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1 destructive differentiation between hemp and cannabis.
2 uivalent cannabis, and 18.28 cm with placebo cannabis.
3 tions, particularly those who frequently use cannabis.
4 al use have regulated production and sale of cannabis.
5 uivalent cannabis, and 19.37 cm with placebo cannabis.
6 procedure to provide evidence of exposure to cannabis.
7 ating the appetite stimulating properties of cannabis.
8 high risk group that used high quantities of cannabis.
9 and consumption of recreational and medical cannabis.
10 ts (N = 26) were healthy occasional users of cannabis.
11 BD-dominant, THC/CBD-equivalent, and placebo cannabis.
12 ogy to unravel the complex phytochemistry of cannabis.
13 .28 to 4.39]; P < .001) but not CBD-dominant cannabis (-0.05 cm [95% CI, -1.49 to 1.39]; P > .99), re
14 ion, the SDLP was 19.03 cm with CBD-dominant cannabis, 19.88 cm with THC-dominant cannabis, 20.59 cm
15 was significantly increased by THC-dominant cannabis (+2.33 cm [95% CI, 0.80 to 3.86]; P < .001) and
16 0 to 3.86]; P < .001) and THC/CBD-equivalent cannabis (+2.83 cm [95% CI, 1.28 to 4.39]; P < .001) but
17 ion, the SDLP was 18.21 cm with CBD-dominant cannabis, 20.59 cm with THC-dominant cannabis, 21.09 cm
18 ominant cannabis, 19.88 cm with THC-dominant cannabis, 20.59 cm with THC/CBD-equivalent cannabis, and
19 ominant cannabis, 20.59 cm with THC-dominant cannabis, 21.09 cm with THC/CBD-equivalent cannabis, and
23 ill be valuable for interrogating effects of cannabis and delineating neural mechanisms that give ris
24 rature review on the evolutionary history of Cannabis and Humulus, including medicinal and industrial
25 nol (THC) is the intoxicating constituent of cannabis and is responsible for the drug's reinforcing e
29 cumulating evidence suggests that the use of cannabis and nicotine and tobacco-related products (NTPs
33 r preclinical studies, nonadult subjects; 3) cannabis and NTP group jointly considered; and 4) neuroc
35 in as it relates to the co-administration of cannabis and NTPs, despite the high prevalence rates of
38 ers an ideal tool for terpenoid profiling of Cannabis and sets the scene for more comprehensive works
39 ers, we test the association between various cannabis and spliff use behaviours and likeliness to smo
40 The decriminalization and legalization of cannabis and the expansion of availability of medical ca
41 ere has been minimal research around various cannabis and tobacco mixing (spliff usage) behaviours an
45 noid receptors, which mediate the actions of cannabis, are abundantly expressed in brain regions know
50 9-THC), the major psychoactive ingredient in cannabis, causes fetal growth restriction, though the me
54 aporized THC-dominant and THC/CBD-equivalent cannabis compared with placebo was significantly greater
56 ctions of synthetic cannabinoids or isolated cannabis constituents that may not capture the complex e
61 sity differences between 89 individuals with cannabis dependence (CD) and 89 matched controls (64 mal
66 rocannabinol, the psychoactive ingredient of cannabis, disrupts autophagy selectively in the striatum
67 es have seen a revolution in legal access to cannabis, driven largely by activists and business inter
71 roducts were detected from both pure THC and cannabis experiments, with the product ratios dependent
73 s (r = -0.55; P = 0.026) and higher previous cannabis exposure (r = 0.52; P = 0.040) were associated
75 ons regarding accurate modeling of perinatal cannabis exposure as well as the need for sex- and age-d
77 valence of detrimental outcomes of perinatal cannabis exposure is likely to increase in tandem with t
78 ledge on the potential effects of adolescent cannabis exposure on brain development and identify pote
79 the immediate and protracted consequences of cannabis exposure on pre- and postnatal development.
80 These results were not explained by past cannabis exposure or current intake of antipsychotic med
83 ng response-contingent delivery of vaporized cannabis extracts containing high concentrations of Delt
87 is increasing as more states are legalizing cannabis for both medicinal and recreational purposes.
88 eviews the use of medicinal and recreational cannabis from a clinical but also a policy and public he
91 a diversity panel derived from the Ecofibre Cannabis germplasm collection, an extreme-phenotype geno
92 alues of structural neuroimaging measures by cannabis group were similar across regions, and any diff
93 us has limited its availability in research; cannabis has been legalized only recently, in some state
94 understanding of the safety and efficacy of cannabis has been limited by decades of worldwide illega
98 disease and the anti-inflammatory effects of cannabis have been investigated in patients with inflamm
99 Over the past 25 years, attitudes toward cannabis have evolved rapidly, with expanding legalizati
101 and the expansion of availability of medical cannabis in North America have led to an increase in can
102 Because of increasing access to and use of cannabis in the general population, along with a high pr
103 mg/2 ml), the key psychoactive ingredient in cannabis, in a set of 16 healthy participants (7 males)
104 any of the concerning health implications of cannabis include cardiovascular diseases, although they
105 striatal glutamate levels may underlie acute cannabis-induced psychosis while lower baseline levels m
108 r optimized SBSE conditions, eight different cannabis inflorescences and a quality control sample wer
110 for the preclinical assessment of volitional cannabis intake and cannabis-seeking behaviors.SIGNIFICA
111 urrent study investigated the association of cannabis involvement with WM performance and associated
113 s particularly timely as the legal status of cannabis is changing in many jurisdictions and the perce
116 d, but the association between state medical cannabis laws and opioid overdose mortality reversed dir
117 d that from 1999 to 2010 states with medical cannabis laws experienced slower increases in opioid ana
118 more restrictive (low-tetrahydrocannabinol) cannabis laws were associated with changes in opioid ove
119 ontinue, but the claim that enacting medical cannabis laws will reduce opioid overdose death should b
121 CANCE STATEMENT With the increasing trend of cannabis legalization and consumption during adolescence
123 drolase (FAAH, C385A), which metabolizes the cannabis-like endocannabinoid anandamide, and dopaminerg
126 ontrast, pre-clinical research suggests that cannabis may affect dopamine via modulation of glutamate
128 However, the effect size for CBD-dominant cannabis may not have excluded clinically important impa
135 tic cannabinoids or active components of the cannabis plant), in addition to significant alterations
137 fferent cannabinoids have been isolated from Cannabis plants, clear physiological effects of only a f
138 the non-psychoactive compound isolated from cannabis plants, was recently approved for treatment of
141 public health impacts of the legalisation of cannabis production, sale, and use in the Americas.
143 ew, we highlight the influence that changing cannabis products have on adolescent health and the impl
147 rapidly changing legal and medical status of cannabis-related compounds, makes understanding how exog
149 C, two biomarkers previously associated with cannabis-related psychiatric risk and subcortical DAergi
151 and 2016 but represented only 0.32% of total cannabis sales in Colorado (in kilograms of tetrahydroca
152 The capitate-stalked glandular trichomes of Cannabis sativa (cannabis), situated on the surfaces of
162 set includes samples from hemp, a variety of Cannabis sativa with the THC concentration below 0.3%.
169 assessment of volitional cannabis intake and cannabis-seeking behaviors.SIGNIFICANCE STATEMENT The ev
171 e field, we have developed a novel method of cannabis self-administration using response-contingent d
174 lked glandular trichomes of Cannabis sativa (cannabis), situated on the surfaces of the bracts of the
175 uggest that their contributions to thirdhand cannabis smoke will be less significant than the role th
176 ahydrocannabinol (THC), a major component of cannabis smoke, with ozone was examined as a pure compou
178 logeny of the CsTPS gene family showed three cannabis-specific clades, including a clade of sesquiter
181 Purple Kush revealed a total of 33 different cannabis terpene synthase (CsTPS) genes, as well as vari
183 isorder is characterised by recurrent use of cannabis that causes significant clinical and functional
184 the increasing availability of high-potency cannabis, this has important implications for public hea
187 atio [OR] 2.78, 95% CI 1.35-5.74; p=0.0059), cannabis use (2.61, 1.11-6.14; p=0.029), other illicit d
188 ease abstinence rates (moderate SOE), reduce cannabis use (low SOE), or increase treatment retention
189 ies (GWAS) of ADHD (n = 53,293) and lifetime cannabis use (n = 32,330) to gain insights into the gene
190 m at baseline, the strongest predictors were cannabis use (OR 2.14, 95% CI 1.04-4.41; p=0.038), other
191 derlie the association, direct evidence that cannabis use affects either acute or chronic striatal do
193 lysis was to investigate the extent to which cannabis use among youths is associated with the risk of
194 tion was 6.1% among women who did not report cannabis use and 12.0% among those reporting use in the
195 echanisms underlying the association between cannabis use and acute or long-lasting psychosis are not
196 With the increasing prevalence of legal cannabis use and availability, there is an urgent need t
197 differences in the prevalence of nonmedical cannabis use and cannabis use disorder among U.S. adults
199 d females) with just one or two instances of cannabis use and carefully matched THC-naive controls.
201 endent negative association between frequent cannabis use and frequent illicit opioid use among PWUD
202 ongitudinal association between frequency of cannabis use and illicit opioid use among people who use
203 s demonstrate a moderate association between cannabis use and physical violence, which remained signi
204 emporal relationship between ADHD and future cannabis use and reinforce the need to consider substanc
205 in North America have led to an increase in cannabis use and the availability of high-potency strain
209 butable fractions (PAFs) for the patterns of cannabis use associated with the highest odds of psychos
212 concurrent and lasting effects of adolescent cannabis use can be observed on important cognitive func
213 ls to the data to estimate which patterns of cannabis use carried the highest odds for psychotic diso
215 equal number (n = 12) of subjects with DSM-5 cannabis use disorder (CUD) and matched healthy controls
217 lthy controls and thirteen participants with cannabis use disorder (CUD) twice after placebo and afte
218 he prevalence of nonmedical cannabis use and cannabis use disorder among U.S. adults with and without
219 of high-potency cannabis is associated with cannabis use disorder and increased susceptibility to ps
221 also reviewing the developmental pathways of cannabis use disorder as well as evidence-based pharmaco
222 l pathological consequences of cannabis use, cannabis use disorder is a clinical diagnosis with high
225 ree times a week) nonmedical use, and DSM-IV cannabis use disorder were estimated for groups with and
226 ding neurobiological systems associated with cannabis use disorder, which often share common neural c
230 (F10.X-19.X), alcohol use disorders (F10.X), cannabis use disorders (F12.X), and polydrug use disorde
232 Retrospective human studies suggest that cannabis use during adolescence is linked to long-term n
233 cit opioid use, and 410 (36%) reported daily cannabis use during at least one 6-month follow-up perio
238 ving legal landscape concerning recreational cannabis use has increased urgency to better understand
240 maturation during adolescence, a period when cannabis use in humans has been linked to subsequent vul
241 cannabis use, with an odds ratio of 7.9 for cannabis use in individuals with ADHD in comparison to i
243 uction in illicit drug use at 38 months (eg, cannabis use in the previous month, 10.7% in the interve
254 e a group increasingly vulnerable to adverse cannabis use outcomes, warranting clinical and public he
258 95% CI 1.02 to 1.07, q = 0.008) for lifetime cannabis use to OR = 1.20 (95% CI 1.16 to 1.23, q = 1.33
261 pregnant women in Ontario, Canada, reported cannabis use was significantly associated with an increa
263 a, alcohol dependence disorder, and lifetime cannabis use) predicted self-harm, with effect sizes ran
265 rding potential pathological consequences of cannabis use, cannabis use disorder is a clinical diagno
266 Risk differences of past-year nonmedical cannabis use, frequent (at least three times a week) non
267 nd very little about the earliest effects of cannabis use, however, because most research is conducte
269 ower changes, head movement, antipsychotics, cannabis use, or IQ, and is not found in other frequency
271 und support that ADHD is causal for lifetime cannabis use, with an odds ratio of 7.9 for cannabis use
272 effect on cognitive deficits associated with cannabis use, yet there is little research on co-use and
279 demographic characteristics between reported cannabis users and nonusers was attenuated using matchin
283 with a high prevalence of CUD among current cannabis users, an urgent need exists for more research
284 NA decay during antiretroviral therapy among cannabis users, compared to those with no drug use.
285 Whether similar alterations exist in human cannabis users, has not yet been demonstrated in vivo.
291 strated that surfaces exposed to side-stream cannabis vapor are positive for THC at quantifiable leve
292 first step in understanding how side-stream cannabis vapor deposits in the environment and potential
293 ndicate that volitional exposure to THC-rich cannabis vapor has bona fide reinforcing properties and
296 ubstantial efforts have been made to develop Cannabis varieties that would produce large amounts of C
297 vs. 8.4%), and visits attributable to edible cannabis were more likely to be due to acute psychiatric
299 and experimental evidence demonstrates that cannabis with high THC concentrations and negligible can
300 e FAAH-inhibitor PF-04457845 in reduction of cannabis withdrawal and cannabis use in men who were dai