| Year |
Citation |
Score |
| 2013 |
Kim J, Geng R, Gallenstein RA, Somers DE. The F-box protein ZEITLUPE controls stability and nucleocytoplasmic partitioning of GIGANTEA. Development (Cambridge, England). 140: 4060-9. PMID 24004949 DOI: 10.1242/Dev.096651 |
0.544 |
|
| 2010 |
Chance MR, Chang J, Liu S, Gokulrangan G, Chen DH, Lindsay A, Geng R, Zheng QY, Alagramam K. Proteomics, bioinformatics and targeted gene expression analysis reveals up-regulation of cochlin and identifies other potential biomarkers in the mouse model for deafness in Usher syndrome type 1F. Human Molecular Genetics. 19: 1515-27. PMID 20097680 DOI: 10.1093/Hmg/Ddq025 |
0.464 |
|
| 2009 |
Tian G, Zhou Y, Hajkova D, Miyagi M, Dinculescu A, Hauswirth WW, Palczewski K, Geng R, Alagramam KN, Isosomppi J, Sankila EM, Flannery JG, Imanishi Y. Clarin-1, encoded by the Usher Syndrome III causative gene, forms a membranous microdomain: possible role of clarin-1 in organizing the actin cytoskeleton. The Journal of Biological Chemistry. 284: 18980-93. PMID 19423712 DOI: 10.1074/Jbc.M109.003160 |
0.33 |
|
| 2004 |
Somers DE, Kim WY, Geng R. The F-box protein ZEITLUPE confers dosage-dependent control on the circadian clock, photomorphogenesis, and flowering time. The Plant Cell. 16: 769-82. PMID 14973171 DOI: 10.1105/Tpc.016808 |
0.56 |
|
| 2003 |
Kim WY, Geng R, Somers DE. Circadian phase-specific degradation of the F-box protein ZTL is mediated by the proteasome. Proceedings of the National Academy of Sciences of the United States of America. 100: 4933-8. PMID 12665620 DOI: 10.1073/Pnas.0736949100 |
0.561 |
|
| Low-probability matches (unlikely to be authored by this person) |
| 2022 |
Xie D, Zhao T, Zhang X, Kui L, Wang Q, Wu Y, Zheng T, Ma P, Zhang Y, Molteni H, Geng R, Yang Y, Li B, Zheng QY. Autophagy Contributes to the Rapamycin-Induced Improvement of Otitis Media. Frontiers in Cellular Neuroscience. 15: 753369. PMID 35153674 DOI: 10.3389/fncel.2021.753369 |
0.265 |
|
| 2013 |
Geng R, Sotomayor M, Kinder KJ, Gopal SR, Gerka-Stuyt J, Chen DH, Hardisty-Hughes RE, Ball G, Parker A, Gaudet R, Furness D, Brown SD, Corey DP, Alagramam KN. Noddy, a mouse harboring a missense mutation in protocadherin-15, reveals the impact of disrupting a critical interaction site between tip-link cadherins in inner ear hair cells. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 33: 4395-404. PMID 23467356 DOI: 10.1523/Jneurosci.4514-12.2013 |
0.237 |
|
| 2014 |
Antonellis PJ, Pollock LM, Chou SW, Hassan A, Geng R, Chen X, Fuchs E, Alagramam KN, Auer M, McDermott BM. ACF7 is a hair-bundle antecedent, positioned to integrate cuticular plate actin and somatic tubulin. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 34: 305-12. PMID 24381291 DOI: 10.1523/Jneurosci.1880-13.2014 |
0.235 |
|
| 2012 |
Geng R, Melki S, Chen DH, Tian G, Furness DN, Oshima-Takago T, Neef J, Moser T, Askew C, Horwitz G, Holt JR, Imanishi Y, Alagramam KN. The mechanosensory structure of the hair cell requires clarin-1, a protein encoded by Usher syndrome III causative gene. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 32: 9485-98. PMID 22787034 DOI: 10.1523/Jneurosci.0311-12.2012 |
0.225 |
|
| 2022 |
Yan B, Xie D, Wu Y, Wang S, Zhang X, Zhao T, Liu L, Ma P, Li G, Yang Y, Zhao Y, Zheng T, Geng R, Li B, Zheng Q. Ferroptosis is involved in PGPS-induced otitis media in C57BL/6 mice. Cell Death Discovery. 8: 217. PMID 35449198 DOI: 10.1038/s41420-022-01025-1 |
0.217 |
|
| 2021 |
Zhao T, Zheng T, Yu H, Hu BH, Hu B, Ma P, Yang Y, Yang N, Hu J, Cao T, Chen G, Yan B, Peshoff M, Hatzoglou M, Geng R, et al. Autophagy impairment as a key feature for acetaminophen-induced ototoxicity. Cell Death & Disease. 12: 3. PMID 33414397 DOI: 10.1038/s41419-020-03328-6 |
0.209 |
|
| 2024 |
Wu Y, Li L, Tang L, Peijnenburg W, Zhang H, Xie D, Geng R, Zheng T, Bi L, Wei X, Chae HJ, Wang L, Zhao L, Li B, Zheng Q. Ototoxicity of polystyrene nanoplastics in mice, HEI-OC1 cells and zebrafish. Frontiers in Molecular Neuroscience. 17: 1345536. PMID 38440220 DOI: 10.3389/fnmol.2024.1345536 |
0.176 |
|
| 2016 |
Alagramam KN, Gopal SR, Geng R, Chen DH, Nemet I, Lee R, Tian G, Miyagi M, Malagu KF, Lock CJ, Esmieu WR, Owens AP, Lindsay NA, Ouwehand K, Albertus F, et al. A small molecule mitigates hearing loss in a mouse model of Usher syndrome III. Nature Chemical Biology. PMID 27110679 DOI: 10.1038/Nchembio.2069 |
0.16 |
|
| 2020 |
Zhao T, Liu X, Sun Z, Zhang J, Zhang X, Wang C, Geng R, Zheng T, Li B, Zheng QY. RNA-seq analysis of potential lncRNAs for age-related hearing loss in a mouse model. Aging. 12. PMID 32335544 DOI: 10.18632/aging.103103 |
0.153 |
|
| 2017 |
Geng R, Omar A, Gopal SR, Chen DH, Stepanyan R, Basch ML, Dinculescu A, Furness DN, Saperstein D, Hauswirth W, Lustig LR, Alagramam KN. Modeling and Preventing Progressive Hearing Loss in Usher Syndrome III. Scientific Reports. 7: 13480. PMID 29044151 DOI: 10.1038/S41598-017-13620-9 |
0.124 |
|
| 2011 |
Alagramam KN, Goodyear RJ, Geng R, Furness DN, van Aken AF, Marcotti W, Kros CJ, Richardson GP. Mutations in protocadherin 15 and cadherin 23 affect tip links and mechanotransduction in mammalian sensory hair cells. Plos One. 6: e19183. PMID 21532990 DOI: 10.1371/Journal.Pone.0019183 |
0.115 |
|
| 2021 |
Zhao T, Ma P, Zhao F, Zheng T, Yan B, Zhang Q, Yuan J, Hu B, Yang Y, Hu J, Geng R, Hu BH, Sun T, Zheng QY, Li B. Phenotypic differences in the inner ears of CBA/CaJ and C57BL/6J mice carrying missense and single base pair deletion mutations in the Cdh23 gene. Journal of Neuroscience Research. PMID 34133797 DOI: 10.1002/jnr.24905 |
0.112 |
|
| 2009 |
Geng R, Geller SF, Hayashi T, Ray CA, Reh TA, Bermingham-McDonogh O, Jones SM, Wright CG, Melki S, Imanishi Y, Palczewski K, Alagramam KN, Flannery JG. Usher syndrome IIIA gene clarin-1 is essential for hair cell function and associated neural activation. Human Molecular Genetics. 18: 2748-60. PMID 19414487 DOI: 10.1093/Hmg/Ddp210 |
0.105 |
|
| 2018 |
Geng R, Furness DN, Muraleedharan CK, Zhang J, Dabdoub A, Lin V, Xu S. The microRNA-183/96/182 Cluster is Essential for Stereociliary Bundle Formation and Function of Cochlear Sensory Hair Cells. Scientific Reports. 8: 18022. PMID 30575790 DOI: 10.1038/S41598-018-36894-Z |
0.104 |
|
| 2010 |
Huertas-Vazquez A, Plaisier CL, Geng R, Haas BE, Lee J, Greevenbroek MM, van der Kallen C, de Bruin TW, Taskinen MR, Alagramam KN, Pajukanta P. A nonsynonymous SNP within PCDH15 is associated with lipid traits in familial combined hyperlipidemia. Human Genetics. 127: 83-9. PMID 19816713 DOI: 10.1007/s00439-009-0749-z |
0.099 |
|
| 2019 |
Geng R, Wang Q, Chen E, Zheng QY. Current Understanding of Host Genetics of Otitis Media. Frontiers in Genetics. 10: 1395. PMID 32117425 DOI: 10.3389/fgene.2019.01395 |
0.094 |
|
| 2023 |
Ma P, Wang S, Geng R, Gong Y, Li M, Xie D, Dong Y, Zheng T, Li B, Zhao T, Zheng Q. MiR-29a-deficiency causes thickening of the basilar membrane and age-related hearing loss by upregulating collagen IV and laminin. Frontiers in Cellular Neuroscience. 17: 1191740. PMID 37275774 DOI: 10.3389/fncel.2023.1191740 |
0.089 |
|
| 2023 |
Kuang X, Zhao W, Wang Q, Sun Z, Xu F, Geng R, Li B, Zheng T, Zheng Q. RNA-seq analysis highlights DNA replication and DNA repair associated with early-onset hearing loss in the cochlea of DBA/2J mice. Life Sciences. 337: 122350. PMID 38103727 DOI: 10.1016/j.lfs.2023.122350 |
0.083 |
|
| 2023 |
Wang S, Li M, Liu P, Dong Y, Geng R, Zheng T, Zheng Q, Li B, Ma P. Col1a1 mediates the focal adhesion pathway affecting hearing in miR-29a mouse model by RNA-seq analysis. Experimental Gerontology. 185: 112349. PMID 38103809 DOI: 10.1016/j.exger.2023.112349 |
0.079 |
|
| 2016 |
Geng R, Noda T, Mulvaney JF, Lin VY, Edge AS, Dabdoub A. Comprehensive Expression of Wnt Signaling Pathway Genes during Development and Maturation of the Mouse Cochlea. Plos One. 11: e0148339. PMID 26859490 DOI: 10.1371/journal.pone.0148339 |
0.075 |
|
| Hide low-probability matches. |