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KIMBERLY ARRINGTON, M.D.
M.D.
Dermatology Physician
NPI: 1417274812IndividualAccepts Medicare
Specialties, Licenses & Credentials
Dermatology PhysicianPrimary
Dermatology
Code: 207N00000X
25MA10674800(NJ)0101254559(VA)75265(MN)
CMS Specialties
PrimaryDERMATOLOGY
Education
GEORGE WASHINGTON UNIVERSITY SCHOOL OF MEDICINE
Class of 2010
Research & Publications (14)
Repeat sternotomy in congenital heart surgery: no longer a risk factor.
PMID 18721579·Ann Thorac Surg·2008
8-other
Optimization of a pyrazoloquinolinone class of Chk1 kinase inhibitors.
PMID 17804227·Bioorg Med Chem Lett·2007
8-other
An inhibitor of the kinesin spindle protein activates the intrinsic apoptotic pathway independently of p53 and de novo protein synthesis.
PMID 17101792·Mol Cell Biol·2007
8-other
3-(Indol-2-yl)indazoles as Chek1 kinase inhibitors: Optimization of potency and selectivity via substitution at C6.
PMID 16978863·Bioorg Med Chem Lett·2006
8-other
Encouraging results for the Contegra conduit in the problematic right ventricle-to-pulmonary artery connection.
PMID 16935124·J Thorac Cardiovasc Surg·2006
8-other
Preliminary experience with the MicroMed DeBakey pediatric ventricular assist device.
PMID 16638555·Semin Thorac Cardiovasc Surg Pediatr Card Surg Annu·2006
8-other
Kinesin spindle protein (KSP) inhibitors. Part 2: the design, synthesis, and characterization of 2,4-diaryl-2,5-dihydropyrrole inhibitors of the mitotic kinesin KSP.
PMID 16439123·Bioorg Med Chem Lett·2006
8-other
Kinesin spindle protein (KSP) inhibitors. Part 3: synthesis and evaluation of phenolic 2,4-diaryl-2,5-dihydropyrroles with reduced hERG binding and employment of a phosphate prodrug strategy for aqueous solubility.
PMID 16439122·Bioorg Med Chem Lett·2006
7-preclinical
Optimization of the indolyl quinolinone class of KDR (VEGFR-2) kinase inhibitors: effects of 5-amido- and 5-sulphonamido-indolyl groups on pharmacokinetics and hERG binding.
PMID 14698157·Bioorg Med Chem Lett·2004
7-preclinical
Discovery and evaluation of 3-(5-thien-3-ylpyridin-3-yl)-1H-indoles as a novel class of KDR kinase inhibitors.
PMID 12941314·Bioorg Med Chem Lett·2003
7-preclinical
Optimization of a pyrazolo[1,5-a]pyrimidine class of KDR kinase inhibitors: improvements in physical properties enhance cellular activity and pharmacokinetics.
PMID 12443771·Bioorg Med Chem Lett·2002
7-preclinical
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
- 8170 33RD AVE S
BLOOMINGTON, MN 55425 - Phone
- (952) 541-2802
Quick Facts
- NPI
- 1417274812
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 3
- Locations
- 2
- Years in Practice
- 16
- Publications
- 14
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