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FAYE RAO, MD
MD
Cardiovascular Disease Physician
NPI: 1508883133IndividualAccepts Medicare
Specialties, Licenses & Credentials
Cardiovascular Disease PhysicianPrimary
Internal Medicine — Cardiovascular Disease
Code: 207RC0000X
036174932(IL)2005016792(MO)29578(AL)
Interventional Cardiology Physician
Internal Medicine — Interventional Cardiology
Code: 207RI0011X
036174932(IL)
CMS Specialties
PrimaryCARDIOVASCULAR DISEASE (CARDIOLOGY)
Education
WAYNE STATE UNIVERSITY SCHOOL OF MEDICINE
Class of 2002
Research & Publications (20)
Enzymatic synthesis of c-di-GMP using a thermophilic diguanylate cyclase.
PMID 19328769·Anal Biochem·2009
8-other
The synthesis and fabrication of horizontally aligned single-walled carbon nanotubes suspended across wide trenches for infrared detecting application.
PMID 19417345·Nanotechnology·2009
8-other
The functional role of a conserved loop in EAL domain-based cyclic di-GMP-specific phosphodiesterase.
PMID 19376848·J Bacteriol·2009
8-other
Adrenergic polymorphism and the human stress response.
PMID 19120120·Ann N Y Acad Sci·2008
7-preclinical
Catalytic mechanism of cyclic di-GMP-specific phosphodiesterase: a study of the EAL domain-containing RocR from Pseudomonas aeruginosa.
PMID 18344366·J Bacteriol·2008
8-other
Catecholamine release-inhibitory peptide catestatin (chromogranin A(352-372)): naturally occurring amino acid variant Gly364Ser causes profound changes in human autonomic activity and alters risk for hypertension.
PMID 17438154·Circulation·2007
8-other
Tyrosine hydroxylase, the rate-limiting enzyme in catecholamine biosynthesis: discovery of common human genetic variants governing transcription, autonomic activity, and blood pressure in vivo.
PMID 17698732·Circulation·2007
4-observational
Renal albumin excretion: twin studies identify influences of heredity, environment, and adrenergic pathway polymorphism.
PMID 17353515·Hypertension·2007
4-observational
Structural insights into the mechanism and inhibition of eukaryotic O-GlcNAc hydrolysis.
PMID 16541109·EMBO J·2006
7-preclinical
Methylxanthine drugs are chitinase inhibitors: investigation of inhibition and binding modes.
PMID 16183021·Chem Biol·2005
8-other
Specificity and affinity of natural product cyclopentapeptide inhibitors against A. fumigatus, human, and bacterial chitinases.
PMID 15664516·Chem Biol·2005
8-other
Crystal structures of allosamidin derivatives in complex with human macrophage chitinase.
PMID 12639956·J Biol Chem·2003
8-other
Malignant and benign pheochromocytoma: chromaffin granule transmitters and the response to medical and surgical treatment.
PMID 12438175·Ann N Y Acad Sci·2002
3-trial
Malignant pheochromocytoma. Chromaffin granule transmitters and response to treatment.
PMID 11116123·Hypertension·2000
3-trial
Natural variation within the neuronal nicotinic acetylcholine receptor cluster on human chromosome 15q24: influence on heritable autonomic traits in twin pairs.
PMID 19671882·J Pharmacol Exp Ther·2009
4-observational
Dopamine D1 receptor (DRD1) genetic polymorphism: pleiotropic effects on heritable renal traits.
PMID 19675531·Kidney Int·2009
4-observational
Chromogranin A regulates renal function by triggering Weibel-Palade body exocytosis.
PMID 19520754·J Am Soc Nephrol·2009
4-observational
Complex trait genetics the role of mechanistic "intermediate phenotypes" and candidate genetic loci.
PMID 18598897·J Am Coll Cardiol·2008
8-other
Electrophysiological effects of ketamine on human atrial myocytes at therapeutically relevant concentrations.
PMID 18671719·Clin Exp Pharmacol Physiol·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
Via practice · 2 locations total
- Address
- 4600 MEMORIAL DR STE W1
BELLEVILLE, IL 62226 - Phone
- (618) 233-3066
Quick Facts
- NPI
- 1508883133
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 4
- Locations
- 2
- Years in Practice
- 24
- Publications
- 20
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