Fiala, André

[["dc.bibliographiccitation.firstpage","952"],["dc.bibliographiccitation.issue","4"],["dc.bibliographiccitation.journal","Cell Reports"],["dc.bibliographiccitation.lastpage","960"],["dc.bibliographiccitation.volume","5"],["dc.contributor.author","Riemensperger, Thomas"],["dc.contributor.author","Issa, Abdul-Raouf"],["dc.contributor.author","Pech, Ulrike"],["dc.contributor.author","Coulom, Helene"],["dc.contributor.author","My-Van Nguyen, My-Van Nguyen"],["dc.contributor.author","Cassar, Marlene"],["dc.contributor.author","Jacquet, Melanie"],["dc.contributor.author","Fiala, Andre"],["dc.contributor.author","Birman, Serge"],["dc.date.accessioned","2018-11-07T09:17:49Z"],["dc.date.available","2018-11-07T09:17:49Z"],["dc.date.issued","2013"],["dc.description.abstract","Expression of the human Parkinson-disease-associated protein alpha-synuclein in all Drosophila neurons induces progressive locomotor deficits. Here, we identify a group of 15 dopaminergic neurons per hemisphere in the anterior medial region of the brain whose disruption correlates with climbing impairments in this model. These neurons selectively innervate the horizontal beta and beta' lobes of the mushroom bodies, and their connections to the Kenyon cells are markedly reduced when they express alpha-synuclein. Using selective mushroom body drivers, we show that blocking or overstimulating neuronal activity in the beta' lobe, but not the beta or gamma lobes, significantly inhibits negative geotaxis behavior. This suggests that modulation of the mushroom body beta' lobes by this dopaminergic pathway is specifically required for an efficient control of startle-induced locomotion in flies."],["dc.identifier.doi","10.1016/j.celrep.2013.10.032"],["dc.identifier.isi","000328266000011"],["dc.identifier.pmid","24239353"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?gs-1/10671"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/28258"],["dc.notes.intern","Merged from goescholar"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Cell Press"],["dc.relation.issn","2211-1247"],["dc.rights","Goescholar"],["dc.rights.uri","https://goescholar.uni-goettingen.de/licenses"],["dc.title","A Single Dopamine Pathway Underlies Progressive Locomotor Deficits in a Drosophila Model of Parkinson Disease"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dc.type.version","published_version"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","1"],["dc.bibliographiccitation.issue","1"],["dc.bibliographiccitation.journal","BMC Neuroscience"],["dc.bibliographiccitation.lastpage","2"],["dc.bibliographiccitation.volume","14"],["dc.contributor.author","Chou, Wen-Chuang"],["dc.contributor.author","Fiala, André"],["dc.contributor.author","Timme, Marc"],["dc.date.accessioned","2014-07-02T10:46:47Z"],["dc.date.accessioned","2021-10-27T13:18:23Z"],["dc.date.available","2014-07-02T10:46:47Z"],["dc.date.available","2021-10-27T13:18:23Z"],["dc.date.issued","2013"],["dc.format.mimetype","application/pdf"],["dc.identifier.doi","10.1186/1471-2202-14-S1-P391"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?gs-1/10416"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/91863"],["dc.language.iso","en"],["dc.notes.intern","Migrated from goescholar"],["dc.publisher","BioMed Central"],["dc.publisher.place","London"],["dc.relation.eissn","1471-2202"],["dc.relation.orgunit","Fakultät für Mathematik und Informatik"],["dc.rights","Goescholar"],["dc.rights.access","openAccess"],["dc.rights.uri","https://goescholar.uni-goettingen.de/licenses"],["dc.title","Heterogeneous connectivity can positively and negatively modulate the correlation between neural representations"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.version","published_version"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.issue","1"],["dc.bibliographiccitation.journal","Scientific Reports"],["dc.bibliographiccitation.volume","12"],["dc.contributor.author","Hancock, Clare E."],["dc.contributor.author","Rostami, Vahid"],["dc.contributor.author","Rachad, El Yazid"],["dc.contributor.author","Deimel, Stephan H."],["dc.contributor.author","Nawrot, Martin P."],["dc.contributor.author","Fiala, André"],["dc.date.accessioned","2022-07-01T07:34:53Z"],["dc.date.available","2022-07-01T07:34:53Z"],["dc.date.issued","2022"],["dc.description.abstract","By learning, through experience, which stimuli coincide with dangers, it is possible to predict outcomes and act pre-emptively to ensure survival. In insects, this process is localized to the mushroom body (MB), the circuitry of which facilitates the coincident detection of sensory stimuli and punishing or rewarding cues and, downstream, the execution of appropriate learned behaviors. Here, we focused our attention on the mushroom body output neurons (MBONs) of the γ-lobes that act as downstream synaptic partners of the MB γ-Kenyon cells (KCs) to ask how the output of the MB γ-lobe is shaped by olfactory associative conditioning, distinguishing this from non-associative stimulus exposure effects, and without the influence of downstream modulation. This was achieved by employing a subcellularly localized calcium sensor to specifically monitor activity at MBON postsynaptic sites. Therein, we identified a robust associative modulation within only one MBON postsynaptic compartment (MBON-γ1pedc > α/β), which displayed a suppressed postsynaptic response to an aversively paired odor. While this MBON did not undergo non-associative modulation, the reverse was true across the remainder of the γ-lobe, where general odor-evoked adaptation was observed, but no conditioned odor-specific modulation. In conclusion, associative synaptic plasticity underlying aversive olfactory learning is localized to one distinct synaptic γKC-to-γMBON connection."],["dc.description.sponsorship"," Deutsche Forschungsgemeinschaft http://dx.doi.org/10.13039/501100001659"],["dc.description.sponsorship"," Georg-August-Universität Göttingen http://dx.doi.org/10.13039/501100003385"],["dc.description.sponsorship","Open-Access-Publikationsfonds 2022"],["dc.identifier.doi","10.1038/s41598-022-14413-5"],["dc.identifier.pii","14413"],["dc.identifier.pmid","35729203"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/112033"],["dc.identifier.url","https://for2705.de/literature/publications/53"],["dc.language.iso","en"],["dc.notes.intern","DOI-Import GROB-581"],["dc.relation","FOR 2705: Dissection of a Brain Circuit: Structure, Plasticity and Behavioral Function of the Drosophila Mushroom Body"],["dc.relation.eissn","2045-2322"],["dc.relation.workinggroup","RG Fiala"],["dc.relation.workinggroup","RG Nawrot"],["dc.rights","CC BY 4.0"],["dc.rights.uri","https://creativecommons.org/licenses/by/4.0"],["dc.title","Visualization of learning-induced synaptic plasticity in output neurons of the Drosophila mushroom body γ-lobe"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.subtype","original_ja"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.journal","eLife"],["dc.bibliographiccitation.volume","8"],["dc.contributor.author","Martelli, Carlotta"],["dc.contributor.author","Fiala, André"],["dc.date.accessioned","2020-12-10T18:48:07Z"],["dc.date.available","2020-12-10T18:48:07Z"],["dc.date.issued","2019"],["dc.identifier.doi","10.7554/eLife.43735"],["dc.identifier.eissn","2050-084X"],["dc.identifier.pmid","31169499"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?gs-1/16448"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/79023"],["dc.language.iso","en"],["dc.notes.intern","DOI Import GROB-354"],["dc.notes.intern","Merged from goescholar"],["dc.rights","CC BY 4.0"],["dc.rights.uri","https://creativecommons.org/licenses/by/4.0"],["dc.title","Slow presynaptic mechanisms that mediate adaptation in the olfactory pathway of Drosophila"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.version","published_version"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.journal","eLife"],["dc.bibliographiccitation.volume","10"],["dc.contributor.author","Prisco, Luigi"],["dc.contributor.author","Deimel, Stephan Hubertus"],["dc.contributor.author","Yeliseyeva, Hanna"],["dc.contributor.author","Fiala, André"],["dc.contributor.author","Tavosanis, Gaia"],["dc.date.accessioned","2022-02-01T10:31:53Z"],["dc.date.available","2022-02-01T10:31:53Z"],["dc.date.issued","2021"],["dc.description.abstract","To identify and memorize discrete but similar environmental inputs, the brain needs to distinguish between subtle differences of activity patterns in defined neuronal populations. The Kenyon cells (KCs) of the Drosophila adult mushroom body (MB) respond sparsely to complex olfactory input, a property that is thought to support stimuli discrimination in the MB. To understand how this property emerges, we investigated the role of the inhibitory anterior paired lateral (APL) neuron in the input circuit of the MB, the calyx. Within the calyx, presynaptic boutons of projection neurons (PNs) form large synaptic microglomeruli (MGs) with dendrites of postsynaptic KCs. Combining electron microscopy (EM) data analysis and in vivo calcium imaging, we show that APL, via inhibitory and reciprocal synapses targeting both PN boutons and KC dendrites, normalizes odour-evoked representations in MGs of the calyx. APL response scales with the PN input strength and is regionalized around PN input distribution. Our data indicate that the formation of a sparse code by the KCs requires APL-driven normalization of their MG postsynaptic responses. This work provides experimental insights on how inhibition shapes sensory information representation in a higher brain centre, thereby supporting stimuli discrimination and allowing for efficient associative memory formation."],["dc.identifier.doi","10.7554/eLife.74172"],["dc.identifier.pmid","34964714"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/98969"],["dc.identifier.url","https://for2705.de/literature/publications/50"],["dc.language.iso","en"],["dc.notes.intern","DOI-Import GROB-517"],["dc.relation","FOR 2705: Dissection of a Brain Circuit: Structure, Plasticity and Behavioral Function of the Drosophila Mushroom Body"],["dc.relation","FOR 2705 | TP 6: The role of gap junctions during mushroom body development and remodeling"],["dc.relation.eissn","2050-084X"],["dc.relation.workinggroup","RG Fiala"],["dc.relation.workinggroup","RG Tavosanis (Developmental Neurobiology)"],["dc.rights","CC BY 4.0"],["dc.rights.uri","http://creativecommons.org/licenses/by/4.0/"],["dc.title","The anterior paired lateral neuron normalizes odour-evoked activity in the Drosophila mushroom body calyx"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.subtype","original_ja"],["dc.type.version","published_version"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.journal","Frontiers in Systems Neuroscience"],["dc.bibliographiccitation.volume","12"],["dc.contributor.author","Sun, Jun"],["dc.contributor.author","Xu, An Qi"],["dc.contributor.author","Giraud, Julia"],["dc.contributor.author","Poppinga, Haiko"],["dc.contributor.author","Riemensperger, Thomas"],["dc.contributor.author","Fiala, André"],["dc.contributor.author","Birman, Serge"],["dc.date.accessioned","2020-12-10T18:44:35Z"],["dc.date.available","2020-12-10T18:44:35Z"],["dc.date.issued","2018"],["dc.description.abstract","Startle-induced locomotion is commonly used in Drosophila research to monitor locomotor reactivity and its progressive decline with age or under various neuropathological conditions. A widely used paradigm is startle-induced negative geotaxis (SING), in which flies entrapped in a narrow column react to a gentle mechanical shock by climbing rapidly upwards. Here we combined in vivo manipulation of neuronal activity and splitGFP reconstitution across cells to search for brain neurons and putative circuits that regulate this behavior. We show that the activity of specific clusters of dopaminergic neurons (DANs) afferent to the mushroom bodies (MBs) modulates SING, and that DAN-mediated SING regulation requires expression of the DA receptor Dop1R1/Dumb, but not Dop1R2/Damb, in intrinsic MB Kenyon cells (KCs). We confirmed our previous observation that activating the MB α'β', but not αβ, KCs decreased the SING response, and we identified further MB neurons implicated in SING control, including KCs of the γ lobe and two subtypes of MB output neurons (MBONs). We also observed that co-activating the αβ KCs antagonizes α'β' and γ KC-mediated SING modulation, suggesting the existence of subtle regulation mechanisms between the different MB lobes in locomotion control. Overall, this study contributes to an emerging picture of the brain circuits modulating locomotor reactivity in Drosophila that appear both to overlap and differ from those underlying associative learning and memory, sleep/wake state and stress-induced hyperactivity."],["dc.identifier.doi","10.3389/fnsys.2018.00006"],["dc.identifier.eissn","1662-5137"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/78518"],["dc.language.iso","en"],["dc.notes.intern","DOI Import GROB-354"],["dc.publisher","Frontiers Media S.A."],["dc.relation.eissn","1662-5137"],["dc.rights","http://creativecommons.org/licenses/by/4.0/"],["dc.title","Neural Control of Startle-Induced Locomotion by the Mushroom Bodies and Associated Neurons in Drosophila"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.artnumber","72"],["dc.bibliographiccitation.journal","Frontiers in Neuroscience"],["dc.bibliographiccitation.volume","5"],["dc.contributor.author","Stoertkuhl, Klemens F."],["dc.contributor.author","Fiala, Andre"],["dc.date.accessioned","2018-11-07T09:01:19Z"],["dc.date.available","2018-11-07T09:01:19Z"],["dc.date.issued","2011"],["dc.description.abstract","Olfaction is one of the most important senses throughout the animal kingdom. It enables animals to discriminate between a wide variety of attractive and repulsive odorants and often plays a decisive role in species specific communication. In recent years the analysis of olfactory systems both invertebrates and invertebrates has attracted much scientific interest. In this context a pivotal question is how the properties and connectivities of individual neurons contribute to a functioning neuronal network that mediates odor-guided behavior. As a novel approach to analyze the role of individual neurons within a circuitry, techniques have been established that make use of light-sensitive proteins. In this review we introduce a non-invasive, optogenetic technique which was used to manipulate the activity of individual neurons in the olfactory system of Drosophila melanogaster larvae. Both channelrhodopsin-2 and the photosensitive adenylyl cyclase PAC alpha in individual olfactory receptor neurons (ORNs) of the olfactory system of Drosophila larvae allows stimulating individual receptor neurons by light. Depending on which particular ORN is optogenetically activated, repulsion or attraction behavior can be induced, indicating which sensory neurons underlie which type of behavior."],["dc.description.sponsorship","Deutsche Forschungsgemeinschaft [SFB 554/A2, STO 283/11]"],["dc.identifier.doi","10.3389/fnins.2011.00072"],["dc.identifier.isi","000209200600068"],["dc.identifier.pmid","21647413"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?gs-1/8730"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/24394"],["dc.notes.intern","Merged from goescholar"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Frontiers Research Foundation"],["dc.relation.issn","1662-453X"],["dc.rights","Goescholar"],["dc.rights.uri","https://goescholar.uni-goettingen.de/licenses"],["dc.title","The smell of blue light: a new approach toward understanding an olfactory neuronal network"],["dc.type","review"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dc.type.version","published_version"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.issue","1"],["dc.bibliographiccitation.journal","Nature Communications"],["dc.bibliographiccitation.volume","12"],["dc.contributor.author","Pooryasin, Atefeh"],["dc.contributor.author","Maglione, Marta"],["dc.contributor.author","Schubert, Marco"],["dc.contributor.author","Matkovic-Rachid, Tanja"],["dc.contributor.author","Hasheminasab, Sayed-mohammad"],["dc.contributor.author","Pech, Ulrike"],["dc.contributor.author","Fiala, André"],["dc.contributor.author","Mielke, Thorsten"],["dc.contributor.author","Sigrist, Stephan J."],["dc.date.accessioned","2021-06-01T09:41:40Z"],["dc.date.available","2021-06-01T09:41:40Z"],["dc.date.issued","2021"],["dc.description.abstract","Abstract The physical distance between presynaptic Ca 2+ channels and the Ca 2+ sensors triggering the release of neurotransmitter-containing vesicles regulates short-term plasticity (STP). While STP is highly diversified across synapse types, the computational and behavioral relevance of this diversity remains unclear. In the Drosophila brain, at nanoscale level, we can distinguish distinct coupling distances between Ca 2+ channels and the (m)unc13 family priming factors, Unc13A and Unc13B. Importantly, coupling distance defines release components with distinct STP characteristics. Here, we show that while Unc13A and Unc13B both contribute to synaptic signalling, they play distinct roles in neural decoding of olfactory information at excitatory projection neuron (ePN) output synapses. Unc13A clusters closer to Ca 2+ channels than Unc13B, specifically promoting fast phasic signal transfer. Reduction of Unc13A in ePNs attenuates responses to both aversive and appetitive stimuli, while reduction of Unc13B provokes a general shift towards appetitive values. Collectively, we provide direct genetic evidence that release components of distinct nanoscopic coupling distances differentially control STP to play distinct roles in neural decoding of sensory information."],["dc.identifier.doi","10.1038/s41467-021-22180-6"],["dc.identifier.pmid","33771998"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/84997"],["dc.identifier.url","https://for2705.de/literature/publications/38"],["dc.language.iso","en"],["dc.notes.intern","DOI-Import GROB-425"],["dc.relation","FOR 2705: Dissection of a Brain Circuit: Structure, Plasticity and Behavioral Function of the Drosophila Mushroom Body"],["dc.relation","FOR 2705 | TP 5: Postsynaptic receptor plasticity and transsynaptic communication in storage of memory components in the mushroom bodies"],["dc.relation.eissn","2041-1723"],["dc.relation.workinggroup","RG Fiala"],["dc.relation.workinggroup","RG Sigrist (Genetics)"],["dc.rights","CC BY 4.0"],["dc.title","Unc13A and Unc13B contribute to the decoding of distinct sensory information in Drosophila"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.subtype","original_ja"],["dc.type.version","published_version"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","2083"],["dc.bibliographiccitation.issue","12"],["dc.bibliographiccitation.journal","Cell Reports"],["dc.bibliographiccitation.lastpage","2095"],["dc.bibliographiccitation.volume","10"],["dc.contributor.author","Pech, Ulrike"],["dc.contributor.author","Revelo, Natalia H."],["dc.contributor.author","Seitz, Katharina J."],["dc.contributor.author","Rizzoli, S. O."],["dc.contributor.author","Fiala, Andre"],["dc.date.accessioned","2017-09-07T11:44:29Z"],["dc.date.available","2017-09-07T11:44:29Z"],["dc.date.issued","2015"],["dc.description.abstract","Drosophila represents a key model organism for dissecting neuronal circuits that underlie innate and adaptive behavior. However, this task is limited by a lack of tools to monitor physiological parameters of spatially distributed, central synapses in identified neurons. We generated transgenic fly strains that express functional fluorescent reporters targeted to either pre-or postsynaptic compartments. Presynaptic Ca2+ dynamics are monitored using synaptophysin-coupled GCaMP3, synaptic transmission is monitored using red fluorescent synaptophysinpHTomato, and postsynaptic Ca2+ dynamics are visualized usingGCaMP3fused with the postsynaptic matrix protein, dHomer. Using two-photon in vivo imaging of olfactory projection neurons, odor-evoked activity across populations of synapses is visualized in the antennal lobe and the mushroom body calyx. Prolonged odor exposure causes odor-specific and differential experience-dependent changes in preand postsynaptic activity at both levels of olfactory processing. The approach advances the physiological analysis of synaptic connections across defined groups of neurons in intact Drosophila."],["dc.identifier.doi","10.1016/j.celrep.2015.02.065"],["dc.identifier.gro","3141936"],["dc.identifier.isi","000352138400014"],["dc.identifier.pmid","25818295"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?gs-1/12108"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/2724"],["dc.language.iso","en"],["dc.notes.intern","WoS Import 2017-03-10"],["dc.notes.intern","Merged from goescholar"],["dc.notes.status","final"],["dc.notes.submitter","PUB_WoS_Import"],["dc.relation.issn","2211-1247"],["dc.rights","CC BY-NC-ND 3.0"],["dc.rights.uri","https://creativecommons.org/licenses/by-nc-nd/3.0"],["dc.title","Optical Dissection of Experience-Dependent Pre- and Postsynaptic Plasticity in the Drosophila Brain"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.subtype","original"],["dc.type.version","published_version"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.artnumber","e24300"],["dc.bibliographiccitation.issue","9"],["dc.bibliographiccitation.journal","PLoS ONE"],["dc.bibliographiccitation.volume","6"],["dc.contributor.author","Niewalda, Thomas"],["dc.contributor.author","Voeller, Thomas"],["dc.contributor.author","Eschbach, Claire"],["dc.contributor.author","Ehmer, Julia"],["dc.contributor.author","Chou, Wen-Chuang"],["dc.contributor.author","Timme, Marc"],["dc.contributor.author","Fiala, Andre"],["dc.contributor.author","Gerber, Bertram"],["dc.date.accessioned","2018-11-07T08:51:47Z"],["dc.date.available","2018-11-07T08:51:47Z"],["dc.date.issued","2011"],["dc.description.abstract","How do physico-chemical stimulus features, perception, and physiology relate? Given the multi-layered and parallel architecture of brains, the question specifically is where physiological activity patterns correspond to stimulus features and/or perception. Perceived distances between six odour pairs are defined behaviourally from four independent odour recognition tasks. We find that, in register with the physico-chemical distances of these odours, perceived distances for 3octanol and n-amylacetate are consistently smallest in all four tasks, while the other five odour pairs are about equally distinct. Optical imaging in the antennal lobe, using a calcium sensor transgenically expressed in only first-order sensory or only second-order olfactory projection neurons, reveals that 3-octanol and n-amylacetate are distinctly represented in sensory neurons, but appear merged in projection neurons. These results may suggest that within-antennal lobe processing funnels sensory signals into behaviourally meaningful categories, in register with the physico-chemical relatedness of the odours."],["dc.identifier.doi","10.1371/journal.pone.0024300"],["dc.identifier.fs","581768"],["dc.identifier.isi","000294803100017"],["dc.identifier.pmid","21931676"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?gs-1/8186"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/22018"],["dc.notes.intern","Merged from goescholar"],["dc.notes.intern","Merged from goescholar"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Public Library Science"],["dc.relation.issn","1932-6203"],["dc.relation.orgunit","Fakultät für Physik"],["dc.rights","CC BY 2.5"],["dc.rights.uri","http://creativecommons.org/licenses/by/2.5/"],["dc.title","A Combined Perceptual, Physico-Chemical, and Imaging Approach to 'Odour-Distances' Suggests a Categorizing Function of the Drosophila Antennal Lobe"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dc.type.version","published_version"],["dspace.entity.type","Publication"]]