Back to Search
JOHN COMMON, DMD
DMD
Dentist
NPI: 1558433581Individual
Specialties, Licenses & Credentials
DentistPrimary
Dentist
Code: 122300000X
1790 0321(SC)
Research & Publications (14)
Clinical and genetic heterogeneity of erythrokeratoderma variabilis.
PMID 16297190·J Invest Dermatol·2005
8-other
Specific loss of connexin 26 expression in ductal sweat gland epithelium associated with the deletion mutation del(GJB6-D13S1830).
PMID 16197390·Clin Exp Dermatol·2005
8-other
Functional studies of human skin disease- and deafness-associated connexin 30 mutations.
PMID 12419304·Biochem Biophys Res Commun·2002
8-other
A case of dermatopathia pigmentosa reticularis with wiry scalp hair and digital fibromatosis resulting from a recurrent KRT14 mutation.
PMID 19040520·Clin Exp Dermatol·2009
5-case
The Human Intermediate Filament Database: comprehensive information on a gene family involved in many human diseases.
PMID 18033728·Hum Mutat·2008
8-other
Stem cell patterns in cell lines derived from head and neck squamous cell carcinoma.
PMID 17944752·J Oral Pathol Med·2007
8-other
Connexin interaction patterns in keratinocytes revealed morphologically and by FRET analysis.
PMID 15769851·J Cell Sci·2005
4-observational
Further evidence for heterozygote advantage of GJB2 deafness mutations: a link with cell survival.
PMID 15235031·J Med Genet·2004
8-other
Defective trafficking and cell death is characteristic of skin disease-associated connexin 31 mutations.
PMID 12165562·Hum Mol Genet·2002
8-other
Diagnosis and confirmation of epidermolytic palmoplantar keratoderma by the identification of mutations in keratin 9 using denaturing high-performance liquid chromatography.
PMID 12072061·Br J Dermatol·2002
8-other
Connexin 26 expression and mutation analysis in epidermal disease.
PMID 12064628·Cell Commun Adhes·2001
7-preclinical
A case of erythrokeratoderma variabilis without mutations in connexin 31.
PMID 11122035·Br J Dermatol·2000
5-case
Recessive mutation in desmoplakin disrupts desmoplakin-intermediate filament interactions and causes dilated cardiomyopathy, woolly hair and keratoderma.
PMID 11063735·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
- 321 N LAUREL ST
SUMMERVILLE, SC 29483 - Phone
- (843) 871-6636
Quick Facts
- NPI
- 1558433581
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 14
Are you this provider?
Claim Your Profile