Showing results (61-70 of 73) with videos related to

Sort By:
Pageof 8
BMC Ophthalmology|February 20, 2020
Protection of retinal function and morphology in MNU-induced retinitis pigmentosa rats by ALDH2: an in-vivo studyWeiming Yan, Pan Long, Dongyu Wei, et al.
Experimental Eye Research|April 8, 2010
A novel middle-wavelength opsin (M-opsin) null-mutation in the retinal cone dysfunction ratBei Xie, Satoshi Nakanishi, Qun Guo, et al.
Biomed Research International|September 23, 2014
CpG island methylator phenotype and prognosis of colorectal cancer in Northeast ChinaXia Li, Fulan Hu, Yibaina Wang, et al.
Journal of Oral & Facial Pain and Headache|February 7, 2019
Long-term Low-Dose Sucrose May Prevent Migraine: Two Double-Blinded Randomized Controlled Pilot TrialsRan Yan, Xin Wang, HaiBo Zhou, et al.
Gene|May 16, 2024
A New Mouse Model for Usher Syndrome Crossing Kunming Mice with CBA/J MiceShaoheng Li, Yihong Jiang, Lei Zhang, et al.
Development and Psychopathology|January 12, 2021
Parental rearing and personality traits as predictors for adolescents with obsessive-compulsive disorder (OCD)Yafeng Zhang, Wei Tian, Chao Wang, et al.
Molecular Vision|February 5, 2008
A naturally-occurring mutation in Cacna1f in a rat model of congenital stationary night blindnessYonghao Gu, Lifeng Wang, Jie Zhou, et al.
Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology|July 2, 2018
A Natural Occurring Mouse Model with Adgrv1 Mutation of Usher Syndrome 2C and Characterization of its Recombinant Inbred StrainsWeiming Yan, Pan Long, Tao Chen, et al.
Pageof 8