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

Subventricular zone astrocytes are neural stem cells in the adult mammalian brain

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Mechanisms and Functional Implications of Adult Neurogenesis

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Astrocytes give rise to new neurons in the adult mammalian hippocampus

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Bmi-1 dependence distinguishes neural stem cell self-renewal from progenitor proliferation

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Neural stem cells confer unique pinwheel architecture to the ventricular surface in neurogenic regions of the adult brain

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Increasing p16INK4a expression decreases forebrain progenitors and neurogenesis during ageing

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Oscillations in Notch Signaling Regulate Maintenance of Neural Progenitors

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Notch signalling limits angiogenic cell behaviour in developing zebrafish arteries

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Neuroanatomy of the Zebrafish Brain

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Late-stage neuronal progenitors in the retina are radial Müller glia that function as retinal stem cells

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Cell types, lineage, and architecture of the germinal zone in the adult dentate gyrus

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Hes genes regulate size, shape and histogenesis of the nervous system by control of the timing of neural stem cell differentiation

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Neural stem cells and neurogenesis in the adult zebrafish brain: Origin, proliferation dynamics, migration and cell fate

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

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Forebrain ependymal cells are Notch-dependent and generate neuroblasts and astrocytes after stroke

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Structural Basis for Cooperativity in Recruitment of MAML Coactivators to Notch Transcription Complexes

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p21 loss compromises the relative quiescence of forebrain stem cell proliferation leading to exhaustion of their proliferation capacity

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Endothelial signalling by the Notch ligand Delta-like 4 restricts angiogenesis

Leslie, J. D., Ariza‐McNaughton, L., Bermange, A. L., Mcadow, R., Johnson, S. L., & Lewis, J. H. (2007) · Development · doi:10.1242/dev.003244 · Cited by 415 · see citing works

Notch regulates cell fate and dendrite morphology of newborn neurons in the postnatal dentate gyrus

Breunig, J. J., Silbereis, J. C., Vaccarino, F. M., Šestan, N., & RAKIC, P. T. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0710156104 · Cited by 402 · see citing works

Conserved and acquired features of adult neurogenesis in the zebrafish telencephalon

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Delta Notch and then? Protein interactions and proposed modes of repression by Hes and Hey bHLH factors

Fischer, A., & Gessler, M. (2007) · Nucleic Acids Research · doi:10.1093/nar/gkm477 · Cited by 400 · see citing works

Simultaneous prospective purification of adult subventricular zone neural stem cells and their progeny

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GFAP transgenic zebrafish

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Growth Suppression of Pre-T Acute Lymphoblastic Leukemia Cells by Inhibition of Notch Signaling

Weng, A. P., Nam, Y., Wolfe, M. S., Pear, W. S., Griffin, J. D., Blacklow, S. C., & Aster, J. C. (2003) · Molecular and Cellular Biology · doi:10.1128/mcb.23.2.655-664.2003 · Cited by 369 · see citing works

Notch-responsive cells initiate the secondary transition in larval zebrafish pancreas

Parsons, M. J., Pisharath, H., Yusuff, S., Moore, J. C., Siekmann, A., Lawson, N., & Leach, S. (2009) · Mechanisms of Development · doi:10.1016/j.mod.2009.07.002 · Cited by 354 · see citing works

Committed Neuronal Precursors Confer Astrocytic Potential on Residual Neural Precursor Cells

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The subcellular locations of p15(Ink4b) and p27(Kip1) coordinate their inhibitory interactions with cdk4 and cdk2.Preprint

Reynisdóttir, I., & Massagué, J. (1997) · Genes & Development · doi:10.1101/gad.11.4.492 · Cited by 332 · see citing works

<i>Ink4a</i> and <i>Arf</i> differentially affect cell proliferation and neural stem cell self-renewal in <i>Bmi1</i>-deficient mice

Bruggeman, S. W. M., Valk-Lingbeek, M. E., van der Stoop, P. P. M., Jacobs, J. J. L., Kieboom, K., Tanger, E., Hulsman, D., Leung, C., Arsenijevic, Y., Marino, S., et al. (2005) · Genes &amp; Development · doi:10.1101/gad.1299305 · Cited by 315 · see citing works

INK4 proteins, a family of mammalian CDK inhibitors with novel biological functions

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Control of the Reversibility of Cellular Quiescence by the Transcriptional Repressor HES1

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

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Identification of aromatase‐positive radial glial cells as progenitor cells in the ventricular layer of the forebrain in zebrafish

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Multiple delta genes and lateral inhibition in zebrafish primary neurogenesis

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Heterogeneity in progenitor cell subtypes in the ventricular zone of the zebrafish adult telencephalon

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Transcription Factor Expression and Notch-Dependent Regulation of Neural Progenitors in the Adult Rat Spinal Cord

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Notch 1 inhibits photoreceptor production in the developing mammalian retina

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Notch1 and its ligands Delta-like and Jagged are expressed and active in distinct cell populations in the postnatal mouse brain

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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

Notch Signaling Regulates the Extent of Hair Cell Regeneration in the Zebrafish Lateral Line

Ma, E. Y., Rubel, E. W., & Raible, D. W. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.4372-07.2008 · Cited by 244 · see citing works

Delta-Notch signaling regulates oligodendrocyte specification

Park, H.-C., & Appel, B. (2003) · Development · doi:10.1242/dev.00576 · Cited by 221 · see citing works

Persistent and high levels of Hes1 expression regulate boundary formation in the developing central nervous system

Baek, J. H., Hatakeyama, J., Sakamoto, S., Ohtsuka, T., & Kageyama, R. (2006) · Development · doi:10.1242/dev.02403 · Cited by 219 · see citing works

Progenitor cell proliferation in the retina is dependent on Notch-independent Sonic hedgehog/Hes1 activity

Wall, D. S., Mears, A. J., McNeill, B., Mazerolle, C. J., Thurig, S., Wang, Y., Kageyama, R., & Wallace, V. A. (2009) · The Journal of Cell Biology · doi:10.1083/jcb.200805155 · Cited by 208 · see citing works

Sustained Notch signaling in progenitors is required for sequential emergence of distinct cell lineages during organogenesisPreprint

Zhu, X., Zhang, J., Tollkühn, J., Ohsawa, R., Bresnick, E. H., Guillemot, F., Kageyama, R., & Rosenfeld, M. G. (2006) · Genes & Development · doi:10.1101/gad.1444706 · Cited by 207 · see citing works

Adult neurogenesis in non‐mammalian vertebrates

Chapouton, P., Jagasia, R., & Bally‐Cuif, L. (2007) · BioEssays · doi:10.1002/bies.20615 · Cited by 201 · see citing works

Mind Bomb 1-Expressing Intermediate Progenitors Generate Notch Signaling to Maintain Radial Glial Cells

Yoon, K., Koo, B., Im, S.-K., Jeong, H., Ghim, J., Kwon, M.-C., Moon, J.-S., Miyata, T., & Kong, Y. (2008) · Neuron · doi:10.1016/j.neuron.2008.03.018 · Cited by 198 · see citing works

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

Takke, C., Dornseifer, P., Weizsäcker, E. V., & Campos-Ortega, J. A. (1999) · Development · doi:10.1242/dev.126.9.1811 · Cited by 192 · see citing works

gfap and nestin reporter lines reveal characteristics of neural progenitors in the adult zebrafish brain

Lam, C. S., März, M., & Strähle, U. (2009) · Developmental Dynamics · doi:10.1002/dvdy.21853 · Cited by 185 · see citing works

Spatiotemporal selectivity of response to Notch1 signals in mammalian forebrain precursors

Chambers, C. B., Peng, Y., Nguyen, H., Gaiano, N., Fishell, G., & Nye, J. S. (2001) · Development · doi:10.1242/dev.128.5.689 · Cited by 184 · see citing works

Notch and MAML Signaling Drives Scl-Dependent Interneuron Diversity in the Spinal Cord

Peng, C., Yajima, H., Burns, C. E., Zon, L. I., Sisodia, S. S., Pfaff, S. L., & Sharma, K. (2007) · Neuron · doi:10.1016/j.neuron.2007.02.019 · Cited by 178 · see citing works

Control of DNA replication and its potential clinical exploitation

Gonzalez, M., Tachibana, K.-E. K., Laskey, R. A., & Coleman, N. (2005) · Nature reviews. Cancer · doi:10.1038/nrc1548 · Cited by 169 · see citing works

Notch Signaling in Astrocytes and Neuroblasts of the Adult Subventricular Zone in Health and after Cortical Injury

Givogri, M. I., de Planell, M., Galbiati, F., Superchi, D., Gritti, A., Vescovi, A. L., de Vellis, J., & Bongarzone, E. R. (2006) · Developmental Neuroscience · doi:10.1159/000090755 · Cited by 145 · see citing works

Notch signalling in development: on equivalence groups and asymmetric developmental potential

Simpson, P. (1997) · Current Opinion in Genetics & Development · doi:10.1016/s0959-437x(97)80083-4 · Cited by 140 · see citing works

Temporally Regulated Asymmetric Neurogenesis Causes Left-Right Difference in the Zebrafish Habenular Structures

Aizawa, H., Goto, M., Sato, T., & Okamoto, H. (2007) · Developmental Cell · doi:10.1016/j.devcel.2006.10.004 · Cited by 128 · 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

Oligodendrocyte Specification in Zebrafish Requires Notch-Regulated Cyclin-Dependent Kinase Inhibitor Function

Park, H., Boyce, J., Shin, J., & Appel, B. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.0981-05.2005 · Cited by 117 · see citing works

Visualization of embryonic neural stem cells using Hes promoters in transgenic mice

Ohtsuka, T., Imayoshi, I., Shimojo, H., Nishi, E., Kageyama, R., & McConnell, S. K. (2005) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2005.09.006 · Cited by 116 · see citing works

FGF induces oscillations of Hes1 expression and Ras/ERK activation

Nakayama, K., Satoh, T., Igari, A., Kageyama, R., & Nishida, E. (2008) · Current Biology · doi:10.1016/j.cub.2008.03.013 · Cited by 114 · see citing works

Notch regulation of progenitor cell behavior in quiescent and regenerating auditory epithelium of mature birds

Daudet, N., Gibson, R. M., Shang, J., Bernard, A., Lewis, J. H., & Stone, J. S. (2008) · Developmental Biology · doi:10.1016/j.ydbio.2008.10.033 · Cited by 98 · see citing works

Notch-independent regulation of Hes-1 expression by c-Jun N-terminal kinase signaling in human endothelial cells

Curry, C. L., Reed, L. L., Nickoloff, B. J., Miele, L., & Foreman, K. E. (2006) · Laboratory Investigation · doi:10.1038/labinvest.3700442 · Cited by 94 · 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

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

Jagged-mediated Notch signaling maintains proliferating neural progenitors and regulates cell diversity in the ventral spinal cord

Yeo, S., & Chitnis, A. B. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0607062104 · Cited by 64 · see citing works

Fgf signaling in the zebrafish adult brain: Association of Fgf activity with ventricular zones but not cell proliferation

Topp, S., Stigloher, C., Komisarczuk, A. Z., Adolf, B., Becker, T. S., & Bally‐Cuif, L. (2008) · The Journal of Comparative Neurology · doi:10.1002/cne.21802 · Cited by 49 · see citing works

Instability of Notch1 and Delta1 mRNAs and reduced Notch activity in vertebrate neuroepithelial cells undergoing S-phase

Cisneros, E., Latasa, M. J., García‐Flores, M., & Frade, J. M. (2008) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2008.01.011 · Cited by 35 · see citing works

Notch resolves mixed neural identities in the zebrafish epiphysis

Cau, E., Quillien, A., & Blader, P. (2008) · Development · doi:10.1242/dev.013482 · Cited by 31 · see citing works

Hes genes regulate size, shape and histogenesis of the nervous system by control of the timing of neural stem cell differentiation

畠山, 淳. (2005) · Medical Entomology and Zoology · Cited by 29 · see citing works

Notch resolves mixed neural identities in the zebrafish epiphysis

Cau, E., Quillien, A., & Blader, P. (2008) · Development · doi:10.1242/dev.026310 · Cited by 7 · see citing works

Molecular regulation of stem cell quiescence

Cheung, T. H., & Rando, T. A. (2013) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3591 · Cited by 1,148 · see citing works

Notch Signaling in Development, Tissue Homeostasis, and Disease

Siebel, C., & Lendahl, U. (2017) · Physiological Reviews · doi:10.1152/physrev.00005.2017 · Cited by 968 · see citing works

Notch Signaling Is Necessary to Maintain Quiescence in Adult Muscle Stem Cells

Bjornson, C. R. R., Cheung, T. H., Liu, L., Tripathi, P. V., Steeper, K. M., & Rando, T. A. (2012) · Stem Cells · doi:10.1002/stem.773 · Cited by 598 · see citing works

A Critical Requirement for Notch Signaling in Maintenance of the Quiescent Skeletal Muscle Stem Cell State

Mourikis, P., Sambasivan, R., Castel, D., Rocheteau, P., Bizzarro, V., & Tajbakhsh, S. (2012) · Stem Cells · doi:10.1002/stem.775 · Cited by 526 · see citing works

The stem cell potential of glia: lessons from reactive gliosis

Robel, S., Berninger, B., & Götz, M. (2011) · Nature reviews. Neuroscience · doi:10.1038/nrn2978 · Cited by 513 · see citing works

Neurogenesis in the embryonic and adult brain: same regulators, different roles

Urbán, N., & Guillemot, F. (2014) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2014.00396 · Cited by 493 · see citing works

Not(ch) just development: Notch signalling in the adult brain

Ables, J. L., Breunig, J. J., Eisch, A. J., & RAKIC, P. T. (2011) · Nature reviews. Neuroscience · doi:10.1038/nrn3024 · Cited by 460 · 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 Neural Stem Cells Bridge Their Niche

Fuentealba, L. C., Obernier, K., & Álvarez-Buylla, A. (2012) · Cell stem cell · doi:10.1016/j.stem.2012.05.012 · Cited by 367 · see citing works

Clinical and Therapeutic Implications of Cancer Stem Cells

Clarke, M. F. (2019) · New England Journal of Medicine · doi:10.1056/nejmra1804280 · Cited by 355 · see citing works

Notch in the Vertebrate Nervous System: An Old Dog with New Tricks

Pierfelice, T. J., Alberi, L. A., & Gaiano, N. (2011) · Neuron · doi:10.1016/j.neuron.2011.02.031 · Cited by 353 · 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

Müller glia: Stem cells for generation and regeneration of retinal neurons in teleost fish

Lenkowski, J. R., & Raymond, P. A. (2014) · Progress in Retinal and Eye Research · doi:10.1016/j.preteyeres.2013.12.007 · Cited by 322 · see citing works

Stem cells living with a Notch

Koch, U., Lehal, R., & Radtke, F. (2013) · Development · doi:10.1242/dev.080614 · Cited by 283 · see citing works

Glial Cells as Progenitors and Stem Cells: New Roles in the Healthy and Diseased Brain

Dimou, L., & Götz, M. (2014) · Physiological Reviews · doi:10.1152/physrev.00036.2013 · Cited by 263 · 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

Heterogeneity in progenitor cell subtypes in the ventricular zone of the zebrafish adult telencephalon

März, M., Chapouton, P., Diotel, N., Vaillant, C., Hesl, B., Takamiya, M., Lam, C. S., Kah, O., Bally‐Cuif, L., & Strähle, U. (2010) · Glia · doi:10.1002/glia.20971 · Cited by 257 · see citing works

Retina regeneration in zebrafish

Wan, J., & Goldman, D. J. (2016) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2016.05.009 · Cited by 247 · see citing works

Adult neurogenesis and neuronal regeneration in the central nervous system of teleost fish

Zupanc, G. K. H., & Sîrbulescu, R. F. (2011) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2011.07854.x · Cited by 248 · see citing works

Different levels of Notch signaling regulate quiescence, renewal and differentiation in pancreatic endocrine progenitors

Ninov, N., Borius, M., & Stainier, D. Y. R. (2012) · Development · doi:10.1242/dev.076000 · Cited by 225 · see citing works

Neurotransmitter-mediated control of neurogenesis in the adult vertebrate brain

Berg, D. A., Belnoue, L., Song, H., & Simon, A. (2013) · Development · doi:10.1242/dev.088005 · Cited by 224 · see citing works

Neuronal regeneration in a zebrafish model of adult brain injury

Kishimoto, N., Shimizu, K., & Sawamoto, K. (2011) · Disease Models & Mechanisms · doi:10.1242/dmm.007336 · Cited by 220 · see citing works

Clonal analysis by distinct viral vectors identifies bona fide neural stem cells in the adult zebrafish telencephalon and characterizes their division properties and fate

Rothenaigner, I., Krecsmarik, M., Hayes, J. A., Bahn, B., Lepier, A., Fortin, G., Götz, M., Jagasia, R., & Bally‐Cuif, L. (2011) · Development · doi:10.1242/dev.058156 · Cited by 193 · see citing works

Stab wound injury of the zebrafish telencephalon: A model for comparative analysis of reactive gliosis

Baumgart, E. V., Barbosa, J. S., Bally-Cuif, L., Götz, M., & Ninkovic, J. (2012) · Glia · doi:10.1002/glia.22269 · Cited by 193 · see citing works

Regenerative response following stab injury in the adult zebrafish telencephalon

März, M., Viales, R. R., Rastegar, S., & Strähle, U. (2011) · Developmental Dynamics · doi:10.1002/dvdy.22710 · Cited by 187 · see citing works

A comparative view of regenerative neurogenesis in vertebrates

Alunni, A., & Bally‐Cuif, L. (2016) · Development · doi:10.1242/dev.122796 · Cited by 189 · see citing works

Live imaging of adult neural stem cell behavior in the intact and injured zebrafish brain

Barbosa, J. S., Sánchez-González, R., Giaimo, R. D., Baumgart, E. V., Theis, F. J., Götz, M., & Ninkovic, J. (2015) · Science · doi:10.1126/science.aaa2729 · Cited by 185 · see citing works

Glial cells in adult neurogenesis

Morrens, J., Broeck, W. V. D., & Kempermann, G. (2011) · Glia · doi:10.1002/glia.21247 · Cited by 180 · see citing works

Neurogenic Subventricular Zone Stem/Progenitor Cells Are Notch1-Dependent in Their Active But Not Quiescent State

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<scp>RNA</scp> ‐seq of the aging brain in the short‐lived fish <i>N. furzeri</i> – conserved pathways and novel genes associated with neurogenesis

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