The world's first wiki where authorship really matters (Nature Genetics, 2008). Due credit and reputation for authors. Imagine a global collaborative knowledge base for original thoughts. Search thousands of articles and collaborate with scientists around the globe.

wikigene or wiki gene protein drug chemical gene disease author authorship tracking collaborative publishing evolutionary knowledge reputation system wiki2.0 global collaboration genes proteins drugs chemicals diseases compound
Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 

Editor

Share

Personal info

View

Links

Table of contents

About

Terms

 

J. Timothy Wright

Dept. of Pediatric Dentistry

School of Dentistry

CB #7450 Brauer Hall

UNC Chapel Hill

USA

[email]@dentistry.unc.edu

Name/email consistency: high

 
 
 
 
 
 
 

Affiliation

  • Dept. of Pediatric Dentistry, School of Dentistry, CB #7450 Brauer Hall, UNC Chapel Hill, USA. 2000 - 2010

References

  1. Oral manifestations in the epidermolysis bullosa spectrum. Wright, J.T. Dermatol. Clin (2010) [Pubmed]
  2. Phenotypic variation in FAM83H-associated amelogenesis imperfecta. Wright, J.T., Frazier-Bowers, S., Simmons, D., Alexander, K., Crawford, P., Han, S.T., Hart, P.S., Hart, T.C. J. Dent. Res. (2009) [Pubmed]
  3. Human and mouse enamel phenotypes resulting from mutation or altered expression of AMEL, ENAM, MMP20 and KLK4. Wright, J.T., Hart, T.C., Hart, P.S., Simmons, D., Suggs, C., Daley, B., Simmer, J., Hu, J., Bartlett, J.D., Li, Y., Yuan, Z.A., Seow, W.K., Gibson, C.W. Cells. Tissues. Organs. (Print) (2009) [Pubmed]
  4. Classifying ectodermal dysplasias: Incorporating the molecular basis and pathways (Workshop II). Wright, J.T., Morris, C., Clements, S.E., D'Souza, R., Gaide, O., Mikkola, M., Zonana, J. Am. J. Med. Genet. A (2009) [Pubmed]
  5. The molecular control of and clinical variations in root formation. Wright, T. Cells. Tissues. Organs. (Print) (2007) [Pubmed]
  6. Human enamel phenotype associated with amelogenesis imperfecta and a kallikrein-4 (g.2142G>A) proteinase mutation. Wright, J.T., Daly, B., Simmons, D., Hong, S., Hart, S.P., Hart, T.C., Atsawasuwan, P., Yamauchi, M. Eur. J. Oral Sci. (2006) [Pubmed]
  7. The molecular etiologies and associated phenotypes of amelogenesis imperfecta. Wright, J.T. Am. J. Med. Genet. A (2006) [Pubmed]
  8. Relationship of phenotype and genotype in X-linked amelogenesis imperfecta. Wright, J.T., Hart, P.S., Aldred, M.J., Seow, K., Crawford, P.J., Hong, S.P., Gibson, C.W., Hart, T.C. Connect. Tissue Res. (2003) [Pubmed]
  9. The genome projects: implications for dental practice and education. Wright, J.T., Hart, T.C. J. Dent. Educ (2002) [Pubmed]
  10. The etch-bleach-seal technique for managing stained enamel defects in young permanent incisors. Wright, J.T. Pediatr. Dent (2002) [Pubmed]
  11. Normal formation and development defects of the human dentition. Wright, J.T. Pediatr. Clin. North Am. (2000) [Pubmed]
 
WikiGenes - Universities