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Cannabinoids and the skeleton: From marijuana to reversal of bone
Cannabinoids and the skeleton: From marijuana to reversal of bone

... Ca2 transients (46). It has been proposed that GPR55 and transient receptor potential vanilloid type 1 receptor (TRPV1) are also involved in endocannabinoid triggering of these events (4749). The main CB1 and CB2 endogenous ligands are N-arachidonoylethanolamine (AEA or anandamide) and 2-arachidon ...
Characteristics and common properties of inhibitors, inducers, and
Characteristics and common properties of inhibitors, inducers, and

Micardis HCT - Boehringer Ingelheim
Micardis HCT - Boehringer Ingelheim

Is there a role for EGFR Tyrosine Kinase Inhibitors in recurrent
Is there a role for EGFR Tyrosine Kinase Inhibitors in recurrent

... Activity with EGFR TKIs has been modest to date in GBM: First generation reversible EGFR inhibitors including gefitinib and erlotinib showed limited activity for several reasons but mainly because these agents were tested in an unselected population. ...
Reward Processing by the Opioid System in the Brain
Reward Processing by the Opioid System in the Brain

Intro to Inhibitors-MM edition-final
Intro to Inhibitors-MM edition-final

Introduction to Inhibitors
Introduction to Inhibitors

Piracetam reverses haloperidol-induced - Tubitak Journals
Piracetam reverses haloperidol-induced - Tubitak Journals

DESIGNING OF POTENTIAL NEW ESTROGEN ANTAGONISTS FOR TREATMENT OF
DESIGNING OF POTENTIAL NEW ESTROGEN ANTAGONISTS FOR TREATMENT OF

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No Slide Title

The Impact of Hepatic Uptake on the Pharmacokinetics of Organic
The Impact of Hepatic Uptake on the Pharmacokinetics of Organic

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Chapter 23

... ◦ Cause volume depletion, sodium excretion, vasodilation of peripheral arterioles ...
Uncoupling between noradrenergic and serotonergic neurons as a
Uncoupling between noradrenergic and serotonergic neurons as a

... hypersensitivity, as displayed by adenylyl cyclase activity coupled to DA in the prefrontal cortex [7]. Interestingly, both the locomotor hyperactivity and the hypersensitivity of cortical D1 receptors were not obtained when dopaminergic cell bodies were destroyed chemically by a 6-hydroxy-dopamine ...
Full text - FNWI (Science) Education Service Centre
Full text - FNWI (Science) Education Service Centre

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Simultaneous Inhibition of Fatty Acid Amide Hydrolase and

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CURRICULUM VITAE

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icrs2015 programme - The International Cannabinoid Research
icrs2015 programme - The International Cannabinoid Research

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Enhancement of Excessive Lever-Pressing After Post
Enhancement of Excessive Lever-Pressing After Post

Can`t I Just Take a Pill For It?
Can`t I Just Take a Pill For It?

Inhibitors of Factor VIIa/Tissue Factor
Inhibitors of Factor VIIa/Tissue Factor

... after parenteral administration, a significant challenge remains in the discovery of an orally bioavailable drug. A successful oral drug will require a careful balance of optimal inhibitor characteristics and drug-like or pharmacokinetic properties, demands that can have contradictory effects on the ...
s - Clayton State University
s - Clayton State University

Antipsychotic drugs reverse the AMPA receptor-stimulated release
Antipsychotic drugs reverse the AMPA receptor-stimulated release

Effects of psilocybin on hippocampal neurogenesis and extinction of
Effects of psilocybin on hippocampal neurogenesis and extinction of

< 1 ... 8 9 10 11 12 13 14 15 16 ... 85 >

Discovery and development of angiotensin receptor blockers

The angiotensin receptor blockers (ARBs), also called angiotensin (AT1) receptor antagonists or sartans, are a group of antihypertensive drugs that act by blocking the effects of the hormone angiotensin II (Ang II) in the body, thereby lowering blood pressure. Their structure is similar to Ang II and they bind to Ang II receptors as inhibitors, e.g., [T24 from Rhys Healthcare].ARBs are widely used drugs in the clinical setting today, their main indications being mild to moderate hypertension, chronic heart failure, secondary stroke prevention and diabetic nephropathy.The discovery and development of ARBs is a demonstrative example of modern rational drug design and how design can be used to gain further knowledge of physiological systems, in this case, the characterization of the subtypes of Ang II receptors.
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