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MICHAEL STRATTON, M.D.
M.D.
Colon & Rectal Surgery Physician
NPI: 1902849011IndividualAccepts Medicare
Specialties, Licenses & Credentials
Colon & Rectal Surgery PhysicianPrimary
Colon & Rectal Surgery
Code: 208C00000X
12728R(LA)
CMS Specialties
PrimaryCOLORECTAL SURGERY (PROCTOLOGY)
Education
INDIANA UNIVERSITY SCHOOL OF MEDICINE
Class of 1992
Research & Publications (20)
A Ca2+-sensing molecular switch based on alternate frame protein folding.
PMID 18947182·ACS Chem Biol·2008
8-other
Impact of insulin-like growth factor-I on migration, proliferation and Akt-ERK signaling in early and late-passages of vascular smooth muscle cells.
PMID 17960499·Cardiovasc Toxicol·2007
7-preclinical
Disparities in the prevalence of medication therapy for hyperlipidemia in the elderly.
PMID 18198974·Consult Pharm·2007
8-other
Lessons learnt from large-scale exon re-sequencing of the X chromosome.
PMID 19297402·Hum Mol Genet·2009
6-review
Newly discovered breast cancer susceptibility loci on 3p24 and 17q23.2.
PMID 19330027·Nat Genet·2009
8-other
Younger age-at-diagnosis for familial malignant testicular germ cell tumor.
PMID 19609727·Fam Cancer·2009
4-observational
Somatic mutations of the histone H3K27 demethylase gene UTX in human cancer.
PMID 19330029·Nat Genet·2009
8-other
Brain sex differences and hormone influences: a moving experience?
PMID 19207813·J Neuroendocrinol·2009
6-review
LKB1/KRAS mutant lung cancers constitute a genetic subset of NSCLC with increased sensitivity to MAPK and mTOR signalling inhibition.
PMID 19165201·Br J Cancer·2009
8-other
A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation.
PMID 19377476·Nat Genet·2009
8-other
Subclonal phylogenetic structures in cancer revealed by ultra-deep sequencing.
PMID 18723673·Proc Natl Acad Sci U S A·2008
8-other
Exclusion of biglycan mutations in a cohort of patients with neuromuscular disorders.
PMID 18602826·Neuromuscul Disord·2008
8-other
In vitro differential sensitivity of melanomas to phenothiazines is based on the presence of codon 600 BRAF mutation.
PMID 18524847·Mol Cancer Ther·2008
8-other
X-linked protocadherin 19 mutations cause female-limited epilepsy and cognitive impairment.
PMID 18469813·Nat Genet·2008
4-observational
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 1811 E BERT KOUNS STE 430
SHREVEPORT, LA 71105 - Phone
- (318) 424-8373
Quick Facts
- NPI
- 1902849011
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 34
- Publications
- 20
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