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1 o15-4513 binding at the diazepam-insensitive benzodiazepine receptor.
2 -dependent protein kinase and the peripheral benzodiazepine receptor.
3 ear independent of binding to the peripheral benzodiazepine receptor.
4 ligand of the mitochondrial peripheral-type benzodiazepine receptor.
5 an antagonist and partial inverse agonist of benzodiazepine receptor.
6 ng component of the mitochondrial peripheral benzodiazepine receptor.
7 achieve sustained binding equilibrium at the benzodiazepine receptors.
8 e binding of RU34347 to diazepam-insensitive benzodiazepine receptors.
9 receptor in the brain and to peripheral 1,4 benzodiazepine receptors.
10 PET imaging with (18)F-FDG, (18)F-peripheral benzodiazepine receptor ((18)F-PBR), and (18)F-florbetap
11 195) is a ligand specific for the peripheral benzodiazepine receptor abundant on macrophages and is e
12 n by bilateral intra-basalis infusion of the benzodiazepine receptor agonist chlordiazepoxide (40 mic
13 interventions, the most evidence exists for benzodiazepine receptor agonist drugs, although persiste
17 We have recently reported that midazolam, a benzodiazepine receptor agonist that is also a short act
20 e with beta-carboline, an anxiogenic inverse benzodiazepine receptor agonist, normalized alcohol pref
21 ilitation of wake-promoting systems, whereas benzodiazepine receptor agonists (BzRAs) such as zolpide
23 to assess the efficacy of benzodiazepines or benzodiazepine receptor agonists or behavioral treatment
26 Insomnia treatments include benzodiazepines, benzodiazepine-receptor agonists, and cognitive behaviou
27 ction of StAR remain unclear; the peripheral benzodiazepine receptor, an OMM protein, appears to be i
29 istribution volume are consistent with fewer benzodiazepine receptors and/or reduced affinity of rece
30 propofol alone, and in combination with the benzodiazepine receptor antagonist flumazenil, into the
32 47 microM, alone and in combination with the benzodiazepine receptor antagonist flumazenil, which has
34 keys were prevented by pretreatment with the benzodiazepine receptor antagonist, RO15-1788, which blo
36 ime-dependent regulation of cortical GABA(A)-benzodiazepine receptors associated with the recovery fr
37 report that Dexras1 binds to the peripheral benzodiazepine receptor-associated protein (PAP7), a pro
38 it was first characterized as the peripheral benzodiazepine receptor because it appears to be respons
39 subjects, a quantitative measure related to benzodiazepine receptor binding (distribution volume) wa
43 mals exposed to stress exhibit a decrease in benzodiazepine receptor binding in the frontal cortex.
44 monstrated reduced dopamine D2 and increased benzodiazepine receptor binding in the striatum of HD an
47 To identify potential abnormalities of brain benzodiazepine receptor binding number and distribution
49 w visualization of a quantitative measure of benzodiazepine receptor binding, are reported to have hi
50 Other agents, such as cyclosporin A and some benzodiazepine receptor-binding agents, have been found
51 adenosine, alone and in combination with the benzodiazepine receptor blocker flumazenil, into the MPA
52 r range, show selectivity toward the central benzodiazepine receptor (BzR) and exhibit structure-affi
54 rontoparietal ACh efflux alone, and with the benzodiazepine receptor (BZR) weak inverse agonist ZK 93
56 e have previously shown reduction of central benzodiazepine receptor (cBZR) binding restricted to the
57 previously shown that reductions of central benzodiazepine receptors (cBZRs) are restricted to the h
58 outflow of glutamate, and implicate the GABA/benzodiazepine receptor complex in the stress-induced ac
60 ty for the gamma-aminobutyric acid A (GABAA)/benzodiazepine receptor complex with efficacies ranging
61 urea series had high affinity for the GABAA/benzodiazepine receptor complex with varying in vitro ef
62 of chloride channel function in the GABA(A)-benzodiazepine receptor complex, or increases in neurona
68 in part via agonist-like actions at GABA(A)/benzodiazepine receptor complexes in the ventral tegment
69 returns ligand binding to both the GABA and benzodiazepine receptor components of the GABAA receptor
71 in gamma-aminobutyric acid type A (GABA(A))-benzodiazepine receptors contribute to the neurobiology
73 ntly that regions of increased and decreased benzodiazepine receptor density may be seen in patients
75 ography with [11C]flumazenil revealed normal benzodiazepine receptor distribution volumes, similar to
77 ACBP required the presence of the peripheral benzodiazepine receptor (for which ACBP is a ligand) to
78 r partial agonist MRK-696, and non-selective benzodiazepine receptor full agonists, midazolam and lor
80 he reduced anxiety was due to differences in benzodiazepine receptor function, the mice were challeng
82 They measured the distribution volume of benzodiazepine receptors in 11 recently detoxified patie
83 e characterised the biphasic response of the benzodiazepine receptor inverse agonist RU34347 in the r
85 ; TSPO), previously known as peripheral-type benzodiazepine receptor, is a high-affinity cholesterol-
86 n (TSPO), previously known as the peripheral benzodiazepine receptor, is a mitochondrial outer membra
87 PO), previously known as the peripheral-type benzodiazepine receptor, is an outer mitochondrial membr
88 PO) (18 kDa), formerly called the peripheral benzodiazepine receptor, is upregulated on activated mic
90 we used positron emission tomography and the benzodiazepine receptor ligand flumazenil labeled with c
91 PET studies with a gamma-aminobutyric acid A-benzodiazepine receptor ligand, (11)C-flumazenil, and th
92 ecarboxamide (PK11195), a typical peripheral benzodiazepine receptor ligand, has been established as
93 in Pgp(+) AML cells and that the peripheral benzodiazepine receptor ligand, PK11195, sensitizes AML
94 n terms of therapeutic drug design, although benzodiazepine receptor ligands are an example of the se
96 e rat mitochondrial outer membrane-localized benzodiazepine receptor (MBR) was expressed in wild-type
98 pounds exhibit functional selectivity at the benzodiazepine receptor of GABA(A) receptor subtypes.
99 within this series had high affinity for the benzodiazepine receptor on the alpha-aminobutyric acid A
100 icate either a toxic effect of alcoholism on benzodiazepine receptors or a vulnerability factor for d
102 ere compared with those of the non-selective benzodiazepine receptor partial agonist MRK-696, and non
103 ive properties of the novel imidazoquinoline benzodiazepine receptor partial agonist, PNU-101017, in
104 olinesterase inhibitor physostigmine nor the benzodiazepine receptor partial inverse agonist FG 7142
105 ivity in the mPFC and BLA in response to the benzodiazepine receptor partial inverse agonist N-methyl
106 tein that interacts with the peripheral-type benzodiazepine receptor (PBR) and cAMP-dependent protein
107 tein that interacts with the peripheral-type benzodiazepine receptor (PBR) and the cAMP-dependent pro
108 To evaluate the utility of the peripheral benzodiazepine receptor (PBR) as a biomarker of neurotox
109 ir applications as nonradioactive peripheral benzodiazepine receptor (PBR) binding probes and photose
111 he role of the mitochondrial peripheral-type benzodiazepine receptor (PBR) in steroidogenesis, we dev
114 ts suggest that the mitochondrial peripheral benzodiazepine receptor (PBR) is not the cellular bindin
115 -carboxamide (PK11195), a typical peripheral benzodiazepine receptor (PBR) ligand, as a selective and
117 tiapoptotic mitochondrial protein peripheral benzodiazepine receptor (PBR) protects neonatal mice aga
118 the carboxyl terminus of the peripheral-type benzodiazepine receptor (PBR), an outer mitochondrial me
119 otein (TSPO), also referred to as peripheral benzodiazepine receptor (PBR), is a crucial 18-kDa outer
125 ), an antagonist to mitochondrial peripheral benzodiazepine receptors (PBRs), with bortezomib trigger
127 photon emission computed tomography and the benzodiazepine receptor radiotracer [123I]iomazenil.
128 in (TSPO; previously known as the peripheral benzodiazepine receptor) remains unclear because its pre
130 sitron-emitting ligand that binds peripheral benzodiazepine receptor sites in activated microglia--us
132 erial homolog of the mammalian mitochondrial benzodiazepine receptor, the tryptophan-rich sensory pro
133 (TSPO), previously known as peripheral-type benzodiazepine receptor; the TSPO-associated protein PAP
135 Ro 15-1788 and [3H]Ro 15-4513 binding to the benzodiazepine receptor was not significantly enhanced b
136 tor with selectivity for the type-I (omega1) benzodiazepine receptor, was studied for efficacy in alt
137 lium has neither GABA(A) nor peripheral-type benzodiazepine receptors, we find that both a diazepam b
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