Effects of adrenoceptor agonists and antagonists on smooth muscle cells and neuromuscular transmission in the guinea-pig renal artery and vein.

le Makita, Y.
Foilsithe 1983

Modulation of noradrenergic transmission in the guinea-pig mesenteric artery: an electrophysiological study.

le Kuriyama, H, Makita, Y
Foilsithe 1983

The presynaptic regulation of noradrenaline release differs in mesenteric arteries of the rabbit and guinea-pig.

le Kuriyama, H, Makita, Y
Foilsithe 1984

Association of keratoconus and Avellino corneal dystrophy

le Igarashi, S, Makita, Y, Hikichi, T, Mori, F, Hanada, K, Yoshida, A
Foilsithe 2003

Actions of isosorbide dinitrate on smooth muscle cells of rabbit vascular tissues.

le Ishikawa, S., Ito, Y., Itoh, T., Kanmura, Y., Kuriyama, H., Makita, Y.
Foilsithe 1983

Transient neonatal diabetes mellitus in an extremely preterm infant

le Nishimaki, S, Yukawa, T, Makita, Y, Honda, H, Kikuchi, N, Minamisawa, S, Yokota, S
Foilsithe 2009

Idiopathic hypoparathyroidism in two patients with 22q11 microdeletion.

le Makita, Y, Masuno, M, Maizumi, K, Tachibana, K, Kuroki, Y, Kurahashi, H
Foilsithe 1995

Onset of spermatogenesis is accelerated by gestational administration of 1,2,3,4,6,7-hexachlorinated naphthalene in male rat offspring.

le Omura, M, Masuda, Y, Hirata, M, Tanaka, A, Makita, Y, Ogata, R, Inoue, N
Foilsithe 2000

De novo mtDNA nt 8993 (T-->G) mutation resulting in Leigh syndrome.

le Takahashi, S, Makita, Y, Oki, J, Miyamoto, A, Yanagawa, J, Naito, E, Goto, Y, Okuno, A
Foilsithe 1998

Identification of COL2A1 mutations in platyspondylic skeletal dysplasia, Torrance type

le Nishimura, G, Nakashima, E, Mabuchi, A, Shimamoto, K, Shimamoto, T, Shimao, Y, Nagai, T, Yamaguchi, T, Kosaki, R, Ohashi, H, Makita, Y, Ikegawa, S
Foilsithe 2004

Common origin of the Val30Met mutation responsible for the amyloidogenic transthyretin type of familial amyloidotic polyneuropathy

le Ohmori, H, Ando, Y, Makita, Y, Onouchi, Y, Nakajima, T, Saraiva, M, Terazaki, H, Suhr, O, Sobue, G, Nakamura, M, Yamaizumi, M, Munar-Ques, M, Inoue, I, Uchino, M, Hata, A
Foilsithe 2004

Sotos syndrome and haploinsufficiency of NSD1: clinical features of intragenic mutations and submicroscopic deletions

le Nagai, T, Matsumoto, N, Kurotaki, N, Harada, N, Niikawa, N, Ogata, T, Imaizumi, K, Kurosawa, K, Kondoh, T, Ohashi, H, Tsukahara, M, Makita, Y, Sugimoto, T, Sonoda, T, Yokoyama, T, Uetake, K, Sakazume, S, Fukushima, Y, Naritomi, K
Foilsithe 2003