| scholarly article | Q13442814 |
| P356 | DOI | 10.1016/S0896-6273(02)00769-9 |
| P698 | PubMed publication ID | 12160747 |
| P50 | author | Hugo J. Bellen | Q22003355 |
| P2093 | author name string | Ian A Meinertzhagen | |
| Ruth Fabian-Fine | |||
| Giuseppa Pennetta | |||
| Peter Robin Hiesinger | |||
| P2860 | cites work | Stereotypic morphology of glutamatergic synapses on identified muscle cells of Drosophila larvae. | Q52453612 |
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| Genetic dissection of structural and functional components of synaptic plasticity. I. Fasciclin II controls synaptic stabilization and growth. | Q45965153 | ||
| Ectopic and increased expression of Fasciclin II alters motoneuron growth cone guidance | Q46045692 | ||
| Synapse-specific control of synaptic efficacy at the terminals of a single neuron | Q46853657 | ||
| Disruption of axonal transport and neuronal viability by amyloid precursor protein mutations in Drosophila. | Q46959740 | ||
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| Drosophila Futsch/22C10 is a MAP1B-like protein required for dendritic and axonal development | Q47071456 | ||
| A genome-wide search for synaptic vesicle cycle proteins in Drosophila | Q47072078 | ||
| Neurobiology. A spine to remember | Q48207358 | ||
| LTP promotes formation of multiple spine synapses between a single axon terminal and a dendrite. | Q52030569 | ||
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| P-element-mediated enhancer detection: a versatile method to study development in Drosophila. | Q52245214 | ||
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| P433 | issue | 2 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | Drosophila | Q312154 |
| neuromuscular junction | Q776995 | ||
| P304 | page(s) | 291-306 | |
| P577 | publication date | 2002-07-01 | |
| P1433 | published in | Neuron | Q3338676 |
| P1476 | title | Drosophila VAP-33A directs bouton formation at neuromuscular junctions in a dosage-dependent manner | |
| P478 | volume | 35 |
| Q27301268 | A Drosophila model of ALS: human ALS-associated mutation in VAP33A suggests a dominant negative mechanism |
| Q44894487 | A Drosophila temperature-sensitive seizure mutant in phosphoglycerate kinase disrupts ATP generation and alters synaptic function. |
| Q36532559 | A Role for MOSPD1 in Mesenchymal Stem Cell Proliferation and Differentiation |
| Q92563853 | A Screen for Synaptic Growth Mutants Reveals Mechanisms That Stabilize Synaptic Strength |
| Q38446556 | A TRPV channel in Drosophila motor neurons regulates presynaptic resting Ca2+ levels, synapse growth, and synaptic transmission |
| Q34107101 | A Trypanosoma brucei protein required for maintenance of the flagellum attachment zone and flagellar pocket ER domains |
| Q24675994 | A conserved ER targeting motif in three families of lipid binding proteins and in Opi1p binds VAP |
| Q35268719 | A fruitful endeavor: modeling ALS in the fruit fly |
| Q34515862 | A genetic screen identifies Tor as an interactor of VAPB in a Drosophila model of amyotrophic lateral sclerosis. |
| Q35981876 | A large-scale RNAi screen identifies functional classes of genes shaping synaptic development and maintenance |
| Q24307582 | A mutation in human VAP-B--MSP domain, present in ALS patients, affects the interaction with other cellular proteins |
| Q24304337 | A mutation in the vesicle-trafficking protein VAPB causes late-onset spinal muscular atrophy and amyotrophic lateral sclerosis |
| Q47198989 | A postsynaptic Pi3K-CII dependent signaling controller for presynaptic homeostatic plasticity. |
| Q41334731 | A presynaptic homeostatic signaling system composed of the Eph receptor, ephexin, Cdc42, and CaV2.1 calcium channels. |
| Q48337086 | AMPA receptors regulate dynamic equilibrium of presynaptic terminals in mature hippocampal networks |
| Q43116922 | Activin signaling functions upstream of Gbb to regulate synaptic growth at the Drosophila neuromuscular junction |
| Q35860341 | Amyotrophic lateral sclerosis-associated mutant VAPBP56S perturbs calcium homeostasis to disrupt axonal transport of mitochondria |
| Q35963706 | An Eph receptor sperm-sensing control mechanism for oocyte meiotic maturation in Caenorhabditis elegans |
| Q89963647 | Axonal Endoplasmic Reticulum Dynamics and Its Roles in Neurodegeneration |
| Q24302479 | Characterization of the Properties of a Novel Mutation in VAPB in Familial Amyotrophic Lateral Sclerosis |
| Q26820443 | Development and plasticity of the Drosophila larval neuromuscular junction |
| Q41479009 | Diminished MTORC1-Dependent JNK Activation Underlies the Neurodevelopmental Defects Associated with Lysosomal Dysfunction |
| Q101237411 | Disruption of Tip60 HAT mediated neural histone acetylation homeostasis is an early common event in neurodegenerative diseases |
| Q35175041 | Downregulation of VAPB expression in motor neurons derived from induced pluripotent stem cells of ALS8 patients |
| Q52746956 | Drosophila Vap-33 is required for axonal localization of Dscam isoforms. |
| Q26863590 | Drosophila as a model for unfolded protein response research |
| Q34022667 | Drosophila melanogaster in the study of human neurodegeneration |
| Q24798261 | Drosophila spastin regulates synaptic microtubule networks and is required for normal motor function |
| Q26765022 | Drosophila tools and assays for the study of human diseases |
| Q24300745 | Electrostatic interaction between oxysterol-binding protein and VAMP-associated protein A revealed by NMR and mutagenesis studies |
| Q38152420 | Embryonic and larval neural connectivity: progressive changes in synapse form and function at the neuromuscular junction mediated by cytoskeletal regulation |
| Q39744176 | Eps15 and Dap160 control synaptic vesicle membrane retrieval and synapse development. |
| Q44524209 | Experience-dependent strengthening of Drosophila neuromuscular junctions. |
| Q24324427 | FFAT rescues VAPA-mediated inhibition of ER-to-Golgi transport and VAPB-mediated ER aggregation |
| Q34708090 | Flightless flies: Drosophila models of neuromuscular disease |
| Q37124490 | Formin-dependent synaptic growth: evidence that Dlar signals via Diaphanous to modulate synaptic actin and dynamic pioneer microtubules |
| Q35744534 | FoxO limits microtubule stability and is itself negatively regulated by microtubule disruption |
| Q37764891 | Functional implications of sterol transport by the oxysterol-binding protein gene family. |
| Q37480373 | Gain-of-function mutations in the ALS8 causative gene VAPB have detrimental effects on neurons and muscles |
| Q47071286 | Genetic analysis of soluble N-ethylmaleimide-sensitive factor attachment protein function in Drosophila reveals positive and negative secretory roles. |
| Q36575025 | Genetics of motor neuron disease |
| Q24337683 | Human VAP-C negatively regulates hepatitis C virus propagation |
| Q37269911 | In vivo assay of presynaptic microtubule cytoskeleton dynamics in Drosophila |
| Q36908231 | Increased levels of phosphoinositides cause neurodegeneration in a Drosophila model of amyotrophic lateral sclerosis |
| Q36782137 | Insights into ALS pathomechanisms: from flies to humans |
| Q30577687 | Interactions between Tau and α-synuclein augment neurotoxicity in a Drosophila model of Parkinson's disease |
| Q47073445 | Investigating the contribution of VAPB/ALS8 loss of function in amyotrophic lateral sclerosis |
| Q41488584 | Kek-6: A truncated-Trk-like receptor for Drosophila neurotrophin 2 regulates structural synaptic plasticity. |
| Q64255599 | Kv2 channels create endoplasmic reticulum / plasma membrane junctions: a brief history of Kv2 channel subcellular localization |
| Q60950728 | Lgl reduces endosomal vesicle acidification and Notch signaling by promoting the interaction between Vap33 and the V-ATPase complex |
| Q27932770 | Ligand-dependent localization and function of ORP-VAP complexes at membrane contact sites. |
| Q37101594 | Microtubule-associated protein 1B (MAP1B)-deficient neurons show structural presynaptic deficiencies in vitro and altered presynaptic physiology |
| Q26853033 | Morphogenesis of the somatic musculature in Drosophila melanogaster |
| Q40084393 | Motor neuron disease-associated mutant vesicle-associated membrane protein-associated protein (VAP) B recruits wild-type VAPs into endoplasmic reticulum-derived tubular aggregates. |
| Q30164261 | Nervous wreck, an SH3 adaptor protein that interacts with Wsp, regulates synaptic growth in Drosophila |
| Q35234991 | Network analyses reveal novel aspects of ALS pathogenesis |
| Q40345993 | Neuronal overexpression of human VAPB slows motor impairment and neuromuscular denervation in a mouse model of ALS. |
| Q43902261 | OSBP- and FAN-mediated sterol requirement for spermatogenesis inDrosophila |
| Q27028029 | On the Teneurin track: a new synaptic organization molecule emerges |
| Q36669868 | Organization of the efferent system and structure of neuromuscular junctions in Drosophila |
| Q37142663 | Phospho-regulation pathways during egg activation in Drosophila melanogaster |
| Q47072233 | Presynaptic N-type calcium channels regulate synaptic growth. |
| Q36873362 | Probing mechanisms that underlie human neurodegenerative diseases in Drosophila |
| Q24321865 | Promotion of neurite extension by protrudin requires its interaction with vesicle-associated membrane protein-associated protein |
| Q33312802 | Protein phosphatase 2Cepsilon is an endoplasmic reticulum integral membrane protein that dephosphorylates the ceramide transport protein CERT to enhance its association with organelle membranes |
| Q36231879 | Protein phosphorylation changes reveal new candidates in the regulation of egg activation and early embryogenesis in D. melanogaster |
| Q43109201 | Proteomic and bioinformatic analysis of epithelial tight junction reveals an unexpected cluster of synaptic molecules |
| Q47325147 | Proteomic profiling of neuronal mitochondria reveals modulators of synaptic architecture. |
| Q28115614 | Protrudin serves as an adaptor molecule that connects KIF5 and its cargoes in vesicular transport during process formation |
| Q52804356 | Rab GTPases and Membrane Trafficking in Neurodegeneration. |
| Q37179079 | Rab11 modulates α-synuclein-mediated defects in synaptic transmission and behaviour |
| Q42098044 | Rab11 rescues synaptic dysfunction and behavioural deficits in a Drosophila model of Huntington's disease |
| Q34999362 | Regulation of synaptic development and function by the Drosophila PDZ protein Dyschronic |
| Q37650236 | Retrograde BMP signaling modulates rapid activity-dependent synaptic growth via presynaptic LIM kinase regulation of cofilin. |
| Q64236022 | SOD1 activity threshold and TOR signalling modulate VAP(P58S) aggregation via reactive oxygen species-induced proteasomal degradation in a model of amyotrophic lateral sclerosis |
| Q35819129 | Secreted VAPB/ALS8 major sperm protein domains modulate mitochondrial localization and morphology via growth cone guidance receptors. |
| Q34005893 | Shared mechanisms between Drosophila peripheral nervous system development and human neurodegenerative diseases |
| Q24626882 | Sperm and oocyte communication mechanisms controlling C. elegans fertility |
| Q40188215 | Structural requirements for VAP-B oligomerization and their implication in amyotrophic lateral sclerosis-associated VAP-B(P56S) neurotoxicity. |
| Q36514656 | Suppression of neurodegeneration and increased neurotransmission caused by expanded full-length huntingtin accumulating in the cytoplasm |
| Q36669894 | Synaptic cytoskeleton at the neuromuscular junction |
| Q28184962 | Synaptojanin is recruited by endophilin to promote synaptic vesicle uncoating |
| Q35186398 | Techniques to dissect cellular and subcellular function in the Drosophila nervous system |
| Q24294526 | The ALS8 protein VAPB interacts with the ER-Golgi recycling protein YIF1A and regulates membrane delivery into dendrites |
| Q46118295 | The ALS8-associated mutant VAPB(P56S) is resistant to proteolysis in neurons |
| Q37787429 | The BMP signaling pathway at the Drosophila neuromuscular junction and its links to neurodegenerative diseases. |
| Q33830458 | The C. elegans VAPB homolog VPR-1 is a permissive signal for gonad development |
| Q26780007 | The Crossroads of Synaptic Growth Signaling, Membrane Traffic and Neurological Disease: Insights from Drosophila |
| Q37771032 | The Drosophila larval neuromuscular junction as a model for scaffold complexes at glutamatergic synapses: benefits and limitations |
| Q90556902 | The Evolutionary History of Ephs and Ephrins: Toward Multicellular Organisms |
| Q33304446 | The LARK RNA-binding protein selectively regulates the circadian eclosion rhythm by controlling E74 protein expression |
| Q26738451 | The Presynaptic Microtubule Cytoskeleton in Physiological and Pathological Conditions: Lessons from Drosophila Fragile X Syndrome and Hereditary Spastic Paraplegias |
| Q24321690 | The amyotrophic lateral sclerosis 8 protein VAPB is cleaved, secreted, and acts as a ligand for Eph receptors |
| Q30574388 | The amyotrophic lateral sclerosis 8 protein, VAP, is required for ER protein quality control |
| Q47405859 | The axonal endoplasmic reticulum: One organelle-many functions in development, maintenance, and plasticity |
| Q47794690 | The large and small SPEN family proteins stimulate axon outgrowth during neurosecretory cell remodeling in Drosophila |
| Q37867604 | The synaptic cytoskeleton in development and disease. |
| Q101451609 | The type II integral ER membrane protein VAP-B homolog in C. elegans is cleaved to release the N-terminal MSP domain to signal non-cell-autonomously |
| Q45974621 | Unrestricted synaptic growth in spinster-a late endosomal protein implicated in TGF-beta-mediated synaptic growth regulation. |
| Q92806485 | VAP-SCRN1 interaction regulates dynamic endoplasmic reticulum remodeling and presynaptic function |
| Q24298739 | VAPB interacts with the mitochondrial protein PTPIP51 to regulate calcium homeostasis |
| Q33797100 | VAPB/ALS8 interacts with FFAT-like proteins including the p97 cofactor FAF1 and the ASNA1 ATPase |
| Q36188594 | Vapb/Amyotrophic lateral sclerosis 8 knock-in mice display slowly progressive motor behavior defects accompanying ER stress and autophagic response |
| Q41821215 | Why Quantification Matters: Characterization of Phenotypes at the Drosophila Larval Neuromuscular Junction |
| Q36513305 | Widespread aggregation of mutant VAPB associated with ALS does not cause motor neuron degeneration or modulate mutant SOD1 aggregation and toxicity in mice |
| Q36451026 | hVAPB, the causative gene of a heterogeneous group of motor neuron diseases in humans, is functionally interchangeable with its Drosophila homologue DVAP-33A at the neuromuscular junction |
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