Michael John Palladino

Affiliations: 
Pharmacology University of Pittsburgh, Pittsburgh, PA, United States 
Area:
Neurodegeneration
Website:
http://www.pharmacology.us/Faculty/MichaelPalladino
Google:
"Michael John Palladino"
Mean distance: 15.35 (cluster 11)
 
SNBCP
Cross-listing: Chemistry Tree

Parents

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Robert A.G. Reenan grad student 2000 University of Connecticut (FlyTree)
 (dADAR, a Drosophila RNA editing enzyme, modifies ion channel transcripts and is required for normal behavior and nervous system integrity.)
Barry Ganetzky post-doc 2003 UW Madison

Children

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Adam Charles Frank research assistant 2003-2007 Pitt
Bartholomew P Roland grad student 2008-2014 University of Pittsburgh School of Medicine (Chemistry Tree)
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Publications

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Drombosky KW, Rode S, Kodali R, et al. (2018) Mutational analysis implicates the amyloid fibril as the toxic entity in Huntington's disease. Neurobiology of Disease
Markantone DM, Towheed A, Crain AT, et al. (2018) Protein coding mitochondrial-targeted RNAs rescue mitochondrial disease in vivo. Neurobiology of Disease
Roland BP, Zeccola AM, Larsen SB, et al. (2016) Structural and Genetic Studies Demonstrate Neurologic Dysfunction in Triosephosphate Isomerase Deficiency Is Associated with Impaired Synaptic Vesicle Dynamics. Plos Genetics. 12: e1005941
Dong W, Zhang X, Liu W, et al. (2015) A conserved polybasic domain mediates plasma membrane targeting of Lgl and its regulation by hypoxia. The Journal of Cell Biology
Roland BP, Amrich CG, Kammerer CJ, et al. (2015) 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
Talsma AD, Chaves JF, LaMonaca A, et al. (2014) Genome-wide screen for modifiers of Na (+) /K (+) ATPase alleles identifies critical genetic loci. Molecular Brain. 7: 89
Chiu WK, Towheed A, Palladino MJ. (2014) Genetically encoded redox sensors. Methods in Enzymology. 542: 263-87
Towheed A, Markantone DM, Crain AT, et al. (2014) Small mitochondrial-targeted RNAs modulate endogenous mitochondrial protein expression in vivo. Neurobiology of Disease. 69: 15-22
Roland BP, Stuchul KA, Larsen SB, et al. (2013) Evidence of a triosephosphate isomerase non-catalytic function crucial to behavior and longevity. Journal of Cell Science. 126: 3151-8
Hrizo SL, Fisher IJ, Long DR, et al. (2013) Early mitochondrial dysfunction leads to altered redox chemistry underlying pathogenesis of TPI deficiency. Neurobiology of Disease. 54: 289-96
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