Dr. George Jackson Snipes M.D.
Pathologist | Anatomic Pathology & Clinical Pathology
3600 Gaston Ave Wadley Tower, #261 Dallas TX, 75246About
Dr. George Snipes is a pathologist practicing in Dallas, TX. Dr. Snipes is a doctor who specializes in the study of bodily fluids and tissues. As a pathologist, Dr. Snipes can help your primary care doctor make a diagnosis about your medical condition. Dr. Snipes 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
Vanderbilt University School of Medicine 1988
Provider Details
Expert Publications
Data provided by the National Library of Medicine- Temporal expression pattern of peripheral myelin protein 22 during in vivo and in
- Intracerebral adenovirus-mediated p53 tumor suppressor gene therapy for experimental human glioma.
- Characterization of chronic bronchopulmonary Pseudomonas aeruginosa infection in resistant and susceptible inbred mouse strains.
- The anatomy and cell biology of peripheral myelin protein-22.
- Common themes in peripheral neuropathy disease genes.
- PMP22 carrying the trembler or trembler-J mutation is intracellularly retained in myelinating Schwann cells.
- Suppression of Rac activity induces apoptosis of human glioma cells but not normal human astrocytes.
- Association of calnexin with mutant peripheral myelin protein-22 ex vivo: a basis for "gain-of-function" ER diseases.
- Isolation of transcriptionally regulated sequences associated with neuronal and non-neuronal cell interactions.
- Phenotypic differences between peripheral myelin protein-22 (PMP22) and myelin protein zero (P0) mutations associated with Charcot-Marie-Tooth-related diseases.
- The gene for the peripheral myelin protein PMP-22 is a candidate for Charcot-Marie-Tooth disease type 1A.
- A leucine-to-proline mutation in the putative first transmembrane domain of the 22-kDa peripheral myelin protein in the trembler-J mouse.
- Continuous electrocorticogram epileptiform discharges due to brain gliosis.
- Molecular mechanisms, diagnosis, and rational approaches to management of and therapy for Charcot-Marie-Tooth disease and related peripheral neuropathies.
- Trembler mouse carries a point mutation in a myelin gene.
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