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JOHN COPPINGER, D.O.
D.O.
Neuromusculoskeletal Medicine & OMM Physician
NPI: 1992083802Individual
Specialties, Licenses & Credentials
Neuromusculoskeletal Medicine & OMM PhysicianPrimary
Neuromusculoskeletal Medicine & OMM
Code: 204D00000X
34005898(OH)02003944A(IN)4078(TN)
Research & Publications (20)
Impact of genotype-first diagnosis: the detection of microdeletion and microduplication syndromes with cancer predisposition by aCGH.
PMID 19365269·Genet Med·2009
8-other
Plk1 and Aurora A regulate the depolymerase activity and the cellular localization of Kif2a.
PMID 19351716·J Cell Sci·2009
8-other
Identification of familial and de novo microduplications of 22q11.21-q11.23 distal to the 22q11.21 microdeletion syndrome region.
PMID 19193630·Hum Mol Genet·2009
8-other
FAM29A promotes microtubule amplification via recruitment of the NEDD1-gamma-tubulin complex to the mitotic spindle.
PMID 19029337·J Cell Biol·2008
8-other
Quantitative mass spectrometry identifies drug targets in cancer stem cell-containing side population.
PMID 18802034·Stem Cells·2008
7-preclinical
RCS1, a substrate of APC/C, controls the metaphase to anaphase transition.
PMID 18757745·Proc Natl Acad Sci U S A·2008
7-preclinical
Comparison of microarray-based detection rates for cytogenetic abnormalities in prenatal and neonatal specimens.
PMID 18646242·Prenat Diagn·2008
4-observational
Bora and the kinase Aurora a cooperatively activate the kinase Plk1 and control mitotic entry.
PMID 18566290·Science·2008
7-preclinical
Expanding the clinical phenotype of the 3q29 microdeletion syndrome and characterization of the reciprocal microduplication.
PMID 18471269·Mol Cytogenet·2008
8-other
DDA3 recruits microtubule depolymerase Kif2a to spindle poles and controls spindle dynamics and mitotic chromosome movement.
PMID 18411309·J Cell Biol·2008
8-other
Plk1- and beta-TrCP-dependent degradation of Bora controls mitotic progression.
PMID 18378770·J Cell Biol·2008
8-other
Neuroimaging findings in children with rare or novel de novo chromosomal anomalies.
PMID 18302267·Birth Defects Res A Clin Mol Teratol·2008
8-other
The identification of microdeletion syndromes and other chromosome abnormalities: cytogenetic methods of the past, new technologies for the future.
PMID 17910076·Am J Med Genet C Semin Med Genet·2007
6-review
Hsp90 cochaperone Aha1 downregulation rescues misfolding of CFTR in cystic fibrosis.
PMID 17110338·Cell·2006
7-preclinical
Detection of low-level mosaicism by array CGH in routine diagnostic specimens.
PMID 17103431·Am J Med Genet A·2006
8-other
Integration of proteomics and genomics in platelets: a profile of platelet proteins and platelet-specific genes.
PMID 14645502·Mol Cell Proteomics·2004
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
- 601 S CONCORD ST STE 102
KNOXVILLE, TN 37919 - Phone
- (856) 440-8759
Quick Facts
- NPI
- 1992083802
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 3
- Locations
- 1
- Publications
- 20
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