Dr. Gregory W. Thomas M.D.
Family Practitioner
1 Grand Ave California Polytechn San Luis Obispo CA, 93407About
Dr. Gregory Thomas is a family practitioner practicing in San Luis Obispo, CA. Dr. Thomas specializes in comprehensive health care for people of all ages. In addition to diagnosing and treating illnesses, family practitioners also put focus on preventative care with routine checkups, tests and personalized coaching on how to maintain a healthy lifestyle. Dr. Thomas possesses immense general knowledge on maintaining health and today, family practitioners provide more care for the underserved and rural populations than any other medical specialty.
Education and Training
Univ of Ca, San Francisco, Sch of Med, San Francisco Ca 1980
University of California 1980
Board Certification
Family MedicineAmerican Board of Family MedicineABFM
Provider Details
Expert Publications
Data provided by the National Library of Medicine- Copper inhibits activated protein C: protective effect of human albumin and an analogue of its high-affinity copper-binding site, d-DAHK.
- Plasma albumin cysteinylation is regulated by cystathionine beta-synthase.
- Inhibitory effect of copper on cystathionine beta-synthase activity: protective effect of an analog of the human albumin N-terminus.
- Commercial human albumin preparations for clinical use are immunosuppressive in vitro.
- Effects of danazol on endothelial cell function and angiogenesis.
- Combined cupric- and cuprous-binding peptides are effective in preventing IL-8 release from endothelial cells and redox reactions.
- Inflammatory Pathways in Knee Osteoarthritis: Potential Targets for Treatment.
- Low Molecular Weight Fraction of Commercial Human Serum Albumin Induces Morphologic and Transcriptional Changes of Bone Marrow-Derived Mesenchymal Stem Cells.
- The low molecular weight fraction of commercial human serum albumin induces acetylation of α-tubulin and reduces transcytosis in retinal endothelial cells.
- The low molecular weight fraction of human serum albumin upregulates COX2, prostaglandin E2, and prostaglandin D2 under inflammatory conditions in osteoarthritic knee synovial fibroblasts.
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