Puneet Opal, MD, PhD - Publications

Northwestern University, Evanston, IL 
Neurodegeneration, Neurology

29 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
2019 Hu YS, Do J, Edamakanti CR, Kini AR, Martina M, Stupp SI, Opal P. Self-assembling vascular endothelial growth factor nanoparticles improve function in spinocerebellar ataxia type 1. Brain : a Journal of Neurology. PMID 30649233 DOI: 10.1093/brain/awy328  0.68
2017 Sun X, Lu B, Han C, Qiu W, Jin Q, Li D, Li Q, Yang Q, Wen Q, Opal P, Kini AR, Crispino JD, Huang Z. ANP32A dysregulation contributes to abnormal megakaryopoiesis in acute megakaryoblastic leukemia. Blood Cancer Journal. 7: 661. PMID 29269781 DOI: 10.1038/s41408-017-0031-x  0.4
2016 Cvetanovic M, Hu YS, Opal P. Mutant Ataxin-1 Inhibits Neural Progenitor Cell Proliferation in SCA1. Cerebellum (London, England). PMID 27306906 DOI: 10.1007/s12311-016-0794-9  0.88
2015 Lowery J, Jain N, Kuczmarski ER, Mahammad S, Goldman A, Gelfand VI, Opal P, Goldman RD. Abnormal Intermediate Filament Organization Alters Mitochondrial Motility in Giant Axonal Neuropathy Fibroblasts. Molecular Biology of the Cell. PMID 26700320 DOI: 10.1091/mbc.E15-09-0627  0.88
2015 Dell'Orco JM, Wasserman AH, Chopra R, Ingram MA, Hu YS, Singh V, Wulff H, Opal P, Orr HT, Shakkottai VG. Neuronal Atrophy Early in Degenerative Ataxia Is a Compensatory Mechanism to Regulate Membrane Excitability. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 35: 11292-307. PMID 26269637 DOI: 10.1523/JNEUROSCI.1357-15.2015  0.88
2015 Cvetanovic M, Ingram M, Orr H, Opal P. Early activation of microglia and astrocytes in mouse models of spinocerebellar ataxia type 1. Neuroscience. 289: 289-99. PMID 25595967 DOI: 10.1016/j.neuroscience.2015.01.003  0.88
2015 Rozenfeld MN, Nemeth AJ, Walker MT, Mohan P, Wang X, Parrish TB, Opal P. An investigation of diffusion imaging techniques in the evaluation of spinocerebellar ataxia and multisystem atrophy. Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia. 22: 166-72. PMID 25439745 DOI: 10.1016/j.jocn.2014.08.006  0.88
2014 Venkatraman A, Hu YS, Didonna A, Cvetanovic M, Krbanjevic A, Bilesimo P, Opal P. The histone deacetylase HDAC3 is essential for Purkinje cell function, potentially complicating the use of HDAC inhibitors in SCA1. Human Molecular Genetics. 23: 3733-45. PMID 24594842 DOI: 10.1093/hmg/ddu081  0.88
2014 Opal P, Orr HT. Animal Models of Spinocerebellar Ataxia Type 1 Movement Disorders: Genetics and Models: Second Edition. 979-990. DOI: 10.1016/B978-0-12-405195-9.00063-9  0.88
2013 Mahammad S, Murthy SN, Didonna A, Grin B, Israeli E, Perrot R, Bomont P, Julien JP, Kuczmarski E, Opal P, Goldman RD. Giant axonal neuropathy-associated gigaxonin mutations impair intermediate filament protein degradation. The Journal of Clinical Investigation. 123: 1964-75. PMID 23585478 DOI: 10.1172/JCI66387  0.88
2013 Opal P, Zoghbi H. The Hereditary Ataxias Emery and Rimoin's Principles and Practice of Medical Genetics. 1-32. DOI: 10.1016/B978-0-12-383834-6.00125-7  0.88
2012 Cvetanovic M, Kular RK, Opal P. LANP mediates neuritic pathology in Spinocerebellar ataxia type 1. Neurobiology of Disease. 48: 526-32. PMID 22884877 DOI: 10.1016/j.nbd.2012.07.024  0.88
2011 Cvetanovic M, Patel JM, Marti HH, Kini AR, Opal P. Vascular endothelial growth factor ameliorates the ataxic phenotype in a mouse model of spinocerebellar ataxia type 1. Nature Medicine. 17: 1445-7. PMID 22001907 DOI: 10.1038/nm.2494  0.88
2010 Kular RK, Gogliotti RG, Opal P. Cpd-1 null mice display a subtle neurological phenotype. Plos One. 5. PMID 20844742 DOI: 10.1371/journal.pone.0012649  0.88
2009 Kular RK, Cvetanovic M, Siferd S, Kini AR, Opal P. Neuronal differentiation is regulated by leucine-rich acidic nuclear protein (LANP), a member of the inhibitor of histone acetyltransferase complex. The Journal of Biological Chemistry. 284: 7783-92. PMID 19136565 DOI: 10.1074/jbc.M806150200  0.88
2008 Paganoni S, Seelaus CA, Ormond KE, Opal P. Association of spinocerebellar ataxia type 3 and spinocerebellar ataxia type 8 microsatellite expansions: genetic counseling implications. Movement Disorders : Official Journal of the Movement Disorder Society. 23: 154-5. PMID 17987652 DOI: 10.1002/mds.21797  0.88
2007 Cvetanovic M, Rooney RJ, Garcia JJ, Toporovskaya N, Zoghbi HY, Opal P. The role of LANP and ataxin 1 in E4F-mediated transcriptional repression. Embo Reports. 8: 671-7. PMID 17557114 DOI: 10.1038/sj.embor.7400983  0.88
2007 Paganoni S, Naidech AM, Opal P. Huntington's disease presenting as postsurgical psychosis. Movement Disorders : Official Journal of the Movement Disorder Society. 22: 1209-10. PMID 17443707 DOI: 10.1002/mds.21522  0.88
2007 Bassuk AG, Chen YZ, Batish SD, Nagan N, Opal P, Chance PF, Bennett CL. In cis autosomal dominant mutation of Senataxin associated with tremor/ataxia syndrome. Neurogenetics. 8: 45-9. PMID 17096168 DOI: 10.1007/s10048-006-0067-8  0.88
2004 Opal P, Garcia JJ, McCall AE, Xu B, Weeber EJ, Sweatt JD, Orr HT, Zoghbi HY. Generation and characterization of LANP/pp32 null mice. Molecular and Cellular Biology. 24: 3140-9. PMID 15060138 DOI: 10.1128/MCB.24.8.3140-3149.2004  0.88
2003 Opal P, Garcia JJ, Propst F, Matilla A, Orr HT, Zoghbi HY. Mapmodulin/leucine-rich acidic nuclear protein binds the light chain of microtubule-associated protein 1B and modulates neuritogenesis. The Journal of Biological Chemistry. 278: 34691-9. PMID 12807913 DOI: 10.1074/jbc.M302785200  0.88
2002 Opal P, Zoghbi HY. The role of chaperones in polyglutamine disease. Trends in Molecular Medicine. 8: 232-6. PMID 12067633 DOI: 10.1016/S1471-4914(02)02310-9  0.88
2002 Opal P, Tintner R, Jankovic J, Leung J, Breakefield XO, Friedman J, Ozelius L. Intrafamilial phenotypic variability of the DYT1 dystonia: from asymptomatic TOR1A gene carrier status to dystonic storm. Movement Disorders : Official Journal of the Movement Disorder Society. 17: 339-45. PMID 11921121 DOI: 10.1002/mds.10096  0.88
2001 Cummings CJ, Sun Y, Opal P, Antalffy B, Mestril R, Orr HT, Dillmann WH, Zoghbi HY. Over-expression of inducible HSP70 chaperone suppresses neuropathology and improves motor function in SCA1 mice. Human Molecular Genetics. 10: 1511-8. PMID 11448943  0.88
1996 Straube-West K, Loomis PA, Opal P, Goldman RD. Alterations in neural intermediate filament organization: functional implications and the induction of pathological changes related to motor neuron disease. Journal of Cell Science. 109: 2319-29. PMID 8886982  0.88
1996 Goldman RD, Khuon S, Chou YH, Opal P, Steinert PM. The function of intermediate filaments in cell shape and cytoskeletal integrity. The Journal of Cell Biology. 134: 971-83. PMID 8769421  0.88
1996 Chou YH, Opal P, Quinlan RA, Goldman RD. The relative roles of specific N- and C-terminal phosphorylation sites in the disassembly of intermediate filament in mitotic BHK-21 cells. Journal of Cell Science. 109: 817-26. PMID 8718673  0.88
1992 Eriksson JE, Opal P, Goldman RD. Intermediate filament dynamics. Current Opinion in Cell Biology. 4: 99-104. PMID 1558758 DOI: 10.1016/0955-0674(92)90065-K  0.88
1991 Goldman RD, Chou YH, Dessev C, Dessev G, Eriksson J, Goldman A, Khuon S, Kohnken R, Lowy M, Miller R, Murphy K, Opal P, Skalli O, Straube K. Dynamic aspects of cytoskeletal and karyoskeletal intermediate filament systems during the cell cycle Cold Spring Harbor Symposia On Quantitative Biology. 56: 629-642. PMID 1819512  0.88
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