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Marijuana, the Endocannabinoid System and the Female Reproductive System

The Yale journal of biology & medicine, 2016-06, Vol.89 (2), p.175-191

Brents, Lisa K

2016

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Phase I hydroxylated metabolites of the K2 synthetic cannabinoid JWH-018 retain in vitro and in vivo cannabinoid 1 receptor affinity and activity

PloS one, 2011-07, Vol.6 (7), p.e21917

2011

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Response to article - alternative interpretation of "there is reduced immunohistochemical staining of placental aromatase in severe neonatal opioid withdrawal syndrome"

The journal of maternal-fetal & neonatal medicine, 2023-12, Vol.36 (1), p.2183469-2183469

2023

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The K2/Spice Phenomenon: emergence, identification, legislation and metabolic characterization of synthetic cannabinoids in herbal incense products

Drug metabolism reviews, 2014-02, Vol.46 (1), p.72-85

2014

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Unifying mechanisms of action of the anticancer activities of triterpenoids and synthetic analogs

Anti-cancer agents in medicinal chemistry, 2012-12, Vol.12 (10), p.1211-1220

2012

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Effects of prenatal opioid exposure and early life adversity on opioid‐induced antinociception

The FASEB journal, 2022-05, Vol.36 (S1), p.n/a

2022

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Cytochrome P450-mediated oxidative metabolism of abused synthetic cannabinoids found in K2/Spice: identification of novel cannabinoid receptor ligands

Drug metabolism and disposition, 2012-11, Vol.40 (11), p.2174-2184

2012

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Deuterated buprenorphine retains pharmacodynamic properties of buprenorphine and resists metabolism to the active metabolite norbuprenorphine in rats

Frontiers in pharmacology, 2023-05, Vol.14, p.1123261-1123261

2023

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Betulinic acid targets YY1 and ErbB2 through cannabinoid receptor-dependent disruption of microRNA-27a:ZBTB10 in breast cancer

Molecular cancer therapeutics, 2012-07, Vol.11 (7), p.1421-1431

2012

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384 Motives for kratom self-medication: contents of public comments solicited by the FDA

Journal of clinical and translational science, 2022-04, Vol.6 (s1), p.72-73

2022

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Differential drug-drug interactions of the synthetic Cannabinoids JWH-018 and JWH-073: implications for drug abuse liability and pain therapy

The Journal of pharmacology and experimental therapeutics, 2013-09, Vol.346 (3), p.350-361

2013

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In Utero Exposure to Norbuprenorphine, a Major Metabolite of Buprenorphine, Induces Fetal Opioid Dependence and Leads to Neonatal Opioid Withdrawal Syndrome

The Journal of pharmacology and experimental therapeutics, 2019-07, Vol.370 (1), p.9-17

2019

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A Major Glucuronidated Metabolite of JWH-018 Is a Neutral Antagonist at CB1 Receptors

Chemical research in toxicology, 2012-04, Vol.25 (4), p.825-827

2012

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481 Interactions between buprenorphine and norbuprenorphine in neonatal opioid withdrawal syndrome

Journal of clinical and translational science, 2023-04, Vol.7 (s1), p.139-140

2023

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Natural prenylated resveratrol analogs arachidin-1 and -3 demonstrate improved glucuronidation profiles and have affinity for cannabinoid receptors

Xenobiotica, 2012-02, Vol.42 (2), p.139-156

2012

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Automated Quantification of Opioid Withdrawal Severity in Neonatal Rat Pups Using Ethovision® XT Software

The FASEB journal, 2020-04, Vol.34 (S1), p.1-1

2020

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2421 Development and validation of a translational rat model of neonatal abstinence syndrome

Journal of clinical and translational science, 2018-06, Vol.2 (S1), p.9-9

2018

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The Effects of P‐glycoprotein Inhibition on Norbuprenorphine‐induced Neonatal Abstinence Syndrome (NAS)

The FASEB journal, 2019-04, Vol.33 (S1), p.663.11-663.11

2019

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The Role of Norbuprenorphine in Buprenorphine‐Induced Neonatal Abstinence Syndrome: A Pilot Study

The FASEB journal, 2017-04, Vol.31 (S1)

2017

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Maternal Delay and Social Discounting Behavior Predicts Impaired Mother‐Infant Bonding, Maternal Stress, and Paternal Involvement

The FASEB journal, 2015-04, Vol.29 (S1)

2015

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Perceived Social Support and Socioeconomic Status Predict Maternal Delay Discounting Behavior and Neural Function in Healthy Postpartum Women

The FASEB journal, 2016-04, Vol.30 (S1)

2016

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The omega and omega‐1 monohydroxyl metabolites of the abused K2/Spice synthetic cannabinoids JWH‐018 and JWH‐ 073 bind with high affinity and act as agonists at human cannabinoid 2 receptors (hCB2s)

The FASEB journal, 2012-04, Vol.26 (S1)

2012

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Effects of the β‐agonist, isoprenaline, on the down‐regulation, functional responsiveness and trafficking of β 2 ‐adrenergic receptors with N‐terminal polymorphisms

Cell biology international, 2012-12, Vol.36 (12), p.1171-1183

2012

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The effects of the β-agonist isoproterenol on the down-regulation, functional responsiveness, and trafficking of β2-adrenergic receptors with amino-terminal polymorphisms

Cell biology international, 2012-01, Vol.36 (12), p.1171-1183

2012

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Effects of the β-agonist, isoprenaline, on the down-regulation, functional responsiveness and trafficking of β2-adrenergic receptors with N-terminal polymorphisms

Cell biology international, 2012-12, Vol.36 (12), p.1171-1183

2012

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Marijuana, the Endocannabinoid System and the Female Reproductive System

Phase I hydroxylated metabolites of the K2 synthetic cannabinoid JWH-018 retain in vitro and in vivo cannabinoid 1 receptor affinity and activity

Response to article - alternative interpretation of "there is reduced immunohistochemical staining of placental aromatase in severe neonatal opioid withdrawal syndrome"

The K2/Spice Phenomenon: emergence, identification, legislation and metabolic characterization of synthetic cannabinoids in herbal incense products

Unifying mechanisms of action of the anticancer activities of triterpenoids and synthetic analogs

Effects of prenatal opioid exposure and early life adversity on opioid‐induced antinociception

Cytochrome P450-mediated oxidative metabolism of abused synthetic cannabinoids found in K2/Spice: identification of novel cannabinoid receptor ligands

Deuterated buprenorphine retains pharmacodynamic properties of buprenorphine and resists metabolism to the active metabolite norbuprenorphine in rats

Betulinic acid targets YY1 and ErbB2 through cannabinoid receptor-dependent disruption of microRNA-27a:ZBTB10 in breast cancer

384 Motives for kratom self-medication: contents of public comments solicited by the FDA

Differential drug-drug interactions of the synthetic Cannabinoids JWH-018 and JWH-073: implications for drug abuse liability and pain therapy

In Utero Exposure to Norbuprenorphine, a Major Metabolite of Buprenorphine, Induces Fetal Opioid Dependence and Leads to Neonatal Opioid Withdrawal Syndrome

A Major Glucuronidated Metabolite of JWH-018 Is a Neutral Antagonist at CB1 Receptors

481 Interactions between buprenorphine and norbuprenorphine in neonatal opioid withdrawal syndrome

Natural prenylated resveratrol analogs arachidin-1 and -3 demonstrate improved glucuronidation profiles and have affinity for cannabinoid receptors

Automated Quantification of Opioid Withdrawal Severity in Neonatal Rat Pups Using Ethovision® XT Software

2421 Development and validation of a translational rat model of neonatal abstinence syndrome

The Effects of P‐glycoprotein Inhibition on Norbuprenorphine‐induced Neonatal Abstinence Syndrome (NAS)

The Role of Norbuprenorphine in Buprenorphine‐Induced Neonatal Abstinence Syndrome: A Pilot Study

Maternal Delay and Social Discounting Behavior Predicts Impaired Mother‐Infant Bonding, Maternal Stress, and Paternal Involvement

Perceived Social Support and Socioeconomic Status Predict Maternal Delay Discounting Behavior and Neural Function in Healthy Postpartum Women

The omega and omega‐1 monohydroxyl metabolites of the abused K2/Spice synthetic cannabinoids JWH‐018 and JWH‐ 073 bind with high affinity and act as agonists at human cannabinoid 2 receptors (hCB2s)

Effects of the β‐agonist, isoprenaline, on the down‐regulation, functional responsiveness and trafficking of β 2 ‐adrenergic receptors with N‐terminal polymorphisms

The effects of the β-agonist isoproterenol on the down-regulation, functional responsiveness, and trafficking of β2-adrenergic receptors with amino-terminal polymorphisms

Effects of the β-agonist, isoprenaline, on the down-regulation, functional responsiveness and trafficking of β2-adrenergic receptors with N-terminal polymorphisms

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