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Newly discovered roles of triosephosphate isomerase including functions within the nucleus

Molecular medicine (Cambridge, Mass.), 2023-01, Vol.29 (1), p.18-18, Article 18

2023

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

Neurobiology of disease, 2018-12, Vol.120, p.126-138

2018

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Neuromuscular dysfunction and pathogenesis in triosephosphate isomerase deficiency

Scientific reports, 2024-08, Vol.14 (1), p.18575-16, Article 18575

2024

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Chemical Targeting of Voltage Sensitive Dyes to Specific Cells and Molecules in the Brain

Journal of the American Chemical Society, 2020-05, Vol.142 (20), p.9285-9301

2020

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A conserved polybasic domain mediates plasma membrane targeting of Lgl and its regulation by hypoxia

The Journal of cell biology, 2015-10, Vol.211 (2), p.273-286

2015

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Modes of metabolic compensation during mitochondrial disease using the Drosophila model of ATP6 dysfunction

PloS one, 2011-10, Vol.6 (10), p.e25823-e25823

2011

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Adaptive substitutions underlying cardiac glycoside insensitivity in insects exhibit epistasis in vivo

eLife, 2019-08, Vol.8

2019

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Identification of protein quality control regulators using a Drosophila model of TPI deficiency

Neurobiology of disease, 2021-05, Vol.152, p.105299-105299, Article 105299

2021

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Structural and Genetic Studies Demonstrate Neurologic Dysfunction in Triosephosphate Isomerase Deficiency Is Associated with Impaired Synaptic Vesicle Dynamics

PLoS genetics, 2016-03, Vol.12 (3), p.e1005941-e1005941

2016

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Itavastatin and resveratrol increase triosephosphate isomerase protein in a newly identified variant of TPI deficiency

Disease models & mechanisms, 2022-05, Vol.15 (5)

2022

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Modeling mitochondrial encephalomyopathy in Drosophila

Neurobiology of disease, 2010-10, Vol.40 (1), p.40-45

Palladino, Michael J

2010

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

Development (Cambridge), 2007-01, Vol.134 (1), p.147-155

2007

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Protein coding mitochondrial-targeted RNAs rescue mitochondrial disease in vivo

Neurobiology of disease, 2018-09, Vol.117, p.203-210

2018

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A-to-I Pre-mRNA Editing in Drosophila Is Primarily Involved in Adult Nervous System Function and Integrity

Cell, 2000-08, Vol.102 (4), p.437-449

2000

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

Neurobiology of disease, 2012-01, Vol.45 (1), p.362-368

2012

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Murine model of triosephosphate isomerase deficiency with anemia and severe neuromuscular dysfunction

Current research in neurobiology, 2022-01, Vol.3, p.100062-100062, Article 100062

2022

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

Neurobiology of disease, 2014-09, Vol.69, p.15-22

2014

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Hsp70- and Hsp90-mediated proteasomal degradation underlies TPIsugarkill pathogenesis in Drosophila

Neurobiology of disease, 2010-12, Vol.40 (3), p.676-683

2010

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Early mitochondrial dysfunction leads to altered redox chemistry underlying pathogenesis of TPI deficiency

Neurobiology of disease, 2013-06, Vol.54, p.289-296

2013

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Sleep and circadian defects in a Drosophila model of mitochondrial encephalomyopathy

Neurobiology of sleep and circadian rhythms, 2019-01, Vol.6, p.44-52

2019

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Novel mutations affecting the Na, K ATPase alpha model complex neurological diseases and implicate the sodium pump in increased longevity

Human genetics, 2009-09, Vol.126 (3), p.431-447

2009

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Predatory fireflies and their toxic firefly prey have evolved distinct toxin resistance strategies

Current biology, 2023-12, Vol.33 (23), p.5160-5168.e7

2023

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

Neurobiology of disease, 2010-10, Vol.40 (1), p.1-3

2010

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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, 2019-09, Vol.1865 (9), p.2257-2266

2019

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Newly discovered roles of triosephosphate isomerase including functions within the nucleus

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

Neuromuscular dysfunction and pathogenesis in triosephosphate isomerase deficiency

Chemical Targeting of Voltage Sensitive Dyes to Specific Cells and Molecules in the Brain

A conserved polybasic domain mediates plasma membrane targeting of Lgl and its regulation by hypoxia

Modes of metabolic compensation during mitochondrial disease using the Drosophila model of ATP6 dysfunction

Adaptive substitutions underlying cardiac glycoside insensitivity in insects exhibit epistasis in vivo

Identification of protein quality control regulators using a Drosophila model of TPI deficiency

Structural and Genetic Studies Demonstrate Neurologic Dysfunction in Triosephosphate Isomerase Deficiency Is Associated with Impaired Synaptic Vesicle Dynamics

Itavastatin and resveratrol increase triosephosphate isomerase protein in a newly identified variant of TPI deficiency

Modeling mitochondrial encephalomyopathy in Drosophila

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

Protein coding mitochondrial-targeted RNAs rescue mitochondrial disease in vivo

A-to-I Pre-mRNA Editing in Drosophila Is Primarily Involved in Adult Nervous System Function and Integrity

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

Murine model of triosephosphate isomerase deficiency with anemia and severe neuromuscular dysfunction

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

Hsp70- and Hsp90-mediated proteasomal degradation underlies TPIsugarkill pathogenesis in Drosophila

Early mitochondrial dysfunction leads to altered redox chemistry underlying pathogenesis of TPI deficiency

Sleep and circadian defects in a Drosophila model of mitochondrial encephalomyopathy

Novel mutations affecting the Na, K ATPase alpha model complex neurological diseases and implicate the sodium pump in increased longevity

Predatory fireflies and their toxic firefly prey have evolved distinct toxin resistance strategies

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

Vesicular glutamate transporter modulates sex differences in dopamine neuron vulnerability to age‐related neurodegeneration

Missense variant in TPI1 (Arg189Gln) causes neurologic deficits through structural changes in the triosephosphate isomerase catalytic site and reduced enzyme levels in vivo

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