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ELLIS WILCOX, MD
MD
Pulmonary Disease Physician
NPI: 1497829634IndividualAccepts Medicare
Specialties, Licenses & Credentials
Pulmonary Disease PhysicianPrimary
Internal Medicine — Pulmonary Disease
Code: 207RP1001X
MA50485(NJ)
Education
OTHER
Class of 1983
Research & Publications (20)
Noncoding mutations of HGF are associated with nonsyndromic hearing loss, DFNB39.
PMID 19576567·Am J Hum Genet·2009
7-preclinical
Overcoming extractability hurdles of a 14C labeled taxane analogue milataxel and its metabolite from xenograft mouse tumor and brain tissues.
PMID 19186016·J Pharm Biomed Anal·2009
7-preclinical
Profound, prelingual nonsyndromic deafness maps to chromosome 10q21 and is caused by a novel missense mutation in the Usher syndrome type IF gene PCDH15.
PMID 19107147·Eur J Hum Genet·2009
8-other
Evidence for a distinct ligand binding site on tubulin discovered through inhibition by GDP of paclitaxel-induced tubulin assembly in the absence of exogenous GTP.
PMID 19161972·Arch Biochem Biophys·2009
8-other
Mutation spectrum of MYO7A and evaluation of a novel nonsyndromic deafness DFNB2 allele with residual function.
PMID 18181211·Hum Mutat·2008
7-preclinical
Accuracy of dose measurements and calculations within and beyond heterogeneous tissues for 6 MV photon fields smaller than 4 cm produced by Cyberknife.
PMID 18649456·Med Phys·2008
8-other
Dosimetric verification of intensity modulated radiation therapy of 172 patients treated for various disease sites: comparison of EBT film dosimetry, ion chamber measurements, and independent MU calculations.
PMID 18973859·Med Dosim·2008
4-observational
Comparison of the epson expression 1680 flatbed and the vidar VXR-16 dosimetry PRO film scanners for use in IMRT dosimetry using gafchromic and radiographic film.
PMID 17278488·Med Phys·2007
4-observational
Using a conceptual framework during learning attenuates the loss of expert-type knowledge structure.
PMID 16848903·BMC Med Educ·2006
8-other
The tip-link antigen, a protein associated with the transduction complex of sensory hair cells, is protocadherin-15.
PMID 16807332·J Neurosci·2006
7-preclinical
Mutations in TRIOBP, which encodes a putative cytoskeletal-organizing protein, are associated with nonsyndromic recessive deafness.
PMID 16385457·Am J Hum Genet·2006
4-observational
'His brain is totally different': an analysis of care-staff explanations of aggressive challenging behaviour and the impact of gendered discourses.
PMID 16573879·Br J Soc Psychol·2006
8-other
A new locus for nonsyndromic deafness DFNB49 maps to chromosome 5q12.3-q14.1.
PMID 15538632·Hum Genet·2005
8-other
DFNB48, a new nonsyndromic recessive deafness locus, maps to chromosome 15q23-q25.1.
PMID 15711797·Hum Genet·2005
8-other
Characterization of a new full length TMPRSS3 isoform and identification of mutant alleles responsible for nonsyndromic recessive deafness in Newfoundland and Pakistan.
PMID 15447792·BMC Med Genet·2004
8-other
Mutations of ESPN cause autosomal recessive deafness and vestibular dysfunction.
PMID 15286153·J Med Genet·2004
7-preclinical
Claudin 14 knockout mice, a model for autosomal recessive deafness DFNB29, are deaf due to cochlear hair cell degeneration.
PMID 12913076·Hum Mol Genet·2003
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
- 409 39TH ST
UNION CITY, NJ 07087 - Phone
- (201) 867-5760
Quick Facts
- NPI
- 1497829634
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 43
- Publications
- 20
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