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Profile Publications (25)
XB-PERS-3229

Publications By Tai Kubo

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Pr-SNTX, a short-chain three-finger toxin from Papuan pigmy mulga snake, is an antagonist of muscle-type nicotinic acetylcholine receptor (α2βδε)., Yamauchi Y, Kimoto H, Yang X, Filkin S, Utkin Y, Kubo T, Inagaki H., Biosci Biotechnol Biochem. January 1, 2016; 80 (1): 158-61.


Functional characterization of Kunitz-type protease inhibitor Pr-mulgins identified from New Guinean Pseudechis australis., Inagaki H, Kimoto H, Yamauchi Y, Toriba M, Kubo T., Toxicon. January 1, 2012; 59 (1): 74-80.


Characterization of voltage-dependent calcium channel blocking peptides from the venom of the tarantula Grammostola rosea., Ono S, Kimura T, Kubo T., Toxicon. September 1, 2011; 58 (3): 265-76.


Enhanced activation of the transient receptor potential channel TRPA1 by ajoene, an allicin derivative., Yassaka RT, Inagaki H, Fujino T, Nakatani K, Kubo T., Neurosci Res. January 1, 2010; 66 (1): 99-105.


Expression cloning of Xenopus zygote arrest 2 (Xzar2) as a novel epidermalization-promoting factor in early embryos of Xenopus laevis., Nakajima Y, Okamoto H, Kubo T., Genes Cells. May 1, 2009; 14 (5): 583-95.   


Effects of 808 nm low-power laser irradiation on the muscle contraction of frog gastrocnemius., Komatsu M, Kubo T, Kogure S, Matsuda Y, Watanabe K., Lasers Surg Med. October 1, 2008; 40 (8): 576-83.


Inhibition of branching and spine maturation by repulsive guidance molecule in cultured cortical neurons., Yoshida J, Kubo T, Yamashita T., Biochem Biophys Res Commun. August 8, 2008; 372 (4): 725-9.


Peptides derived from repulsive guidance molecule act as antagonists., Suda M, Hata K, Sawada A, Nakamura Y, Kubo T, Yamaguchi A, Yamashita T., Biochem Biophys Res Commun. July 4, 2008; 371 (3): 501-4.


Cloning and functional characterization of squid voltage-dependent Ca2+ channel beta subunits: involvement of N-terminal sequences in differential modulation of the current., Kimura T, Kubo T., Neurosci Res. May 1, 2003; 46 (1): 105-17.


Functional identification of a cloned squid presynaptic voltage-dependent calcium channel., Kimura T, Kubo T., Neuroreport. December 20, 2002; 13 (18): 2389-93.


Cumulative inactivation and the pore domain in the Kv1 channels., Shimizu Y, Kubo T, Furukawa Y., Pflugers Arch. March 1, 2002; 443 (5-6): 720-30.


In vitro effects of estradiol and aromatase inhibitor treatment on sex differentiation in Xenopus laevis gonads., Miyata S, Kubo T., Gen Comp Endocrinol. July 1, 2000; 119 (1): 105-10.


Gene structure and chromosome mapping of mouse transcription elongation factor S-II (Tcea1)., Ito T, Seldin MF, Taketo MM, Kubo T, Natori S., Gene. February 22, 2000; 244 (1-2): 55-63.


Anchoring proteins confer G protein sensitivity to an inward-rectifier K(+) channel through the GK domain., Hibino H, Inanobe A, Tanemoto M, Fujita A, Doi K, Kubo T, Hata Y, Takai Y, Kurachi Y., EMBO J. January 4, 2000; 19 (1): 78-83.


Preferential expression of the gene for a putative inositol 1,4,5-trisphosphate receptor homologue in the mushroom bodies of the brain of the worker honeybee Apis mellifera L., Kamikouchi A, Takeuchi H, Sawata M, Ohashi K, Natori S, Kubo T., Biochem Biophys Res Commun. January 6, 1998; 242 (1): 181-6.


Inhibition of gastrulation in Xenopus embryos by an antibody against a cathepsin L-like protease., Miyata S, Kubo T., Dev Growth Differ. February 1, 1997; 39 (1): 111-5.


Up- and down-modulation of a cloned Aplysia K+ channel (AKv1.1a) by the activators of protein kinase C., Furukawa Y, Kim HN, Kubo T., Zoolog Sci. February 1, 1995; 12 (1): 35-44.


A new class of noninactivating K+ channels from aplysia capable of contributing to the resting potential and firing patterns of neurons., Zhao B, Rassendren F, Kaang BK, Furukawa Y, Kubo T, Kandel ER., Neuron. November 1, 1994; 13 (5): 1205-13.


Selective effector coupling of muscarinic acetylcholine receptor subtypes., Fukuda K, Kubo T, Maeda A, Akiba I, Bujo H, Nakai J, Mishina M, Higashida H, Neher E, Marty A., Trends Pharmacol Sci. December 1, 1989; Suppl 4-10.


Location of a region of the muscarinic acetylcholine receptor involved in selective effector coupling., Kubo T, Bujo H, Akiba I, Nakai J, Mishina M, Numa S., FEBS Lett. December 5, 1988; 241 (1-2): 119-25.


Different sensitivities to agonist of muscarinic acetylcholine receptor subtypes., Bujo H, Nakai J, Kubo T, Fukuda K, Akiba I, Maeda A, Mishina M, Numa S., FEBS Lett. November 21, 1988; 240 (1-2): 95-100.


Selective coupling with K+ currents of muscarinic acetylcholine receptor subtypes in NG108-15 cells., Fukuda K, Higashida H, Kubo T, Maeda A, Akiba I, Bujo H, Mishina M, Numa S., Nature. September 22, 1988; 335 (6188): 355-8.


Primary structure of porcine muscarinic acetylcholine receptor III and antagonist binding studies., Akiba I, Kubo T, Maeda A, Bujo H, Nakai J, Mishina M, Numa S., FEBS Lett. August 1, 1988; 235 (1-2): 257-61.


Molecular distinction between muscarinic acetylcholine receptor subtypes., Fukuda K, Kubo T, Akiba I, Maeda A, Mishina M, Numa S., Nature. June 18, 1987; 327 (6123): 623-5.


Cloning, sequencing and expression of complementary DNA encoding the muscarinic acetylcholine receptor., Kubo T, Fukuda K, Mikami A, Maeda A, Takahashi H, Mishina M, Haga T, Haga K, Ichiyama A, Kangawa K., Nature. October 2, 1986; 323 (6087): 411-6.

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