her4 , a zebrafish homologue of the Drosophila neurogenic gene E(spl) , is a target of NOTCH signalling

Stages of embryonic development of the zebrafish

Kimmel, C. B., Ballard, W. W., Kimmel, S. R., Ullmann, B., & Schilling, T. F. (1995) · Developmental Dynamics · doi:10.1002/aja.1002030302 · Cited by 12,037 · see citing works

Interactions between heterologous helix-loop-helix proteins generate complexes that bind specifically to a common DNA sequence

Murre, C., Page-McCaw, P., Vaessin, H., Caudy, M. A., Jan, L. Y., Jan, Y. N., Cabrera, C. V., Buskin, J. N., Hauschka, S. D., Lassar, A. B., et al. (1989) · Cell · doi:10.1016/0092-8674(89)90434-0 · Cited by 1,815 · see citing works

Expression of achaete-scute homolog 3 in Xenopus embryos converts ectodermal cells to a neural fate.Preprint

Turner, D. L., & Weintraub, H. (1994) · Genes & Development · doi:10.1101/gad.8.12.1434 · Cited by 1,023 · see citing works

Avian hairy Gene Expression Identifies a Molecular Clock Linked to Vertebrate Segmentation and Somitogenesis

Palmeirim, I., Henrique, D., Ish‐Horowicz, D., & Pourquié, O. (1997) · Cell · doi:10.1016/s0092-8674(00)80451-1 · Cited by 951 · see citing works

Identification of neurogenin, a vertebrate neuronal determination gene.

Ma, Q.-F., Kintner, C., & Anderson, D. J. (1996) · Cell · doi:10.1016/s0092-8674(00)81321-5 · Cited by 874 · see citing works

The choice of cell fate in the epidermis of Drosophila

Heitzler, P., & Simpson, P. (1991) · Cell · doi:10.1016/0092-8674(91)90263-x · Cited by 750 · see citing works

Primary neurogenesis in Xenopus embryos regulated by a homologue of the Drosophila neurogenic gene Delta

Chitnis, A. B., Henrique, D., Lewis, J. H., Ish‐Horowicz, D., & Kintner, C. R. (1995) · Nature · doi:10.1038/375761a0 · Cited by 675 · see citing works

Identification of separate slow and fast muscle precursor cells in vivo, prior to somite formation

Devoto, S. H., Melançon, E., Eisen, J. S., & Westerfield, M. (1996) · Development · doi:10.1242/dev.122.11.3371 · Cited by 667 · see citing works

Two mammalian helix-loop-helix factors structurally related to Drosophila hairy and Enhancer of split.Preprint

Sasai, Y., Kageyama, R., Tagawa, Y., Shigemoto, R., & Nakanishi, S. (1992) · Genes & Development · doi:10.1101/gad.6.12b.2620 · Cited by 665 · see citing works

Suppressor of hairless directly activates transcription of enhancer of split complex genes in response to Notch receptor activity.Preprint

Bailey, A. M., & Posakony, J. W. (1995) · Genes & Development · doi:10.1101/gad.9.21.2609 · Cited by 592 · see citing works

Groucho is required for Drosophila neurogenesis, segmentation, and sex determination and interacts directly with hairy-related bHLH proteins

Paroush, Z. (1994) · Cell · doi:10.1016/0092-8674(94)90070-1 · Cited by 568 · see citing works

LIN-12/Notch signaling: lessons from worms and fliesPreprint

Greenwald, I. (1998) · Genes & Development · doi:10.1101/gad.12.12.1751 · Cited by 541 · see citing works

On the phenotype and development of mutants of early neurogenesis inDrosophila melanogaster

Lehmann, R., Jim�nez, F., Dietrich, U., & Campos-Ortega, J. A. (1983) · Development Genes and Evolution · doi:10.1007/bf00848482 · Cited by 494 · see citing works

Intrinsic activity of the lin-12 and Notch intracellular domains in vivo

Struhl, G., Fitzgerald, K. J., & Greenwald, I. (1993) · Cell · doi:10.1016/0092-8674(93)90424-o · Cited by 466 · see citing works

Maintenance of neuroepithelial progenitor cells by Delta–Notch signalling in the embryonic chick retina

Henrique, D., Hirsinger, E., Adam, J., Roux, I., Pourquié, O., Ish‐Horowicz, D., & Lewis, J. H. (1997) · Current Biology · doi:10.1016/s0960-9822(06)00293-4 · Cited by 431 · see citing works

The neurogenic suppressor of hairless DNA-binding protein mediates the transcriptional activation of the enhancer of split complex genes triggered by Notch signaling.Preprint

Lecourtois, M., & Schweisguth, F. (1995) · Genes & Development · doi:10.1101/gad.9.21.2598 · Cited by 430 · see citing works

Antineurogenic phenotypes induced by truncated Notch proteins indicate a role in signal transduction and may point to a novel function for Notch in nuclei.Preprint

Lieber, T., Kidd, S., Alcamo, E., Corbin, V., & Young, M. W. (1993) · Genes & Development · doi:10.1101/gad.7.10.1949 · Cited by 421 · see citing works

Specific truncations of Drosophila Notch define dominant activated and dominant negative forms of the receptor

Rebay, I., Fehon, R. G., & Artavanis‐Tsakonas, S. (1993) · Cell · doi:10.1016/0092-8674(93)90423-n · Cited by 413 · see citing works

Expression of an extracellular deletion of Xotch diverts cell fate in Xenopus embryos

Coffman, C. R., Skoglund, P., Harris, W. A., & Kintner, C. R. (1993) · Cell · doi:10.1016/0092-8674(93)90247-n · Cited by 369 · see citing works

The WRPW Motif of the Hairy-Related Basic Helix-Loop-Helix Repressor Proteins Acts as a 4-Amino-Acid Transcription Repression and Protein-Protein Interaction Domain

Fisher, A. L., Ohsako, S., & Caudy, M. A. (1996) · Molecular and Cellular Biology · doi:10.1128/mcb.16.6.2670 · Cited by 353 · see citing works

Genes of the Enhancer of split and achaete-scute complexes are required for a regulatory loop between Notch and Delta during lateral signalling in Drosophila

Heitzler, P., Bourouis, M., Ruel, L., Carteret, C., & Simpson, P. (1996) · Development · doi:10.1242/dev.122.1.161 · Cited by 334 · see citing works

Zebrafish elav/HuC homologue as a very early neuronal marker

Kim, C., Ueshima, E., Muraoka, O., Tanaka, H., Yeo, S., Huh, T., & Miki, N. (1996) · Neuroscience Letters · doi:10.1016/0304-3940(96)13021-4 · Cited by 317 · see citing works

Molecular characterization of a rat negative regulator with a basic helix-loop-helix structure predominantly expressed in the developing nervous system.

Akazawa, C., Sasai, Y., Nakanishi, S., & Kageyama, R. (1992) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)36694-3 · Cited by 299 · see citing works

The basic-helix-loop-helix domain of Drosophila lethal of scute protein is sufficient for proneural function and activates neurogenic genes

Hinz, U., Giebel, B., & Campos‐Ortega, J. A. (1994) · Cell · doi:10.1016/0092-8674(94)90174-0 · Cited by 299 · see citing works

The Xenopus homolog of Drosophila Suppressor of Hairless mediates Notch signaling during primary neurogenesis

Wettstein, D. A., Turner, D. L., & Kintner, C. R. (1997) · Development · doi:10.1242/dev.124.3.693 · Cited by 287 · see citing works

Multiple delta genes and lateral inhibition in zebrafish primary neurogenesis

Haddon, C., Smithers, L. E., Schneider‐Maunoury, S., Coche, T. G., Henrique, D., & Lewis, J. H. (1998) · Development · doi:10.1242/dev.125.3.359 · Cited by 266 · see citing works

Closely related transcripts encoded by the neurogenic gene complex enhancer of split of Drosophila melanogaster.

Klämbt, C., Knust, E., Tietze, K., & Campos‐Ortega, J. A. (1989) · The EMBO Journal · doi:10.1002/j.1460-2075.1989.tb03365.x · Cited by 264 · see citing works

Zebrafish primary neurons initiate expression of the LIM homeodomain protein Isl-1 at the end of gastrulation

Korzh, V. P., Edlund, H., & Thor, S. (1993) · Development · doi:10.1242/dev.118.2.417 · Cited by 250 · see citing works

The activity of Neurogenin1 is controlled by local cues in the zebrafish embryo

Blader, P., Fischer, N., Gradwohl, G., Guillemot, F., & Strähle, U. (1997) · Development · doi:10.1242/dev.124.22.4557 · Cited by 243 · see citing works

The Drosophila hairy protein acts in both segmentation and bristle patterning and shows homology to N‐myc.

Rushlow, C., Hogan, A., Pinchin, S. M., Howe, K. M., Lardelli, M. T., & Ish‐Horowicz, D. (1989) · The EMBO Journal · doi:10.1002/j.1460-2075.1989.tb08461.x · Cited by 240 · see citing works

deadpan, an essential pan-neural gene in Drosophila, encodes a helix-loop-helix protein similar to the hairy gene product.Preprint

Bier, E., Vaessin, H., Younger, S. H., Jan, L. Y., & Jan, Y. N. (1992) · Genes & Development · doi:10.1101/gad.6.11.2137 · Cited by 239 · see citing works

Developmental regulation of Islet‐1 mRNA expression during neuronal differentiation in embryonic zebrafish

Inoue, A., Takahashi, M., Hatta, K., Hotta, Y., & Okamoto, H. (1994) · Developmental Dynamics · doi:10.1002/aja.1001990102 · Cited by 232 · see citing works

Specificity for the Hairy/Enhancer of split Basic Helix-Loop-Helix (bHLH) Proteins Maps outside the bHLH Domain and Suggests Two Separable Modes of Transcriptional Repression

Dawson, S. R., Turner, D. L., Weintraub, H. M., & Parkhurst, S. M. (1995) · Molecular and Cellular Biology · doi:10.1128/mcb.15.12.6923 · Cited by 221 · see citing works

Seven genes of the Enhancer of split complex of Drosophila melanogaster encode helix-loop-helix proteins.

Knust, E., Schrons, H., Grawe, F., & Campos‐Ortega, J. A. (1992) · Genetics · doi:10.1093/genetics/132.2.505 · Cited by 216 · see citing works

Sensitivity of proneural genes to lateral inhibition affects the pattern of primary neurons in Xenopus embryos

Chitnis, A. B., & Kintner, C. R. (1996) · Development · doi:10.1242/dev.122.7.2295 · Cited by 178 · see citing works

The Enhancer of split [E(spl)] locus of Drosophila encodes seven independent helix-loop-helix proteins.

Delidakis, C., & Artavanis‐Tsakonas, S. (1992) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.89.18.8731 · Cited by 174 · see citing works

Expression domains of a zebrafish homologue of the Drosophila pair-rule gene hairy correspond to primordia of alternating somites

Müller, M., Weizsäcker, E. V., & Campos‐Ortega, J. A. (1996) · Development · doi:10.1242/dev.122.7.2071 · Cited by 163 · see citing works

Lateral inhibition mediated by the Drosophila neurogenic gene delta is enhanced by proneural proteins.

Kunisch, M., Haenlin, M., & Campos‐Ortega, J. A. (1994) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.91.21.10139 · Cited by 159 · see citing works

Functional interactions of neurogenic genes of Drosophila melanogaster.

de la Concha, A., Dietrich, U., Weigel, D., & Campos‐Ortega, J. A. (1988) · Genetics · doi:10.1093/genetics/118.3.499 · Cited by 158 · see citing works

Regulation of neuronal specification in the zebrafish spinal cord by Delta function

Appel, B., & Eisen, J. S. (1998) · Development · doi:10.1242/dev.125.3.371 · Cited by 156 · see citing works

A zebrafish homologue of the Drosophila neurogenic gene Notch and its pattern of transcription during early embryogenesis

Bierkamp, C., & Campos‐Ortega, J. A. (1993) · Mechanisms of Development · doi:10.1016/0925-4773(93)90027-u · Cited by 148 · see citing works

Three novel Notch genes in zebrafish: implications for vertebrate Notch gene evolution and function

Westin, J., & Lardelli, M. (1997) · Development Genes and Evolution · doi:10.1007/s004270050091 · Cited by 134 · see citing works

Overexpression of a zebrafish homologue of the Drosophila neurogenic gene Delta perturbs differentiation of primary neurons and somite development

Dornseifer, P., Takke, C., & Campos‐Ortega, J. A. (1997) · Mechanisms of Development · doi:10.1016/s0925-4773(97)00037-3 · Cited by 134 · see citing works

Persistent Expression of Genes of the Enhancer of Split Complex Suppresses Neural Development in Drosophila

Nakao, K., & Campos‐Ortega, J. A. (1996) · Neuron · doi:10.1016/s0896-6273(00)80046-x · Cited by 130 · see citing works

Direct downstream targets of proneural activators in the imaginal disc include genes involved in lateral inhibitory signaling.Preprint

Singson, A. W., Leviten, M. W., Bang, A. G., Hua, X. H., & Posakony, J. W. (1994) · Genes & Development · doi:10.1101/gad.8.17.2058 · Cited by 120 · see citing works

Molecular analysis of the neurogenic locus Enhancer of split of Drosophila melanogaster

Knust, E., Tietze, K., & Campos‐Ortega, J. A. (1987) · The EMBO Journal · doi:10.1002/j.1460-2075.1987.tb02757.x · Cited by 119 · see citing works

Enhancer of splitD, a dominant mutation of Drosophila, and its use in the study of functional domains of a helix-loop-helix protein.

Tietze, K., Oellers, N., & Knust, E. (1992) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.89.13.6152 · Cited by 113 · see citing works

bHLH proteins encoded by theEnhancer of split complex ofDrosophila negatively interfere with transcriptional activation mediated by proneural genes

Oellers, N., Dehio, M., & Knust, E. (1994) · Molecular and General Genetics MGG · doi:10.1007/bf00583897 · Cited by 111 · see citing works

Cell autonomy of expression of neurogenic genes of Drosophila melanogaster.

Technau, G. M., & Campos‐Ortega, J. A. (1987) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.84.13.4500 · Cited by 107 · see citing works

Evolutionarily Conserved Sequences of Striated Muscle Myosin Heavy Chain Isoforms

Miller, J. B., Teal, S., & Stockdale, F. E. (1989) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)51604-5 · Cited by 83 · see citing works

Neuroectodermal transcription of the Drosophila neurogenic genes E(spl) and HLH-m5 is regulated by proneural genes

Kramatschek, B., & Campos‐Ortega, J. A. (1994) · Development · doi:10.1242/dev.120.4.815 · Cited by 80 · see citing works

Functional dissection of the Drosophila Enhancer of split protein, a suppressor of neurogenesis

Giebel, B., & Campos‐Ortega, J. A. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.12.6250 · Cited by 76 · see citing works

Point Mutations in the Drosophila hairy Gene Demonstrate In Vivo Requirements for Basic, Helix-Loop-Helix, and WRPW Domains

Wainwright, S. M., & Ish‐Horowicz, D. (1992) · Molecular and Cellular Biology · doi:10.1128/mcb.12.6.2475 · Cited by 75 · see citing works

Notch-related genes in animal development

Lardelli, M., Williams, R. T. P., & Lendahl, U. (1995) · The International Journal of Developmental Biology · doi:10.1387/ijdb.8645561 · Cited by 57 · see citing works

Inhibition of cell fate in Drosophila by Enhancer of split genes

Tata, F., & Hartley, D. A. (1995) · Mechanisms of Development · doi:10.1016/0925-4773(95)00377-0 · Cited by 53 · see citing works

Genomic regions regulating early embryonic expression of the Drosophila neurogenic gene Delta

Haenlin, M., Kunisch, M., Kramatschek, B., & Campos‐Ortega, J. A. (1994) · Mechanisms of Development · doi:10.1016/0925-4773(94)90099-x · Cited by 46 · see citing works

Transcription of a zebrafish gene of the hairy-Enhancer of split family delineates the midbrain anlage in the neural plate

Müller, M., Weizsäcker, E. V., & Campos‐Ortega, J. A. (1996) · Development Genes and Evolution · doi:10.1007/s004270050041 · Cited by 42 · see citing works

A zebrafish Id homologue and its pattern of expression during embryogenesis

Sawai, S., & Campos‐Ortega, J. A. (1997) · Mechanisms of Development · doi:10.1016/s0925-4773(97)00071-3 · Cited by 28 · see citing works

The HLH domain of a zebrafish hE12 homologue can partially substitute for functions of the HLH domain of Drosophiladaughterless

Wülbeck, C., Fromental-Ramain, C., & Campos‐Ortega, J. A. (1994) · Mechanisms of Development · doi:10.1016/0925-4773(94)90077-9 · Cited by 24 · see citing works

Two zebrafish homologues of the Drosophila neurogenic gene groucho and their pattern of transcription during early embryogenesis

Wülbeck, C., & Campos‐Ortega, J. A. (1997) · Development Genes and Evolution · doi:10.1007/s004270050103 · Cited by 23 · see citing works

Homeotic duplication of the pelvic body segment in regenerating tadpole tails induced by retinoic acid

Müller, G. B., Streicher, J., & Müller, R. J. (1996) · Development Genes and Evolution · doi:10.1007/s004270050062 · Cited by 22 · see citing works

HES and HERP families: Multiple effectors of the notch signaling pathway

Iso, T., Kedes, L., & Hamamori, Y. (2003) · Journal of Cellular Physiology · doi:10.1002/jcp.10208 · Cited by 1,240 · see citing works

Notch signaling is required for arterial-venous differentiation during embryonic vascular development

Lawson, N. D., Scheer, N., Pham, V. N., Kim, C., Chitnis, A. B., Campos‐Ortega, J. A., & Weinstein, B. M. (2001) · Development · doi:10.1242/dev.128.19.3675 · Cited by 915 · see citing works

Mind Bomb Is a Ubiquitin Ligase that Is Essential for Efficient Activation of Notch Signaling by Delta

Itoh, M., Kim, C., Palardy, G. R., Oda, T., Jiang, Y., Maust, D. T., Yeo, S., Lorick, K. L., Wright, G. J., Ariza‐McNaughton, L., et al. (2003) · Developmental Cell · doi:10.1016/s1534-5807(02)00409-4 · Cited by 779 · see citing works

The Hes gene family: repressors and oscillators that orchestrate embryogenesis

Kageyama, R., Ohtsuka, T., & Kobayashi, T. (2007) · Development · doi:10.1242/dev.000786 · Cited by 683 · see citing works

A γ‐secretase inhibitor blocks Notch signaling in vivo and causes a severe neurogenic phenotype in zebrafish

Geling, A., Steiner, H., Willem, M., Bally‐Cuif, L., & Haass, C. (2002) · The EMBO Reports · doi:10.1093/embo-reports/kvf124 · Cited by 497 · see citing works

Regeneration of the adult zebrafish brain from neurogenic radial glia-type progenitors

Kroehne, V., Freudenreich, D., Hans, S., Kaslin, J., & Brand, M. (2011) · Development · doi:10.1242/dev.072587 · Cited by 448 · see citing works

Vertebrate hairy and Enhancer of split related proteins: transcriptional repressors regulating cellular differentiation and embryonic patterning

Davis, R. L., & Turner, D. L. (2001) · Oncogene · doi:10.1038/sj.onc.1205094 · Cited by 387 · see citing works

Neurogenesis in zebrafish – from embryo to adult

Viales, R. R., Strähle, U., & Scholpp, S. (2013) · Neural Development · doi:10.1186/1749-8104-8-3 · Cited by 374 · see citing works

Adult neurogenesis and brain regeneration in zebrafish

Kızıl, Ç., Kaslin, J., Kroehne, V., & Brand, M. (2011) · Developmental Neurobiology · doi:10.1002/dneu.20918 · Cited by 346 · see citing works

Regulation of Neurogenesis by Interkinetic Nuclear Migration through an Apical-Basal Notch Gradient

Bene, F. D., Wehman, A. M., Link, B. A., & Baier, H. (2008) · Cell · doi:10.1016/j.cell.2008.07.017 · Cited by 339 · see citing works

Cloning, expression analysis, and chromosomal localization of murine and human homologues of aXenopus Mix gene

Robb, L. G., Hartley, L., Begley, C. G., Brodnicki, T. C., Copeland, N. G., Gilbert, D. J., Jenkins, N. A., & Elefanty, A. G. (2000) · Developmental Dynamics · doi:10.1002/1097-0177(2000)9999:9999 · Cited by 78 · see citing works

HRT1, HRT2, and HRT3: A New Subclass of bHLH Transcription Factors Marking Specific Cardiac, Somitic, and Pharyngeal Arch Segments

Nakagawa, O., Nakagawa, M., Richardson, J. A., Olson, E. N., & Srivastava, D. (1999) · Developmental Biology · doi:10.1006/dbio.1999.9454 · Cited by 282 · see citing works

HB-EGF is Necessary and Sufficient for Müller Glia Dedifferentiation and Retina Regeneration

Wan, J., Ramachandran, R., & Goldman, D. (2012) · Developmental Cell · doi:10.1016/j.devcel.2011.11.020 · Cited by 262 · see citing works

Notch activity levels control the balance between quiescence and recruitment of adult neural stem cells

Chapouton, P., Skupien, P., Hesl, B., Coolen, M., Moore, J. C., Madelaine, R., Kremmer, E., Faus-Kessler, T., Blader, P., Lawson, N. D., et al. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.6170-09.2010 · Cited by 259 · see citing works

Notch signaling regulates cardiomyocyte proliferation during zebrafish heart regeneration

Zhao, L., Borikova, A. L., Ben-Yair, R., Guner‐Ataman, B., MacRae, C. A., Lee, R. T., Burns, C. G., & Burns, C. E. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1311705111 · Cited by 255 · see citing works

An instructive function for Notch in promoting gliogenesis in the zebrafish retina

Scheer, N., Groth, A., Hans, S., & Campos‐Ortega, J. A. (2001) · Development · doi:10.1242/dev.128.7.1099 · Cited by 245 · see citing works

HERP, a Novel Heterodimer Partner of HES/E(spl) in Notch Signaling

Iso, T., Sartorelli, V., Poizat, C. I., Iezzi, S., Wu, H., Chung, G., Kedes, L., & Hamamori, Y. (2001) · Molecular and Cellular Biology · doi:10.1128/mcb.21.17.6080-6089.2001 · Cited by 217 · see citing works

HERP, a New Primary Target of Notch Regulated by Ligand Binding

Iso, T., Sartorelli, V., Chung, G., Shichinohe, T., Kedes, L., & Hamamori, Y. (2001) · Molecular and Cellular Biology · doi:10.1128/mcb.21.17.6071-6079.2001 · Cited by 191 · see citing works

Nrarp is a novel intracellular component of the Notch signaling pathwayPreprint

Lamar, E., Deblandre, G. A., Wettstein, D. A., Gawantka, V., Pollet, N., Niehrs, C., & Kintner, C. R. (2001) · Genes & Development · doi:10.1101/gad.908101 · Cited by 188 · see citing works

Delta/Notch signaling promotes formation of zebrafish neural crest by repressing Neurogenin 1 function

Cornell, R. A., & Eisen, J. S. (2002) · Development · doi:10.1242/dev.129.11.2639 · Cited by 185 · see citing works

Notch Signalling Synchronizes the Zebrafish Segmentation Clock but Is Not Needed To Create Somite Boundaries

Özbudak, E. M., & Lewis, J. H. (2008) · PLoS Genetics · doi:10.1371/journal.pgen.0040015 · Cited by 167 · see citing works

Multiple roles for Gata5 in zebrafish endoderm formation

Reiter, J. F., Kikuchi, Y., & Stainier, D. Y. R. (2001) · Development · doi:10.1242/dev.128.1.125 · Cited by 172 · see citing works

Two linkedhairy/Enhancer of split-related zebrafish genes,her1andher7, function together to refine alternating somite boundaries

Henry, C. A., Urban, M. K., Dill, K. K., Merlie, J. P., Page, M. F., Kimmel, C. B., & Amacher, S. L. (2002) · Development · doi:10.1242/dev.129.15.3693 · Cited by 164 · see citing works

Formation of the Ascidian Epidermal Sensory Neurons: Insights into the Origin of the Chordate Peripheral Nervous System

Pasini, A., Amiel, A., Rothbächer, U., Roure, A., Lemaire, P., & Darras, S. (2006) · PLoS Biology · doi:10.1371/journal.pbio.0040225 · Cited by 152 · see citing works

Fluorescent protein expression driven by her4 regulatory elements reveals the spatiotemporal pattern of Notch signaling in the nervous system of zebrafish embryos

Yeo, S., Kim, M., Kim, H.-S., Huh, T., & Chitnis, A. B. (2006) · Developmental Biology · doi:10.1016/j.ydbio.2006.10.020 · Cited by 154 · see citing works

her1, a zebrafish pair-rule like gene, acts downstream of notch signalling to control somite development

Takke, C., & Campos‐Ortega, J. A. (1999) · Development · doi:10.1242/dev.126.13.3005 · Cited by 153 · see citing works

Hes6 acts in a positive feedback loop with the neurogenins to promote neuronal differentiation

Koyano‐Nakagawa, N., Kim, J., Anderson, D. J., & Kintner, C. R. (2000) · Development · doi:10.1242/dev.127.19.4203 · Cited by 149 · see citing works

Expression of proneural and neurogenic genes in the zebrafish lateral line primordium correlates with selection of hair cell fate in neuromasts

Itoh, M., & Chitnis, A. B. (2001) · Mechanisms of Development · doi:10.1016/s0925-4773(01)00308-2 · Cited by 143 · see citing works

Notch Activation Regulates the Segregation and Differentiation of Rhombomere Boundary Cells in the Zebrafish Hindbrain

Cheng, Y., Amoyel, M., Qiu, X., Jiang, Y., Xu, Q., & Wilkinson, D. G. (2004) · Developmental Cell · doi:10.1016/s1534-5807(04)00097-8 · Cited by 141 · see citing works

Identification and Expression of a Novel Family of bHLH cDNAs Related to Drosophila Hairy and Enhancer of Split

Kokubo, H., Lun, Y., & Johnson, R. L. (1999) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.1999.0880 · Cited by 139 · see citing works

Notch3 signaling gates cell cycle entry and limits neural stem cell amplification in the adult pallium

Alunni, A., Krecsmarik, M., Bosco, A., Galant, S., Pan, L., Moens, C. B., & Bally‐Cuif, L. (2013) · Development · doi:10.1242/dev.095018 · Cited by 135 · see citing works

Jagged2a-Notch Signaling Mediates Cell Fate Choice in the Zebrafish Pronephric Duct

Ma, M., & Jiang, Y. (2007) · PLoS Genetics · doi:10.1371/journal.pgen.0030018 · Cited by 134 · see citing works

Hes1 but not Hes5 regulates an astrocyte versus oligodendrocyte fate choice in glial restricted precursors

Wu, Y.-Y., Liu, Y., Levine, E., & Rao, M. S. (2003) · Developmental Dynamics · doi:10.1002/dvdy.10278 · Cited by 138 · see citing works

Nemo-like kinase suppresses Notch signalling by interfering with formation of the Notch active transcriptional complex

Ishitani, T., Hirao, T., Suzuki, M., Isoda, M., Ishitani, S., Harigaya, K., Kitagawa, M., Matsumoto, K., & Itoh, M. (2010) · Nature Cell Biology · doi:10.1038/ncb2028 · Cited by 131 · see citing works

Notch signalling regulates left-right asymmetry through ciliary length control

Lopes, S. S., Lourenço, R., Pacheco, L. G. C. A., Moreno, N., Kreiling, J. A., & Saúde, L. (2010) · Development · doi:10.1242/dev.054452 · Cited by 126 · see citing works

The genetics and embryology of zebrafish metamerism

Holley, S. A. (2007) · Developmental Dynamics · doi:10.1002/dvdy.21162 · Cited by 123 · see citing works

Notch–Delta signaling is required for spatial patterning and Müller glia differentiation in the zebrafish retina

Bernardos, R. L., Lentz, S. I., Wolfe, M. S., & Raymond, P. A. (2004) · Developmental Biology · doi:10.1016/j.ydbio.2004.11.018 · Cited by 117 · see citing works

Notch activity in the nervous system: to switch or not switch?

Cau, E., & Blader, P. (2009) · Neural Development · doi:10.1186/1749-8104-4-36 · Cited by 109 · see citing works

Histone deacetylase 1 is required to repress Notch target gene expression during zebrafish neurogenesis and to maintain the production of motoneurones in response to hedgehog signalling

Cunliffe, V. T. (2004) · Development · doi:10.1242/dev.01166 · Cited by 111 · see citing works

Notch‐regulated oligodendrocyte specification from radial glia in the spinal cord of zebrafish embryos

Kim, H., Shin, J., Kim, S., Poling, J., Park, H., & Appel, B. (2008) · Developmental Dynamics · doi:10.1002/dvdy.21620 · Cited by 99 · see citing works

Basal body proteins regulate Notch signaling via endosomal trafficking

Leitch, C. C., Lodh, S., Prieto-Echagüe, V., Badano, J. L., & Zaghloul, N. A. (2014) · Journal of Cell Science · doi:10.1242/jcs.130344 · Cited by 98 · see citing works

Ciliopathy proteins regulate paracrine signaling by modulating proteasomal degradation of mediators

Liu, Y. P., Tsai, I.-C., Morleo, M., Oh, E. C. T., Leitch, C. C., Massa, F., Lee, B., Parker, D. S., Finley, D. J., Zaghloul, N. A., et al. (2014) · Journal of Clinical Investigation · doi:10.1172/jci71898 · Cited by 94 · see citing works

Common and Distinct Features of Adult Neurogenesis and Regeneration in the Telencephalon of Zebrafish and Mammals

Diotel, N., Lübke, L., Strähle, U., & Rastegar, S. (2020) · Frontiers in Neuroscience · doi:10.3389/fnins.2020.568930 · Cited by 93 · see citing works

Neural stem cell quiescence and stemness are molecularly distinct outputs of the Notch3 signalling cascade in the vertebrate adult brain

Than‐Trong, E., Ortica, S., Mella, S., Nepal, C., Alunni, A., & Bally‐Cuif, L. (2018) · Development · doi:10.1242/dev.161034 · Cited by 88 · see citing works

Dual Roles of Notch in Regulation of Apically Restricted Mitosis and Apicobasal Polarity of Neuroepithelial Cells

Ohata, S., Aoki, R., Kinoshita, S., Yamaguchi, M., Tsuruoka-Kinoshita, S., Tanaka, H., Wada, H., Watabe, S., Tsuboi, T., Masai, I., et al. (2011) · Neuron · doi:10.1016/j.neuron.2010.12.026 · Cited by 92 · see citing works

Identification of cis regulatory features in the embryonic zebrafish genome through large-scale profiling of H3K4me1 and H3K4me3 binding sites

Aday, A. W., Zhu, L. J., Lakshmanan, A., Wang, J., & Lawson, N. D. (2011) · Developmental Biology · doi:10.1016/j.ydbio.2011.03.007 · Cited by 90 · see citing works

Mib-Jag1-Notch signalling regulates patterning and structural roles of the notochord by controlling cell-fate decisions

Yamamoto, M., Morita, R., Mizoguchi, T., Matsuo, H., Isoda, M., Ishitani, T., Chitnis, A. B., Matsumoto, K., Crump, J. G., Hozumi, K., et al. (2010) · Development · doi:10.1242/dev.051011 · Cited by 90 · see citing works

Nrarp functions to modulate neural-crest-cell differentiation by regulating LEF1 protein stability

Ishitani, T., Matsumoto, K., Chitnis, A. B., & Itoh, M. (2005) · Nature Cell Biology · doi:10.1038/ncb1311 · Cited by 89 · see citing works

bHLH transcription factor Her5 links patterning to regional inhibition of neurogenesis at the midbrain-hindbrain boundary

Geling, A., Itoh, M., Tallafuß, A., Chapouton, P., Tannhäuser, B., Kuwada, J. Y., Chitnis, A. B., & Bally‐Cuif, L. (2003) · Development · doi:10.1242/dev.00375 · Cited by 87 · see citing works

Notch signaling regulates neural precursor allocation and binary neuronal fate decisions in zebrafish

Shin, J., Poling, J., Park, H., & Appel, B. (2007) · Development · doi:10.1242/dev.001602 · Cited by 87 · see citing works

Sequence and embryonic expression of deltaC in the zebrafish

Smithers, L. E., Haddon, C., Jiang, Y., & Lewis, J. H. (2000) · Mechanisms of Development · doi:10.1016/s0925-4773(99)00231-2 · Cited by 86 · see citing works

Evolutionary Conservation of the Presumptive Neural Plate Markers AmphiSox1/2/3 and AmphiNeurogenin in the Invertebrate Chordate Amphioxus

Holland, L. Z., Schubert, M., Holland, N. D., & Neuman, T. (2000) · Developmental Biology · doi:10.1006/dbio.2000.9810 · Cited by 86 · see citing works

her5expression reveals a pool of neural stem cells in the adult zebrafish midbrain

Chapouton, P., Adolf, B., Leucht, C., Tannhäuser, B., Ryu, S., Driever, W., & Bally‐Cuif, L. (2006) · Development · doi:10.1242/dev.02573 · Cited by 84 · see citing works

Atoh1a expression must be restricted by Notch signaling for effective morphogenesis of the posterior lateral line primordium in zebrafish

Matsuda, M., & Chitnis, A. B. (2010) · Development · doi:10.1242/dev.052761 · Cited by 81 · see citing works

Patterning of proneuronal and inter-proneuronal domains byhairy- andenhancer of split-related genes in zebrafish neuroectoderm

Bae, Y., Shimizu, T., & Hibi, M. (2005) · Development · doi:10.1242/dev.01710 · Cited by 79 · see citing works

A quantitative analysis of the kinetics of Gal4 activator and effector gene expression in the zebrafish

Scheer, N., Riedl, I., Warren, J. T., Kuwada, J. Y., & Campos‐Ortega, J. A. (2002) · Mechanisms of Development · doi:10.1016/s0925-4773(01)00621-9 · Cited by 75 · see citing works

Expression of Hairy/enhancer of split genes in neural progenitors and neurogenesis domains of the adult zebrafish brain

Chapouton, P., Webb, K. J., Stigloher, C., Alunni, A., Adolf, B., Hesl, B., Topp, S., Kremmer, E., & Bally‐Cuif, L. (2011) · The Journal of Comparative Neurology · doi:10.1002/cne.22599 · Cited by 73 · see citing works

Activation of Xenopus Genes Required for Lateral Inhibition and Neuronal Differentiation during Primary Neurogenesis

Koyano‐Nakagawa, N., Wettstein, D. A., & Kintner, C. R. (1999) · Molecular and Cellular Neuroscience · doi:10.1006/mcne.1999.0783 · Cited by 73 · see citing works

Genome-wide loss-of-function analysis of deubiquitylating enzymes for zebrafish development

Tse, W. K. F., Eisenhaber, B., Ho, S. H., Ng, Q., Eisenhaber, F., & Jiang, Y. (2009) · BMC Genomics · doi:10.1186/1471-2164-10-637 · Cited by 72 · see citing works

Her5 acts as a prepattern factor that blocks neurogenin1 and coe2 expression upstream of Notch to inhibit neurogenesis at the midbrain-hindbrain boundary

Geling, A., Plessy, C., Rastegar, S., Strähle, U., & Bally‐Cuif, L. (2004) · Development · doi:10.1242/dev.01093 · Cited by 71 · see citing works

Mutations in FAM50A suggest that Armfield XLID syndrome is a spliceosomopathy

Lee, Y., Khan, K., Uhas, K. A., Srikanth, S., Thompson, N., Pardo, M., Yu, L., Norris, J. W., Peng, Y., Gripp, K. W., et al. (2020) · Nature Communications · doi:10.1038/s41467-020-17452-6 · Cited by 71 · see citing works

let-7 MicroRNA-Mediated Regulation of Shh Signaling and the Gene Regulatory Network Is Essential for Retina Regeneration

Kaur, S. J., Gupta, S., Chaudhary, M., Khursheed, M. A., Mitra, S., Kurup, A. J., & Ramachandran, R. (2018) · Cell Reports · doi:10.1016/j.celrep.2018.04.002 · Cited by 66 · see citing works

Activator-to-Repressor Conversion of T-Box Transcription Factors by the Ripply Family of Groucho/TLE-Associated Mediators

Kawamura, A., Koshida, S., & Takada, S. (2008) · Molecular and Cellular Biology · doi:10.1128/mcb.01754-07 · Cited by 67 · see citing works

MiRNA expression analysis during normal zebrafish development and following inhibition of the Hedgehog and Notch signaling pathways

Thatcher, E. J., Flynt, A. S., Li, N., Patton, J. R., & Patton, J. G. (2007) · Developmental Dynamics · doi:10.1002/dvdy.21211 · Cited by 66 · see citing works

Three modules of zebrafish Mind bomb work cooperatively to promote Delta ubiquitination and endocytosis

Chen, W., & Corliss, D. C. (2004) · Developmental Biology · doi:10.1016/j.ydbio.2003.11.010 · Cited by 65 · see citing works

her3, a zebrafish member of thehairy-E(spl)family, is repressed by Notch signalling

Hans, S., Scheer, N., Riedl, I., Weizsäcker, E. V., Blader, P., & Campos‐Ortega, J. A. (2004) · Development · doi:10.1242/dev.01167 · Cited by 64 · see citing works

Interaction with Notch determines endocytosis of specific Delta ligands in zebrafish neural tissue

Matsuda, M., & Chitnis, A. B. (2008) · Development · doi:10.1242/dev.027938 · Cited by 59 · see citing works

Identification of NKL, a novel Gli-Kruppel zinc-finger protein that promotes neuronal differentiation

Lamar, E., Kintner, C. R., & Goulding, M. (2001) · Development · doi:10.1242/dev.128.8.1335 · Cited by 59 · see citing works

Her9 represses neurogenic fate downstream of Tbx1 and retinoic acid signaling in the inner ear

Radosevic, M., Robert‐Moreno, A., Coolen, M., Bally‐Cuif, L., & Alsina, B. (2011) · Development · doi:10.1242/dev.056093 · Cited by 56 · see citing works

Lunatic fringe promotes the lateral inhibition of neurogenesis

Nikolaou, N., Watanabe‐Asaka, T., Gerety, S. S., Distel, M., Köster, R. W., & Wilkinson, D. G. (2009) · Development · doi:10.1242/dev.034736 · Cited by 57 · see citing works

A Nuclear Role for miR-9 and Argonaute Proteins in Balancing Quiescent and Activated Neural Stem Cell States

Katz, S., Cussigh, D., Urbán, N., Blomfield, I. M., Guillemot, F., Bally‐Cuif, L., & Coolen, M. (2016) · Cell Reports · doi:10.1016/j.celrep.2016.09.088 · Cited by 53 · see citing works

Homologues of c-hairy1 (her9) and lunatic fringe in zebrafish are expressed in the developing central nervous system, but not in the presomitic mesoderm

Leve, C., Gajewski, M., Rohr, K. B., & Tautz, D. (2001) · Development Genes and Evolution · doi:10.1007/s00427-001-0181-4 · Cited by 55 · see citing works

Delta-Notch signaling induces hypochord development in zebrafish

Latimer, A. J., Dong, X., Markov, Y., & Appel, B. (2002) · Development · doi:10.1242/dev.129.11.2555 · Cited by 53 · see citing works

The characterization of zebrafish antimorphic mib alleles reveals that Mib and Mind bomb-2 (Mib2) function redundantly

Zhang, C., Li, Q., Lim, C.-H., Qiu, X., & Jiang, Y. (2007) · Developmental Biology · doi:10.1016/j.ydbio.2007.01.034 · Cited by 52 · see citing works

Interference with splicing of Presenilin transcripts has potent dominant negative effects on Presenilin activity

Nornes, S., Newman, M., Verdile, G., Wells, S., Stoick-Cooper, C. L., Tucker, B., Frederich-Sleptsova, I., Martins, R. N., & Lardelli, M. T. (2007) · Human Molecular Genetics · doi:10.1093/hmg/ddm317 · Cited by 51 · see citing works

Patterning and cell fate in the inner ear: a case for N otch in the chicken embryo

Neves, J., Abelló, G., Petrovic, J., & Giráldez, F. (2012) · Development Growth & Differentiation · doi:10.1111/dgd.12016 · Cited by 50 · see citing works

Notch signaling regulates midline cell specification and proliferation in zebrafish

Latimer, A. J., & Appel, B. (2006) · Developmental Biology · doi:10.1016/j.ydbio.2006.05.039 · Cited by 50 · see citing works

Embryonic origin and lineage hierarchies of the neural progenitor subtypes building the zebrafish adult midbrain

Galant, S., Furlan, G., Coolen, M., Dirian, L., Foucher, I., & Bally‐Cuif, L. (2016) · Developmental Biology · doi:10.1016/j.ydbio.2016.09.022 · Cited by 50 · see citing works

Completing the set of h/E(spl) cyclic genes in zebrafish: her12 and her15 reveal novel modes of expression and contribute to the segmentation clock

Shankaran, S. S., Sieger, D., Schröter, C. J., Czepe, C., Pauly, M.-C., Laplante, M. A., Becker, T. S., Oates, A. C., & Gajewski, M. (2007) · Developmental Biology · doi:10.1016/j.ydbio.2007.01.004 · Cited by 50 · see citing works

Characterization of expanded intermediate cell mass in zebrafish chordin morphant embryos

Leung, A. Y. H., Mendenhall, E. M., Kwan, T. T. F., Liang, R., Eckfeldt, C. E., Chen, E. Y., Hammerschmidt, M., Grindley, S., Ekker, S. C., & Verfaillie, C. M. (2004) · Developmental Biology · doi:10.1016/j.ydbio.2004.09.032 · Cited by 50 · see citing works

Characterization and Developmental Expression of the Amphioxus Homolog of Notch (AmphiNotch): Evolutionary Conservation of Multiple Expression Domains in Amphioxus and Vertebrates

Holland, L. Z., Abi‐Rached, L., Tamme, R., Holland, N. D., Inoko, H., Shiina, T., Burgtorf, C., & Lardelli, M. T. (2001) · Developmental Biology · doi:10.1006/dbio.2001.0160 · Cited by 49 · see citing works

Notch signaling can regulate endoderm formation in zebrafish

Kikuchi, Y., Verkade, H. M., Reiter, J. F., Kim, C., Chitnis, A. B., Kuroiwa, A., & Stainier, D. Y. R. (2004) · Developmental Dynamics · doi:10.1002/dvdy.10483 · Cited by 49 · see citing works

Mecp2 regulates neural cell differentiation by suppressing the Id1 to Her2 axis in zebrafish

Gao, H. F., Bu, Y., Wu, Q., Wang, X., Chang, N., Lei, L., Chen, S., Liu, D. N., Zhu, X., Hu, K., et al. (2015) · Journal of Cell Science · doi:10.1242/jcs.167874 · Cited by 48 · see citing works

Perineurial Glia Require Notch Signaling during Motor Nerve Development but Not Regeneration

Binari, L. A., Lewis, G. M., & Kucenas, S. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.4893-12.2013 · Cited by 48 · see citing works

Identification of neural progenitor pools by E(Spl) factors in the embryonic and adult brain

Stigloher, C., Chapouton, P., Adolf, B., & Bally‐Cuif, L. (2007) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2007.10.032 · Cited by 48 · see citing works

Two zebrafish Notch-dependenthairy/Enhancer-of-split-relatedgenes,her6andher4, are required to maintain the coordination of cyclic gene expression in the presomitic mesoderm

Pasini, A., Jiang, Y., & Wilkinson, D. G. (2004) · Development · doi:10.1242/dev.01031 · Cited by 46 · see citing works

Notch Signaling Can Inhibit Xath5 Function in the Neural Plate and Developing Retina

Schneider, M. L., Turner, D. L., & Vetter, M. L. (2001) · Molecular and Cellular Neuroscience · doi:10.1006/mcne.2001.1040 · Cited by 45 · see citing works

Coregulation of anterior and posterior mesendodermal development by a hairy-related transcriptional repressorPreprint

Bally-Cuif, L., Goutel, C., Wassef, M., Wurst, W., & Rosa, F. (2000) · Genes & Development · doi:10.1101/gad.14.13.1664 · Cited by 45 · see citing works

Specification and positioning of the anterior neuroectoderm in deuterostome embryos

Range, R. (2014) · genesis · doi:10.1002/dvg.22759 · Cited by 43 · see citing works

her11 is involved in the somitogenesis clock in zebrafish

Sieger, D., Tautz, D., & Gajewski, M. (2004) · Development Genes and Evolution · doi:10.1007/s00427-004-0427-z · Cited by 43 · see citing works

Antagonizing Activity of Chick Grg4 against Tectum-Organizing Activity

Sugiyama, S., Funahashi, J., & Nakamura, H. (2000) · Developmental Biology · doi:10.1006/dbio.2000.9643 · Cited by 41 · see citing works

Neuroepithelial cells require fucosylated glycans to guide the migration of vagus motor neuron progenitors in the developing zebrafish hindbrain

Ohata, S., Kinoshita, S., Aoki, R., Tanaka, H., Wada, H., Tsuruoka-Kinoshita, S., Tsuboi, T., Watabe, S., & Okamoto, H. (2009) · Development · doi:10.1242/dev.033290 · Cited by 40 · see citing works

notch3 is essential for oligodendrocyte development and vascular integrity in zebrafish

Zaucker, A., Mercurio, S., Sternheim, N., Talbot, W. S., & Marlow, F. L. (2013) · Disease Models & Mechanisms · doi:10.1242/dmm.012005 · Cited by 40 · see citing works

Combined activity of the two Gli2 genes of zebrafish play a major role in Hedgehog signaling during zebrafish neurodevelopment.

Ke, Z., Kondrichin, I., Gong, Z., & Korzh, V. (2008) · Molecular and cellular neurosciences · doi:10.1016/j.mcn.2007.10.013 · Cited by 40 · see citing works

A Self-Organizing miR-132/Ctbp2 Circuit Regulates Bimodal Notch Signals and Glial Progenitor Fate Choice during Spinal Cord Maturation

Salta, E., Lau, P., Frigerio, C. S., Coolen, M., Bally‐Cuif, L., & Strooper, B. D. (2014) · Developmental Cell · doi:10.1016/j.devcel.2014.07.006 · Cited by 38 · see citing works

Single-cell RNA sequencing unravels the transcriptional network underlying zebrafish retina regeneration

Celotto, L., Rost, F., Machate, A., Bläsche, J., Dahl, A., Weber, A., Hans, S., & Brand, M. (2023) · eLife · doi:10.7554/elife.86507 · Cited by 36 · see citing works

The Notch-effectorHRT1gene plays a role in glomerular development and patterning of theXenopuspronephros anlagen

Taelman, V. F., Campenhout, C. V., Sölter, M., Pieler, T., & Bellefroid, E. (2006) · Development · doi:10.1242/dev.02458 · Cited by 37 · see citing works

her9 promotes floor plate development in zebrafish

Latimer, A. J., Shin, J., & Appel, B. (2005) · Developmental Dynamics · doi:10.1002/dvdy.20264 · Cited by 37 · see citing works

Dner inhibits neural progenitor proliferation and induces neuronal and glial differentiation in zebrafish

Hsieh, F.-Y., Ma, T., Shih, H., Lin, S., Huang, C.-W., Wang, H.-Y., & Cheng, Y. (2013) · Developmental Biology · doi:10.1016/j.ydbio.2013.01.007 · Cited by 36 · see citing works

Comparative analysis of her genes during fish somitogenesis suggests a mouse/chick-like mode of oscillation in medaka

Gajewski, M., Elmasri, H., Girschick, M., Sieger, D., & Winkler, C. (2006) · Development Genes and Evolution · doi:10.1007/s00427-006-0059-6 · Cited by 36 · see citing works

Fluorescent protein expression driven by her4 regulatory elements reveals the spatiotemporal pattern of Notch signaling in the nervous system of zebrafish embryos

Yeo, S., Kim, M., Kim, H.-S., Huh, T., & Chitnis, A. B. (2006) · Developmental Biology · doi:10.1016/j.ydbio.2006.10.020 · Cited by 154 · see citing works

Genetic Mechanism That Defines the Characteristic Neurogenesis Patterns in the Neural Plate Using Hes/her Genes During Early Vertebrate Development

Ohyanagi, T., Tokizaki, H., Sato, T., Tsuruoka, M., & Yamasu, K. (2025) · genesis · doi:10.1002/dvg.70015 · Cited by 2 · see citing works

Zebrafish Her8a Is Activated by Su(H)-Dependent Notch Signaling and Is Essential for the Inhibition of Neurogenesis

Chung, P.-C., Lin, W.-S., Scotting, P. J., Hsieh, F.-Y., Wu, H., & Cheng, Y. (2011) · PLoS ONE · doi:10.1371/journal.pone.0019394 · Cited by 26 · see citing works

Zebrafish Her8a Is Activated by Su(H)-Dependent Notch Signaling and Is Essential for the Inhibition of

Chung, P.-C., Lin, W.-S., Scotting, P. J., Hsieh, F.-Y., Wu, H.-L., & Cheng, Y.-C. (2011)

her3, a zebrafish member of thehairy-E(spl)family, is repressed by Notch signalling

Hans, S., Scheer, N., Riedl, I., Weizsäcker, E. V., Blader, P., & Campos‐Ortega, J. A. (2004) · Development · doi:10.1242/dev.01167 · Cited by 64 · see citing works