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1                                              CBG also catalyzes a variety of transglycosylation react
2                                              CBG also enhanced verbal memory relative to placebo.
3                                              CBG may represent a novel option to reduce stress and an
4 ved and supported in silico by modeling of a CBG-GalNAc-transferase (GalNAc-T) complex with various R
5                              In songbirds, a CBG circuit regulates moment-by-moment variability in so
6  cannabidivarin (CBDV), cannabigerolic acid (CBG-A) into cannabigerol (CBG), and d-9-tetrahydrocannab
7 targeted modifications of the human alpha1AT-CBG locus on the regulation of cell-specific gene activi
8 e chromatin structure of the entire alpha1AT/CBG locus was reorganized to an expressing cell-typical
9                           Human alpha1AT and CBG gene expression was activated in rat hepatoma microc
10 f targeted modifications of the alpha1AT and CBG loci on the regulation of gene activity and chromati
11  cells results in activation of alpha1AT and CBG transcription and chromatin reorganization of the en
12  resulted in activation of both alpha1AT and CBG transcription and gene activation was accompanied by
13                        However, alpha1AT and CBG transcription could be rescued by transfecting the c
14  of alpha1AT; three MARs are between ATR and CBG and one MAR is within the CBG gene itself.
15  ATR and approximately 40 kb between ATR and CBG.
16 imal subcluster includes alpha 1AT, ATR, and CBG; it occupies approximately 90 kb of genomic DNA, wit
17 KHN, and 47.63 +/- 22.40 KHN for PG, BG, and CBG, respectively.
18        While THC is an illicit drug, CBD and CBG are legal substances that have a variety of unique p
19  is whether RS can be used to detect CBD and CBG in hemp, as well as enable confirmatory differentiat
20  that would produce large amounts of CBD and CBG.
21                                CBD, CBN, and CBG demonstrated the lowest hepatotoxic potential, as ev
22 t and quantify CBD, CBDV, Delta(9)-THCV, and CBG in biological matrices.
23         We report here that the alpha1AT-ATR-CBG region contains five distinct MARs.
24  teeth were treated with a conventional bur (CBG) or chemomechanical agents - Papacarie Duo (PG) and
25                                Cannabigerol (CBG) is a phytocannabinoid increasing in popularity, wit
26 N), Cannabichromene (CBC), and Cannabigerol (CBG) using the Emulate Quad-Culture Liver-Chip model.
27 nabivarin (Delta(9)-THCV), and cannabigerol (CBG).
28  (THC), cannabidiol (CBD), and cannabigerol (CBG).
29 ids, namely cannabidiol (CBD), cannabigerol (CBG), and cannabichromene, as potential leads for novel
30 annabinoids-cannabidiol (CBD), cannabigerol (CBG), and cannabinol (CBN)-effectively inhibit Nav1.8, s
31 nnabigerolic acid (CBG-A) into cannabigerol (CBG), and d-9-tetrahydrocannabinolic acid (THC-A) into d
32 ion, using spectral unmixing, green beta-cat-CBG was deconvoluted from a red TCF-dependent FLuc repor
33 -cat click beetle green luciferase (beta-cat-CBG).
34       Gene order within this interval is cen-CBG-ATR-alpha 1 AT-KAL-PCI-AACT-tel.
35                    As expected, on cleavage, CBG undergoes the irreversible S-to-R serpin transition,
36 e secreted by Pseudomonas aeruginosa cleaves CBG in zebra finch plasma within its reactive center loo
37   Cannabigerols (CBGA and its decarboxylated CBG molecule) have pharmacological profiles similar to C
38 ased plasma corticosterone (CORT), decreased CBG, aphagia and adipsia 24 h after IS.
39  on increased CBT, increased CORT, decreased CBG, adipsia, or aphagia 24 h after IS.
40 ive and exoglycosidase-treated blood-derived CBG of healthy individuals were monitored by gel electro
41 e-blind administration of 20 mg hemp-derived CBG or placebo tincture (T0).
42  RCL-centric glycoprofiling of serum-derived CBG to elucidate the Asn347-glycans and then used molecu
43 ss, and the daily number of visits from each CBG to these four categories of POIs were calculated dur
44  plasma CBG production, and anti-zebra finch CBG antibodies cross-react with CBGs in other birds, ext
45 cosylation of this asparagine in zebra finch CBG does not influence its steroid-binding affinity, but
46                      Recombinant zebra finch CBG steroid-binding properties reflect those of the natu
47 stitutions of amino acids within zebra finch CBG that are conserved only in birds reveal how they con
48 ensitivity was 2 ng/mL for CBDV, 4 ng/mL for CBG and THCV, and 7 ng/mL for CBD.
49 ary to derive correct kinetic parameters for CBG.
50 he development of therapeutic strategies for CBG-related vocal and motor disorders.
51                      Cortical-basal ganglia (CBG) circuits are critical for motor learning and perfor
52 d dysfunction of the cortical-basal ganglia (CBG) song circuit.
53 bol PI) and corticosteroid-binding globulin (CBG) are part of a cluster of six serine protease inhibi
54 cation, the corticosteroid-binding globulin (CBG) binding affinity of the well-known steroid data set
55             Corticosteroid-binding globulin (CBG) delivers anti-inflammatory cortisol to inflamed tis
56             Corticosteroid-binding globulin (CBG) delivers anti-inflammatory cortisol to inflamed tis
57             Corticosteroid-binding globulin (CBG) was isolated from chicken serum and identified by m
58 symbol PI), corticosteroid-binding globulin (CBG), alpha 1-antichymotrypsin (AACT), and protein C inh
59 ne encoding corticosteroid-binding globulin (CBG), and the chromatin organization of this approximate
60 y a serpin, corticosteroid-binding globulin (CBG), and their normally equilibrated release can be fur
61 ins such as corticosterone binding globulin (CBG), aphagia and adipsia.
62 pha1AT) and corticosteroid-binding globulin (CBG), as well as an antitrypsin-related sequence termed
63 hat encodes corticosteroid-binding globulin (CBG).
64 m levels of corticosteroid binding globulin (CBG).
65 ich encodes corticosteroid-binding globulin (CBG).
66             Corticosteroid binding globulin (CBG; SERPINA6) binds >85% of circulating glucocorticoids
67                  Cytosolic beta-glucosidase (CBG) from mammalian liver is known for its broad substra
68 kidney contain a cytosolic beta-glucosidase (CBG) that hydrolyses various beta-d-glycosides, but whos
69  was modeled at the U.S. Census block group (CBG) level using building energy models, outdoor weather
70 e formation of a conjugated bis-guanidinate (CBG)-supported aluminum dihydride complex, i.e., LAlH(2)
71  birds, extending opportunities to study how CBG regulates the actions of glucocorticoids and sex ste
72 here the crystal structures of cleaved human CBG (cCBG) at 1.8-A resolution and its complex with cort
73 e the first heterologous expression of human CBG, a system that facilitated a detailed assessment of
74               These data indicate that human CBG hydrolyses a broad range of dietary glucosides and m
75 our findings show that augmented bursting in CBG circuitry drives plasticity in well-learned motor sk
76 n basal CORT (5 microg/dl) and a decrease in CBG (30% decrease).
77 s, with many DHSs around alpha1AT but few in CBG.
78                                A full-length CBG cDNA (cbg-1) was cloned from a human liver cDNA libr
79 ion acceptor specificity of guinea pig liver CBG by several methods.
80     Klf15-deficient mice have profoundly low CBG, reduced plasma corticosteroid binding capacity, and
81 tryptophan that anchors ligands in mammalian CBG steroid-binding sites is replaced by an asparagine.
82  of Molecular Cell Biology and Genetics (MPI-CBG) in Dresden.
83 ch is in a helix-like conformation in native CBG, unwinds and grossly perturbs the hormone binding si
84  was enhanced by sialoglycans on neighboring CBG N-sites.
85 nd documented activation of alpha1AT but not CBG gene expression.
86 cate that the transglycosylation activity of CBG derives from the formation of a covalently linked en
87             Targeted proteolytic cleavage of CBG by neutrophil elastase (NE; ELANE) significantly red
88 cebo, there was a significant main effect of CBG on overall reductions in anxiety as well as reductio
89 f this study was to examine acute effects of CBG on anxiety, stress, and mood.
90 ered by the cleavage of the reactive loop of CBG.
91                              Measurements of CBG mRNA in zebra finch tissues indicate that liver is t
92   We also report spectroscopic signatures of CBG, cannabigerolic acid (CBGA), THC, delta-9-tetrahydro
93 gar intermediate and that the specificity of CBG for transglycosylation reactions is different from i
94 oral trends and meteorology, and matching on CBG of residence, year, month, and weekday of the advers
95  cells failed to activate either alpha1AT or CBG transcription, and chromatin remodeling failed to oc
96 3) that of the park census block group (park CBG).
97                               In particular, CBG shows significant promise due to its ability to effe
98 utic potential of cannabinoids, particularly CBG, as agents that may attenuate pain via block of Nav1
99 dicate that liver is the main site of plasma CBG production, and anti-zebra finch CBG antibodies cros
100                          Zebra finch and rat CBG crystal structures in complex with cortisol resemble
101                                  Recombinant CBG was then used to determine roles of RCL O-glycosylat
102                              The recombinant CBG (reCBG) was purified from the supernatant using a si
103 cts are completely rescued by reconstituting CBG, supporting that KLF15 works primarily through CBG t
104 l elastase (NE; ELANE) significantly reduces CBG binding affinity, potentially increasing 'free' gluc
105 nclusion, we report on biologically relevant CBG RCL glycosylation events, which improve our understa
106 Phylogenetic comparisons show that reptilian CBG orthologs share this unexpected property.
107 sites (Thr338/Thr342/Thr345/Ser350) of serum CBG close to the NE-targeted Val344-Thr345 cleavage site
108                 In conclusion, site-specific CBG N-glycosylation regulates the bioavailability of cor
109  covalent enzyme-sugar intermediate and that CBG will transfer sugar residues to primary hydroxyls an
110                             We conclude that CBG has adapted an allosteric mechanism of the serpins t
111                  These studies indicate that CBG employs a two-step catalytic mechanism with the form
112 pounds such as the CBD derivative, 2 and the CBG derivative, 11, significantly reduced cytokine level
113 er, combined with circuit dysfunction in the CBG song system, offers a model for genetic manipulation
114 etween ATR and CBG and one MAR is within the CBG gene itself.
115 t firing in LMAN, the output nucleus of this CBG circuit, actively drives acute song variability, but
116 upporting that KLF15 works primarily through CBG to control plasma corticosterone homeostasis.
117  of various Asn(347) glycoforms of uncleaved CBG indicated that multiple Asn(347) glycan features are
118 ation is still required to better understand CBG glycobiology.
119 l of the visitor census block group (visitor CBG) and 3) that of the park census block group (park CB
120 Secondary objectives were to examine whether CBG produces subjective drug effects or motor and cognit
121 ve biomarkers are two distinct groups, while CBG is associated with some biomarkers from both groups.
122 us tissue was removed in a shorter time with CBG (median = 54.0 seconds) than the time required for c

 
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