Literature DB >> 16911293

L457F missense mutation within the 2B rod domain of keratin 9 in a Japanese family with epidermolytic palmoplantar keratoderma.

A Kon1, N Ito, Y Kudo, K Nomura, K Yoneda, K Hanada, I Hashimoto, K Takagaki.   

Abstract

Entities:  

Mesh：

Substances：

Year:  2006        PMID： 16911293     DOI： 10.1111/j.1365-2133.2006.07358.x

Source DB:  PubMed          Journal:  Br J Dermatol        ISSN： 0007-0963            Impact factor:   9.302


× No keyword cloud information.
  4 in total

1.  Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families.

Authors:  Naveed Wasif; Syed Kamran ul-Hassan Naqvi; Sulman Basit; Nadir Ali; Muhammad Ansar; Wasim Ahmad
Journal:  Hum Genet       Date:  2010-12-28       Impact factor: 4.132

Review 2.  Keratin gene mutations in disorders of human skin and its appendages.

Authors:  Jean Christopher Chamcheu; Imtiaz A Siddiqui; Deeba N Syed; Vaqar M Adhami; Mirjana Liovic; Hasan Mukhtar
Journal:  Arch Biochem Biophys       Date:  2010-12-19       Impact factor: 4.013

3.  Mutations in the keratin 9 gene in Pakistani families with epidermolytic palmoplantar keratoderma.

Authors:  Y Shimomura; M Wajid; J Weiser; L Kraemer; A M Christiano
Journal:  Clin Exp Dermatol       Date:  2010-10       Impact factor: 3.470

Review 4.  The molecular basis of human keratin disorders.

Authors:  Meral Julia Arin
Journal:  Hum Genet       Date:  2009-02-27       Impact factor: 4.132
  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.