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WILLIAM WILCOX, D.M.D.
D.M.D.
Dentist
NPI: 1366479164Individual
Specialties, Licenses & Credentials
DentistPrimary
Dentist
Code: 122300000X
5068(CT)
Research & Publications (20)
FGFR3 promotes synchondrosis closure and fusion of ossification centers through the MAPK pathway.
PMID 18923003·Hum Mol Genet·2009
7-preclinical
High molecular weight FGF2: the biology of a nuclear growth factor.
PMID 18850066·Cell Mol Life Sci·2009
6-review
Fibroblast growth factor inhibits interferon gamma-STAT1 and interleukin 6-STAT3 signaling in chondrocytes.
PMID 18950705·Cell Signal·2009
7-preclinical
Lysosomal Disease Network's "WORLD Symposium 2009". Introduction.
PMID 19083251·Mol Genet Metab·2009
8-other
Experimental comparison of tracking algorithms in the presence of aircraft boundary-layer distortions for emulated free-space laser communication links.
PMID 19107161·Appl Opt·2009
8-other
Fabry disease: progression of nephropathy, and prevalence of cardiac and cerebrovascular events before enzyme replacement therapy.
PMID 19218538·Nephrol Dial Transplant·2009
8-other
Emulation of dynamic wavefront disturbances using a deformable mirror.
PMID 19259183·Opt Express·2009
8-other
A novel interaction between fibroblast growth factor receptor 3 and the p85 subunit of phosphoinositide 3-kinase: activation-dependent regulation of ERK by p85 in multiple myeloma cells.
PMID 19286672·Hum Mol Genet·2009
8-other
AORN Interviews . . . William H. Wilcox: part one of two-part Interview. Interview by Patricia C. Seifert.
PMID 19499630·AORN J·2009
8-other
AORN interviews...William H Wilcox. Interview by Patricia C Seifert.
PMID 19606573·AORN J·2009
8-other
Analysis of STAT1 activation by six FGFR3 mutants associated with skeletal dysplasia undermines dominant role of STAT1 in FGFR3 signaling in cartilage.
PMID 19088846·PLoS One·2008
7-preclinical
Gerodermia osteodysplastica is caused by mutations in SCYL1BP1, a Rab-6 interacting golgin.
PMID 18997784·Nat Genet·2008
8-other
WITHDRAWN: Familial Degenerative Encephalopathy with Intracranial Calcification and Metaphyseal Dysplasia.
PMID 19016590·J Bone Miner Res·2008
8-other
Reversible leukoencephalopathy with acute neurological deterioration and permanent residua in classical homocystinuria: A case report.
PMID 18210212·J Inherit Metab Dis·2008
8-other
Characterization of Fabry disease in 352 pediatric patients in the Fabry Registry.
PMID 18596579·Pediatr Res·2008
8-other
Living and loving "decent": religion and relationship quality among urban parents.
PMID 18784851·Soc Sci Res·2008
8-other
Evaluation of prenatal-onset osteochondrodysplasias by ultrasonography: a retrospective and prospective analysis.
PMID 18627037·Am J Med Genet A·2008
8-other
Females with Fabry disease frequently have major organ involvement: lessons from the Fabry Registry.
PMID 18037317·Mol Genet Metab·2008
8-other
Gain-of-function mutations in TRPV4 cause autosomal dominant brachyolmia.
PMID 18587396·Nat Genet·2008
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
- 1005 FARMINGTON AVE
WEST HARTFORD, CT 06107 - Phone
- (860) 232-7270
Quick Facts
- NPI
- 1366479164
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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