Dr. Stanley A Lightfoot MD
Pathologist | Cytopathology
921 Ne 13th St Oklahoma City OK, 73104About
Dr. Stanley Lightfoot is a pathologist practicing in Oklahoma City, OK. Dr. Lightfoot is a doctor who specializes in the study of bodily fluids and tissues. As a pathologist, Dr. Lightfoot can help your primary care doctor make a diagnosis about your medical condition. Dr. Lightfoot may perform a tissue biopsy to determine if a patient has cancer, practice genetic testing, and complete a number of laboratory examinations. Pathologists can also perform autopsies which can determine a persons cause of death and gain information about genetic progression of a disease.
Education and Training
University of Texas Southwestern Medical Center Southwestern Medical School 1963
Board Certification
PathologyAmerican Board of PathologyABP
Provider Details
Expert Publications
Data provided by the National Library of Medicine- A history of physician payment policies under Medicare.
- Practice expenses.
- Surgeons make public policy.
- Many general surgery work values increased.
- Medicare volume performance standards and Part B spending.
- Therapeutic treatment of DMBA-induced mammary tumors with PPAR ligands.
- cDNA cloning, DNA binding, and evolution of mammalian transcription factor IIIA.
- Antitumor activity of SS(dsFv)PE38 and SS1(dsFv)PE38, recombinant antimesothelin immunotoxins against human gynecologic cancers grown in organotypic culture in vitro.
- DNA ploidy and markovian analysis of neoplastic progression in experimental pancreatic cancer.
- Soy isoflavones prevent ovariectomy-induced atherosclerotic lesions in Golden Syrian hamster model of postmenopausal hyperlipidemia.
- Flaxseed reduces plasma cholesterol and atherosclerotic lesion formation in ovariectomized Golden Syrian hamsters.
- Expression of prohibitin 3' untranslated region suppressor RNA alters morphology and inhibits motility of breast cancer cells.
- Stress induced in heart and other tissues by rat dermal exposure to JP-8 fuel.
- Dried plum prevents bone loss in a male osteoporosis model via IGF-I and the RANK pathway.
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