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AMIN BARAKAT, MD
MD
Pediatrics Physician
NPI: 1861572588Individual
Specialties, Licenses & Credentials
Pediatrics PhysicianPrimary
Pediatrics
Code: 208000000X
VA27650(VA)
Research & Publications (20)
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
The cinnamyl alcohol dehydrogenase gene family in Populus: phylogeny, organization, and expression.
PMID 19267902·BMC Plant Biol·2009
8-other
Large-scale identification of microRNAs from a basal eudicot (Eschscholzia californica) and conservation in flowering plants.
PMID 17635767·Plant J·2007
8-other
Molecular evolutionary analyses of the Arabidopsis L7 ribosomal protein gene family.
PMID 17889453·Gene·2007
8-other
Effect of cerium oxide nanoparticles on inflammation in vascular endothelial cells.
PMID 19558244·Inhal Toxicol·2009
8-other
Metals in surface sediments and marine bivalves of the Hadhramout coastal area, Gulf of Aden, Yemen.
PMID 19081581·Mar Pollut Bull·2009
7-preclinical
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
Mutations in the protamine locus: association with spermatogenic failure?
PMID 19602509·Mol Hum Reprod·2009
8-other
Uptake and inflammatory effects of nanoparticles in a human vascular endothelial cell line.
PMID 19552347·Res Rep Health Eff Inst·2009
8-other
Examining requirement for formation of functional Presenilin proteins and their processing events in vivo.
PMID 19191327·Genesis·2009
7-preclinical
Carrier frequencies of mutations/polymorphisms in the connexin 26 gene (GJB2) in the Moroccan population.
PMID 19072567·Genet Test·2008
8-other
No association between T222P/LGR8 mutation and cryptorchidism in the Moroccan population.
PMID 18772597·Horm Res·2008
8-other
Dragging along: the glycocalyx and vascular endothelial cell mechanotransduction.
PMID 18403731·Circ Res·2008
7-preclinical
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
The effective concentration 50 (EC50) for propofol with 70% xenon versus 70% nitrous oxide.
PMID 18292426·Anesth Analg·2008
4-observational
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
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 107 N VIRGINIA AVE
FALLS CHURCH, VA 22046 - Phone
- (703) 532-4446
Quick Facts
- NPI
- 1861572588
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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