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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