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Cell & Bioscience|June 28, 2023
Spatiotemporal control of genome engineering in cone photoreceptorsNan-Kai Wang, Pei-Kang Liu, Yang Kong, et al.International Journal of Molecular Sciences|August 7, 2021
Mouse Models of Achromatopsia in Addressing Temporal "Point of No Return" in Gene-TherapyNan-Kai Wang, Pei-Kang Liu, Yang Kong, et al.Developmental Cell|January 22, 2009
Scara5 is a ferritin receptor mediating non-transferrin iron deliveryJau Yi Li, Neal Paragas, Renee M Ned, et al.Plos Genetics|March 12, 2015
Effects on murine behavior and lifespan of selectively decreasing expression of mutant huntingtin allele by supt4h knockdownHui-Min Cheng, Yijuang Chern, I-Hui Chen, et al.Cellular and Molecular Life Sciences : CMLS|April 13, 2019
Mechanisms of neurodegeneration in a preclinical autosomal dominant retinitis pigmentosa knock-in model with a RhoD190N mutationJavier Sancho-Pelluz, Xuan Cui, Winston Lee, et al.The Journal of Clinical Investigation|November 15, 2016
Reprogramming metabolism by targeting sirtuin 6 attenuates retinal degenerationLijuan Zhang, Jianhai Du, Sally Justus, et al.Human Molecular Genetics|February 23, 2022
Long-term vitamin A supplementation in a preclinical mouse model for RhoD190N-associated retinitis pigmentosaXuan Cui, Hye Jin Kim, Chia-Hua Cheng, et al.Elife|June 4, 2017
Transcription factor TFCP2L1 patterns cells in the mouse kidney collecting ductsMax Werth, Kai M Schmidt-Ott, Thomas Leete, et al.Science Translational Medicine|October 16, 2024
Melatonin receptor 1A variants as genetic cause of idiopathic osteoporosisBrygida Bisikirska, Rossella Labella, Alvaro Cuesta-Dominguez, et al.Cell Reports Methods|April 27, 2022
GEM-IL: A highly responsive fluorescent lactate indicatorRamsey Bekdash, Jose R Quejada, Shunnosuke Ueno, et al.Pageof 9