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Li Jiang - Publications

Affiliations: 
Ophthalmology University of Utah, Salt Lake City, UT 
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17 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2022 Ren ZL, Zhang HB, Li L, Yang ZL, Jiang L. Characterization of two novel knock-in mouse models of syndromic retinal ciliopathy carrying hypomorphic mutations. Zoological Research. 43: 442-456. PMID 35503560 DOI: 10.24272/j.issn.2095-8137.2021.387  0.672
2020 Xu H, Qu C, Gan L, Sun K, Tan J, Liu X, Jiang Z, Tian W, Liu W, Zhang S, Yang Y, Jiang L, Zhu X, Zhang L. Deletion of the Impg2 gene causes the degeneration of rod and cone cells in mice. Human Molecular Genetics. PMID 32242237 DOI: 10.1093/hmg/ddaa062  0.38
2019 Guo X, Li J, Wang Q, Shu Y, Wang J, Chen L, Zhang H, Shi Y, Yang J, Lu F, Jiang L, Qu C, Gong B. Identification of CRB1 mutations in two Chinese consanguineous families exhibiting autosomal recessive retinitis pigmentosa. Molecular Medicine Reports. PMID 31322236 DOI: 10.3892/mmr.2019.10495  0.594
2018 Yang Y, Liu W, Sun K, Jiang L, Zhu X. Tmem30a deficiency leads to retinal rod bipolar cell degeneration. Journal of Neurochemistry. PMID 30548540 DOI: 10.1111/jnc.14643  0.302
2016 Ronquillo CC, Hanke-Gogokhia C, Revelo MP, Frederick JM, Jiang L, Baehr W. 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. PMID 27328943 DOI: 10.1096/Fj.201600511R  0.673
2015 Jiang L, Tam BM, Ying G, Wu S, Hauswirth WW, Frederick JM, Moritz OL, Baehr W. 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. PMID 26229057 DOI: 10.1096/Fj.15-275677  0.604
2015 Jiang L, Wei Y, Ronquillo CC, Marc RE, Yoder BK, Frederick JM, Baehr W. Heterotrimeric kinesin-2 (KIF3) mediates transition zone and axoneme formation of mouse photoreceptors. The Journal of Biological Chemistry. 290: 12765-78. PMID 25825494 DOI: 10.1074/Jbc.M115.638437  0.748
2015 Zhang H, Hanke-Gogokhia C, Jiang L, Li X, Wang P, Gerstner CD, Frederick JM, Yang Z, Baehr W. Mistrafficking of prenylated proteins causes retinitis pigmentosa 2. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. 29: 932-42. PMID 25422369 DOI: 10.1096/Fj.14-257915  0.716
2014 Jiang L, Frederick JM, Baehr W. RNA interference gene therapy in dominant retinitis pigmentosa and cone-rod dystrophy mouse models caused by GCAP1 mutations. Frontiers in Molecular Neuroscience. 7: 25. PMID 24778606 DOI: 10.3389/Fnmol.2014.00025  0.62
2013 Lai CW, Kolesnikov AV, Frederick JM, Blake DR, Jiang L, Stewart JS, Chen CK, Barrow JR, Baehr W, Kefalov VJ, Willardson BM. 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. PMID 23637185 DOI: 10.1523/Jneurosci.5001-12.2013  0.525
2013 Jiang L, Li TZ, Boye SE, Hauswirth WW, Frederick JM, Baehr W. RNAi-mediated gene suppression in a GCAP1(L151F) cone-rod dystrophy mouse model. Plos One. 8: e57676. PMID 23472098 DOI: 10.1371/Journal.Pone.0057676  0.631
2011 Jiang L, Zhang H, Dizhoor AM, Boye SE, Hauswirth WW, Frederick JM, Baehr W. Long-term RNA interference gene therapy in a dominant retinitis pigmentosa mouse model. Proceedings of the National Academy of Sciences of the United States of America. 108: 18476-81. PMID 22042849 DOI: 10.1073/Pnas.1112758108  0.678
2011 Vázquez-Chona FR, Swan A, Ferrell WD, Jiang L, Baehr W, Chien WM, Fero M, Marc RE, Levine EM. Proliferative reactive gliosis is compatible with glial metabolic support and neuronal function. Bmc Neuroscience. 12: 98. PMID 21985191 DOI: 10.1186/1471-2202-12-98  0.548
2010 Jiang L, Baehr W. GCAP1 mutations associated with autosomal dominant cone dystrophy. Advances in Experimental Medicine and Biology. 664: 273-82. PMID 20238026 DOI: 10.1007/978-1-4419-1399-9_31  0.534
2008 Jiang L, Wheaton D, Bereta G, Zhang K, Palczewski K, Birch DG, Baehr W. A novel GCAP1(N104K) mutation in EF-hand 3 (EF3) linked to autosomal dominant cone dystrophy. Vision Research. 48: 2425-32. PMID 18706439 DOI: 10.1016/J.Visres.2008.07.016  0.57
2005 Jiang L, Katz BJ, Yang Z, Zhao Y, Faulkner N, Hu J, Baird J, Baehr W, Creel DJ, Zhang K. Autosomal dominant cone dystrophy caused by a novel mutation in the GCAP1 gene (GUCA1A). Molecular Vision. 11: 143-51. PMID 15735604  0.566
2005 Yang Z, Alvarez BV, Chakarova C, Jiang L, Karan G, Frederick JM, Zhao Y, Sauvé Y, Li X, Zrenner E, Wissinger B, Hollander AI, Katz B, Baehr W, Cremers FP, et al. Mutant carbonic anhydrase 4 impairs pH regulation and causes retinal photoreceptor degeneration. Human Molecular Genetics. 14: 255-65. PMID 15563508 DOI: 10.1093/Hmg/Ddi023  0.567
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