Judy Shih-Hwa Liu - Publications

Affiliations: 
2010-2017 Center for Neuroscience Research Children's National Medical Center, Washington, DC, United States 
 2017- Neurology/ MCB Brown University, Providence, RI 
Area:
neuronal differentiation, doublecortin, polarity, epilepsy, circadian rhythms

41 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
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  0.48
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  0.704
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  0.564
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  0.578
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  0.67
2021 Chan F, Liu J. Molecular regulation of brain metabolism underlying circadian epilepsy. Epilepsia. PMID 33395505 DOI: 10.1111/epi.16796  0.543
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  0.424
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  0.485
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  0.514
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  0.475
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  0.564
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  0.73
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  0.612
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  0.363
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  0.672
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  0.349
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  0.579
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  0.526
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  0.379
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  0.649
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  0.417
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  0.364
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  0.413
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  0.714
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  0.552
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  0.717
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  0.398
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  0.431
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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