| P2093 | author name string | Michael J Palladino | |
| | Aaron D Talsma | |
| | Alexandra LaMonaca | |
| | Emily D Wieczorek | |
| | John F Chaves | |
| P2860 | cites work | Drosophila neurotrophins reveal a common mechanism for nervous system formation | Q21563556 |
| | Signal-induced ubiquitination of IkappaBalpha by the F-box protein Slimb/beta-TrCP | Q21666110 |
| | dDYRK2: a novel dual-specificity tyrosine-phosphorylation-regulated kinase in Drosophila | Q24530188 |
| | Vilse, a conserved Rac/Cdc42 GAP mediating Robo repulsion in tracheal cells and axons | Q24562721 |
| | De novo mutations in ATP1A3 cause alternating hemiplegia of childhood | Q24600468 |
| | Drosophila model of human inherited triosephosphate isomerase deficiency glycolytic enzymopathy | Q24676326 |
| | Cloning and characterization of a potassium-dependent sodium/calcium exchanger in Drosophila | Q24684797 |
| | Toll-6 and Toll-7 function as neurotrophin receptors in the Drosophila melanogaster CNS | Q27313234 |
| | Modes of metabolic compensation during mitochondrial disease using the Drosophila model of ATP6 dysfunction | Q27317174 |
| | Rapid-onset dystonia-parkinsonism: linkage to chromosome 19q13 | Q28141878 |
| | Alternating hemiplegia of childhood: early characteristics and evolution of a neurodevelopmental syndrome | Q28236896 |
| | Temperature-sensitive paralytic mutations demonstrate that synaptic exocytosis requires SNARE complex assembly and disassembly | Q28281473 |
| | Alpha3Na+/K+-ATPase is a neuronal receptor for agrin | Q28577669 |
| | The mle(napts) RNA helicase mutation in drosophila results in a splicing catastrophe of the para Na+ channel transcript in a region of RNA editing. | Q52170282 |
| | A gradient of cytoplasmic Cactus degradation establishes the nuclear localization gradient of the dorsal morphogen in Drosophila. | Q52199100 |
| | A Drosophila NSF mutant | Q52537194 |
| | Intermediate form between alternating hemiplegia of childhood and rapid-onset dystonia-parkinsonism. | Q53847409 |
| | Using FlyAtlas to identify better Drosophila melanogaster models of human disease | Q29615721 |
| | Analysis of temperature-sensitive mutants reveals new genes involved in the courtship song of Drosophila | Q30498638 |
| | Regulation of Drosophila TRPL channels by immunophilin FKBP59. | Q30701605 |
| | Molecular cloning and functional expression of the first insect FMRFamide receptor | Q30846705 |
| | Characterization of the Drosophila melanogaster ribosomal proteome | Q33252898 |
| | Conservation of the protein composition and electron microscopy structure of Drosophila melanogaster and human spliceosomal complexes | Q33382329 |
| | A Drosophila behavioral mutant, down and out (dao), is defective in an essential regulator of Erg potassium channels. | Q33777996 |
| | Glutactin, a novel Drosophila basement membrane-related glycoprotein with sequence similarity to serine esterases. | Q33919372 |
| | Subunit contributions to histone methyltransferase activities of fly and worm polycomb group complexes | Q33924962 |
| | Ouabain, a steroid hormone that signals with slow calcium oscillations. | Q33949448 |
| | Genetic screens to identify elements of the decapentaplegic signaling pathway in Drosophila. | Q33964215 |
| | Na+,K+-ATPase: structure, mechanism, and regulation. | Q34017236 |
| | Drosophila as a model for epilepsy: bss is a gain-of-function mutation in the para sodium channel gene that leads to seizures | Q34152362 |
| | Evidence for a separate type of migraine with aura: sporadic hemiplegic migraine | Q34179270 |
| | A Sod2 null mutation confers severely reduced adult life span in Drosophila | Q34287545 |
| | Presynaptic alpha2delta-3 is required for synaptic morphogenesis independent of its Ca2+-channel functions | Q34378519 |
| | Drosophila couch potato mutants exhibit complex neurological abnormalities including epilepsy phenotypes | Q34572732 |
| | The mei-P26 gene encodes a RING finger B-box coiled-coil-NHL protein that regulates seizure susceptibility in Drosophilia | Q34573468 |
| | Neuropathology in Drosophila membrane excitability mutants | Q34587578 |
| | Genetic modifiers of the Drosophila NSF mutant, comatose, include a temperature-sensitive paralytic allele of the calcium channel alpha1-subunit gene, cacophony | Q34609325 |
| | A genetic screen for suppressors and enhancers of the Drosophila PAN GU cell cycle kinase identifies cyclin B as a target | Q34613014 |
| | Temperature-sensitive paralytic mutants are enriched for those causing neurodegeneration in Drosophila. | Q34615437 |
| | Protons at the gate: DEG/ENaC ion channels help us feel and remember | Q34623311 |
| | Epithelial sodium channel/degenerin family of ion channels: a variety of functions for a shared structure. | Q34711250 |
| | A Cullin1-based SCF E3 ubiquitin ligase targets the InR/PI3K/TOR pathway to regulate neuronal pruning. | Q34998125 |
| | Neurophysiological defects in temperature-sensitive paralytic mutants of Drosophila melanogaster | Q35024840 |
| | Molecular characterization and functional expression of the DSC1 channel | Q35057907 |
| | The Na,K-ATPase | Q35233980 |
| | Na,K-ATPase: isoform structure, function, and expression | Q35233983 |
| | MicroRNA transgene overexpression complements deficiency-based modifier screens in Drosophila | Q35748253 |
| | A novel Drosophila SOD2 mutant demonstrates a role for mitochondrial ROS in neurodevelopment and disease | Q36206004 |
| | The regulatory complex of Drosophila melanogaster 26S proteasomes. Subunit composition and localization of a deubiquitylating enzyme | Q36342543 |
| | Tombola, a tesmin/TSO1-family protein, regulates transcriptional activation in the Drosophila male germline and physically interacts with always early | Q36437286 |
| | Conversion of neurons and glia to external-cell fates in the external sensory organs of Drosophila hamlet mutants by a cousin-cousin cell-type respecification | Q37413205 |
| | Novel mutations affecting the Na, K ATPase alpha model complex neurological diseases and implicate the sodium pump in increased longevity | Q37470011 |
| | A Drosophila mutant with a temperature-sensitive block in nerve conduction | Q37593423 |
| | Sporadic and familial hemiplegic migraine: pathophysiological mechanisms, clinical characteristics, diagnosis, and management | Q37860502 |
| | Drosophila painless is a Ca2+-requiring channel activated by noxious heat | Q39933446 |
| | Synaptic transmission reversibly conditioned by single-gene mutation in Drosophila melanogaster | Q39981184 |
| | Distinct roles for N-ethylmaleimide-sensitive fusion protein (NSF) suggested by the identification of a second Drosophila NSF homolog. | Q40464131 |
| | A mutation of the Drosophila sodium pump alpha subunit gene results in bang-sensitive paralysis | Q41045006 |
| | The Drosophila Na,K-ATPase alpha-subunit gene: gene structure, promoter function and analysis of a cold-sensitive recessive-lethal mutation | Q41116922 |
| | Molecular characterization of daughterless, a Drosophila sex determination gene with multiple roles in development | Q41261560 |
| | Cyclic nucleotide phosphodiesterases in Drosophila melanogaster. | Q41889474 |
| | Connectin: a homophilic cell adhesion molecule expressed on a subset of muscles and the motoneurons that innervate them in Drosophila | Q42020417 |
| | Metabolic disruption in Drosophila bang-sensitive seizure mutants | Q42421200 |
| | Partially reversible cortical metabolic dysfunction in familial hemiplegic migraine with prolonged aura | Q43126261 |
| | Sightless has homology to transmembrane acyltransferases and is required to generate active Hedgehog protein | Q43709883 |
| | In vivo modification of Na(+),K(+)-ATPase activity in Drosophila | Q43787373 |
| | Characterization of a novel Drosophila melanogaster galectin. Expression in developing immune, neural, and muscle tissues | Q43865563 |
| | Axon pruning during Drosophila metamorphosis: evidence for local degeneration and requirement of the ubiquitin-proteasome system | Q44485246 |
| | Contribution of Drosophila DEG/ENaC genes to salt taste | Q44505350 |
| | The Drosophila easily shocked gene: a mutation in a phospholipid synthetic pathway causes seizure, neuronal failure, and paralysis. | Q46028601 |
| | Seizure suppression by top1 mutations in Drosophila. | Q46535283 |
| | Mutations in the K+/Cl- cotransporter gene kazachoc (kcc) increase seizure susceptibility in Drosophila. | Q46619464 |
| | Mutations in a Drosophila alpha2delta voltage-gated calcium channel subunit reveal a crucial synaptic function | Q46825820 |
| | Blood-brain barrier defects associated with Rbp9 mutation | Q47070293 |
| | Regulation of the Hedgehog and Wingless signalling pathways by the F-box/WD40-repeat protein Slimb | Q47070747 |
| | Drosophila exocyst components Sec5, Sec6, and Sec15 regulate DE-Cadherin trafficking from recycling endosomes to the plasma membrane | Q47070861 |
| | A typical N-terminal extensions confer novel regulatory properties on GTP cyclohydrolase isoforms in Drosophila melanogaster | Q47071156 |
| | Neural dysfunction and neurodegeneration in Drosophila Na+/K+ ATPase alpha subunit mutants. | Q47071329 |
| | Plexin A-Semaphorin-1a Reverse Signaling Regulates Photoreceptor Axon Guidance inDrosophila | Q47071412 |
| | Cloning and characterization of a Na+-driven anion exchanger (NDAE1). A new bicarbonate transporter | Q47071843 |
| | DAMB, a novel dopamine receptor expressed specifically in Drosophila mushroom bodies | Q47072027 |
| | Genetic dissection of monoamine neurotransmitter synthesis in Drosophila | Q47072222 |
| | Cloning and functional characterization of a novel dopamine receptor from Drosophila melanogaster. | Q47072444 |
| | Bi-directional signaling by Semaphorin 1a during central synapse formation in Drosophila | Q47072460 |
| | Transcriptional and post-transcriptional control mechanisms coordinate the onset of spermatid differentiation with meiosis I in Drosophila. | Q47072624 |
| | Rasp, a putative transmembrane acyltransferase, is required for Hedgehog signaling | Q47072725 |
| | Mutations in Drosophila sec15 reveal a function in neuronal targeting for a subset of exocyst components | Q47072877 |
| | Synaptic function modulated by changes in the ratio of synaptotagmin I and IV. | Q47933649 |
| | The Drosophila erg K+ channel polypeptide is encoded by the seizure locus | Q48054809 |
| | A Component of Calcium-activated Potassium Channels Encoded by the Drosophila slo Locus | Q48215777 |
| | Molecular analysis of the para locus, a sodium channel gene in Drosophila | Q48287063 |
| | A population-based study of familial hemiplegic migraine suggests revised diagnostic criteria | Q48599309 |
| P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
| P6216 | copyright status | copyrighted | Q50423863 |
| P304 | page(s) | 89 | |
| P577 | publication date | 2014-12-05 | |
| P1433 | published in | Molecular Brain | Q6895938 |
| P1476 | title | Genome-wide screen for modifiers of Na (+) /K (+) ATPase alleles identifies critical genetic loci | |
| P478 | volume | 7 | |