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 genome-engineered tool set for Drosophila TGF-β/BMP signaling studies

Ell, C.-M., Safyan, A., Chayengia, M., Kustermann, M. M. M., Lorenz, J., Schächtle, M., & Pyrowolakis, G. (2024) · Development · doi:10.1242/dev.204222 · Cited by 1

Ambivalent partnership of the Drosophila posterior class Hox protein Abdominal-B with Extradenticle and Homothorax

Curt, J. R., Martín, P., Foronda, D., Hudry, B., Kannan, R., Shetty, S., Merabet, S., Saurin, A. J., Graba, Y., & Sánchez‐Herrero, E. (2025) · PLoS Genetics · doi:10.1371/journal.pgen.1011355 · Cited by 1

The deubiquitinase USP36 funtions through catalytic-dependent and catalytic-independent mechanisms in Drosophila

Coirry, C., Manessier, J., Clot, C., Mortier, M., Fauvarque, M., & Taillebourg, E. (2025) · Genetics · doi:10.1093/genetics/iyaf131 · Cited by 1

Tuning mitotic recombination with patterned DNA nicks for precision mosaic analysis

Shen, Y., Yeung, A. T., Wang, B., Yeh, C.-T., Ditchfield, P., Korn, E., & Han, C. (2026) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2531265123 · Cited by 1

A genetic circuit that extends the useful range of a BMP morphogen arose alongside insect wing evolution

Huang, A., Cocconi, L., Nicholls-Mindlin, B., Alexandre, C., Salbreux, G., & Vincent, J. (2025) · Current Biology · doi:10.1016/j.cub.2025.10.059 · Cited by 1

DIL-CRISPR: a practical approach to mitigate G0 mosaic lethality in insect gene editing

Nishizawa, H., & Daimon, T. (2026) · Insect Biochemistry and Molecular Biology · doi:10.1016/j.ibmb.2026.104492 · Cited by 1

The Drosophila maternal-effect gene abnormal oocyte ( ao ) does not repress histone gene expression

Takenaka, R., Albanese, E. H., Simmerman, S. M., Verghese, S., Maddox, M. A. E., de la Cruz, A. F., Young, J. M., Schmidt, C. A., Rieder, L. E., & Malik, H. S. (2026) · Genetics · doi:10.1093/genetics/iyag036 · Cited by 1

A genome-wide MAGIC kit for recombinase-independent mosaic analysis in Drosophila

Shen, Y., Yeung, A. T., Ditchfield, P., Korn, E., CLEMENTS, R. G. H., Chen, X., Wang, B., Huang, Z., Sheen, M., Jarman, P. A., et al. (2026) · eLife · doi:10.7554/elife.108453.3 · Cited by 1

Embedded CRISPRi Enhances Gene‐Silencing Efficiency in Drosophila

Fu, P., Zhang, X., Zhou, Y., Zheng, J., Sun, A., Zhuang, K., Bao, W., & Gao, G. (2026) · Advanced Science · doi:10.1002/advs.202515849 · Cited by 1

Spen and Nito prevent dedifferentiation of intermediate progenitors by maintaining Notch target expression in stem cells at low levels

Li, X., Lu, W., Connell, M., Deng, X., Chen, R., & Zhu, S. (2026) · Cell Reports · doi:10.1016/j.celrep.2026.117194 · Cited by 1

Transient residence of the repulsive client Shutdown in Yb bodies plays a critical role in Piwi-piRISC biogenesis and maintaining fertility

Hirakata, S., Fukaya, T., Fujita, A., Kosako, H., & Siomi, M. C. (2026) · Molecular Cell · doi:10.1016/j.molcel.2026.03.003 · Cited by 1

The actin crosslinker Fimbrin is required for force sensing at tricellular junctions

Taneja, N., Looney, C. A., Moubarak, M. F., McGovern, M. J., Yeoh, K., & Zallen, J. A. (2026) · Developmental Cell · doi:10.1016/j.devcel.2026.07.001 · Cited by 4

Ana1/Cep295 regulates centriole elongation via Cep135 and microtubules

Wang, Z., Qian, Y., Wang, X., Ng, Q., Zhang, H., Wu, Y., Liu, Z., & Feng, Z. (2026) · The Journal of Cell Biology · doi:10.1083/jcb.202504094 · Cited by 1

Drosophila cytoplasmic dynein

Neisch, A. L., Avery, A. W., Li, M.-G., & Hays, T. S. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-809471-6.00021-8 · Cited by 1

Efficient Synthesis of Mutants Using Genetic Crosses

Pratapa, A., Jalihal, A. P., Ravi, S. S., & Murali, T. M. (2018) · ACM International Conference on Bioinformatics, Computational Biology, and Health Informatics (ACM-BCB) · doi:10.1145/3233547.3233556

Methods for Creating Fly Models to Understand the Molecular Mechanisms Underlying Neurological Diseases

Nandan, J., & Nagarkar-Jaiswal, S. (2019) · Springer eBooks · doi:10.1007/978-981-13-2218-1_2 · Cited by 1

Despite its sequence identity with canonical H4, Drosophila H4r product is enriched at specific chromatin regions

Ábrahám, A., Villányi, Z., Zsindely, N., Nagy, G., Szabó, Á., Bodai, L., Henn, L., & Boros, I. (2022) · Scientific Reports · doi:10.1038/s41598-022-09026-x · Cited by 1

COLUMNS

(2015) · Asia-Pacific Biotech News · doi:10.1142/s0219030315000439 · Cited by 1

DMKPs provide a generalizable strategy for studying genes required for reproduction or viability in nontraditional model organisms

Laursen, W. J., Busby, R., Sarkissian, T., Chang, E. C., & Garrity, P. (2023) · Genetics · doi:10.1093/genetics/iyad057 · Cited by 1

Drosophila as Model System to Study Ras-Mediated Oncogenesis: The Case of the Tensin Family of Proteins

Martín-Bermudo, M. D., Millán, A. M.-A., Beatty, J. S., & Valencia-Expósito, A. (2023) · Genes · doi:10.3390/genes14071502 · Cited by 1

Palmitoylation of proteolipid protein M6 promotes tricellular junction assembly in epithelia of Drosophila

Schleutker, R., & Luschnig, S. (2024) · Journal of Cell Science · doi:10.1242/jcs.261916 · Cited by 1

Targeted Mutagenesis

Choi, K. (2024) · KAIST research series · doi:10.1007/978-981-97-0830-7_9 · Cited by 1

Drosophila Robo3 guides longitudinal axons partially independently of its cytodomain

Agcaoili, J., & Evans, T. A. (2024) · PubMed Central · doi:10.17912/micropub.biology.001228 · Cited by 1

CrisprBuildr: an open-source application for CRISPR-mediated genome engineering in Drosophila melanogaster

Horsley, N., Sythoff, A. V. B., Delgado, M., Liu, S. J., & Cabernard, C. (2025) · G3 Genes Genomes Genetics · doi:10.1093/g3journal/jkaf251 · Cited by 1

Principles and Applications of RNA-Based Genome Editing for Crop Improvement

Kumar, M. N., Kumar, V. V. S., Watts, A., & Chinnusamy, V. (2021) · Concepts and strategies in plant sciences · doi:10.1007/978-3-030-64994-4_12 · Cited by 1

Highly efficient CRISPR/Cas9-mediated tissue specific mutagenesis in DrosophilaPreprint

Poe, A. R., Wang, B., Sapar, M. L., Ji, H., Li, K., Onabajo, T., Fazliyeva, R., Gibbs, M., Qiu, Y., Hu, Y., et al. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/268482 · Cited by 1

PI31 is an adaptor protein for proteasome transport in axons and required for synaptic development and functionPreprint

Liu, K., Jones, S., Minis, A., Rodriguez, J., Molina, H., & Steller, H. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/364463 · Cited by 1

A comprehensive genetic characterisation of the mitochondrial Ca2+ uniporter in DrosophilaPreprint

Tufi, R., Gleeson, T., von Stockum, S., Hewitt, V. L., Lee, J., Terriente-Félix, A., Sánchez-Martínez, Á., Ziviani, E., & Whitworth, A. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.17863/cam.38469 · Cited by 1

CAMIO for deletion analysis of endogenous DNA sequences in multicellular organismsPreprint

Chen, H.-M., García‐Marqués, J., Sugino, K., Wei, D., Miyares, R. L., & Lee, T. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/658088 · Cited by 1

Stop codon readthrough of a POU transcription factor regulates steroidogenesis and developmental transitionsPreprint

Zhao, Y., Lindberg, B. G., Esfahani, S. S., Tang, X., Piazza, S., & Engström, Y. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.05.30.125401 · Cited by 1

APC/C-Vihar regulates centrosome activity and stability in the Drosophila germlinePreprint

Braun, A. L., Meghini, F., Villa-Fombuena, G., Guermont, M., Fernández‐Martínez, E., Glover, D. M., Martin-Bermudo, M. D., González‐Reyes, A., & Kimata, Y. (2017) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/202465 · Cited by 1

High levels of Dorsal transcription factor downregulate, not promote, snail expression by regulating enhancer actionPreprint

Irizarry, J., McGehee, J. M., & Stathopoulos, A. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.01.11.426256 · Cited by 1

Co-option of immune effectors by the hormonal signalling system triggering metamorphosis in Drosophila melanogasterPreprint

Nunes, C., Koyama, T., & Sucena, É. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.05.22.444626 · Cited by 1

Oxoglutarate dehydrogenase coordinates myofibril growth by maintaining amino acid homeostasisPreprint

González‐Morales, N., Marescal, O., Szikora, S., Erdélyi, M., Bíró, P., Correia‐Mesquita, T. O., Mihály, J., & Schöck, F. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.12.13.472149 · Cited by 1

Intellectual disability-associated disruption of O-GlcNAcylation impairs neuronal development and cognitive function in DrosophilaPreprint

Fencková, M., Muha, V., Mariappa, D., Catinozzi, M., Czajewski, I., Blok, L. E. R., Ferenbach, A. T., Storkebaum, E., Schenck, A., & van Aalten, D. M. F. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.01.10.475726 · Cited by 1

Insect asynchronous flight requires neural circuit de-synchronization by electrical synapsesPreprint

Hürkey, S., Niemeyer, N., Schleimer, J., Ryglewski, S., Schreiber, S., & Duch, C. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.02.02.478622 · Cited by 1

Molecular and functional characterization of the Drosophila melanogaster conserved smORFomePreprint

Bosch, J. A., Keith, N., Escobedo, F., Fisher, W. W., LaGraff, J. T., Rabasco, J. T., Wan, K. H., Weiszmann, R., Hu, Y., Kondo, S., et al. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.04.24.489283 · Cited by 1

In vivo seamless genetic engineering via CRISPR-triggered single-strand annealingPreprint

Aguilar, G., Bauer, M., Viganò, M., Schnider, S. T., Brügger, L. E., Jiménez‐Jiménez, C., Guerrero, I., & Affolter, M. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.06.17.496589 · Cited by 1

A temperature-tolerant CRISPR base editor mediates highly efficient and precise gene inactivation in vivoPreprint

Doll, R. M., Boutros, M., & Port, F. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.12.13.520203 · Cited by 1

Systematic characterization of Drosophila RhoGEF/GAP localizations uncovers regulators of mechanosensing and junction formation during epithelial cell divisionPreprint

di Pietro, F., Osswald, M., Heras, J. M. D. L., Cristo, I., López-Gay, J. M., Wang, Z., Pelletier, S., Gaugué, I., Leroy, A., Martin, C. A., et al. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.12.29.522184 · Cited by 1

split-intein Gal4 provides intersectional genetic labeling that is fully repressible by Gal80Preprint

Ewen‐Campen, B., Luan, H., Xu, J. Q., Singh, R., Joshi, N., Thakkar, T., Berger, B., White, B. H., & Perrimon, N. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.03.24.534001 · Cited by 1

Loss of Mitochondrial Enoyl CoA Reductase causes elevated ceramide levels and impairs iron metabolismPreprint

Dutta, D., Kanca, O., Byeon, S. K., Marcogliese, P. C., Zuo, Z., Shridharan, R. V., Park, J. H., Undiagnosed Diseases Network, Lin, G., Ge, M. J., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.04.14.536458 · Cited by 1

A force-sensitive mutation reveals a spindle assembly checkpoint-independent role for dynein in anaphase progressionPreprint

Salvador-Garcia, D., Li, J., Hensley, A. M., Gölcük, M., Gallaud, E., Chaaban, S., Port, F., Vagnoni, A., Planelles-Herrero, V. J., McClintock, M. A., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.08.03.551815 · Cited by 1

Chromosome Structure II: Stem-loops and circle-loopsPreprint

Ke, W., Fujioka, M., Schedl, P. D., & Jaynes, J. B. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.01.02.573928 · Cited by 1

Epg5 links proteotoxic stress due to defective autophagic clearance and epileptogenesis in Drosophila and Vici Syndrome patientsPreprint

Deneubourg, C., Dafsari, H. S., Lowe, S. A., Martinez-Cotrina, A., Mazaud, D., Park, S. H., Vergani, V., Maroofian, R., Averdunk, L., Karimiani, E. G., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.04.23.590762 · Cited by 1

sisterless A is required for activation of Sex lethal in the Drosophila germlinePreprint

Goyal, R., Baxter, E. M., & Doren, M. V. (2024) · eLife · doi:10.7554/elife.100491.1 · Cited by 1

A library of lineage-specific driver lines connects developing neuronal circuits to behavior in the Drosophila Ventral Nerve CordPreprint

Soffers, J. H., Beck, E., Sytkowski, D. J., Maughan, M. E., Devasi, D., Zhu, Y. Z., Wilson, B. A., Chen, Y., Erclik, T., Truman, J. W., et al. (2025) · eLife · doi:10.7554/elife.106042.1 · Cited by 1

A library of lineage-specific driver lines connects developing neuronal circuits to behavior in the Drosophila Ventral Nerve CordPreprint

Soffers, J. H., Beck, E., Sytkowski, D. J., Maughan, M. E., Devarakonda, D., Zhu, Y. Z., Wilson, B. A., Chen, Y., Erclik, T., Truman, J. W., et al. (2025) · eLife · doi:10.7554/elife.106042.2 · Cited by 1

The structure of Egalitarian in complex with the K10 mRNA localization signal reveals a modular binding surface required for functionPreprint

Hong, Z., Li, J., Mühle, J., & Bono, F. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.08.03.668247 · Cited by 1

A genome-wide MAGIC kit for recombinase-independent mosaic analysis in DrosophilaPreprint

Shen, Y., Yeung, A. T., Ditchfield, P., Korn, E., CLEMENTS, R. G. H., Chen, X., Wang, B., Sheen, M., Jarman, P. A., & Han, C. (2025) · eLife · doi:10.7554/elife.108453.1 · Cited by 1

A Na + -selective receptor enables state-dependent plasticity in high-salt tastePreprint

Qu, G., Wang, B., & Chen, Y. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.10.07.680871 · Cited by 1

The Fd4 transcription factor translates transient spatial cues in progenitors into long-term lineage identityPreprint

Lai, S.-L., & Doe, C. Q. (2025) · eLife · doi:10.7554/elife.109188.1 · Cited by 1

Chromatin priming and Hunchback recruitment integrate spatial and temporal cues in Drosophila neuroblastsPreprint

Bhattacharya, A., Rao, H., & Sen, S. (2026) · eLife · doi:10.7554/elife.110150.1 · Cited by 1

Reversible Actin modifications by Mical and SelR regulate dynamic actomyosin ring functions during cell wound repairPreprint

Nakamura, M., Hui, J., & Parkhurst, S. M. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.07.05.736623 · Cited by 1

A More Accessible Drosophila Genome to Study Fly CNS Development: A Dissertation

Chen, H.-M. (2015) · eScholarship@UMassChan · doi:10.13028/m2401r

Determination of the phylogenetic range of Sex combs reduced activity in Drosophila melanogaster

Garofalo, L. E. (2015) · Scholarship@Western (Western University)

A Genetic Test of a Model for Two Activities of Fushi Tarazu Protein in Drosophila Melanogaster

Briek, A. (2016) · Scholarship@Western (Western University)

Investigation of Novel Circuits Involved in Virgin Female Receptivity of Drosophila melanogaster

Herrmann, D. (2015) · Portuguese National Funding Agency for Science, Research and Technology (RCAAP Project by FCT)

A Drosophila melanogaster poszt-meiotikus spermatogenezisében szerepet játszó gének vizsgálata

Vedelek, V. (2017) · doi:10.14232/phd.3111

CRISPR-Based Perturbation of Gene Function in Drosophila Cells

Housden, B. E., Ewen‐Campen, B., Mohr, S. E., & Perrimon, N. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-809473-0.00009-9

From chromosomes to genomes: new insights with emerging techniques

Ponrathnam, T., & Mishra, R. K. (2018) · The Nucleus · doi:10.1007/s13237-018-0242-y

Development of versatile genetic tools to study a DYRK family kinase in Caenorhabditis elegans

Wang, Y. (2015)

Creating Tools to Determine Whether Katanin 60 Affects Female Rejection of Males in Drosophila

Isaacson, J. (2018) · Scholarship@Western (Western University) · Cited by 1

Parental Allele-Specific Protein Expression in Single Cells In Vivo

Lo, C.-A., & Chen, B. E. (2018) · doi:10.1101/413849

Understanding Nuage-mitochondrial Coupling in Drosophila piRNA Biogenesis

Ge, T. (2018) · The Journal of the American Medical Association (JAMA) Network (American Medical Association) · doi:10.13028/2v5a-rs66

Behavioural Evaluation of the Anticonvulsant Properties of the Traditional Medicine Anonna Senegalensis on Para bss Drosophila melanogaster MutantsPreprint

Dare, S. S., Merlo, E., Ekanem, P. E., & Berni, J. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/519322

A Rab11-GEF Parcas recruits Rab11 onto recycling endosomes for rhodopsin transport in Drosophila photoreceptorsPreprint

Otsuka, Y., Satoh, T., Nakayama, N., Inaba, R., & Satoh, A. K. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/561563

Localization of Chitin Synthase in Drosophila Melanogaster

Naimi, W. A. (2016) · doi:10.18130/v38397

Enhancing autophagy by redox regulation extends lifespan in DrosophilaPreprint

Lennicke, C., Bjedov, I., Grönke, S., Menger, K. E., James, A. M., Castillo-Quan, J. I., van Leeuwen, L. A. G., Foley, A., Buricova, M., Adcott, J., et al. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/790378

CRISPR Technique for Gene Deletions in Drosophila

Patnaik, A., & Mishra, M. (2019) · Springer protocols handbooks/Springer protocols · doi:10.1007/978-1-4939-9756-5_15

EFFECT EVALUATION IN ENGINEERING PROGRAM

Gayathiri, A., Balasubramanian, A., & Sakthiselvan, P. (2015) · INTERNATIONAL JOURNAL OF INDUSTRIAL ENGINEERING RESEARCH AND DEVELOPMENT · doi:10.34218/ijierd.6.2.2015.003

MAGIC: Mosaic Analysis by gRNA-Induced Crossing-overPreprint

Allen, S. E., Koreman, G. T., Sarkar, A., Wang, B., Wolfner, M. F., & Han, C. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.06.26.174045

CRISPR: A Revolutionary Technique... For Humans?

Barroma, C. (2020) · MacEwan University Student eJournal · doi:10.31542/muse.v4i1.1866

Axon-secreted chemokine-like Orion is a signal for astrocyte infiltration during neuronal remodelingPreprint

Boulanger, A., Thinat, C., Zuchner, S. L., Fradkin, L. G., Lortat‐Jacob, H., & Dura, J. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.11.23.394049

Evaluation of genetic engineering and genome editing tools to develop multifactorial reproductive sterility or killing sperm systems for the improvement of the Sterile Insect Technique

Eckermann, K. N. (2020) · doi:10.53846/goediss-8321

Functional analysis of caspase cleavable proteoforms from the Drosophila GSK-3 gene shaggyPreprint

Korona, D., Nightingale, D. J. H., Fabre, B., Nelson, M. G., Fischer, B., Johnson, G., Hubbard, S. J., Lilley, K. S., & Russell, S. R. H. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.12.22.423955

Altering the Temporal Regulation of One Transcription Factor Drives Sensory Trade-OffsPreprint

Ramaekers, A., Claeys, A., Kapun, M., Jan, J., Wolf, R., Flatt, T., Buchner, E., & Hassan, B. A. (2018) · SSRN Electronic Journal · doi:10.2139/ssrn.3241721

The Phylogenetic Roots of Addiction: Compulsive Drug Seeking, Natural and Drug-Sensitive Reward, and the Acquisition of Learned Habits

Huber, R., & Jacobson, D. (2020) · Brain Behavior and Evolution · doi:10.1159/000517121

A Drosophila P 5B ‐Type ATPase is Required for Polyamine Transport

von Kalm, L., & Brown, D. (2019) · The FASEB Journal · doi:10.1096/fasebj.2019.33.1_supplement.476.31

Gelsolin and dCryAB act downstream of muscle identity genes and contribute to preventing muscle splitting and branching in DrosophilaPreprint

Bertin, B., Renaud, Y., Jagla, T., Lavergne, G., Dondi, C., Ponte, J. P. D., Junion, G., & Jagla, K. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/784546

A SUMO-dependent regulatory switch connects the piRNA pathway to the heterochromatin machinery in DrosophilaPreprint

Andreev, V. I., Yu, C., Wang, J., Schnabl, J., Tirián, L., Gehre, M., Handler, D., Duchek, P., Novatchkova, M., Baumgartner, L., et al. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.07.27.453956

Regulation of sexually dimorphic abdominal courtship behaviors in Drosophila by the Tlx/tailless -like nuclear receptor, DissatisfactionPreprint

Duckhorn, J. C., Cande, J., Metkus, M. C., Song, H., Altamirano, S., Stern, D. L., & Shirangi, T. R. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.08.09.455671

Sex-biased regulation of body size by nutrient-responsive signaling pathways in Drosophila

Millington, J. W. (2021) · cIRcle (University of British Columbia) · doi:10.14288/1.0401369

Transcription Factor Control of Dendrite Targeting via Combinatorial Cell-Surface CodesPreprint

Luo, L., Xie, Q., Li, J., Li, H., Udeshi, N. D., Svinkina, T., Kohani, S., Guajardo, R., Mani, D. R., Xu, C., et al. (2021) · Research Square · doi:10.21203/rs.3.rs-983283/v1

25.基礎代謝に影響を及ぼす因子に関する研究 : 就中季節・結核・癩・脳下垂体前葉移植・冷蔵植皮及び胸部交感神経遮断の影響に就て

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