Optimized CRISPR/Cas tools for efficient germline and somatic genome engineering in Drosophila

A Programmable Dual-RNA–Guided DNA Endonuclease in Adaptive Bacterial Immunity

Jinek, M., Chylinski, K., Fonfara, I., Hauer, M., Doudna, J. A., & Charpentier, E. (2012) · Science · doi:10.1126/science.1225829 · Cited by 17,116

Targeted gene expression as a means of altering cell fates and generating dominant phenotypes

Brand, A. H., & Perrimon, N. (1993) · Development · doi:10.1242/dev.118.2.401 · Cited by 9,510

RNA-Guided Human Genome Engineering via Cas9

Mali, P., Yang, L., Esvelt, K. M., Aach, J., Guell, M., DiCarlo, J. E., Norville, J. E., & Church, G. M. (2013) · Science · doi:10.1126/science.1232033 · Cited by 9,210

Mutations affecting segment number and polarity in Drosophila

Nüsslein‐Volhard, C., & Wieschaus, E. F. (1980) · Nature · doi:10.1038/287795a0 · Cited by 4,370

One-step generation of mice carrying mutations in multiple genes by CRISPR/Cas-mediated genome engineering

Wang, H., Yang, H., Shivalila, C. S., Dawlaty, M. M., Cheng, A. W., Zhang, F., & Jaenisch, R. (2013) · Cell · doi:10.1016/j.cell.2013.04.025 · Cited by 3,495

Double nicking by RNA-guided CRISPR Cas9 for enhanced genome editing specificity

Ran, F. A., Hsu, P. D., Lin, C.-Y., Gootenberg, J. S., Konermann, S., Trevino, A. E., Scott, D. A., Inoue, A., Matoba, S., Zhang, Y., et al. (2013) · Cell · doi:10.1016/j.cell.2013.08.021 · Cited by 3,299

High-Frequency off-Target Mutagenesis Induced by CRISPR-Cas Nucleases in Human Cells

Fu, Y., Foden, J. A., Khayter, C., Maeder, M. L., Reyon, D., Joung, J. K., & Sander, J. D. (2013) · Nature Biotechnology · doi:10.1038/nbt.2623 · Cited by 3,292

RNA-programmed genome editing in human cells

Jinek, M., East, A., Cheng, A., Lin, S., Ma, E., & Doudna, J. (2013) · eLife · doi:10.7554/elife.00471 · Cited by 2,098

Improving CRISPR-Cas nuclease specificity using truncated guide RNAs

Fu, Y., Sander, J. D., Reyon, D., Cascio, V. M., & Joung, J. K. (2014) · Nature Biotechnology · doi:10.1038/nbt.2808 · Cited by 1,993 · cited 1×

An optimized transgenesis system for Drosophila using germ-line-specific φC31 integrases

Bischof, J., Maeda, R., Hediger, M., Karch, F., & Basler, K. (2007) · Proceedings of the National Academy of Sciences of the United States of America · doi:10.1073/pnas.0611511104 · Cited by 1,959

A novel mistranslating tRNA model in Drosophila melanogaster has diverse, sexually dimorphic effects

Isaacson, J., Berg, M. D., Charles, B., Jagiello, J., Villén, J., Brandl, C. J., & Moehring, A. J. (2022) · G3 Genes Genomes Genetics · doi:10.1093/g3journal/jkac035 · Cited by 9

Evolution of casein kinase 1 and functional analysis of new doubletime mutants in Drosophila

Thakkar, N., Giesecke, A. V., Bazalová, O., Martinek, J., Smýkal, V., Stanewsky, R., & Doležel, D. (2022) · Frontiers in Physiology · doi:10.3389/fphys.2022.1062632 · Cited by 9

Plk4 Is a Novel Substrate of Protein Phosphatase 5

Ábrahám, E., Réthi‐Nagy, Z., Vilmos, P., Sinka, R., & Lipinszki, Z. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24032033 · Cited by 9

The USP46 deubiquitylase complex increases Wingless/Wnt signaling strength by stabilizing Arrow/LRP6

Spencer, Z. T., Ng, V. H., Benchabane, H., Siddiqui, G. S., Duwadi, D., Maines, B., Bryant, J. M., Schwarzkopf, A., Yuan, K., Kassel, S. N., et al. (2023) · Nature Communications · doi:10.1038/s41467-023-41843-0 · Cited by 9

Drosophila melanogaster: A Valuable Genetic Model Organism to Elucidate the Biology of Retinitis Pigmentosa

Lehmann, M., Knust, E., & Hebbar, S. (2018) · Methods in molecular biology · doi:10.1007/978-1-4939-8669-9_16 · Cited by 8

Behavioral screening defines three molecular Parkinsonism subgroups in DrosophilaPreprint

Kaempf, N., Valadas, J. S., Robberechts, P., Schoovaerts, N., Praschberger, R., Ortega, A., Kilic, A., Chabot, D., Pech, U., Kuenen, S., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.08.27.609924 · Cited by 9

Wnt/Wingless signaling promotes lipid mobilization through signal-induced transcriptional repression

Liu, M., Hemba-Waduge, R.-U.-S., Li, X., Huang, X., Liu, T.-H., Han, X., Wang, Y., & Ji, J.-Y. (2024) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2322066121 · Cited by 12

CRISPR/Cas9 Based Cell-Type Specific Gene Knock-Out in Arabidopsis Roots

Li, M., Niu, X., Li, S., Fu, S., Li, Q., Xu, M., Wang, C., & Wu, S. (2023) · Plants · doi:10.3390/plants12122365 · Cited by 8

Redesigning the Drosophila histone gene cluster: an improved genetic platform for spatiotemporal manipulation of histone function

Crain, A. T., Nevil, M., Leatham-Jensen, M. P., Reeves, K. B., Matera, A. G., McKay, D. J., & Duronio, R. J. (2024) · Genetics · doi:10.1093/genetics/iyae117 · Cited by 10

Tackling hepatitis B Virus with CRISPR/Cas9: advances, challenges, and delivery strategies

Nair, D. M., Vajravelu, L. K., Thulukanam, J., Panneerselvam, V. P., Vimala, P. B., & Lathakumari, R. H. (2024) · Virus Genes · doi:10.1007/s11262-024-02105-3 · Cited by 10

A candidate loss-of-function variant in SGIP1 causes synaptic dysfunction and recessive parkinsonism

Decet, M., Scott, P., Kuenen, S., Meftah, D., Swerts, J., Calatayud, C., Gallego, S. F., Kaempf, N., Nachman, E., Praschberger, R., et al. (2024) · Cell Reports Medicine · doi:10.1016/j.xcrm.2024.101749 · Cited by 8

Transferable approaches to CRISPR-Cas9 induced genome editing in non-model insects: a brief guide

Ahmed, H. M. M., Zheng, L., & Hunnekuhl, V. S. (2025) · Frontiers in Zoology · doi:10.1186/s12983-025-00566-2 · Cited by 8

Introduction of a point mutation in the KRAS gene of in vitro fertilized porcine zygotes via electroporation of the CRISPR/Cas9 system with single‐stranded oligodeoxynucleotides

Wittayarat, M., Hirata, M., Namula, Z., Sato, Y., Nguyen, N. T., Le, Q. A., Lin, Q., Takebayashi, K., Tanihara, F., & Otoi, T. (2021) · Animal Science Journal · doi:10.1111/asj.13534 · Cited by 8

An actin-related protein that is most highly expressed in Drosophila testes is critical for embryonic development

Schroeder, C. M., Tomlin, S. A., Natividad, I. M., Valenzuela, J. R., Young, J. M., & Malik, H. S. (2021) · eLife · doi:10.7554/elife.71279 · Cited by 8

Tace/ADAM17 is a bi-directional regulator of axon guidance that coordinates distinct Frazzled and Dcc receptor signaling outputs

Zang, Y., Chaudhari, K., & Bashaw, G. J. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.111785 · Cited by 8

α-Tubulin acetylation at lysine 40 regulates dendritic arborization and larval locomotion by promoting microtubule stability in Drosophila

Niu, X., Mao, C., Wang, S., Wang, X., Zhang, Y., Hu, J., Bi, R., Liu, Z., & Jin, S. (2023) · PLoS ONE · doi:10.1371/journal.pone.0280573 · Cited by 8

Stuxnet fine-tunes Notch dose during development using a functional Polycomb response element

He, T., Fan, Y., Du, J., Yi, M., Li, Y., Liu, M., & Zhu, A. J. (2023) · Development · doi:10.1242/dev.201297 · Cited by 8

A force-sensitive mutation reveals a non-canonical role for dynein in anaphase progression

Salvador-Garcia, D., Jin, L., Hensley, A. M., Gölcük, M., Gallaud, E., Chaaban, S., Port, F., Vagnoni, A., Planelles-Herrero, V. J., McClintock, M. A., et al. (2024) · The Journal of Cell Biology · doi:10.1083/jcb.202310022 · Cited by 7

Establishment of pupal color as a screening marker and activity analysis of six U6 promoters in Zeugodacus cucurbitae using the white pupae gene

Fan, Z., Wu, Y., Zha, X., Ma, S., Ma, L., Liang, L., Lin, X.-W., & Yan, R. (2025) · Pest Management Science · doi:10.1002/ps.8692 · Cited by 8

Clonal analysis of gene loss of function and tissue-specific gene deletion in zebrafish via CRISPR/Cas9 technology

Santis, F. D., Donato, V. D., & Bene, F. D. (2016) · Methods in cell biology · doi:10.1016/bs.mcb.2016.03.006 · Cited by 8

Bxb1 phage recombinase assists genome engineering in Drosophila melanogaster

Voutev, R., & Mann, R. S. (2017) · BioTechniques · doi:10.2144/000114494 · Cited by 8

GATA factor genes in the Drosophila midgut embryo

de Madrid, B. H., & Casanova, J. (2018) · PLoS ONE · doi:10.1371/journal.pone.0193612 · Cited by 8

Anchor Away – A Fast, Reliable and Reversible Technique To Inhibit Proteins in Drosophila melanogaster

Bosch, P. S., Pepperl, J., & Basler, K. (2020) · G3: Genes, Genomes, Genetics · doi:10.1534/g3.120.401055 · Cited by 7

Drosophila melanogaster as a Model of Developmental Genetics: Modern Approaches and Prospects

Нефедова, Л. Н. (2020) · Russian Journal of Developmental Biology · doi:10.1134/s1062360420040050 · Cited by 8

The expression of Drosophila melanogaster Hox gene Ultrabithorax is not overtly regulated by the intronic long noncoding RNA lncRNA:PS4 in a wild-type genetic background

Hermann, A., Kosman, D., McGinnis, W. J., & Tour, E. (2021) · G3 Genes Genomes Genetics · doi:10.1093/g3journal/jkab374 · Cited by 8

CRISPR/Cas9-mediated tissue-specific knockout and cDNA rescue using sgRNAs that target exon-intron junctions in Drosophila melanogaster

Chilian, M., Parra, K. V., Sandoval, A., Ramírez, J. D., & Yoon, W. H. (2022) · STAR Protocols · doi:10.1016/j.xpro.2022.101465 · Cited by 8

Dispersive forces and resisting spot welds by alternative homolog conjunction govern chromosome shape in Drosophila spermatocytes during prophase I

Vernizzi, L., & Lehner, C. F. (2022) · PLoS Genetics · doi:10.1371/journal.pgen.1010327 · Cited by 8

GTPase-activating protein TBC1D5 coordinates with retromer to constrain synaptic growth by inhibiting BMP signaling

Zhou, X., Gan, G., Sun, Y., Ou, M., Geng, J., Wang, J., Yang, X., Huang, S., Jia, D., Xie, W., et al. (2022) · Journal of genetics and genomics/Journal of Genetics and Genomics · doi:10.1016/j.jgg.2022.11.009 · Cited by 8

The Osiris family genes function as novel regulators of the tube maturation process in the Drosophila trachea

Scholl, A., Ndoja, I., Dhakal, N., Morante, D., Ivan, A., Newman, D., Mossington, T., Clemans, C., Surapaneni, S., Powers, M. R., et al. (2023) · PLoS Genetics · doi:10.1371/journal.pgen.1010571 · Cited by 8

Drosophila melanogaster and its nephrocytes: A versatile model for glomerular research

Odenthal, J., & Brinkkoetter, P. T. (2019) · Methods in cell biology · doi:10.1016/bs.mcb.2019.03.011 · Cited by 8

Neural Changes Underlying Rapid Fly Song EvolutionPreprint

Ding, Y., Lillvis, J. L., Cande, J., Berman, G. J., Arthur, B. J., Xu, M., Dickson, B. J., & Stern, D. L. (2017) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/238147 · Cited by 8

A Pandas complex adapted for piRNA-guided transposon silencingPreprint

Zhao, K., Cheng, S., Miao, N., Xu, P., Lu, X., Zhang, Y., Wang, M., Ouyang, X., Yuan, X., Liu, W., et al. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/608273 · Cited by 8

2-Locus Cleave and Rescue selfish elements harness a recombination rate-dependent generational clock for self limiting gene drivePreprint

Oberhofer, G., Ivy, T., & Hay, B. A. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.07.09.196253 · Cited by 8

Synaptic deregulation of cholinergic projection neurons causes olfactory dysfunction across 5 fly Parkinsonism modelsPreprint

Pech, U., Janssens, J., Schoovaerts, N., Kuenen, S., Makhzami, S., Hulselmans, G. J., Poovathingal, S. K., Bademosi, A. T., Swerts, J., Vilain, S., et al. (2024) · eLife · doi:10.7554/elife.98348.1 · Cited by 8

Germline Editing of Drosophila Using CRISPR-Cas9-Based Cytosine and Adenine Base Editors

Thakkar, N., Hejzlarova, A., Brabec, V., & Doležel, D. (2023) · The CRISPR Journal · doi:10.1089/crispr.2023.0026 · Cited by 7

Molecular and functional characterization of the Drosophila melanogaster conserved smORFome

Bosch, J. A., Keith, N., Escobedo, F., Fisher, W. W., LaGraff, J. T., Rabasco, J. T., Wan, K. H., Weiszmann, R., Wu, Y., Hu, Y., et al. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.113311 · Cited by 7

The potential use of Drosophila as an in vivo model organism for COVID-19-related research: a review

Demir, E. (2021) · Turkish journal of biology = Turk biyoloji dergisi · doi:10.3906/biy-2104-26 · Cited by 6

The Role of Drosophila CtIP in Homology-Directed Repair of DNA Double-Strand Breaks

Yannuzzi, I., Butler, M. A., Fernandez, J., & LaRocque, J. R. (2021) · Genes · doi:10.3390/genes12091430 · Cited by 8

CRISPR-/Cas9-Mediated Precise and Efficient Genome Editing in Drosophila

Nyberg, K. G., & Carthew, R. W. (2022) · Methods in molecular biology · doi:10.1007/978-1-0716-2541-5_6 · Cited by 7

Peptidoglycan recognition in Drosophila is mediated by LysMD3/4

Snee, M. J., Wever, J., Guyton, J., Beehler-Evans, R., Yokoyama, C. C., & Micchelli, C. A. (2023) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2023.104758 · Cited by 7

Allelic strengths of encephalopathy-associated UBA5 variants correlate between in vivo and in vitro assays

Pan, X., Alvarez, A. N., Ma, M., Lu, S., Crawford, M. W., Briere, L. C., Kanca, O., Yamamoto, S., Sweetser, D. A., Wilson, J. L., et al. (2023) · eLife · doi:10.7554/elife.89891 · Cited by 7

CRISPR‐Cas: von einem bakteriellen adaptiven Immunsystem zu einem vielseitigen Werkzeug für die Gentechnik

Kirchner, M., & Schneider, S. (2015) · Angewandte Chemie · doi:10.1002/ange.201504741 · Cited by 7

The importance of a halotyrosine dehalogenase for Drosophila fertility

Phatarphekar, A., Su, Q., Eun, S. H., Chen, X., & Rokita, S. E. (2018) · Journal of Biological Chemistry · doi:10.1074/jbc.ra118.003364 · Cited by 7

Perspectives on gene expression regulation techniques in Drosophila

Xu, R., Wang, X., Shen, D., Sun, J., Qiao, H., Wang, F., Liu, L., & Ni, J. (2019) · Journal of genetics and genomics/Journal of Genetics and Genomics · doi:10.1016/j.jgg.2019.03.006 · Cited by 7

CAMIO: a transgenic CRISPR pipeline to create diverse targeted genome deletions in Drosophila

Chen, H.-M., García‐Marqués, J., Sugino, K., Wei, D., Miyares, R. L., & Lee, T. (2020) · Nucleic Acids Research · doi:10.1093/nar/gkaa177 · Cited by 8

Optogenetic approaches for understanding homeostatic and degenerative processes in Drosophila

Lim, W. K., Kaur, P., Huang, H., Jo, R. S., Ramamoorthy, A., Ng, L. F., Suresh, J., Maisha, F. I., Mathuru, A. S., & Tolwinski, N. S. (2021) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-021-03836-4 · Cited by 7

Compensatory replacement of the BigH1 variant histone by canonical H1 supports normal embryonic development in DrosophilaPreprint

Li, K. K., Han, D., Chen, F., Li, R., Zhou, B., Bai, Y., Yuan, K., & Rong, Y. S. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/789735 · Cited by 7

Balanced synapse-to-synapse short-term plasticity ensures constant transmitter release

Aghi, K., Schultz, R., Stowers, R. S., Liu, W. Y., Mendonça, P. R. F., Li, R., Bakshinska, D., Newman, Z. L., & Isacoff, E. Y. (2025) · Current Biology · doi:10.1016/j.cub.2025.05.024 · Cited by 7

Vostok: A looping factor for the organization of the regulatory genome in the Drosophila brain

Hu, J. H., Li, X., Ломаев, Д. В., Vorobyeva, N. E., Levine, M., Erokhin, M., & Chetverina, D. (2025) · Molecular Cell · doi:10.1016/j.molcel.2025.05.020 · Cited by 6

Defining the roles of the Integrator, NEXT, and nuclear exosome complexes in Drosophila oogenesis

Lee, Y., Biasini, A., Tipping, C., Hong, S. H., & Zamore, P. D. (2025) · Cell Reports · doi:10.1016/j.celrep.2025.116329 · Cited by 6

The ubiquitin thioesterase YOD1 ameliorates mutant Huntingtin induced pathology in Drosophila

Farkas, A., Zsindely, N., Nagy, G., Kovács, L., Deák, P., & Bodai, L. (2023) · Scientific Reports · doi:10.1038/s41598-023-49241-8 · Cited by 6

Conditional chemoconnectomics (cCCTomics) as a strategy for efficient and conditional targeting of chemical transmission

Mao, R., Yu, J., Deng, B., Dai, X., Du, Y., Du, S., Zhang, W., & Rao, Y. (2023) · eLife · doi:10.7554/elife.91927 · Cited by 6

Same rule, different genes: Blimp1 is a pair-rule gene in the milkweed bug Oncopeltus fasciatus

Reding, K., Chung, M. C., Heath, A., Hotopp, J. C. D., & Pick, L. (2024) · Science Advances · doi:10.1126/sciadv.adq9045 · Cited by 6

Glial Derived TGF-β Instructs Axon Midline Stopping

Marmor‐Kollet, N., Gutman, I., Issman-Zecharya, N., & Schuldiner, O. (2019) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2019.00232 · Cited by 6

A novel non‐invasive identification of genome editing mutants from insect exuviae

Wang, X., Li, J., Wang, T., Yang, Y., Zhang, H., Zhou, M., Kang, L., & Wei, L. (2021) · Insect Science · doi:10.1111/1744-7917.12914 · Cited by 6

Secreted C-type lectin regulation of neuromuscular junction synaptic vesicle dynamics modulates coordinated movement

Bhimreddy, M., Rushton, E., Kopke, D. L., & Broadie, K. S. (2021) · Journal of Cell Science · doi:10.1242/jcs.257592 · Cited by 6

EGFRAP encodes a new negative regulator of the EGFR acting in both normal and oncogenic EGFR/Ras-driven tissue morphogenesis

Beatty, J. S., Molnar, C., Luque, C. M., de Celis, J. F., & Martin-Bermudo, M. D. (2021) · PLoS Genetics · doi:10.1371/journal.pgen.1009738 · Cited by 6

Evolutionary diversification reveals distinct somatic versus germline cytoskeletal functions of the Arp2 branched actin nucleator protein

Stromberg, K. A., Spain, T., Tomlin, S. A., Powell, J., Amarillo, K. D., & Schroeder, C. M. (2023) · Current Biology · doi:10.1016/j.cub.2023.10.055 · Cited by 6

Insights into unique features of Drosophila CYP4G enzymes

Kefi, M., Konstantinos, P., Balabanidou, V., Sarafoglou, C., Tsakireli, D., Douris, V., Monastirioti, M., Maréchal, J., Feyereisen, R., & VONTAS, J. G. (2023) · Insect Biochemistry and Molecular Biology · doi:10.1016/j.ibmb.2023.104041 · Cited by 6

Allelic strengths of encephalopathy-associated UBA5 variants correlate between in vivo and in vitro assays

Pan, X., Alvarez, A. N., Ma, M., Lu, S., Crawford, M. W., Briere, L. C., Kanca, O., Yamamoto, S., Sweetser, D. A., Wilson, J. L., et al. (2023) · eLife · doi:10.7554/elife.89891.3 · Cited by 6

The FAM114A proteins are adaptors for the recycling of Golgi enzymes

Welch, L. G., Muschalik, N., & Munro, S. (2024) · Journal of Cell Science · doi:10.1242/jcs.262160 · Cited by 6

Transcriptional coupling of telomeric retrotransposons with the cell cycle

Liu, M., Xie, X., Li, X., Ren, X., Sun, J. L., Lin, Z. N., Hemba-Waduge, R.-U.-S., & Ji, J. (2025) · Science Advances · doi:10.1126/sciadv.adr2299 · Cited by 6

A Family of Auxiliary Subunits of the TRP Cation Channel Encoded by the Complex inaF Locus

Chen, Z., & Montell, C. (2020) · Genetics · doi:10.1534/genetics.120.303268 · Cited by 6

R7 photoreceptor axon targeting depends on the relative levels of lost and found expression in R7 and its synaptic partners

Douthit, J., Hairston, A., Lee, G., Morrison, C. A., Holguera, I., & Treisman, J. E. (2021) · eLife · doi:10.7554/elife.65895 · Cited by 6

A Novel Neuron-Specific Regulator of the V-ATPase in Drosophila

Dulac, A., Issa, A.-R., Sun, J., Matassi, G., Jonas, C., Rahmani, Z., Chérif‐Zahar, B., Cattaert, D., & Birman, S. (2021) · eNeuro · doi:10.1523/eneuro.0193-21.2021 · Cited by 6

Characterization of enhancer fragments in Drosophila robo2

Hauptman, G., Reichert, M. C., Rhida, M. A. A., & Evans, T. A. (2022) · Fly · doi:10.1080/19336934.2022.2126259 · Cited by 6

Nanoscaled RIM clustering at presynaptic active zones revealed by endogenous tagging

Mrestani, A., Dannhäuser, S., Pauli, M., Kollmannsberger, P., Hübsch, M., Morris, L., Langenhan, T., Heckmann, M., & Paul, M. M. (2023) · Life Science Alliance · doi:10.26508/lsa.202302021 · Cited by 7

Cloning and functional characterizations of an apoptogenic Hid gene in the Scuttle Fly, Megaselia scalaris (Diptera; Phoridae)

Yoo, S., Lam, H. R., Lee, C., Lee, G., & Park, J. H. (2016) · Gene · doi:10.1016/j.gene.2016.11.043 · Cited by 6

An Efficient Strategy for Generating Tissue-specific Binary Transcription Systems in Drosophila by Genome Editing

Du, L., Zhou, A., Sohr, A., & Roy, S. (2018) · Journal of Visualized Experiments · doi:10.3791/58268 · Cited by 6

Axin proteolysis by Iduna is required for the regulation of stem cell proliferation and intestinal homeostasis in Drosophila

Gültekin, Y., & Steller, H. (2019) · Development · doi:10.1242/dev.169284 · Cited by 6

Characterisation of protein isoforms encoded by the Drosophila Glycogen Synthase Kinase 3 gene shaggy

Korona, D., Nightingale, D. J. H., Fabre, B., Nelson, M. G., Fischer, B., Johnson, G., Lees, J., Hubbard, S. J., Lilley, K. S., & Russell, S. R. H. (2020) · PLoS ONE · doi:10.1371/journal.pone.0236679 · Cited by 6

TADs Pair Homologous Chromosomes to Promote Interchromosomal Gene RegulationPreprint

Viets, K., Sauria, M. E. G., Chernoff, C., Anderson, C., Tran, S., Dove, A., Goyal, R., Voortman, L., Gordus, A. G., Taylor, J., et al. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/445627 · Cited by 6

A home and rescue gene drive efficiently spreads and persists in populationsPreprint

Kandul, N. P., Liu, J., Bennett, J. B., Marshall, J. M., & Akbari, O. S. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.08.21.261610 · Cited by 6

Centrocortin potentiates co-translational localization of its mRNA to the centrosome via dyneinPreprint

Zein-Sabatto, H., Brockett, J. S., Jin, L., Husbands, C. A., Lee, J., Fang, J., Buehler, J., Bullock, S. L., & Lerit, D. A. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.08.09.607365 · Cited by 6

Structure-optimized sgRNA selection with PlatinumCRISPr for efficient Cas9 generation of knockoutsPreprint

Haussmann, I. U., Dix, T. C., McQuarrie, D. W. J., Dezi, V., Hans, A. I., Arnold, R. R., & Soller, M. (2024) · Genome Research · doi:10.1101/gr.279479.124 · Cited by 6

Dissecting the enhancer gene regulatory network in early Drosophila spermatogenesis

y Sanchez, P. V. N., Sekhar, P. S., Yildirim, K., Lange, T., Kreplin, L. Z., Boopathy, V. M., de Souza, S. R., Dammer, K., Ibberson, D., Wang, Q., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-62046-9 · Cited by 5

Specification of the endocrine primordia controlling insect moulting and metamorphosis by the JAK/STAT signalling pathway

García-Ferrés, M., Sánchez-Higueras, C., Espinosa, J. M., & Hombría, J. C. (2022) · PLoS Genetics · doi:10.1371/journal.pgen.1010427 · Cited by 5

Tropical super flies: Integrating Cas9 into Drosophila ananassae and its phenotypic effects

Yılmaz, V. M., Ramnarine, T. J. S., Königer, A., Mussgnug, S., & Grath, S. (2023) · Journal of Insect Physiology · doi:10.1016/j.jinsphys.2023.104516 · Cited by 5

The proximal enhancer of the snail gene mediates negative autoregulatory feedback in Drosophila melanogaster

Dunipace, L., McGehee, J. M., Irizarry, J., & Stathopoulos, A. (2025) · Genetics · doi:10.1093/genetics/iyaf058 · Cited by 5

Frameshift mutations of YPEL3 alter the sensory circuit function in Drosophila

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