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Ren ZL, Zhang HB, Li L, et al. (2022) Characterization of two novel knock-in mouse models of syndromic retinal ciliopathy carrying hypomorphic mutations. Zoological Research. 43: 442-456 |
Xu H, Qu C, Gan L, et al. (2020) Deletion of the Impg2 gene causes the degeneration of rod and cone cells in mice. Human Molecular Genetics |
Guo X, Li J, Wang Q, et al. (2019) Identification of CRB1 mutations in two Chinese consanguineous families exhibiting autosomal recessive retinitis pigmentosa. Molecular Medicine Reports |
Yang Y, Liu W, Sun K, et al. (2018) Tmem30a deficiency leads to retinal rod bipolar cell degeneration. Journal of Neurochemistry |
Ronquillo CC, Hanke-Gogokhia C, Revelo MP, et al. (2016) Ciliopathy-associated IQCB1/NPHP5 protein is required for mouse photoreceptor outer segment formation. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology |
Jiang L, Tam BM, Ying G, et al. (2015) Kinesin family 17 (osmotic avoidance abnormal-3) is dispensable for photoreceptor morphology and function. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology |
Jiang L, Wei Y, Ronquillo CC, et al. (2015) Heterotrimeric kinesin-2 (KIF3) mediates transition zone and axoneme formation of mouse photoreceptors. The Journal of Biological Chemistry. 290: 12765-78 |
Zhang H, Hanke-Gogokhia C, Jiang L, et al. (2015) Mistrafficking of prenylated proteins causes retinitis pigmentosa 2. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. 29: 932-42 |
Jiang L, Frederick JM, Baehr W. (2014) RNA interference gene therapy in dominant retinitis pigmentosa and cone-rod dystrophy mouse models caused by GCAP1 mutations. Frontiers in Molecular Neuroscience. 7: 25 |
Lai CW, Kolesnikov AV, Frederick JM, et al. (2013) Phosducin-like protein 1 is essential for G-protein assembly and signaling in retinal rod photoreceptors. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 33: 7941-51 |