Search Results - "Welsby, Philip J"
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The Effect of Cryoprotectants and Storage Conditions on the Transfection Efficiency, Stability, and Safety of Lipid‐Based Nanoparticles for mRNA and DNA Delivery
Published in Advanced healthcare materials (01-07-2023)“…Lipid‐based nanoparticles have recently shown great promise, establishing themselves as the gold standard in delivering novel RNA therapeutics. However,…”
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Intracellular mechanisms underlying the nicotinic enhancement of LTP in the rat dentate gyrus
Published in The European journal of neuroscience (01-01-2009)“…We have previously shown that activation of nicotinic acetylcholine receptors (nAChRs) enhanced long‐term potentiation (LTP) in the rat dentate gyrus in vitro…”
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3
Discovery of Potent Multikinase Type-II Inhibitors Targeting CDK5 in the DFG-out Inactive State with Promising Potential against Glioblastoma
Published in Journal of medicinal chemistry (09-05-2024)“…Kinases have proven valuable targets in successful cancer drug discovery projects, but not yet for malignant brain tumors where type-II inhibition of…”
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4
Multidisciplinary docking, kinetics and X-ray crystallography studies of baicalein acting as a glycogen phosphorylase inhibitor and determination of its’ potential against glioblastoma in cellular models
Published in Chemico-biological interactions (01-09-2023)“…Glycogen phosphorylase (GP) is the rate-determining enzyme in the glycogenolysis pathway. Glioblastoma (GBM) is amongst the most aggressive cancers of the…”
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Enhanced detection of receptor constitutive activity in the presence of regulators of G protein signaling: applications to the detection and analysis of inverse agonists and low-efficacy partial agonists
Published in Molecular pharmacology (01-05-2002)“…Fusion proteins between the human 5-hydroxytryptamine (5-HT)(1A) receptor and either wild type or certain pertussis toxin-resistant forms of G(o1)alpha and…”
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6
Beta-amyloid blocks high frequency stimulation induced LTP but not nicotine enhanced LTP
Published in Neuropharmacology (01-07-2007)“…Nicotine has been postulated to be a possible neuroprotective agent in Alzheimer's Disease (AD). In the present studies, the effect of beta-amyloid (Aβ) was…”
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A Mechanism for the Direct Regulation of T-Type Calcium Channels by Ca2+/Calmodulin-Dependent Kinase II
Published in The Journal of neuroscience (05-11-2003)“…Low-voltage-activated (LVA) Ca2+ channels are widely distributed throughout the CNS and are important determinants of neuronal excitability, initiating…”
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8
Molecular basis for the modulation of native T-type Ca2+ channels in vivo by Ca2+/calmodulin-dependent protein kinase II
Published in The Journal of clinical investigation (01-09-2006)“…Ang II receptor activation increases cytosolic Ca2+ levels to enhance the synthesis and secretion of aldosterone, a recently identified early pathogenic…”
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9
Regulation of the avidity of ternary complexes containing the human 5‐HT1A receptor by mutation of a receptor contact site on the interacting G protein α subunit
Published in British journal of pharmacology (01-10-2002)“…Fusion proteins were constructed between the human 5‐HT1A receptor and pertussis toxin‐resistant forms of both Gi1α and Go1α mutated at residue351 from…”
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P51PREPARATION OF ASIATIC ACID LOADED NANOPARTICLES FOR DELIVERY ACROSS THE BLOOD BRAIN BARRIER AND ITS EFFECTS ON GLIOBLASTOMA CELLS IN VITRO
Published in Neuro-oncology (Charlottesville, Va.) (01-10-2014)“…INTRODUCTION: Drug delivery across tight junctions of the blood brain barrier poses a significant challenge to glioma treatment. Biodegradable nanoparticles…”
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P51 PREPARATION OF ASIATIC ACID LOADED NANOPARTICLES FOR DELIVERY ACROSS THE BLOOD BRAIN BARRIER AND ITS EFFECTS ON GLIOBLASTOMA CELLS IN VITRO
Published in Neuro-oncology (Charlottesville, Va.) (01-10-2014)“…INTRODUCTION: Drug delivery across tight junctions of the blood brain barrier poses a significant challenge to glioma treatment. Biodegradable nanoparticles…”
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Journal Article -
12
Regulation of the avidity of ternary complexes containing the human 5‐HT 1A receptor by mutation of a receptor contact site on the interacting G protein α subunit
Published in British journal of pharmacology (02-02-2009)“…Fusion proteins were constructed between the human 5‐HT 1A receptor and pertussis toxin‐resistant forms of both G i1 α and G o1 α mutated at residue 351 from…”
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Journal Article -
13
Molecular basis for the modulation of native T-type Ca super(2+) channels in vivo by Ca super(2+) /calmodulin-dependent protein kinase II
Published in The Journal of clinical investigation (01-09-2006)“…Ang II receptor activation increases cytosolic Ca super(2+) levels to enhance the synthesis and secretion of aldosterone, a recently identified early…”
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Regulation of the avidity of ternary complexes containing the human 5-HT(1A) receptor by mutation of a receptor contact site on the interacting G protein alpha subunit
Published in British journal of pharmacology (01-10-2002)“…1 Fusion proteins were constructed between the human 5-HT(1A) receptor and pertussis toxin-resistant forms of both G(i1)alpha and G(o1)alpha mutated at…”
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Journal Article -
16
Regulation of the avidity of ternary complexes containing the human 5-HT1A receptor by mutation of a receptor contact site on the interacting G protein [alpha] subunit
Published in British journal of pharmacology (01-10-2002)“…1 Fusion proteins were constructed between the human 5-HT(1A) receptor and pertussis toxin-resistant forms of both G(i1)alpha and G(o1)alpha mutated at…”
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Journal Article -
17
A Mechanism for the Direct Regulation of T-Type Calcium Channels by Ca 2+ /Calmodulin-Dependent Kinase II
Published in The Journal of neuroscience (05-11-2003)“…Low-voltage-activated (LVA) Ca 2+ channels are widely distributed throughout the CNS and are important determinants of neuronal excitability, initiating…”
Get full text
Journal Article -
18
Pharmacological characterisation of the human 5-HT1A receptor and its inhibitory G protein fusions
Published 01-01-2001“…Fusion proteins between the human 5-HTIA receptor and wild type and pertussis toxin resistant forms of the Gi1α and Gi1α proteins were constructed and stably…”
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Dissertation