Neural Stem Cells Confer Unique Pinwheel Architecture to the Ventricular Surface in Neurogenic Regions of the Adult Brain

The Ki-67 protein: From the known and the unknown

Scholzen, T. E., & Gerdes, J. (2000) · Journal of Cellular Physiology · doi:10.1002/(sici)1097-4652(200003)182:3 · Cited by 4,707

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

Doetsch, F., Caillé, I., Lim, D. A., García-Verdugo, J. M., & Alvarez-Buylla, A. (1999) · Cell · doi:10.1016/s0092-8674(00)80783-7 · Cited by 3,898

A transcriptome database for astrocytes, neurons, and oligodendrocytes: a new resource for understanding brain development and function

Cahoy, J. D., Emery, B., Kaushal, A., Foo, L. C., Zamanian, J. L., Christopherson, K. S., Xing, Y., Lubischer, J. L., Krieg, P. A., Krupenko, S. A., et al. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.4178-07.2008 · Cited by 3,129

Mechanisms and Functional Implications of Adult Neurogenesis

Zhao, C., Deng, W., & Gage, F. H. (2008) · Cell · doi:10.1016/j.cell.2008.01.033 · Cited by 3,007

Mode of cell migration to the superficial layers of fetal monkey neocortex

Rakic, P. (1972) · Journal of Comparative Neurology · doi:10.1002/cne.901450105 · Cited by 2,170

Neurons derived from radial glial cells establish radial units in neocortex

Noctor, S. C., Flint, A. C., Weissman, T. A., Dammerman, R. S., & Kriegstein, A. R. (2001) · Nature · doi:10.1038/35055553 · Cited by 2,016

Cellular Composition and Three-Dimensional Organization of the Subventricular Germinal Zone in the Adult Mammalian Brain

Doetsch, F. K., García‐Verdugo, J. M., & Álvarez-Buylla, A. (1997) · Journal of Neuroscience · doi:10.1523/jneurosci.17-13-05046.1997 · Cited by 1,909

Direct isolation of human central nervous system stem cells

Uchida, N., Buck, D. W., He, D., Reitsma, M. J., Masek, M., Phan, T. V., Tsukamoto, A. S., Gage, F. H., & Weissman, I. L. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.97.26.14720 · Cited by 1,829

Endothelial Cells Stimulate Self-Renewal and Expand Neurogenesis of Neural Stem Cells

Shen, Q., Goderie, S. K., Jin, L., Karanth, N., Sun, Y., Abramova, N. E., Vincent, P. A., Pumiglia, K. M., & Temple, S. (2004) · Science · doi:10.1126/science.1095505 · Cited by 1,574

Vertebrate Smoothened functions at the primary cilium

Corbit, K. C., Aanstad, P., Singla, V., Norman, A. R., Stainier, D. Y. R., & Reiter, J. F. (2005) · Nature · doi:10.1038/nature04117 · Cited by 1,481

EGF induces CREB and ERK activation at the wall of the mouse lateral ventricles

Gampe, K., Brill, M. S., Momma, S., Götz, M., & Zimmermann, H. (2010) · Brain Research · doi:10.1016/j.brainres.2010.11.040 · Cited by 24

Protective Mechanism and Treatment of Neurogenesis in Cerebral Ischemia

Li, W., Ye, A., Ao, L., Zhou, L., Yan, Y., Hu, Y., Fang, W., & Li, Y. (2020) · Neurochemical Research · doi:10.1007/s11064-020-03092-1 · Cited by 25

Genes causing congenital hydrocephalus: Their chromosomal characteristics of telomere proximity and DNA compositions

McKnight, I., Hart, C., Park, I., & Shim, J. W. (2020) · Experimental Neurology · doi:10.1016/j.expneurol.2020.113523 · Cited by 24

To Become or Not to Become Tumorigenic: Subventricular Zone Versus Hippocampal Neural Stem Cells

Fontán‐Lozano, Á., Morcuende, S., de Carrizosa, M. A. D., Benítez‐Temiño, B., Mejı́as, R., & Matarredona, E. R. (2020) · Frontiers in Oncology · doi:10.3389/fonc.2020.602217 · Cited by 28

A novel stem cell type at the basal side of the subventricular zone maintains adult neurogenesis

Baur, K., Abdullah, Y., Mandl, C., Hölzl‐Wenig, G., Shi, Y., Schmidt-Edelkraut, U., Khatri, P. R., Hagenston, A. M., Irmler, M., Beckers, J., et al. (2022) · EMBO Reports · doi:10.15252/embr.202154078 · Cited by 22

Connexin 43-mediated neurovascular interactions regulate neurogenesis in the adult brain subventricular zone

Genet, N., Genet, G., Chavkin, N. W., Paila, U., Fang, J. S., Vasavada, H. H., Goldberg, J. S., Acharya, B. R., Bhatt, N. S., Baker, K. L., et al. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.112371 · Cited by 25

Autophagy in neural stem cells and glia for brain health and diseases

Nagayach, A., & Wang, C. (2023) · Neural Regeneration Research · doi:10.4103/1673-5374.382227 · Cited by 30

Increased doublecortin (DCX) expression and incidence of DCX-immunoreactive multipolar cells in the subventricular zone-olfactory bulb system of suicides

Maheu, M., Devorak, J., Freibauer, A., Davoli, M. A., Turecki, G., & Mechawar, N. (2015) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2015.00074 · Cited by 25

Long-term hydrocephalus alters the cytoarchitecture of the adult subventricular zone

Campos-Ordoñez, T., Herranz‐Pérez, V., Chaichana, K. L., Rincón-Torroella, J., Rigamonti, D., García‐Verdugo, J. M., Quiñones‐Hinojosa, A., & González-Pérez, Ó. (2014) · Experimental Neurology · doi:10.1016/j.expneurol.2014.05.011 · Cited by 25

Endothelial cells regulate p53-dependent apoptosis of neural progenitors after irradiation

Lu, F., Li, Y., Aubert, I., & Wong, C. S. (2012) · Cell Death and Disease · doi:10.1038/cddis.2012.59 · Cited by 25

Developmental dynamics of neurogenesis and gliogenesis in the postnatal mammalian brain in health and disease: Historical and future perspectives

Nakafuku, M., & del Águila, Á. (2019) · Wiley Interdisciplinary Reviews Developmental Biology · doi:10.1002/wdev.369 · Cited by 25

Live Imaging of Adult Neural Stem Cells in Rodents

Ortega, F., & Costa, M. R. (2016) · Frontiers in Neuroscience · doi:10.3389/fnins.2016.00078 · Cited by 23

Adult neurogenesis and reproductive functions in mammals

Migaud, M., Butruille, L., Duittoz, A. H., Pillon, D., & Batailler, M. (2016) · Theriogenology · doi:10.1016/j.theriogenology.2016.04.044 · Cited by 24

Assessing the Role of Ependymal and Vascular Cells as Sources of Extracellular Cues Regulating the Mouse Ventricular-Subventricular Zone Neurogenic Niche

Quaresima, S., Istiaq, A., Jono, H., Cacci, E., Ohta, K., & Lupo, G. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.845567 · Cited by 26

A simple method to obtain pure cultures of multiciliated ependymal cells from adult rodents

Grondona, J. M., Granados‐Durán, P., Fernández‐Llebrez, P., & López-Ávalos, M. D. (2012) · Histochemistry and Cell Biology · doi:10.1007/s00418-012-1008-2 · Cited by 24

Postnatal Neurogenesis

Walton, R. M. (2011) · Veterinary Pathology · doi:10.1177/0300985811414035 · Cited by 24

Seasonal reorganization of hypothalamic neurogenic niche in adult sheep

Butruille, L., Batailler, M., Mazur, D., Prévot, V., & Migaud, M. (2017) · Brain Structure and Function · doi:10.1007/s00429-017-1478-z · Cited by 24

Erratum to: Anosmin-1 over-expression increases adult neurogenesis in the subventricular zone and neuroblast migration to the olfactory bulb

García‐González, D., Murcia‐Belmonte, V., Esteban, P. F., Ortega, F., Díaz, D., Sánchez-Vera, I., Lebrón‐Galán, R., Escobar, L., Martínez‐Millán, L., Weruaga, E., et al. (2016) · Brain Structure and Function · doi:10.1007/s00429-016-1300-3 · Cited by 24

Glioma stem cells: turpis omen in nomen? (the evil in the name?)

Binda, E., Reynolds, B., & Vescovi, A. L. (2014) · Journal of Internal Medicine · doi:10.1111/joim.12254 · Cited by 23

How Necessary is the Vasculature in the Life of Neural Stem and Progenitor Cells? Evidence from Evolution, Development and the Adult Nervous System

Koutsakis, C., & Kazanis, I. (2016) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2016.00035 · Cited by 23

The role of inflammation in subventricular zone cancer

Bardella, C., Al‐Shammari, A. R., Soares, L. C., Tomlinson, I. P. M., O’Neill, E. E., & Szele, F. G. (2018) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2018.04.007 · Cited by 23

Physical Binding of Endothelial MCAM and Neural Transmembrane Protease Matriptase—Novel Cell Adhesion in Neural Stem cell Vascular Niche

Tung, H., & Lee, S.-L. (2017) · Scientific Reports · doi:10.1038/s41598-017-05131-4 · Cited by 23

Loss of p73 in ependymal cells during the perinatal period leads to aqueductal stenosis

Fujitani, M., Sato, R., & Yamashita, T. (2017) · Scientific Reports · doi:10.1038/s41598-017-12105-z · Cited by 23

Neural stem cell heterogeneity in the mammalian forebrain

Adams, K. V., & Morshead, C. M. (2018) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2018.06.005 · Cited by 26

Developmental cues and persistent neurogenic potential within an in vitro neural niche

Pierret, C., Morrison, J. A., Rath, P., Zigler, R. E., Engel, L. A., Fairchild, C. L. A., Shi, H., MARUNIAK, J. A., & Kirk, M. D. (2010) · BMC Developmental Biology · doi:10.1186/1471-213x-10-5 · Cited by 22

The laser lesion of the mouse visual cortex as a model to study neural extracellular matrix remodeling during degeneration, regeneration and plasticity of the CNS

Roll, L., Mittmann, T., Eysel, U. T., & Faissner, A. (2012) · Cell and Tissue Research · doi:10.1007/s00441-011-1313-4 · Cited by 22

Anchoring stem cells in the niche by cell adhesion molecules

Xi, R. (2009) · Cell Adhesion & Migration · doi:10.4161/cam.3.4.8604 · Cited by 23

The vasculature of neurogenic niches: Properties and function

Karakatsani, A., Álvarez-Vergara, M. I., & de Almodóvar, C. R. (2023) · Cells and Development · doi:10.1016/j.cdev.2023.203841 · Cited by 25

The Matrix Receptor CD44 Is Present in Astrocytes throughout the Human Central Nervous System and Accumulates in Hypoxia and Seizures

Al‐Dalahmah, O., Sosunov, A. A., Sun, Y., Liu, Y., Akpan, N., Madden, N., Connolly, E. S., Troy, C. M., McKhann, G. M., & Goldman, J. E. (2024) · Cells · doi:10.3390/cells13020129 · Cited by 22

The Olfactory System as a Puzzle: Playing With Its Pieces

Díaz, D., Gómez, C., Muñoz-Castañeda, R., Baltanás, F. C., Alonso, J. R., & Weruaga, E. (2013) · The Anatomical Record · doi:10.1002/ar.22748 · Cited by 22

Making neurons from mature glia: A far-fetched dream?

Berninger, B. (2009) · Neuropharmacology · doi:10.1016/j.neuropharm.2009.11.004 · Cited by 22

Neural Stem Cells and Transplantation Studies in Parkinson’s Disease

Pardal, R., & López‐Barneo, J. (2012) · Advances in experimental medicine and biology · doi:10.1007/978-1-4614-2098-9_14 · Cited by 22

Direct and efficient transfection of mouse neural stem cells and mature neurons by in vivo mRNA electroporation

Bugeon, S., de Chevigny, A., Boutin, C., Coré, N., Wild, S., Bosio, A., Cremer, H., & Béclin, C. (2017) · Development · doi:10.1242/dev.151381 · Cited by 22

Application of amniotic fluid stem cells in repairing sciatic nerve injury in minipigs

Su, C.-F., Chang, L., Kao, C., Lee, D.-C., Cho, K., Kuo, L., Chang, H., Wang, Y., & Chiu, I. (2017) · Brain Research · doi:10.1016/j.brainres.2017.11.010 · Cited by 22

Reconstituting neurovascular unit based on the close relations between neural stem cells and endothelial cells: an effective method to explore neurogenesis and angiogenesis

Hongjin, W., Chen, H., Baoxiang, J., Shiqi, Y., & Xu, X. (2019) · Reviews in the Neurosciences · doi:10.1515/revneuro-2019-0023 · Cited by 22

Sensory Neuroblast Quiescence Depends on Vascular Cytoneme Contacts and Sensory Neuronal Differentiation Requires Initiation of Blood Flow

Taberner, L., Bañón, A., & Alsina, B. (2020) · Cell Reports · doi:10.1016/j.celrep.2020.107903 · Cited by 20

Physiological Interactions between Microglia and Neural Stem Cells in the Adult Subependymal Niche

Sirerol-Piquer, M. S., Belenguer, G., Morante‐Redolat, J. M., Duart-Abadía, P., Pérez‐Villalba, A., & Fariñas, I. (2019) · Neuroscience · doi:10.1016/j.neuroscience.2019.01.009 · Cited by 23

SARS-CoV-2 and the central nervous system: Emerging insights into hemorrhage-associated neurological consequences and therapeutic considerations

Mitra, J., Kodavati, M. M., Provasek, V. E., Rao, K. S. J., MITRA, S. P., Hamilton, D. J., Horner, P. J., Vahidy, F., Britz, G. W., Kent, T. A., et al. (2022) · Ageing Research Reviews · doi:10.1016/j.arr.2022.101687 · Cited by 20

Prostaglandin E2 induces glutamate release from subventricular zone astrocytes

Dave, K. A., Platel, J., Huang, F., Tian, D., Stamboulian-Platel, S., & Bordey, A. (2010) · Neuron Glia Biology · doi:10.1017/s1740925x10000244 · Cited by 21

Ciliogenic RFX transcription factors regulate FGF1 gene promoter

Hsu, Y., Kao, C., Chung, Y., Chen, M., & Chiu, I. (2012) · Journal of Cellular Biochemistry · doi:10.1002/jcb.24127 · Cited by 23

Epidermal Growth Factor Treatment of the Adult Brain Subventricular Zone Leads to Focal Microglia/Macrophage Accumulation and Angiogenesis

Lindberg, O. R., Brederlau, A., & Kuhn, H. G. (2014) · Stem Cell Reports · doi:10.1016/j.stemcr.2014.02.003 · Cited by 21

Osteogenic and Neurogenic Stem Cells in Their Own Place: Unraveling Differences and Similarities Between Niches

Lattanzi, W., Parolisi, R., Barba, M., & Bonfanti, L. (2015) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2015.00455 · Cited by 21

Synaptic Regulator α-Synuclein in Dopaminergic Fibers Is Essentially Required for the Maintenance of Subependymal Neural Stem Cells

Pérez‐Villalba, A., Sirerol-Piquer, M. S., Belenguer, G., Soriano‐Cantón, R., Muñoz‐Manchado, A. B., Villadiego, J., Alarcón-Arís, D., Soria, F. N., Dehay, B., Bézard, E., et al. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.2276-17.2017 · Cited by 21

Oxidative DNA Damage Signalling in Neural Stem Cells in Alzheimer’s Disease

Kieroń, M., Żekanowski, C., Falk, A., & Wężyk, M. (2019) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2019/2149812 · Cited by 22

Deciphering neural heterogeneity through cell lineage tracing

Figueres‐Oñate, M., Sánchez‐González, R., & López‐Mascaraque, L. (2020) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-020-03689-3 · Cited by 20

Integrin Alpha 6: Anchors Away for Glioma Stem Cells

Corsini, N. S., & Martín-Villalba, A. (2010) · Cell stem cell · doi:10.1016/j.stem.2010.04.003 · Cited by 21

Neural stem cell relay from B1 to B2 cells in the adult mouse ventricular-subventricular zone

Cebrián‐Silla, A., Nascimento, M. A., Mancia, W., González-Granero, S., Romero-Rodriguez, R., Obernier, K., Steffen, D. M., Lim, D. A., García‐Verdugo, J. M., & Álvarez-Buylla, A. (2025) · Cell Reports · doi:10.1016/j.celrep.2025.115264 · Cited by 22

Paracrine regulation of neural stem cells in the subependymal zone.

Porlan, E., Pérez-Villalba, A., Delgado, A. C., & Ferrón, S. (2013) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2012.10.001 · Cited by 22

Regulation of Asymmetric Cell Division in Mammalian Neural Stem and Cancer Precursor Cells

Daynac, M., & Petritsch, C. K. (2017) · Results and problems in cell differentiation · doi:10.1007/978-3-319-53150-2_17 · Cited by 21

Ependyma‐expressed CCN1 restricts the size of the neural stem cell pool in the adult ventricular‐subventricular zone

Wu, J., Tian, W., Liu, Y., Wang, H. J., Zheng, J., Wang, X., Pan, H., Li, J., Luo, J., Yang, X., et al. (2020) · The EMBO Journal · doi:10.15252/embj.2019101679 · Cited by 20

Dysfunction of the proteoglycan Tsukushi causes hydrocephalus through altered neurogenesis in the subventricular zone in mice

Ito, N., Riyadh, M. A., Ahmad, S. A. I., Hattori, S., Kanemura, Y., Kiyonari, H., Abe, T., Furuta, Y., Shinmyo, Y., Kaneko, N., et al. (2021) · Science Translational Medicine · doi:10.1126/scitranslmed.aay7896 · Cited by 20

Neurogenesis and Viral Infection

Ihunwo, A. O., Perego, J., Martino, G., Vicenzi, E., & Panina‐Bordignon, P. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.826091 · Cited by 21

Radial stem astrocytes (aka neural stem cells): Identity, development, physio‐pathology, and therapeutic potential

Yeh, C., Wu, K., Huang, G., & Verkhratsky, A. (2023) · Acta Physiologica · doi:10.1111/apha.13967 · Cited by 20

Neurogenesis in the Adult Mammalian Brain: How Much Do We Need, How Much Do We Have?

Kazanis, I. (2012) · Current topics in behavioral neurosciences · doi:10.1007/7854_2012_227 · Cited by 20

JAM-C is an Apical Surface Marker for Neural Stem Cells

Stelzer, S., Worlitzer, M. M. A., Bahnassawy, L., Hemmer, K., Rugani, K., Werthschulte, I., Schön, A.-L., Brinkmann, B., Bunk, E. C., Palm, T., et al. (2011) · Stem Cells and Development · doi:10.1089/scd.2011.0274 · Cited by 20

Distinct Requirements for Extracellular and Intracellular MMP12 in the Development of the Adult V-SVZ Neural Stem Cell Niche

Shan, X., Tomlinson, L., Yang, Q., & Colognato, H. (2018) · Stem Cell Reports · doi:10.1016/j.stemcr.2018.01.038 · Cited by 20

The Surface Proteome of Adult Neural Stem Cells in Zebrafish Unveils Long-Range Cell-Cell Connections and Age-Related Changes in Responsiveness to IGF

Obermann, J., Wagner, F. M., Kociaj, A., Zambusi, A., Ninkovic, J., Hauck, S. M., & Chapouton, P. (2019) · Stem Cell Reports · doi:10.1016/j.stemcr.2018.12.005 · Cited by 21

Targeting Protein Kinase C in Glioblastoma Treatment

Geribaldi‐Doldán, N., Hervás-Corpión, I., Gómez‐Oliva, R., Domínguez‐García, S., Ruiz, F. A., Lozano, I. I., Carrascal, L., Pardillo-Díaz, R., Gil-Salú, J. L., Nunez‐Abades, P., et al. (2021) · Biomedicines · doi:10.3390/biomedicines9040381 · Cited by 21

Developmental Origin of Neural Stem Cells: The Glial Cell That Could

Grabel, L. B. (2012) · Stem Cell Reviews and Reports · doi:10.1007/s12015-012-9349-8 · Cited by 22

Mcidas and GemC1/Lynkeas specify embryonic radial glial cells

Kyrousi, C., Lalioti, M., Skavatsou, E., Lygerou, Z., & Taraviras, S. L. (2016) · Neurogenesis · doi:10.1080/23262133.2016.1172747 · Cited by 20

A cell population that strongly expresses the CB1 cannabinoid receptor in the ependyma of the rat spinal cord

García‐Ovejero, D., Arévalo‐Martín, Á., Paniagua‐Torija, B., Sierra‐Palomares, Y., & Molina‐Holgado, E. (2012) · The Journal of Comparative Neurology · doi:10.1002/cne.23184 · Cited by 19

Regenerative potential of the brain: Composition and forming of regulatory microenvironment in neurogenic niches

Komleva, Y. K., Kuvacheva, N. V., Malinocskaya, N. A., Gorina, Y. V., Lopatina, O. L., Тепляшина, Е. А., Пожиленкова, Е. А., Zamay, A. S., Morgun, A. V., & Salmina, A. B. (2016) · Human Physiology · doi:10.1134/s0362119716080077 · Cited by 19

The Strange Case of Jekyll and Hyde: Parallels Between Neural Stem Cells and Glioblastoma-Initiating Cells

Bakhshinyan, D., Savage, N. J., Salim, S. K., Venugopal, C., & Singh, S. K. (2021) · Frontiers in Oncology · doi:10.3389/fonc.2020.603738 · Cited by 21

Glioblastoma disrupts the ependymal wall and extracellular matrix structures of the subventricular zone

Norton, E. S., Whaley, L. A., Ulloa-Navas, M. J., García-Tárraga, P., Meneses, K. M., Lara-Velazquez, M. A., Zarco, N., Carrano, A., Quiñones‐Hinojosa, A., García‐Verdugo, J. M., et al. (2022) · Fluids and Barriers of the CNS · doi:10.1186/s12987-022-00354-8 · Cited by 19

The Organism as the Niche: Physiological States Crack the Code of Adult Neural Stem Cell Heterogeneity

Chaker, Z., Makarouni, E., & Doetsch, F. K. (2024) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev-cellbio-120320-040213 · Cited by 21

Ectopic ependymal cells in striatum accompany neurogenesis in a rat model of stroke

Danilov, A. I., Kokaia, Z., & Lindvall, O. (2012) · Neuroscience · doi:10.1016/j.neuroscience.2012.03.062 · Cited by 19

γ-Aminobutyric A Receptor (GABAAR) Regulates Aquaporin 4 Expression in the Subependymal Zone

Li, Y., Schmidt-Edelkraut, U., Poetz, F., Oliva, I., Mandl, C., Hölzl‐Wenig, G., Schönig, K., Bartsch, D., & Ciccolini, F. (2014) · Journal of Biological Chemistry · doi:10.1074/jbc.m114.618686 · Cited by 19

Targeted activation of primitive neural stem cells in the mouse brain

Reeve, R. L., Yammine, S. Z., DeVeale, B., & van der Kooy, D. (2016) · European Journal of Neuroscience · doi:10.1111/ejn.13228 · Cited by 19

Regulation of Adult Neurogenesis by the Fragile X Family of RNA Binding Proteins

Patzlaff, N. E., Shen, M., & Zhao, X. (2017) · Brain Plasticity · doi:10.3233/bpl-170061 · Cited by 18

Topographical Analysis of the Subependymal Zone Neurogenic Niche

Falcão, A. M., Palha, J. A., Ferreira, A. C., Marques, F., Sousa, N., & Sousa, J. C. (2012) · PLoS ONE · doi:10.1371/journal.pone.0038647 · Cited by 19

Morphological and Behavioral Changes in the Pathogenesis of a Novel Mouse Model of Communicating Hydrocephalus

McMullen, A. B., Baidwan, G. S., & McCarthy, K. D. (2012) · PLoS ONE · doi:10.1371/journal.pone.0030159 · Cited by 19

Neuroblast niche position is controlled by PI3-kinase dependent DE-Cadherin adhesion

Doyle, S. E., Pahl, M. C., Siller, K. H., Ardiff, L., & Siegrist, S. E. (2017) · Development · doi:10.1242/dev.136713 · Cited by 17

Cellular and molecular attributes of neural stem cell niches in adult zebrafish brain

Anand, S. K., & Mondal, A. C. (2017) · Developmental Neurobiology · doi:10.1002/dneu.22508 · Cited by 19

VEGF: A potential target for hydrocephalus

Shim, J. W., Sandlund, J., & Madsen, J. R. (2014) · Cell and Tissue Research · doi:10.1007/s00441-014-1978-6 · Cited by 17

Cumulative Damage: Cell Death in Posthemorrhagic Hydrocephalus of Prematurity

Sevensky, R., Newville, J., Tang, H. L., Robinson, S., & Jantzie, L. L. (2021) · Cells · doi:10.3390/cells10081911 · Cited by 19

Astrocytes in Ageing

Verkhratsky, A., & Semyanov, A. V. (2023) · Sub-cellular biochemistry/Subcellular biochemistry · doi:10.1007/978-3-031-26576-1_11 · Cited by 20

Spatial Distribution of Prominin-1 (CD133) – Positive Cells within Germinative Zones of the Vertebrate Brain

Jászai, J., Graupner, S., Tanaka, E. M., Funk, R. H. W., Huttner, W. Β., Brand, M., & Corbeil, D. (2013) · PLoS ONE · doi:10.1371/journal.pone.0063457 · Cited by 18

Switching on mTORC1 induces neurogenesis but not proliferation in neural stem cells of young mice

Mahoney, C., Feliciano, D. M., Bordey, A., & Hartman, N. W. (2016) · Neuroscience Letters · doi:10.1016/j.neulet.2015.12.042 · Cited by 18

Escargot controls the sequential specification of two tracheal tip cell types by suppressing FGF signaling in Drosophila

Miao, G., & Hayashi, S. (2016) · Development · doi:10.1242/dev.133322 · Cited by 18

PTEN Signaling in the Postnatal Perivascular Progenitor Niche Drives Medulloblastoma Formation

Zhu, G. G., Rankin, S. L., Larson, J. D., Zhu, X., Chow, L. M. L., Qu, C., Zhang, J., Ellison, D. W., & Baker, S. J. (2016) · Cancer Research · doi:10.1158/0008-5472.can-16-1991 · Cited by 18

The adult human subventricular zone: partial ependymal coverage and proliferative capacity of cerebrospinal fluid

de Sonnaville, S. F. A. M., van Strien, M. E., Middeldorp, J., Sluijs, J. A., van den Berge, S. A., Moeton, M., Donega, V., van Berkel, A. A., Deering, T., Filippis, L. D., et al. (2020) · Brain Communications · doi:10.1093/braincomms/fcaa150 · Cited by 18

De novo expression of parvalbumin in ependymal cells in response to brain injury promotes ependymal remodeling and wound repair

Szabolcsi, V., & Celio, M. R. (2014) · Glia · doi:10.1002/glia.22768 · Cited by 18

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Pardal, R., & Barneo, J. L. (2016) · Development Growth & Differentiation · doi:10.1111/dgd.12283 · Cited by 18

Methods of reactivation and reprogramming of neural stem cells for neural repair

Tian, Z., Zhao, Q., Biswas, S., & Deng, W. (2017) · Methods · doi:10.1016/j.ymeth.2017.08.014 · Cited by 18

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Mateo, E. M., Tonino, R. P. B., Cantó, A., Monroy‐Noyola, A., Miranda, M., Soria, J. M., & Esparza, M. Á. G. (2022) · Toxins · doi:10.3390/toxins14090624 · Cited by 17

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Schiffer, D., Mellai, M., Annovazzi, L., Piazzi, A., Monzeglio, O., & Caldera, V. (2012) · Stem Cell Discovery · doi:10.4236/scd.2012.23017 · Cited by 17

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Heywood, R. M., Marcus, H. J., Ryan, D. J., Piccirillo, S. G. M., Al-Mayhani, T. M. F., & Watts, C. (2012) · Acta Neurochirurgica · doi:10.1007/s00701-012-1338-9 · Cited by 16

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Stratton, J. A., Shah, P. T., Sinha, S., Crowther, E., & Biernaskie, J. A. (2019) · FEBS Journal · doi:10.1111/febs.14930 · Cited by 16

BMP signaling suppresses Gemc1 expression and ependymal differentiation of mouse telencephalic progenitors

Omiya, H., Yamaguchi, S., Watanabe, T., Kuniya, T., Harada, Y., Kawaguchi, D., & Gotoh, Y. (2021) · Scientific Reports · doi:10.1038/s41598-020-79610-6 · Cited by 16

Enteric neurons show a primary cilium

Bartolomé, M. J. L., Cantarero, I., Castiella, T., Soriano‐Navarro, M., García‐Verdugo, J. M., & Junquera, C. (2012) · Journal of Cellular and Molecular Medicine · doi:10.1111/j.1582-4934.2012.01657.x · Cited by 17

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Habela, C. W., Yoon, K.-J., Kim, N.-S., Taga, A., Bell, K., Bergles, D. E., Maragakis, N. J., Ming, G.-L., & Song, H. (2020) · The Journal of Neuroscience · doi:10.1523/jneurosci.2249-19.2020 · Cited by 16

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Dawes, W. J. (2022) · Frontiers in Pediatrics · doi:10.3389/fped.2022.887606 · Cited by 16

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Demir, M., & Laywell, E. D. (2015) · Frontiers in Neuroscience · doi:10.3389/fnins.2015.00093 · Cited by 16

Vascular niche contribution to age-associated neural stem cell dysfunction

Apple, D. M., & Kokovay, E. (2017) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00154.2017 · Cited by 18

Endothelinergic cells in the subependymal region of mice

Castañeda, M. M., Cubilla, M. A., López-Vicchi, M. M., & Suburo, Á. M. (2010) · Brain Research · doi:10.1016/j.brainres.2010.01.056 · Cited by 16

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Zhu, C., Mahesula, S., Temple, S., & Kokovay, E. (2019) · Stem Cell Reports · doi:10.1016/j.stemcr.2018.11.022 · Cited by 16

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Devaraju, K., Barnabé‐Heider, F., Kokaia, Z., & Lindvall, O. (2013) · Experimental Cell Research · doi:10.1016/j.yexcr.2013.08.028 · Cited by 15

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Acabchuk, R. L., Sun, Y., Wolferz, R., Eastman, M. B., Lennington, J. B., Shook, B. A., Wu, Q., & Conover, J. C. (2015) · Journal of Visualized Experiments · doi:10.3791/52328 · Cited by 20

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Bachor, T. P., Karbanová, J., Büttner, E., Bermúdez, V., Marquioni‐Ramella, M. D., Carmeliet, P., Corbeil, D., & Suburo, Á. M. (2017) · Neurobiology of Disease · doi:10.1016/j.nbd.2017.07.010 · Cited by 15

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Rodríguez-Jiménez, F. J., Clemente, E., Moreno‐Manzano, V., & Erceg, S. (2019) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2019.00334 · Cited by 15

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Whalley, K. (2008) · Nature reviews. Neuroscience · doi:10.1038/nrn2517 · Cited by 1

Epithelial organization of the adult neural stem cell niche

Mirzadeh, Z. (2008) · eScholarship (California Digital Library)

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Lim, D. A., & Álvarez-Buylla, A. (2014) · Trends in Neurosciences · doi:10.1016/j.tins.2014.08.006 · Cited by 191

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Alvarez-Buylla, A., Kohwi, M., Nguyen, T. M., & Merkle, F. T. (2008) · Cold Spring Harbor Symposia on Quantitative Biology · doi:10.1101/sqb.2008.73.019 · Cited by 194

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Fuentealba, L. C., Obernier, K., & Álvarez-Buylla, A. (2012) · Cell stem cell · doi:10.1016/j.stem.2012.05.012 · Cited by 389