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LOUIS BENTLEY, MD
MD
Pediatrics Physician
NPI: 1265471429Individual
Specialties, Licenses & Credentials
Pediatrics PhysicianPrimary
Pediatrics
Code: 208000000X
1600911205(UT)
Research & Publications (20)
The imprinted region on human chromosome 7q32 extends to the carboxypeptidase A gene cluster: an imprinted candidate for Silver-Russell syndrome.
PMID 12676894·J Med Genet·2003
8-other
Identification of antigenic regions on VP2 of African horsesickness virus serotype 3 by using phage-displayed epitope libraries.
PMID 10725425·J Gen Virol·2000
7-preclinical
Tbx22null mice have a submucous cleft palate due to reduced palatal bone formation and also display ankyloglossia and choanal atresia phenotypes.
PMID 19648291·Hum Mol Genet·2009
7-preclinical
Expression of an activating mutation in the gene encoding the KATP channel subunit Kir6.2 in mouse pancreatic beta cells recapitulates neonatal diabetes.
PMID 19065048·J Clin Invest·2009
7-preclinical
Disparities in children's oral health and access to care.
PMID 17993213·J Calif Dent Assoc·2007
8-other
A simple method for the production of plasmid DNA in bioreactors.
PMID 16988462·Methods Mol Med·2006
6-review
Association of phosphodiesterase 4D polymorphisms with ischemic stroke in a US population stratified by hypertension status.
PMID 16675738·Stroke·2006
8-other
Experiences and concerns among patients being treated for atypical chest pain.
PMID 16137547·Eur J Intern Med·2005
8-other
Doublets and low-frequency fatigue in potentiated human muscle.
PMID 16128697·Acta Physiol Scand·2005
8-other
Association of the dopamine transporter (DAT1) 10/10-repeat genotype with ADHD symptoms and response inhibition in a general population sample.
PMID 15809660·Mol Psychiatry·2005
4-observational
A genetic and physiological study of impaired glucose homeostasis control in C57BL/6J mice.
PMID 15729571·Diabetologia·2005
4-observational
A new mouse model of type 2 diabetes, produced by N-ethyl-nitrosourea mutagenesis, is the result of a missense mutation in the glucokinase gene.
PMID 15161764·Diabetes·2004
7-preclinical
DDC and COBL, flanking the imprinted GRB10 gene on 7p12, are biallelically expressed.
PMID 12514746·Mamm Genome·2002
4-observational
Chromosome 7p disruptions in Silver Russell syndrome: delineating an imprinted candidate gene region.
PMID 12384779·Hum Genet·2002
8-other
ERBB receptor signaling promotes ependymoma cell proliferation and represents a potential novel therapeutic target for this disease.
PMID 12374672·Clin Cancer Res·2002
4-observational
Recruiting physicians and long-term viability: perspectives of physicians and practice managers.
PMID 12199496·J Health Care Finance·2002
8-other
Characterisation of the growth regulating gene IMP3, a candidate for Silver-Russell syndrome.
PMID 12161597·J Med Genet·2002
7-preclinical
Identification and characterization of an imprinted antisense RNA (MESTIT1) in the human MEST locus on chromosome 7q32.
PMID 12095916·Hum Mol Genet·2002
8-other
Cloning and characterization of Igsf9 in mouse and human: a new member of the immunoglobulin superfamily expressed in the developing nervous system.
PMID 11991715·Genomics·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
- Address
- 2000 S 900 E
SALT LAKE CITY, UT 84105 - Phone
- (801) 464-7600
Quick Facts
- NPI
- 1265471429
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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