Neurophysiological defects in temperature-sensitive paralytic mutants of Drosophila melanogaster
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Modification of a hydrophobic layer by a point mutation in syntaxin 1A regulates the rate of synaptic vesicle fusionStructural and Genetic Studies Demonstrate Neurologic Dysfunction in Triosephosphate Isomerase Deficiency Is Associated with Impaired Synaptic Vesicle DynamicsDrosophila sodium channel mutations: Contributions to seizure-susceptibilitySeizures are regulated by ubiquitin-specific peptidase 9 X-linked (USP9X), a de-ubiquitinaseThe gene for soluble N-ethylmaleimide sensitive factor attachment protein alpha is mutated in hydrocephaly with hop gait (hyh) miceGrowth factor-induced binding of dynamin to signal transduction proteins involves sorting to distinct and separate proline-rich dynamin sequences.Lithium-Responsive Seizure-Like Hyperexcitability Is Caused by a Mutation in the Drosophila Voltage-Gated Sodium Channel Gene paralytic.An automated system for quantitative analysis of Drosophila larval locomotion.Pickpocket is a DEG/ENaC protein required for mechanical nociception in Drosophila larvae.Automated quantification of locomotion, social interaction, and mate preference in Drosophila mutants.Molecular Chaperone Calnexin Regulates the Function of Drosophila Sodium Channel Paralytic.Molecular characterization of eag: a gene affecting potassium channels in Drosophila melanogasterTwo sodium-channel genes in Drosophila: implications for channel diversity.Biogenesis of Golgi stacks in imaginal discs of Drosophila melanogaster.Enhancer of seizure: a new genetic locus in Drosophila melanogaster defined by interactions with temperature-sensitive paralytic mutationsEvidence that the Drosophila olfactory mutant smellblind defines a novel class of sodium channel mutation.Fate mapping multi-focus phenotypesGenetic studies of membrane excitability in Drosophila: lethal interaction between two temperature-sensitive paralytic mutationsA remarkably stable TipE gene cluster: evolution of insect Para sodium channel auxiliary subunits.Drosophila as a model for epilepsy: bss is a gain-of-function mutation in the para sodium channel gene that leads to seizures.Loss of Hsp70 in Drosophila is pleiotropic, with effects on thermotolerance, recovery from heat shock and neurodegeneration.Neuropathology in Drosophila membrane excitability mutantsGenetic modifiers of the Drosophila NSF mutant, comatose, include a temperature-sensitive paralytic allele of the calcium channel alpha1-subunit gene, cacophony.Partitioning of N-ethylmaleimide-sensitive fusion (NSF) protein function in Drosophila melanogaster: dNSF1 is required in the nervous system, and dNSF2 is required in mesodermGenetic analysis of a synaptic calcium channel in Drosophila: intragenic modifiers of a temperature-sensitive paralytic mutant of cacophonyA genetic screen for synaptic transmission mutants mapping to the right arm of chromosome 3 in Drosophila.A neuroprotective function of NSF1 sustains autophagy and lysosomal trafficking in Drosophilawasted away, a Drosophila mutation in triosephosphate isomerase, causes paralysis, neurodegeneration, and early deathTolerance to anesthesia depends on synaptic proteins.Death following traumatic brain injury in Drosophila is associated with intestinal barrier dysfunction.A role for dynamin in triggering ethanol tolerance.Dissecting the Genetic Architecture of Behavior in Drosophila melanogaster.Cellular functions of NSF: not just SNAPs and SNAREs.Reversible alteration in the neuromuscular junctions of Drosophila melanogaster bearing a temperature-sensitive mutation, shibireA novel Drosophila SOD2 mutant demonstrates a role for mitochondrial ROS in neurodevelopment and diseaseReversible control of synaptic transmission in a single gene mutant of Drosophila melanogaster.Reversible blockage of membrane retrieval and endocytosis in the garland cell of the temperature-sensitive mutant of Drosophila melanogaster, shibirets1.Disruption of Endocytosis with the Dynamin Mutant shibirets1 Suppresses Seizures in DrosophilaSequential SNARE disassembly and GATE-16-GOS-28 complex assembly mediated by distinct NSF activities drives Golgi membrane fusion.A knock-in model of human epilepsy in Drosophila reveals a novel cellular mechanism associated with heat-induced seizure.
P2860
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P2860
Neurophysiological defects in temperature-sensitive paralytic mutants of Drosophila melanogaster
description
1976 nî lūn-bûn
@nan
1976 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
1976 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
1976年の論文
@ja
1976年論文
@yue
1976年論文
@zh-hant
1976年論文
@zh-hk
1976年論文
@zh-mo
1976年論文
@zh-tw
1976年论文
@wuu
name
Neurophysiological defects in ...... nts of Drosophila melanogaster
@ast
Neurophysiological defects in ...... nts of Drosophila melanogaster
@en
type
label
Neurophysiological defects in ...... nts of Drosophila melanogaster
@ast
Neurophysiological defects in ...... nts of Drosophila melanogaster
@en
prefLabel
Neurophysiological defects in ...... nts of Drosophila melanogaster
@ast
Neurophysiological defects in ...... nts of Drosophila melanogaster
@en
P2860
P921
P356
P1476
Neurophysiological defects in ...... nts of Drosophila melanogaster
@en
P2093
P2860
P304
P356
10.1073/PNAS.73.9.3253
P407
P577
1976-09-01T00:00:00Z