Dr. Lawrence Joe Wilson DC
Chiropractor
10769 Woodside Ave 109 Santee CA, 92071About
Dr. Lawrence Wilson is a Chiropractor practicing in Santee, CA. Dr. Wilson specializes in preventing, diagnosing, and treating conditions associated with the neuromusculoskeletal system, while improving each patients functionality and quality of life. Conditions treated include sciatica, neck pain, and arthritis pain, among many others. Dr. Wilson seeks to reduce pain and discomfort through manipulation and adjustment of the spine.
Provider Details
Expert Publications
Data provided by the National Library of Medicine- Simplified staurosporine analogs as potent JAK3 inhibitors.
- Mild and efficient Lewis acid-promoted detritylation in the synthesis of N-hydroxy amides: a concise synthesis of (-)-Cobactin T.
- beta-N-Biaryl ether sulfonamide hydroxamates as potent gelatinase inhibitors: part 2. Optimization of alpha-amino substituents.
- beta-N-Biaryl ether sulfonamide hydroxamates as potent gelatinase inhibitors: part 1. Design, synthesis, and lead identification.
- Virtual screening to successfully identify novel janus kinase 3 inhibitors: a sequential focused screening approach.
- Synthetic staurosporines via a ring closing metathesis strategy as potent JAK3 inhibitors and modulators of allergic responses.
- Recent patents regarding the discovery of small molecule CXCR4 antagonists.
- Synthesis, structural activity-relationships, and biological evaluation of novel amide-based allosteric binding site antagonists in NR1A/NR2B N-methyl-D-aspartate receptors.
- Recent patents in the discovery of small molecule inhibitors of JAK3.
- Discovery of novel Cobactin-T based matrix metalloproteinase inhibitors via a ring closing metathesis strategy.
- Discovery of tetrahydroisoquinoline-based CXCR4 antagonists.
- Anti-HIV small-molecule binding in the peptide subpocket of the CXCR4:CVX15 crystal structure.
- Context-dependent GluN2B-selective inhibitors of NMDA receptor function are neuroprotective with minimal side effects.
- Discovery of novel N-aryl piperazine CXCR4 antagonists.
- Pyrazolo-Piperidines Exhibit Dual Inhibition of CCR5/CXCR4 HIV Entry and Reverse Transcriptase.
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