Ito M - Search Results

1

Case of hypohidrotic ectodermal dysplasia caused by a large deletion mutation in the EDA gene.

Hayashi R, Farooq M, Fujikawa H, Fujimoto A, Hashimoto T, Ito M, Shimomura Y. Hayashi R, et al. Among authors: ito m. J Dermatol. 2013 Apr;40(4):281-3. doi: 10.1111/1346-8138.12077. Epub 2013 Jan 7. J Dermatol. 2013. PMID: 23293949 No abstract available.

2

hKAP1.6 and hKAP1.7, two novel human high sulfur keratin-associated proteins are expressed in the hair follicle cortex.

Shimomura Y, Aoki N, Rogers MA, Langbein L, Schweizer J, Ito M. Shimomura Y, et al. Among authors: ito m. J Invest Dermatol. 2002 Feb;118(2):226-31. doi: 10.1046/j.0022-202x.2001.01653.x. J Invest Dermatol. 2002. PMID: 11841537 Free article.

3

Polymorphisms in the human high sulfur hair keratin-associated protein 1, KAP1, gene family.

Shimomura Y, Aoki N, Schweizer J, Langbein L, Rogers MA, Winter H, Ito M. Shimomura Y, et al. Among authors: ito m. J Biol Chem. 2002 Nov 22;277(47):45493-501. doi: 10.1074/jbc.M206398200. Epub 2002 Sep 11. J Biol Chem. 2002. PMID: 12228244 Free article.

4

Characterization of human keratin-associated protein 1 family members.

Shimomura Y, Aoki N, Rogers MA, Langbein L, Schweizer J, Ito M. Shimomura Y, et al. Among authors: ito m. J Investig Dermatol Symp Proc. 2003 Jun;8(1):96-9. doi: 10.1046/j.1523-1747.2003.12180.x. J Investig Dermatol Symp Proc. 2003. PMID: 12895003 Free article. Review.

5

A rare case of hypohidrotic ectodermal dysplasia caused by compound heterozygous mutations in the EDAR gene.

Shimomura Y, Sato N, Miyashita A, Hashimoto T, Ito M, Kuwano R. Shimomura Y, et al. Among authors: ito m. J Invest Dermatol. 2004 Oct;123(4):649-55. doi: 10.1111/j.0022-202X.2004.23405.x. J Invest Dermatol. 2004. PMID: 15373768 Free article.

6

Size polymorphisms in the human ultrahigh sulfur hair keratin-associated protein 4, KAP4, gene family.

Kariya N, Shimomura Y, Ito M. Kariya N, et al. Among authors: ito m. J Invest Dermatol. 2005 Jun;124(6):1111-8. doi: 10.1111/j.0022-202X.2005.23662.x. J Invest Dermatol. 2005. PMID: 15955084 Free article.

7

Human hair keratin-associated proteins.

Shimomura Y, Ito M. Shimomura Y, et al. Among authors: ito m. J Investig Dermatol Symp Proc. 2005 Dec;10(3):230-3. doi: 10.1111/j.1087-0024.2005.10112.x. J Investig Dermatol Symp Proc. 2005. PMID: 16382671 Free article.

8

Mutations in the desmoglein 4 gene are associated with monilethrix-like congenital hypotrichosis.

Shimomura Y, Sakamoto F, Kariya N, Matsunaga K, Ito M. Shimomura Y, et al. Among authors: ito m. J Invest Dermatol. 2006 Jun;126(6):1281-5. doi: 10.1038/sj.jid.5700113. J Invest Dermatol. 2006. PMID: 16439973 Free article.

9

Mutations in the LIPH gene in three Japanese families with autosomal recessive woolly hair/hypotrichosis.

Shimomura Y, Ito M, Christiano AM. Shimomura Y, et al. Among authors: ito m. J Dermatol Sci. 2009 Dec;56(3):205-7. doi: 10.1016/j.jdermsci.2009.08.005. Epub 2009 Nov 4. J Dermatol Sci. 2009. PMID: 19892526 Free PMC article. No abstract available.

10

Hypohidrotic ectodermal dysplasia caused by a missense mutation in the EDA gene.

Fujimoto A, Farooq M, Sato N, Masui Y, Fujikawa H, Ito M, Shimomura Y. Fujimoto A, et al. Among authors: ito m. Eur J Dermatol. 2011 Sep-Oct;21(5):801-3. doi: 10.1684/ejd.2011.1460. Eur J Dermatol. 2011. PMID: 21715252 No abstract available.

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