Glial lipid droplets and neurodegeneration in a Drosophila model of complex I deficiency.

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Mito-Nuclear Interactions Affecting Lifespan and Neurodegeneration in a Drosophila Model of Leigh Syndrome.Lipid Droplet, a Key Player in Host-Parasite Interactions.

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P2860

Glial lipid droplets and neurodegeneration in a Drosophila model of complex I deficiency.

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Glial lipid droplets and neurodegeneration in a Drosophila model of complex I deficiency.

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Glial lipid droplets and neurodegeneration in a Drosophila model of complex I deficiency.

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label

Glial lipid droplets and neurodegeneration in a Drosophila model of complex I deficiency.

@en

Glial lipid droplets and neurodegeneration in a Drosophila model of complex I deficiency.

@nl

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Glial lipid droplets and neurodegeneration in a Drosophila model of complex I deficiency.

@en

Glial lipid droplets and neurodegeneration in a Drosophila model of complex I deficiency.

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P1476

Glial lipid droplets and neurodegeneration in a Drosophila model of complex I deficiency

@en

P2093

Bilal Khalil

http://www.w3.org/2001/XMLSchema#string

Marie Thérèse Besson

http://www.w3.org/2001/XMLSchema#string

Marie-Jeanne Cabirol-Pol

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P2860

The first nuclear-encoded complex I mutation in a patient with Leigh syndrome.

Loss of Swiss cheese/neuropathy target esterase activity causes disruption of phosphatidylcholine homeostasis and neuronal and glial death in adult Drosophila.

Subacute necrotizing encephalomyelopathy in an infant

Glial cells as intrinsic components of non-cell-autonomous neurodegenerative disease

Lipid droplets at a glance

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

Functional conservation for lipid storage droplet association among Perilipin, ADRP, and TIP47 (PAT)-related proteins in mammals, Drosophila, and Dictyostelium

Enhanced neuronal glucose transporter expression reveals metabolic choice in a HD Drosophila model

Mutations in the mitochondrial methionyl-tRNA synthetase cause a neurodegenerative phenotype in flies and a recessive ataxia (ARSAL) in humans

Proteomic and metabolomic analyses of mitochondrial complex I-deficient mouse model generated by spontaneous B2 short interspersed nuclear element (SINE) insertion into NADH dehydrogenase (ubiquinone) Fe-S protein 4 (Ndufs4) gene

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874-888

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scholarly article

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10.1002/GLIA.23290

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P433

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P478

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Catherine Faivre-Sarrailh

Thomas Rival

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2017-12-29T00:00:00Z

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29285794

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P921

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Glial lipid droplets and neurodegeneration in a Drosophila model of complex I deficiency.

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P2860

P2860

Glial lipid droplets and neurodegeneration in a Drosophila model of complex I deficiency.

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P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698

P921

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698

P921