Year |
Citation |
Score |
2023 |
Yang L, Borne F, Betz A, Aardema ML, Zhen Y, Peng J, Visconti R, Wu M, Roland BP, Talsma AD, Palladino MJ, Petschenka G, Andolfatto P. Predatory fireflies and their toxic firefly prey have evolved distinct toxin resistance strategies. Current Biology : Cb. PMID 37989309 DOI: 10.1016/j.cub.2023.10.063 |
0.706 |
|
2019 |
Taverner AM, Yang L, Barile ZJ, Lin B, Peng J, Pinharanda AP, Rao AS, Roland BP, Talsma AD, Wei D, Petschenka G, Palladino MJ, Andolfatto P. Adaptive substitutions underlying cardiac glycoside insensitivity in insects exhibit epistasis . Elife. 8. PMID 31453806 DOI: 10.7554/Elife.48224 |
0.728 |
|
2019 |
Roland BP, Richards KR, Hrizo SL, Eicher S, Barile ZJ, Chang TC, Savon G, Bianchi P, Fermo E, Ricerca BM, Tortorolo L, Vockley J, VanDemark AP, Palladino MJ. Missense variant in TPI1 (Arg189Gln) causes neurologic deficits through structural changes in the triosephosphate isomerase catalytic site and reduced enzyme levels in vivo. Biochimica Et Biophysica Acta. Molecular Basis of Disease. PMID 31075491 DOI: 10.1016/J.Bbadis.2019.05.002 |
0.755 |
|
2019 |
Fogle KJ, Mobini CL, Paseos AS, Palladino MJ. Sleep and circadian defects in a model of mitochondrial encephalomyopathy. Neurobiology of Sleep and Circadian Rhythms. 6: 44-52. PMID 30868108 DOI: 10.1016/J.Nbscr.2019.01.003 |
0.313 |
|
2019 |
Fogle KJ, Smith AR, Satterfield SL, Gutierrez AC, Hertzler JI, McCardell CS, Shon JH, Barile ZJ, Novak MO, Palladino MJ. Ketogenic and anaplerotic dietary modifications ameliorate seizure activity in Drosophila models of mitochondrial encephalomyopathy and glycolytic enzymopathy. Molecular Genetics and Metabolism. PMID 30683556 DOI: 10.1016/J.Ymgme.2019.01.008 |
0.318 |
|
2019 |
Taverner AM, Yang L, Barile ZJ, Lin B, Peng J, Pinharanda AP, Rao AS, Roland BP, Talsma AD, Wei D, Petschenka G, Palladino MJ, Andolfatto P. Author response: Adaptive substitutions underlying cardiac glycoside insensitivity in insects exhibit epistasis in vivo Elife. DOI: 10.7554/Elife.48224.029 |
0.702 |
|
2018 |
Drombosky KW, Rode S, Kodali R, Jacob TC, Palladino MJ, Wetzel R. Mutational analysis implicates the amyloid fibril as the toxic entity in Huntington's disease. Neurobiology of Disease. PMID 30171891 DOI: 10.1016/J.Nbd.2018.08.019 |
0.302 |
|
2018 |
Markantone DM, Towheed A, Crain AT, Collins JM, Celotto AM, Palladino MJ. Protein coding mitochondrial-targeted RNAs rescue mitochondrial disease in vivo. Neurobiology of Disease. PMID 29908326 DOI: 10.1016/J.Nbd.2018.06.009 |
0.38 |
|
2016 |
Fogle KJ, Hertzler JI, Shon JH, Palladino MJ. The ATP-sensitive K channel is seizure protective and required for effective dietary therapy in a model of mitochondrial encephalomyopathy. Journal of Neurogenetics. 1-12. PMID 27868454 DOI: 10.1080/01677063.2016.1252765 |
0.309 |
|
2016 |
Roland BP, Zeccola AM, Larsen SB, Amrich CG, Talsma AD, Stuchul KA, Heroux A, Levitan ES, VanDemark AP, Palladino MJ. Structural and Genetic Studies Demonstrate Neurologic Dysfunction in Triosephosphate Isomerase Deficiency Is Associated with Impaired Synaptic Vesicle Dynamics. Plos Genetics. 12: e1005941. PMID 27031109 DOI: 10.1371/Journal.Pgen.1005941 |
0.735 |
|
2015 |
Roland BP, Amrich CG, Kammerer CJ, Stuchul KA, Larsen SB, Rode S, Aslam AA, Heroux A, Wetzel R, VanDemark AP, Palladino MJ. Triosephosphate isomerase I170V alters catalytic site, enhances stability and induces pathology in a Drosophila model of TPI deficiency. Biochimica Et Biophysica Acta. 1852: 61-9. PMID 25463631 DOI: 10.1016/J.Bbadis.2014.10.010 |
0.753 |
|
2014 |
Talsma AD, Chaves JF, LaMonaca A, Wieczorek ED, Palladino MJ. Genome-wide screen for modifiers of Na (+) /K (+) ATPase alleles identifies critical genetic loci. Molecular Brain. 7: 89. PMID 25476251 DOI: 10.1186/S13041-014-0089-3 |
0.401 |
|
2014 |
Towheed A, Markantone DM, Crain AT, Celotto AM, Palladino MJ. Small mitochondrial-targeted RNAs modulate endogenous mitochondrial protein expression in vivo. Neurobiology of Disease. 69: 15-22. PMID 24807207 DOI: 10.1016/J.Nbd.2014.04.017 |
0.36 |
|
2013 |
Roland BP, Stuchul KA, Larsen SB, Amrich CG, Vandemark AP, Celotto AM, Palladino MJ. Evidence of a triosephosphate isomerase non-catalytic function crucial to behavior and longevity. Journal of Cell Science. 126: 3151-8. PMID 23641070 DOI: 10.1242/Jcs.124586 |
0.744 |
|
2013 |
Hrizo SL, Fisher IJ, Long DR, Hutton JA, Liu Z, Palladino MJ. Early mitochondrial dysfunction leads to altered redox chemistry underlying pathogenesis of TPI deficiency. Neurobiology of Disease. 54: 289-96. PMID 23318931 DOI: 10.1016/J.Nbd.2012.12.020 |
0.373 |
|
2012 |
Celotto AM, Liu Z, Vandemark AP, Palladino MJ. A novel Drosophila SOD2 mutant demonstrates a role for mitochondrial ROS in neurodevelopment and disease. Brain and Behavior. 2: 424-34. PMID 22950046 DOI: 10.1002/Brb3.73 |
0.363 |
|
2012 |
Liu Z, Celotto AM, Romero G, Wipf P, Palladino MJ. Genetically encoded redox sensor identifies the role of ROS in degenerative and mitochondrial disease pathogenesis. Neurobiology of Disease. 45: 362-8. PMID 21889980 DOI: 10.1016/J.Nbd.2011.08.022 |
0.338 |
|
2011 |
Celotto AM, Chiu WK, Van Voorhies W, Palladino MJ. Modes of metabolic compensation during mitochondrial disease using the Drosophila model of ATP6 dysfunction. Plos One. 6: e25823. PMID 21991365 DOI: 10.1371/Journal.Pone.0025823 |
0.341 |
|
2010 |
Hrizo SL, Palladino MJ. Hsp70- and Hsp90-mediated proteasomal degradation underlies TPI sugarkill pathogenesis in Drosophila. Neurobiology of Disease. 40: 676-83. PMID 20727972 DOI: 10.1016/J.Nbd.2010.08.011 |
0.374 |
|
2010 |
Burton EA, Palladino MJ. Of fish, flies, worms and men: powerful approaches to neuropsychiatric disease using genetic models. Neurobiology of Disease. 40: 1-3. PMID 20654715 DOI: 10.1016/J.Nbd.2010.07.009 |
0.33 |
|
2010 |
Palladino MJ. Modeling mitochondrial encephalomyopathy in Drosophila. Neurobiology of Disease. 40: 40-5. PMID 20472065 DOI: 10.1016/J.Nbd.2010.05.009 |
0.343 |
|
2009 |
Ashmore LJ, Hrizo SL, Paul SM, Van Voorhies WA, Beitel GJ, Palladino MJ. Novel mutations affecting the Na, K ATPase alpha model complex neurological diseases and implicate the sodium pump in increased longevity. Human Genetics. 126: 431-47. PMID 19455355 DOI: 10.1007/S00439-009-0673-2 |
0.392 |
|
2008 |
Seigle JL, Celotto AM, Palladino MJ. Degradation of functional triose phosphate isomerase protein underlies sugarkill pathology. Genetics. 179: 855-62. PMID 18458110 DOI: 10.1534/Genetics.108.087551 |
0.419 |
|
2008 |
Fergestad T, Olson L, Patel KP, Miller R, Palladino MJ, Ganetzky B. Neuropathology in Drosophila mutants with increased seizure susceptibility. Genetics. 178: 947-56. PMID 18245348 DOI: 10.1534/Genetics.107.082115 |
0.69 |
|
2007 |
Paul SM, Palladino MJ, Beitel GJ. A pump-independent function of the Na,K-ATPase is required for epithelial junction function and tracheal tube-size control. Development (Cambridge, England). 134: 147-55. PMID 17164420 DOI: 10.1242/Dev.02710 |
0.321 |
|
2006 |
Celotto AM, Frank AC, Seigle JL, Palladino MJ. Drosophila model of human inherited triosephosphate isomerase deficiency glycolytic enzymopathy. Genetics. 174: 1237-46. PMID 16980388 DOI: 10.1534/Genetics.106.063206 |
0.678 |
|
2006 |
Celotto AM, Frank AC, McGrath SW, Fergestad T, Van Voorhies WA, Buttle KF, Mannella CA, Palladino MJ. Mitochondrial encephalomyopathy in Drosophila. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 26: 810-20. PMID 16421301 DOI: 10.1523/Jneurosci.4162-05.2006 |
0.647 |
|
2006 |
Fergestad T, Ganetzky B, Palladino MJ. Neuropathology in Drosophila membrane excitability mutants. Genetics. 172: 1031-42. PMID 16272407 DOI: 10.1534/Genetics.105.050625 |
0.692 |
|
2005 |
Celotto AM, Palladino MJ. Drosophila: a "model" model system to study neurodegeneration. Molecular Interventions. 5: 292-303. PMID 16249525 DOI: 10.1124/Mi.5.5.9 |
0.313 |
|
2003 |
Palladino MJ, Bower JE, Kreber R, Ganetzky B. Neural dysfunction and neurodegeneration in Drosophila Na+/K+ ATPase alpha subunit mutants. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 23: 1276-86. PMID 12598616 DOI: 10.1523/Jneurosci.23-04-01276.2003 |
0.703 |
|
2002 |
Palladino MJ, Hadley TJ, Ganetzky B. Temperature-sensitive paralytic mutants are enriched for those causing neurodegeneration in Drosophila. Genetics. 161: 1197-208. PMID 12136022 |
0.688 |
|
2000 |
Palladino MJ, Keegan LP, O'Connell MA, Reenan RA. A-to-I pre-mRNA editing in Drosophila is primarily involved in adult nervous system function and integrity. Cell. 102: 437-49. PMID 10966106 DOI: 10.1016/S0092-8674(00)00049-0 |
0.759 |
|
2000 |
Palladino MJ, Keegan LP, O'Connell MA, Reenan RA. dADAR, a Drosophila double-stranded RNA-specific adenosine deaminase is highly developmentally regulated and is itself a target for RNA editing. Rna (New York, N.Y.). 6: 1004-18. PMID 10917596 DOI: 10.1017/S1355838200000248 |
0.75 |
|
2000 |
Hanrahan CJ, Palladino MJ, Ganetzky B, Reenan RA. RNA editing of the Drosophila para Na(+) channel transcript. Evolutionary conservation and developmental regulation. Genetics. 155: 1149-60. PMID 10880477 |
0.736 |
|
1999 |
Hanrahan CJ, Palladino MJ, Bonneau LJ, Reenan RA. RNA editing of a Drosophila sodium channel gene. Annals of the New York Academy of Sciences. 868: 51-66. PMID 10414281 DOI: 10.1111/J.1749-6632.1999.Tb11273.X |
0.745 |
|
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