelah, M. M., Zani, F., Incerti, M., 
 Vicini, P. (2010). Synthesis and biological evaluation of tetracyclic fluoroquinolones as antibacterial and anticancer agents. Bioorganic & Medicinal Chemistry, 18(16), 5873-5884. doi:10.1016/j.bmc.2010.06.098Aldred, K. J., Schwanz, H. A., Li, G., Williamson, B. H., McPherson, S. A., Turnbough, C. L., 
 Osheroff, N. (2015). Activity of Quinolone CP-115,955 Against Bacterial and Human Type II Topoisomerases Is Mediated by Different Interactions. Biochemistry, 54(5), 1278-1286. doi:10.1021/bi501073vPommier, Y., Leo, E., Zhang, H., & Marchand, C. (2010). DNA Topoisomerases and Their Poisoning by Anticancer and Antibacterial Drugs. Chemistry & Biology, 17(5), 421-433. doi:10.1016/j.chembiol.2010.04.012Palumbo, M., Gatto, B., Zagotto, G., & PalĂč, G. (1993). On the mechanism of action of quinolone drugs. Trends in Microbiology, 1(6), 232-235. doi:10.1016/0966-842x(93)90138-hPaul, M., Gafter-Gvili, A., Fraser, A., & Leibovici, L. (2007). The anti-cancer effects of quinolone antibiotics? European Journal of Clinical Microbiology & Infectious Diseases, 26(11), 825-831. doi:10.1007/s10096-007-0375-4Perrone, C. E. (2002). Inhibition of Human Topoisomerase IIalpha by Fluoroquinolones and Ultraviolet A Irradiation. Toxicological Sciences, 69(1), 16-22. doi:10.1093/toxsci/69.1.16Lhiaubet-Vallet, V., Bosca, F., & Miranda, M. A. (2009). Photosensitized DNA Damage: The Case of Fluoroquinolones. Photochemistry and Photobiology, 85(4), 861-868. doi:10.1111/j.1751-1097.2009.00548.xMarrot, L., BelaĂŻdi, J. P., Jones, C., Perez, P., Meunier, J. R., Riou, L., & Sarasin, A. (2003). Molecular Responses to Photogenotoxic Stress Induced by the Antibiotic Lomefloxacin in Human Skin Cells: From DNA Damage to Apoptosis. Journal of Investigative Dermatology, 121(3), 596-606. doi:10.1046/j.1523-1747.2003.12422.xMeunier, J.-R., Sarasin, A., & Marrot, L. (2002). Photogenotoxicity of Mammalian Cells: A Review of the Different Assays for In Vitro Testing¶. Photochemistry and Photobiology, 75(5), 437. doi:10.1562/0031-8655(2002)0752.0.co;2Martinez, L. J., Li, G., & Chignell, C. F. (1997). Photogeneration of Fluoride by the Fluoroquinolone Antimicrobial Agents Lomefloxacin and Fleroxacin. Photochemistry and Photobiology, 65(3), 599-602. doi:10.1111/j.1751-1097.1997.tb08612.xChignell, C. F., Haseman, J. K., Sik, R. H., Tennant, R. W., & Trempus, C. S. (2003). Photocarcinogenesis in the Tg.AC Mouse: Lomefloxacin and 8-Methoxypsoralen¶†. Photochemistry and Photobiology, 77(1), 77. doi:10.1562/0031-8655(2003)0772.0.co;2Fasani, E., Profumo, A., & Albini, A. (1998). Structure and Medium-Dependent Photodecomposition of Fluoroquinolone Antibiotics. Photochemistry and Photobiology, 68(5), 666-674. doi:10.1111/j.1751-1097.1998.tb02527.xJeffrey, A. M., Shao, L., Brendler-Schwaab, S. Y., SchlĂŒter, G., & Williams, G. M. (2000). Photochemical mutagenicity of phototoxic and photochemically carcinogenic fluoroquinolones in comparison with the photostable moxifloxacin. Archives of Toxicology, 74(9), 555-559. doi:10.1007/s002040000162Spratt, T. E., Schultz, S. S., Levy, D. E., Chen, D., SchlĂŒter, G., & Williams, G. M. (1999). Different Mechanisms for the Photoinduced Production of Oxidative DNA Damage by Fluoroquinolones Differing in Photostability. Chemical Research in Toxicology, 12(9), 809-815. doi:10.1021/tx980224jReus, A. A., Usta, M., Kenny, J. D., Clements, P. J., Pruimboom-Brees, I., Aylott, M., 
 Krul, C. A. . (2012). The in vivo rat skin photomicronucleus assay: phototoxicity and photogenotoxicity evaluation of six fluoroquinolones. Mutagenesis, 27(6), 721-729. doi:10.1093/mutage/ges038Soldevila, S., & Bosca, F. (2012). Photoreactivity of Fluoroquinolones: Nature of Aryl Cations Generated in Water. Organic Letters, 14(15), 3940-3943. doi:10.1021/ol301694pCuquerella, M. C., Miranda, M. A., & BoscĂĄ, F. (2006). Generation of Detectable Singlet Aryl Cations by Photodehalogenation of Fluoroquinolones. The Journal of Physical Chemistry B, 110(13), 6441-6443. doi:10.1021/jp060634dFreccero, M., Fasani, E., Mella, M., Manet, I., Monti, S., & Albini, A. (2008). Modeling the Photochemistry of the Reference Phototoxic Drug Lomefloxacin by Steady-State and Time-Resolved Experiments, and DFT and Post-HF Calculations. Chemistry - A European Journal, 14(2), 653-663. doi:10.1002/chem.200701099Albini, A., & Monti, S. (2003). Photophysics and photochemistry of fluoroquinolones. Chemical Society Reviews, 32(4), 238. doi:10.1039/b209220bFasani, E., Manet, I., Capobianco, M. L., Monti, S., Pretali, L., & Albini, A. (2010). Fluoroquinolones as potential photochemotherapeutic agents: covalent addition to guanosine monophosphate. Organic & Biomolecular Chemistry, 8(16), 3621. doi:10.1039/c0ob00056fSoldevila, S., Cuquerella, M. C., & Bosca, F. (2014). Understanding of the Photoallergic Properties of Fluoroquinolones: Photoreactivity of Lomefloxacin with Amino Acids and Albumin. Chemical Research in Toxicology, 27(4), 514-523. doi:10.1021/tx400377sSoldevila, S., Consuelo Cuquerella, M., Lhiaubet-Vallet, V., Edge, R., & Bosca, F. (2014). Seeking the mechanism responsible for fluoroquinolone photomutagenicity: a pulse radiolysis, steady-state, and laser flash photolysis study. Free Radical Biology and Medicine, 67, 417-425. doi:10.1016/j.freeradbiomed.2013.11.027Domagala, J. M., Heifetz, C. L., Hutt, M. P., Mich, T. F., Nichols, J. B., Solomon, M., & Worth, D. F. (1988). 1-Substituted 7-[3-[(ethylamino)methyl]-1-pyrrolidinyl]-6,8-difluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acids. New quantitative structure activity relationships at N1 for the quinolone antibacterials. Journal of Medicinal Chemistry, 31(5), 991-1001. doi:10.1021/jm00400a017Schmidt, R., Tanielian, C., Dunsbach, R., & Wolff, C. (1994). Phenalenone, a universal reference compound for the determination of quantum yields of singlet oxygen O2(1Δg) sensitization. Journal of Photochemistry and Photobiology A: Chemistry, 79(1-2), 11-17. doi:10.1016/1010-6030(93)03746-4Garcia-Lainez, G., MartĂ­nez-Reig, A. M., Limones-Herrero, D., Consuelo JimĂ©nez, M., Miranda, M. A., & Andreu, I. (2018). Photo(geno)toxicity changes associated with hydroxylation of the aromatic chromophores during diclofenac metabolism. Toxicology and Applied Pharmacology, 341, 51-55. doi:10.1016/j.taap.2018.01.005Palumbo, F., Garcia-Lainez, G., Limones-Herrero, D., Coloma, M. D., Escobar, J., JimĂ©nez, M. C., 
 Andreu, I. (2016). Enhanced photo(geno)toxicity of demethylated chlorpromazine metabolites. Toxicology and Applied Pharmacology, 313, 131-137. doi:10.1016/j.taap.2016.10.024Martinez, L. J., Sik, R. H., & Chignell, C. F. (1998). Fluoroquinolone Antimicrobials: Singlet Oxygen, Superoxide and Phototoxicity. Photochemistry and Photobiology, 67(4), 399-403. doi:10.1111/j.1751-1097.1998.tb05217.xFasani, E., Monti, S., Manet, I., Tilocca, F., Pretali, L., Mella, M., & Albini, A. (2009). Inter- and Intramolecular Photochemical Reactions of Fleroxacin. Organic Letters, 11(9), 1875-1878. doi:10.1021/ol900189vBelvedere, A., BoscĂĄ, F., Catalfo, A., Cuquerella, M. C., de Guidi, G., & Miranda, M. A. (2002). Type II Guanine Oxidation Photoinduced by the Antibacterial Fluoroquinolone Rufloxacin in Isolated DNA and in 2‘-Deoxyguanosine. Chemical Research in Toxicology, 15(9), 1142-1149. doi:10.1021/tx025530iCuquerella, M. C., BoscĂĄ, F., Miranda, M. A., Belvedere, A., Catalfo, A., & de Guidi, G. (2003). Photochemical Properties of Ofloxacin Involved in Oxidative DNA Damage:  A Comparison with Rufloxacin. Chemical Research in Toxicology, 16(4), 562-570. doi:10.1021/tx034006oMonti, S., & Sortino, S. (2002). Laser flash photolysis study of photoionization in fluoroquinolones. Photochemical & Photobiological Sciences, 1(11), 877-881. doi:10.1039/b206750aSeto, Y., Inoue, R., Ochi, M., Gandy, G., Yamada, S., & Onoue, S. (2011). Combined Use of In Vitro Phototoxic Assessments and Cassette Dosing Pharmacokinetic Study for Phototoxicity Characterization of Fluoroquinolones. The AAPS Journal, 13(3). doi:10.1208/s12248-011-9292-7Sauvaigo, S., Douki, T., Odin, F., Caillat, S., Ravanat, J.-L., & Cadet, J. (2001). Analysis of Fluoroquinolone-mediated Photosensitization of 2â€Č-Deoxyguanosine, Calf Thymus and Cellular DNA: Determination of Type-I, Type-II and Triplet–Triplet Energy Transfer Mechanism Contribution¶. Photochemistry and Photobiology, 73(3), 230. doi:10.1562/0031-8655(2001)0732.0.co;2Cuquerella, M. C., Lhiaubet-Vallet, V., Cadet, J., & Miranda, M. A. (2012). Benzophenone Photosensitized DNA Damage. Accounts of Chemical Research, 45(9), 1558-1570. doi:10.1021/ar300054

    MYOD-SKP2 axis boosts tumorigenesis in fusion negative rhabdomyosarcoma by preventing differentiation through p57Kip2^{Kip2} targeting

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    Rhabdomyosarcomas (RMS) are pediatric mesenchymal-derived malignancies encompassing PAX3/7-FOXO1 Fusion Positive (FP)-RMS, and Fusion Negative (FN)-RMS with frequent RAS pathway mutations. RMS express the master myogenic transcription factor MYOD that, whilst essential for survival, cannot support differentiation. Here we discover SKP2, an oncogenic E3-ubiquitin ligase, as a critical pro-tumorigenic driver in FN-RMS. We show that SKP2 is overexpressed in RMS through the binding of MYOD to an intronic enhancer. SKP2 in FN-RMS promotes cell cycle progression and prevents differentiation by directly targeting p27Kip1^{Kip1} and p57Kip2^{Kip2}, respectively. SKP2 depletion unlocks a partly MYOD-dependent myogenic transcriptional program and strongly affects stemness and tumorigenic features and prevents in vivo tumor growth. These effects are mirrored by the investigational NEDDylation inhibitor MLN4924. Results demonstrate a crucial crosstalk between transcriptional and post-translational mechanisms through the MYOD-SKP2 axis that contributes to tumorigenesis in FN-RMS. Finally, NEDDylation inhibition is identified as a potential therapeutic vulnerability in FN-RMS

    Calibration of the Logarithmic-Periodic Dipole Antenna (LPDA) Radio Stations at the Pierre Auger Observatory using an Octocopter

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    An in-situ calibration of a logarithmic periodic dipole antenna with a frequency coverage of 30 MHz to 80 MHz is performed. Such antennas are part of a radio station system used for detection of cosmic ray induced air showers at the Engineering Radio Array of the Pierre Auger Observatory, the so-called Auger Engineering Radio Array (AERA). The directional and frequency characteristics of the broadband antenna are investigated using a remotely piloted aircraft (RPA) carrying a small transmitting antenna. The antenna sensitivity is described by the vector effective length relating the measured voltage with the electric-field components perpendicular to the incoming signal direction. The horizontal and meridional components are determined with an overall uncertainty of 7.4^{+0.9}_{-0.3} % and 10.3^{+2.8}_{-1.7} % respectively. The measurement is used to correct a simulated response of the frequency and directional response of the antenna. In addition, the influence of the ground conductivity and permittivity on the antenna response is simulated. Both have a negligible influence given the ground conditions measured at the detector site. The overall uncertainties of the vector effective length components result in an uncertainty of 8.8^{+2.1}_{-1.3} % in the square root of the energy fluence for incoming signal directions with zenith angles smaller than 60{\deg}.Comment: Published version. Updated online abstract only. Manuscript is unchanged with respect to v2. 39 pages, 15 figures, 2 table

    Multi-resolution anisotropy studies of ultrahigh-energy cosmic rays detected at the Pierre Auger Observatory

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    We report a multi-resolution search for anisotropies in the arrival directions of cosmic rays detected at the Pierre Auger Observatory with local zenith angles up to 80∘80^\circ and energies in excess of 4 EeV (4×10184 \times 10^{18} eV). This search is conducted by measuring the angular power spectrum and performing a needlet wavelet analysis in two independent energy ranges. Both analyses are complementary since the angular power spectrum achieves a better performance in identifying large-scale patterns while the needlet wavelet analysis, considering the parameters used in this work, presents a higher efficiency in detecting smaller-scale anisotropies, potentially providing directional information on any observed anisotropies. No deviation from isotropy is observed on any angular scale in the energy range between 4 and 8 EeV. Above 8 EeV, an indication for a dipole moment is captured; while no other deviation from isotropy is observed for moments beyond the dipole one. The corresponding pp-values obtained after accounting for searches blindly performed at several angular scales, are 1.3×10−51.3 \times 10^{-5} in the case of the angular power spectrum, and 2.5×10−32.5 \times 10^{-3} in the case of the needlet analysis. While these results are consistent with previous reports making use of the same data set, they provide extensions of the previous works through the thorough scans of the angular scales.Comment: Published version. Added journal reference and DOI. Added Report Numbe

    Measurement of the cosmic ray spectrum above 4×10184{\times}10^{18} eV using inclined events detected with the Pierre Auger Observatory

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    A measurement of the cosmic-ray spectrum for energies exceeding 4×10184{\times}10^{18} eV is presented, which is based on the analysis of showers with zenith angles greater than 60∘60^{\circ} detected with the Pierre Auger Observatory between 1 January 2004 and 31 December 2013. The measured spectrum confirms a flux suppression at the highest energies. Above 5.3×10185.3{\times}10^{18} eV, the "ankle", the flux can be described by a power law E−γE^{-\gamma} with index Îł=2.70±0.02 (stat)±0.1 (sys)\gamma=2.70 \pm 0.02 \,\text{(stat)} \pm 0.1\,\text{(sys)} followed by a smooth suppression region. For the energy (EsE_\text{s}) at which the spectral flux has fallen to one-half of its extrapolated value in the absence of suppression, we find Es=(5.12±0.25 (stat)−1.2+1.0 (sys))×1019E_\text{s}=(5.12\pm0.25\,\text{(stat)}^{+1.0}_{-1.2}\,\text{(sys)}){\times}10^{19} eV.Comment: Replaced with published version. Added journal reference and DO

    Ultrahigh-energy neutrino follow-up of Gravitational Wave events GW150914 and GW151226 with the Pierre Auger Observatory

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    On September 14, 2015 the Advanced LIGO detectors observed their first gravitational-wave (GW) transient GW150914. This was followed by a second GW event observed on December 26, 2015. Both events were inferred to have arisen from the merger of black holes in binary systems. Such a system may emit neutrinos if there are magnetic fields and disk debris remaining from the formation of the two black holes. With the surface detector array of the Pierre Auger Observatory we can search for neutrinos with energy above 100 PeV from point-like sources across the sky with equatorial declination from about -65 deg. to +60 deg., and in particular from a fraction of the 90% confidence-level (CL) inferred positions in the sky of GW150914 and GW151226. A targeted search for highly-inclined extensive air showers, produced either by interactions of downward-going neutrinos of all flavors in the atmosphere or by the decays of tau leptons originating from tau-neutrino interactions in the Earth's crust (Earth-skimming neutrinos), yielded no candidates in the Auger data collected within ±500\pm 500 s around or 1 day after the coordinated universal time (UTC) of GW150914 and GW151226, as well as in the same search periods relative to the UTC time of the GW candidate event LVT151012. From the non-observation we constrain the amount of energy radiated in ultrahigh-energy neutrinos from such remarkable events.Comment: Published version. Added journal reference and DOI. Added Report Numbe
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