Takeichi T - Search Results

1

Ceramide Analysis in Combination With Genetic Testing May Provide a Precise Diagnosis for Self-Healing Collodion Babies.

Takeichi T, Ohno Y, Tanahashi K, Ito Y, Shiraishi K, Utsunomiya R, Yoshida S, Ikeda K, Nomura H, Morizane S, Sayama K, Ogi T, Muro Y, Kihara A, Akiyama M. Takeichi T, et al. J Lipid Res. 2022 Dec;63(12):100308. doi: 10.1016/j.jlr.2022.100308. Epub 2022 Nov 1. J Lipid Res. 2022. PMID: 36332686 Free PMC article.

2

Overexpression of LEDGF/DFS70 induces IL-6 via p38 activation in HaCaT cells, similar to that seen in the psoriatic condition.

Takeichi T, Sugiura K, Muro Y, Matsumoto K, Ogawa Y, Futamura K, Kaminuma O, Hashimoto N, Shimoyama Y, Saito H, Tomita Y. Takeichi T, et al. J Invest Dermatol. 2010 Dec;130(12):2760-7. doi: 10.1038/jid.2010.203. Epub 2010 Jul 15. J Invest Dermatol. 2010. PMID: 20631726 Free article.

3

LEDGF/DFS70 activates the MK2/IL6/STAT3 pathway in HaCaT.

Takeichi T, Sugiura K, Muro Y, Ogawa Y, Akiyama M. Takeichi T, et al. J Dermatol Sci. 2011 Sep;63(3):203-5. doi: 10.1016/j.jdermsci.2011.05.004. Epub 2011 May 20. J Dermatol Sci. 2011. PMID: 21676593 No abstract available.

4

Prevalent founder mutation c.736T>A of LIPH in autosomal recessive woolly hair of Japanese leads to variable severity of hypotrichosis in adulthood.

Tanahashi K, Sugiura K, Takeichi T, Takama H, Shinkuma S, Shimizu H, Akiyama M. Tanahashi K, et al. Among authors: takeichi t. J Eur Acad Dermatol Venereol. 2013 Sep;27(9):1182-4. doi: 10.1111/j.1468-3083.2012.04526.x. Epub 2012 Mar 26. J Eur Acad Dermatol Venereol. 2013. PMID: 22449147

5

Sporadic VACTERL association in a Japanese family with Sjögren-Larsson syndrome.

Takeichi T, Sugiura K, Arai H, Ishii K, Kono M, Akiyama M. Takeichi T, et al. Acta Derm Venereol. 2013 Sep 4;93(5):579-80. doi: 10.2340/00015555-1526. Acta Derm Venereol. 2013. PMID: 23450279 Free article. No abstract available.

6

The novel CTSC homozygous nonsense mutation p.Lys106X in a patient with Papillon-Lefèvre syndrome with all permanent teeth remaining at over 40 years of age.

Kobayashi T, Sugiura K, Takeichi T, Akiyama M. Kobayashi T, et al. Among authors: takeichi t. Br J Dermatol. 2013 Oct;169(4):948-50. doi: 10.1111/bjd.12429. Br J Dermatol. 2013. PMID: 23662908 No abstract available.

7

The majority of generalized pustular psoriasis without psoriasis vulgaris is caused by deficiency of interleukin-36 receptor antagonist.

Sugiura K, Takemoto A, Yamaguchi M, Takahashi H, Shoda Y, Mitsuma T, Tsuda K, Nishida E, Togawa Y, Nakajima K, Sakakibara A, Kawachi S, Shimizu M, Ito Y, Takeichi T, Kono M, Ogawa Y, Muro Y, Ishida-Yamamoto A, Sano S, Matsue H, Morita A, Mizutani H, Iizuka H, Muto M, Akiyama M. Sugiura K, et al. Among authors: takeichi t. J Invest Dermatol. 2013 Nov;133(11):2514-2521. doi: 10.1038/jid.2013.230. Epub 2013 May 22. J Invest Dermatol. 2013. PMID: 23698098 Free article.

8

Lamellar ichthyosis in a collodion baby caused by CYP4F22 mutations in a non-consanguineous family outside the Mediterranean.

Sugiura K, Takeichi T, Tanahashi K, Ito Y, Kosho T, Saida K, Uhara H, Okuyama R, Akiyama M. Sugiura K, et al. Among authors: takeichi t. J Dermatol Sci. 2013 Nov;72(2):193-5. doi: 10.1016/j.jdermsci.2013.06.008. Epub 2013 Jun 28. J Dermatol Sci. 2013. PMID: 23871423 No abstract available.

9

Next generation diagnostics of heritable connective tissue disorders.

Salam A, Simpson MA, Stone KL, Takeichi T, Nanda A, Akiyama M, McGrath JA. Salam A, et al. Among authors: takeichi t. Matrix Biol. 2014 Jan;33:35-40. doi: 10.1016/j.matbio.2013.06.004. Epub 2013 Jul 26. Matrix Biol. 2014. PMID: 23896220 Free article. Review.

10

Impact of next generation sequencing on diagnostics in a genetic skin disease clinic.

Takeichi T, Nanda A, Liu L, Salam A, Campbell P, Fong K, Akiyama M, Ozoemena L, Stone KL, Al-Ajmi H, Simpson MA, McGrath JA. Takeichi T, et al. Exp Dermatol. 2013 Dec;22(12):825-31. doi: 10.1111/exd.12276. Exp Dermatol. 2013. PMID: 24279917

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