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GEORGE SNIPES, M.D.
M.D.
Anatomic Pathology & Clinical Pathology Physician
NPI: 1508861527IndividualAccepts Medicare
Specialties, Licenses & Credentials
Anatomic Pathology & Clinical Pathology PhysicianPrimary
Pathology — Anatomic Pathology & Clinical Pathology
Code: 207ZP0102X
L5567(TX)
Neuropathology Physician
Pathology — Neuropathology
Code: 207ZN0500X
L5567(TX)
CMS Specialties
PrimaryPATHOLOGY
Education
VANDERBILT UNIVERSITY SCHOOL OF MEDICINE
Class of 1988
Research & Publications (10)
Expanded CTG repeats within the DMPK 3' UTR causes severe skeletal muscle wasting in an inducible mouse model for myotonic dystrophy.
PMID 18272483·Proc Natl Acad Sci U S A·2008
7-preclinical
Oral curcumin mitigates the clinical and neuropathologic phenotype of the Trembler-J mouse: a potential therapy for inherited neuropathy.
PMID 17701891·Am J Hum Genet·2007
7-preclinical
Upregulation of hypoxia-inducible factor (HIF)-1alpha and HIF-2alpha in leptomeningeal vascular malformations of Sturge-Weber syndrome.
PMID 17204940·J Neuropathol Exp Neurol·2007
4-observational
Curcumin treatment abrogates endoplasmic reticulum retention and aggregation-induced apoptosis associated with neuropathy-causing myelin protein zero-truncating mutants.
PMID 16252242·Am J Hum Genet·2005
8-other
An 8.5-kb segment of the PMP22 promoter responds to loss of axon signals during Wallerian degeneration, but does not respond to specific axonal signals during nerve regeneration.
PMID 15723356·J Neurosci Res·2005
7-preclinical
Molecular mechanisms, diagnosis, and rational approaches to management of and therapy for Charcot-Marie-Tooth disease and related peripheral neuropathies.
PMID 14577517·J Investig Med·2003
6-review
Phenotypic differences between peripheral myelin protein-22 (PMP22) and myelin protein zero (P0) mutations associated with Charcot-Marie-Tooth-related diseases.
PMID 12901701·J Neuropathol Exp Neurol·2003
4-observational
Association of calnexin with mutant peripheral myelin protein-22 ex vivo: a basis for "gain-of-function" ER diseases.
PMID 12119418·Proc Natl Acad Sci U S A·2002
7-preclinical
Suppression of Rac activity induces apoptosis of human glioma cells but not normal human astrocytes.
PMID 11929835·Cancer Res·2002
8-other
PMP22 carrying the trembler or trembler-J mutation is intracellularly retained in myelinating Schwann cells.
PMID 11114256·Neurobiol Dis·2000
7-preclinical
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 3600 GASTON AVE, WADLEY TOWER, #261
DALLAS, TX 75246 - Phone
- (214) 823-6492
Quick Facts
- NPI
- 1508861527
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 2
- Locations
- 1
- Years in Practice
- 38
- Publications
- 10
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