Ihara K - Search Results

1

Neuroendocrine phenotypes in a boy with 5q14 deletion syndrome implicate the regulatory roles of myocyte-specific enhancer factor 2C in the postnatal hypothalamus.

Sakai Y, Ohkubo K, Matsushita Y, Akamine S, Ishizaki Y, Torisu H, Ihara K, Sanefuji M, Kim MS, Lee KU, Shaw CA, Lim J, Nakabeppu Y, Hara T. Sakai Y, et al. Among authors: ihara k. Eur J Med Genet. 2013 Sep;56(9):475-83. doi: 10.1016/j.ejmg.2013.06.009. Epub 2013 Jul 5. Eur J Med Genet. 2013. PMID: 23832106

2

Perforin defects of primary haemophagocytic lymphohistiocytosis in Japan.

Suga N, Takada H, Nomura A, Ohga S, Ishii E, Ihara K, Ohshima K, Hara T. Suga N, et al. Among authors: ihara k. Br J Haematol. 2002 Feb;116(2):346-9. doi: 10.1046/j.1365-2141.2002.03266.x. Br J Haematol. 2002. PMID: 11841437 Free article.

3

A case of growth hormone and gonadotropin deficiency associated with unilateral anophthalmia, microphallus, cryptorchidism, and mental retardation.

Miyako K, Takemoto M, Ihara K, Kuromaru R, Kohno H, Hara T. Miyako K, et al. Among authors: ihara k. Endocr J. 2002 Feb;49(1):15-20. doi: 10.1507/endocrj.49.15. Endocr J. 2002. PMID: 12008745 Free article.

4

Contribution of the interleukin 4 gene to susceptibility to subacute sclerosing panencephalitis.

Inoue T, Kira R, Nakao F, Ihara K, Bassuny WM, Kusuhara K, Nihei K, Takeshita K, Hara T. Inoue T, et al. Among authors: ihara k. Arch Neurol. 2002 May;59(5):822-7. doi: 10.1001/archneur.59.5.822. Arch Neurol. 2002. PMID: 12020266

5

A functional polymorphism in fas (CD95/APO-1) gene promoter associated with systemic lupus erythematosus.

Kanemitsu S, Ihara K, Saifddin A, Otsuka T, Takeuchi T, Nagayama J, Kuwano M, Hara T. Kanemitsu S, et al. Among authors: ihara k. J Rheumatol. 2002 Jun;29(6):1183-8. J Rheumatol. 2002. PMID: 12064832

6

Association study of the NRAMP1 gene promoter polymorphism and early-onset type 1 diabetes.

Bassuny WM, Ihara K, Matsuura N, Ahmed S, Kohno H, Kuromaru R, Miyako K, Hara T. Bassuny WM, et al. Among authors: ihara k. Immunogenetics. 2002 Jul;54(4):282-5. doi: 10.1007/s00251-002-0459-3. Epub 2002 Jun 14. Immunogenetics. 2002. PMID: 12136340

7

Dominant expression of interleukin 10 but not interferon gamma in CD4(-)CD8(-)alphabetaT cells of autoimmune lymphoproliferative syndrome.

Ohga S, Nomura A, Takahata Y, Ihara K, Takada H, Wakiguchi H, Kudo Y, Hara T. Ohga S, et al. Among authors: ihara k. Br J Haematol. 2002 Nov;119(2):535-8. doi: 10.1046/j.1365-2141.2002.03848.x. Br J Haematol. 2002. PMID: 12406097 Free article.

8

Founder effect of the C9 R95X mutation in Orientals.

Khajoee V, Ihara K, Kira R, Takemoto M, Torisu H, Sakai Y, Guanjun J, Hee PM, Tokunaga K, Hara T. Khajoee V, et al. Among authors: ihara k. Hum Genet. 2003 Mar;112(3):244-8. doi: 10.1007/s00439-002-0870-8. Epub 2003 Jan 9. Hum Genet. 2003. PMID: 12596049

9

Cytokine imbalance in hyper-IgE syndrome: reduced expression of transforming growth factor beta and interferon gamma genes in circulating activated T cells.

Ohga S, Nomura A, Ihara K, Takahata Y, Suga N, Akeda H, Shibata R, Okamura J, Kinukawa N, Hara T. Ohga S, et al. Among authors: ihara k. Br J Haematol. 2003 Apr;121(2):324-31. doi: 10.1046/j.1365-2141.2003.04267.x. Br J Haematol. 2003. PMID: 12694256 Free article.

10

Inducible and endothelial constitutive nitric oxide synthase gene polymorphisms in Kawasaki disease.

Khajoee V, Kariyazono H, Ohno T, Ihara K, Mizuno Y, Kusuhara K, Hara T. Khajoee V, et al. Among authors: ihara k. Pediatr Int. 2003 Apr;45(2):130-4. doi: 10.1046/j.1442-200x.2003.01684.x. Pediatr Int. 2003. PMID: 12709136

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