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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 

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Ken Arita

Department of Dermatology

Hokkaido University Graduate School of Medicine

Sapporo

Japan

[email]@med.hokudai.ac.jp

Name/email consistency: high

 
 
 
 
 
 
 

Affiliation

  • Department of Dermatology, Hokkaido University Graduate School of Medicine, Sapporo, Japan. 2002 - 2006

References

  1. A novel N14Y mutation in Connexin26 in keratitis-ichthyosis-deafness syndrome: analyses of altered gap junctional communication and molecular structure of N terminus of mutated Connexin26. Arita, K., Akiyama, M., Aizawa, T., Umetsu, Y., Segawa, I., Goto, M., Sawamura, D., Demura, M., Kawano, K., Shimizu, H. Am. J. Pathol. (2006) [Pubmed]
  2. Erythrokeratoderma variabilis without connexin 31 or connexin 30.3 gene mutation: immunohistological, ultrastructural and genetic studies. Arita, K., Akiyama, M., Tsuji, Y., Onozuka, T., Shimizu, H. Acta Derm. Venereol. (2003) [Pubmed]
  3. Changes in gap junction distribution and connexin expression pattern during human fetal skin development. Arita, K., Akiyama, M., Tsuji, Y., McMillan, J.R., Eady, R.A., Shimizu, H. J. Histochem. Cytochem. (2002) [Pubmed]
 
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