Ohara O - Search Results

1

Two novel HSD3B2 missense mutations with diverse residual enzymatic activities for Δ5-steroids.

Takasawa K, Ono M, Hijikata A, Matsubara Y, Katsumata N, Takagi M, Morio T, Ohara O, Kashimada K, Mizutani S. Takasawa K, et al. Among authors: ohara o. Clin Endocrinol (Oxf). 2014 Jun;80(6):782-9. doi: 10.1111/cen.12394. Epub 2014 Jan 16. Clin Endocrinol (Oxf). 2014. PMID: 24372086

2

Post-transcriptional effects of phorbol 12-myristate 13-acetate on transcriptome of U937 cells.

Kitamura H, Nakagawa T, Takayama M, Kimura Y, Hijikata A, Ohara O. Kitamura H, et al. Among authors: ohara o. FEBS Lett. 2004 Dec 3;578(1-2):180-4. doi: 10.1016/j.febslet.2004.11.008. FEBS Lett. 2004. PMID: 15581638 Free article.

3

Construction of quantitative proteome reference maps of mouse spleen and lymph node based on two-dimensional gel electrophoresis.

Kimura Y, Yokoyama R, Ishizu Y, Nishigaki T, Murahashi Y, Hijikata A, Kitamura H, Ohara O. Kimura Y, et al. Among authors: ohara o. Proteomics. 2006 Jul;6(13):3833-44. doi: 10.1002/pmic.200500586. Proteomics. 2006. PMID: 16767787

4

Genome-wide identification and characterization of transcripts translationally regulated by bacterial lipopolysaccharide in macrophage-like J774.1 cells.

Kitamura H, Ito M, Yuasa T, Kikuguchi C, Hijikata A, Takayama M, Kimura Y, Yokoyama R, Kaji T, Ohara O. Kitamura H, et al. Among authors: ohara o. Physiol Genomics. 2008 Mar 14;33(1):121-32. doi: 10.1152/physiolgenomics.00095.2007. Epub 2008 Jan 29. Physiol Genomics. 2008. PMID: 18230670

5

Two brothers with ataxia-telangiectasia-like disorder with lung adenocarcinoma.

Uchisaka N, Takahashi N, Sato M, Kikuchi A, Mochizuki S, Imai K, Nonoyama S, Ohara O, Watanabe F, Mizutani S, Hanada R, Morio T. Uchisaka N, et al. Among authors: ohara o. J Pediatr. 2009 Sep;155(3):435-8. doi: 10.1016/j.jpeds.2009.02.037. J Pediatr. 2009. PMID: 19732584

6

Unique activation status of peripheral blood mononuclear cells at acute phase of Kawasaki disease.

Ikeda K, Yamaguchi K, Tanaka T, Mizuno Y, Hijikata A, Ohara O, Takada H, Kusuhara K, Hara T. Ikeda K, et al. Among authors: ohara o. Clin Exp Immunol. 2010 May;160(2):246-55. doi: 10.1111/j.1365-2249.2009.04073.x. Epub 2009 Dec 15. Clin Exp Immunol. 2010. PMID: 20015095 Free PMC article.

7

Mutation@A Glance: an integrative web application for analysing mutations from human genetic diseases.

Hijikata A, Raju R, Keerthikumar S, Ramabadran S, Balakrishnan L, Ramadoss SK, Pandey A, Mohan S, Ohara O. Hijikata A, et al. Among authors: ohara o. DNA Res. 2010 Jun;17(3):197-208. doi: 10.1093/dnares/dsq010. Epub 2010 Apr 1. DNA Res. 2010. PMID: 20360267 Free PMC article.

8

Analysis of mutations and recombination activity in RAG-deficient patients.

Asai E, Wada T, Sakakibara Y, Toga A, Toma T, Shimizu T, Nampoothiri S, Imai K, Nonoyama S, Morio T, Muramatsu H, Kamachi Y, Ohara O, Yachie A. Asai E, et al. Among authors: ohara o. Clin Immunol. 2011 Feb;138(2):172-7. doi: 10.1016/j.clim.2010.11.005. Epub 2010 Dec 4. Clin Immunol. 2011. PMID: 21131235

9

Detection of base substitution-type somatic mosaicism of the NLRP3 gene with >99.9% statistical confidence by massively parallel sequencing.

Izawa K, Hijikata A, Tanaka N, Kawai T, Saito MK, Goldbach-Mansky R, Aksentijevich I, Yasumi T, Nakahata T, Heike T, Nishikomori R, Ohara O. Izawa K, et al. Among authors: ohara o. DNA Res. 2012 Apr;19(2):143-52. doi: 10.1093/dnares/dsr047. Epub 2012 Jan 24. DNA Res. 2012. PMID: 22279087 Free PMC article.

10

A novel Wiskott-Aldrich syndrome protein mutation in an infant with thrombotic thrombocytopenic purpura.

Kawasaki Y, Toyoda H, Otsuki S, Iwasa T, Iwamoto S, Azuma E, Itoh-Habe N, Wada H, Fujimura Y, Morio T, Imai K, Mitsuiki N, Ohara O, Komada Y. Kawasaki Y, et al. Among authors: ohara o. Eur J Haematol. 2013 Feb;90(2):164-8. doi: 10.1111/ejh.12057. Epub 2013 Jan 7. Eur J Haematol. 2013. PMID: 23237501

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