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Biological & Pharmaceutical Bulletin|May 8, 2020
Abnormal Vascular Phenotypes Associated with the Timing of Interruption of Retinal Vascular Development in RatsRyo Kondo, Ayuki Nakano, Daiki Asano, et al.
The Journal of Clinical Endocrinology and Metabolism|September 4, 2008
Transient congenital hypothyroidism caused by biallelic mutations of the dual oxidase 2 gene in Japanese patients detected by a neonatal screening programYoshihiro Maruo, Hiroko Takahashi, Ikumi Soeda, et al.
Biological & Pharmaceutical Bulletin|October 2, 2008
Attenuation of cataract progression by A-3922, a dihydrobenzofuran derivative, in streptozotocin-induced diabetic ratsMaki Saito, Mayumi Ueo, Sokichi Kametaka, et al.
Experimental Eye Research|January 18, 2018
Retinal neuronal cell loss prevents abnormal retinal vascular growth in a rat model of retinopathy of prematurityAyuki Nakano, Daiki Asano, Ryo Kondo, et al.
The Journal of Pediatrics|March 22, 2014
Bilirubin uridine diphosphate-glucuronosyltransferase variation is a genetic basis of breast milk jaundiceYoshihiro Maruo, Yoriko Morioka, Hiroshi Fujito, et al.
European Journal of Pharmacology|April 8, 2014
Activation of the TRPV1 channel attenuates N-methyl-D-aspartic acid-induced neuronal injury in the rat retinaKenji Sakamoto, Taiyo Kuroki, Yui Okuno, et al.
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