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MICHAEL SHAHBAZIAN, M.D.
M.D.
Interventional Pain Medicine Physician
NPI: 1417091133IndividualAccepts Medicare
Specialties, Licenses & Credentials
Interventional Pain Medicine PhysicianPrimary
Pain Medicine — Interventional Pain Medicine
Code: 208VP0014X
A91591(CA)
Education
OTHER
Class of 2002
Research & Publications (14)
Functions of site-specific histone acetylation and deacetylation.
PMID 17362198·Annu Rev Biochem·2007
6-review
Histone H2B ubiquitylation controls processive methylation but not monomethylation by Dot1 and Set1.
PMID 16039595·Mol Cell·2005
8-other
A comparative evaluation of Cone Beam Computed Tomography (CBCT) and Multi-Slice CT (MSCT) Part I. On subjective image quality.
PMID 19410409·Eur J Radiol·2010
4-observational
A commutable cytomegalovirus calibrator is required to improve the agreement of viral load values between laboratories.
PMID 19574467·Clin Chem·2009
8-other
Reduced proportion of Purkinje cells expressing paternally derived mutant Mecp2308 allele in female mouse cerebellum is not due to a skewed primary pattern of X-chromosome inactivation.
PMID 15888476·Hum Mol Genet·2005
7-preclinical
Identification of MeCP2 mutations in a series of females with autistic disorder.
PMID 12770674·Pediatr Neurol·2003
5-case
Balanced X chromosome inactivation patterns in the Rett syndrome brain.
PMID 12210344·Am J Med Genet·2002
8-other
Rett syndrome and MeCP2: linking epigenetics and neuronal function.
PMID 12442230·Am J Hum Genet·2002
6-review
Mice with truncated MeCP2 recapitulate many Rett syndrome features and display hyperacetylation of histone H3.
PMID 12160743·Neuron·2002
7-preclinical
Insight into Rett syndrome: MeCP2 levels display tissue- and cell-specific differences and correlate with neuronal maturation.
PMID 11809720·Hum Mol Genet·2002
7-preclinical
Reduction of Purkinje cell pathology in SCA1 transgenic mice by p53 deletion.
PMID 11741393·Neurobiol Dis·2001
7-preclinical
Evidence for stem-cell niches in the tracheal epithelium.
PMID 11415930·Am J Respir Cell Mol Biol·2001
7-preclinical
Molecular genetics of Rett syndrome and clinical spectrum of MECP2 mutations.
PMID 11262731·Curr Opin Neurol·2001
6-review
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 366 SAN MIGUEL DR STE 210
NEWPORT BEACH, CA 92660 - Phone
- (949) 207-9494
Quick Facts
- NPI
- 1417091133
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 24
- Publications
- 14
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