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Cell Biology of the Mitochondrion

Genetics (Austin), 2017-11, Vol.207 (3), p.843-871

2017

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Mitochondrial Complex I Deficiency Increases Protein Acetylation and Accelerates Heart Failure

Cell metabolism, 2013-08, Vol.18 (2), p.239-250

2013

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mTOR Inhibition Alleviates Mitochondrial Disease in a Mouse Model of Leigh Syndrome

Science (American Association for the Advancement of Science), 2013-12, Vol.342 (6165), p.1524-1528

2013

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Region-Specific Defects of Respiratory Capacities in the Ndufs4(KO) Mouse Brain

PloS one, 2016-01, Vol.11 (1), p.e0148219-e0148219

2016

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Altered anesthetic sensitivity of mice lacking Ndufs4, a subunit of mitochondrial complex I

PloS one, 2012-08, Vol.7 (8), p.e42904-e42904

2012

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A Putative Cation Channel and Its Novel Regulator: Cross-Species Conservation of Effects on General Anesthesia

Current biology, 2007-04, Vol.17 (7), p.624-629

2007

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Relevance of experimental paradigms of anesthesia induced neurotoxicity in the mouse

PloS one, 2019-03, Vol.14 (3), p.e0213543

2019

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Glutamatergic Neurotransmission Links Sensitivity to Volatile Anesthetics with Mitochondrial Function

Current biology, 2016-08, Vol.26 (16), p.2194-2201

2016

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Regional knockdown of NDUFS4 implicates a thalamocortical circuit mediating anesthetic sensitivity

PloS one, 2017-11, Vol.12 (11), p.e0188087-e0188087

2017

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Mechanisms underlying neonate-specific metabolic effects of volatile anesthetics

eLife, 2021-07, Vol.10

2021

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Leukocytes mediate disease pathogenesis in the Ndufs4(KO) mouse model of Leigh syndrome

JCI insight, 2022-03, Vol.7 (5)

2022

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Complex I Function Is Defective in Complex IV-deficient Caenorhabditis elegans

The Journal of biological chemistry, 2009-03, Vol.284 (10), p.6425-6435

2009

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A Drosophila model of mitochondrial disease caused by a complex I mutation that uncouples proton pumping from electron transfer

Disease models & mechanisms, 2014-10, Vol.7 (10), p.1165-1174

2014

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The genetics of isoflurane-induced developmental neurotoxicity

Neurotoxicology and teratology, 2017-03, Vol.60, p.40-49

2017

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Tether mutations that restore function and suppress pleiotropic phenotypes of the C. elegans isp-1(qm150) Rieske iron–sulfur protein

Proceedings of the National Academy of Sciences - PNAS, 2015-11, Vol.112 (45), p.E6148-E6148

2015

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Optical Reversal of Halothane-Induced Immobility in C. elegans

Current biology, 2011-12, Vol.21 (24), p.2070-2076

2011

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A primordial target: Mitochondria mediate both primary and collateral anesthetic effects of volatile anesthetics

Experimental Biology and Medicine, 2023-04, Vol.248 (7), p.545-552

2023

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Mitochondrial Oxidative Phosphorylation Is Defective in the Long-lived Mutant clk-1

The Journal of biological chemistry, 2004-12, Vol.279 (52), p.54479-54486

2004

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Mitochondrial defects and anesthetic sensitivity

Anesthesiology (Philadelphia), 2002-05, Vol.96 (5), p.1268-1270

2002

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The effects of complex I function and oxidative damage on lifespan and anesthetic sensitivity in Caenorhabditis elegans

Mechanisms of ageing and development, 2004-06, Vol.125 (6), p.455-464

2004

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Anesthetic Hypersensitivity in a Case-Controlled Series of Patients With Mitochondrial Disease

Anesthesia and analgesia, 2021-10, Vol.133 (4), p.924-932

2021

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Mitochondrial Function in Astrocytes Is Essential for Normal Emergence from Anesthesia in Mice

Anesthesiology (Philadelphia), 2019-03, Vol.130 (3), p.423-434

2019

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Potassium Leak Channels and Mitochondrial Complex I Interact in Glutamatergic Interneurons of the Mouse Spinal Cord

Anesthesiology (Philadelphia), 2024-04, Vol.140 (4), p.715

2024

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Isoflurane inhibition of endocytosis is an anesthetic mechanism of action

Current biology, 2022-07, Vol.32 (14), p.3016-3032.e3

2022

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Regional metabolic signatures in the Ndufs4(KO) mouse brain implicate defective glutamate/α-ketoglutarate metabolism in mitochondrial disease

Molecular genetics and metabolism, 2020-06, Vol.130 (2), p.118-132

2020

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Cell Biology of the Mitochondrion

Mitochondrial Complex I Deficiency Increases Protein Acetylation and Accelerates Heart Failure

mTOR Inhibition Alleviates Mitochondrial Disease in a Mouse Model of Leigh Syndrome

Region-Specific Defects of Respiratory Capacities in the Ndufs4(KO) Mouse Brain

Altered anesthetic sensitivity of mice lacking Ndufs4, a subunit of mitochondrial complex I

A Putative Cation Channel and Its Novel Regulator: Cross-Species Conservation of Effects on General Anesthesia

Relevance of experimental paradigms of anesthesia induced neurotoxicity in the mouse

Glutamatergic Neurotransmission Links Sensitivity to Volatile Anesthetics with Mitochondrial Function

Regional knockdown of NDUFS4 implicates a thalamocortical circuit mediating anesthetic sensitivity

Mechanisms underlying neonate-specific metabolic effects of volatile anesthetics

Leukocytes mediate disease pathogenesis in the Ndufs4(KO) mouse model of Leigh syndrome

Complex I Function Is Defective in Complex IV-deficient Caenorhabditis elegans

A Drosophila model of mitochondrial disease caused by a complex I mutation that uncouples proton pumping from electron transfer

The genetics of isoflurane-induced developmental neurotoxicity

Tether mutations that restore function and suppress pleiotropic phenotypes of the C. elegans isp-1(qm150) Rieske iron–sulfur protein

Optical Reversal of Halothane-Induced Immobility in C. elegans

A primordial target: Mitochondria mediate both primary and collateral anesthetic effects of volatile anesthetics

Mitochondrial Oxidative Phosphorylation Is Defective in the Long-lived Mutant clk-1

Mitochondrial defects and anesthetic sensitivity

The effects of complex I function and oxidative damage on lifespan and anesthetic sensitivity in Caenorhabditis elegans

Anesthetic Hypersensitivity in a Case-Controlled Series of Patients With Mitochondrial Disease

Mitochondrial Function in Astrocytes Is Essential for Normal Emergence from Anesthesia in Mice

Potassium Leak Channels and Mitochondrial Complex I Interact in Glutamatergic Interneurons of the Mouse Spinal Cord

Isoflurane inhibition of endocytosis is an anesthetic mechanism of action

Regional metabolic signatures in the Ndufs4(KO) mouse brain implicate defective glutamate/α-ketoglutarate metabolism in mitochondrial disease

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