PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 7929453-9 1994 Thus, the subunit combinations alpha 1 beta 2 gamma 2 and alpha 2 beta 3 gamma 2 represent two main GABAA receptor subtypes, which together amount to 75-85% of the diazepam-sensitive GABAA receptors. Diazepam 164-172 adrenoceptor alpha 1D Homo sapiens 31-38 15926867-1 2005 Non-selective benzodiazepine (BZ) binding-site full agonists, exemplified by diazepam, act by enhancing the inhibitory effects of GABA at GABA(A) receptors containing either an alpha1, -2, -3 or -5 subunit. Diazepam 77-85 adrenoceptor alpha 1D Homo sapiens 177-197 11100148-3 2000 Here we show that, with low concentrations of GABA, diazepam produces a biphasic potentiation for the alpha1beta2gamma2-receptor channel, with distinct components in the nanomolar and micromolar concentration ranges. Diazepam 52-60 adrenoceptor alpha 1D Homo sapiens 102-119 8592140-6 1996 The alpha 1 subunit contributes the high-affinity binding of [3H]Ro 15-1788 (flumazenil) and the diazepam-sensitive binding of [3H]Ro 15-4513. Diazepam 97-105 adrenoceptor alpha 1D Homo sapiens 4-11 14660012-2 2003 Exposure (48 and/or 96 h) of human embryonic kidney (HEK 293) cells stably expressing recombinant alpha1beta2gamma2s GABA(A) receptors for gamma-aminobutyric (GABA, 1 mM) and muscimol (100 microM), but not for diazepam (1 microM), enhanced the maximum number (B(max)) of [3H]flunitrazepam binding sites without affecting their affinity (K(d)). Diazepam 210-218 adrenoceptor alpha 1D Homo sapiens 98-115 12494402-10 2003 Diazepam with affinity for alpha1, alpha2, alpha3, and alpha5 subunits inhibited the binding in all brain regions. Diazepam 0-8 adrenoceptor alpha 1D Homo sapiens 27-61 11306694-6 2001 Of the diazepam-sensitive GABA(A) receptors (alpha1, alpha2, alpha3, alpha5), alpha5 showed the most divergence, being discriminated by zolpidem in terms of very low affinity, and CL218,872 and CGS9895 with different efficacies. Diazepam 7-15 adrenoceptor alpha 1D Homo sapiens 45-51 10728882-10 2000 Cells transfected with alpha1 and gamma2S cDNAs displayed small diazepam and loreclezole responsive GABA-activated currents. Diazepam 64-72 adrenoceptor alpha 1D Homo sapiens 23-41 8145733-7 1994 The apparent potency of GABA was increased 2-fold by diazepam with alpha 1 beta 2 gamma 2 receptors, 3-fold with alpha 3 beta 2 gamma 2 receptors, and 5-fold with alpha 1 alpha 3 beta 2 gamma 2 receptors. Diazepam 53-61 adrenoceptor alpha 1D Homo sapiens 67-89 8145733-7 1994 The apparent potency of GABA was increased 2-fold by diazepam with alpha 1 beta 2 gamma 2 receptors, 3-fold with alpha 3 beta 2 gamma 2 receptors, and 5-fold with alpha 1 alpha 3 beta 2 gamma 2 receptors. Diazepam 53-61 adrenoceptor alpha 1D Homo sapiens 67-74 17805947-4 2008 On the other hand, the docking of diazepam to alpha1/gamma2 interface revealed five multi-member conformational clusters in the binding site and model 1 seemed to represent the correct orientation of diazepam in the binding site. Diazepam 34-42 adrenoceptor alpha 1D Homo sapiens 46-59 7681869-7 1993 Whole-cell currents recorded from cells coexpressing alpha 1 beta 1 gamma 2S subunits were three to four times larger than those recorded from cells coexpressing alpha 1 beta 1 subunits, and they were always enhanced by coapplied diazepam. Diazepam 230-238 adrenoceptor alpha 1D Homo sapiens 53-60 7681869-7 1993 Whole-cell currents recorded from cells coexpressing alpha 1 beta 1 gamma 2S subunits were three to four times larger than those recorded from cells coexpressing alpha 1 beta 1 subunits, and they were always enhanced by coapplied diazepam. Diazepam 230-238 adrenoceptor alpha 1D Homo sapiens 162-169 29138471-3 2017 In the absence of alpha1 subunits, a receptor was formed that was gated by GABA and modulated by diazepam similarly. Diazepam 97-105 adrenoceptor alpha 1D Homo sapiens 18-24 29138471-8 2017 Thus, the beta2 subunit can take over the role of the alpha1 subunit for the formation of both sites, its minus side for the GABA binding site and its plus side for the diazepam binding site. Diazepam 169-177 adrenoceptor alpha 1D Homo sapiens 54-60 17805947-4 2008 On the other hand, the docking of diazepam to alpha1/gamma2 interface revealed five multi-member conformational clusters in the binding site and model 1 seemed to represent the correct orientation of diazepam in the binding site. Diazepam 200-208 adrenoceptor alpha 1D Homo sapiens 46-59 17377772-3 2007 Human embryonic kidney (HEK 293) cells stably expressing recombinant alpha1beta2gamma2s GABA(A) receptors were exposed for 72 h to a high concentration of diazepam (50 microM) in the absence or presence of other drugs. Diazepam 155-163 adrenoceptor alpha 1D Homo sapiens 69-86 17087982-2 2007 Most 1,4-BZs like diazepam recognize all GABA(A)/BZ receptors containing the alpha1-3 or alpha5 together with any beta and the gamma2 subunit. Diazepam 18-26 adrenoceptor alpha 1D Homo sapiens 77-85