Tools for neuroanatomy and neurogenetics in Drosophila

By B. Pfeiffer, Arnim Jenett, Ann Hammonds, Teri-Tb Ngo, S. Misra, C. Murphy, Audra L. Scully, Joseph W. Carlson, K. Wan, T. Laverty and 7 more. Proceedings of the National Academy of Sciences of the United States of America, 2008

956 citations recorded by the source corpus.

Subfields: Cellular and Molecular Neuroscience, Molecular Biology, Plant Science

View Paper: https://www.semanticscholar.org/paper/61c7c7a956cf197a5bdce00b31170ecdf5d40d37

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Citations in the corpus

Fly motion vision. (2010, background): “Controlled and standardized expression levels in well-defined and small sets of neurons are highly desirable, such as those resulting from enhancer fragment lines currently being produced (Pfeiffer et al. 2008).”
The neuronal architecture of the mushroom body provides a logic for associative learning (2014, methodology): “…primers SM(1A) and BI(1S) (Alekseyenko et al., 2010) and cloned into pBPp65ADZpw and pBPZpGAL4DBDw using the Gateway system as previously described (Pfeiffer et al., 2008, 2010). pJFRC225-5xUAS-IVS-myr::smGFP-FLAG in VK00005 and pJFRC200-10xUAS-IVS-myr::smGFP-HA in attP18 are described by…”
Dissecting neural pathways for forgetting in Drosophila olfactory aversive memory (2015, methodology): “To further distinguish different subsets of PAM-DANs, we took advantage of Gal80 lines derived from R24E12 and R48B04, two drivers that overlapped with NP2397 in PAM-β′1 and in other PAM-DANs, respectively (Fig.”
The Q System: A Repressible Binary System for Transgene Expression, Lineage Tracing and Mosaic Analysis (2010, neutral): “…to QF-SV40) and has enabled fly transgenesis using constructs that proved toxic with QF-SV40 (CJP and LL, unpublished results). pattB-DSCP-QF-SV40 The DSCP from pBPGUw (Pfeiffer et al., 2008) was PCR amplified to include EcoRI/MfeI restriction sites and ligated into the EcoRI site of pattB-QF-sv40.”
Mushroom body efferent neurons responsible for aversive olfactory memory retrieval in Drosophila (2011, methodology): “4), constructed as described in reference [27] (see methods).”
Cell-type Specific Labeling of Synapses in vivo through Synaptic Tagging with Recombination (STaR) (2014, background): “…UAS > stop > myr-tdTomato in su(Hw)attP2; (16) UAS-R in attP2 (Nern et al., 2011); (17) UAS-myr-GFP in attP40; (18) UAS-myr-tdTomato in su(Hw)attP2 (Pfeiffer et al., 2008); (19) R27G05-FLP2::PEST in attp40 (PanLN-FLP); (20) R20C11-Gal4 (R7); (21) R24C08-Gal4 (Tm9); (22) R53C12Gal4 (Mi1); (23)…”
Genetic manipulation of genes and cells in the nervous system of the fruit fly (2011, methodology): “Obviously, enhancer trap screens or enhancer fusion lines could be created for LexA and QF (Pfeiffer et al., 2008).”
Genome-Wide Quantitative Enhancer Activity Maps Identified by STARR-seq (2013, neutral): “sampling depth) or its specific design to be a ‘promiscuous’ core promoter (22).”
A single pair of neurons links sleep to memory consolidation in Drosophila melanogaster (2015, methodology): “A modified version of pBPGUw (Pfeiffer et al., 2008), pBPGUw-R1R3-p10 was used for gateway recombination and injection into flies where it was targeted to the attP40 landing site on the second chromosome.”
Patterns of growth, axonal extension and axonal arborization of neuronal lineages in the developing Drosophila brain. (2009, background): “Large scale screens are underway to attain this goal (Pfeiffer et al., 2008).”