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EMILY RAO, MD
MD
Pediatric Hematology & Oncology Physician
NPI: 1679919948Individual
Specialties, Licenses & Credentials
Pediatric Hematology & Oncology PhysicianPrimary
Pediatrics — Pediatric Hematology-Oncology
Code: 2080P0207X
D87595(MD)
CMS Specialties
PrimaryPEDIATRIC MEDICINE
Education
PENNSYLVANIA STATE UNIVERSITY COLLEGE OF MEDICINE
Class of 2013
Research & Publications (17)
CD4-anchoring HIV-1 fusion inhibitor with enhanced potency and in vivo stability.
PMID 19097993·J Biol Chem·2009
7-preclinical
Closing two doors of viral entry: intramolecular combination of a coreceptor- and fusion inhibitor of HIV-1.
PMID 18452606·Virol J·2008
7-preclinical
CCR5 small-molecule antagonists and monoclonal antibodies exert potent synergistic antiviral effects by cobinding to the receptor.
PMID 17392523·Mol Pharmacol·2007
7-preclinical
The effect of immunosuppressive drug rapamycin on regulatory CD4+CD25+Foxp3+T cells in mice.
PMID 17331841·Transpl Immunol·2007
7-preclinical
The second extracellular loop of CCR5 contains the dominant epitopes for highly potent anti-human immunodeficiency virus monoclonal antibodies.
PMID 17242138·Antimicrob Agents Chemother·2007
8-other
Compatibility of porcine and human interleukin 2: implications for xenotransplantation.
PMID 16925666·Xenotransplantation·2006
7-preclinical
Carbohydrate-electrolyte feedings and 1 h time trial cycling performance.
PMID 15673100·Int J Sport Nutr Exerc Metab·2004
3-trial
The short stature homeodomain protein SHOX induces cellular growth arrest and apoptosis and is expressed in human growth plate chondrocytes.
PMID 15145945·J Biol Chem·2004
8-other
Familial growth and skeletal features associated with SHOX haploinsufficiency.
PMID 14513875·J Pediatr Endocrinol Metab·2003
8-other
Comparative assessment of DNA fingerprinting techniques (RAPD, ISSR and AFLP) for genetic analysis of cashew (Anacardium occidentale L.) accessions of India.
PMID 12834051·Genome·2003
4-observational
Prevalence of mutations in the short stature homeobox containing gene (SHOX) in Madelung deformity of childhood.
PMID 12362035·J Med Genet·2002
4-observational
Differential divergence of three human pseudoautosomal genes and their mouse homologs: implications for sex chromosome evolution.
PMID 11731500·Genome Res·2001
4-observational
The Leri-Weill and Turner syndrome homeobox gene SHOX encodes a cell-type specific transcriptional activator.
PMID 11751690·Hum Mol Genet·2001
8-other
Monitoring of Multimode Imaging Devices by use of Optical Low-Coherence Reflectometers in Reflection and Transmission Modes.
PMID 18345118·Appl Opt·2000
8-other
A member of a gene family on Xp22.3, VCX-A, is deleted in patients with X-linked nonspecific mental retardation.
PMID 10903929·Am J Hum Genet·2000
8-other
The short stature homeobox gene SHOX is involved in skeletal abnormalities in Turner syndrome.
PMID 10749976·Hum Mol Genet·2000
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
- 720 RUTLAND AVE # ROSS1125
BALTIMORE, MD 21205 - Phone
- (410) 955-6513
Quick Facts
- NPI
- 1679919948
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 13
- Publications
- 17
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