| Year |
Citation |
Score |
| 2024 |
Deng L, Jiang H, Lin J, Xu D, Qi A, Guo Q, Li PP, Wang X, Liu JS, Fu X, Li P. Clock knockout in inhibitory neurons reduces predisposition to epilepsy and influences anxiety-like behaviors in mice. Neurobiology of Disease. 193: 106457. PMID 38423191 DOI: 10.1016/j.nbd.2024.106457 |
0.549 |
|
| 2023 |
Kavanaugh BC, Elacio J, Best CR, St Pierre DG, Pescosolido MF, Ouyang Q, Caruso P, Buch K, Biedermann J, Bradley RS, Liu JS, Jones RN, Morrow EM. Christianson Syndrome across the Lifespan: An International Longitudinal Study in Children, Adolescents, and Adults. Medrxiv : the Preprint Server For Health Sciences. PMID 37987014 DOI: 10.1101/2023.11.11.23298218 |
0.479 |
|
| 2023 |
Pescosolido MF, Ouyang Q, Liu JS, Morrow EM. Live-Imaging Detection of Multivesicular Body-Plasma Membrane Fusion and Exosome Release in Cultured Primary Neurons. Methods in Molecular Biology (Clifton, N.J.). 2683: 213-220. PMID 37300778 DOI: 10.1007/978-1-0716-3287-1_17 |
0.47 |
|
| 2022 |
Cheon S, Culver AM, Bagnell AM, Ritchie FD, Vacharasin JM, McCord MM, Papendorp CM, Chukwurah E, Smith AJ, Cowen MH, Moreland TA, Ghate PS, Davis SW, Liu JS, Lizarraga SB. Counteracting epigenetic mechanisms regulate the structural development of neuronal circuitry in human neurons. Molecular Psychiatry. PMID 35210569 DOI: 10.1038/s41380-022-01474-1 |
0.706 |
|
| 2021 |
Pescosolido MF, Ouyang Q, Liu JS, Morrow EM. Loss of Christianson Syndrome Na+/H+ Exchanger 6 () Causes Abnormal Endosome Maturation and Trafficking Underlying Lysosome Dysfunction in Neurons. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. PMID 34526390 DOI: 10.1523/JNEUROSCI.1244-20.2021 |
0.565 |
|
| 2021 |
Fu X, Liu JS, Li P. Stopping the Clock on Seizures! Trends in Neurosciences. PMID 33965214 DOI: 10.1016/j.tins.2021.04.002 |
0.579 |
|
| 2021 |
Li P, Li L, Yu B, Wang X, Wang Q, Lin J, Zheng Y, Zhu J, He M, Xia Z, Tu M, Liu JS, Lin Z, Fu X. Doublecortin facilitates the elongation of the somatic Golgi apparatus into proximal dendrites. Molecular Biology of the Cell. mbcE19090530. PMID 33405953 DOI: 10.1091/mbc.E19-09-0530 |
0.671 |
|
| 2021 |
Chan F, Liu J. Molecular regulation of brain metabolism underlying circadian epilepsy. Epilepsia. PMID 33395505 DOI: 10.1111/epi.16796 |
0.544 |
|
| 2020 |
Mohammad S, Page SJ, Wang L, Ishii S, Li P, Sasaki T, Basha A, Salzberg A, Quezado Z, Imamura F, Nishi H, Isaka K, Corbin JG, Liu JS, Kawasawa YI, et al. Kcnn2 blockade reverses learning deficits in a mouse model of fetal alcohol spectrum disorders. Nature Neuroscience. PMID 32203497 DOI: 10.1038/S41593-020-0592-Z |
0.423 |
|
| 2019 |
Ouyang Q, Kavanaugh BC, Joesch-Cohen L, Dubois B, Wu Q, Schmidt M, Baytas O, Pastore SF, Harripaul R, Mishra S, Hussain A, Kim KH, Holler-Managan YF, Ayub M, Mir A, ... ... Liu JS, et al. GPT2 mutations in autosomal recessive developmental disability: extending the clinical phenotype and population prevalence estimates. Human Genetics. PMID 31471722 DOI: 10.1007/S00439-019-02057-X |
0.484 |
|
| 2019 |
Kavanaugh BC, Warren EB, Baytas O, Schmidt M, Merck D, Buch K, Liu JS, Phornphutkul C, Caruso P, Morrow EM. Longitudinal MRI findings in patient with SLC25A12 pathogenic variants inform disease progression and classification. American Journal of Medical Genetics. Part A. PMID 31403263 DOI: 10.1002/Ajmg.A.61322 |
0.515 |
|
| 2019 |
Pescosolido MF, Kavanaugh BC, Pochet N, Schmidt M, Jerskey BA, Rogg JM, De Jager PL, Young-Pearse TL, Liu JS, Morrow EM. Complex Neurological Phenotype in Female Carriers of Mutations. Molecular Neuropsychiatry. 5: 98-108. PMID 31192222 DOI: 10.1159/000496341 |
0.474 |
|
| 2018 |
Yap CC, Digilio L, Kruczek K, Roszkowska M, Fu XQ, Liu JS, Winckler B. A dominant dendrite phenotype caused by the disease-associated G253D mutation in doublecortin (DCX) is not due to its endocytosis defect. The Journal of Biological Chemistry. PMID 30291144 DOI: 10.1074/Jbc.Ra118.004462 |
0.565 |
|
| 2017 |
Li P, Fu X, Smith NA, Ziobro J, Curiel J, Tenga MJ, Martin B, Freedman S, Cea-Del Rio CA, Oboti L, Tsuchida TN, Oluigbo C, Yaun A, Magge SN, O'Neill B, ... ... Liu JS, et al. Loss of CLOCK Results in Dysfunction of Brain Circuits Underlying Focal Epilepsy. Neuron. 96: 387-401.e6. PMID 29024662 DOI: 10.1016/J.Neuron.2017.09.044 |
0.733 |
|
| 2017 |
Curiel J, Rodríguez Bey G, Takanohashi A, Bugiani M, Fu X, Wolf NI, Nmezi B, Schiffmann R, Bugaighis M, Pierson T, Helman G, Simons C, van der Knaap MS, Liu J, Padiath Q, et al. TUBB4A mutations result in specific neuronal and oligodendrocytic defects that closely match clinically distinct phenotypes. Human Molecular Genetics. PMID 28973395 DOI: 10.1093/Hmg/Ddx338 |
0.613 |
|
| 2017 |
Ho CY, Ames HM, Tipton A, Vezina G, Liu JS, Scafidi J, Torii M, Rodriguez FJ, du Plessis A, DeBiasi RL. Differential Neuronal Susceptibility and Apoptosis in Congenital ZIKV Infection. Annals of Neurology. PMID 28556287 DOI: 10.1002/Ana.24968 |
0.368 |
|
| 2017 |
Son AI, Fu X, Suto F, Liu JS, Hashimoto-Torii K, Torii M. Proteome dynamics during postnatal mouse corpus callosum development. Scientific Reports. 7: 45359. PMID 28349996 DOI: 10.1038/Srep45359 |
0.552 |
|
| 2017 |
Lischinsky JE, Sokolowski K, Peijun L, Esumi S, Kamal Y, Goodrich M, Oboti L, Hammond TR, Krishnamoorthy M, Feldman D, Huntsman M, Liu J, Corbin JG. Embryonic transcription factor expression in mice predicts medial amygdala neuronal identity and sex-specific responses to innate behavioral cues. Elife. 6. PMID 28244870 DOI: 10.7554/Elife.21012 |
0.673 |
|
| 2016 |
Chakraborti S, Natarajan K, Curiel J, Janke C, Liu J. The emerging role of the tubulin code: From the tubulin molecule to neuronal function and disease. Cytoskeleton (Hoboken, N.J.). PMID 26934450 DOI: 10.1002/Cm.21290 |
0.35 |
|
| 2016 |
Fu X, Brown KJ, Rayavarapu S, Nagaraju K, Liu JS. The use of proteomic analysis to study trafficking defects in axons. Methods in Cell Biology. 131: 151-62. PMID 26794512 DOI: 10.1016/Bs.Mcb.2015.06.009 |
0.578 |
|
| 2015 |
Nawabi H, Belin S, Cartoni R, Williams PR, Wang C, Latremolière A, Wang X, Zhu J, Taub DG, Fu X, Yu B, Gu X, Woolf CJ, Liu JS, Gabel CV, et al. Doublecortin-Like Kinases Promote Neuronal Survival and Induce Growth Cone Reformation via Distinct Mechanisms. Neuron. PMID 26526391 DOI: 10.1016/J.Neuron.2015.10.005 |
0.588 |
|
| 2014 |
Pescosolido MF, Stein DM, Schmidt M, El Achkar CM, Sabbagh M, Rogg JM, Tantravahi U, McLean RL, Liu JS, Poduri A, Morrow EM. Genetic and phenotypic diversity of NHE6 mutations in Christianson syndrome. Annals of Neurology. 76: 581-93. PMID 25044251 DOI: 10.1002/Ana.24225 |
0.525 |
|
| 2013 |
Falnikar A, Tole S, Liu M, Liu JS, Baas PW. Polarity in migrating neurons is related to a mechanism analogous to cytokinesis. Current Biology : Cb. 23: 1215-20. PMID 23791725 DOI: 10.1016/J.Cub.2013.05.027 |
0.382 |
|
| 2013 |
Fu X, Brown KJ, Yap CC, Winckler B, Jaiswal JK, Liu JS. Doublecortin (Dcx) family proteins regulate filamentous actin structure in developing neurons. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 33: 709-21. PMID 23303949 DOI: 10.1523/Jneurosci.4603-12.2013 |
0.593 |
|
| 2012 |
Liu JS, Schubert CR, Fu X, Fourniol FJ, Jaiswal JK, Houdusse A, Stultz CM, Moores CA, Walsh CA. Molecular basis for specific regulation of neuronal kinesin-3 motors by doublecortin family proteins. Molecular Cell. 47: 707-21. PMID 22857951 DOI: 10.1016/J.Molcel.2012.06.025 |
0.65 |
|
| 2012 |
Yap CC, Vakulenko M, Kruczek K, Motamedi B, Digilio L, Liu JS, Winckler B. Doublecortin (DCX) mediates endocytosis of neurofascin independently of microtubule binding. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 32: 7439-53. PMID 22649224 DOI: 10.1523/Jneurosci.5318-11.2012 |
0.418 |
|
| 2011 |
Liu ZH, Li PJ, Chen QL, Meng DM, Guo ZG, Liu JS. [Prognostic value of heart-fatty acid-binding protein for myocardial infarction in early post operative period after off-pump coronary artery bypass grafting]. Zhongguo Wei Zhong Bing Ji Jiu Yi Xue = Chinese Critical Care Medicine = Zhongguo Weizhongbing Jijiuyixue. 23: 370-1. PMID 21672390 |
0.362 |
|
| 2011 |
Liu JS. Molecular genetics of neuronal migration disorders. Current Neurology and Neuroscience Reports. 11: 171-8. PMID 21222180 DOI: 10.1007/S11910-010-0176-5 |
0.415 |
|
| 2010 |
Liu JS, Walsh CA. Rare genetic causes of lissencephaly may implicate microtubule-based transport in the pathogenesis of cortical dysplasias Epilepsia. 51: 67. DOI: 10.1111/J.1528-1167.2010.02853.X |
0.493 |
|
| 2008 |
Sepp KJ, Hong P, Lizarraga SB, Liu JS, Mejia LA, Walsh CA, Perrimon N. Identification of neural outgrowth genes using genome-wide RNAi. Plos Genetics. 4: e1000111. PMID 18604272 DOI: 10.1371/Journal.Pgen.1000111 |
0.715 |
|
| 2007 |
Zhang Y, Ryan JA, Di Cesare PE, Liu J, Walsh CA, You Z. Doublecortin is expressed in articular chondrocytes. Biochemical and Biophysical Research Communications. 363: 694-700. PMID 17897623 DOI: 10.1016/J.Bbrc.2007.09.030 |
0.433 |
|
| 2007 |
Friocourt G, Liu JS, Antypa M, Rakic S, Walsh CA, Parnavelas JG. Both doublecortin and doublecortin-like kinase play a role in cortical interneuron migration. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 27: 3875-83. PMID 17409252 DOI: 10.1523/Jneurosci.4530-06.2007 |
0.554 |
|
| 2006 |
Deuel TA, Liu JS, Corbo JC, Yoo SY, Rorke-Adams LB, Walsh CA. Genetic interactions between doublecortin and doublecortin-like kinase in neuronal migration and axon outgrowth. Neuron. 49: 41-53. PMID 16387638 DOI: 10.1016/J.Neuron.2005.10.038 |
0.719 |
|
| 2001 |
Liu JS, Zhao ML, Brosnan CF, Lee SC. Expression of inducible nitric oxide synthase and nitrotyrosine in multiple sclerosis lesions. The American Journal of Pathology. 158: 2057-66. PMID 11395383 DOI: 10.1016/S0002-9440(10)64677-9 |
0.397 |
|
| 2000 |
Liu JS, John GR, Sikora A, Lee SC, Brosnan CF. Modulation of interleukin-1beta and tumor necrosis factor alpha signaling by P2 purinergic receptors in human fetal astrocytes. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 20: 5292-9. PMID 10884313 |
0.633 |
|
| 2000 |
McManus CM, Liu JS, Hahn MT, Hua LL, Brosnan CF, Berman JW, Lee SC. Differential induction of chemokines in human microglia by type I and II interferons. Glia. 29: 273-80. PMID 10642753 DOI: 10.1002/(Sici)1098-1136(20000201)29:3<273::Aid-Glia8>3.0.Co;2-9 |
0.427 |
|
| 1999 |
John GR, Scemes E, Suadicani SO, Liu JS, Charles PC, Lee SC, Spray DC, Brosnan CF. IL-1beta differentially regulates calcium wave propagation between primary human fetal astrocytes via pathways involving P2 receptors and gap junction channels. Proceedings of the National Academy of Sciences of the United States of America. 96: 11613-8. PMID 10500225 DOI: 10.1073/Pnas.96.20.11613 |
0.642 |
|
| 1999 |
Sikora A, Liu J, Brosnan C, Buell G, Chessel I, Bloom BR. Cutting edge: purinergic signaling regulates radical-mediated bacterial killing mechanisms in macrophages through a P2X7-independent mechanism. Journal of Immunology (Baltimore, Md. : 1950). 163: 558-61. PMID 10395640 |
0.419 |
|
| 1998 |
Liu JS, Amaral TD, Brosnan CF, Lee SC. IFNs are critical regulators of IL-1 receptor antagonist and IL-1 expression in human microglia. Journal of Immunology (Baltimore, Md. : 1950). 161: 1989-96. PMID 9712071 |
0.407 |
|
| 1998 |
Hua LL, Liu JS, Brosnan CF, Lee SC. Selective inhibition of human glial inducible nitric oxide synthase by interferon-beta: implications for multiple sclerosis. Annals of Neurology. 43: 384-7. PMID 9506556 DOI: 10.1002/Ana.410430317 |
0.43 |
|
| 1997 |
Brosnan CF, Lee SC, Liu J. Regulation of inducible nitric oxide synthase expression in human glia: implications for inflammatory central nervous system diseases. Biochemical Society Transactions. 25: 679-83. PMID 9191181 |
0.43 |
|
| 1996 |
Liu J, Zhao ML, Brosnan CF, Lee SC. Expression of type II nitric oxide synthase in primary human astrocytes and microglia: role of IL-1beta and IL-1 receptor antagonist. Journal of Immunology (Baltimore, Md. : 1950). 157: 3569-76. PMID 8871657 |
0.441 |
|
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