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AYMAN BARAKAT M.D.
M.D.
Medical Oncology Physician
NPI: 1134320328IndividualAccepts Medicare
Specialties, Licenses & Credentials
Medical Oncology PhysicianPrimary
Internal Medicine — Medical Oncology
Code: 207RX0202X
ME120092(FL)
Education
OTHER
Class of 2002
Research & Publications (20)
Examining requirement for formation of functional Presenilin proteins and their processing events in vivo.
PMID 19191327·Genesis·2009
7-preclinical
Metals in surface sediments and marine bivalves of the Hadhramout coastal area, Gulf of Aden, Yemen.
PMID 19081581·Mar Pollut Bull·2009
7-preclinical
Comparison of the transcriptomes of American chestnut (Castanea dentata) and Chinese chestnut (Castanea mollissima) in response to the chestnut blight infection.
PMID 19426529·BMC Plant Biol·2009
4-observational
Uptake and inflammatory effects of nanoparticles in a human vascular endothelial cell line.
PMID 19552347·Res Rep Health Eff Inst·2009
8-other
The cinnamyl alcohol dehydrogenase gene family in Populus: phylogeny, organization, and expression.
PMID 19267902·BMC Plant Biol·2009
8-other
Mutations in the protamine locus: association with spermatogenic failure?
PMID 19602509·Mol Hum Reprod·2009
8-other
Effect of cerium oxide nanoparticles on inflammation in vascular endothelial cells.
PMID 19558244·Inhal Toxicol·2009
8-other
In vitro model assemblies to study the impact of lignin-carbohydrate interactions on the enzymatic conversion of xylan.
PMID 19655790·Biomacromolecules·2009
8-other
Comparison of next generation sequencing technologies for transcriptome characterization.
PMID 19646272·BMC Genomics·2009
4-observational
Shear stress and 17beta-estradiol modulate cerebral microvascular endothelial Na-K-Cl cotransporter and Na/H exchanger protein levels.
PMID 17959724·Am J Physiol Cell Physiol·2008
7-preclinical
The analysis of three markers flanking GJB2 gene suggests a single origin of the most common 35delG mutation in the Moroccan population.
PMID 18952066·Biochem Biophys Res Commun·2008
8-other
Absence of GJB3 and GJB6 mutations in Moroccan familial and sporadic patients with autosomal recessive non-syndromic deafness.
PMID 18809214·Int J Pediatr Otorhinolaryngol·2008
8-other
A novel mutation in the Espin gene causes autosomal recessive nonsyndromic hearing loss but no apparent vestibular dysfunction in a Moroccan family.
PMID 18973245·Am J Med Genet A·2008
8-other
Supramolecular organization of heteroxylan-dehydrogenation polymers (synthetic lignin) nanoparticles.
PMID 18211003·Biomacromolecules·2008
4-observational
Role of ultrasonic shear rate estimation errors in assessing inflammatory response and vascular risk.
PMID 18207310·Ultrasound Med Biol·2008
8-other
Trophoblasts and shear stress induce an asymmetric distribution of icam-1 in uterine endothelial cells.
PMID 18211542·Am J Reprod Immunol·2008
7-preclinical
The effective concentration 50 (EC50) for propofol with 70% xenon versus 70% nitrous oxide.
PMID 18292426·Anesth Analg·2008
4-observational
Dragging along: the glycocalyx and vascular endothelial cell mechanotransduction.
PMID 18403731·Circ Res·2008
7-preclinical
No association between T222P/LGR8 mutation and cryptorchidism in the Moroccan population.
PMID 18772597·Horm Res·2008
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
- 7154 MEDICAL CENTER DR
SPRING HILL, FL 34608 - Phone
- (352) 596-1926
Quick Facts
- NPI
- 1134320328
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 24
- Publications
- 20
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