Progression of the cell cycle through mitosis leads to abortion of nascent transcripts

A gene complex controlling segmentation in Drosophila

Lewis, E. B. (1978) · Nature · doi:10.1038/276565a0 · Cited by 3,813

A non-radioactive in situ hybridization method for the localization of specific RNAs in Drosophila embryos reveals translational control of the segmentation gene hunchback

Tautz, D., & Pfeifle, C. (1989) · Chromosoma · doi:10.1007/bf00291041 · Cited by 2,518

The embryonic development of Drosophila melanogaster

Campos‐Ortega, J. A., & Hartenstein, V. (1938) · PROTOPLASMA · doi:10.1007/bf01613769 · Cited by 2,156

Cyclin synthesis drives the early embryonic cell cycle

Murray, A. W., & Kirschner, M. W. (1989) · Nature · doi:10.1038/339275a0 · Cited by 1,177

The role of cyclin synthesis and degradation in the control of maturation promoting factor activity

Murray, A. W., Solomon, M. J., & Kirschner, M. W. (1989) · Nature · doi:10.1038/339280a0 · Cited by 1,094

Studies of nuclear and cytoplasmic behaviour during the five mitotic cycles that precede gastrulation in Drosophila embryogenesis

Foe, V. E., & Alberts, B. (1983) · Journal of Cell Science · doi:10.1242/jcs.61.1.31 · Cited by 1,056

Genetic control of cell division patterns in the Drosophila embryo

Edgar, B. A., & O’Farrell, P. H. (1989) · Cell · doi:10.1016/0092-8674(89)90183-9 · Cited by 577

Mitotic domains reveal early commitment of cells in Drosophila embryos

Foe, V. E. (1989) · Trends in Genetics · doi:10.1016/0168-9525(89)90120-0 · Cited by 562

Synthesis of RNA and protein during mitosis in mammalian tissue culture cells

Prescott, D. M., & Bender, M. A. (1962) · Experimental Cell Research · doi:10.1016/0014-4827(62)90176-3 · Cited by 499

The three postblastoderm cell cycles of Drosophila embryogenesis are regulated in G2 by string

Edgar, B. A., & O’Farrell, P. H. (1990) · Cell · doi:10.1016/0092-8674(90)90012-4 · Cited by 437

Remodeling of regulatory nucleoprotein complexes on the Xenopus hsp70 promoter during meiotic maturation of the Xenopus oocyte

Landsberger, N., & Wolffe, A. P. (1997) · The EMBO Journal · doi:10.1093/emboj/16.14.4361 · Cited by 30

Superresolution light microscopy of the Drosophila histone locus body reveals a core–shell organization associated with expression of replication–dependent histone genes

Kemp, J. P., Yang, X., Domiński, Z., Marzluff, W. F., & Duronio, R. J. (2021) · Molecular Biology of the Cell · doi:10.1091/mbc.e20-10-0645 · Cited by 29

Visualizing mRNA by in situ hybridization using 'high resolution' and sensitive tyramide signal amplification

Wilkie, G. S., & Davis, I. (1998) · Technical Tips Online · doi:10.1016/s1366-2120(08)70110-7 · Cited by 29

Regulation of RNA Polymerase II Termination by Phosphorylation of Gdown1

Guo, J., Turek, M. E., & Price, D. H. (2014) · Journal of Biological Chemistry · doi:10.1074/jbc.m113.537662 · Cited by 26

A Multiscale Investigation of Bicoid-Dependent Transcriptional Events in Drosophila Embryos

He, F., Ren, J., Wang, W., & Ma, J. (2011) · PLoS ONE · doi:10.1371/journal.pone.0019122 · Cited by 28

Drosophila JAK/STAT Pathway Reveals Distinct Initiation and Reinforcement Steps in Early Transcription of Sxl

Avila, F. W., & Erickson, J. W. (2007) · Current Biology · doi:10.1016/j.cub.2007.02.038 · Cited by 28

Totipotency or multipotentiality of cultured cells: Applications and progress

Campbell, K., & Wilmut, I. (1997) · Theriogenology · doi:10.1016/s0093-691x(96)00340-8 · Cited by 28

The relationship between growth and pattern formation

Bryant, S. V., & Gardiner, D. M. (2016) · Regeneration · doi:10.1002/reg2.55 · Cited by 27

The DNA-to-cytoplasm ratio broadly activates zygotic gene expression in Xenopus

Jukam, D., Kapoor, R. R., Straight, A. F., & Skotheim, J. M. (2021) · Current Biology · doi:10.1016/j.cub.2021.07.035 · Cited by 26

Complex gene organization of synaptic protein SNAP-25 in Drosophila melanogaster

Risinger, C., Deitcher, D. L., Lundell, I., Schwarz, T. L., & Larhammar, D. (1997) · Gene · doi:10.1016/s0378-1119(97)00106-6 · Cited by 27

The Spatiotemporal Control of Zygotic Genome Activation

Gentsch, G. E., Owens, N. D. L., & Smith, J. C. (2019) · iScience · doi:10.1016/j.isci.2019.06.013 · Cited by 28

From mother to embryo: A molecular perspective on zygotic genome activation

Wu, E., & Vastenhouw, N. L. (2020) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/bs.ctdb.2020.02.002 · Cited by 28

Initiation of DNA replication in xenopus egg extracts

Arias, E. E. (2004) · Frontiers in bioscience · doi:10.2741/1457 · Cited by 25

Relationship between expression of serendipity α and cellularisation of the Drosophila embryo as revealed by interspecific transformation

Koraichi, S. I., Schweisguth, F., de Billy, G., & Vincent, A. (1993) · Development · doi:10.1242/dev.119.2.471 · Cited by 25

Nascent transcriptome reveals orchestration of zygotic genome activation in early embryogenesis

Chen, H., & Good, M. C. (2022) · Current Biology · doi:10.1016/j.cub.2022.07.078 · Cited by 28

TriTag: an integrative tool to correlate chromatin dynamics and gene expression in living cells

Xu, H., Wang, J., Liang, Y., Fu, Y., Li, S., Huang, J., Xu, H., Zou, W., & Chen, B. (2020) · Nucleic Acids Research · doi:10.1093/nar/gkaa1170 · Cited by 23

Hyper-active RAS/MAPK introduces cancer-specific mitotic vulnerabilities

Herman, J., Romain, R. R., Hoellerbauer, P., Shirnekhi, H. K., King, D. C., DeLuca, K. F., Nishimura, E. O., Paddison, P. J., & DeLuca, J. G. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2208255119 · Cited by 21

Dampened regulates the activating potency of Bicoid and the embryonic patterning outcome in Drosophila

Liu, J., & Ma, J. (2013) · Nature Communications · doi:10.1038/ncomms3968 · Cited by 24

Transcriptional Regulation During Zygotic Genome Activation in Zebrafish and Other Anamniote Embryos

Wragg, J. W., & Müller, F. (2016) · Advances in genetics · doi:10.1016/bs.adgen.2016.05.001 · Cited by 25

Cell Cycle Remodeling and Zygotic Gene Activation at the Midblastula Transition

Zhang, M., Skirkanich, J., Lampson, M. A., & Klein, P. S. (2016) · Advances in experimental medicine and biology · doi:10.1007/978-3-319-46095-6_9 · Cited by 23

Analysis of CpG islands of trophoblast giant cells by restriction landmark genomic scanning

Ohgane, J., Aikawa, J.-I., Ogura, A., Hattori, N., Ogawa, T., & Shiota, K. (1998) · Developmental Genetics · doi:10.1002/(sici)1520-6408(1998)22:2 · Cited by 67

Modulation of transcription burst amplitude underpins dosage compensation in the Drosophila embryo

Beadle, L. F., Zhou, H., Rattray, M., & Ashe, H. L. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.112382 · Cited by 21

Setting the stage for development: the maternal-to-zygotic transition in Drosophila

Harrison, M. M., Marsh, A. J., & Rushlow, C. A. (2023) · Genetics · doi:10.1093/genetics/iyad142 · Cited by 25

P-TEFb, the Super Elongation Complex and Mediator Regulate a Subset of Non-paused Genes during Early Drosophila Embryo Development

Dahlberg, O., Shilkova, O., Tang, M., Holmqvist, P.-H., & Mannervik, M. (2015) · PLoS Genetics · doi:10.1371/journal.pgen.1004971 · Cited by 23

Flying the RNA Nest: Drosophila Reveals Novel Insights into the Transcriptome Dynamics of Early Development

Lefebvre, F. A., & Lécuyer, É. (2018) · Journal of Developmental Biology · doi:10.3390/jdb6010005 · Cited by 22

Activation‐induced cytidine deaminase can target multiple topologies of double‐stranded DNA in a transcription‐independent manner

Branton, S., Ghorbani, A., Bolt, B. N., Fifield, H., Berghuis, L., & Larijani, M. (2020) · The FASEB Journal · doi:10.1096/fj.201903036rr · Cited by 22

Changes in gene expression in response to polyamine depletion indicates selective stabilization of mRNAs

Veress, I., HAGHIGHI, S., Pulkka, A. E., & Pajunen, A. (2000) · Biochemical Journal · doi:10.1042/0264-6021:3460185 · Cited by 22

Asymmetric localization of Drosophila pair‐rule transcripts from displaced nuclei: evidence for directional nuclear export.

Francis-Lang, H., Davis, I., & Ish‐Horowicz, D. (1996) · The EMBO Journal · doi:10.1002/j.1460-2075.1996.tb00396.x · Cited by 22

Minimal synthetic enhancers reveal control of the probability of transcriptional engagement and its timing by a morphogen gradient

Álamos, S., Reimer, A. E., Westrum, C., Turner, M. A., Talledo, P., Zhao, J., Luu, E., & García, H. G. (2023) · Cell Systems · doi:10.1016/j.cels.2022.12.008 · Cited by 26

Mitotic progression, arrest, exit or death relies on centromere structural integrity, rather than de novo transcription

Novais-Cruz, M., Abad, M. A., van IJcken, W. F. J., Galjart, N., Jeyaprakash, A. A., Maiato, H., & Ferrás, C. (2018) · eLife · doi:10.7554/elife.36898 · Cited by 20

3′– UTR ‐dependent regulation of m RNA turnover is critical for differential distribution patterns of cyclic gene m RNA s

Nitanda, Y., Matsui, T., Matta, T., Higami, A., Kohno, K., Nakahata, Y., & Bessho, Y. (2013) · FEBS Journal · doi:10.1111/febs.12582 · Cited by 20

Principles of genome activation in the early embryo

Zhou, C. Y., & Heald, R. (2023) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2023.102062 · Cited by 22

Uncovering a Dynamic Feature of the Transcriptional Regulatory Network for Anterior-Posterior Patterning in the Drosophila Embryo

Liu, J., & Ma, J. (2013) · PLoS ONE · doi:10.1371/journal.pone.0062641 · Cited by 19

Two otu transcripts are selectively localised in Drosophila oogenesis by a mechanism that requires a function of the otu protein

Tirronen, M., Lahti, V.-P., Heino, T. I., & Roos, C. (1995) · Mechanisms of Development · doi:10.1016/0925-4773(95)00390-m · Cited by 19

Pinning Down Transcription: Regulation of RNA Polymerase II Activity During the Cell Cycle

Xu, Y., & Manley, J. L. (2004) · Cell Cycle · doi:10.4161/cc.3.4.769 · Cited by 19

Metaphase fragility of the human RNU1 and RNU2 loci is induced by actinomycin D through a p53-dependent pathway

Yu, A. (1998) · Human Molecular Genetics · doi:10.1093/hmg/7.4.609 · Cited by 19

Cell-specific expression of preproenkephalin intronic heteronuclear RNA in the rat forebrain

Brooks, P. J., Funabashi, T., Kleopoulos, S. P., Mobbs, C. V., & Pfaff, D. W. (1993) · Molecular Brain Research · doi:10.1016/0169-328x(93)90144-e · Cited by 19

Identification and characterization of a gene activated by the deformed homeoprotein

Mahaffey, J. W., Jones, D. F., Hickel, J. A., & Griswold, C. M. (1993) · Development · doi:10.1242/dev.118.1.203 · Cited by 19

The nonlinear dynamics and fluctuations of mRNA levels in cell cycle coupled transcription

Sun, Q., Jiao, F., Lin, G., Yu, J., & Tang, M. (2019) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1007017 · Cited by 17

Control of DNA replication: A new facet of Hox proteins?

Miotto, B., & Graba, Y. (2010) · BioEssays · doi:10.1002/bies.201000048 · Cited by 18

Transcription and splicing dynamics during early Drosophila development

Prudêncio, P., Savisaar, R., Rebelo, K., Martinho, R. G., & Carmo‐Fonseca, M. (2021) · RNA · doi:10.1261/rna.078933.121 · Cited by 19

Adenovirus Type 12-Induced Fragility of the Human RNU2 Locus Requires p53 Function

Li, Z., Yu, A., & Weiner, A. M. (1998) · Journal of Virology · doi:10.1128/jvi.72.5.4183-4191.1998 · Cited by 18

Maternal Groucho and bHLH repressors amplify the dose-sensitive X chromosome signal in Drosophila sex determination

Lu, H., Kozhina, E., Mahadevaraju, S., Yang, D., Avila, F. W., & Erickson, J. W. (2008) · Developmental Biology · doi:10.1016/j.ydbio.2008.08.012 · Cited by 19

Geminin Is Required for Zygotic Gene Expression at the Xenopus Mid-Blastula Transition

Kerns, S. L., Schultz, K. M., Barry, K. A., Thorne, T., & McGarry, T. J. (2012) · PLoS ONE · doi:10.1371/journal.pone.0038009 · Cited by 16

Genetic control of morphogenesis - Hox induced organogenesis of the posterior spiracles

Hombría, J. C., Rivas, M. L., & Sotillos, S. (2009) · The International Journal of Developmental Biology · doi:10.1387/ijdb.072421jc · Cited by 17

A Developmental Program Truncates Long Transcripts to Temporally Regulate Cell Signaling

Sandler, J. E., Irizarry, J., Stepanik, V. A., Dunipace, L., Amrhein, H., & Stathopoulos, A. (2018) · Developmental Cell · doi:10.1016/j.devcel.2018.11.019 · Cited by 17

Lighting up the central dogma for predictive developmental biology

García, H. G., Berrocal, A., Kim, Y. J., Martini, G. D., & Zhao, J. (2019) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/bs.ctdb.2019.10.010 · Cited by 19

The regulation and potential functions of intronic satellite DNA

Fingerhut, J. M., & Yamashita, Y. M. (2022) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2022.04.010 · Cited by 17

G2 arrest of cell cycle ensures a determination process of sensory mother cell formation in Drosophila

Kimura, K., Usui-Ishihara, A., & Usui, K. (1997) · Development Genes and Evolution · doi:10.1007/s004270050108 · Cited by 17

Oligonucleotide probes detect splicing variants insituinDrosophilaembryos

Artero, R. D., Akam, M. E., & Pérez‐Alonso, M. (1992) · Nucleic Acids Research · doi:10.1093/nar/20.21.5687 · Cited by 17

Stage, tissue, and cell specific distribution of alternative Ultrabithorax mRNAs and protein isoforms in the Drosophila embryo

L�pez, A. J., Artero, R. D., & P�rez-Alonso, M. (1996) · Development Genes and Evolution · doi:10.1007/bf00377226 · Cited by 17

Hes7 3′UTR is required for somite segmentation function

Fujimuro, T., Matsui, T., Nitanda, Y., Matta, T., Sakumura, Y., Saito, M., Kohno, K., Nakahata, Y., & Bessho, Y. (2014) · Scientific Reports · doi:10.1038/srep06462 · Cited by 17

The Drosophila RCC1 homolog, Bj1 , regulates nucleocytoplasmic transport and neural differentiation during Drosophila development

Shi, W., & Skeath, J. B. (2004) · Developmental Biology · doi:10.1016/j.ydbio.2004.02.011 · Cited by 16

Mitotic delay dependent survival identifies components of cell cycle control in the Drosophila blastoderm

Ruden, D. M., & Jäckle, H. (1995) · Development · doi:10.1242/dev.121.1.63 · Cited by 16

TriTag: an integrative tool to correlate chromatin dynamics and gene expression in living cells

Xu, H., Wang, J., Liang, Y., Fu, Y., Li, S., Huang, J., Xu, H., Zou, W., & Chen, B. (2020) · Nucleic Acids Research · doi:10.1093/nar/gkaa906 · Cited by 15

SVD Identifies Transcript Length Distribution Functions from DNA Microarray Data and Reveals Evolutionary Forces Globally Affecting GBM Metabolism

Bertagnolli, N. M., Drake, J. A., Tennessen, J. M., & Alter, O. (2013) · PLoS ONE · doi:10.1371/journal.pone.0078913 · Cited by 15

Stepwise Progression of Embryonic Patterning

Sandler, J. E., & Stathopoulos, A. (2016) · Trends in Genetics · doi:10.1016/j.tig.2016.04.004 · Cited by 14

Spatiotemporal relationships between a novel Drosophila stripe expressing gene and known segmentation genes by simultaneous visualization of transcript patterns

Hartmann, C., & J�ckle, H. (1995) · Chromosoma · doi:10.1007/bf00347690 · Cited by 13

Brd4 and P300 regulate zygotic genome activation through histone acetylationPreprint

Chan, S.-H., Tang, Y., Miao, L.-Y., Darwich-Codore, H., Vejnar, C., Beaudoin, J.-D., Musaev, D., Fernández, J. P., Moreno-Mateos, M., & Giráldez, A. (2018) · bioRxiv · doi:10.1101/369231 · Cited by 12

Three Drosophila Hox Complex microRNAs Do Not Have Major Effects on Expression of Evolutionarily Conserved Hox Gene Targets during Embryogenesis

Lemons, D., Paré, A. C., & McGinnis, W. J. (2012) · PLoS ONE · doi:10.1371/journal.pone.0031365 · Cited by 14

Detection of RNA-DNA association by a proximity ligation-based method

Petruk, S., Fenstermaker, T. K., Black, K. L., Brock, H. W., & Mazo, A. (2016) · Scientific Reports · doi:10.1038/srep27313 · Cited by 14

Localized expression of a novel micropia-like element in the blastoderm of Drosophila melanogaster is dependent on the anterior morphogen bicoid

Frommer, G., Schuh, R., & Jäckle, H. (1994) · Chromosoma · doi:10.1007/bf00352316 · Cited by 14

stringcdc25 and cyclin E are required for patterned histone expression at different stages of Drosophila embryonic development

Lanzotti, D. J., Kupsco, J., Marzluff, W. F., & Duronio, R. J. (2004) · Developmental Biology · doi:10.1016/j.ydbio.2004.06.019 · Cited by 13

Do imprinted genes have few and small introns?

Haig, D. (1996) · BioEssays · doi:10.1002/bies.950180504 · Cited by 13

Drosophila as a Model System for Studying of the Evolution and Functional Specialization of the Y Chromosome

Kotov, A. A., Bazylev, S. S., Adashev, V. E., Shatskikh, A. S., & Olenina, L. V. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23084184 · Cited by 13

Stochastic Modeling of Expression Kinetics Identifies Messenger Half-Lives and Reveals Sequential Waves of Co-ordinated Transcription and Decay

Cacace, F., Paci, P., Cusimano, V., Germani, A., & Farina, L. (2012) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1002772 · Cited by 13

Stochastic model for gene transcription onDrosophila melanogasterembryos

Prata, G. N., Hornos, J. E. M., & Ramos, A. F. (2016) · Physical review. E · doi:10.1103/physreve.93.022403 · Cited by 12

Chemical Embryology Redux: Metabolic Control of Development

Song, Y., & Shvartsman, S. Y. (2020) · Trends in Genetics · doi:10.1016/j.tig.2020.05.007 · Cited by 12

Autocrine insulin pathway signaling regulates actin dynamics in cell wound repair

Nakamura, M., Verboon, J. M., Allen, T. E., Blanco, M. A., Liu, R., Dominguez, A. N. M., Delrow, J. J., & Parkhurst, S. M. (2020) · PLoS Genetics · doi:10.1371/journal.pgen.1009186 · Cited by 12

Control of tissue development and cell diversity by cell cycle-dependent transcriptional filtering

Chakra, M. A., Isserlin, R., Tran, T. N., & Bader, G. D. (2021) · eLife · doi:10.7554/elife.64951 · Cited by 11

Ultrastructural localization of transcription sites, DNA, and RNA reveals a concentric arrangement of structural and functional domains in plant nucleolonema

Yano, H., & Sato, S. (2000) · PROTOPLASMA · doi:10.1007/bf01279058 · Cited by 12

Intron dynamics reveal principles of gene regulation during the maternal-to-zygotic transition

Riemondy, K. A., Henriksen, J. C., & Rissland, O. S. (2023) · RNA · doi:10.1261/rna.079168.122 · Cited by 12

Mesoscale, long-time mixing of chromosomes and its connection to polymer dynamics

Bajpai, G., & Safran, S. A. (2023) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1011142 · Cited by 11

Nuclear export restricts Gdown1 to a mitotic function

Ball, C. B., Parida, M., Santana, J. F., Spector, B. M., Suarez, G. A., & Price, D. H. (2022) · Nucleic Acids Research · doi:10.1093/nar/gkac015 · Cited by 10

Pollination: Sexual Mimicry Abounds

Schiestl, F. P. (2010) · Current Biology · doi:10.1016/j.cub.2010.10.019 · Cited by 11

Transcription elongation in the human c-myc gene is governed by overall transcription initiation levels in Xenopus oocytes.

Spencer, C. A., & Kilvert, M. A. (1993) · Molecular and Cellular Biology · doi:10.1128/mcb.13.2.1296 · Cited by 11

Co-transcriptional splicing facilitates transcription of gigantic genes

Fingerhut, J. M., Lannes, R., Whitfield, T. W., Thiru, P., & Yamashita, Y. M. (2024) · PLoS Genetics · doi:10.1371/journal.pgen.1011241 · Cited by 10

Evolutionarily conserved positive and negative cis-acting elements control the blastoderm-specific expression of the Drosophila serendipity α cellularisation gene

Koraichi, S. I., Schweisguth, F., Jullien, D., Kücherer, C., Lepesant, J., & Vincent, A. (1995) · Mechanisms of Development · doi:10.1016/0925-4773(94)00304-6 · Cited by 10

A Drosophila melanogaster chromosome 2L repeat is expressed in the male germ line

Russell, S. R. H., & Kaiser, K. (1994) · Chromosoma · doi:10.1007/bf00364727 · Cited by 10

A Spatial Point Pattern Analysis in Drosophila Blastoderm Embryos Evaluating the Potential Inheritance of Transcriptional States

He, F., & Ma, J. (2013) · PLoS ONE · doi:10.1371/journal.pone.0060876 · Cited by 9

Modulation of temporal dynamics of gene transcription by activator potency in theDrosophilaembryo

Liu, J., & Ma, J. (2015) · Development · doi:10.1242/dev.126946 · Cited by 11

Biochemical Fractionation of Time-Resolved Drosophila Embryos Reveals Similar Transcriptomic Alterations in Replication Checkpoint and Histone mRNA Processing Mutants

Lefebvre, F. A., Bouvrette, L. P. B., Bergalet, J., & Lécuyer, É. (2017) · Journal of Molecular Biology · doi:10.1016/j.jmb.2017.01.022 · Cited by 8

The maternal‐zygotic transition and zygotic activation of the Mnemiopsis leidyi genome occurs within the first three cleavage cycles

Davidson, P. L., Koch, B. J., Schnitzler, C. E., Henry, J. J., Martindale, M. Q., Baxevanis, A. D., & Browne, W. E. (2017) · Molecular Reproduction and Development · doi:10.1002/mrd.22926 · Cited by 9

Chapter 3 Genotype–Phenotype Mapping

Atallah, J., & Larsen, E. (2009) · International review of cytology · doi:10.1016/s1937-6448(09)78003-7 · Cited by 8

Release of Histone H3K4-reading transcription factors from chromosomes in mitosis is independent of adjacent H3 phosphorylation

Harris, R. J., Heer, M., Levasseur, M. D., Cartwright, T. N., Weston, B., Mitchell, J. L., Coxhead, J., Gaughan, L., Prendergast, L., Rico, D., et al. (2023) · Nature Communications · doi:10.1038/s41467-023-43115-3 · Cited by 9

Imaging developmental cell cycles

Kohrman, A. Q., Kim, R., & Pósfai, E. (2021) · Biophysical Journal · doi:10.1016/j.bpj.2021.04.035 · Cited by 10

Contribution of transcription to animal early development

Wang, J., & Davis, R. E. (2014) · Transcription · doi:10.4161/21541264.2014.967602 · Cited by 8

Cell growth and differentiation from the perspective of dynamical organization of cellular and subcellular processes

Aon, M. A., & Cortassa, S. C. (1995) · Progress in Biophysics and Molecular Biology · doi:10.1016/0079-6107(95)00010-0 · Cited by 7

Spatial localization of pre-mRNA transcription and processing within the nucleus

Carter, K. C. (1994) · Current Opinion in Biotechnology · doi:10.1016/0958-1669(94)90078-7 · Cited by 8

Incorporation of CENP-A/CID into centromeres during early Drosophila embryogenesis does not require RNA polymerase II–mediated transcription

Ghosh, S., & Lehner, C. F. (2022) · Chromosoma · doi:10.1007/s00412-022-00767-2 · Cited by 7

How gene expression in fast‐proliferating cells keeps pace

Martinho, R. G., Guilgur, L. G., & Prudêncio, P. (2015) · BioEssays · doi:10.1002/bies.201400195 · Cited by 8

Pure early zygotic genes in the Asian malaria mosquito Anopheles stephensi

Wu, Y., Hu, W., Biedler, J. K., Chen, X., & Tu, Z. J. (2018) · Parasites & Vectors · doi:10.1186/s13071-018-3220-y · Cited by 7

Patterning in Limbs: The Resolution of Positional Confrontations

Bryant, S. V., Hayamizu, T. F., & Gardiner, D. M. (1993) · Springer eBooks · doi:10.1007/978-1-4615-2433-5_6 · Cited by 7

Developmental control of cell division in leech embryos

Bissen, S. T. (1997) · BioEssays · doi:10.1002/bies.950190305 · Cited by 7

Polytene chromosomes show normal gene activity but some mRNAs are abnormally accumulated in the pseudonurse cell nuclei of Drosophila melanogaster otu mutants

Heino, T. I., Lahti, V.-P., Tirronen, M., & Roos, C. (1995) · Chromosoma · doi:10.1007/bf00352225 · Cited by 7

DNA replication times the cell cycle and contributes to the mid-blastula transition in Drosophila embryos

(2009) · SciVee · doi:10.4016/13415.01 · Cited by 7

Landscape and regulation of mRNA translation in the early C. elegans embryo

Shukla, Y., Ghatpande, V., Hu, C., Dickinson, D. J., & Cenik, C. (2025) · Cell Reports · doi:10.1016/j.celrep.2025.115778 · Cited by 6

A dual‐function SNF2 protein drives chromatid resolution and nascent transcript removal in mitosis

Carmo, C., Coelho, J., Silva, R. D., Tavares, A., Boavida, A., Gaetani, P., Guilgur, L. G., Martinho, R. G., & Oliveira, R. A. (2023) · EMBO Reports · doi:10.15252/embr.202256463 · Cited by 6

DNA topology and genome organization in higher eukaryotes: A model

Gaillard, C., & Strauss, F. (2006) · Journal of Theoretical Biology · doi:10.1016/j.jtbi.2006.07.001 · Cited by 6

Global Mitotic Transcription and Reactivation during Mitotic Exit: A Potential Epigenetic Mechanism

Palozola, K. C. (2017) · ScholarlyCommons (University of Pennsylvania)

Distinct regulation across the transcription cycle drives mitotic transcriptional silencingPreprint

Gaetani, P., Tavares, A., Paixão, T., & Oliveira, R. A. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.10.12.758451

Coupling of zygotic transcription to mitotic control at theDrosophilamid-blastula transition

Lu, X., Li, J., Elemento, O., Tavazoie, S., & Wieschaus, E. F. (2009) · Development · doi:10.1242/dev.034421 · Cited by 122

A Developmental Program Truncates Long Transcripts to Temporally Regulate Cell Signaling

Sandler, J. E., Irizarry, J., Stepanik, V. A., Dunipace, L., Amrhein, H., & Stathopoulos, A. (2018) · Developmental Cell · doi:10.1016/j.devcel.2018.11.019 · Cited by 17

Mitotic Transcription and Waves of Gene Reactivation During Mitotic Exit

Palozola, K. C., Donahue, G., Liu, H., Grant, G., Becker, J., Coté, A., Yu, H.-T., Raj, A., & Zaret, K. (2017) · Science · doi:10.1126/science.aal4671 · Cited by 245