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1

Garfield, Joshua B. B., and Gavan P. McNally. "The effects of FG7142 on overexpectation of Pavlovian fear conditioning." Behavioral Neuroscience 123, no. 1 (2009): 75–85. http://dx.doi.org/10.1037/a0013814.

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Peris, Joanna, and James D. Scott. "FG7142 causes opposite changes in [3H]GABA release from nigrocollicular regions." Pharmacology Biochemistry and Behavior 44, no. 2 (February 1993): 333–38. http://dx.doi.org/10.1016/0091-3057(93)90470-e.

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Little, H. "Chronic benzodiazepine treatment increases the effects of the inverse agonist FG7142." Neuropharmacology 27, no. 4 (April 1988): 383–89. http://dx.doi.org/10.1016/0028-3908(88)90147-5.

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Glushankov, P. G., V. S. Vorob'ev, and V. G. Skrebitskii. "Effect of the ?-carboline derivative FG7142 on inhibition in hippocampal slices." Bulletin of Experimental Biology and Medicine 100, no. 6 (December 1985): 1715–18. http://dx.doi.org/10.1007/bf00836318.

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Murphy, B. "Clozapine Reverses the Spatial Working Memory Deficits Induced by FG7142 in Monkeys." Neuropsychopharmacology 16, no. 6 (June 1997): 433–37. http://dx.doi.org/10.1016/s0893-133x(97)00019-5.

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Major, Christine A., Brian J. Kelly, Melinda A. Novak, Matthew D. Davenport, Karen M. Stonemetz, and Jerrold S. Meyer. "The anxiogenic drug FG7142 increases self-injurious behavior in male rhesus monkeys (Macaca mulatta)." Life Sciences 85, no. 21-22 (November 2009): 753–58. http://dx.doi.org/10.1016/j.lfs.2009.10.003.

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Takamatsu, Hiroyuki, Akihiro Noda, Akeo Kurumaji, Yoshihiro Murakami, Mitsuyoshi Tatsumi, Rikiya Ichise, and Shintaro Nishimura. "A PET study following treatment with a pharmacological stressor, FG7142, in conscious rhesus monkeys." Brain Research 980, no. 2 (August 2003): 275–80. http://dx.doi.org/10.1016/s0006-8993(03)02987-1.

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Tang, Helen H. Y., Gavan P. McNally, and Rick Richardson. "The effects of FG7142 on two types of forgetting in 18-day-old rats." Behavioral Neuroscience 121, no. 6 (2007): 1421–25. http://dx.doi.org/10.1037/0735-7044.121.6.1421.

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Kurumaji, Akeo, Takashi Ito, Sumikazu Ishii, and Toru Nishikawa. "Effects of FG7142 and immobilization stress on the gene expression in the neocortex of mice." Neuroscience Research 62, no. 3 (November 2008): 155–59. http://dx.doi.org/10.1016/j.neures.2008.08.001.

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Birnbaum, S. G., D. M. Podell, and A. F. T. Arnsten. "Noradrenergic alpha-2 receptor agonists reverse working memory deficits induced by the anxiogenic drug, FG7142, in rats." Pharmacology Biochemistry and Behavior 67, no. 3 (November 2000): 397–403. http://dx.doi.org/10.1016/s0091-3057(00)00306-3.

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Taylor, Stuart C., Amanda L. Johnston, Lucy J. Wilks, Jane M. Nicholass, Sandra E. File та Hilary J. Little. "Kindling with the β-Carboline FG7142 Suggests Separation between Changes in Seizure Threshold and Anxiety-Related Behaviour". Neuropsychobiology 19, № 4 (1988): 195–201. http://dx.doi.org/10.1159/000118460.

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Stanford, S. C., D. Gettins, and H. J. Littel. "Adverse effects on rat cardiac function ex vivo after repeated administration of the benzodiazepine partial inverse agonist, FG7142." British Journal of Pharmacology 99, no. 3 (March 1990): 441–44. http://dx.doi.org/10.1111/j.1476-5381.1990.tb12946.x.

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Ferretti, Valeria, Paola Gilli та Pier Andrea Borea. "Structural features controlling the binding of β-carbolines to the benzodiazepine receptor". Acta Crystallographica Section B Structural Science 60, № 4 (19 липня 2004): 481–89. http://dx.doi.org/10.1107/s0108768104013564.

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β-Carbolines are a class of drug which can interact with a high affinity with the benzodiazepine (BDZ) binding site of the GABAA receptor. The present paper, aimed at obtaining a deeper insight into the structure–properties relationships of this class of molecules, reports the crystal structures of four β-carbolines: ZK93423 (3-carboethoxy-4-methoxymethyl-6-benzyloxy-β-carboline), ZK91296 (3-carboethoxy-4-methoxymethyl-5-benzyloxy-β-carboline), FG7142 (N-methyl-3-carbamoyl-β-carboline) and the low-affinity ligand harmine hydrochloride (1-methyl-7-methoxy-β-carboline). This set of structural da
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14

Kohno, Shin-ichi, Kinzo Matsumoto, Kazuma Ojima, and Hiroshi Watanabe. "Flumazenil but not FG7142 attenuates the decrease in pentobarbital sleep produced by activation of central noradrenergic systems in mice." Japanese Journal of Pharmacology 73 (1997): 171. http://dx.doi.org/10.1016/s0021-5198(19)45185-8.

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Matsumoto, Kinzo, Shin-Ichi Kohno, Kazuma Ojima, and Hiroshi Watanabe. "Flumazenil but not FG7142 reverses the decrease in pentobarbital sleep caused by activation of central noradrenergic systems in mice." Brain Research 754, no. 1-2 (April 1997): 325–28. http://dx.doi.org/10.1016/s0006-8993(97)00176-5.

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16

Dazzi, Laura, Stefania Ladu, Francesca Spiga, Giada Vacca, Antonella Rivano, Luigi Pira, and Giovanni Biggio. "Chronic treatment with imipramine or mirtazapine antagonizes stress- and FG7142-induced increase in cortical norepinephrine output in freely moving rats." Synapse 43, no. 1 (November 30, 2001): 70–77. http://dx.doi.org/10.1002/syn.10024.

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17

Casarrubea, Maurizio, Giuseppe Di Giovanni, and Giuseppe Crescimanno. "Effects of Different Anxiety Levels on the Behavioral Patternings Investigated through T-pattern Analysis in Wistar Rats Tested in the Hole-Board Apparatus." Brain Sciences 11, no. 6 (May 27, 2021): 714. http://dx.doi.org/10.3390/brainsci11060714.

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The Hole-Board is an ethologically based tool for investigating the anxiety-related behavior of rats following manipulation of the central anxiety level. The present paper aims to assess behavioral patterning following pharmacological manipulation of emotional assets in Wistar rats tested in this experimental apparatus. For this purpose, the behavior of three groups of rats injected with saline, diazepam or FG7142 was evaluated using conventional quantitative and multivariate T-pattern analyses. The results demonstrate that quantitative analyses of individual components of the behavior, disjoi
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18

Yeung, Michelle, Lily Lu, Adam M. Hughes, Dallas Treit та Clayton T. Dickson. "FG7142, yohimbine, and βCCE produce anxiogenic-like effects in the elevated plus-maze but do not affect brainstem activated hippocampal theta". Neuropharmacology 75 (грудень 2013): 47–52. http://dx.doi.org/10.1016/j.neuropharm.2013.06.027.

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Stanford, S. Clare, Stuart C. Taylor та Hilary J. Little. "Chronic desipramine treatment prevents the upregulation of cortical β-receptors caused by a single dose of the benzodiazepine inverse agonist FG7142". European Journal of Pharmacology 139, № 2 (липень 1987): 225–32. http://dx.doi.org/10.1016/0014-2999(87)90255-x.

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20

Casarrubea, Maurizio, Fabiana Faulisi, Massimiliano Pensabene, Claudio Mendola, Riccardo Dell’Utri, Maurizio Cardaci, Andrea Santangelo, and Giuseppe Crescimanno. "Effects of the benzodiazepine inverse agonist FG7142 on the structure of anxiety-related behavior of male Wistar rats tested in hole board." Psychopharmacology 234, no. 3 (November 12, 2016): 381–91. http://dx.doi.org/10.1007/s00213-016-4474-8.

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21

Stanford, S. C., H. A. Baldwin, and S. E. File. "Effects of a single or repeated administration of the benzodiazepine inverse agonist FG7142 on behaviour and cortical adrenoceptor binding in the rat." Psychopharmacology 98, no. 3 (July 1989): 417–24. http://dx.doi.org/10.1007/bf00451698.

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Rüsch, Dirk, та Stuart A. Forman. "Classic Benzodiazepines Modulate the Open–Close Equilibrium in α1β2γ2Lγ-Aminobutyric Acid Type A Receptors". Anesthesiology 102, № 4 (1 квітня 2005): 783–92. http://dx.doi.org/10.1097/00000542-200504000-00014.

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Background Classic benzodiazepine agonists induce their clinical effects by binding to a site on gamma-aminobutyric acid type A (GABAA) receptors and enhancing receptor activity. There are conflicting data regarding whether the benzodiazepine site is allosterically coupled to gamma-aminobutyric acid binding versus the channel open-close (gating) equilibrium. The authors tested the hypothesis that benzodiazepine site ligands modulate alpha1beta2gamma2L GABAA receptor gating both in the absence of orthosteric agonists and when the orthosteric sites are occupied. Methods GABAA receptors were reco
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23

Little, H. J., M. Andreasen, and J. D. C. Lambert. "Chronic treatment with a benzodiazepine agonist in vivo increases the actions of the benzodiazepine partial inverse agonist, FG7142, on the hippocampal slice in vitro." Brain Research 573, no. 2 (February 1992): 243–50. http://dx.doi.org/10.1016/0006-8993(92)90769-6.

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24

Schultz, John L., Michael Weber, Jayla Allen, and Kevin W. Bradley. "Evaluation of Weed Management Programs and Response of FG72 Soybean to HPPD-Inhibiting Herbicides." Weed Technology 29, no. 4 (December 2015): 653–64. http://dx.doi.org/10.1614/wt-d-14-00067.1.

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Field experiments were conducted at two locations in Missouri in 2012 and 2013 to evaluate herbicide programs in 4-hydroxyphenylpyruvate dioxygenase (HPPD)-inhibitor-resistant soybean, referred to as FG72 soybean, and their tolerance to four HPPD-inhibiting herbicides. At the Columbia location, PRE followed by (fb) POST and two-pass POST treatments provided 97% or greater control of all weeds except ivyleaf morningglory. At Moberly in 2012, PRE fb POST treatments provided 95% or greater control and 100% biomass reduction (BR) of glyphosate-resistant (GR) waterhemp, with the exception of isoxaf
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25

Xie, Zixin, Shiying Zou, Wentao Xu, Xu Liu, Kunlun Huang, and Xiaoyun He. "No subchronic toxicity of multiple herbicide-resistant soybean FG72 in Sprague-Dawley rats by 90-days feeding study." Regulatory Toxicology and Pharmacology 94 (April 2018): 299–305. http://dx.doi.org/10.1016/j.yrtph.2018.02.004.

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Köppel, René, Thomas Bucher, Anna Frei, and Hans-Ulrich Waiblinger. "Droplet digital PCR versus multiplex real-time PCR method for the detection and quantification of DNA from the four transgenic soy traits MON87769, MON87708, MON87705 and FG72, and lectin." European Food Research and Technology 241, no. 4 (June 18, 2015): 521–27. http://dx.doi.org/10.1007/s00217-015-2481-3.

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Taiwe, Germain Sotoing, Arielle Larissa Ndieudieu Kouamou, Armelle Rosalie Mbang Ambassa, Joseph Renaud Menanga, Thierry Bang Tchoya, and Paul Desire Djomeni Dzeufiet. "Evidence for the involvement of the GABA-ergic pathway in the anticonvulsant activity of the roots bark aqueous extract of Anthocleista djalonensis A. Chev. (Loganiaceae)." Journal of Basic and Clinical Physiology and Pharmacology 28, no. 5 (January 1, 2017). http://dx.doi.org/10.1515/jbcpp-2017-0048.

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AbstractBackground:The root bark ofMethods:To investigate the anticonvulsant effects and the possible mechanisms of this plant, an aqueous extract ofResults:This extract significantly protected mice against bicuculline-induced motor seizures. It provided 80% protection against picrotoxin-induced tonic-clonic seizures, and strongly antagonized convulsions induced by pilocarpine. AEAD also protected 100% of mice against pentylenetetrazole-induced seizures. Flumazenil, a central benzodiazepine receptor antagonist and FG7142, a partial inverse agonist in the benzodiazepine site of the GABAConclusi
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"Soja FG72 Tolérant Deux Herbicides (MST-FG 72-2)." International Food Risk Analysis Journal, 2014, 1. http://dx.doi.org/10.5772/59036.

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"Double Herbicide Tolerant Soybean Event FG72 (MST-FG 72-2)." International Food Risk Analysis Journal, 2014, 1. http://dx.doi.org/10.5772/59035.

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"Scientific Opinion on an application (EFSA‐GMO‐BE‐2011‐98) for the placing on the market of herbicide‐tolerant genetically modified soybean FG72 for food and feed uses, import and processing under Regulation (EC) No 1829/2003 from Bayer CropScience." EFSA Journal 13, no. 7 (July 2015). http://dx.doi.org/10.2903/j.efsa.2015.4167.

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Naegeli, Hanspeter, Andrew Nicholas Birch, Josep Casacuberta, Adinda De Schrijver, Mikołaj Antoni Gralak, Philippe Guerche, Huw Jones, et al. "Scientific opinion on application EFSA‐GMO‐NL‐2013‐120 for authorisation of genetically modified soybean FG72 × A5547‐127 for food and feed uses, import and processing submitted in accordance with Regulation (EC) No 1829/2003 by Bayer CropScience LP and M.S. Technologies LLC." EFSA Journal 15, no. 4 (April 2017). http://dx.doi.org/10.2903/j.efsa.2017.4744.

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