Okada S - Search Results

1

IRAK4 Deficiency Presenting with Anti-NMDAR Encephalitis and HHV6 Reactivation.

Nishimura S, Kobayashi Y, Ohnishi H, Moriya K, Tsumura M, Sakata S, Mizoguchi Y, Takada H, Kato Z, Sancho-Shimizu V, Picard C, Irani SR, Ohara O, Casanova JL, Puel A, Ishikawa N, Okada S, Kobayashi M. Nishimura S, et al. Among authors: okada s. J Clin Immunol. 2021 Jan;41(1):125-135. doi: 10.1007/s10875-020-00885-5. Epub 2020 Oct 20. J Clin Immunol. 2021. PMID: 33083971 Free PMC article.

2

A comparison of the defective granulopoiesis in childhood cyclic neutropenia and in severe congenital neutropenia.

Sera Y, Kawaguchi H, Nakamura K, Sato T, Habara M, Okada S, Ishikawa N, Kojima S, Katoh O, Kobayashi M. Sera Y, et al. Among authors: okada s. Haematologica. 2005 Aug;90(8):1032-41. Haematologica. 2005. PMID: 16079102

3

[X-linked hypogammaglobulinemia with growth hormone deficiency].

Okada S, Miyagawa S, Nishimura S, Kobayashi M, Nishi Y. Okada S, et al. Nihon Rinsho. 2006 May 28;Suppl 1:67-9. Nihon Rinsho. 2006. PMID: 16776095 Review. Japanese. No abstract available.

4

Steroid-dependent ACTH-produced thymic carcinoid: regulation of POMC gene expression by cortisol via methylation of its promoter region.

Mizoguchi Y, Kajiume T, Miyagawa S, Okada S, Nishi Y, Kobayashi M. Mizoguchi Y, et al. Among authors: okada s. Horm Res. 2007;67(5):257-62. doi: 10.1159/000098548. Epub 2007 Jan 12. Horm Res. 2007. PMID: 17220632

5

The novel IFNGR1 mutation 774del4 produces a truncated form of interferon-gamma receptor 1 and has a dominant-negative effect on interferon-gamma signal transduction.

Okada S, Ishikawa N, Shirao K, Kawaguchi H, Tsumura M, Ohno Y, Yasunaga S, Ohtsubo M, Takihara Y, Kobayashi M. Okada S, et al. J Med Genet. 2007 Aug;44(8):485-91. doi: 10.1136/jmg.2007.049635. Epub 2007 May 18. J Med Genet. 2007. PMID: 17513528 Free PMC article.

6

A novel mutation (Gln433Glu) in exon 12 combined with the G insertion in exon 13 causes severe factor XI deficiency in Japanese patients.

Ishikawa N, Okada S, Sato T, Yasunaga S, Ohtsubo M, Takihara Y, Kobayashi M. Ishikawa N, et al. Among authors: okada s. Blood Coagul Fibrinolysis. 2007 Jul;18(5):519-23. doi: 10.1097/MBC.0b013e328133f553. Blood Coagul Fibrinolysis. 2007. PMID: 17581330

7

Polycomb-group complex 1 acts as an E3 ubiquitin ligase for Geminin to sustain hematopoietic stem cell activity.

Ohtsubo M, Yasunaga S, Ohno Y, Tsumura M, Okada S, Ishikawa N, Shirao K, Kikuchi A, Nishitani H, Kobayashi M, Takihara Y. Ohtsubo M, et al. Among authors: okada s. Proc Natl Acad Sci U S A. 2008 Jul 29;105(30):10396-401. doi: 10.1073/pnas.0800672105. Epub 2008 Jul 23. Proc Natl Acad Sci U S A. 2008. PMID: 18650381 Free PMC article.

8

Development of a new enzymatic diagnosis method for very-long-chain Acyl-CoA dehydrogenase deficiency by detecting 2-hexadecenoyl-CoA production and its application in tandem mass spectrometry-based selective screening and newborn screening in Japan.

Tajima G, Sakura N, Shirao K, Okada S, Tsumura M, Nishimura Y, Ono H, Hasegawa Y, Hata I, Naito E, Yamaguchi S, Shigematsu Y, Kobayashi M. Tajima G, et al. Among authors: okada s. Pediatr Res. 2008 Dec;64(6):667-72. doi: 10.1203/PDR.0b013e318187cc44. Pediatr Res. 2008. PMID: 18670371

9

Molecular pathogenesis of a novel mutation, G108D, in short-chain acyl-CoA dehydrogenase identified in subjects with short-chain acyl-CoA dehydrogenase deficiency.

Shirao K, Okada S, Tajima G, Tsumura M, Hara K, Yasunaga S, Ohtsubo M, Hata I, Sakura N, Shigematsu Y, Takihara Y, Kobayashi M. Shirao K, et al. Among authors: okada s. Hum Genet. 2010 Jun;127(6):619-28. doi: 10.1007/s00439-010-0822-7. Epub 2010 Apr 8. Hum Genet. 2010. PMID: 20376488 Review.

10

[Hematological malignancies in congenital neutropenia].

Okada S, Nakamura K, Kobayashi M. Okada S, et al. Rinsho Ketsueki. 2010 Jul;51(7):553-8. Rinsho Ketsueki. 2010. PMID: 20693776 Review. Japanese. No abstract available.

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