The DOI matches its Crossref record; 53 of the 53 references it cites were found in a registry or an index.
A gradient of cytoplasmic Cactus degradation establishes the nuclear localization gradient of the dorsal morphogen in Drosophila
Open accessAbstract
Dorsoventral axis formation in the Drosophila embryo is established by a signal transduction pathway that comprises the products of at least 12 maternal genes. Two of these genes, dorsal and cactus, show homology to the mammalian transcription factor NF-kappa B and its inhibitor I kappa B, respectively. As in the case for I kappa B and NF-kappa B, Cactus inhibits Dorsal by retaining it in the cytoplasm. In response to the signal produced and transmitted by the products of the other genes, Dorsal translocates to the nucleus preferentially on the ventral side of the embryo. Here, we show that Cactus forms a cytoplasmic concentration gradient inversely correlated to the nuclear translocation gradient of Dorsal. Deletions of the N-terminus and C-terminus of Cactus reveal that two modes of degradation control cactus activity: signal-induced degradation and signal-independent degradation, respectively. Genetic evidence indicates that degradation of Cactus is required, but not sufficient to translocates Dorsal completely into the nucleus.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“Toll signaling likely potentiates Dorsal nuclear translocation in a Cactus-independent manner, as even in cactus mutants, Dorsal is not fully nuclear on the dorsal side of the embryo”
From Graded dorsal and differential gene regulation in the Drosophila embryo. (2009) · cites this paper as Bergmann et al. 1996
Citations
Cites
Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4
LAEMMLI, U. K. (1970) · Nature · doi:10.1038/227680a0 · Cited by 249,961
Amino Acid Sequences Common to Rapidly Degraded Proteins: The PEST Hypothesis
Rogers, S. W., Wells, R., & Rechsteiner, M. (1986) · Science · doi:10.1126/science.2876518 · Cited by 2,541
The embryonic development of Drosophila melanogaster
Campos‐Ortega, J. A., & Hartenstein, V. (1938) · PROTOPLASMA · doi:10.1007/bf01613769 · Cited by 2,156
IκB: a Specific Inhibitor of the NF-κB Transcription Factor
Baeuerle, P. A., & Baltimore, D. (1988) · Science · doi:10.1126/science.3140380 · Cited by 2,154
Palombella, V. J., Rando, O. J., Goldberg, A. L., & Maniatis, T. (1994) · Cell · doi:10.1016/s0092-8674(94)90482-0 · Cited by 2,089
Rel/NF-kappa B/I kappa B family: intimate tales of association and dissociation.Preprint
Verma, I. M., Stevenson, J. K., Schwarz, E. M., Antwerp, D. V., & Miyamoto, S. (1995) · Genes & Development · doi:10.1101/gad.9.22.2723 · Cited by 1,696
Control of IκB-α Proteolysis by Site-Specific, Signal-Induced Phosphorylation
Brown, K., Gerstberger, S., Carlson, L., Franzoso, G., & Siebenlist, U. (1995) · Science · doi:10.1126/science.7878466 · Cited by 1,434
Chen, Z., Hagler, J., Palombella, V. J., Melandri, F. D., Scherer, D. C., Ballard, D. W., & Maniatis, T. (1995) · Genes & Development · doi:10.1101/gad.9.13.1586 · Cited by 1,270
NF-κB Controls Expression of Inhibitor IκBα: Evidence for an Inducible Autoregulatory Pathway
Sun, S., Ganchi, P. A., Ballard, D. W., & Greene, W. C. (1993) · Science · doi:10.1126/science.8096091 · Cited by 1,108
Rapid proteolysis of IκB-α is necessary for activation of transcription factor NF-κB
Henkel, T., Machleidt, T., Alkalay, I., Krönke, M., Ben‐Neriah, Y., & Baeuerle, P. A. (1993) · Nature · doi:10.1038/365182a0 · Cited by 1,085
Cited by
Sorted by citations
NF-κB signaling pathways in mammalian and insect innate immunityPreprint
Silverman, N. S., & Maniatis, T. (2001) · Genes & Development · doi:10.1101/gad.909001 · Cited by 904
Toll receptors in innate immunity.
Imler, J., & Hoffmann, J. (2001) · Trends in Cell Biology · doi:10.1016/s0962-8924(01)02004-9 · Cited by 474
Function of reactive oxygen species during animal development: Passive or active?
Covarrubias, L., Hernández-García, D., Schnabel, D., Vidal, E. S., & Castro‐Obregón, S. (2008) · Developmental Biology · doi:10.1016/j.ydbio.2008.04.041 · Cited by 418
Regulated nuclear import of Rel proteins in the Drosophila immune response
Wu, L. P., & Anderson, K. (1998) · Nature · doi:10.1038/32195 · Cited by 324
A role for the Drosophila Toll/Cactus pathway in larval hematopoiesis
Qiu, P., Pan, P. C., & Govind, S. (1998) · Development · doi:10.1242/dev.125.10.1909 · Cited by 277
NF- B in the Immune Response of DrosophilaPreprint
Hétru, C., & Hoffmann, J. A. (2009) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a000232 · Cited by 252
Dorsoventral Axis Formation in the Drosophila Embryo—Shaping and Transducing a Morphogen Gradient
Moussian, B., & Roth, S. (2005) · Current Biology · doi:10.1016/j.cub.2005.10.026 · Cited by 245
Manfruelli, P., Reichhart, J., Steward, R., Hoffmann, J. A., & Lemaître, B. (1999) · EMBO Journal · doi:10.1093/emboj/18.12.3380 · Cited by 228
Pal, S., Leger, R. J. S., & Wu, L. P. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m605927200 · Cited by 224
NF-κB/Rel Proteins and the Humoral Immune Responses of Drosophila melanogaster
Ganesan, S., Aggarwal, K., Paquette, N., & Silverman, N. S. (2010) · Current topics in microbiology and immunology · doi:10.1007/82_2010_107 · Cited by 204
Positive and negative regulation of the Drosophila immune response
Aggarwal, K., & Silverman, N. S. (2008) · BMB Reports · doi:10.5483/bmbrep.2008.41.4.267 · Cited by 197
Mosquito immune defenses against Plasmodium infection
Cirimotich, C. M., Dong, Y., Garver, L. S., Sim, S., & Dimopoulos, G. (2009) · Developmental & Comparative Immunology · doi:10.1016/j.dci.2009.12.005 · Cited by 197
Thoetkiattikul, H., Beck, M. H., & Strand, M. R. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0505240102 · Cited by 151
Oligomerisation of Tube and Pelle leads to nuclear localisation of dorsal.
Grosshans, J., Schnorrer, F., & Nüsslein-Volhard, C. (1999) · Mechanisms of Development · doi:10.1016/s0925-4773(98)00236-6 · Cited by 139
Self-citationGraded dorsal and differential gene regulation in the Drosophila embryo.
Reeves, G. T., & Stathopoulos, A. (2009) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a000836 · Cited by 119
In Vivo Regulation of the IκB Homologuecactus during the Immune Response ofDrosophila *
Nicolas, E., Reichhart, J., Hoffmann, J., & Lemaître, B. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.17.10463 · Cited by 110
Control of development and immunity by Rel transcription factors in Drosophila
Govind, S. (1999) · Oncogene · doi:10.1038/sj.onc.1203223 · Cited by 110
Nuclear import of the Drosophila Rel protein Dorsal is regulated by phosphorylationPreprint
Drier, E. A., Huang, L., & Steward, R. (1999) · Genes & Development · doi:10.1101/gad.13.5.556 · Cited by 103
Edwards, D. N., Towb, P., & Wasserman, S. A. (1997) · Development · doi:10.1242/dev.124.19.3855 · Cited by 104
Is there any kind of adaptive immunity in invertebrates?
Arala-Chaves, M. P., & Sequeira, T. (2000) · Aquaculture · doi:10.1016/s0044-8486(00)00430-0 · Cited by 95
Briggs, L. J., Stein, D., Goltz, J. S., Corrigan, V. C., Efthymiadis, A., Hübner, S., & Jans, D. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.35.22745 · Cited by 98
Self-citationRoth, P., Xylourgidis, N., Sabri, N., Uv, A., Fornerod, M. W. J., & Samakovlis, C. (2003) · The Journal of Cell Biology · doi:10.1083/jcb.200304046 · Cited by 86
Nuclear factor-kappa B pathways in Drosophila
Minakhina, S., & Steward, R. (2006) · Oncogene · doi:10.1038/sj.onc.1209940 · Cited by 85
Chen, G., Handel, K., & Roth, S. (2000) · Development · doi:10.1242/dev.127.23.5145 · Cited by 85
Mykles, D. L. (1998) · International review of cytology · doi:10.1016/s0074-7696(08)62181-6 · Cited by 84
DeLotto, R., DeLotto, Y., Steward, R., & Lippincott-Schwartz, J. (2007) · Development · doi:10.1242/dev.010934 · Cited by 82
Ganguly, A., Jiang, J., & Ip, Y. T. (2005) · Development · doi:10.1242/dev.01903 · Cited by 81
Avila, A., Silverman, N., Diaz-Meco, M., & Moscat, J. (2002) · Molecular and Cellular Biology · doi:10.1128/mcb.22.24.8787-8795.2002 · Cited by 80
Liu, Z.-P., Galindo, R. L., & Wasserman, S. A. (1997) · Genes & Development · doi:10.1101/gad.11.24.3413 · Cited by 70
NF-κB, IκB, and IRAK Control Glutamate Receptor Density at the Drosophila NMJ
Heckscher, E. S., Fetter, R. D., Marek, K. W., Albin, S. D., & Davis, G. W. (2007) · Neuron · doi:10.1016/j.neuron.2007.08.005 · Cited by 72
Falabella, P., Varricchio, P., Provost, B., Espagne, E., Ferrarese, R., Grimaldi, A., de Eguileor, M., Fimiani, G., Ursini, M. V., Malva, C., et al. (2006) · Journal of General Virology · doi:10.1099/vir.0.82306-0 · Cited by 65
Role for Sumoylation in Systemic Inflammation and Immune Homeostasis in Drosophila Larvae
Paddibhatla, I., Lee, M. J., Kalamarz, M. E., Ferrarese, R., & Govind, S. (2010) · PLoS Pathogens · doi:10.1371/journal.ppat.1001234 · Cited by 63
Recruitment of Tube and Pelle to signaling sites at the surface of the Drosophila embryo
Towb, P., Galindo, R. L., & Wasserman, S. A. (1998) · Development · doi:10.1242/dev.125.13.2443 · Cited by 61
An anteroposterior Dorsal gradient in the Drosophila embryo
Huang, A. M., Rusch, J., & Levine, M. (1997) · Genes & Development · doi:10.1101/gad.11.15.1963 · Cited by 59
Maternal control of the Drosophila dorsal–ventral body axis
Stein, D. S., & Stevens, L. M. (2014) · Wiley Interdisciplinary Reviews Developmental Biology · doi:10.1002/wdev.138 · Cited by 58
Self-citationCritical Role of RelB Serine 368 for Dimerization and p100 Stabilization
Maier, H. J., Marienfeld, R. B., Wirth, T., & Baumann, B. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m301521200 · Cited by 57
Phosphorylation modulates direct interactions between the Toll receptor, Pelle kinase and Tube
Shen, B., & Manley, J. L. (1998) · Development · doi:10.1242/dev.125.23.4719 · Cited by 56
Toll signaling: the enigma variations
Wasserman, S. A. (2000) · Current Opinion in Genetics & Development · doi:10.1016/s0959-437x(00)00118-0 · Cited by 55
Chiu, H., Ring, B. C., Sorrentino, R. P., Kalamarz, M. E., Garza, D., & Govind, S. (2005) · Developmental Biology · doi:10.1016/j.ydbio.2005.08.008 · Cited by 51
Fernandez‐Becker, N., Großhans, J., Goltz, J. S., & Stein, D. (2001) · Development · doi:10.1242/dev.128.15.2963 · Cited by 49
Self-citationThe IRAK Homolog Pelle Is the Functional Counterpart of IκB Kinase in the Drosophila Toll Pathway
Daigneault, J., Klemetsaune, L., & Wasserman, S. A. (2013) · PLoS ONE · doi:10.1371/journal.pone.0075150 · Cited by 49
The Toll gene in Drosophila pattern formation.
Nüsslein-Volhard, C. (2021) · Trends in Genetics · doi:10.1016/j.tig.2021.09.006 · Cited by 42
Self-citationird1 is a Vps15 homologue important for antibacterial immune responses in Drosophila
Wu, J., Randle, K. E., & Wu, L. P. (2006) · Cellular Microbiology · doi:10.1111/j.1462-5822.2006.00853.x · Cited by 48
Spätzle regulates the shape of the Dorsal gradient in the Drosophila embryo
Morisato, D. (2001) · Development · doi:10.1242/dev.128.12.2309 · Cited by 46
Genetic determinants of antiviral immunity in dipteran insects – Compiling the experimental evidence
Machado, S. R., van der Most, T., & Miesen, P. (2021) · Developmental & Comparative Immunology · doi:10.1016/j.dci.2021.104010 · Cited by 45
Dynamic BMP signaling polarized by Toll patterns the dorsoventral axis in a hemimetabolous insect
Sachs, L., Chen, Y.-T., Drechsler, A., Lynch, J., Panfilio, K. A., Lässig, M., Berg, J., & Roth, S. (2015) · eLife · doi:10.7554/elife.05502 · Cited by 44
Lack of an Antibacterial Response Defect in Drosophila Toll-9 Mutant
Narbonne-Reveau, K., Charroux, B., & Royet, J. (2011) · PLoS ONE · doi:10.1371/journal.pone.0017470 · Cited by 43
Conservation and Divergence in Molecular Mechanisms of Axis Formation
Lall, S., & Patel, N. H. (2001) · Annual Review of Genetics · doi:10.1146/annurev.genet.35.102401.090832 · Cited by 43
Dong, X., Zhao, H. L., Li, J., Tian, Y., Zeng, H., Ramos, M. A., Hu, T. S., & Xu, Q. (2020) · iScience · doi:10.1016/j.isci.2020.101749 · Cited by 42
Lin, P., Huang, L. H., & Steward, R. (2000) · Mechanisms of Development · doi:10.1016/s0925-4773(00)00314-2 · Cited by 42
Stein, D., Goltz, J. S., Jurcsak, J., & Stevens, L. M. (1998) · Development · doi:10.1242/dev.125.11.2159 · Cited by 42
Self-citationCactus-independent regulation of Dorsal nuclear import by the ventral signal
Drier, E. A., Govind, S., & Steward, R. (2000) · Current Biology · doi:10.1016/s0960-9822(99)00267-5 · Cited by 42
Krapfen/dMyd88 is required for the establishment of dorsoventral pattern in the Drosophila embryo
Charatsi, I., Luschnig, S., Bartoszewski, S., Nüsslein‐Volhard, C., & Moussian, B. (2003) · Mechanisms of Development · doi:10.1016/s0925-4773(02)00410-0 · Cited by 40
Self-citationÖzüak, O., Buchta, T., Roth, S., & Lynch, J. (2014) · Current Biology · doi:10.1016/j.cub.2014.08.035 · Cited by 39
A multimeric complex and the nuclear targeting of the Drosophila Rel protein Dorsal
Yang, J., & Steward, R. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.26.14524 · Cited by 37
Maxton-Küchenmeister, J., Handel, K., Schmidt‐Ott, U., Roth, S., & Jäckle, H. (1999) · Mechanisms of Development · doi:10.1016/s0925-4773(99)00041-6 · Cited by 37
Novel Roles for the NF-κB Signaling Pathway in Regulating Neuronal Function
Boersma, M. C. H., & Meffert, M. K. (2008) · Science Signaling · doi:10.1126/stke.16pe7 · Cited by 34
Bracovirus gene products are highly divergent from insect proteins
Bézier, A., Herbinière, J., Serbielle, C., Lesobre, J., Wincker, P., Huguet, E., & Drezen, J. (2008) · Archives of Insect Biochemistry and Physiology · doi:10.1002/arch.20219 · Cited by 35
Combinatorial patterning mechanisms in the Drosophila embryo
Chopra, V. S., & Levine, M. (2009) · Briefings in Functional Genomics and Proteomics · doi:10.1093/bfgp/elp026 · Cited by 39
Chen, L.-Y., Wang, J.-C., Hyvert, Y., Lin, H.-P., Perrimon, N., Imler, J., & Hsu, J. (2006) · Current Biology · doi:10.1016/j.cub.2006.05.050 · Cited by 38
A facilitated diffusion mechanism establishes the Drosophila Dorsal gradient
Carrell-Noel, S., O'Connell, M. D., Jacobsen, T. L., Allen, A. E., Smith, S. M., & Reeves, G. T. (2017) · Development · doi:10.1242/dev.155549 · Cited by 28
AP-1, but not NF-κB, is required for efficient steroid-triggered cell death in Drosophila
Lehmann, M., Jiang, C., Ip, Y. T., & Thummel, C. S. (2002) · Cell Death and Differentiation · doi:10.1038/sj.cdd.4401003 · Cited by 26
Conserved Spätzle/Toll signaling in dorsoventral patterning of Xenopus embryos
Armstrong, N. J., Steinbeißer, H., Prothmann, C., DeLotto, R., & Rupp, R. A. W. (1998) · Mechanisms of Development · doi:10.1016/s0925-4773(98)00003-3 · Cited by 26
Signaling between somatic follicle cells and the germline patterns the egg and embryo of Drosophila
Merkle, J. A., Wittes, J., & Schüpbach, T. (2019) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/bs.ctdb.2019.10.004 · Cited by 25
Regulation of Easter activity is required for shaping the Dorsal gradient in theDrosophilaembryo
Chang, A. J., & Morisato, D. (2002) · Development · doi:10.1242/dev.00161 · Cited by 24
Proteolysis and developmental signal transduction
Ye, Y., & Fortini, M. (2000) · Seminars in Cell and Developmental Biology · doi:10.1006/scdb.2000.0167 · Cited by 25
Fontenele, M., Carneiro, K., Agrellos, R., de Oliveira, D. M. P., Oliveira-Silva, A., Vieira, V., Negreiros, É., Machado, E. A., & Araujo, H. M. (2009) · Mechanisms of Development · doi:10.1016/j.mod.2009.04.005 · Cited by 23
Calpain A modulates Toll responses by limited Cactus/IκB proteolysis
Fontenele, M., Lim, B., Oliveira, D., Buffolo, M., Perlman, D. H., Schüpbach, T., & Araujo, H. (2013) · Molecular Biology of the Cell · doi:10.1091/mbc.e13-02-0113 · Cited by 25
Formation, interpretation, and regulation of the Drosophila Dorsal/NF-κB gradient
Schloop, A. E., Bandodkar, P. U., & Reeves, G. T. (2019) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/bs.ctdb.2019.11.007 · Cited by 23
Genome-wide screen for modifiers of Na + /K + ATPase alleles identifies critical genetic loci
Talsma, A. D., Chaves, J. F., LaMonaca, A., Wieczorek, E. D., & Palladino, M. J. (2014) · Molecular Brain · doi:10.1186/s13041-014-0089-3 · Cited by 19
O’Connell, M. D., & Reeves, G. T. (2015) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1004159 · Cited by 17
fusilli, an Essential Gene with a Maternal Role in Drosophila Embryonic Dorsal–Ventral Patterning
Wakabayashi-Ito, N., Belvin, M. P., Bluestein, D. A., & Anderson, K. V. (2001) · Developmental Biology · doi:10.1006/dbio.2000.9954 · Cited by 18
Wulczyn, F. G., Krappmann, D., & Scheidereit, C. (1998) · Nucleic Acids Research · doi:10.1093/nar/26.7.1724 · Cited by 18
Cardoso, M. A., Fontenele, M., Lim, B., Bisch, P. M., Shvartsman, S. Y., & Araujo, H. M. (2017) · Development · doi:10.1242/dev.145557 · Cited by 16
Progress and potential of Drosophila protein interaction maps
Stanyon, C. A., & Finley, R. L. (2000) · Pharmacogenomics · doi:10.1517/14622416.1.4.417 · Cited by 15
Oxidative stress and oxidative damage-induced cell death
Madkour, L. H. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-822481-6.00008-6 · Cited by 15
A tissue communication network coordinating innate immune response during muscle stress
Green, N., Walker, J., Bontrager, A., Zych, M., & Geisbrecht, E. (2018) · Journal of Cell Science · doi:10.1242/jcs.217943 · Cited by 10
Ehrlichia chaffeensis Infections in Drosophila melanogaster
Luce-Fedrow, A., Ohlen, T. V. V., & Chapes, S. (2009) · Infection and Immunity · doi:10.1128/iai.00594-09 · Cited by 13
Yorkie-Cactus (IκBα)-JNK axis promotes tumor growth and progression in Drosophila
Snigdha, K., Singh, A., & Kango-Singh, M. (2021) · Oncogene · doi:10.1038/s41388-021-01831-4 · Cited by 11
Stevens, L. M., Kim, G., Koromila, T., Steele, J., McGehee, J. M., Stathopoulos, A., & Stein, D. S. (2021) · PLoS Genetics · doi:10.1371/journal.pgen.1009544 · Cited by 11
Self-citationSUMOylation of Dorsal attenuates Toll/NF-κB signaling
Hegde, S., Sreejan, A., Gadgil, C. J., & Ratnaparkhi, G. (2021) · bioRxiv · doi:10.1093/genetics/iyac081 · Cited by 7
The role of micro RNAs (miRNAs) in the regulation of Drosophila melanogaster’s innate immunity
Lu, M. Y., & Chtarbanova, S. (2022) · Fly · doi:10.1080/19336934.2022.2149204 · Cited by 10
The Roles and Mechanisms of ROS, Oxidative Stress, and Oxidative Damage
Madkour, L. H. (2020) · Nanomedicine and nanotoxicology · doi:10.1007/978-3-030-37297-2_4 · Cited by 8
Schloop, A. E., Carrell-Noel, S., Friedman, J., Thomas, A., & Reeves, G. T. (2020) · Developmental Biology · doi:10.1016/j.ydbio.2020.01.011 · Cited by 8
Barros, C. D. T., Cardoso, M., Bisch, P., Araujo, H., & Lopes, F. P. (2020) · bioRxiv · doi:10.1371/journal.pcbi.1009040 · Cited by 5
Flores-saaib, R., & Courey, A. (2007) · Cell Biochemistry and Biophysics · doi:10.1385/cbb:33:1:1 · Cited by 8
Spatiotemporal dynamics of NF-κB/Dorsal inhibitor IκBα/Cactus in Drosophila blastoderm embryos
Schloop, A. E., Hiremath, S., Shaikh, R., Dima, S. S., Lizardo, L., Bhakta, A., Williams, C., & Reeves, G. T. (2025) · iScience · doi:10.1016/j.isci.2025.112854 · Cited by 5
IKKϵ Signaling: Not Just NF-κB
Bergmann, A. (2006) · Current Biology · doi:10.1016/j.cub.2006.07.010 · Cited by 5
Self-citationSchiffmann, Y. (2012) · Progress in Biophysics and Molecular Biology · doi:10.1016/j.pbiomolbio.2012.04.005 · Cited by 5
Dorsal/NF-κB exhibits a dorsal-to-ventral mobility gradient in the Drosophila embryoPreprint
Asafen, H. A., Clark, N. M., Goyal, E., Dima, S., Chen, H.-Y., Jacobsen, T., Sozzani, R., & Reeves, G. T. (2018) · bioRxiv · doi:10.1101/320754 · Cited by 6
Pers, D., Buchta, T., Özüak, O., Roth, S., & Lynch, J. (2022) · Journal of Developmental Biology · doi:10.3390/jdb10010007 · Cited by 2
Signaling Cascades, Gradients, and Gene Networks in Dorsal/Ventral Patterning
Ratnaparkhi, G. S., & Courey, A. J. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-405945-0.00008-9 · Cited by 3
Hepatic encephalpathy: new concepts of pathogenesis, biological basis and outcome.
Daif, A. (2002) · PubMed · Cited by 2
Alaouna, M. (2013) · University of the Witwatersrand, Johannesburg Institutional Repository on DSpace (University of the Witwatersrand, Johannesburg) · Cited by 2
Dorsal/NF-κB exhibits a dorsal-to-ventral mobility gradient in the Drosophila embryoPreprint
Asafen, H. A., Clark, N. M., Goyal, E., Jacobsen, T. L., Dima, S. S., Chen, H.-Y., Sozzani, R., & Reeves, G. T. (2024) · eLife · doi:10.7554/elife.100462.1 · Cited by 2
Calpain Proteases and the Evolving Signaling Network in Insect Embryonic Patterning
Julio, A. H. F., & Araujo, H. M. (2025) · Journal of Experimental Zoology Part B Molecular and Developmental Evolution · doi:10.1002/jez.b.23307 · Cited by 1
Mechanisms for controlling Dorsal nuclear levels
McGehee, J. M., & Stathopoulos, A. (2024) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2024.1436369 · Cited by 1
Bug Versus Bug: Humoral Immune Responses in Drosophila melanogaster
Ertürk-Hasdemir, D., Paquette, N., Aggarwal, K., & Silverman, N. S. (2007) · Nucleic acids and molecular biology · doi:10.1007/978-3-540-73930-2_3 · Cited by 1
Mesoderm Formation in the Drosophila Embryo
Wakabayashi-Ito, N., & Ip, Y. (2006) · Springer eBooks · doi:10.1007/0-387-32963-3_3 · Cited by 1
Vertebrate rel proteins exhibit dorsal‐like activities in early Drosophila embryogenesis
Prothmann, C., Armstrong, N. J., Roth, S., & Rupp, R. A. W. (2006) · Developmental Dynamics · doi:10.1002/dvdy.20713 · Cited by 1
Metadata
- Authors
- Bergmann, A., Stein, D., Geisler, R., Hagenmaier, S., Schmid, B., Fernandez, N., Schnell, B., & Nüsslein-Volhard, C.
- Affiliations
- Max Planck Institute for Developmental Biology (DE)
- Albert Einstein College of Medicine (US)
- Corresponding author
- Bergmann, Andreas
- Venue
- Mechanisms of Development
- Publisher
- Elsevier BV
- Published
- 1996-11
- Volume
- 60
- Issue
- 1
- Pages
- 109-123
- ISSN
- 0925-4773 (ISSN-L)
- OpenAlex
- W2057381460
- Cited by
- 119
- References
- 53
- Citations by year
- 2026: 1 · 2025: 3 · 2024: 3 · 2022: 3 · 2021: 6 · 2020: 4 · 2019: 3 · 2018: 2 · 2017: 2 · 2015: 4 · 2014: 4 · 2013: 3 · 2012: 3
- FWCI
- 2.42
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Mechanisms of Development (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › NF-κB Signaling Pathways
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Chromatin Dynamics
- Keywords
- cactus, Dorsal, cytoplasmic degradation, NF-κB, IκB, maternal genes, Drosophila embryo, protein degradation
- MeSH terms
- Animals, Cell Nucleus, Cytoplasm, DNA-Binding Proteins, Drosophila, Immunohistochemistry, Membrane Glycoproteins, Mutation, Nuclear Proteins, Phosphoproteins, Receptors, Cell Surface, Transcription Factors, Genes, Insect, Sequence Deletion, In Situ Hybridization, Gene Expression Regulation, Developmental, Insect Proteins, Body Patterning, Drosophila Proteins, Toll-Like Receptors
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review