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NANCY LESLIE, M.D.
M.D.
NPI: 1356372783IndividualAccepts Medicare
Specialties, Licenses & Credentials
Clinical Genetics (M.D.) PhysicianPrimary
Medical Genetics — Clinical Genetics (M.D.)
Code: 207SG0201X
35.049232(OH)
CMS Specialties
PrimaryPEDIATRIC MEDICINE
Education
WASHINGTON UNIVERSITY SCHOOL OF MEDICINE
Class of 1979
Research & Publications (20)
UDP-galactose pyrophosphorylase in mice with galactose-1-phosphate uridyltransferase deficiency.
PMID 15862277·Mol Genet Metab·2005
7-preclinical
Functional analysis of the mouse galactose-1-phosphate uridyl transferase (GALT)promoter.
PMID 11161826·Mol Genet Metab·2001
7-preclinical
Prdx1 inhibits tumorigenesis via regulating PTEN/AKT activity.
PMID 19369943·EMBO J·2009
7-preclinical
Early treatment with alglucosidase alpha prolongs long-term survival of infants with Pompe disease.
PMID 19542901·Pediatr Res·2009
2-rct
A novel hereditary spastic paraplegia with dystonia linked to chromosome 2q24-2q31.
PMID 19006192·Mov Disord·2009
8-other
PtdIns5P protects Akt from dephosphorylation through PP2A inhibition.
PMID 19576174·Biochem Biophys Res Commun·2009
8-other
Clinical outcomes after long-term treatment with alglucosidase alfa in infants and children with advanced Pompe disease.
PMID 19287243·Genet Med·2009
3-trial
Understanding PTEN regulation: PIP2, polarity and protein stability.
PMID 18794881·Oncogene·2008
6-review
Prolactin signaling through the short form of its receptor represses forkhead transcription factor FOXO3 and its target gene galt causing a severe ovarian defect.
PMID 17975019·Mol Endocrinol·2008
7-preclinical
Suppression of PTEN function increases breast cancer chemotherapeutic drug resistance while conferring sensitivity to mTOR inhibitors.
PMID 18332865·Oncogene·2008
8-other
PTEN posttranslational inactivation and hyperactivation of the PI3K/Akt pathway sustain primary T cell leukemia viability.
PMID 18830414·J Clin Invest·2008
8-other
Use of Akt inhibitor and a drug-resistant mutant validates a critical role for protein kinase B/Akt in the insulin-dependent regulation of glucose and system A amino acid uptake.
PMID 18669636·J Biol Chem·2008
7-preclinical
Enzyme reconstitution/replacement therapy for lysosomal storage diseases.
PMID 18025928·Curr Opin Pediatr·2007
6-review
Mutations in the MPV17 gene are responsible for rapidly progressive liver failure in infancy.
PMID 17694548·Hepatology·2007
5-case
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 3333 BURNET AVE, ML 4006
CINCINNATI, OH 45229 - Phone
- (513) 636-4760
Quick Facts
- NPI
- 1356372783
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 47
- Publications
- 20
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