Higaki K - Search Results

1

The orientation of primary cilia during the wound response in 3Y1 cells.

Katsumoto T, Higaki K, Ohno K, Onodera K. Katsumoto T, et al. Among authors: higaki k. Biol Cell. 1994;81(1):17-21. doi: 10.1016/0248-4900(94)90050-7. Biol Cell. 1994. PMID: 7987238

2

Cell-cycle dependent biosynthesis and localization of p53 protein in untransformed human cells.

Katsumoto T, Higaki K, Ohno K, Onodera K. Katsumoto T, et al. Among authors: higaki k. Biol Cell. 1995;84(3):167-73. doi: 10.1016/0248-4900(96)89426-3. Biol Cell. 1995. PMID: 8720437

3

Accumulation of cholesterol and GM2 ganglioside in cells cultured in the presence of progesterone: an implication for the basic defect in Niemann-Pick disease type C.

Sato M, Akaboshi S, Katsumoto T, Taniguchi M, Higaki K, Tai T, Sakuraba H, Ohno K. Sato M, et al. Among authors: higaki k. Brain Dev. 1998 Jan;20(1):50-2. doi: 10.1016/s0387-7604(97)00099-5. Brain Dev. 1998. PMID: 9533562

4

Ubiquitin-proteasome system impairment caused by a missense cardiac myosin-binding protein C mutation and associated with cardiac dysfunction in hypertrophic cardiomyopathy.

Bahrudin U, Morisaki H, Morisaki T, Ninomiya H, Higaki K, Nanba E, Igawa O, Takashima S, Mizuta E, Miake J, Yamamoto Y, Shirayoshi Y, Kitakaze M, Carrier L, Hisatome I. Bahrudin U, et al. Among authors: higaki k. J Mol Biol. 2008 Dec 26;384(4):896-907. doi: 10.1016/j.jmb.2008.09.070. Epub 2008 Oct 7. J Mol Biol. 2008. PMID: 18929575

5

Impairment of ubiquitin-proteasome system by E334K cMyBPC modifies channel proteins, leading to electrophysiological dysfunction.

Bahrudin U, Morikawa K, Takeuchi A, Kurata Y, Miake J, Mizuta E, Adachi K, Higaki K, Yamamoto Y, Shirayoshi Y, Yoshida A, Kato M, Yamamoto K, Nanba E, Morisaki H, Morisaki T, Matsuoka S, Ninomiya H, Hisatome I. Bahrudin U, et al. Among authors: higaki k. J Mol Biol. 2011 Nov 4;413(4):857-78. doi: 10.1016/j.jmb.2011.09.006. Epub 2011 Sep 12. J Mol Biol. 2011. PMID: 21939669

6

Antisense suppression of TSC1 gene product, hamartin, enhances neurite outgrowth in NGF-treated PC12h cells.

Floricel F, Higaki K, Maki H, Nanba E, Ninomiya H, Ohno K. Floricel F, et al. Among authors: higaki k. Brain Dev. 2007 Sep;29(8):502-9. doi: 10.1016/j.braindev.2007.01.007. Epub 2007 Mar 21. Brain Dev. 2007. PMID: 17376623

7

Chaperone activity of bicyclic nojirimycin analogues for Gaucher mutations in comparison with N-(n-nonyl)deoxynojirimycin.

Luan Z, Higaki K, Aguilar-Moncayo M, Ninomiya H, Ohno K, García-Moreno MI, Ortiz Mellet C, García Fernández JM, Suzuki Y. Luan Z, et al. Among authors: higaki k. Chembiochem. 2009 Nov 23;10(17):2780-92. doi: 10.1002/cbic.200900442. Chembiochem. 2009. PMID: 19830760

8

A Fluorescent sp2-iminosugar with pharmacological chaperone activity for gaucher disease: synthesis and intracellular distribution studies.

Luan Z, Higaki K, Aguilar-Moncayo M, Li L, Ninomiya H, Nanba E, Ohno K, García-Moreno MI, Ortiz Mellet C, García Fernández JM, Suzuki Y. Luan Z, et al. Among authors: higaki k. Chembiochem. 2010 Nov 22;11(17):2453-64. doi: 10.1002/cbic.201000323. Chembiochem. 2010. PMID: 21064079

9

Molecular basis of 1-deoxygalactonojirimycin arylthiourea binding to human α-galactosidase a: pharmacological chaperoning efficacy on Fabry disease mutants.

Yu Y, Mena-Barragán T, Higaki K, Johnson JL, Drury JE, Lieberman RL, Nakasone N, Ninomiya H, Tsukimura T, Sakuraba H, Suzuki Y, Nanba E, Mellet CO, García Fernández JM, Ohno K. Yu Y, et al. Among authors: higaki k. ACS Chem Biol. 2014 Jul 18;9(7):1460-9. doi: 10.1021/cb500143h. Epub 2014 May 12. ACS Chem Biol. 2014. PMID: 24783948

10

[Niemann-Pick disease [type A and B] (acid sphingomyelinase deficiencies)].

Higaki K, Ohno K. Higaki K, et al. Ryoikibetsu Shokogun Shirizu. 1998;(19 Pt 2):360-2. Ryoikibetsu Shokogun Shirizu. 1998. PMID: 9645083 Review. Japanese. No abstract available.

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