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ANDREW PAIGE, DMD
Orthodontics and Dentofacial Orthopedics Dentistry
NPI: 1750177739Individual
Specialties, Licenses & Credentials
Orthodontics and Dentofacial Orthopedics DentistryPrimary
Dentist — Orthodontics and Dentofacial Orthopedics
Code: 1223X0400X
DE61526215(WA)
Research & Publications (16)
PPM1D is a potential therapeutic target in ovarian clear cell carcinomas.
PMID 19293255·Clin Cancer Res·2009
8-other
WWOX gene expression abolishes ovarian cancer tumorigenicity in vivo and decreases attachment to fibronectin via integrin alpha3.
PMID 19458077·Cancer Res·2009
7-preclinical
Cortical and subcortical networks in human secondarily generalized tonic-clonic seizures.
PMID 19339252·Brain·2009
8-other
Clinical use of ictal SPECT in secondarily generalized tonic-clonic seizures.
PMID 19339251·Brain·2009
4-observational
Homozygous deletions may be markers of nearby heterozygous mutations: The complex deletion at FRA16D in the HCT116 colon cancer cell line removes exons of WWOX.
PMID 18273838·Genes Chromosomes Cancer·2008
8-other
Structural and functional neuroimaging correlates of depression in temporal lobe epilepsy.
PMID 17215168·Epilepsy Behav·2007
8-other
WWOX mRNA expression profile in epithelial ovarian cancer supports the role of WWOX variant 1 as a tumour suppressor, although the role of variant 4 remains unclear.
PMID 15870886·Int J Oncol·2005
8-other
Localizing value of ictal-interictal SPECT analyzed by SPM (ISAS).
PMID 16146441·Epilepsia·2005
4-observational
Positive and negative network correlations in temporal lobe epilepsy.
PMID 15084494·Cereb Cortex·2004
3-trial
Redefining tumour suppressor genes: exceptions to the two-hit hypothesis.
PMID 14618262·Cell Mol Life Sci·2003
6-review
Defects in whirlin, a PDZ domain molecule involved in stereocilia elongation, cause deafness in the whirler mouse and families with DFNB31.
PMID 12833159·Nat Genet·2003
7-preclinical
WWOX: a candidate tumor suppressor gene involved in multiple tumor types.
PMID 11572989·Proc Natl Acad Sci U S A·2001
7-preclinical
A 700-kb physical map of a region of 16q23.2 homozygously deleted in multiple cancers and spanning the common fragile site FRA16D.
PMID 10749141·Cancer Res·2000
8-other
A deletion on chromosome 4 cosegregates with the whirler deafness mutation: exclusion of Orm1 as a candidate.
PMID 10602993·Mamm Genome·2000
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
- 7530 164TH AVE NE STE A250
REDMOND, WA 98052 - Phone
- (425) 861-9685
Quick Facts
- NPI
- 1750177739
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 16
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