Kondo N - Search Results

1

Selective utilization of nonhomologous end-joining and homologous recombination DNA repair pathways during nervous system development.

Orii KE, Lee Y, Kondo N, McKinnon PJ. Orii KE, et al. Among authors: kondo n. Proc Natl Acad Sci U S A. 2006 Jun 27;103(26):10017-22. doi: 10.1073/pnas.0602436103. Epub 2006 Jun 15. Proc Natl Acad Sci U S A. 2006. PMID: 16777961 Free PMC article.

2

Recurrent genomic alterations characterize medulloblastoma arising from DNA double-strand break repair deficiency.

Frappart PO, Lee Y, Russell HR, Chalhoub N, Wang YD, Orii KE, Zhao J, Kondo N, Baker SJ, McKinnon PJ. Frappart PO, et al. Among authors: kondo n. Proc Natl Acad Sci U S A. 2009 Feb 10;106(6):1880-5. doi: 10.1073/pnas.0806882106. Epub 2009 Jan 21. Proc Natl Acad Sci U S A. 2009. PMID: 19164512 Free PMC article.

3

Structural basis for the multiple interactions of the MyD88 TIR domain in TLR4 signaling.

Ohnishi H, Tochio H, Kato Z, Orii KE, Li A, Kimura T, Hiroaki H, Kondo N, Shirakawa M. Ohnishi H, et al. Among authors: kondo n. Proc Natl Acad Sci U S A. 2009 Jun 23;106(25):10260-5. doi: 10.1073/pnas.0812956106. Epub 2009 Jun 8. Proc Natl Acad Sci U S A. 2009. PMID: 19506249 Free PMC article.

4

Developmental changes of radiological findings in Fukuyama-type congenital muscular dystrophy.

Kato Z, Morimoto M, Orii KE, Kato T, Kondo N. Kato Z, et al. Among authors: kondo n. Pediatr Radiol. 2010 Dec;40 Suppl 1:S127-9. doi: 10.1007/s00247-010-1724-5. Epub 2010 Jun 23. Pediatr Radiol. 2010. PMID: 20571791

5

Changes of autonomic nervous system function in patients with breath-holding spells treated with iron.

Orii KE, Kato Z, Osamu F, Funato M, Kubodera U, Inoue R, Shimozawa N, Kondo N. Orii KE, et al. Among authors: kondo n. J Child Neurol. 2002 May;17(5):337-40. doi: 10.1177/088307380201700505. J Child Neurol. 2002. PMID: 12150579

6

STXBP1 mutations in early infantile epileptic encephalopathy with suppression-burst pattern.

Saitsu H, Kato M, Okada I, Orii KE, Higuchi T, Hoshino H, Kubota M, Arai H, Tagawa T, Kimura S, Sudo A, Miyama S, Takami Y, Watanabe T, Nishimura A, Nishiyama K, Miyake N, Wada T, Osaka H, Kondo N, Hayasaka K, Matsumoto N. Saitsu H, et al. Among authors: kondo n. Epilepsia. 2010 Dec;51(12):2397-405. doi: 10.1111/j.1528-1167.2010.02728.x. Epub 2010 Sep 30. Epilepsia. 2010. PMID: 20887364 Free article.

7

Liver-specific silencing of the human gene encoding succinyl-CoA: 3-ketoacid CoA transferase.

Orii KE, Fukao T, Song XQ, Mitchell GA, Kondo N. Orii KE, et al. Among authors: kondo n. Tohoku J Exp Med. 2008 Jul;215(3):227-36. doi: 10.1620/tjem.215.227. Tohoku J Exp Med. 2008. PMID: 18648183 Free article.

8

Comparison of mitochondrial A3243G mutation loads in easily accessible samples from a family with maternally inherited diabetes and deafness.

Fukao T, Kondo M, Yamamoto T, Orii KE, Kondo N. Fukao T, et al. Among authors: kondo n, kondo m. Mol Med Rep. 2009 Jan-Feb;2(1):69-72. doi: 10.3892/mmr_00000063. Mol Med Rep. 2009. PMID: 21475792

9

Spinal muscular atrophy type 1 with anti-acetylcholine receptor antibody.

Kato Z, Funato M, Orii KE, Saito K, Kondo N. Kato Z, et al. Among authors: kondo n. Eur J Pediatr. 2002 May;161(5):293-4. doi: 10.1007/s00431-002-0937-5. Epub 2002 Mar 13. Eur J Pediatr. 2002. PMID: 12012229 No abstract available.

10

A transient lesion in the corpus callosum during rotavirus infection.

Kato Z, Orii KE, Morimoto M, Sasai H, Funato M, Sawatari S, Kuwabara H, Kondo N. Kato Z, et al. Among authors: kondo n. Pediatr Neurol. 2009 Dec;41(6):467-9; author reply 469. doi: 10.1016/j.pediatrneurol.2009.07.006. Pediatr Neurol. 2009. PMID: 19931174 Review. No abstract available.

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