| Year |
Citation |
Score |
| 2022 |
Zhi L, Zhao J, Jaffe D, Chen Y, Wang N, Qin Q, Seifert EL, Li C, Zhang H. Measurement of Oxygen Consumption Rate in Acute Striatal Slices from Adult Mice. Journal of Visualized Experiments : Jove. PMID 35758711 DOI: 10.3791/63379 |
0.403 |
|
| 2022 |
Shenoy SA, Zheng S, Liu W, Dai Y, Liu Y, Hou Z, Mori S, Tang Y, Cheng J, Duan W, Li C. A novel and accurate full-length HTT mouse model for Huntington's disease. Elife. 11. PMID 35023827 DOI: 10.7554/eLife.70217 |
0.755 |
|
| 2019 |
Yang X, Bayat V, DiDonato N, Zhao Y, Zarnegar B, Siprashvili Z, Lopez-Pajares V, Sun T, Tao S, Li C, Rump A, Khavari P, Lu B. Genetic and genomic studies of pathogenic EXOSC2 mutations in the newly described disease SHRF implicate the autophagy pathway in disease pathogenesis. Human Molecular Genetics. PMID 31628467 DOI: 10.1093/Hmg/Ddz251 |
0.403 |
|
| 2018 |
Zhi L, Qin Q, Muqeem T, Seifert EL, Liu W, Zheng S, Li C, Zhang H. Loss of PINK1 causes age-dependent decrease of dopamine release and mitochondrial dysfunction. Neurobiology of Aging. 75: 1-10. PMID 30504091 DOI: 10.1016/J.Neurobiolaging.2018.10.025 |
0.44 |
|
| 2014 |
Chen BB, Coon TA, Glasser JR, Zou C, Ellis B, Das T, McKelvey AC, Rajbhandari S, Lear T, Kamga C, Shiva S, Li C, Pilewski JM, Callio J, Chu CT, et al. E3 ligase subunit Fbxo15 and PINK1 kinase regulate cardiolipin synthase 1 stability and mitochondrial function in pneumonia. Cell Reports. 7: 476-87. PMID 24703837 DOI: 10.1016/J.Celrep.2014.02.048 |
0.357 |
|
| 2013 |
Cannon JR, Geghman KD, Tapias V, Sew T, Dail MK, Li C, Greenamyre JT. Expression of human E46K-mutated α-synuclein in BAC-transgenic rats replicates early-stage Parkinson's disease features and enhances vulnerability to mitochondrial impairment. Experimental Neurology. 240: 44-56. PMID 23153578 DOI: 10.1016/J.Expneurol.2012.11.007 |
0.761 |
|
| 2012 |
Zheng S, Geghman K, Shenoy S, Li C. Retake the center stage--new development of rat genetics. Journal of Genetics and Genomics = Yi Chuan Xue Bao. 39: 261-8. PMID 22749013 DOI: 10.1016/J.Jgg.2012.05.003 |
0.654 |
|
| 2012 |
Huang Y, Shenoy S, Lu B, Liu W, Li C. Kinase signaling dysfunction in Parkinson's disease: a reverse genetic approach in Drosophila. Journal of Neurogenetics. 26: 158-67. PMID 22486164 DOI: 10.3109/01677063.2012.672499 |
0.787 |
|
| 2012 |
Xu Q, Shenoy S, Li C. Mouse models for LRRK2 Parkinson's disease. Parkinsonism & Related Disorders. 18: S186-9. PMID 22166430 DOI: 10.1016/S1353-8020(11)70058-X |
0.789 |
|
| 2011 |
Geghman K, Li C. Practical considerations of genetic rodent models for neurodegenerative diseases. Methods in Molecular Biology (Clifton, N.J.). 793: 185-93. PMID 21913101 DOI: 10.1007/978-1-61779-328-8_12 |
0.753 |
|
| 2011 |
Liu W, Acín-Peréz R, Geghman KD, Manfredi G, Lu B, Li C. Pink1 regulates the oxidative phosphorylation machinery via mitochondrial fission. Proceedings of the National Academy of Sciences of the United States of America. 108: 12920-4. PMID 21768365 DOI: 10.1073/Pnas.1107332108 |
0.717 |
|
| 2011 |
Dagda RK, Gusdon AM, Pien I, Strack S, Green S, Li C, Van Houten B, Cherra SJ, Chu CT. Mitochondrially localized PKA reverses mitochondrial pathology and dysfunction in a cellular model of Parkinson's disease. Cell Death and Differentiation. 18: 1914-23. PMID 21637291 DOI: 10.1038/Cdd.2011.74 |
0.462 |
|
| 2010 |
Vives-Bauza C, Zhou C, Huang Y, Cui M, de Vries RL, Kim J, May J, Tocilescu MA, Liu W, Ko HS, Magrané J, Moore DJ, Dawson VL, Grailhe R, Dawson TM, ... Li C, et al. PINK1-dependent recruitment of Parkin to mitochondria in mitophagy. Proceedings of the National Academy of Sciences of the United States of America. 107: 378-83. PMID 19966284 DOI: 10.1073/Pnas.0911187107 |
0.417 |
|
| 2009 |
Li Y, Liu W, Oo TF, Wang L, Tang Y, Jackson-Lewis V, Zhou C, Geghman K, Bogdanov M, Przedborski S, Beal MF, Burke RE, Li C. Mutant LRRK2(R1441G) BAC transgenic mice recapitulate cardinal features of Parkinson's disease. Nature Neuroscience. 12: 826-8. PMID 19503083 DOI: 10.1038/Nn.2349 |
0.755 |
|
| 2009 |
Liu W, Vives-Bauza C, AcÃn-Peréz- R, Yamamoto A, Tan Y, Li Y, Magrané J, Stavarache MA, Shaffer S, Chang S, Kaplitt MG, Huang XY, Beal MF, Manfredi G, Li C. PINK1 defect causes mitochondrial dysfunction, proteasomal deficit and alpha-synuclein aggregation in cell culture models of Parkinson's disease. Plos One. 4: e4597. PMID 19242547 DOI: 10.1371/Journal.Pone.0004597 |
0.447 |
|
| 2007 |
Kim Y, Zhou P, Qian L, Chuang JZ, Lee J, Li C, Iadecola C, Nathan C, Ding A. MyD88-5 links mitochondria, microtubules, and JNK3 in neurons and regulates neuronal survival. The Journal of Experimental Medicine. 204: 2063-74. PMID 17724133 DOI: 10.1084/Jem.20070868 |
0.307 |
|
| 2005 |
Li C, Beal MF. Leucine-rich repeat kinase 2: a new player with a familiar theme for Parkinson's disease pathogenesis. Proceedings of the National Academy of Sciences of the United States of America. 102: 16535-6. PMID 16275903 DOI: 10.1073/Pnas.0508350102 |
0.519 |
|
| 2005 |
Gu X, Li C, Wei W, Lo V, Gong S, Li SH, Iwasato T, Itohara S, Li XJ, Mody I, Heintz N, Yang XW. Pathological cell-cell interactions elicited by a neuropathogenic form of mutant Huntingtin contribute to cortical pathogenesis in HD mice. Neuron. 46: 433-44. PMID 15882643 DOI: 10.1016/J.Neuron.2005.03.025 |
0.365 |
|
| 2005 |
Sang TK, Li C, Liu W, Rodriguez A, Abrams JM, Zipursky SL, Jackson GR. Inactivation of Drosophila Apaf-1 related killer suppresses formation of polyglutamine aggregates and blocks polyglutamine pathogenesis. Human Molecular Genetics. 14: 357-72. PMID 15590702 DOI: 10.1093/Hmg/Ddi032 |
0.332 |
|
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