Modeling mitochondrial encephalomyopathy in Drosophila

od Palladino, Michael J.
Izdano 2010

Cleavage of mispaired heteroduplex DNA substrates by numerous restriction enzymes

od Langhans, Mark T., Palladino, Michael J.
Izdano 2008

Hsp70 and Hsp90 mediated proteasomal degradation underlies TPI(sugarkill) pathogenesis in Drosophila

od Hrizo, Stacy L., Palladino, Michael J.
Izdano 2010

Of fish, flies, worms and men: powerful approaches to neuropsychiatric disease using genetic models

od Burton, Edward A., Palladino, Michael J.
Izdano 2010

Neuropathology in Drosophila Membrane Excitability Mutants

od Fergestad, Tim, Ganetzky, Barry, Palladino, Michael J.
Izdano 2006

Temperature-sensitive paralytic mutants are enriched for those causing neurodegeneration in Drosophila.

od Palladino, Michael J, Hadley, Tricia J, Ganetzky, Barry
Izdano 2002

A pump-independent function of the Na,K-ATPase is required for epithelial junction function and tracheal tube-size control

od Paul, Sarah M., Palladino, Michael J., Beitel, Greg J.
Izdano 2007

Degradation of Functional Triose Phosphate Isomerase Protein Underlies sugarkill Pathology

od Seigle, Jacquelyn L., Celotto, Alicia M., Palladino, Michael J.
Izdano 2008

Neural Dysfunction and Neurodegeneration inDrosophila Na(+)/K(+) ATPase Alpha Subunit Mutants

od Palladino, Michael J., Bower, Jill E., Kreber, Robert, Ganetzky, Barry
Izdano u J Neurosci (2003)

Sleep and circadian defects in a Drosophila model of mitochondrial encephalomyopathy

od Fogle, Keri J., Mobini, Catherina L., Paseos, Abygail S., Palladino, Michael J.
Izdano u Neurobiol Sleep Circadian Rhythms (2019)

Drosophila Model of Human Inherited Triosephosphate Isomerase Deficiency Glycolytic Enzymopathy

od Celotto, Alicia M., Frank, Adam C., Seigle, Jacquelyn L., Palladino, Michael J.
Izdano 2006

Modes of Metabolic Compensation during Mitochondrial Disease Using the Drosophila Model of ATP6 Dysfunction

od Celotto, Alicia M., Chiu, Wai Kan, Van Voorhies, Wayne, Palladino, Michael J.
Izdano 2011

Genetically encoded redox sensor identifies the role of ROS in degenerative and mitochondrial disease pathogenesis

od Liu, Zhaohui, Celotto, Alicia M., Romero, Guillermo, Wipf, Peter, Palladino, Michael J.
Izdano 2011

A novel Drosophila SOD2 mutant demonstrates a role for mitochondrial ROS in neurodevelopment and disease

od Celotto, Alicia M, Liu, Zhaohui, VanDemark, Andrew P, Palladino, Michael J
Izdano 2012

The ATP-sensitive K channel is seizure protective and required for effective dietary therapy in a model of mitochondrial encephalomyopathy

od Fogle, Keri J., Hertzler, J. Ian, Shon, Joy H., Palladino, Michael J.
Izdano u J Neurogenet (2016)

Small mitochondrial-targeted RNAs modulate endogenous mitochondrial protein expression in vivo

od Towheed, Atif, Markantone, Desiree M., Crain, Aaron T., Celotto, Alicia M., Palladino, Michael J.
Izdano 2014

Neuropathology in Drosophila Mutants With Increased Seizure Susceptibility

od Fergestad, Tim, Olson, Lisa, Patel, Khelan P., Miller, Rosie, Palladino, Michael J., Ganetzky, Barry
Izdano 2008

Genome-wide screen for modifiers of Na(+)/K(+)ATPase alleles identifies critical genetic loci

od Talsma, Aaron D, Chaves, John F, LaMonaca, Alexandra, Wieczorek, Emily D, Palladino, Michael J
Izdano u Mol Brain (2014)

Mutational analysis implicates the amyloid fibril as the toxic entity in Huntington’s disease

od Drombosky, Kenneth W., Rode, Sascha, Kodali, Ravi, Jacob, Tija C., Palladino, Michael J., Wetzel, Ronald
Izdano u Neurobiol Dis (2018)

Protein coding mitochondrial-targeted RNAs rescue mitochondrial disease in vivo

od Markantone, Desiree M., Towheed, Atif, Crain, Aaron T., Collins, Jessica M., Celotto, Alicia M., Palladino, Michael J.
Izdano u Neurobiol Dis (2018)