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MARILYN CORBETT, MD
MD
Anesthesiology Physician
NPI: 1962496646Individual
Specialties, Licenses & Credentials
Anesthesiology PhysicianPrimary
Anesthesiology
Code: 207L00000X
178894-1205(UT)
Research & Publications (20)
A drowsiness detection system for pilots: Optalert.
PMID 19198203·Aviat Space Environ Med·2009
8-other
Aerosol immunization with NYVAC and MVA vectored vaccines is safe, simple, and immunogenic.
PMID 18270165·Proc Natl Acad Sci U S A·2008
7-preclinical
An alphaTropomyosin mutation alters dimer preference in nemaline myopathy.
PMID 15562513·Ann Neurol·2005
4-observational
A mutation in alpha-tropomyosin(slow) affects muscle strength, maturation and hypertrophy in a mouse model for nemaline myopathy.
PMID 11157795·Hum Mol Genet·2001
7-preclinical
Prescription of anti-influenza drugs for healthy adults: a systematic review and meta-analysis.
PMID 19665930·Lancet Infect Dis·2009
1-meta
Short-acting 5-(trifluoromethyl)pyrido[4,3-d]pyrimidin-4(3H)-one derivatives as orally-active calcium-sensing receptor antagonists.
PMID 19625189·Bioorg Med Chem Lett·2009
7-preclinical
Identifying predictors of medically-attended injuries to young children: do child or parent behavioural attributes matter?
PMID 19651992·Inj Prev·2009
8-other
A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation.
PMID 19377476·Nat Genet·2009
8-other
GP attitudes and self-reported behaviour in primary care consultations for low back pain.
PMID 19546118·Fam Pract·2009
8-other
The genetic landscape of intellectual disability arising from chromosome X.
PMID 19556021·Trends Genet·2009
6-review
Synthesis and structure based optimization of novel Akt inhibitors.
PMID 18456494·Bioorg Med Chem Lett·2008
7-preclinical
X-linked protocadherin 19 mutations cause female-limited epilepsy and cognitive impairment.
PMID 18469813·Nat Genet·2008
4-observational
The Saccharomyces cerevisiae actin cytoskeletal component Bsp1p has an auxiliary role in actomyosin ring function and in the maintenance of bud-neck structure.
PMID 18430924·Genetics·2008
8-other
"Do as I say, not as I do": family influences on children's safety and risk behaviors.
PMID 18643008·Health Psychol·2008
8-other
Rapid cell-cycle reentry and cell death after acute inactivation of the retinoblastoma gene product in postnatal cochlear hair cells.
PMID 18178626·Proc Natl Acad Sci U S A·2008
7-preclinical
Involvement of DPP-IV catalytic residues in enzyme-saxagliptin complex formation.
PMID 18227430·Protein Sci·2008
8-other
Submicroscopic duplications of the hydroxysteroid dehydrogenase HSD17B10 and the E3 ubiquitin ligase HUWE1 are associated with mental retardation.
PMID 18252223·Am J Hum Genet·2008
8-other
Photoreduction of the active site of the metalloprotein putidaredoxin by synchrotron radiation.
PMID 17704563·Acta Crystallogr D Biol Crystallogr·2007
8-other
Mutations in UPF3B, a member of the nonsense-mediated mRNA decay complex, cause syndromic and nonsyndromic mental retardation.
PMID 17704778·Nat Genet·2007
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
- 3838 S 700 E, SUITE 200
SALT LAKE CITY, UT 84106 - Phone
- (801) 261-4988
Quick Facts
- NPI
- 1962496646
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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