The Concise Guide to PHARMACOLOGY 2013/14: transporters. - Test2 - elhamkhani - TriplyDB

The Concise Guide to PHARMACOLOGY 2013/14: transporters.

The Concise Guide to PHARMACOLOGY 2013/14: transporters.

http://www.wikidata.org/entity/Q30486743

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Sphingosine-1-Phosphate Receptor-2 Antagonists: Therapeutic Potential and Potential Risks The effects of microRNA on the absorption, distribution, metabolism and excretion of drugs Role of the MPTP in conditioning the heart - translatability and mechanism Anaesthetics as cardioprotectants: translatability and mechanism Something old, something new and something very old: drugs for treating type 2 diabetes p38 MAPK in cardioprotection - are we there yet?Are cannabidiol and Δ(9) -tetrahydrocannabivarin negative modulators of the endocannabinoid system? A systematic review Potassium Channelopathies and Gastrointestinal Ulceration Dopamine receptors - IUPHAR Review 13 Developmental rodent models of fear and anxiety: from neurobiology to pharmacology.Mechanisms to medicines: elucidating neural and molecular substrates of fear extinction to identify novel treatments for anxiety disorders Regulatory role of the cannabinoid CB2 receptor in stress-induced neuroinflammation in mice.TRP channels in the skin.The histone acetylranseferase hMOF acetylates Nrf2 and regulates anti-drug responses in human non-small cell lung cancer Increased drug resistance is associated with reduced glucose levels and an enhanced glycolysis phenotype.The TRPC channel blocker SKF 96365 inhibits glioblastoma cell growth by enhancing reverse mode of the Na(+) /Ca(2+) exchanger and increasing intracellular Ca(2+).Nucleoside transporters and human organic cation transporter 1 determine the cellular handling of DNA-methyltransferase inhibitors.Lysophospholipid receptor nomenclature review: IUPHAR Review 8.Purinergic neuromuscular transmission in the gastrointestinal tract; functional basis for future clinical and pharmacological studies Pharmacological manipulations in animal models of anorexia and binge eating in relation to humans.Fluoxetine elevates allopregnanolone in female rat brain but inhibits a steroid microsomal dehydrogenase rather than activating an aldo-keto reductase.Stereochemistry of mephedrone neuropharmacology: enantiomer-specific behavioural and neurochemical effects in rats Pharmacological profile of novel psychoactive benzofurans.Multimodal antidepressant vortioxetine increases frontal cortical oscillations unlike escitalopram and duloxetine--a quantitative EEG study in rats.Utilizing hydrogen sulfide as a novel anti-cancer agent by targeting cancer glycolysis and pH imbalance.Identification of novel insulin mimetic drugs by quantitative total internal reflection fluorescence (TIRF) microscopy.Pharmacokinetics, metabolism, and excretion of cycloastragenol, a potent telomerase activator in rats.Synthetic (+)-antroquinonol exhibits dual actions against insulin resistance by triggering AMP kinase and inhibiting dipeptidyl peptidase IV activities Hydrogen peroxide stimulation of CFTR reveals an Epac-mediated, soluble AC-dependent cAMP amplification pathway common to GPCR signalling Molecular targets of the multifunctional iron-chelating drug, M30, in the brains of mouse models of type 2 diabetes mellitus Selective Na(+) /Ca(2+) exchanger inhibition prevents Ca(2+) overload-induced triggered arrhythmias Neuroprotective effects of the anti-cancer drug sunitinib in models of HIV neurotoxicity suggests potential for the treatment of neurodegenerative disorders.A non-erythropoietic peptide derivative of erythropoietin decreases susceptibility to diet-induced insulin resistance in mice.In vitro, in vivo and ex vivo characterization of ibrutinib: a potent inhibitor of the efflux function of the transporter MRP1.Orexin/hypocretin role in reward: implications for opioid and other addictions Targeting two-pore domain K(+) channels TREK-1 and TASK-3 for the treatment of depression: a new therapeutic concept.Ionic mechanisms underlying the negative chronotropic action of propofol on sinoatrial node automaticity in guinea pig heart Preventing leptin resistance by blocking angiotensin II AT1 receptors in diet-induced obese rats.Molecular mechanisms governing different pharmacokinetics of ginsenosides and potential for ginsenoside-perpetrated herb-drug interactions on OATP1B3.Presynaptic adenosine A2A receptors dampen cannabinoid CB1 receptor-mediated inhibition of corticostriatal glutamatergic transmission

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P2860

The Concise Guide to PHARMACOLOGY 2013/14: transporters.

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2013 nî lūn-bûn

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2013 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2013 թվականի դեկտեմբերին հրատարակված գիտական հոդված

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2013年の論文

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2013年論文

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2013年論文

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2013年論文

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2013年論文

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2013年論文

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2013年论文

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The Concise Guide to PHARMACOLOGY 2013/14: transporters.

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CGTP Collaborators

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Helen E Benson

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SLC37A1 and SLC37A2 are phosphate-linked, glucose-6-phosphate antiporters

Evaluation of expression and function of the H+/myo-inositol transporter HMIT

Cloning and functional expression of a human Na(+) and Cl(-)-dependent neutral and cationic amino acid transporter B(0+)

Molecular cloning and functional expression of the human Golgi UDP-N-acetylglucosamine transporter

Cloning of the human thiamine transporter, a member of the folate transporter family

A new gene, encoding an anion transporter, is mutated in sialic acid storage diseases

Mutations in ATP2C1, encoding a calcium pump, cause Hailey-Hailey disease

Molecular cloning and characterization of multispecific organic anion transporter 4 expressed in the placenta

VMAT2: a dynamic regulator of brain monoaminergic neuronal function interacting with drugs of abuse

The vesicular amine transporter family (SLC18): amine/proton antiporters required for vesicular accumulation and regulated exocytotic secretion of monoamines and acetylcholine

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10.1111/BPH.12450

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8

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170

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Michael Spedding

Steve Alexander

Joanna L. Sharman

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2013-12-01T00:00:00Z

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262046556

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24528242

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3892292

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