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CRAIG BODDY, M.D.
M.D.
Hematology & Oncology Physician
NPI: 1265796270IndividualAccepts Medicare
Specialties, Licenses & Credentials
Hematology & Oncology PhysicianPrimary
Internal Medicine — Hematology & Oncology
Code: 207RH0003X
MD-19733(HI)
CMS Specialties
PrimaryHEMATOLOGY/ONCOLOGY
Education
UNIVERSITY OF ILLINOIS COLLEGE OF MED (CHI/PEOR/ROCK/CHM-URB)
Class of 2012
Research & Publications (18)
A thioesterase from an iterative fungal polyketide synthase shows macrocyclization and cross coupling activity and may play a role in controlling iterative cycling through product offloading.
PMID 19530704·Biochemistry·2009
8-other
Polyketide synthase thioesterases catalyze rapid hydrolysis of peptidyl thioesters.
PMID 19188064·Bioorg Med Chem Lett·2009
4-observational
Biomimetic transannular oxa-conjugate addition approach to the 2,6-disubstituted dihydropyran of laulimalide yields an unprecedented transannular oxetane.
PMID 19159194·J Org Chem·2009
8-other
Examining the role of hydrogen bonding interactions in the substrate specificity for the loading step of polyketide synthase thioesterase domains.
PMID 18850723·Biochemistry·2008
8-other
Orthogonal ligation: a three piece assembly of a PNA-peptide-PNA conjugate.
PMID 18688310·Chem Commun (Camb)·2008
8-other
A new mechanism for benzopyrone formation in aromatic polyketide biosynthesis.
PMID 17625867·J Am Chem Soc·2007
8-other
Sialic acid and N-acyl sialic acid analog production by fermentation of metabolically and genetically engineered Escherichia coli.
PMID 17551639·Org Biomol Chem·2007
8-other
The thioesterase domain from the pimaricin and erythromycin biosynthetic pathways can catalyze hydrolysis of simple thioester substrates.
PMID 17428661·Bioorg Med Chem Lett·2007
8-other
Total biosynthesis of antitumor nonribosomal peptides in Escherichia coli.
PMID 16799553·Nat Chem Biol·2006
8-other
Precursor-directed biosynthesis of epothilone in Escherichia coli.
PMID 15198579·J Am Chem Soc·2004
8-other
Understanding substrate specificity of polyketide synthase modules by generating hybrid multimodular synthases.
PMID 12923197·J Biol Chem·2003
8-other
Epothilone C macrolactonization and hydrolysis are catalyzed by the isolated thioesterase domain of epothilone polyketide synthase.
PMID 12643694·J Am Chem Soc·2003
8-other
Atropselective macrocyclization of diaryl ether ring systems: application to the synthesis of vancomycin model systems.
PMID 12197747·J Am Chem Soc·2002
8-other
Extending synthetic access to proteins with a removable acyl transfer auxiliary.
PMID 11971712·J Am Chem Soc·2002
8-other
Pharmacist involvement with warfarin dosing for inpatients.
PMID 11344589·Pharm World Sci·2001
8-other
Does CIP Nomenclature Adequately Handle Molecules with Multiple Stereoelements? A Case Study of Vancomycin and Cognates We would like to thank Professor Dieter Hellwinkel for pointing out to us the stereochemical discrepancies in our review6 and elsewhere in the literature, and Kurt Mislow for stimulating and useful discussions.
PMID 11241596·Angew Chem Int Ed Engl·2001
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
- 888 S KING ST
HONOLULU, HI 96813 - Phone
- (808) 522-4333
Quick Facts
- NPI
- 1265796270
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 14
- Publications
- 18
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