Shigihara T - Search Results

1

Human villous trophoblasts express and secrete placenta-specific microRNAs into maternal circulation via exosomes.

Luo SS, Ishibashi O, Ishikawa G, Ishikawa T, Katayama A, Mishima T, Takizawa T, Shigihara T, Goto T, Izumi A, Ohkuchi A, Matsubara S, Takeshita T, Takizawa T. Luo SS, et al. Among authors: shigihara t. Biol Reprod. 2009 Oct;81(4):717-29. doi: 10.1095/biolreprod.108.075481. Epub 2009 Jun 3. Biol Reprod. 2009. PMID: 19494253

2

Transcriptome profile of Trypanosoma cruzi-infected cells: simultaneous up- and down-regulation of proliferation inhibitors and promoters.

Shigihara T, Hashimoto M, Shindo N, Aoki T. Shigihara T, et al. Parasitol Res. 2008 Mar;102(4):715-22. doi: 10.1007/s00436-007-0819-x. Epub 2007 Dec 5. Parasitol Res. 2008. PMID: 18058129

3

Gene expression profile in diabetic KK/Ta mice.

Fan Q, Shike T, Shigihara T, Tanimoto M, Gohda T, Makita Y, Wang LN, Horikoshi S, Tomino Y. Fan Q, et al. Among authors: shigihara t. Kidney Int. 2003 Dec;64(6):1978-85. doi: 10.1046/j.1523-1755.2003.00312.x. Kidney Int. 2003. PMID: 14633120 Free article.

4

Two distinct pathways of p16 gene inactivation in gallbladder cancer.

Tadokoro H, Shigihara T, Ikeda T, Takase M, Suyama M. Tadokoro H, et al. Among authors: shigihara t. World J Gastroenterol. 2007 Dec 21;13(47):6396-403. doi: 10.3748/wjg.v13.i47.6396. World J Gastroenterol. 2007. PMID: 18081229 Free PMC article.

5

[Unilaterally dominant chronic idiopathic interstitial pneumonia complicated by pulmonary thromboembolism].

Takeshita K, Shigihara T, Shimizu T, Sato N, Matsubara H, Nishio K, Yamaguchi K. Takeshita K, et al. Among authors: shigihara t. Nihon Kokyuki Gakkai Zasshi. 1999 Nov;37(11):948-52. Nihon Kokyuki Gakkai Zasshi. 1999. PMID: 18217321 Japanese.

6

Mutations of ATP2C1 in Japanese patients with Hailey-Hailey disease: intrafamilial and interfamilial phenotype variations and lack of correlation with mutation patterns.

Ikeda S, Shigihara T, Mayuzumi N, Yu X, Ogawa H. Ikeda S, et al. Among authors: shigihara t. J Invest Dermatol. 2001 Dec;117(6):1654-6. doi: 10.1046/j.0022-202x.2001.01596.x. J Invest Dermatol. 2001. PMID: 11886536 Free article.

7

R162W mutation of keratin 9 in a family with autosomal dominant palmoplantar keratoderma with unique histologic features.

Mayuzumi N, Shigihara T, Ikeda S, Ogawa H. Mayuzumi N, et al. Among authors: shigihara t. J Investig Dermatol Symp Proc. 1999 Sep;4(2):150-2. doi: 10.1038/sj.jidsp.5640199. J Investig Dermatol Symp Proc. 1999. PMID: 10536990 Free article.

8

Recurrent R156H mutation of KRT10 in a Japanese family with bullous congenital ichthyosiform erythroderma.

Mayuzumi N, Shigihara T, Ikeda S, Ogawa H. Mayuzumi N, et al. Among authors: shigihara t. J Eur Acad Dermatol Venereol. 2000 Jul;14(4):304-6. doi: 10.1046/j.1468-3083.2000.00101.x. J Eur Acad Dermatol Venereol. 2000. PMID: 11204523

9

Mutations in ATP2A2 in patients with Darier's disease.

Ikeda S, Mayuzumi N, Shigihara T, Epstein EH Jr, Goldsmith LA, Ogawa H. Ikeda S, et al. Among authors: shigihara t. J Invest Dermatol. 2003 Sep;121(3):475-7. doi: 10.1046/j.1523-1747.2003.12400.x. J Invest Dermatol. 2003. PMID: 12925202 Free article. No abstract available.

10

Mutations in ATP2C1, encoding a calcium pump, cause Hailey-Hailey disease.

Hu Z, Bonifas JM, Beech J, Bench G, Shigihara T, Ogawa H, Ikeda S, Mauro T, Epstein EH Jr. Hu Z, et al. Among authors: shigihara t. Nat Genet. 2000 Jan;24(1):61-5. doi: 10.1038/71701. Nat Genet. 2000. PMID: 10615129

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

53 results

Search Page