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Biochemical and Biophysical Research Communications|August 14, 2018
Optineurin E50K triggers BDNF deficiency-mediated mitochondrial dysfunction in retinal photoreceptor cell lineMyoung Sup Shim, Keun-Young Kim, Mark Noh, et al.
European Journal of Radiology|July 29, 2025
Impact of the use of deep-learning 3D camera on workflow and patient positioning in CT examinationsAkio Ito, Yoshifumi Noda, Nobuyuki Kawai, et al.
Ophthalmology|January 10, 2018
Early Patterns of Macular Degeneration in ABCA4-Associated RetinopathyKamron N Khan, Melissa Kasilian, Omar A R Mahroo, et al.
Japanese Journal of Ophthalmology|April 5, 2016
Novel mutations in the gene for α-subunit of retinal cone cyclic nucleotide-gated channels in a Japanese patient with congenital achromatopsiaKazuki Kuniyoshi, Sanae Muraki-Oda, Hisao Ueyama, et al.
Investigative Ophthalmology & Visual Science|December 24, 2003
Purification, molecular cloning, and expression of a novel growth-promoting factor for retinal pigment epithelial cells, REF-1/TFPI-2Yasuhiko Tanaka, Jun Utsumi, Mizuo Matsui, et al.
Abdominal Radiology (New York)|January 20, 2026
Improved visualization of pancreas and tumor boundaries using high-frequency kernels with deep-learning image reconstruction at high-strength levelNobuyuki Kawai, Yoshifumi Noda, Tetsuro Kaga, et al.
Abdominal Radiology (New York)|August 25, 2025
Optimal trigger threshold with the bolus-tracking technique for the renal CT angiography protocolMasashi Asano, Yoshifumi Noda, Nobuyuki Kawai, et al.
Abdominal Radiology (New York)|July 29, 2026
Impact of image reconstruction algorithms on histogram analysis of iodine concentration for assessing chemotherapy response in pancreatic ductal adenocarcinomaMasashi Asano, Yoshifumi Noda, Nobuyuki Kawai, et al.
Scientific Reports|September 21, 2016
CCT2 Mutations Evoke Leber Congenital Amaurosis due to Chaperone Complex InstabilityYuriko Minegishi, XunLun Sheng, Kazutoshi Yoshitake, et al.
Scientific Reports|November 15, 2018
Compound heterozygous splice site variants in the SCLT1 gene highlight an additional candidate locus for Senior-Løken syndromeSatoshi Katagiri, Takaaki Hayashi, Kazutoshi Yoshitake, et al.
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