Sakai N - Search Results

1

Chemical chaperone treatment for galactosialidosis: Effect of NOEV on β-galactosidase activities in fibroblasts.

Hossain MA, Higaki K, Shinpo M, Nanba E, Suzuki Y, Ozono K, Sakai N. Hossain MA, et al. Among authors: sakai n. Brain Dev. 2016 Feb;38(2):175-80. doi: 10.1016/j.braindev.2015.07.006. Epub 2015 Aug 7. Brain Dev. 2016. PMID: 26259553

2

Analysis of recombinant human saposin A expressed by Pichia pastoris.

Yamada M, Inui K, Hamada D, Nakahira K, Yanagihara K, Sakai N, Nishigaki T, Ozono K, Yanagihara I. Yamada M, et al. Among authors: sakai n. Biochem Biophys Res Commun. 2004 May 28;318(2):588-93. doi: 10.1016/j.bbrc.2004.04.069. Biochem Biophys Res Commun. 2004. PMID: 15120640

3

Involvement of phosphoinositide 3-kinase signaling pathway in chondrocytic differentiation of ATDC5 cells: application of a gene-trap mutagenesis.

Ihara-Watanabe M, Uchihashi T, Miyauchi Y, Sakai N, Yamagata M, Ozono K, Michigami T. Ihara-Watanabe M, et al. Among authors: sakai n. J Cell Biochem. 2004 Oct 1;93(2):418-26. doi: 10.1002/jcb.20185. J Cell Biochem. 2004. PMID: 15368367

4

Skeletal defects in ringelschwanz mutant mice reveal that Lrp6 is required for proper somitogenesis and osteogenesis.

Kokubu C, Heinzmann U, Kokubu T, Sakai N, Kubota T, Kawai M, Wahl MB, Galceran J, Grosschedl R, Ozono K, Imai K. Kokubu C, et al. Among authors: sakai n. Development. 2004 Nov;131(21):5469-80. doi: 10.1242/dev.01405. Epub 2004 Oct 6. Development. 2004. PMID: 15469977

5

A novel mutation in the PTPN11 gene in a patient with Noonan syndrome and rapidly progressive hypertrophic cardiomyopathy.

Takahashi K, Kogaki S, Kurotobi S, Nasuno S, Ohta M, Okabe H, Wada K, Sakai N, Taniike M, Ozono K. Takahashi K, et al. Among authors: sakai n. Eur J Pediatr. 2005 Aug;164(8):497-500. doi: 10.1007/s00431-005-1679-y. Epub 2005 May 12. Eur J Pediatr. 2005. PMID: 15889278

6

Novel mutation of gene coding for glial fibrillary acidic protein in a Japanese patient with Alexander disease.

Kawai M, Sakai N, Miyake S, Tsukamoto H, Akagi M, Inui K, Mushiake S, Taniike M, Ozono K. Kawai M, et al. Among authors: sakai n. Brain Dev. 2006 Jan;28(1):60-2. doi: 10.1016/j.braindev.2005.03.011. Epub 2005 Sep 15. Brain Dev. 2006. PMID: 16168595

7

Six novel mutations detected in the GALC gene in 17 Japanese patients with Krabbe disease, and new genotype-phenotype correlation.

Xu C, Sakai N, Taniike M, Inui K, Ozono K. Xu C, et al. Among authors: sakai n. J Hum Genet. 2006;51(6):548-554. doi: 10.1007/s10038-006-0396-3. Epub 2006 Apr 11. J Hum Genet. 2006. PMID: 16607461

8

Involvement of nuclear factor I transcription/replication factor in the early stage of chondrocytic differentiation.

Uchihashi T, Kimata M, Tachikawa K, Koshimizu T, Okada T, Ihara-Watanabe M, Sakai N, Kogo M, Ozono K, Michigami T. Uchihashi T, et al. Among authors: sakai n. Bone. 2007 Dec;41(6):1025-35. doi: 10.1016/j.bone.2007.08.028. Epub 2007 Aug 30. Bone. 2007. PMID: 17904922

9

Sleep disordered breathing in childhood-onset acid maltase deficiency.

Nabatame S, Taniike M, Sakai N, Kato-Nishimura K, Mohri I, Kagitani-Shimono K, Okinaga T, Tachibana N, Ozono K. Nabatame S, et al. Among authors: sakai n. Brain Dev. 2009 Mar;31(3):234-9. doi: 10.1016/j.braindev.2008.03.007. Epub 2008 May 21. Brain Dev. 2009. PMID: 18495398

10

Lrp6 hypomorphic mutation affects bone mass through bone resorption in mice and impairs interaction with Mesd.

Kubota T, Michigami T, Sakaguchi N, Kokubu C, Suzuki A, Namba N, Sakai N, Nakajima S, Imai K, Ozono K. Kubota T, et al. Among authors: sakai n. J Bone Miner Res. 2008 Oct;23(10):1661-71. doi: 10.1359/jbmr.080512. J Bone Miner Res. 2008. PMID: 18505367 Free article.

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