Showing results (81-90 of 128) with videos related to
Sort By:
Pageof 13
BMC Endocrine Disorders|January 13, 2016
Successful every-other-day liothyronine therapy for severe resistance to thyroid hormone beta with a novel THRB mutation; case reportYoshihiro Maruo, Asami Mori, Yoriko Morioka, et al.Biological & Pharmaceutical Bulletin|May 3, 2007
Vasodilation of retinal arteriole mediated by corticotropin-releasing factor receptor is impaired in streptozotocin-induced diabetic ratsYoshiko Kaneko, Maki Saito, Asami Mori, et al.World Journal of Pediatrics : WJP|April 30, 2015
A novel large deletion (exons 12, 13) and a missense mutation (p.G46R) in the PAH in a Japanese patient with phenylketonuriaYoshihiro Maruo, Masafumi Suzaki, Katsuyuki Matsui, et al.European Journal of Pharmacology|July 8, 2015
Involvement of prostaglandin I(2) in nitric oxide-induced vasodilation of retinal arterioles in ratsAsami Mori, Ryo Namekawa, Masami Hasebe, et al.Journal of Ocular Pharmacology and Therapeutics : the Official Journal of the Association for Ocular Pharmacology and Therapeutics|June 27, 2007
Vasodilator effects of fasudil, a Rho-kinase inhibitor, on retinal arterioles in stroke-prone spontaneously hypertensive ratsNami Okamura, Maki Saito, Asami Mori, et al.Journal of Pharmacological Sciences|April 9, 2018
Establishment of an abnormal vascular patterning model in the mouse retinaAkane Morita, Shohei Sawada, Asami Mori, et al.European Journal of Pharmacology|July 9, 2017
Opioid receptor activation is involved in neuroprotection induced by TRPV1 channel activation against excitotoxicity in the rat retinaKenji Sakamoto, Taiyo Kuroki, Tomonori Sagawa, et al.Vascular Pharmacology|July 1, 2008
Beta-adrenoceptor-mediated vasodilation of retinal blood vessels is reduced in streptozotocin-induced diabetic ratsTaisuke Nakazawa, Ayumi Sato, Asami Mori, et al.Biological & Pharmaceutical Bulletin|March 10, 2015
Preventive effects of rapamycin on inflammation and capillary degeneration in a rat model of NMDA-induced retinal injuryYuto Aoki, Tsutomu Nakahara, Daiki Asano, et al.Human Genetics|September 21, 2004
Two linked polymorphic mutations (A(TA)7TAA and T-3279G) of UGT1A1 as the principal cause of Gilbert syndromeYoshihiro Maruo, Carlos D'Addario, Asami Mori, et al.Pageof 13