Glover, David M.

Combined from CaltechAUTHORS

• Sperling, Alexis L. and Fabian, Daniel K., et el. (2024) Protocol for preparing Drosophila genomic DNA to create chromosome-level de novo genome assemblies; STAR Protocols; Vol. 5; No. 2; 102974; PMCID PMC11002874; 10.1016/j.xpro.2024.102974
• Sperling, Alexis L. and Glover, David M. (2023) Protocol for screening facultative parthenogenesis in Drosophila; STAR Protocols; Vol. 4; No. 4; 102585; PMCID PMC10520562; 10.1016/j.xpro.2023.102585
• Sperling, A. L. and Glover, D. M. (2023) Aneuploidy during development in facultative parthenogenetic Drosophila; Heredity; 10.1038/s41437-023-00664-z
• Bao, Min and Cornwall-Scoones, Jake, et el. (2023) Stem cell-derived synthetic embryos self-assemble by exploiting cadherin codes and cortical tension; Nature Cell Biology; Vol. 24; No. 9; 1341-2349; PMCID PMC9481465; 10.1038/s41556-022-00984-y
• Sperling, Alexis L. and Fabian, Daniel K., et el. (2023) A genetic basis for facultative parthenogenesis in Drosophila; Current Biology; 10.1016/j.cub.2023.07.006
• Sperling, A. L. and Glover, D. M. (2023) Parthenogenesis in dipterans: a genetic perspective; Proceedings of the Royal Society of London. Series B, Biological Sciences; Vol. 290; No. 1995; Art. No. 20230261; PMCID PMC10031431; 10.1098/rspb.2023.0261
• Santos, Inês B. and Wainman, Alan, et el. (2023) Mob4 is essential for spermatogenesis in Drosophila melanogaster; 10.1101/2023.02.05.527206
• Amadei, Gianluca and Glover, David M. (2023) Behind the developing brains and beating hearts of stem cell-derived embryo models; Open Biology; Vol. 13; No. 1; Art. No. rsob.220325; PMCID PMC9833437; 10.1098/rsob.220325
• Kovacs, Levente and Fatalska, Agnieszka, et el. (2022) Targeting Drosophila Sas6 to mitochondria reveals its high affinity for Gorab; Biology Open; Vol. 11; No. 11; Art. No. bio059545; PMCID PMC9836085; 10.1242/bio.059545
• Amadei, Gianluca and Handford, Charlotte E., et el. (2022) Embryo model completes gastrulation to neurulation and organogenesis; Nature; Vol. 610; No. 7930; 143-153; PMCID PMC9534772; 10.1038/s41586-022-05246-3
• Bao, Min and Cornwall-Scoones, Jake, et el. (2022) Stem cell-derived synthetic embryos self-assemble by exploiting cadherin codes and cortical tension; Nature Cell Biology; Vol. 24; No. 9; 1341-1349; PMCID PMC9481465; 10.1038/s41556-022-00984-y
• Amadei, Gianluca and Handford, Charlotte E., et el. (2022) Stem cell-derived mouse embryos develop within an extra-embryonic yolk sac to form anterior brain regions and a beating heart; 10.1101/2022.08.01.502375
• Braun, A. L. and Fabian, D. K., et el. (2022) Virgin Birth: A genetic basis for facultative parthenogenesis; 10.1101/2022.03.13.484157
• Lattao, Ramona and Rangone, Hélène, et el. (2021) Mauve/LYST limits fusion of lysosome-related organelles and promotes centrosomal recruitment of microtubule nucleating proteins; Developmental Cell; Vol. 56; No. 7; 1000-1013; PMCID PMC8024676; 10.1016/j.devcel.2021.02.019
• Fatalska, Agnieszka and Stepinac, Emma, et el. (2021) The dimeric Golgi protein Gorab binds to Sas6 as a monomer to mediate centriole duplication; eLife; Vol. 10; Art. No. e57241; PMCID PMC8009671; 10.7554/elife.57241
• Karman, Zoltan and Rethi-Nagy, Zsuzsanna, et el. (2020) Novel perspectives of target-binding by the evolutionarily conserved PP4 phosphatase; Open Biology; Vol. 10; No. 12; Art. No. 200343; PMCID PMC7776573; 10.1098/rsob.200343
• Fatalska, Agnieszka and Dzhindzhev, Nikola S., et el. (2020) Interaction interface in the C-terminal parts of centriole proteins Sas6 and Ana2; Open Biology; Vol. 10; No. 11; Art. No. 200221; PMCID PMC7729032; 10.1098/rsob.200221
• Panda, Pallavi and Kovacs, Levente, et el. (2020) Tissue specific requirement of Drosophila Rcd4 for centriole duplication and ciliogenesis; Journal of Cell Biology; Vol. 219; No. 8; Art. No. e201912154; PMCID PMC7401805; 10.1083/jcb.201912154
• Weatherbee, Bailey A. T. and Glover, David M., et el. (2020) Expression of SARS-CoV-2 receptor ACE2 and the protease TMPRSS2 suggests susceptibility of the human embryo in the first trimester; Open Biology; Vol. 10; No. 8; 200162; PMCID PMC7479935; 10.1098/rsob.200162
• Glover, David M. (2020) Open Biology in a new decade; Open Biology; Vol. 10; No. 2; Art. No. 200025; PMCID PMC7058933; 10.1098/rsob.200025
• Sozen, Berna and Cox, Andy L., et el. (2019) Self-Organization of Mouse Stem Cells into an Extended Potential Blastoid; Developmental Cell; Vol. 51; No. 6; 698-712; PMCID PMC10291877; 10.1016/j.devcel.2019.11.014
• Glover, David M. (2019) 2018: a year in review for Open Biology; Open Biology; Vol. 9; No. 1; Art. No. 190015; PMCID PMC6367131; 10.1098/rsob.190015
• Hupalowska, Anna and Jedrusik, Agnieszka, et el. (2018) CARM1 and Paraspeckles Regulate Pre-implantation Mouse Embryo Development; Cell; Vol. 175; No. 7; 1902-1916.e13; PMCID PMC6292842; 10.1016/j.cell.2018.11.027
• Sozen, Berna and Amadei, Gianluca, et el. (2018) Self-assembly of embryonic and two extra-embryonic stem cell types into gastrulating embryo-like structures; Nature Cell Biology; Vol. 20; No. 8; 979-989; 10.1038/s41556-018-0147-7
• Kovacs, Levente and Chao-Chu, Jennifer, et el. (2018) Gorab is a Golgi protein required for structure and duplication of Drosophila centrioles; Nature Genetics; Vol. 50; No. 7; 1021-1031; PMCID PMC6097609; 10.1038/s41588-018-0149-1
• Grant, Rhys and Abdelbaki, Ahmed, et el. (2018) Constitutive regulation of mitochondrial morphology by Aurora A kinase depends on a predicted cryptic targeting sequence at the N-terminus; Open Biology; Vol. 8; No. 6; Art. No. 170272; PMCID PMC6030116; 10.1098/rsob.170272
• Glover, David M. (2018) New Year's revolution; Open Biology; Vol. 8; No. 1; Art. No. 180005; PMCID PMC5795058; 10.1098/rsob.180005
• Dzhindzhev, Nikola S. and Tzolovsky, George, et el. (2017) Two-step phosphorylation of Ana2 by Plk4 is required for the sequential loading of Ana2 and Sas6 to initiate procentriole formation; Open Biology; Vol. 7; No. 12; Art. No. 170247; PMCID PMC5746551; 10.1098/rsob.170247
• Bury, Leah and Coelho, Paula A., et el. (2017) Plk4 and Aurora A cooperate in the initiation of acentriolar spindle assembly in mammalian oocytes; Journal of Cell Biology; Vol. 216; No. 11; 3571-3590; PMCID PMC5674873; 10.1083/jcb.201606077
• Lattao, Ramona and Kovacs, Levente, et el. (2017) The Centrioles, Centrosomes, Basal Bodies, and Cilia of Drosophila melanogaster; Genetics; Vol. 206; No. 1; 33-53; PMCID PMC5419478; 10.1534/genetics.116.198168
• Pérez de Castro, Ignacio and Carmena, Mar, et el. (2017) Editorial: Aurora Kinases: Classical Mitotic Roles, Non-Canonical Functions and Translational Views; Frontiers in Oncology; Vol. 7; Art. No. 48; PMCID PMC5360697; 10.3389/fonc.2017.00048
• Glover, David M. (2017) A new world for Open Biology; Open Biology; Vol. 7; No. 1; Art. No. 170002; PMCID PMC5303283; 10.1098/rsob.170002
• Sechi, Stefano and Frappaolo, Anna, et el. (2017) Rab1 interacts with GOLPH3 and controls Golgi structure and contractile ring constriction during cytokinesis in Drosophila melanogaster; Open Biology; Vol. 7; No. 1; Art. No. 160257; PMCID PMC5303273; 10.1098/rsob.160257
• Meghini, Francesco and Martins, Torcato, et el. (2016) Targeting of Fzr/Cdh1 for timely activation of the APC/C at the centrosome during mitotic exit; Nature Communications; Vol. 7; Art. No. 12607; PMCID PMC5007356; 10.1038/ncomms12607
• Richter, Magdalena M. and Poznanski, Jaroslaw, et el. (2016) Network of protein interactions within the Drosophila inner kinetochore; Open Biology; Vol. 6; No. 2; Art. No. 150238; PMCID PMC4772809; 10.1098/rsob.150238
• Glover, David M. (2016) Editorial bring in the new!; Open Biology; Vol. 6; No. 1; Art. No. 150264; PMCID PMC4736829; 10.1098/rsob.150264
• Fu, Jingyan and Lipinszki, Zoltan, et el. (2016) Conserved molecular interactions in centriole-to-centrosome conversion; Nature Cell Biology; Vol. 18; No. 1; 87-99; PMCID PMC4719191; 10.1038/ncb3274
• Coelho, Paula A. and Bury, Leah, et el. (2015) Over-expression of Plk4 induces centrosome amplification, loss of primary cilia and associated tissue hyperplasia in the mouse; Open Biology; Vol. 5; No. 12; Art. No. 150209; PMCID PMC4703062; 10.1098/rsob.150209
• Carmena, Mar and Earnshaw, William C., et el. (2015) The Dawn of Aurora Kinase Research: From Fly Genetics to the Clinic; Frontiers in Cell and Developmental Biology; Vol. 3; Art. No. 73; PMCID PMC4646952; 10.3389/fcell.2015.00073
• Haider, Syed and Lipinszki, Zoltan, et el. (2015) DAPPER: a data-mining resource for protein-protein interactions; BioData Mining; Vol. 8; Art. no. 30; PMCID PMC4581157; 10.1186/s13040-015-0063-3
• Chen, Chin-Chi and Bowers, Sarion, et el. (2015) Establishment of Centromeric Chromatin by the CENP-A Assembly Factor CAL1 Requires FACT-Mediated Transcription; Developmental Cell; Vol. 34; No. 1; 73-84; PMCID PMC4495351; 10.1016/j.devcel.2015.05.012
• Edlich-Muth, Christian and Artero, Jean-Baptiste, et el. (2015) The Pentameric Nucleoplasmin Fold Is Present in Drosophila FKBP39 and a Large Number of Chromatin-Related Proteins; Journal of Molecular Biology; Vol. 427; No. 10; 1949-1963; PMCID PMC4414354; 10.1016/j.jmb.2015.03.010
• Glover, David M. (2015) The 350th anniversary of scientific publishing: van Leeuwenhoek, the most prolific author of the Philosophical Transactions of the Royal Society; Open Biology; Vol. 5; No. 4; Art. No. 150044; PMCID PMC4422129; 10.1098/rsob.150044
• Jedrusik, Agnieszka and Cox, Andy, et el. (2015) Maternal-zygotic knockout reveals a critical role of Cdx2 in the morula to blastocyst transition; Developmental Biology; Vol. 398; No. 2; 147-152; PMCID PMC4319684; 10.1016/j.ydbio.2014.12.004
• Fu, Jingyan and Hagan, Iain M., et el. (2015) The Centrosome and Its Duplication Cycle; Cold Spring Harbor Perspectives in Biology; Vol. 7; No. 2; Art. No. a015800; PMCID PMC4315929; 10.1101/cshperspect.a015800
• Lipinszki, Zoltan and Lefevre, Stephane, et el. (2015) Centromeric binding and activity of Protein Phosphatase 4; Nature Communications; Vol. 6; Art. No. 5894; PMCID PMC4354016; 10.1038/ncomms6894
• Dzhindzhev, Nikola S. and Tzolovsky, George, et el. (2014) Plk4 Phosphorylates Ana2 to Trigger Sas6 Recruitment and Procentriole Formation; Current Biology; Vol. 24; No. 21; 2526-2532; PMCID PMC4229625; 10.1016/j.cub.2014.08.061
• Alqarni, Saad S. M. and Murthy, Andal, et el. (2014) Insight into the Architecture of the NuRD Complex: Structure of the RbAp48-MTA1 Subcomplex; Journal of Biological Chemistry; Vol. 289; No. 32; 21844-21855; PMCID PMC4139204; 10.1074/jbc.m114.558940
• Riparbelli, Maria G. and Gottardo, Marco, et el. (2014) Inhibition of Polo kinase by BI2536 affects centriole separation during Drosophila male meiosis; Cell Cycle; Vol. 13; No. 13; 2064-2072; PMCID PMC4111698; 10.4161/cc.29083
• Savoian, Matthew S. and Glover, David M. (2014) Differing requirements for Augmin in male meiotic and mitotic spindle formation in Drosophila; Open Biology; Vol. 4; No. 5; Art. No. 140047; PMCID PMC4042853; 10.1098/rsob.140047
• Coelho, Paula A. and Bury, Leah, et el. (2013) Spindle Formation in the Mouse Embryo Requires Plk4 in the Absence of Centrioles; Developmental Cell; Vol. 27; No. 5; 586-597; PMCID PMC3898710; 10.1016/j.devcel.2013.09.029
• Takeda, Tetsuya and Robinson, Iain M., et el. (2013) Drosophila F-BAR protein Syndapin contributes to coupling the plasma membrane and contractile ring in cytokinesis; Open Biology; Vol. 3; No. 8; Art. No. 130081; PMCID PMC3758542; 10.1098/rsob.130081
• Earnshaw, W. C. and Allshire, R. C., et el. (2013) Esperanto for histones: CENP-A, not CenH3, is the centromeric histone H3 variant; Chromosome Research; Vol. 21; No. 2; 101-106; PMCID PMC3627038; 10.1007/s10577-013-9347-y
• Fu, Jingyan and Glover, David M. (2012) Structured illumination of the interface between centriole and peri-centriolar material; Open Biology; Vol. 2; No. 8; Art. No. 120104; PMCID PMC3438536; 10.1098/rsob.120104
• Capalbo, Luisa and Montembault, Emilie, et el. (2012) The chromosomal passenger complex controls the function of endosomal sorting complex required for transport-III Snf7 proteins during cytokinesis; Open Biology; Vol. 2; No. 5; Art. No. 120070; PMCID PMC3376741; 10.1098/rsob.120070
• Delgehyr, Nathalie and Wieland, Uta, et el. (2012) Drosophila Mgr, a Prefoldin subunit cooperating with von Hippel Lindau to regulate tubulin stability; Proceedings of the National Academy of Sciences of the United States of America; Vol. 109; No. 15; 5729-5734; PMCID PMC3326472; 10.1073/pnas.1108537109
• Delgehyr, Nathalie and Rangone, Hélène, et el. (2012) Klp10A, a Microtubule-Depolymerizing Kinesin-13, Cooperates with CP110 to Control Drosophila Centriole Length; Current Biology; Vol. 22; No. 6; 502-509; 10.1016/j.cub.2012.01.046
• Glover, David M. (2012) The overlooked greatwall: a new perspective on mitotic control; Open Biology; Vol. 2; No. 3; Art. No. 120023; PMCID PMC3382961; 10.1098/rsob.120023
• Venkei, Zsolt and Przewloka, Marcin R., et el. (2012) Spatiotemporal dynamics of Spc105 regulates the assembly of the Drosophila kinetochore; Open Biology; Vol. 2; No. 2; Art. No. 110032; PMCID PMC3352094; 10.1098/rsob.110032
• Carmena, Mar and Pinson, Xavier, et el. (2012) The Chromosomal Passenger Complex Activates Polo Kinase at Centromeres; PLoS Biology; Vol. 10; No. 1; Art. No. e1001250; PMCID PMC3265468; 10.1371/journal.pbio.1001250
• Bassi, Zuni I. and Verbrugghe, Koen J., et el. (2011) Sticky/Citron kinase maintains proper RhoA localization at the cleavage site during cytokinesis; Journal of Cell Biology; Vol. 195; No. 4; 595-603; PMCID PMC3257531; 10.1083/jcb.201105136
• Capalbo, Luisa and D'Avino, Pier Paolo, et el. (2011) Rab5 GTPase controls chromosome alignment through Lamin disassembly and relocation of the NuMA-like protein Mud to the poles during mitosis; Proceedings of the National Academy of Sciences of the United States of America; Vol. 108; No. 42; 17343-17348; PMCID PMC3198372; 10.1073/pnas.1103720108
• Meng, Zheng and Capalbo, Luisa, et el. (2011) Role for casein kinase 1 in the phosphorylation of Claspin on critical residues necessary for the activation of Chk1; Molecular Biology of the Cell; Vol. 22; No. 16; 2834-2847; PMCID PMC3154880; 10.1091/mbc.E11-01-0048
• Rangone, Hélène and Wegel, Eva, et el. (2011) Suppression of Scant Identifies Endos as a Substrate of Greatwall Kinase and a Negative Regulator of Protein Phosphatase 2A in Mitosis; PLOS Genetics; Vol. 7; No. 8; Art. No. e1002225; PMCID PMC3154957; 10.1371/journal.pgen.1002225
• Przewloka, Marcin R. and Venkei, Zsolt, et el. (2011) CENP-C Is a Structural Platform for Kinetochore Assembly; Current Biology; Vol. 21; No. 5; 399-405; 10.1016/j.cub.2011.02.005
• Venkei, Zsolt and Przewloka, Marcin R., et el. (2011) Drosophila Mis12 Complex Acts as a Single Functional Unit Essential for Anaphase Chromosome Movement and a Robust Spindle Assembly Checkpoint; Genetics; Vol. 187; No. 1; 131-140; PMCID PMC3018309; 10.1534/genetics.110.119628
• Montembault, Emilie and Zhang, Wei, et el. (2010) Nessun Dorma, a novel centralspindlin partner, is required for cytokinesis in Drosophila spermatocytes; Journal of Cell Biology; Vol. 191; No. 7; 1351-1365; PMCID PMC3010078; 10.1083/jcb.201007060
• Sharif, Bedra and Na, Jie, et el. (2010) The chromosome passenger complex is required for fidelity of chromosome transmission and cytokinesis in meiosis of mouse oocytes; Journal of Cell Science; Vol. 123; No. 24; 4292-4300; PMCID PMC2995614; 10.1242/jcs.067447
• Higgins, Julie and Midgley, Carol, et el. (2010) Human ASPM participates in spindle organisation, spindle orientation and cytokinesis; BMC Cell Biology; Vol. 11; Art. No. 85; PMCID PMC2988714; 10.1186/1471-2121-11-85
• Wang, Shudong and Griffiths, Gary, et el. (2010) Discovery and Characterization of 2-Anilino-4- (Thiazol-5-yl)Pyrimidine Transcriptional CDK Inhibitors as Anticancer Agents; Chemistry and Biology; Vol. 17; No. 10; 1111-1121; 10.1016/j.chembiol.2010.07.016
• Burrows, Carla and Abd Latip, Normala, et el. (2010) The RNA binding protein Larp1 regulates cell division, apoptosis and cell migration; Nucleic Acids Research; Vol. 38; No. 16; 5542-5553; PMCID PMC2938220; 10.1093/nar/gkq294
• Ahmed, Ahmed Ashour and Lu, Zhen, et el. (2010) SIK2 Is a Centrosome Kinase Required for Bipolar Mitotic Spindle Formation that Provides a Potential Target for Therapy in Ovarian Cancer; Cancer Cell; Vol. 18; No. 2; 109-121; PMCID PMC3954541; 10.1016/j.ccr.2010.06.018
• Romé, Pierre and Montembault, Emilie, et el. (2010) Aurora A contributes to p150ᵍⁱᵘᵉᵈ phosphorylation and function during mitosis; Journal of Cell Biology; Vol. 189; No. 4; 651-659; PMCID PMC2872913; 10.1083/jcb.201001144
• Morris, Samantha A. and Teo, Roy T. Y., et el. (2010) Origin and formation of the first two distinct cell types of the inner cell mass in the mouse embryo; Proceedings of the National Academy of Sciences of the United States of America; Vol. 107; No. 14; 6364-6369; PMCID PMC2852013; 10.1073/pnas.0915063107
• Savoian, Matthew S. and Glover, David M. (2010) Drosophila Klp67A binds prophase kinetochores to subsequently regulate congression and spindle length; Journal of Cell Science; Vol. 123; No. 5; 767-776; 10.1242/jcs.055905
• Wu, Qiang and Bruce, Alexander W., et el. (2009) CARM1 Is Required in Embryonic Stem Cells to Maintain Pluripotency and Resist Differentiation; Stem Cells; Vol. 27; No. 11; 2637-2645; PMCID PMC4135545; 10.1002/stem.131
• Blagden, Sarah P. and Gatt, Melanie K., et el. (2009) Drosophila Larp associates with poly(A)-binding protein and is required for male fertility and syncytial embryo development; Developmental Biology; Vol. 334; No. 1; 186-197; 10.1016/j.ydbio.2009.07.016
• Cunha-Ferreira, Inês and Rodrigues-Martins, Ana, et el. (2009) The SCF/Slimb Ubiquitin Ligase Limits Centrosome Amplification through Degradation of SAK/PLK4; Current Biology; Vol. 19; No. 1; 43-49; 10.1016/j.cub.2008.11.037
• Bettencourt-Dias, Mónica and Glover, David M. (2009) SnapShot: Centriole Biogenesis; Cell; Vol. 136; No. 1; 188.e1-188.e2; 10.1016/j.cell.2008.12.035
• Archambault, Vincent and D'Avino, Pier Paolo, et el. (2008) Sequestration of Polo kinase to microtubules by phosphopriming-independent binding to Map205 is relieved by phosphorylation at a CDK site in mitosis; Genes and Development; Vol. 22; No. 19; 2707-2720; PMCID PMC2559908; 10.1101/gad.486808
• Archambault, Vincent and Chen, Feng, et el. (2008) A Bitter PP1 Fights the Sweet Polo; Molecular Cell; Vol. 30; No. 5; 541-542; 10.1016/j.molcel.2008.05.012
• D'Avino, Pier Paolo and Takeda, Tetsuya, et el. (2008) Interaction between Anillin and RacGAP50C connects the actomyosin contractile ring with spindle microtubules at the cell division site; Journal of Cell Science; Vol. 121; No. 8; 1151-1158; 10.1242/jcs.026716
• Archambault, Vincent and Glover, David M. (2008) Yeast Polo-like kinase substrates are nailed with the right tools; Genome Biology; Vol. 9; Art.No. 203; PMCID PMC2395232; 10.1186/gb-2008-9-1-203
• Archambault, Vincent and Zhao, Xinbei, et el. (2007) Mutations in Drosophila Greatwall/Scant Reveal Its Roles in Mitosis and Meiosis and Interdependence with Polo Kinase; PLOS Genetics; Vol. 3; No. 11; Art. No. e200; PMCID PMC2065886; 10.1371/journal.pgen.0030200
• Rodrigues-Martins, Ana and Bettencourt-Dias, Mónica, et el. (2007) DSAS-6 Organizes a Tube-like Centriole Precursor, and Its Absence Suggests Modularity in Centriole Assembly; Current Biology; Vol. 17; No. 17; 1465-1472; 10.1016/j.cub.2007.07.034
• D'Avino, Pier Paolo and Archambault, Vincent, et el. (2007) Recruitment of Polo Kinase to the Spindle Midzone during Cytokinesis Requires the Feo/Klp3A Complex; PLoS ONE; Vol. 2; No. 6; Art. No. e572; PMCID PMC1894651; 10.1371/journal.pone.0000572
• Przewloka, Marcin R. and Zhang, Wei, et el. (2007) Molecular Analysis of Core Kinetochore Composition and Assembly in Drosophila melanogaster; PLoS ONE; Vol. 2; No. 5; Art. No. e478; PMCID PMC1868777; 10.1371/journal.pone.0000478
• Rodrigues-Martins, A. and Riparbelli, M., et el. (2007) Revisiting the Role of the Mother Centriole in Centriole Biogenesis; Science; Vol. 316; No. 5827; 1046-1050; 10.1126/science.1142950
• Chen, Feng and Archambault, Vincent, et el. (2007) Multiple Protein Phosphatases Are Required for Mitosis in Drosophila; Current Biology; Vol. 17; No. 4; 293-303; 10.1016/j.cub.2007.01.068
• D'Avino, Pier Paolo and Savoian, Matthew S., et el. (2006) RacGAP50C is sufficient to signal cleavage furrow formation during cytokinesis; Journal of Cell Science; Vol. 119; No. 21; 4402-4408; 10.1242/jcs.03210
• Gatt, Melanie K. and Glover, David M. (2006) The Drosophila phosphatidylinositol transfer protein encoded by vibrator is essential to maintain cleavage-furrow ingression in cytokinesis; Journal of Cell Science; Vol. 119; No. 11; 2225-2235; 10.1242/jcs.02933
• Laycock, Joseph E. and Savoian, Matthew S., et el. (2006) Antagonistic activities of Klp10A and Orbit regulate spindle length, bipolarity and function in vivo; Journal of Cell Science; Vol. 119; No. 11; 2354-2361; 10.1242/jcs.02957
• Petretti, Clotilde and Savoian, Matthew, et el. (2006) PITSLRE/CDK11ᵖ⁵⁸ protein kinase promotes centrosome maturation and bipolar spindle formation; EMBO Reports; Vol. 7; No. 4; 418-424; PMCID PMC1456919; 10.1038/sj.embor.7400639
• Soares, Miguel L. and Haraguchi, Seiki, et el. (2005) Functional studies of signaling pathways in peri-implantation development of the mouse embryo by RNAi; BMC Developmental Biology; Vol. 5; Art. No. 28; PMCID PMC1363358; 10.1186/1471-213x-5-28
• Bettencourt-Dias, M. and Rodrigues-Martins, A., et el. (2005) SAK/PLK4 Is Required for Centriole Duplication and Flagella Development; Current Biology; Vol. 15; No. 24; 2199-2207; 10.1016/j.cub.2005.11.042
• Page, Andrew R. and Kovacs, Andras, et el. (2005) Spotted-dick, a zinc-finger protein of Drosophila required for expression of Orc4 and S phase; EMBO Journal; Vol. 24; No. 24; 4304-4315; PMCID PMC1356331; 10.1038/sj.emboj.7600890
• Gatt, Melanie K. and Savoian, Matthew S., et el. (2005) Klp67A destabilises pre-anaphase microtubules but subsequently is required to stabilise the central spindle; Journal of Cell Science; Vol. 118; No. 12; 2671-2682; 10.1242/jcs.02410
• D'Avino, Pier Paolo and Savoian, Matthew S., et el. (2005) Cleavage furrow formation and ingression during animal cytokinesis: a microtubule legacy; Journal of Cell Science; Vol. 118; No. 8; 1549-1558; 10.1242/jcs.02335
• Plusa, Berenika and Hadjantonakis, Anna-Katerina, et el. (2005) The first cleavage of the mouse zygote predicts the blastocyst axis; Nature; Vol. 434; No. 7031; 391-395; 10.1038/nature03388
• Riparbelli, Maria Giovanna and Inoue, Yoshihiro, et el. (2005) parva germina, a gene involved in germ cell maintenance during male and female Drosophila gametogenesis; Developmental Dynamics; Vol. 232; No. 3; 835-844; 10.1002/dvdy.20190
• Plusa, Berenika and Frankenberg, Stephen, et el. (2005) Downregulation of Par3 and aPKC function directs cells towards the ICM in the preimplantation mouse embryo; Journal of Cell Science; Vol. 118; No. 3; 505-515; 10.1242/jcs.01666
• Bettencourt-Dias, M. and Giet, R., et el. (2004) Genome-wide survey of protein kinases required for cell cycle progression; Nature; Vol. 432; No. 7020; 980-987; 10.1038/nature03160
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