Dr. Ronald Joseph Knox O.D.
Optometrist | Low Vision Rehabilitation
10000 Watson Rd Suite 2p Saint Louis MO, 63126About
Dr. Ronald Knox is an optometrist practicing in Saint Louis, MO. Dr. Knox specializing in providing eye care services to patients. As an optometrist, Dr. Knox performs eye exams, tests vision, corrects vision by prescribing eye glasses or contacts, detects certain eye disorders and manages and treats vision problems. Optometrists often work closely with ophthalmologists who may need to further treat patients with surgical procedures.
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Expert Publications
Data provided by the National Library of Medicine- Fluorine substitution can block CYP3A4 metabolism-dependent inhibition: identification of (S)-N-[1-(4-fluoro-3- morpholin-4-ylphenyl)ethyl]-3- (4-fluorophenyl)acrylamide as an orally bioavailable KCNQ2 opener devoid of CYP3A4 metabolism-dependent inh
- (S)-N-[1-(4-cyclopropylmethyl-3,4-dihydro-2H-benzo[1,4]oxazin-6-yl)-ethyl]-3-(2-fluoro-phenyl)-acrylamide is a potent and efficacious KCNQ2 opener which inhibits induced hyperexcitability of rat hippocampal neurons.
- Activation of a calcium entry pathway by sodium pyrithione in the bag cell neurons of Aplysia.
- A thallium-sensitive, fluorescence-based assay for detecting and characterizing potassium channel modulators in mammalian cells.
- A store-operated Ca(2+) influx pathway in the bag cell neurons of Aplysia.
- Comparative effects of sodium pyrithione evoked intracellular calcium elevation in rodent and primate ventral horn motor neurons.
- Discovery of D1 Dopamine Receptor Positive Allosteric Modulators:
- Design and Synthesis of a New Series of 4-Heteroarylamino-1'-azaspiro[oxazole-5,3'-bicyclo[2.2.2]octanes as α7 Nicotinic Receptor Agonists. 1. Development of Pharmacophore and Early Structure-Activity Relationship.
- Development of 4-Heteroarylamino-1'-azaspiro[oxazole-5,3'-bicyclo[2.2.2]octanes] as α7 Nicotinic Receptor Agonists.
- B-973, a novel piperazine positive allosteric modulator of the α7 nicotinic acetylcholine receptor.
- Development of New Benzenesulfonamides As Potent and Selective Na1.7 Inhibitors for the Treatment of Pain.
- BMS-933043, a Selective α7 nAChR Partial Agonist for the Treatment of Cognitive Deficits Associated with Schizophrenia.
- Discovery of non-zwitterionic aryl sulfonamides as Na1.7 inhibitors with efficacy in preclinical behavioral models and translational measures of nociceptive neuron activation.
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Nearest Hospitals
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