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Translational Vision Science & Technology|June 15, 2021
Retinal Features of Family Members With Familial Exudative Vitreoretinopathy Caused By Mutations in KIF11 GeneHiroyuki Kondo, Itsuka Matsushita, Tatsuo Nagata, et al.Plos One|March 25, 2015
Potentiation of epidermal growth factor-mediated oncogenic transformation by sialidase NEU3 leading to Src activationKoji Yamamoto, Kohta Takahashi, Kazuhiro Shiozaki, et al.Nihon Shokakibyo Gakkai Zasshi = the Japanese Journal of Gastro-Enterology|April 9, 2023
[A case of hepatitis C virus-related mixed cryoglobulinemic vasculitis with chronic diarrhea]Fumitaka Mizuno, Takayoshi Fujita, Masaya Morii, et al.The British Journal of Radiology|January 7, 2009
Quality of portal verification radiography using EC-L film in electron beam therapyM Kawai, T Tada, M Hosono, et al.Modern Rheumatology|September 24, 2008
An adult case of Henoch-Schönlein purpura complicating common peroneal nerve mononeuropathyKei Ohnuma, Osamu Hosono, Hiroshi Kawasaki, et al.Cytotechnology|November 13, 2008
Prior stimulation of antigen-presenting cells with Lactobacillus regulates excessive antigen-specific cytokine responses in vitro when compared with BacteroidesMasato Tsuda, Akira Hosono, Tsutomu Yanagibashi, et al.European Spine Journal : Official Publication of the European Spine Society, the European Spinal Deformity Society, and the European Section of the Cervical Spine Research Society|June 6, 2007
Kinematics of the lumbar spine in trunk rotation: in vivo three-dimensional analysis using magnetic resonance imagingRyutaro Fujii, Hironobu Sakaura, Yoshihiro Mukai, et al.Journal of Cardiology Cases|November 29, 2023
A case of constrictive pericarditis with a milk of calcium pericardial effusion undergoing surgical treatmentShojiro Hirano, Masaya Shinohara, Rine Nakanishi, et al.Journal of the American Chemical Society|November 23, 2019
Low-Temperature Synthesis of Perovskite Oxynitride-Hydrides as Ammonia Synthesis CatalystsMasaaki Kitano, Jun Kujirai, Kiya Ogasawara, et al.Human Genome Variation|November 1, 2019
Retinal structure in Leber's congenital amaurosis caused by RPGRIP1 mutationsDaisuke Miyamichi, Sachiko Nishina, Katsuhiro Hosono, et al.Pageof 257