2023
Townson, JM., Gomez-Lamarca, MJ., Santa Cruz Mateos, C. and Bray, SJ., 2023. OptIC-Notch reveals mechanism that regulates receptor interactions with CSL. Development, v. 150
Doi: http://doi.org/10.1242/dev.201785
2022
Logeay, R., Géminard, C., Lassus, P., Rodríguez-Vázquez, M., Kantar, D., Heron-Milhavet, L., Fischer, B., Bray, SJ., Colinge, J. and Djiane, A., 2022. Mechanisms underlying the cooperation between loss of epithelial polarity and Notch signaling during neoplastic growth in Drosophila. Development, v. 149
Doi: 10.1242/dev.200110
2021
Falo-Sanjuan, J. and Bray, SJ., 2021. Membrane architecture and adherens junctions contribute to strong Notch pathway activation
Doi: 10.1101/2021.05.26.445755
2019
Koca, Y., Housden, BE., Gault, WJ., Bray, SJ. and Mlodzik, M., 2019. Notch signaling coordinates ommatidial rotation in the Drosophila eye via transcriptional regulation of the EGF-Receptor ligand Argos. Sci Rep, v. 9
Doi: http://doi.org/10.1038/s41598-019-55203-w
2018
Boukhatmi, H. and Bray, S., 2018. A population of adult satellite-like cells in Drosophila is maintained through a switch in RNA-isoforms. Elife, v. 7
Doi: http://doi.org/10.7554/eLife.35954
2017
Terriente-Félix, A., Pérez, L., Bray, SJ., Nebreda, AR. and Milán, M., 2017. A $\textit{Drosophila }$ model of myeloproliferative neoplasm reveals a feed-forward loop in the JAK pathway mediated by p38 MAPK signalling. Disease Models & Mechanisms, v. 10
Doi: http://doi.org/10.1242/dmm.028118
Yao, L., Wang, S., Westholm, JO., Dai, Q., Matsuda, R., Hosono, C., Bray, S., Lai, EC. and Samakovlis, C., 2017. Genome-wide identification of Grainy head targets in Drosophila reveals regulatory interactions with the POU domain transcription factor Vvl. Development, v. 144
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Chan, SKK., Cerda-Moya, G., Stojnic, R., Millen, K., Fischer, B., Fexova, S., Skalska, L., Gomez-Lamarca, M., Pillidge, Z., Russell, S. and Bray, SJ., 2017. Role of co-repressor genomic landscapes in shaping the Notch response. PLoS Genet, v. 13
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2016
Zacharioudaki, E., Housden, BE., Garinis, G., Stojnic, R., Delidakis, C. and Bray, SJ., 2016. Genes implicated in stem cell identity and temporal programme are directly targeted by Notch in neuroblast tumours. Development, v. 143
Doi: http://doi.org/10.1242/dev.126326
Slaninova, V., Krafcikova, M., Perez-Gomez, R., Steffal, P., Trantirek, L., Bray, SJ. and Krejci, A., 2016. Notch stimulates growth by direct regulation of genes involved in the control of glycolysis and the tricarboxylic acid cycle. Open Biol, v. 6
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2015
Zaessinger, S., Zhou, Y., Bray, SJ., Tapon, N. and Djiane, A., 2015. Drosophila MAGI interacts with RASSF8 to regulate E-Cadherin-based adherens junctions in the developing eye. Development, v. 142
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Skalska, L., Stojnic, R., Li, J., Fischer, B., Cerda-Moya, G., Sakai, H., Tajbakhsh, S., Russell, S., Adryan, B. and Bray, SJ., 2015. Chromatin signatures at Notch-regulated enhancers reveal large-scale changes in H3K56ac upon activation. EMBO J, v. 34
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Gomez-Lamarca, MJ., Snowdon, LA., Seib, E., Klein, T. and Bray, SJ., 2015. Rme-8 depletion perturbs Notch recycling and predisposes to pathogenic signaling. J Cell Biol, v. 210
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Gomez-Lamarca, M., Snowdon, LA., Seib, E., Klein, T. and Bray, S., 2015. Rme-8 depletion perturbs Notch recycling and predisposes to pathogenic signaling. J Cell Biol, v. 210
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2014
Torella, R., Li, J., Kinrade, E., Cerda-Moya, G., Contreras, AN., Foy, R., Stojnic, R., Glen, RC., Kovall, RA., Adryan, B. and Bray, SJ., 2014. A combination of computational and experimental approaches identifies DNA sequence constraints associated with target site binding specificity of the transcription factor CSL. Nucleic Acids Res, v. 42
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Djiane, A., Zaessinger, S., Babaoğlan, AB. and Bray, SJ., 2014. Notch inhibits Yorkie activity in Drosophila wing discs. PLoS One, v. 9
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Lowe, N., Rees, JS., Roote, J., Ryder, E., Armean, IM., Johnson, G., Drummond, E., Spriggs, H., Drummond, J., Magbanua, JP., Naylor, H., Sanson, B., Bastock, R., Huelsmann, S., Trovisco, V., Landgraf, M., Knowles-Barley, S., Armstrong, JD., White-Cooper, H., Hansen, C., Phillips, RG., UK Drosophila Protein Trap Screening Consortium, , Lilley, KS., Russell, S. and St Johnston, D., 2014. Analysis of the expression patterns, subcellular localisations and interaction partners of Drosophila proteins using a pigP protein trap library. Development, v. 141
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Pézeron, G., Millen, K., Boukhatmi, H. and Bray, S., 2014. Notch directly regulates the cell morphogenesis genes Reck, talin and trio in adult muscle progenitors. J Cell Sci, v. 127
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Simón, R., Aparicio, R., Housden, BE., Bray, S. and Busturia, A., 2014. Drosophila p53 controls Notch expression and balances apoptosis and proliferation Apoptosis, v. 19
Doi: http://doi.org/10.1007/s10495-014-1000-5
Wong, CC., Martincorena, I., Rust, AG., Rashid, M., Alifrangis, C., Alexandrov, LB., Tiffen, JC., Kober, C., Chronic Myeloid Disorders Working Group of the International Cancer Genome Consortium, , Green, AR., Massie, CE., Nangalia, J., Lempidaki, S., Döhner, H., Döhner, K., Bray, SJ., McDermott, U., Papaemmanuil, E., Campbell, PJ. and Adams, DJ., 2014. Inactivating CUX1 mutations promote tumorigenesis. Nat Genet, v. 46
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Housden, BE., Terriente-Felix, A. and Bray, SJ., 2014. Context-dependent enhancer selection confers alternate modes of notch regulation on argos. Mol Cell Biol, v. 34
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Zacharioudaki, E. and Bray, SJ., 2014. Tools and methods for studying Notch signaling in Drosophila melanogaster. Methods, v. 68
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Simón, R., Aparicio, R., Housden, BE., Bray, S. and Busturia, A., 2014. Drosophila p53 controls Notch expression and balances apoptosis and proliferation. Apoptosis, v. 19
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Housden, BE., Li, J. and Bray, SJ., 2014. Visualizing Notch signaling in vivo in Drosophila tissues. Methods Mol Biol, v. 1187
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Li, J., Housden, BE. and Bray, SJ., 2014. Notch signaling assays in Drosophila cultured cell lines. Methods Mol Biol, v. 1187
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2013
Moshkin, YM., Kan, TW., Goodfellow, H., Bezstarosti, K., Maeda, RK., Pilyugin, M., Karch, F., Bray, S., Demmers, JAA. and Verrijzer, CP., 2013. Erratum to Histone Chaperones ASF1 and NAP1 Differentially Modulate Removal of Active Histone Marks by LID-RPD3 Complexes during NOTCH Silencing [Molecular Cell, 35, (September 24, 2009), 782-793] Molecular Cell, v. 51
Doi: http://doi.org/10.1016/j.molcel.2013.06.015
Djiane, A., Krejci, A., Bernard, F., Fexova, S., Millen, K. and Bray, SJ., 2013. Dissecting the mechanisms of Notch induced hyperplasia. EMBO J, v. 32
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Housden, BE., Fu, AQ., Krejci, A., Bernard, F., Fischer, B., Tavaré, S., Russell, S. and Bray, SJ., 2013. Transcriptional dynamics elicited by a short pulse of notch activation involves feed-forward regulation by E(spl)/Hes genes. PLoS Genet, v. 9
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Terriente-Felix, A., Li, J., Collins, S., Mulligan, A., Reekie, I., Bernard, F., Krejci, A. and Bray, S., 2013. Notch cooperates with Lozenge/Runx to lock haemocytes into a differentiation programme. Development, v. 140
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Djiane, A., Krejci, A., Bernard, F., Fexova, S., Millen, K. and Bray, SJ., 2013. Dissecting the mechanisms of Notch induced hyperplasia EMBO Journal, v. 32
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Babaoğlan, AB., Housden, BE., Furriols, M. and Bray, SJ., 2013. Deadpan contributes to the robustness of the notch response. PLoS One, v. 8
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Fu, AQ., Russell, S., Bray, SJ. and Tavaré, S., 2013. Bayesian clustering of replicated time-course gene expression data with weak signals Annals of Applied Statistics, v. 7
Doi: 10.1214/13-AOAS650
2012
Endo, K., Karim, MR., Taniguchi, H., Krejci, A., Kinameri, E., Siebert, M., Ito, K., Bray, SJ. and Moore, AW., 2012. Chromatin modification of Notch targets in olfactory receptor neuron diversification NAT NEUROSCI, v. 15
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Housden, BE., Millen, K. and Bray, SJ., 2012. Drosophila Reporter Vectors Compatible with ΦC31 Integrase Transgenesis Techniques and Their Use to Generate New Notch Reporter Fly Lines. G3 (Bethesda), v. 2
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Capilla, A., Johnson, R., Daniels, M., Benavente, M., Bray, SJ. and Galindo, MI., 2012. Planar cell polarity controls directional Notch signaling in the Drosophila leg Development (Cambridge), v. 139
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2011
Bending, D., Newland, S., Krejcí, A., Phillips, JM., Bray, S. and Cooke, A., 2011. Epigenetic changes at Il12rb2 and Tbx21 in relation to plasticity behavior of Th17 cells. J Immunol, v. 186
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Endo, K., Karim, MR., Taniguchi, H., Krejci, A., Kinameri, E., Siebert, M., Ito, K., Bray, SJ. and Moore, AW., 2011. Chromatin modification of Notch targets in olfactory receptor neuron diversification Nature Neuroscience,
Djiane, A., Shimizu, H., Wilkin, M., Mazleyrat, S., Jennings, MD., Avis, J., Bray, S. and Baron, M., 2011. Su(dx) E3 ubiquitin ligase-dependent and -independent functions of polychaetoid, the Drosophila ZO-1 homologue. J Cell Biol, v. 192
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2010
Bernard, F., Krejci, A., Housden, B., Adryan, B. and Bray, SJ., 2010. Specificity of Notch pathway activation: twist controls the transcriptional output in adult muscle progenitors. Development, v. 137
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Endo, K., Karim, MR., Krejci, A., Kinameri, E., Seibert, M., Ito, K., Bray, SJ. and Moore, AW., 2010. Modification of the Notch transcriptional response by Hamlet/Evi1 maximizes Drosophila olfactory sensory neuron diversity NEUROSCIENCE RESEARCH, v. 68
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Pines, MK., Housden, BE., Bernard, F., Bray, SJ. and Röper, K., 2010. The cytolinker Pigs is a direct target and a negative regulator of Notch signalling. Development, v. 137
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Monastirioti, M., Giagtzoglou, N., Koumbanakis, KA., Zacharioudaki, E., Deligiannaki, M., Wech, I., Almeida, M., Preiss, A., Bray, S. and Delidakis, C., 2010. Drosophila Hey is a target of Notch in asymmetric divisions during embryonic and larval neurogenesis DEVELOPMENT, v. 137
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2009
Moshkin, YM., Kan, TW., Goodfellow, H., Bezstarosti, K., Maeda, RK., Pilyugin, M., Karch, F., Bray, SJ., Demmers, JAA. and Verrijzer, CP., 2009. Histone Chaperones ASF1 and NAP1 Differentially Modulate Removal of Active Histone Marks by LID-RPD3 Complexes during NOTCH Silencing MOL CELL, v. 35
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Krejčí, A., Bernard, F., Housden, B., Collins, S. and Bray, SJ., 2009. Erratum: Direct response to notch activation: Signaling crosstalk and incoherent logic (Science Signaling (2009) 2 (er3)) Science Signaling, v. 2
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Krejcí, A., Bernard, F., Housden, BE., Collins, S. and Bray, SJ., 2009. Direct response to Notch activation: signaling crosstalk and incoherent logic. Sci Signal, v. 2
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Benitez, E., Bray, SJ., Rodriguez, I. and Guerrero, I., 2009. Lines is required for normal operation of Wingless, Hedgehog and Notch pathways during wing development DEVELOPMENT, v. 136
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2008
Bray, SJ., Takada, S., Harrison, E., Shen, S-C. and Ferguson-Smith, AC., 2008. The atypical mammalian ligand Delta-like homologue 1 (Dlk1) can regulate Notch signalling in Drosophila. BMC Dev Biol, v. 8
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Narasimha, M., Uv, A., Krejci, A., Brown, NH. and Bray, SJ., 2008. Grainy head promotes expression of septate junction proteins and influences epithelial morphogenesis. J Cell Sci, v. 121
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2007
Krejcí, A. and Bray, S., 2007. Notch activation stimulates transient and selective binding of Su(H)/CSL to target enhancers. Genes Dev, v. 21
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Goodfellow, H., Krejcí, A., Moshkin, Y., Verrijzer, CP., Karch, F. and Bray, SJ., 2007. Gene-specific targeting of the histone chaperone asf1 to mediate silencing. Dev Cell, v. 13
Doi: http://doi.org/10.1016/j.devcel.2007.08.021
2006
Glittenberg, M., Pitsouli, C., Garvey, C., Delidakis, C. and Bray, S., 2006. Role of conserved intracellular motifs in Serrate signalling, cis-inhibition and endocytosis. EMBO J, v. 25
Doi: http://doi.org/10.1038/sj.emboj.7601337
2005
Nagel, AC., Krejci, A., Tenin, G., Bravo-Patino, A., Bray, S., Maier, D. and Preiss, A., 2005. Hairless-mediated repression of Notch target genes requires the combined activity of Groucho and CtBP corepressors MOL CELL BIOL, v. 25
Doi: http://doi.org/10.1128/MCB.25.23.10433-10441.2005
Hatini, V., Green, RB., Lengyel, JA., Bray, SJ. and DiNardo, S., 2005. The drumstick/lines/bowl regulatory pathway links antagonistic Hedgehog and Wingless signaling inputs to epidermal cell differentiation GENE DEV, v. 19
Doi: http://doi.org/10.1101/gad.1268005
2003
de Celis Ibeas, JM. and Bray, SJ., 2003. Bowl is required downstream of Notch for elaboration of distal limb patterning. Development, v. 130
Doi: http://doi.org/10.1242/dev.00833
Hemphala, J., Uv, A., Cantera, R., Bray, S. and Samakovlis, C., 2003. Grainy head controls apical membrane growth and tube elongation in response to Branchless/FGF signalling DEVELOPMENT, v. 130
Doi: http://doi.org/10.1242/dev.00218
2002
Bagni, C., Bray, S., Gogos, JA., Kafatos, FC. and Hsu, T., 2002. The Drosophila zinc finger transcription factor CF2 is a myogenic marker downstream of MEF2 during muscle development MECH DEVELOP, v. 117
Strutt, D., Johnson, R., Cooper, K. and Bray, S., 2002. Asymmetric localization of frizzled and the determination of notch-dependent cell fate in the Drosophila eye CURR BIOL, v. 12
2001
2000
Bray, S. and Stein, D., 2000. Developmental biology - Post-expressionist flies NATURE, v. 407
Cooper, MT., Tyler, DM., Furriols, M., Chalkiadaki, A., Delidakis, C. and Bray, S., 2000. Spatially restricted factors cooperate with notch in the regulation of Enhancer of split genes. Dev Biol, v. 221
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de Celis, JF. and Bray, SJ., 2000. The Abruptex domain of Notch regulates negative interactions between Notch, its ligands and Fringe DEVELOPMENT, v. 127
1999
Wech, I., Bray, S., Delidakis, C. and Preiss, A., 1999. Distinct expression patterns of different Enhancer of split bHLH genes during embryogenesis of Drosophila melanogaster DEV GENES EVOL, v. 209
Cooper, MT. and Bray, SJ., 1999. Frizzled regulation of Notch signalling polarizes cell fate in the Drosophila eye. Nature, v. 397
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Jennings, BH., Tyler, DM. and Bray, SJ., 1999. Target specificities of Drosophila enhancer of split basic helix-loop-helix proteins. Mol Cell Biol, v. 19
Doi: http://doi.org/10.1128/MCB.19.7.4600
Ligoxygakis, P., Bray, SJ., Apidianakis, Y. and Delidakis, C., 1999. Ectopic expression of individual E(spl) genes has differential effects on different cell fate decisions and underscores the biphasic requirement for Notch activity in wing margin establishment in Drosophila DEVELOPMENT, v. 126
1998
Prokop, A., Bray, S., Harrison, E. and Technau, GM., 1998. Homeotic regulation of segment-specific differences in neuroblast numbers and proliferation in the Drosophila central nervous system MECH DEVELOP, v. 74
de Celis, JF., Tyler, DM., de Celis, J. and Bray, SJ., 1998. Notch signalling mediates segmentation of the Drosophila leg. Development, v. 125
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1997
Eastman, DS., Slee, R., Skoufos, E., Bangalore, L., Bray, S. and Delidakis, C., 1997. Synergy between suppressor of hairless and notch in regulation of enhancer of split m gamma and m delta expression MOL CELL BIOL, v. 17
Bray, SJ., 1997. Expression and function of Enhancer of split bHLH proteins during Drosophila neurogenesis. Perspect Dev Neurobiol, v. 4
Uv, AE., Harrison, EJ. and Bray, SJ., 1997. Tissue-specific splicing and functions of the Drosophila transcription factor Grainyhead. Mol Cell Biol, v. 17
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de Celis, JF., Bray, S. and Garcia-Bellido, A., 1997. Notch signalling regulates veinlet expression and establishes boundaries between veins and interveins in the Drosophila wing. Development, v. 124
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de Celis, JF. and Bray, S., 1997. Feed-back mechanisms affecting Notch activation at the dorsoventral boundary in the Drosophila wing. Development, v. 124
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1996
Jennings, B. and Bray, SJ., 1996. Function of enhancer of split proteins in the notch signalling pathway MOL BIOL CELL, v. 7
de Celis, JF., Garcia-Bellido, A. and Bray, SJ., 1996. Activation and function of Notch at the dorsal-ventral boundary of the wing imaginal disc. Development, v. 122
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Ebling, FJ., Maywood, ES., Mehta, M., Hancock, DC., McNulty, S., De Bono, J., Bray, SJ. and Hastings, MH., 1996. FosB in the suprachiasmatic nucleus of the Syrian and Siberian hamster. Brain Res Bull, v. 41
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de Celis, JF., de Celis, J., Ligoxygakis, P., Preiss, A., Delidakis, C. and Bray, S., 1996. Functional relationships between Notch, Su(H) and the bHLH genes of the E(spl) complex: the E(spl) genes mediate only a subset of Notch activities during imaginal development. Development, v. 122
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1995
JENNINGS, B., DECELIS, J., DELIDAKIS, C., PREISS, A. and BRAY, S., 1995. ROLE OF NOTCH AND ACHAETE-SCUTE COMPLEX IN THE EXPRESSION OF ENHANCER OF SPLIT BHLH PROTEINS DEVELOPMENT, v. 121
Tannahill, D., Bray, S. and Harris, WA., 1995. A Drosophila E(spł) gene is "neurogenic" in Xenopus: a green fluorescent protein study. Dev Biol, v. 168
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1994
Uv, AE., Thompson, CR. and Bray, SJ., 1994. The Drosophila tissue-specific factor Grainyhead contains novel DNA-binding and dimerization domains which are conserved in the human protein CP2. Mol Cell Biol, v. 14
Doi: http://doi.org/10.1128/mcb.14.6.4020-4031.1994
Jennings, B., Preiss, A., Delidakis, C. and Bray, S., 1994. The Notch signalling pathway is required for Enhancer of split bHLH protein expression during neurogenesis in the Drosophila embryo. Development, v. 120
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1991
Bray, SJ. and Kafatos, FC., 1991. Developmental function of Elf-1: an essential transcription factor during embryogenesis in Drosophila. Genes Dev, v. 5
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1989
BRAY, SJ., BURKE, B., BROWN, NH. and HIRSH, J., 1989. EMBRYONIC EXPRESSION PATTERN OF A FAMILY OF DROSOPHILA PROTEINS THAT INTERACT WITH A CENTRAL NERVOUS-SYSTEM REGULATORY ELEMENT GENE DEV, v. 3
Johnson, WA., McCormick, CA., Bray, SJ. and Hirsh, J., 1989. A neuron-specific enhancer of the Drosophila dopa decarboxylase gene. Genes Dev, v. 3
Doi: http://doi.org/10.1101/gad.3.5.676
1988
Bray, SJ., Johnson, WA., Hirsh, J., Heberlein, U. and Tjian, R., 1988. A cis-acting element and associated binding factor required for CNS expression of the Drosophila melanogaster dopa decarboxylase gene. EMBO J, v. 7
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1986
SCHOLNICK, SB., BRAY, SJ., MORGAN, BA., MCCORMICK, CA. and HIRSH, J., 1986. CNS AND HYPODERM REGULATORY ELEMENTS OF THE DROSOPHILA-MELANOGASTER DOPA DECARBOXYLASE GENE SCIENCE, v. 234
BRAY, SJ. and HIRSH, J., 1986. THE DROSOPHILA-VIRILIS DOPA DECARBOXYLASE GENE IS DEVELOPMENTALLY REGULATED WHEN INTEGRATED INTO DROSOPHILA-MELANOGASTER EMBO J, v. 5
BRAY, SJ., SCHOLNICK, SB., MORGAN, BA., BEALL, CJ. and HIRSH, J., 1986. SEQUENCES AND SPLICES GOVERNING CNS EXPRESSION OF THE DROSOPHILA DOPA DECARBOXYLASE GENE DDC BIOL BULL, v. 170
1985
Standart, NM., Bray, SJ., George, EL., Hunt, T. and Ruderman, JV., 1985. The small subunit of ribonucleotide reductase is encoded by one of the most abundant translationally regulated maternal RNAs in clam and sea urchin eggs. J Cell Biol, v. 100
Doi: http://doi.org/10.1083/jcb.100.6.1968
Sjöberg, BM., Eklund, H., Fuchs, JA., Carlson, J., Standart, NM., Ruderman, JV., Bray, SJ. and Hunt, T., 1985. Identification of the stable free radical tyrosine residue in ribonucleotide reductase. A sequence comparison. FEBS Lett, v. 183
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1984
Ballinger, DG., Bray, SJ. and Hunt, T., 1984. Studies of the kinetics and ionic requirements for the phosphorylation of ribosomal protein S6 after fertilization of Arbacia punctulata eggs. Dev Biol, v. 101
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1983
GEORGE, EL., BRAY, S., ROSENTHAL, ET. and HUNT, T., 1983. A MAJOR MATERNALLY ENCODED K-41 PROTEIN IN BOTH SPISULA AND ARBACIA BINDS TO AN ANTI-TUBULIN AFFINITY COLUMN BIOL BULL, v. 165
Bray, S. and Falo Sanjuan, J., Notch-dependent and -independent transcription are modulated by tissue movements at gastrulation eLife,
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Bray, S., OptIC Notch reveals mechanism that regulates receptor interactions with CSL Development,
Bray, SJ., Gomez Lamarca, M., Falo Sanjuan, J., Stojnic, R., Cerda Moya, G., Jones, M., Pillidge, Z., O'Holleran, K., Abdul Rehman, S., Muresan, L., Rhett, K., Payre, F., Bystricky, K., Baloul, S., Valenti, P. and Yuan, Z., Activation of the Notch signalling pathway in vivo elicits changes in CSL nuclear dynamics Developmental Cell,
Zacharioudaki, E., Falo Sanjuan, J. and Bray, S., Mi-2/NuRD complex protects stem cell progeny from mitogenic Notch signalling eLife,
Pillidge, Z. and Bray, S., SWI/SNF chromatin remodeling controls Notch-responsive enhancer accessibility EMBO Reports,
Feng, S., Zacharioudaki, E., Millen, K. and Bray, S., The SLC36 transporter Pathetic is required for neural stem cell proliferation and for brain growth under nutrition restriction Neural Development,
Bray, S., Falo-Sanjuan, J., Garcia, H. and Lammers, N., Enhancer priming enables fast and sustained transcriptional responses to Notch signaling Developmental Cell,
Falo Sanjuan, J. and Bray, S., Decoding the Notch Signal Development Growth and Differentiation,
Bray, S., Martins, T., Lea, S., Handford, P., Meng, Y., Korona, B., Suckling, R. and Johnson, S., The conserved C2 phospholipid-binding Domain in Delta contributes to robust Notch signalling EMBO Reports,
Bray, S., Boukhatmi, H., Martins, T., Pillidge, Z. and Kamenova, T., Notch mediates inter-tissue communication to promote tumorigenesis. Current Biology,
Bray, S. and Falo Sanjuan, J., Membrane architecture and adherens junctions contribute to strong Notch pathway activation Development,
