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CHARLES MCKEOWN, MD
MD
Internal Medicine Physician
NPI: 1902048929Individual
Specialties, Licenses & Credentials
Internal Medicine PhysicianPrimary
Internal Medicine
Code: 207R00000X
MD00018968(WA)
Research & Publications (20)
Impact of pretreated Switchgrass and biomass carbohydrates on Clostridium thermocellum ATCC 27405 cellulosome composition: a quantitative proteomic analysis.
PMID 19384422·PLoS One·2009
8-other
Evaluation of affinity-tagged protein expression strategies using local and global isotope ratio measurements.
PMID 19459691·J Proteome Res·2009
8-other
Atypical teratoid/rhabdoid tumor arising from the third cranial nerve.
PMID 18769285·J Neuroophthalmol·2008
5-case
MSI-H 'medullary type' adenocarcinoma complicating ileal Crohn's disease; further molecular insight into Crohn's-related carcinogenesis.
PMID 18315608·Histopathology·2008
5-case
A general system for studying protein-protein interactions in Gram-negative bacteria.
PMID 18590317·J Proteome Res·2008
8-other
Tropomodulin1 is required in the heart but not the yolk sac for mouse embryonic development.
PMID 18927466·Circ Res·2008
7-preclinical
Familial multiple pterygium syndrome (MPS) is not associated with CHRNG gene mutation.
PMID 17431910·Am J Med Genet A·2007
5-case
Construction and evaluation of a Clostridium thermocellum ATCC 27405 whole-genome oligonucleotide microarray.
PMID 18478424·Appl Biochem Biotechnol·2007
8-other
Determining the political influence of nurses who work in the field of hepatitis C: a Delphi survey.
PMID 17584338·J Clin Nurs·2007
8-other
Addressing the challenges of genetic screening for deafness.
PMID 17550533·Clin Otolaryngol·2007
8-other
Structural insights into the p97-Ufd1-Npl4 complex.
PMID 17202270·Proc Natl Acad Sci U S A·2007
8-other
Mutations in genes encoding ribonuclease H2 subunits cause Aicardi-Goutières syndrome and mimic congenital viral brain infection.
PMID 16845400·Nat Genet·2006
4-observational
Conformational changes in the AAA ATPase p97-p47 adaptor complex.
PMID 16601695·EMBO J·2006
7-preclinical
The transmembrane protein meckelin (MKS3) is mutated in Meckel-Gruber syndrome and the wpk rat.
PMID 16415887·Nat Genet·2006
7-preclinical
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 7812 W RIVER BLVD
PASCO, WA 99301 - Phone
- (509) 947-4981
Quick Facts
- NPI
- 1902048929
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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