Neuropathology in Drosophila mutants with increased seizure susceptibility. - Wikidata - wikimedia - TriplyDB

Neuropathology in Drosophila mutants with increased seizure susceptibility.

Neuropathology in Drosophila mutants with increased seizure susceptibility.

http://www.wikidata.org/entity/Q36470506

about

The Microtubule Regulatory Protein Stathmin Is Required to Maintain the Integrity of Axonal Microtubules in Drosophila Modes of metabolic compensation during mitochondrial disease using the Drosophila model of ATP6 dysfunction SDHAF4 promotes mitochondrial succinate dehydrogenase activity and prevents neurodegeneration.Rescue of easily shocked mutant seizure sensitivity in Drosophila adults.Effects of oxygen concentration and pressure on Drosophila melanogaster: oxidative stress, mitochondrial activity, and survivorship.Maintaining the brain: insight into human neurodegeneration from Drosophila melanogaster mutants Mechanisms explaining transitions between tonic and phasic firing in neuronal populations as predicted by a low dimensional firing rate model Small mitochondrial-targeted RNAs modulate endogenous mitochondrial protein expression in vivo.The alternative oxidase AOX does not rescue the phenotype of tko25t mutant flies Mutations in prickle orthologs cause seizures in flies, mice, and humans.Death following traumatic brain injury in Drosophila is associated with intestinal barrier dysfunction.A new model to study sleep deprivation-induced seizure.Mechanical and temperature stressor-induced seizure-and-paralysis behaviors in Drosophila bang-sensitive mutants A novel Drosophila SOD2 mutant demonstrates a role for mitochondrial ROS in neurodevelopment and disease Probing mechanisms that underlie human neurodegenerative diseases in Drosophila Accelerated bang recovery in Drosophila genderblind mutants Drosophila melanogaster as a model organism of brain diseases Novel mutations affecting the Na, K ATPase alpha model complex neurological diseases and implicate the sodium pump in increased longevity.The Histone Demethylase KDM5 Activates Gene Expression by Recognizing Chromatin Context through Its PHD Reader Motif.A mutation in Drosophila Aldolase causes temperature-sensitive paralysis, shortened lifespan, and neurodegeneration.Sialyltransferase regulates nervous system function in Drosophila.Lipid metabolic perturbation is an early-onset phenotype in adult spinster mutants: a Drosophila model for lysosomal storage disorders.

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P2860

Neuropathology in Drosophila mutants with increased seizure susceptibility.

http://www.wikidata.org/entity/Q36470506

description

2008 nî lūn-bûn

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2008年の論文

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2008年学术文章

@wuu

2008年学术文章

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2008年学术文章

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2008年学术文章

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2008年学术文章

@zh-sg

2008年學術文章

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2008年學術文章

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2008年學術文章

@zh-hant

name

Neuropathology in Drosophila mutants with increased seizure susceptibility.

@ast

Neuropathology in Drosophila mutants with increased seizure susceptibility.

@en

type

label

Neuropathology in Drosophila mutants with increased seizure susceptibility.

@ast

Neuropathology in Drosophila mutants with increased seizure susceptibility.

@en

prefLabel

Neuropathology in Drosophila mutants with increased seizure susceptibility.

@ast

Neuropathology in Drosophila mutants with increased seizure susceptibility.

@en

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GENETICS.107.082115

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Neuropathology in Drosophila mutants with increased seizure susceptibility.

@en

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Barry Ganetzky

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

Khelan P Patel

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

Lisa Olson

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

Michael J Palladino

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

Rosie Miller

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

Tim Fergestad

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P2860

Role of adenine nucleotide translocator 1 in mtDNA maintenance

Antiepileptic drugs and apoptotic neurodegeneration in the developing brain

An energy budget for signaling in the grey matter of the brain

Recovery and Characterization of Temperature-Sensitive Mutations Affecting Adult Viability in DROSOPHILA MELANOGASTER.

Do epileptic seizures damage the brain?

Myoclonus epilepsy and ragged-red fibres (MERRF). 1. A clinical, pathological, biochemical, magnetic resonance spectrographic and positron emission tomographic study.

Progressive hippocampal and extrahippocampal atrophy in drug resistant epilepsy.

Metabolic parameters of epilepsy: adjuncts to established antiepileptic drug therapy.

Mitochondrial disorders: clinical and genetic features.

Mitochondrial respiratory chain disorders II: neurodegenerative disorders and nuclear gene defects.

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10.1534/GENETICS.107.082115

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