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JAMES COMPTON, M.D.
M.D.
Internal Medicine Physician
NPI: 1336133321Individual
Specialties, Licenses & Credentials
Internal Medicine PhysicianPrimary
Internal Medicine
Code: 207R00000X
R2D22(MO)
Research & Publications (20)
Serious as a heart attack: health-related content of late-night comedy television.
PMID 16548705·Health Commun·2006
8-other
Caregiver strain and youth suicide attempt: Are they related?
PMID 19527155·Suicide Life Threat Behav·2009
8-other
Bladder cryoablation in a porcine model: evaluation of three surgical approaches and cryolesion predictability.
PMID 19322940·J Endourol·2009
7-preclinical
Prevalence and nonrandom distribution of exonic mutations in interferon regulatory factor 6 in 307 families with Van der Woude syndrome and 37 families with popliteal pterygium syndrome.
PMID 19282774·Genet Med·2009
8-other
Oligonucleotide array CGH studies in myeloproliferative neoplasms: comparison with JAK2V617F mutational status and conventional chromosome analysis.
PMID 18937974·Leuk Res·2009
4-observational
Pharmacokinetics of rebaudioside A and stevioside after single oral doses in healthy men.
PMID 18555578·Food Chem Toxicol·2008
4-observational
An intronic mutation in DKC1 in an infant with Høyeraal-Hreidarsson syndrome.
PMID 18627054·Am J Med Genet A·2008
5-case
Salmonella infections in the common raccoon (Procyon lotor) in western Pennsylvania.
PMID 18596136·J Clin Microbiol·2008
7-preclinical
Long-term estrogen therapy and 5-HT(2A) receptor binding in postmenopausal women; a single photon emission tomography (SPET) study.
PMID 17956758·Horm Behav·2008
4-observational
Pinpointing pseurotins from a marine-derived Aspergillus as tools for chemical genetics using a synthetic lethality yeast screen.
PMID 17929896·J Nat Prod·2007
8-other
Identification of a variant HLA-A*3401 allele, A*340102, in an educational DNA typing sample.
PMID 17868254·Tissue Antigens·2007
8-other
A structured simple form for ordering genetic tests is needed to ensure coupling of clinical detail (phenotype) with DNA variants (genotype) to ensure utility in publication and databases.
PMID 17726697·Hum Mutat·2007
8-other
Four Classes of Structurally Unusual Peptides from Two Marine-Derived Fungi: Structures and Bioactivities.
PMID 18820723·Tetrahedron·2007
8-other
Augmentation of sertraline with prolonged exposure in the treatment of posttraumatic stress disorder.
PMID 17075912·J Trauma Stress·2006
4-observational
Loss-of-function mutations in the gene encoding filaggrin cause ichthyosis vulgaris.
PMID 16444271·Nat Genet·2006
8-other
Estrogen-triggered delays in mammary gland gene expression during the estrous cycle: evidence for a novel timing system.
PMID 16899557·J Endocrinol·2006
7-preclinical
Common loss-of-function variants of the epidermal barrier protein filaggrin are a major predisposing factor for atopic dermatitis.
PMID 16550169·Nat Genet·2006
8-other
Transcriptional induction of cholinesterase expression and protection against chemical warfare nerve agents.
PMID 16429504·Chem Biol Interact·2005
7-preclinical
Using jasplakinolide to turn on pathways that enable the isolation of new chaetoglobosins from Phomospis asparagi.
PMID 16309305·J Nat Prod·2005
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
- 3915 WATSON RD
SAINT LOUIS, MO 63109 - Phone
- (314) 881-0300
Quick Facts
- NPI
- 1336133321
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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