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MICHELLE EMI, M.D.
M.D.
Internal Medicine Physician
NPI: 1962755298Individual
Specialties, Licenses & Credentials
Internal Medicine PhysicianPrimary
Internal Medicine
Code: 207R00000X
G73265(CA)
Research & Publications (20)
Association of nucleotide variations in the apolipoprotein B48 receptor gene (APOB48R) with hypercholesterolemia.
PMID 15830122·J Hum Genet·2005
4-observational
Association of single nucleotide polymorphisms in the promoter region of the pro-opiomelanocortin gene (POMC) with low bone mineral density in adult women.
PMID 15864412·J Hum Genet·2005
4-observational
Nucleotide variations in genes encoding plasminogen activator inhibitor-2 and serine proteinase inhibitor B10 associated with prostate cancer.
PMID 16172807·J Hum Genet·2005
8-other
Targeted therapy against Bcl-2-related proteins in breast cancer cells.
PMID 16280040·Breast Cancer Res·2005
7-preclinical
Amplification, up-regulation and over-expression of C3G (CRK SH3 domain-binding guanine nucleotide-releasing factor) in non-small cell lung cancers.
PMID 15138850·J Hum Genet·2004
8-other
Functional impairment of two novel mutations detected in lipoprotein-associated phospholipase A2 (Lp-PLA2) deficiency patients.
PMID 15148590·J Hum Genet·2004
7-preclinical
Up-regulation of transcriptional factor E2F1 in papillary and anaplastic thyroid cancers.
PMID 15118916·J Hum Genet·2004
8-other
The important role for betaVLDLs binding at the fourth cysteine of first ligand-binding domain in the low-density lipoprotein receptor.
PMID 15459764·J Hum Genet·2004
4-observational
Soluble epoxide hydrolase variant (Glu287Arg) modifies plasma total cholesterol and triglyceride phenotype in familial hypercholesterolemia: intrafamilial association study in an eight-generation hyperlipidemic kindred.
PMID 14673705·J Hum Genet·2004
8-other
Hypercholesterolemia associated with splice-junction variation of inter-alpha-trypsin inhibitor heavy chain 4 (ITIH4) gene.
PMID 14661079·J Hum Genet·2004
8-other
A promoter SNP (-1323T>C) in G-substrate gene (GSBS) correlates with hypercholesterolemia.
PMID 12955585·J Hum Genet·2003
4-observational
Association of natural tooth loss with genetic variation at the human matrix Gla protein locus in elderly women.
PMID 12721790·J Hum Genet·2003
4-observational
Hypertriglyceridemia associated with amino acid variation Asn985Tyr of the RP1 gene.
PMID 12764676·J Hum Genet·2003
4-observational
Nucleotide variations in genes encoding carbonic anhydrase 8 and 10 associated with femoral bone mineral density in Japanese female with osteoporosis.
PMID 19172221·J Bone Miner Metab·2009
8-other
Genetic polymorphisms of paraoxonase-1 are associated with chronic kidney disease in Japanese women.
PMID 19357718·Kidney Int·2009
8-other
Skin tube reconstruction for esophageal defect due to postoperative complication.
PMID 19379922·Ann Thorac Surg·2009
5-case
Genetic association between aldehyde dehydrogenase 2 (ALDH2) variation and high-density lipoprotein cholesterol (HDL-C) among non-drinkers in two large population samples in Japan.
PMID 18776700·J Atheroscler Thromb·2008
8-other
Salt consumption-dependent association of the GNB3 gene polymorphism with type 2 DM.
PMID 18656447·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
- 19950 RINALDI ST, SUITE 300
PORTER RANCH, CA 91326 - Phone
- (818) 271-2400
Quick Facts
- NPI
- 1962755298
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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