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NATALIE LESLIE, MD
MD
Student in an Organized Health Care Education/Training Program
NPI: 1538916051Individual
Specialties, Licenses & Credentials
Student in an Organized Health Care Education/Training ProgramPrimary
Student in an Organized Health Care Education/Training Program
Code: 390200000X
Research & Publications (20)
Clinical outcomes after long-term treatment with alglucosidase alfa in infants and children with advanced Pompe disease.
PMID 19287243·Genet Med·2009
3-trial
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
Early treatment with alglucosidase alpha prolongs long-term survival of infants with Pompe disease.
PMID 19542901·Pediatr Res·2009
2-rct
Prdx1 inhibits tumorigenesis via regulating PTEN/AKT activity.
PMID 19369943·EMBO J·2009
7-preclinical
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
Understanding PTEN regulation: PIP2, polarity and protein stability.
PMID 18794881·Oncogene·2008
6-review
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
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
Loss of PTEN selectively desensitizes upstream IGF1 and insulin signaling.
PMID 17486056·Oncogene·2007
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
Association of carnitine deficiency in Indian continuous ambulatory peritoneal dialysis patients with anemia, erythropoietin use, residual renal function, and diabetes mellitus.
PMID 17556311·Perit Dial Int·2007
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
- 593 EDDY ST
PROVIDENCE, RI 02903 - Phone
- (401) 444-8450
Quick Facts
- NPI
- 1538916051
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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