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Heather Valentine

Researcher at Johns Hopkins University

Publications -  35
Citations -  1539

Heather Valentine is an academic researcher from Johns Hopkins University. The author has contributed to research in topics: Electroencephalography & Radioligand. The author has an hindex of 18, co-authored 35 publications receiving 1410 citations. Previous affiliations of Heather Valentine include Johns Hopkins University School of Medicine.

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Neurotrophic actions of nonimmunosuppressive analogues of immunosuppressive drugs FK506, rapamycin and cyclosporin A.

TL;DR: The striking potency of these agents, their bioavailability and the dissociation of neurotrophic from immunosuppressant actions argue for their therapeutic relevance in the treatment of neurodegenerative diseases.
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Neurotrophic immunophilin ligands stimulate structural and functional recovery in neurodegenerative animal models

TL;DR: In the central nervous system, GPI-1046 promoted protection and/or sprouting of serotonin-containing nerve fibers in somatosensory cortex following parachloroamphetamine treatment and induced regenerative sprouting from spared nigrostriatal dopaminergic neurons following 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine toxicity in mice or 6-hydroxydopamine toxicity in rats.
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Synthesis and biodistribution of [11C]A-836339, a new potential radioligand for PET imaging of cannabinoid type 2 receptors (CB2)

TL;DR: The radiosynthesis of [11C]A-836339 via its desmethyl precursor as a candidate radioligand for imaging CB2 receptors with positron-emission tomography (PET) establishes a proof of principle thatCB2 receptors binding in the neuro inflammation and related disorders can be measured in vivo.
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Human brain imaging of α7 nAChR with [(18)F]ASEM: a new PET radiotracer for neuropsychiatry and determination of drug occupancy.

TL;DR: The characteristics of [18F]ASEM are consistent with the ability to quantify α7-nAChR in the human brain and is suitable for imaging neuropsychiatric disorders and target engagement (receptor occupancy) of potential α 7-n AChR drugs.