Year |
Citation |
Score |
2023 |
Tejwani L, Ravindra NG, Lee C, Cheng Y, Nguyen B, Luttik K, Ni L, Zhang S, Morrison LM, Gionco J, Xiang Y, Yoon J, Ro H, Haidery F, Grijalva RM, ... ... Lim J, et al. Longitudinal single-cell transcriptional dynamics throughout neurodegeneration in SCA1. Neuron. PMID 38016472 DOI: 10.1016/j.neuron.2023.10.039 |
0.469 |
|
2023 |
Tejwani L, Jung Y, Kokubu H, Sowmithra S, Ni L, Lee C, Sanders B, Lee PJ, Xiang Y, Luttik K, Soriano A, Yoon J, Park J, Ro HH, Ju H, ... ... Lim J, et al. Reduction of Nemo-like kinase increases lysosome biogenesis and ameliorates TDP-43-related neurodegeneration. The Journal of Clinical Investigation. PMID 37384409 DOI: 10.1172/JCI138207 |
0.685 |
|
2022 |
Gauhar Z, Tejwani L, Abdullah U, Saeed S, Shafique S, Badshah M, Choi J, Dong W, Nelson-Williams C, Lifton RP, Lim J, Raja GK. A Novel Missense Mutation in Co-Segregates with Cerebellar Ataxia in a Consanguineous Pakistani Family. Cells. 11. PMID 36231052 DOI: 10.3390/cells11193090 |
0.75 |
|
2022 |
Luttik K, Tejwani L, Ju H, Driessen T, Smeets CJLM, Edamakanti CR, Khan A, Yun J, Opal P, Lim J. Differential effects of Wnt-β-catenin signaling in Purkinje cells and Bergmann glia in spinocerebellar ataxia type 1. Proceedings of the National Academy of Sciences of the United States of America. 119: e2208513119. PMID 35969780 DOI: 10.1073/pnas.2208513119 |
0.717 |
|
2022 |
Olmos V, Gogia N, Luttik K, Haidery F, Lim J. The extra-cerebellar effects of spinocerebellar ataxia type 1 (SCA1): looking beyond the cerebellum. Cellular and Molecular Life Sciences : Cmls. 79: 404. PMID 35802260 DOI: 10.1007/s00018-022-04419-7 |
0.305 |
|
2022 |
Gogia N, Ni L, Olmos V, Haidery F, Luttik K, Lim J. Exploring the Role of Posttranslational Modifications in Spinal and Bulbar Muscular Atrophy. Frontiers in Molecular Neuroscience. 15: 931301. PMID 35726299 DOI: 10.3389/fnmol.2022.931301 |
0.368 |
|
2021 |
Dong T, Tejwani L, Jung Y, Kokubu H, Luttik K, Driessen TM, Lim J. Microglia regulate brain Progranulin levels through the endocytosis-lysosomal pathway. Jci Insight. PMID 34618685 DOI: 10.1172/jci.insight.136147 |
0.752 |
|
2020 |
Khalid M, Raza H, M Driessen T, J Lee P, Tejwani L, Sami A, Nawaz M, Mehmood Baig S, Lim J, Kaukab Raja G. Genetic Risk of Autism Spectrum Disorder in a Pakistani Population. Genes. 11. PMID 33076578 DOI: 10.3390/genes11101206 |
0.719 |
|
2020 |
Tejwani L, Lim J. Pathogenic mechanisms underlying spinocerebellar ataxia type 1. Cellular and Molecular Life Sciences : Cmls. PMID 32306062 DOI: 10.1007/s00018-020-03520-z |
0.756 |
|
2018 |
Khalid M, Driessen TM, Lee JS, Tejwani L, Rasool A, Saqlain M, Shiaq PA, Hanif M, Nawaz A, DeWan AT, Raja GK, Lim J. Association of CACNA1C with bipolar disorder among the Pakistani population. Gene. PMID 29684488 DOI: 10.1016/J.Gene.2018.04.061 |
0.722 |
|
2017 |
Tejwani L, Lim J. Hunting for the mutant without the MAP(K). Cell Research. PMID 29134957 DOI: 10.1038/cr.2017.140 |
0.741 |
|
2015 |
Todd TW, Kokubu H, Miranda HC, Cortes CJ, La Spada AR, Lim J. Nemo-like kinase is a novel regulator of spinal and bulbar muscular atrophy. Elife. 4. PMID 26308581 DOI: 10.7554/eLife.08493 |
0.307 |
|
2014 |
Ju H, Kokubu H, Lim J. Beyond the glutamine expansion: influence of posttranslational modifications of ataxin-1 in the pathogenesis of spinocerebellar ataxia type 1. Molecular Neurobiology. 50: 866-74. PMID 24752589 DOI: 10.1007/s12035-014-8703-z |
0.368 |
|
2013 |
Sakai Y, Ohkubo K, Matsushita Y, Akamine S, Ishizaki Y, Torisu H, Ihara K, Sanefuji M, Kim MS, Lee KU, Shaw CA, Lim J, Nakabeppu Y, Hara T. Neuroendocrine phenotypes in a boy with 5q14 deletion syndrome implicate the regulatory roles of myocyte-specific enhancer factor 2C in the postnatal hypothalamus. European Journal of Medical Genetics. 56: 475-83. PMID 23832106 DOI: 10.1016/J.Ejmg.2013.06.009 |
0.435 |
|
2013 |
Kim S, Chahrour M, Ben-Shachar S, Lim J. Ube3a/E6AP is involved in a subset of MeCP2 functions. Biochemical and Biophysical Research Communications. 437: 67-73. PMID 23791832 DOI: 10.1016/J.Bbrc.2013.06.036 |
0.712 |
|
2013 |
Ju H, Kokubu H, Todd TW, Kahle JJ, Kim S, Richman R, Chirala K, Orr HT, Zoghbi HY, Lim J. Polyglutamine disease toxicity is regulated by Nemo-like kinase in spinocerebellar ataxia type 1. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 33: 9328-36. PMID 23719801 DOI: 10.1523/Jneurosci.3465-12.2013 |
0.71 |
|
2011 |
Kahle JJ, Gulbahce N, Shaw CA, Lim J, Hill DE, Barabási AL, Zoghbi HY. Comparison of an expanded ataxia interactome with patient medical records reveals a relationship between macular degeneration and ataxia. Human Molecular Genetics. 20: 510-27. PMID 21078624 DOI: 10.1093/Hmg/Ddq496 |
0.724 |
|
2010 |
Duvick L, Barnes J, Ebner B, Agrawal S, Andresen M, Lim J, Giesler GJ, Zoghbi HY, Orr HT. SCA1-like disease in mice expressing wild-type ataxin-1 with a serine to aspartic acid replacement at residue 776. Neuron. 67: 929-35. PMID 20869591 DOI: 10.1016/J.Neuron.2010.08.022 |
0.583 |
|
2008 |
Lim J, Jafar-Nejad H, Hsu YC, Choi KW. Novel function of the class I bHLH protein Daughterless in the negative regulation of proneural gene expression in the Drosophila eye. Embo Reports. 9: 1128-33. PMID 18758436 DOI: 10.1038/Embor.2008.166 |
0.365 |
|
2008 |
Lim J, Crespo-Barreto J, Jafar-Nejad P, Bowman AB, Richman R, Hill DE, Orr HT, Zoghbi HY. Opposing effects of polyglutamine expansion on native protein complexes contribute to SCA1. Nature. 452: 713-8. PMID 18337722 DOI: 10.1038/Nature06731 |
0.734 |
|
2007 |
Al-Ramahi I, Pérez AM, Lim J, Zhang M, Sorensen R, de Haro M, Branco J, Pulst SM, Zoghbi HY, Botas J. dAtaxin-2 mediates expanded Ataxin-1-induced neurodegeneration in a Drosophila model of SCA1. Plos Genetics. 3: e234. PMID 18166084 DOI: 10.1371/Journal.Pgen.0030234 |
0.593 |
|
2007 |
Lim J, Lee OK, Hsu YC, Singh A, Choi KW. Drosophila TRAP230/240 are essential coactivators for Atonal in retinal neurogenesis. Developmental Biology. 308: 322-30. PMID 17585897 DOI: 10.1016/J.Ydbio.2007.05.029 |
0.35 |
|
2006 |
Lam YC, Bowman AB, Jafar-Nejad P, Lim J, Richman R, Fryer JD, Hyun ED, Duvick LA, Orr HT, Botas J, Zoghbi HY. ATAXIN-1 interacts with the repressor Capicua in its native complex to cause SCA1 neuropathology. Cell. 127: 1335-47. PMID 17190598 DOI: 10.1016/J.Cell.2006.11.038 |
0.748 |
|
2006 |
Lim J, Hao T, Shaw C, Patel AJ, Szabó G, Rual JF, Fisk CJ, Li N, Smolyar A, Hill DE, Barabási AL, Vidal M, Zoghbi HY. A protein-protein interaction network for human inherited ataxias and disorders of Purkinje cell degeneration. Cell. 125: 801-14. PMID 16713569 DOI: 10.1016/J.Cell.2006.03.032 |
0.686 |
|
2005 |
Rual JF, Venkatesan K, Hao T, Hirozane-Kishikawa T, Dricot A, Li N, Berriz GF, Gibbons FD, Dreze M, Ayivi-Guedehoussou N, Klitgord N, Simon C, Boxem M, Milstein S, Rosenberg J, ... ... Lim J, et al. Towards a proteome-scale map of the human protein-protein interaction network. Nature. 437: 1173-8. PMID 16189514 DOI: 10.1038/Nature04209 |
0.545 |
|
2004 |
Lim J, Choi KW. Induction and autoregulation of the anti-proneural gene Bar during retinal neurogenesis in Drosophila. Development (Cambridge, England). 131: 5573-80. PMID 15496446 DOI: 10.1242/Dev.01426 |
0.323 |
|
2003 |
Lim J, Choi KW. Bar homeodomain proteins are anti-proneural in the Drosophila eye: transcriptional repression of atonal by Bar prevents ectopic retinal neurogenesis. Development (Cambridge, England). 130: 5965-74. PMID 14573515 DOI: 10.1242/Dev.00818 |
0.355 |
|
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