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D. DYE, M.D.
M.D.
Family Medicine Physician
NPI: 1437192903IndividualAccepts Medicare
Specialties, Licenses & Credentials
Family Medicine PhysicianPrimary
Family Medicine
Code: 207Q00000X
16529(OK)
CMS Specialties
PrimaryFAMILY PRACTICE
Education
UNIVERSITY OF OKLAHOMA COLLEGE OF MEDICINE
Class of 1987
Research & Publications (20)
Human organ/tissue growth algorithms that include obese individuals and black/white population organ weight similarities from autopsy data.
PMID 19267313·J Toxicol Environ Health A·2009
8-other
hShroom1 links a membrane bound protein to the actin cytoskeleton.
PMID 19137261·Cell Mol Life Sci·2009
7-preclinical
Inhibition of prostate cancer cell growth by second-site androgen receptor antagonists.
PMID 19574450·Proc Natl Acad Sci U S A·2009
7-preclinical
Differential presentation of protein interaction surfaces on the androgen receptor defines the pharmacological actions of bound ligands.
PMID 19389631·Chem Biol·2009
8-other
Mutations and polymorphisms of the skeletal muscle alpha-actin gene (ACTA1).
PMID 19562689·Hum Mutat·2009
8-other
Mutations in TPM3 are a common cause of congenital fiber type disproportion.
PMID 18300303·Ann Neurol·2008
8-other
Histologic evidence of repetitive blunt force abdominal trauma in four pediatric fatalities.
PMID 18808370·J Forensic Sci·2008
5-case
Duty and liability surrounding clinical internships: What every internship coordinator should know.
PMID 17036673·J Allied Health·2006
8-other
Novel slow-skeletal myosin (MYH7) mutation in the original myosin storage myopathy kindred.
PMID 16684601·Neuromuscul Disord·2006
5-case
Severe nemaline myopathy caused by mutations of the stop codon of the skeletal muscle alpha actin gene (ACTA1).
PMID 16945536·Neuromuscul Disord·2006
5-case
A geometric switching approach toward thermal activation of metalloenediynes.
PMID 16244733·Chem Commun (Camb)·2005
8-other
Reexamination of lead(II) coordination preferences in sulfur-rich sites: implications for a critical mechanism of lead poisoning.
PMID 15984876·J Am Chem Soc·2005
8-other
Myosin storage myopathy: slow skeletal myosin (MYH7) mutation in two isolated cases.
PMID 15699387·Neurology·2005
5-case
Reconsideration of Arthrobacter ilicis (Mandel et al. 1961) Collins et al. 1982 as a plant-pathogenic species. Proposal to emend the authority and description of the species. Request for an opinion.
PMID 14742500·Int J Syst Evol Microbiol·2004
8-other
Reactivity of the hydrido/nitrosyl radical MHCl(NO)(CO)(P(i)Pr(3))(2), M = Ru, Os.
PMID 14704087·Inorg Chem·2004
8-other
Actin mutations are one cause of congenital fibre type disproportion.
PMID 15468086·Ann Neurol·2004
4-observational
Mutations in the slow skeletal muscle fiber myosin heavy chain gene (MYH7) cause laing early-onset distal myopathy (MPD1).
PMID 15322983·Am J Hum Genet·2004
4-observational
9,10-Anthracene dicarboxylate bridged complexes with M2 quadruply bonded dimetal units: [[M2(O2CtBu)3]2(mu-9,10-An(CO2)2)], where M = Mo or W.
PMID 15252513·Dalton Trans·2004
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 1401 N 4TH AVE, SUITE 201
PURCELL, OK 73080 - Phone
- (405) 527-5400
Quick Facts
- NPI
- 1437192903
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 39
- Publications
- 20
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