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ADAM IRVINE, DMD
DMD
Oral and Maxillofacial Surgery (Dentist)
NPI: 1922366939Individual
Specialties, Licenses & Credentials
Oral and Maxillofacial Surgery (Dentist)Primary
Dentist — Oral and Maxillofacial Surgery
Code: 1223S0112X
0001(ZZ)
Research & Publications (20)
Copy-number mutations on chromosome 17q24.2-q24.3 in congenital generalized hypertrichosis terminalis with or without gingival hyperplasia.
PMID 19463983·Am J Hum Genet·2009
8-other
Towards a unified classification of the ectodermal dysplasias: opportunities outweigh challenges.
PMID 19681131·Am J Med Genet A·2009
6-review
CCN3: a key growth regulator in Chronic Myeloid Leukaemia.
PMID 19623482·J Cell Commun Signal·2009
8-other
Proteasome proteolytic profile is linked to Bcr-Abl expression.
PMID 19157685·Exp Hematol·2009
8-other
Carrier status for the common R501X and 2282del4 filaggrin mutations is not associated with hearing phenotypes in 5,377 children from the ALSPAC cohort.
PMID 19492053·PLoS One·2009
8-other
A rapid and sensitive method for measuring cell adhesion.
PMID 19370401·J Cell Commun Signal·2009
8-other
Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis.
PMID 19122663·Nat Genet·2009
5-case
Meta-analysis of filaggrin polymorphisms in eczema and asthma: robust risk factors in atopic disease.
PMID 19501237·J Allergy Clin Immunol·2009
1-meta
The treatment of viral warts with topical cidofovir 1%: our experience of seven paediatric patients.
PMID 19067689·Br J Dermatol·2009
8-other
Filaggrin in the frontline: role in skin barrier function and disease.
PMID 19386895·J Cell Sci·2009
7-preclinical
A homozygous frameshift mutation in the mouse Flg gene facilitates enhanced percutaneous allergen priming.
PMID 19349982·Nat Genet·2009
7-preclinical
TN-TIES: A system for extracting temporal information from emergency department triage notes.
PMID 18998945·AMIA Annu Symp Proc·2008
8-other
Juvenile localised scleroderma: a retrospective review of response to systemic treatment.
PMID 18941862·Ir J Med Sci·2008
8-other
Report on the fifth international workshop on the CCN family of genes.
PMID 19156540·J Cell Commun Signal·2008
8-other
The role of filaggrin loss-of-function mutations in atopic dermatitis.
PMID 18769192·Curr Opin Allergy Clin Immunol·2008
6-review
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 11018 ALBURY PARK LN
TOMBALL, TX 77375 - Phone
- (281) 687-2628
Quick Facts
- NPI
- 1922366939
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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