The origins of the circumventricular organs

Cyclopia and defective axial patterning in mice lacking Sonic hedgehog gene function

Chiang, C. C., Litingtung, Y., Lee, E., Young, K. E., Corden, J. L., Westphal, H., & Beachy, P. A. (1996) · Nature · doi:10.1038/383407a0 · Cited by 3,062 · see citing works

IgG marker of optic-spinal multiple sclerosis binds to the aquaporin-4 water channel

Lennon, V. A., Kryzer, T. J., Pittock, S. J., Verkman, A. S., & Hinson, S. R. (2005) · The Journal of Experimental Medicine · doi:10.1084/jem.20050304 · Cited by 2,288 · see citing works

Dwarf locus mutants lacking three pituitary cell types result from mutations in the POU-domain gene pit-1

Li, S., Crenshaw, E. B., Rawson, E. J., Simmons, D. M., Swanson, L. W., & Rosenfeld, M. G. (1990) · Nature · doi:10.1038/347528a0 · Cited by 1,194 · see citing works

Melatonin: an ancient molecule that makes oxygen metabolically tolerable

Manchester, L. C., Coto‐Montes, A. M., Boga, J. A., Andersen, L. P. H., Zhou, Z., Galano, A., Vriend, J. P., Tan, D. X., & Reiter, R. J. (2015) · Journal of Pineal Research · doi:10.1111/jpi.12267 · Cited by 954 · see citing works

Mutations in the homeobox gene HESX1/Hesx1 associated with septo-optic dysplasia in human and mouse

Dattani, M., Martı́nez-Barberá, J. P., Thomas, P. Q., Brickman, J. M., Gupta, R., Mårtensson, I., Toresson, H., Fox, M., Wales, J. K., Hindmarsh, P. C., et al. (1998) · Nature Genetics · doi:10.1038/477 · Cited by 790 · see citing works

Central mechanisms of osmosensation and systemic osmoregulation

Bourque, C. W. (2008) · Nature reviews. Neuroscience · doi:10.1038/nrn2400 · Cited by 703 · see citing works

Forebrain and midbrain regions are deleted in Otx2−/− mutants due to a defective anterior neuroectoderm specification during gastrulation

Acampora, D., Mazan, S., Lallemand, Y., Avantaggiato, V., Maury, M., Simeone, A., & Brûlet, P. (1995) · Development · doi:10.1242/dev.121.10.3279 · Cited by 702 · see citing works

Mouse Otx2 functions in the formation and patterning of rostral head.Preprint

Matsuo, I., Kuratani, S., Kimura, C., Takeda, N., & Aizawa, S. (1995) · Genes & Development · doi:10.1101/gad.9.21.2646 · Cited by 690 · see citing works

Structure and functions of the GNAT superfamily of acetyltransferases

Vetting, M. W., de Carvalho, L. P. S., Yu, M. C., Hegde, S. S., Magnet, S., Roderick, S. L., & Blanchard, J. S. (2004) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2004.09.003 · Cited by 631 · see citing works

Melatonin as a chronobiotic

Arendt, J., & Skene, D. J. (2005) · Sleep Medicine Reviews · doi:10.1016/j.smrv.2004.05.002 · Cited by 629 · see citing works

Otx2 homeobox gene controls retinal photoreceptor cell fate and pineal gland development

Nishida, A., Furukawa, A., Koike, C., Tano, Y., Aizawa, S., Matsuo, I., & Furukawa, T. (2003) · Nature Neuroscience · doi:10.1038/nn1155 · Cited by 607 · see citing works

Pax2 contributes to inner ear patterning and optic nerve trajectory

Torres, M., Gómez‐Pardo, E., & Gruß, P. (1996) · Development · doi:10.1242/dev.122.11.3381 · Cited by 603 · see citing works

Vertebrate Cranial Placodes I. Embryonic Induction

Baker, C. V. H., & Bronner-Fraser, M. E. (2001) · Developmental Biology · doi:10.1006/dbio.2001.0156 · Cited by 589 · see citing works

Mutations in PROP1 cause familial combined pituitary hormone deficiency

Wu, W., Cogan, J. D., Pfäffle, R. W., Dasen, J. S., Frisch, H., O’Connell, S. M., Flynn, S. E., Brown, M. R., Mullis, P. E., Parks, J. S., et al. (1998) · Nature Genetics · doi:10.1038/ng0298-147 · Cited by 562 · see citing works

Human pineal physiology and functional significance of melatonin

Macchi, M. M., & Bruce, J. N. (2004) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2004.08.001 · Cited by 545 · see citing works

Six3 repression of Wnt signaling in the anterior neuroectoderm is essential for vertebrate forebrain developmentPreprint

Lagutin, O. V., Zhu, C. C., Kobayashi, D., Topczewski, J., Shimamura, K., Puelles, L., Russell, H. R. C., McKinnon, P. J., Solnica‐Krezel, L., & Oliver, G. C. (2003) · Genes & Development · doi:10.1101/gad.1059403 · Cited by 528 · see citing works

Transcriptional Codes and the Control of Neuronal Identity

Shirasaki, R., & Pfaff, S. L. (2002) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.25.112701.142916 · Cited by 522 · see citing works

A targeted mouse Otx2 mutation leads to severe defects in gastrulation and formation of axial mesoderm and to deletion of rostral brain

Ang, S., Jin, O., Rhinn, M., Daigle, N., Stevenson, L., & Rossant, J. (1996) · Development · doi:10.1242/dev.122.1.243 · Cited by 501 · see citing works

Multistep signaling requirements for pituitary organogenesis in vivoPreprint

Treier, M., Gleiberman, A. S., O’Connell, S. M., Szeto, D. P., McMahon, J. A., McMahon, A. P., & Rosenfeld, M. G. (1998) · Genes & Development · doi:10.1101/gad.12.11.1691 · Cited by 495 · see citing works

Early Steps in the Development of the Forebrain

Wilson, S. W., & Houart, C. (2004) · Developmental Cell · doi:10.1016/s1534-5807(04)00027-9 · Cited by 460 · see citing works

Specification of Pituitary Cell Lineages by the LIM Homeobox Gene Lhx3

SHENG, H. Z., Zhadanov, A. B., Mosinger, B. J., Fujii, T., Bertuzzi, S., Grinberg, A., Lee, E. J., Huang, S.-P., Mahon, K. A., & Westphal, H. (1996) · Science · doi:10.1126/science.272.5264.1004 · Cited by 456 · see citing works

Regulation of vascular morphogenesis by Notch signalingPreprint

Roca, C., & Adams, R. H. (2007) · Genes & Development · doi:10.1101/gad.1589207 · Cited by 440 · see citing works

Axon Guidance Molecules in Vascular PatterningPreprint

Adams, R. H., & Eichmann, A. (2010) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a001875 · Cited by 407 · see citing works

Mapping of the early neural primordium in quail-chick chimeras

Couly, G. F., & Douarin, N. M. L. (1985) · Developmental Biology · doi:10.1016/0012-1606(85)90101-0 · Cited by 400 · see citing works

Integrated FGF and BMP signaling controls the progression of progenitor cell differentiation and the emergence of pattern in the embryonic anterior pituitary

Ericson, J., Norlin, S., Jessell, T. M., & Edlund, H. (1998) · Development · doi:10.1242/dev.125.6.1005 · Cited by 395 · see citing works

Functional and developmental analysis of the blood–brain barrier in zebrafish

Jeong, J.-Y., Kwon, H.-B., Ahn, J.-C., Kang, D., Kwon, S., Park, J. A., & Kim, K.-W. (2007) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2007.10.043 · Cited by 391 · see citing works

Induction and specification of cranial placodes

Schlosser, G. (2006) · Developmental Biology · doi:10.1016/j.ydbio.2006.03.009 · Cited by 389 · see citing works

Conserved sensory-neurosecretory cell types in annelid and fish forebrain: insights into hypothalamus evolution

Tessmar-Raible, K., Raible, F., Christodoulou, F., Guy, K., Rembold, M., Hausen, H., & Arendt, D. (2007) · Cell · doi:10.1016/j.cell.2007.04.041 · Cited by 384 · see citing works

Multistep Control of Pituitary Organogenesis

SHENG, H. Z., Moriyama, K., Yamashita, T., Li, H., Potter, S. S., Mahon, K. A., & Westphal, H. (1997) · Science · doi:10.1126/science.278.5344.1809 · Cited by 382 · see citing works

Choroid plexus: biology and pathology

Wolburg, H., & Paulus, W. (2009) · Acta Neuropathologica · doi:10.1007/s00401-009-0627-8 · Cited by 376 · see citing works

Overview and introduction: The blood–brain barrier in health and disease

Abbott, N. J., & Friedman, A. (2012) · Epilepsia · doi:10.1111/j.1528-1167.2012.03696.x · Cited by 364 · see citing works

Dose-dependent functions of Fgf8 in regulating telencephalic patterning centers

Storm, E. E., Garel, S., Borello, U., Hébert, J. M., Martı́nez, S., McConnell, S. K., Martin, G. R., & Rubenstein, J. L. R. (2006) · Development · doi:10.1242/dev.02324 · Cited by 361 · see citing works

Mapping of the early neural primordium in quail-chick chimeras

Couly, G. F., & Douarin, N. M. L. (1987) · Developmental Biology · doi:10.1016/0012-1606(87)90118-7 · Cited by 352 · see citing works

The habenular nuclei: a conserved asymmetric relay station in the vertebrate brain

Bianco, I. H., & Wilson, S. W. (2008) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2008.0213 · Cited by 344 · see citing works

Neurogenesis in the ependymal layer of the adult rat 3rd ventricle

Xu, Y., Tamamaki, N., Noda, T., Kimura, K., Itokazu, Y., Matsumoto, N., Dezawa, M., & Idé, C. (2005) · Experimental Neurology · doi:10.1016/j.expneurol.2004.12.021 · Cited by 331 · see citing works

Formation of Rathke’s pouch requires dual induction from the diencephalon

Takuma, N., SHENG, H. Z., Furuta, Y., Ward, J. M., Sharma, K., Hogan, B. L. M., Pfaff, S. L., Westphal, H., Kimura, S., & Mahon, K. A. (1998) · Development · doi:10.1242/dev.125.23.4835 · Cited by 328 · see citing works

Embryonic signaling centers expressing BMP, WNT and FGF proteins interact to pattern the cerebral cortex

Shimogori, T., Banuchi, V., Ng, H., Strauss, J. B., & Grove, E. (2004) · Development · doi:10.1242/dev.01428 · Cited by 317 · see citing works

The pan-Pituitary Activator of Transcription, Ptx1 (Pituitary Homeobox 1), Acts in Synergy with SF-1 and Pit1 and Is an Upstream Regulator of the Lim-Homeodomain Gene Lim3/Lhx3

Tremblay, J., Lanctôt, C., & Drouin, J. (1998) · Molecular Endocrinology · doi:10.1210/mend.12.3.0073 · Cited by 315 · see citing works

α-Tanycytes of the adult hypothalamic third ventricle include distinct populations of FGF-responsive neural progenitors

Robins, S. C., Stewart, I., McNay, D. E., Taylor, V., Giachino, C., Goetz, M., Ninkovic, J., Briancon, N., Maratos-Flier, E., Flier, J. S., et al. (2013) · Nature Communications · doi:10.1038/ncomms3049 · Cited by 306 · see citing works

Order and coherence in the fate map of the zebrafish nervous system

Woo, K., & Fraser, S. E. (1995) · Development · doi:10.1242/dev.121.8.2595 · Cited by 301 · see citing works

Hedgehog signaling is required for pituitary gland development

Treier, M., O’Connell, S. M., Gleiberman, A. S., Price, J. A., Szeto, D. P., Burgess, R., Chuang, P., McMahon, A. P., & Rosenfeld, M. G. (2001) · Development · doi:10.1242/dev.128.3.377 · Cited by 299 · see citing works

Tanycyte-like cells form a blood-cerebrospinal fluid barrier in the circumventricular organs of the mouse brain

Langlet, F., Mullier, A., Bouret, S. G., Prevot, V., & Dehouck, B. (2013) · Journal of Comparative Neurology · doi:10.1002/cne.23355 · Cited by 295 · see citing works

Cooperation of BMP7 and SHH in the Induction of Forebrain Ventral Midline Cells by Prechordal Mesoderm

Dale, J. K., Vesque, C., Lints, T., Sampath, T. K., Furley, A. J., Dodd, J., & Placzek, M. (1997) · Cell · doi:10.1016/s0092-8674(00)80334-7 · Cited by 295 · see citing works

Coordinate regulation and synergistic actions of BMP4, SHH and FGF8 in the rostral prosencephalon regulate morphogenesis of the telencephalic and optic vesicles

Ohkubo, Y., Chiang, C. C., & Rubenstein, J. L. R. (2002) · Neuroscience · doi:10.1016/s0306-4522(01)00616-9 · Cited by 289 · see citing works

Mapping of the presumptive brain regions in the neural plate of Xenopus laevis

Eagleson, G. W., & Harris, W. A. (1990) · Journal of Neurobiology · doi:10.1002/neu.480210305 · Cited by 285 · see citing works

The anatomy and innervation of the mammalian pineal gland

Møller, M., & Baeres, F. M. M. (2002) · Cell and Tissue Research · doi:10.1007/s00441-002-0580-5 · Cited by 284 · see citing works

From nerve net to nerve ring, nerve cord and brain — evolution of the nervous system

Arendt, D., Tosches, M. A., & Marlow, H. (2016) · Nature Reviews Neuroscience · doi:10.1038/nrn.2015.15 · Cited by 279 · see citing works

A mutation in the Gsk3–binding domain of zebrafish Masterblind/Axin1 leads to a fate transformation of telencephalon and eyes to diencephalonPreprint

Heisenberg, C., Houart, C., Take-uchi, M., Rauch, G.-J., Young, N., Coutinho, P., Masai, I., Caneparo, L., Concha, M. L., Geisler, R., et al. (2001) · Genes & Development · doi:10.1101/gad.194301 · Cited by 265 · see citing works

The Area Postrema: A Brain Monitor and Integrator of Systemic Autonomic State

Price, C. J., Hoyda, T. D., & Ferguson, A. V. (2008) · The Neuroscientist · doi:10.1177/1073858407311100 · Cited by 257 · see citing works

The evolution of irradiance detection: melanopsin and the non-visual opsins

Peirson, S. N., Halford, S., & Foster, F. (2009) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2009.0050 · Cited by 253 · see citing works

Heterogeneity of the blood-brain barrier

Wilhelm, I., Nyúl‐Tóth, Á., Suciu, M., Hermenean, A. O., & Krizbai, I. A. (2016) · Tissue Barriers · doi:10.1080/21688370.2016.1143544 · Cited by 246 · see citing works

Pituitary homeobox 2, a novel member of the bicoid-related family of homeobox genes, is a potential regulator of anterior structure formation

Gage, P. J., & Camper, S. A. (1997) · Human Molecular Genetics · doi:10.1093/hmg/6.3.457 · Cited by 235 · see citing works

Nomenclature and location of avian hypothalamic nuclei and associated circumventricular organs

Kuenzel, W. J., & van Tienhoven, A. (1982) · The Journal of Comparative Neurology · doi:10.1002/cne.902060309 · Cited by 221 · see citing works

Patterning of the chick forebrain anlage by the prechordal plate

Pera, E. M., & Kessel, M. (1997) · Development · doi:10.1242/dev.124.20.4153 · Cited by 210 · see citing works

A new scenario of hypothalamic organization: rationale of new hypotheses introduced in the updated prosomeric model

Puelles, L., & Rubenstein, J. L. R. (2015) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2015.00027 · Cited by 204 · see citing works

Regulation of a remote Shh forebrain enhancer by the Six3 homeoprotein

Jeong, Y., Leskow, F. C., El-Jaick, K. B., Roessler, E., Muenke, M., Yocum, A. K., Dubourg, C., Li, X., Geng, X., Oliver, G. C., et al. (2008) · Nature Genetics · doi:10.1038/ng.230 · Cited by 202 · see citing works

Specification of dorsal telencephalic character by sequential Wnt and FGF signaling

Gunhaga, L., Marklund, M., Sjödal, M., Hsieh, J.-C., Jessell, T. M., & Edlund, H. (2003) · Nature Neuroscience · doi:10.1038/nn1068 · Cited by 197 · see citing works

Haploinsufficiency of Six3 Fails to Activate Sonic hedgehog Expression in the Ventral Forebrain and Causes Holoprosencephaly

Geng, X., Speirs, C. K., Lagutin, O. V., Inbal, A., Liu, W., Solnica‐Krezel, L., Jeong, Y., Epstein, D. J., & Oliver, G. C. (2008) · Developmental Cell · doi:10.1016/j.devcel.2008.07.003 · Cited by 190 · see citing works

The saccus vasculosus of fish is a sensor of seasonal changes in day length

Nakane, Y., Ikegami, K., Iigo, M., Ono, H., Takeda, K., Takahashi, D., Uesaka, M., Kimijima, M., Hashimoto, R., Arai, N., et al. (2013) · Nature Communications · doi:10.1038/ncomms3108 · Cited by 189 · see citing works

The preplacodal region: an ectodermal domain with multipotential progenitors that contribute to sense organs and cranial sensory ganglia

Streit, A. (2007) · The International Journal of Developmental Biology · doi:10.1387/ijdb.072327as · Cited by 186 · see citing works

The Role of Organizers in Patterning the Nervous System

Kiecker, C. M., & Lumsden, A. (2012) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-062111-150543 · Cited by 185 · see citing works

Ventromedial Arcuate Nucleus Communicates Peripheral Metabolic Information to the Suprachiasmatic Nucleus

Yi, C., van der Vliet, J., Dai, J., Guangfu, Y., Li-qiang, R., & Buijs, R. M. (2005) · Endocrinology · doi:10.1210/en.2005-1051 · Cited by 184 · see citing works

The role of Pax6 in forebrain development

Georgala, P. A., Carr, C. B., & Price, D. J. (2011) · Developmental Neurobiology · doi:10.1002/dneu.20895 · Cited by 183 · see citing works

Isolation and developmental expression of the amphioxus Pax-6 gene (AmphiPax-6): insights into eye and photoreceptor evolution

Glardon, S., Holland, L. Z., Gehring, W. J., & Holland, N. D. (1998) · Development · doi:10.1242/dev.125.14.2701 · Cited by 182 · see citing works

Fate Map of the Avian Anterior Forebrain at the Four-Somite Stage, Based on the Analysis of Quail–Chick Chimeras

Cobos, I., Shimamura, K., Rubenstein, J. L. R., Martı́nez, S., & Puelles, L. (2001) · Developmental Biology · doi:10.1006/dbio.2001.0423 · Cited by 182 · see citing works

The median preoptic nucleus: front and centre for the regulation of body fluid, sodium, temperature, sleep and cardiovascular homeostasis

McKinley, M. J., Yao, S. T., Uschakov, A., McAllen, R. M., Rundgren, M., & Martelli, D. (2015) · Acta Physiologica · doi:10.1111/apha.12487 · Cited by 180 · see citing works

Distinct neural mechanisms for the control of thirst and salt appetite in the subfornical organ

Matsuda, T., Hiyama, T. Y., Niimura, F., Matsusaka, T., Fukamizu, A., Kobayashi, K., Kobayashi, K., & Noda, M. (2016) · Nature Neuroscience · doi:10.1038/nn.4463 · Cited by 178 · see citing works

Evolution and development of interhemispheric connections in the vertebrate forebrain

Suárez, R., Gobius, I., & Richards, L. J. (2014) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2014.00497 · Cited by 175 · see citing works

Survey of the Development and Comparative Morphology of the Pineal Organ

Oksche, A. (1965) · Progress in brain research · doi:10.1016/s0079-6123(08)63445-7 · Cited by 170 · see citing works

Polymicrogyria and absence of pineal gland due to PAX6 mutation

Mitchell, T. N., Free, S. L., Williamson, K. A., Stevens, J., Churchill, A., Hanson, I. M., Shorvon, S. D., Moore, A. T., van Heyningen, V., & Sisodiya, S. M. (2003) · Annals of Neurology · doi:10.1002/ana.10576 · Cited by 163 · see citing works

Otx5 regulates genes that show circadian expression in the zebrafish pineal complex

Gamse, J. T., Shen, Y.-C., Thisse, C., Thisse, B., Raymond, P. A., Halpern, M. E., & Liang, J. O. (2001) · Nature Genetics · doi:10.1038/ng793 · Cited by 160 · see citing works

Pax6 is essential for establishing ventral-dorsal cell boundaries in pituitary gland development

Kioussi, C., O’Connell, S. M., St‐Onge, L., Treier, M., Gleiberman, A. S., Gruß, P., & Rosenfeld, M. G. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.25.14378 · Cited by 159 · see citing works

Role of aquaporin-4 water channel in the development and integrity of the blood-brain barrier

Nico, B., Frigeri, A., Nicchia, G. P., Quondamatteo, F., Herken, R., Errede, M., Ribatti, D., Svelto, M., & Roncali, L. (2001) · Journal of Cell Science · doi:10.1242/jcs.114.7.1297 · Cited by 154 · see citing works

The homeobox gene Otx2 in development and disease

Béby, F., & Lamonerie, T. (2013) · Experimental Eye Research · doi:10.1016/j.exer.2013.03.007 · Cited by 148 · see citing works

Evolution of photosensory pineal organs in new light: the fate of neuroendocrine photoreceptors

Ekström, P., & Meissl, H. (2003) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2003.1303 · Cited by 146 · see citing works

Night/Day Changes in Pineal Expression of >600 Genes

Bailey, M. J., Coon, S. L., Carter, D., Humphries, A., Kim, J., Shi, Q., Gaildrat, P., Morin, F., Ganguly, S., Hogenesch, J. B., et al. (2008) · Journal of Biological Chemistry · doi:10.1074/jbc.m808394200 · Cited by 142 · see citing works

Differentiation of the brain vasculature: the answer came blowing by the Wnt

Liebner, S., & Plate, K. H. (2010) · Vascular Cell · doi:10.1186/2040-2384-2-1 · Cited by 138 · see citing works

floating head and masterblind Regulate Neuronal Patterning in the Roof of the Forebrain

Masai, I., Heisenberg, C., Barth, K., MacDonald, R. E., Adamek, S., & Wilson, S. W. (1997) · Neuron · doi:10.1016/s0896-6273(01)80045-3 · Cited by 136 · see citing works

Melatonin Signaling Controls Circadian Swimming Behavior in Marine Zooplankton

Tosches, M. A., Bucher, D. B., Vopálenský, P., & Arendt, D. (2014) · Cell · doi:10.1016/j.cell.2014.07.042 · Cited by 134 · see citing works

Novel FGF8 mutations associated with recessive holoprosencephaly, craniofacial defects, and hypothalamo-pituitary dysfunction.

McCabe, M., Gaston-Massuet, C., Tziaferi, V., Gregory, L., Alatzoglou, K. S., Signore, M., Puelles, E., Gerrelli, D., Farooqi, I., Raza, J., et al. (2011) · Journal of Clinical Endocrinology and Metabolism · doi:10.1210/jc.2011-0454 · Cited by 132 · see citing works

Pituitary Gland Development and Disease

Davis, S. W., Ellsworth, B. S., Millan, M. I. P., Gergics, P., Schade, V., Foyouzi, N., Brinkmeier, M. L., Mortensen, A. H., & Camper, S. A. (2013) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/b978-0-12-416021-7.00001-8 · Cited by 131 · see citing works

Combinatorial function of the homeodomain proteins Nkx2.1 and Gsh2 in ventral telencephalic patterning

Corbin, J. G., Rutlin, M. L., Gaiano, N., & Fishell, G. (2003) · Development · doi:10.1242/dev.00717 · Cited by 131 · see citing works

Recent advances in central congenital hypothyroidism

Schoenmakers, N., Alatzoglou, K. S., Chatterjee, V. K., & Dattani, M. T. (2015) · Journal of Endocrinology · doi:10.1530/joe-15-0341 · Cited by 125 · see citing works

A deficiency in RFX3 causes hydrocephalus associated with abnormal differentiation of ependymal cells

Baas, D., Meiniel, A., Benadiba, C., Bonnafé, E., Meiniel, O., Reith, W., & Durand, B. (2006) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2006.05002.x · Cited by 118 · see citing works

Protein components of the blood–brain barrier (BBB) in the mediobasal hypothalamus

Gregory, E. N., Gömüç, B., & Meister, B. (2008) · Journal of Chemical Neuroanatomy · doi:10.1016/j.jchemneu.2008.06.002 · Cited by 116 · see citing works

SOX2 regulates the hypothalamic-pituitary axis at multiple levels

Jayakody, S. A., Andoniadou, C. L., Gaston‐Massuet, C., Signore, M., Cariboni, A. M., Bouloux, P. M., Tissier, P. L., Pevny, L., Dattani, M., & Martı́nez-Barberá, J. P. (2012) · Journal of Clinical Investigation · doi:10.1172/jci64311 · Cited by 115 · see citing works

WNT signaling affects gene expression in the ventral diencephalon and pituitary gland growth

Potok, M. A., Cha, K. B., Hunt, A., Brinkmeier, M. L., Leitges, M., Kispert, A., & Camper, S. A. (2008) · Developmental Dynamics · doi:10.1002/dvdy.21511 · Cited by 111 · see citing works

Noradrenergic neurons in the zebrafish hindbrain are induced by retinoic acid and requiretfap2afor expression of the neurotransmitter phenotype

Holzschuh, J., Barrallo‐Gimeno, A., Ettl, A.-K., Dürr, K., Knapik, E. W., & Driever, W. (2003) · Development · doi:10.1242/dev.00816 · Cited by 110 · see citing works

The transcription factor Pax6 is required for development of the diencephalic dorsal midline secretory radial glia that form the subcommissural organ

Estivill‐Torrús, G., Vitalis, T., Fernández‐Llebrez, P., & Price, D. J. (2001) · Mechanisms of Development · doi:10.1016/s0925-4773(01)00527-5 · Cited by 106 · see citing works

islet Reveals Segmentation in the Amphioxus Hindbrain Homolog

Jackman, W. R., Langeland, J. A., & Kimmel, C. B. (2000) · Developmental Biology · doi:10.1006/dbio.2000.9630 · Cited by 105 · see citing works

The evolution and nomenclature of GnRH-type and corazonin-type neuropeptide signaling systems

Zandawala, M., Tian, S., & Elphick, M. R. (2018) · General and Comparative Endocrinology · doi:10.1016/j.ygcen.2017.06.007 · Cited by 105 · see citing works

Hypothalamus as an Endocrine Organ

Clarke, I. J. (2014) · Comprehensive physiology · doi:10.1002/cphy.c140019 · Cited by 104 · see citing works

Altered Forebrain and Hindbrain Development in Mice Mutant for theGsh-2Homeobox Gene

Szucsik, J. C., Witte, D. P., Li, H., Pixley, S. K., Small, K. M., & Potter, S. S. (1997) · Developmental Biology · doi:10.1006/dbio.1997.8733 · Cited by 104 · see citing works

Disruption of SoxB1-Dependent Sonic hedgehog Expression in the Hypothalamus Causes Septo-optic Dysplasia

Zhao, L., Zevallos, S. E., Rizzoti, K., Jeong, Y., Lovell-Badge, R. H., & Epstein, D. J. (2012) · Developmental Cell · doi:10.1016/j.devcel.2011.12.023 · Cited by 104 · see citing works

Transient dwarfism and hypogonadism in mice lacking Otx1 reveal prepubescent stage-specific control of pituitary levels of GH, FSH and LH

Acampora, D., Mazan, S., Tuorto, F., Avantaggiato, V., Tremblay, J., Lazzaro, D., Carlo, A. D., Mariano, A., Macchia, P. E., Corte, G., et al. (1998) · Development · doi:10.1242/dev.125.7.1229 · Cited by 100 · see citing works

WNT5A signaling affects pituitary gland shape

Cha, K. B., Douglas, K. R., Potok, M. A., Liang, H., Jones, S. N., & Camper, S. A. (2004) · Mechanisms of Development · doi:10.1016/j.mod.2003.12.002 · Cited by 97 · see citing works

Protein components of the blood–brain barrier (BBB) in the brainstem area postrema–nucleus tractus solitarius region

Maolood, N., & Meister, B. (2008) · Journal of Chemical Neuroanatomy · doi:10.1016/j.jchemneu.2008.12.007 · Cited by 94 · see citing works

Developmental Angiogenesis of the Central Nervous System

Mancuso, M. R., Kuhnert, F., & Kuo, C. J. (2008) · Lymphatic Research and Biology · doi:10.1089/lrb.2008.1014 · Cited by 93 · see citing works

Msx1is required for dorsal diencephalon patterning

Bach, A., Lallemand, Y., Nicola, M., Ramos, C., Mathis, L., Maufras, M., & Robert, B. (2003) · Development · doi:10.1242/dev.00609 · Cited by 90 · see citing works

Neuromyelitis optica

Matiello, M., Jacob, A., Wingerchuk, D. M., & Weinshenker, B. G. (2007) · Current Opinion in Neurology · doi:10.1097/wco.0b013e32814f1c6b · Cited by 89 · see citing works

Heterogeneous vascular permeability and alternative diffusion barrier in sensory circumventricular organs of adult mouse brain

Morita, S., Furube, E., Mannari, T., Okuda, H., Tatsumi, K., Wanaka, A., & Miyata, S. (2016) · Cell and Tissue Research · doi:10.1007/s00441-015-2207-7 · Cited by 88 · see citing works

Neuronal and Neuroendocrine Expression oflim3,a LIM Class Homeobox Gene, Is Altered in Mutant Zebrafish with Axial Signaling Defects

Glasgow, E. F., Karavanov, A. A., & Dawid, I. B. (1997) · Developmental Biology · doi:10.1006/dbio.1997.8761 · Cited by 88 · see citing works

Evolution of arylalkylamine N-acetyltransferase: emergence and divergence.

Coon, S., & Klein, D. (2006) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2006.03.039 · Cited by 88 · see citing works

Direct and indirect requirements of Shh/Gli signaling in early pituitary development

Wang, Y., Martin, J. F., & Bai, C. B. (2010) · Developmental Biology · doi:10.1016/j.ydbio.2010.09.024 · Cited by 88 · see citing works

Expression and function of nr4a2, lmx1b, and pitx3in zebrafish dopaminergic and noradrenergic neuronal development

Filippi, A., Dürr, K., Ryu, S., Willaredt, M. A., Holzschuh, J., & Driever, W. (2007) · BMC Developmental Biology · doi:10.1186/1471-213x-7-135 · Cited by 87 · see citing works

Novel HESX1 Mutations Associated with a Life-Threatening Neonatal Phenotype, Pituitary Aplasia, but Normally Located Posterior Pituitary and No Optic Nerve Abnormalities

Sobrier, M., Maghnie, M., Luton, M., Secco, A., Iorgi, N. D., Lorini, R., & Amselem, S. (2006) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2006-0426 · Cited by 84 · see citing works

Pivotal role of median eminence tanycytes for hypothalamic function and neurogenesis

Rizzoti, K., & Lovell-Badge, R. H. (2016) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2016.08.020 · Cited by 79 · see citing works

Comparative Morphology of the Vertebrate Pineal Complex

Vollrath, L. (1979) · Progress in brain research · doi:10.1016/s0079-6123(08)62909-x · Cited by 78 · see citing works

Pituitary development: a complex, temporal regulated process dependent on specific transcriptional factors

Moraes, D. C., Vaisman, M., Conceição, F. L., & Ortiga-Carvalho, T. M. (2012) · Journal of Endocrinology · doi:10.1530/joe-12-0229 · Cited by 76 · see citing works

Genetic interaction between the homeobox transcription factors HESX1 and SIX3 is required for normal pituitary development

Gaston‐Massuet, C., Andoniadou, C. L., Signore, M., Sajedi, E., Bird, S., Turner, J. M. A., & Martı́nez-Barberá, J. P. (2008) · Developmental Biology · doi:10.1016/j.ydbio.2008.08.008 · Cited by 74 · see citing works

Ontogenetical development of the chick and duck subcommissural organ

Schoebitz, K., Garrido, O., Heinrichs, M., Speer, L., & Rodr�guez, E. M. (1986) · Histochemistry and Cell Biology · doi:10.1007/bf00493417 · Cited by 73 · see citing works

Inhibition of Sox2-dependent activation of <i>Shh</i> in the ventral diencephalon by Tbx3 is required for formation of the neurohypophysis

Trowe, M.-O., Zhao, L., Weiss, A.-C., Christoffels, V., Epstein, D. J., & Kispert, A. (2013) · Development · doi:10.1242/dev.094524 · Cited by 72 · see citing works

The pineal gland and geographical distribution of animals

Ralph, C. L. (1975) · International Journal of Biometeorology · doi:10.1007/bf01451040 · Cited by 72 · see citing works

Windows of the brain: Towards a developmental biology of circumventricular and other neurohemal organs

Joly, J., Osório, J., Alunni, A., Auger, H., Kano, S., & Rétaux, S. (2007) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2007.06.001 · Cited by 72 · see citing works

Expression of the Homeobox Genes OTX2 and OTX1 in the Early Developing Human Brain

Larsen, K. B., Lutterodt, M. C., Møllgård, K., & Møller, M. (2010) · Journal of Histochemistry & Cytochemistry · doi:10.1369/jhc.2010.955757 · Cited by 72 · see citing works

A Median Third Eye: Pineal Gland Retraces Evolution of Vertebrate Photoreceptive Organs †

Mano, H., & Fukada, Y. (2006) · Photochemistry and Photobiology · doi:10.1562/2006-02-24-ir-813 · Cited by 71 · see citing works

The role of Otx and Otp genes in brain development

Acampora, D., Postiglione, M. P., Avantaggiato, V., Bonito, M. D., & Simeone, A. (2000) · The International Journal of Developmental Biology · doi:10.1387/ijdb.11061431 · Cited by 69 · see citing works

Tanycytes As Regulators of Seasonal Cycles in Neuroendocrine Function

Lewis, J. E., & Ebling, F. J. P. (2017) · Frontiers in Neurology · doi:10.3389/fneur.2017.00079 · Cited by 67 · see citing works

Differentiation of cerebellar cell identities in absence of Fgf signalling in zebrafish Otx morphants

Foucher, I., Mione, M., Simeone, A., Acampora, D., Bally‐Cuif, L., & Houart, C. (2006) · Development · doi:10.1242/dev.02352 · Cited by 65 · see citing works

A role of the LIM-homeobox gene Lhx2 in the regulation of pituitary development

Zhao, Y., Mailloux, C. M., Hermesz, E., Palkovits, M., & Westphal, H. (2009) · Developmental Biology · doi:10.1016/j.ydbio.2009.11.002 · Cited by 65 · see citing works

Understanding How the Subcommissural Organ and Other Periventricular Secretory Structures Contribute via the Cerebrospinal Fluid to Neurogenesis

Guerra, M. M., González, C., Caprile, T., Jara, M., Vío, K., Muñoz, R. I., Rodríguez, S., & Rodríguez, E. M. (2015) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2015.00480 · Cited by 65 · see citing works

On the Origin and Evolution of the Tripartite Brain

Hirth, F. (2010) · Brain Behavior and Evolution · doi:10.1159/000320218 · Cited by 64 · see citing works

The secretory ependymal cells of the subcommissural organ: Which role in hydrocephalus?

Meiniel, A. (2006) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2006.10.021 · Cited by 62 · see citing works

Molecular genetics of the developing neuroendocrine hypothalamus

Szarek, E., Cheah, P.-S., Schwartz, J., & Thomas, P. Q. (2010) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2010.04.002 · Cited by 62 · see citing works

PAX6 aniridia and interhemispheric brain anomalies.

Abouzeid, H., Youssef, M. A., ElShakankiri, N., Hauser, P. M., Munier, F. L., & Schorderet, D. F. (2009) · PubMed Central · Cited by 61 · see citing works

A Brain-Hatschek's Pit Connection in Amphioxus

Gorbman, A., Nozaki, M., & Kubokawa, K. (1999) · General and Comparative Endocrinology · doi:10.1006/gcen.1998.7193 · Cited by 61 · see citing works

The Prethalamus Is Established during Gastrulation and Influences Diencephalic Regionalization

Staudt, N. D., & Houart, C. (2007) · PLoS Biology · doi:10.1371/journal.pbio.0050069 · Cited by 61 · see citing works

The circumventricular organs.

Kaur, C., & Ling, E.-A. (2017) · PubMed · doi:10.14670/hh-11-881 · Cited by 61 · see citing works

Tbx2b is required for the development of the parapineal organ

Snelson, C. D., Santhakumar, K., Halpern, M. E., & Gamse, J. T. (2008) · Development · doi:10.1242/dev.016576 · Cited by 60 · see citing works

Drastic neofunctionalization associated with evolution of the timezyme AANAT 500 Mya

Falcón, J., Coon, S. L., Laurence Besseau, A., Cazaméa-Catalan, D., Fuentès, M., Magnanou, É., Paulin, C.-H., Bœuf, G., Sauzet, S., Jørgensen, E. H., et al. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1312634110 · Cited by 59 · see citing works

New Insights on Saccus vasculosus Evolution: A Developmental and Immunohistochemical Study in Elasmobranchs

Sueiro, C., Carrera, I., Ferreiro‐Galve, S., Molíst, P., Adrio, F., Anadón, R., & Rodríguez‐Moldes, I. (2007) · Brain Behavior and Evolution · doi:10.1159/000104309 · Cited by 56 · see citing works

Developmental and Diurnal Dynamics of Pax4 Expression in the Mammalian Pineal Gland: Nocturnal Down-Regulation Is Mediated by Adrenergic-Cyclic Adenosine 3′,5′-Monophosphate Signaling

Rath, M. F., Bailey, M. J., Kim, J., Ho, A. K., Gaildrat, P., Coon, S. L., Møller, M., & Klein, D. C. (2008) · Endocrinology · doi:10.1210/en.2008-0882 · Cited by 55 · see citing works

SCO-ping Out the Mechanisms Underlying the Etiology of Hydrocephalus

Huh, M. S., Todd, M. A. M., & Picketts, D. J. (2009) · Physiology · doi:10.1152/physiol.00039.2008 · Cited by 55 · see citing works

Xotx5b, a new member of the Otx gene family, may be involved in anterior and eye development in Xenopus laevis

Vignali, R., Colombetti, S., Lupo, G., Zhang, W., Stachel, S. E., Harland, R. M., & Barsacchi, G. (2000) · Mechanisms of Development · doi:10.1016/s0925-4773(00)00367-1 · Cited by 53 · see citing works

Zinc-containing afferent projections to the rat corticomedial amygdaloid complex: A retrograde tracing study

Christensen, M.-K., & Frederickson, C. J. (1998) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19981026)400:3 · Cited by 53 · see citing works

The role of homeodomain transcription factors in heritable pituitary disease

Prince, K. L., Walvoord, E. C., & Rhodes, S. J. (2011) · Nature Reviews Endocrinology · doi:10.1038/nrendo.2011.119 · Cited by 53 · see citing works

Deletion of OTX2 in neural ectoderm delays anterior pituitary development

Mortensen, A. H., Schade, V., Lamonerie, T., & Camper, S. A. (2014) · Human Molecular Genetics · doi:10.1093/hmg/ddu506 · Cited by 53 · see citing works

Choline acetyltransferase-immunoreactive neurons in the developing rat retina

Kim, I., Lee, E.-J., Kim, M.-K., Park, D., & Chun, M. (2000) · The Journal of Comparative Neurology · doi:10.1002/1096-9861(20001127)427:4 · Cited by 50 · see citing works

Mechanisms regulating angiogenesis underlie seasonal control of pituitary function

Castle-Miller, J., Bates, D. O., & Tortonese, D. J. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1618917114 · Cited by 50 · see citing works

A survey of occurrence of about seventeen circumventricular organs in brains of various vertebrates with special reference to lower groups.

Tsuneki, K. (1986) · PubMed · Cited by 49 · see citing works

Circumventricular Organs

Scherrmann, J. M. (2010) · Springer eBooks · doi:10.1007/978-3-540-68706-1_1096 · Cited by 48 · see citing works

Cadherin-10 is a novel blood–brain barrier adhesion molecule in human and mouse

Williams, M. J., Lowrie, M. B., Bennett, J. P., Firth, J. A., & Clark, P. (2005) · Brain Research · doi:10.1016/j.brainres.2005.07.078 · Cited by 45 · see citing works

Pheromonal stimulation of spawning release of gametes by gonadotropin releasing hormone in the chiton, Mopalia sp.

Gorbman, A., Whiteley, A. H., & Kavanaugh, S. I. (2003) · General and Comparative Endocrinology · doi:10.1016/s0016-6480(02)00647-0 · Cited by 44 · see citing works

Physiological roles for the subfornical organ: a dynamic transcriptome shaped by autonomic state

Hindmarch, C. C. T., & Ferguson, A. V. (2015) · The Journal of Physiology · doi:10.1113/jp270726 · Cited by 44 · see citing works

Direct and indirect roles of Fgf3 and Fgf10 in innervation and vascularisation of the vertebrate hypothalamic neurohypophysis

Liu, F., Pogoda, H., Pearson, C. A., Ohyama, K., Löhr, H., Hammerschmidt, M., & Placzek, M. (2013) · Development · doi:10.1242/dev.080226 · Cited by 44 · see citing works

Homeobox Genes in the Rodent Pineal Gland: Roles in Development and Phenotype Maintenance

Rath, M. F., Rohde, K., Klein, D. C., & Møller, M. (2012) · Neurochemical Research · doi:10.1007/s11064-012-0906-y · Cited by 43 · see citing works

Pax6 Is Implicated in Murine Pituitary Endocrine Function

Bentley, C. A., Zidehsarai, M. P., Grindley, J. C., Parlow, A. F., Barth, S., & Roberts, V. J. (1999) · Endocrine · doi:10.1385/endo:10:2:171 · Cited by 43 · see citing works

Role of the subcommissural organ in the pathogenesis of congenital hydrocephalus in the HTx rat

Ortloff, A., Vío, K., Guerra, M., Jaramillo, K., Kaehne, T., Jones, H. C., McAllister, J. P., & Rodríguez, E. M. (2013) · Cell and Tissue Research · doi:10.1007/s00441-013-1615-9 · Cited by 42 · see citing works

Msx1-Deficient Mice Fail to Form Prosomere 1 Derivatives, Subcommissural Organ, and Posterior Commissure and Develop Hydrocephalus

Fernández‐Llebrez, P., Grondona, J. M., Pérez, J., López‐Aranda, M. F., Estivill‐Torrús, G., Llebrez-Zayas, P., Soriano, E. R., Ramos, C., Lallemand, Y., Bach, A., et al. (2004) · Journal of Neuropathology & Experimental Neurology · doi:10.1093/jnen/63.6.574 · Cited by 42 · see citing works

The Lengthening of a Giant Protein: When, How, and Why?

Meiniel, O., Meiniel, R., Lalloué, F., Didier, R., Jauberteau, M., Meiniel, A., & Petit, D. P. (2007) · Journal of Molecular Evolution · doi:10.1007/s00239-007-9055-3 · Cited by 40 · see citing works

The Lhx9 homeobox gene controls pineal gland development and prevents postnatal hydrocephalus

Yamazaki, F., Møller, M., Fu, C., Clokie, S. J. H., Zykovich, A., Coon, S. L., Klein, D. C., & Rath, M. F. (2014) · Brain Structure and Function · doi:10.1007/s00429-014-0740-x · Cited by 38 · see citing works

Postnatal distribution of Glut1 glucose transporter and relative capillary density in blood-brain barrier structures and circumventricular organs during development

Zeller, K., Vogel, J., & Kuschinsky, W. (1996) · Developmental Brain Research · doi:10.1016/0165-3806(95)00177-8 · Cited by 36 · see citing works

Glucose-responsive neurons in the subfornical organ of the rat—a novel site for direct CNS monitoring of circulating glucose

Medeiros, N., Dai, L., & Ferguson, A. V. (2011) · Neuroscience · doi:10.1016/j.neuroscience.2011.11.028 · Cited by 36 · see citing works

Heterogeneous occurrence of aquaporin-4 in the ependyma and in the circumventricular organs in rat and chicken

Goren, O., Adorjan, I., & Kálmán, M. (2006) · Anatomy and Embryology · doi:10.1007/s00429-005-0067-8 · Cited by 35 · see citing works

Pax6 regulates the formation of the habenular nuclei by controlling the temporospatial expression of Shhin the diencephalon in vertebrates

Chatterjee, M., Guo, Q., Weber, S., Scholpp, S., & Li, J. Y. H. (2014) · BMC Biology · doi:10.1186/1741-7007-12-13 · Cited by 32 · see citing works

Congenital Hydrocephalus and Abnormal Subcommissural Organ Development in Sox3 Transgenic Mice

Lee, K., Tan, J., Morris, M. B., Rizzoti, K., Hughes, J., Cheah, P.-S., Felquer, F. A., Liu, X., Piltz, S., Lovell-Badge, R. H., et al. (2012) · PLoS ONE · doi:10.1371/journal.pone.0029041 · Cited by 32 · see citing works

Chicken lateral septal organ and other circumventricular organs form in a striatal subdomain abutting the molecular striatopallidal border

Bardet, S. M., Cobos, I., Puelles, E., Martinez-de-la-Torre, M., & Puelles, L. (2006) · The Journal of Comparative Neurology · doi:10.1002/cne.21121 · Cited by 30 · see citing works

The Subcommissural Organ and the Development of the Posterior Commissure

Grondona, J. M., Hoyo-Becerra, C., Visser, R., Fernández‐Llebrez, P., & López-Ávalos, M. D. (2012) · International review of cytology · doi:10.1016/b978-0-12-394307-1.00002-3 · Cited by 29 · see citing works

Hypothalamus as an Endocrine Organ

Clarke, I. J. (2015) · Comprehensive physiology · doi:10.1002/j.2040-4603.2015.tb00605.x · Cited by 28 · see citing works

Expression patterns of Shh, Ptc2, Raldh3, Pitx2, Isl1, Lim3 and Pax6 in the developing chick hypophyseal placode and Rathke’s pouch

Sjödal, M., & Gunhaga, L. (2008) · Gene Expression Patterns · doi:10.1016/j.gep.2008.06.007 · Cited by 27 · see citing works

The human subfornical organ: an anatomic and ultrastructural study.

Mh, M., & Farmer, P. (1985) · PubMed · Cited by 27 · see citing works

Evolution of AANAT: expansion of the gene family in the cephalochordate amphioxus

Pavlı́ček, J., Sauzet, S., Laurence Besseau, A., Coon, S. L., Weller, J. L., Bœuf, G., Gaildrat, P., Omelchenko, M. V., Koonin, E. V., Falcón, J., et al. (2010) · BMC Evolutionary Biology · doi:10.1186/1471-2148-10-154 · Cited by 26 · see citing works

Aquaporin-1 in blood vessels of rat circumventricular organs

Wilson, A. J., Carati, C. J., Gannon, B. J., Haberberger, R. V., & Chataway, T. (2010) · Cell and Tissue Research · doi:10.1007/s00441-010-0927-2 · Cited by 26 · see citing works

Thyrotropin-releasing hormone concentrations in different regions of the chicken brain and pituitary: an ontogenetic study

Geris, K. L., D’Hondt, E., Kühn, E. R., & Darras, V. (1999) · Brain Research · doi:10.1016/s0006-8993(98)01281-5 · Cited by 24 · see citing works

Origin and early development of the chicken adenohypophysis

Sánchez‐Arrones, L., Ferrán, J. L., Hidalgo‐Sánchez, M., & Puelles, L. (2015) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2015.00007 · Cited by 24 · see citing works

Newly identified patterns of Pax2 expression in the developing mouse forebrain

Fotaki, V., Price, D. J., & Mason, J. O. (2008) · BMC Developmental Biology · doi:10.1186/1471-213x-8-79 · Cited by 23 · see citing works

Early development of the human area postrema and subfornical organ

Castañeyra-Perdomo, A., Meyer, G., & Heylings, D. J. (1992) · The Anatomical Record · doi:10.1002/ar.1092320416 · Cited by 21 · see citing works

Ontogeny of the Saccus Vasculosus, a Seasonal Sensor in Fish

Maeda, R., Shimo, T., Nakane, Y., Nakao, N., & Yoshimura, T. (2015) · Endocrinology · doi:10.1210/en.2015-1415 · Cited by 17 · see citing works

Neurohumoral Integration of Cardiovascular Function by the Lamina Terminalis

Cancelliere, N. M., Black, E. A. E., & Ferguson, A. V. (2015) · Current Hypertension Reports · doi:10.1007/s11906-015-0602-9 · Cited by 16 · see citing works

GABAergic systems in the nucleus tractus solitarius regulate noradrenaline release in the subfornical organ area in the rat

Tanaka, J., Mashiko, N., Kawakami, A., Ushigome, A., & Nomura, M. (2002) · Autonomic Neuroscience · doi:10.1016/s1566-0702(02)00152-2 · Cited by 16 · see citing works

Attenuated drinking response induced by angiotensinergic activation of subfornical organ projections to the paraventricular nucleus in estrogen-treated rats

Tanaka, J., Kariya, K., Miyakubo, H., Sakamaki, K., & Nomura, M. (2002) · Neuroscience Letters · doi:10.1016/s0304-3940(02)00203-3 · Cited by 15 · see citing works

Differential Cellular Responses to Hedgehog Signalling in Vertebrates—What is the Role of Competence?

Kiecker, C., Graham, A., & Logan, M. (2016) · Journal of Developmental Biology · doi:10.3390/jdb4040036 · Cited by 6 · see citing works

LIM homeodomain proteins Islet‐1 and Lim‐3 expressions in the developing pineal gland of chick embryo by immunohistochemistry

Zhang, J., Liu, J., Wu, Y., & Cui, S. (2006) · Journal of Pineal Research · doi:10.1111/j.1600-079x.2006.00363.x · Cited by 5 · see citing works

Circumventricular Organs

Anderson, J. W., & Ferguson, A. V. (2003) · Humana Press eBooks · doi:10.1385/1-59259-108-6:309 · Cited by 5 · see citing works

Multiple forms of glycoproteins in the secretory product of the bovine subcommissural organ - an ancient glial structure

Lehmann, W., Wagner, U., & Naumann, W. W. (2001) · Acta Histochemica · doi:10.1078/0065-1281-00583 · Cited by 3 · see citing works

A high-resolution transcriptomic and spatial atlas of cell types in the whole mouse brain

Yao, Z., van Velthoven, C. T. J., Kunst, M., Zhang, M., McMillen, D., Lee, C., Jung, W., Goldy, J., Abdelhak, A., Aitken, M., et al. (2023) · Nature · doi:10.1038/s41586-023-06812-z · Cited by 1,194 · see citing works

A Comprehensive Review on the Role of the Gut Microbiome in Human Neurological Disorders

Sorboni, S. G., Moghaddam, H. S., Jafarzadeh-Esfehani, R., & Soleimanpour, S. (2022) · Clinical Microbiology Reviews · doi:10.1128/cmr.00338-20 · Cited by 562 · see citing works

The Glymphatic System: A Novel Component of Fundamental Neurobiology

Hablitz, L. M., & Nedergaard, M. (2021) · Journal of Neuroscience · doi:10.1523/jneurosci.0619-21.2021 · Cited by 480 · see citing works

The Bioavailability of Drugs—The Current State of Knowledge

Stielow, M., Witczyńska, A., Kubryń, N., Fijałkowski, Ł., Nowaczyk, J., & Nowaczyk, A. (2023) · Molecules · doi:10.3390/molecules28248038 · Cited by 426 · see citing works

Brain-wide cell-type-specific transcriptomic signatures of healthy ageing in mice

Jin, K., Yao, Z., van Velthoven, C. T. J., Kaplan, E. S., Glattfelder, K. J., Barlow, S. T., Boyer, G., Carey, D., Casper, T., Chakka, A. B., et al. (2025) · Nature · doi:10.1038/s41586-024-08350-8 · Cited by 146 · see citing works

Basic physiology of the blood-brain barrier in health and disease: a brief overview

Kaya, M., & Ahıshalı, B. (2020) · Tissue Barriers · doi:10.1080/21688370.2020.1840913 · Cited by 120 · see citing works

Structure and Function of the Blood–Brain Barrier (BBB)

Benz, F., & Liebner, S. (2020) · Handbook of experimental pharmacology · doi:10.1007/164_2020_404 · Cited by 97 · see citing works

Low wnt/β-catenin signaling determines leaky vessels in the subfornical organ and affects water homeostasis in mice

Benz, F., Wichitnaowarat, V., Lehmann, M., Germano, R. F. V., Mihova, D., Macas, J., Adams, R. H., Taketo, M. M., Plate, K.-H., Guérit, S., et al. (2019) · eLife · doi:10.7554/elife.43818 · Cited by 85 · see citing works

Osteocyte-derived sclerostin impairs cognitive function during ageing and Alzheimer’s disease progression

Shi, T., Shen, S., Shi, Y., Wang, Q., Zhang, G., Lin, J., Chen, J., Bai, F., Zhang, L., Wang, Y., et al. (2024) · Nature Metabolism · doi:10.1038/s42255-024-00989-x · Cited by 87 · see citing works

Developmental regulation of barrier‐ and non‐barrier blood vessels in the CNS

Ben‐Zvi, A., & Liebner, S. (2021) · Journal of Internal Medicine · doi:10.1111/joim.13263 · Cited by 62 · see citing works

Revisiting the pineal gland: a review of calcification, masses, precocious puberty, and melatonin functions

Patel, S., Rahmani, B., Gandhi, J., Seyam, O., Joshi, G. S., Reid, I., Smith, N. L., Waltzer, W. C., & Khan, S. A. (2019) · International Journal of Neuroscience · doi:10.1080/00207454.2019.1692838 · Cited by 63 · see citing works

Visceral adiposity, inflammation, and hippocampal function in obesity

Stranahan, A. M. (2021) · Neuropharmacology · doi:10.1016/j.neuropharm.2021.108920 · Cited by 63 · see citing works

Circumventricular Organs and Parasite Neurotropism: Neglected Gates to the Brain?

Bentivoglio, M., Kristensson, K., & Rottenberg, M. E. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.02877 · Cited by 59 · see citing works

Form and Function of the Vertebrate and Invertebrate Blood-Brain Barriers

Dunton, A. D., Göpel, T., Ho, D. H., & Burggren, W. W. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms222212111 · Cited by 55 · see citing works

Impact of P-Glycoprotein Function on the Brain Kinetics of the Weak Substrate 11C-Metoclopramide Assessed with PET Imaging in Humans

Tournier, N., Bauer, M., Pichler, V., Nics, L., Klebermass, E., Bamminger, K., Matzneller, P., Weber, M., Karch, R., Caillé, F., et al. (2019) · Journal of Nuclear Medicine · doi:10.2967/jnumed.118.219972 · Cited by 49 · see citing works

Central regulation of body fluid homeostasis

Noda, M., & Matsuda, T. (2022) · Proceedings of the Japan Academy Series B · doi:10.2183/pjab.98.016 · Cited by 47 · see citing works

Understanding glucose metabolism and insulin action at the blood–brain barrier: Implications for brain health and neurodegenerative diseases

Zhu, Y., Verkhratsky, A., Chen, H., & Yi, C. (2025) · Acta Physiologica · doi:10.1111/apha.14283 · Cited by 49 · see citing works

Thymus-Pineal Gland Axis: Revisiting Its Role in Human Life and Ageing

Rezzani, R., Franco, C., Hardeland, R., & Rodella, L. F. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21228806 · Cited by 37 · see citing works

Genetic and epigenetic characterization of posterior pituitary tumors

Schmid, S., Solomon, D. A., Pérez, E., Thieme, A., Kleinschmidt-DeMasters, B. K., Giannini, C., Reinhardt, A., Asa, S. L., Mete, Ö., Stichel, D., et al. (2021) · Acta Neuropathologica · doi:10.1007/s00401-021-02377-1 · Cited by 32 · see citing works

Hypertension, blood–brain barrier disruption and changes in intracranial pressure

Colombari, E., Biancardi, V. C., Colombari, D. S. A., Katayama, P. L., Medeiros, F., Aitken, A. V., Xavier, C. H., Pedrino, G. R., & Евгеньевич, Б. Д. (2025) · The Journal of Physiology · doi:10.1113/jp285058 · Cited by 35 · see citing works

Obesity, Metabolic Syndrome and Disorders of Energy Balance

Han, J. C., & Weiss, R. (2021) · Elsevier eBooks · doi:10.1016/b978-0-323-62520-3.00024-5 · Cited by 27 · see citing works

Physiology, Blood Brain Barrier

Gawdi, R., & Emmady, P. D. (2020) · StatPearls · Cited by 26 · see citing works

Aquaporins: Gatekeepers of Fluid Dynamics in Traumatic Brain Injury

Czyżewski, W., Litak, J., Sobstyl, J., Mandat, T. S., Torres, K., & Staśkiewicz, G. J. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25126553 · Cited by 25 · see citing works

Novel molecular subtypes of intracranial germ cell tumors expand therapeutic opportunities

Li, B., Zhao, S., Li, S., Li, C., Liu, W., Li, L., Cui, B., Liu, X., Chen, H., Zhang, J., et al. (2024) · Neuro-Oncology · doi:10.1093/neuonc/noae038 · Cited by 21 · see citing works

The Enigmatic Reissner’s Fiber and the Origin of Chordates

Aboitiz, F., & Montiel, J. F. (2021) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2021.703835 · Cited by 18 · see citing works

Central regulation of glucose metabolism in an insulin‐dependent and ‐independent manner

Fujikawa, T. (2021) · Journal of Neuroendocrinology · doi:10.1111/jne.12941 · Cited by 19 · see citing works

Primary papillary epithelial tumour of the sella: expanding the spectrum of TTF‐1‐positive sellar lesions

Roncaroli, F., Chatterjee, D., Giannini, C., Pereira, M., Rosa, S. L., Brouland, J., Gnanalingham, K. K., GALLI, C., Fernandes, B., Lania, A. G., et al. (2020) · Neuropathology and Applied Neurobiology · doi:10.1111/nan.12622 · Cited by 17 · see citing works

Central nervous system disorders after use of dolutegravir: evidence from preclinical and clinical studies

Jakimiuk, A. A., Piechal, A., Wiercińska‐Drapało, A., Nowaczyk, A., & Mirowska-Guzel, D. M. (2023) · Pharmacological Reports · doi:10.1007/s43440-023-00515-y · Cited by 16 · see citing works

The organum vasculosum of the lamina terminalis and subfornical organ: regulation of thirst

Wang, J., Lv, F., Yin, W., Gao, Z., Liu, H., Wang, Z., & Sun, J. (2023) · Frontiers in Neuroscience · doi:10.3389/fnins.2023.1223836 · Cited by 15 · see citing works

Endogenous amylin contributes to birth of microglial cells in arcuate nucleus of hypothalamus and area postrema during fetal development

Lutz, T. A., & Foll, C. L. (2019) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00004.2019 · Cited by 15 · see citing works

Camel regulates development of the brain ventricular system

Yang, S., Emelyanov, A., You, M., Sin, M., & Korzh, V. P. (2020) · Cell and Tissue Research · doi:10.1007/s00441-020-03270-1 · Cited by 15 · see citing works

Development of a Therapeutic Peptide for Cachexia Suggests a Platform Approach for Drug-like Peptides

Gruber, K. A., Ji, R.-L., Gallazzi, F., Jiang, S., Doren, S. R. V., Tao, Y., & Newton‐Northup, J. (2022) · ACS Pharmacology & Translational Science · doi:10.1021/acsptsci.1c00270 · Cited by 14 · see citing works

Salient brain entities labelled in P2rx7-EGFP reporter mouse embryos include the septum, roof plate glial specializations and circumventricular ependymal organs

Ortega, F., Gómez‐Villafuertes, R., Benito-León, M., de la Torre, M. M., Olivos-Oré, L. A., Arribas-Blázquez, M., Gómez‐Gaviro, M. V., Azcorra, A., Desco, M., Artalejo, A. R., et al. (2021) · Brain Structure and Function · doi:10.1007/s00429-020-02204-5 · Cited by 14 · see citing works

Imaging the pituitary in psychopathologies: a review of in vivo magnetic resonance imaging studies

Anastassiadis, C., Jones, S. L., & Pruessner, J. C. (2019) · Brain Structure and Function · doi:10.1007/s00429-019-01942-5 · Cited by 14 · see citing works

Origin and development of circumventricular organs in living vertebrate

Korzh, V. P., & Kondrychyn, I. (2019) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2019.10.010 · Cited by 13 · see citing works

Microglia in Circumventricular Organs: The Pineal Gland Example

Muñoz, E. M. (2022) · ASN NEURO · doi:10.1177/17590914221135697 · Cited by 13 · see citing works

Area Postrema: Fetal Maturation, Tumors, Vomiting Center, Growth, Role in Neuromyelitis Optica

Sarnat, H. B., Flores‐Sarnat, L., & Boltshauser, E. (2018) · Pediatric Neurology · doi:10.1016/j.pediatrneurol.2018.12.006 · Cited by 13 · see citing works

Role of aldosterone and mineralocorticoid receptor (MR) in addiction: A scoping review

Pince, C. L., Whiting, K. E., Wang, T., Lékó, A. H., Farinelli, L. A., Cooper, D., Farokhnia, M., Vendruscolo, L. F., & Leggio, L. (2023) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2023.105427 · Cited by 12 · see citing works

A critique on the theory of homeostasis.

Luca, L. A. D. (2022) · Physiology and Behavior · doi:10.1016/j.physbeh.2022.113712 · Cited by 10 · see citing works

The Microbiome–Neurodegeneration Interface: Mechanisms, Evidence, and Future Directions

Böckels, L., Alexa, D., Antal, D. C., Gațcan, C., Alecu, C., Kacani, K., Cretu, R. A., Piseru, E.-A., Bîlcu, R. V., & Cuciureanu, D. I. (2026) · Cells · doi:10.3390/cells15020135 · Cited by 12 · see citing works

Regulation of the blood-brain barrier function by peripheral cues in health and disease

Devraj, K., Kulkarni, O. P., & Liebner, S. (2024) · Metabolic Brain Disease · doi:10.1007/s11011-024-01468-8 · Cited by 13 · see citing works

Improving Eflornithine Oral Bioavailability and Brain Uptake by Modulating Intercellular Junctions With an E-cadherin Peptide

Yang, S., Chen, Y., Feng, M., Rodriguez, L., Wu, J. Q., & Wang, M. Z. (2019) · Journal of Pharmaceutical Sciences · doi:10.1016/j.xphs.2019.09.015 · Cited by 10 · see citing works

Cell-type specific molecular signatures of aging revealed in a brain-wide transcriptomic cell-type atlasPreprint

Jin, K., Yao, Z., van Velthoven, C. T. J., Kaplan, E. S., Glattfelder, K. J., Barlow, S. T., Boyer, G., Carey, D., Casper, T., Chakka, A. B., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.07.26.550355 · Cited by 10 · see citing works

Interference with systemic negative feedback as a potential mechanism for nonmonotonic dose-responses of endocrine-disrupting chemicals

Shi, Z., Xiao, S., & Zhang, Q. (2025) · Toxicological Sciences · doi:10.1093/toxsci/kfaf060 · Cited by 9 · see citing works

Pineal progenitors originate from a non-neural territory limited by FGF signalling

Staudt, N. D., Giger, F. A., Fielding, T., Hutt, J. A., Foucher, I., Snowden, V., Hellich, A., Kiecker, C. M., & Houart, C. (2019) · Development · doi:10.1242/dev.171405 · Cited by 9 · see citing works

Signaling within the pineal gland: A parallelism with the central nervous system

Altamirano, L. E. F., Freites, C. L., Vásquez, E., & Muñoz, E. M. (2018) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2018.11.004 · Cited by 9 · see citing works

Nanoparticles Navigating the Intranasal Route: Innovative Approaches in Neurodegenerative Diseases

Borbolla‐Jiménez, F. V., Gutiérrez-Ruíz, S. C., Hernández‐Parra, H., Peña‐Corona, S. I., Tamez-González, A., Rivas-Amores, R. D., Magaña, J. J., & Leyva‐Gómez, G. (2025) · Journal of Nanotechnology · doi:10.1155/jnt/7697122 · Cited by 7 · see citing works

Parallel trajectories in the discovery of the SCN‐OVLT and pituitary portal pathways: Legacies of Geoffrey Harris

Silver, R., Yao, Y., Roy, R. K., & Stern, J. E. (2023) · Journal of Neuroendocrinology · doi:10.1111/jne.13245 · Cited by 8 · see citing works

Hypocortisolemic ASIA: a vaccine- and chronic infection-induced syndrome behind the origin of long COVID and myalgic encephalomyelitis

Ruiz-Pablos, M., Paiva, B., & Zabaleta, A. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1422940 · Cited by 7 · see citing works

Neuropathological links between T2DM and LOAD: systematic review and meta-analysis

Lemche, E., Hortobágyi, T., Kiecker, C. M., & Turkheimer, F. (2025) · Physiological Reviews · doi:10.1152/physrev.00040.2024 · Cited by 8 · see citing works

Early-life sodium deprivation programs long-term changes in ingestive behaviors and energy expenditure in C57BL/6J mice

Ziegler, A. A., Lawton, S. B. R., Grobe, C. C., Reho, J. J., Freudinger, B. P., Burnett, C. M.-L., Nakagawa, P., Grobe, J. L., & Segar, J. L. (2023) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00137.2023 · Cited by 7 · see citing works

A bioinspired model of short-term satiety of hunger influenced by food properties in virtual creatures

Gómez-Martínez, D. G., Ramos, M. A., del Valle‐Padilla, J. L., Rosales, J.-H., Robles, F., & Ramos, F. (2020) · Cognitive Systems Research · doi:10.1016/j.cogsys.2020.10.008 · Cited by 7 · see citing works

The circle of Willis revisited: Forebrain dehydration sensing facilitated by the anterior communicating artery

Fenrich, M., Habjanović, K., Kajan, J., & Heffer, M. (2020) · BioEssays · doi:10.1002/bies.202000115 · Cited by 6 · see citing works

The Phylotypic Brain of Vertebrates, from Neural Tube Closure to Brain Diversification

Senovilla-Ganzo, R., & García‐Moreno, F. (2024) · Brain Behavior and Evolution · doi:10.1159/000537748 · Cited by 6 · see citing works

Profiling metabolome of mouse embryonic cerebrospinal fluid following maternal immune activation

Petrova, B., Lacey, T. E., Culhane, A. J., Cui, J., Brook, J. R., Raskind, A. B., Misra, A., Lehtinen, M. K., & Kanarek, N. (2024) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2024.107749 · Cited by 9 · see citing works

The Intricate Relationship between Melatonin and Breast Cancer: A Short Review

Pistioli, L., Katsarelias, D., Audisio, R. A., & Bagge, R. O. (2021) · Chirurgia · doi:10.21614/chirurgia.116.2suppl.s24 · Cited by 6 · see citing works

A novel feature of the ancient organ: A possible involvement of the subcommissural organ in neurogenic/gliogenic potential in the adult brain

Inada, H., Corales, L. G., & Osumi, N. (2023) · Frontiers in Neuroscience · doi:10.3389/fnins.2023.1141913 · Cited by 5 · see citing works

Identification of New Ketamine Metabolites and Their Detailed Distribution in the Mammalian Brain

Vallianatou, T., Anselmo, C. D. S., Tsiara, I., Bèchet, N. B., Lundgaard, I., & Globisch, D. (2024) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.4c00051 · Cited by 4 · see citing works

Development of the neurohypophysis: A major neuroendocrine interface

Ramesh, A. R., Nedunchezhian, N., Ali, M. H., Pęcherz, S., Kowalewska, N., & Anbalagan, S. (2025) · Journal of Neuroendocrinology · doi:10.1111/jne.70125 · Cited by 3 · see citing works

Early and isolated breast cancer metastasis to the pituitary: A case report and systematic review

Rasiah, N. P., Albakr, A. A., Kosteniuk, S., & Starreveld, Y. P. (2022) · Surgical Neurology International · doi:10.25259/sni_1053_2021 · Cited by 3 · see citing works

Metabolomics of Mouse Embryonic CSF Following Maternal Immune ActivationPreprint

Petrova, B., Lacey, T. E., Culhane, A. J., Cui, J., Raskin, A., Misra, A., Lehtinen, M. K., & Kanarek, N. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.12.06.570507 · Cited by 3 · see citing works

Modification of the Bacterial Metabolites by the Host after Absorption, and Consequences for the Peripheral Tissues’ Metabolism, Physiology, and Physiopathology

Blachier, F. (2023) · Springer eBooks · doi:10.1007/978-3-031-26322-4_5 · Cited by 2 · see citing works

Histological examination of neuroanatomical and ocular structures in the Gambian Sun squirrel ( Heliosciurus gambianus Ogilby, 1835) for understanding arboreal adaptations

Fatola, O. I., Aribisala, K. C., Gilbert, T. T., Njasi, M. K., Abeje, J. I., Aina, O. O., & Olopade, J. O. (2025) · The Anatomical Record · doi:10.1002/ar.25684 · Cited by 2 · see citing works

Hypothalamic Median Eminence Thyrotropin-Releasing Hormone-Degrading Ectoenzyme Activity Is Dispensable for Basal Thyroid Axis Activity in Lean Rodents

Rodríguez-Rodríguez, A., Uribe, R. M., Cote-Vélez, A., Joseph‐Bravo, P., & Charli, J. (2025) · Cells · doi:10.3390/cells14100725 · Cited by 2 · see citing works

Sensory Circumventricular Organ Insulin Signaling in Cardiovascular and Metabolic Regulation

Kim, H. R., Jeong, J. K., & Young, C. N. (2025) · Current Issues in Molecular Biology · doi:10.3390/cimb47080595 · Cited by 2 · see citing works

Material considerations for delivering therapeutics across the blood–brain barrier

Zoba, A. N., & Tringides, C. M. (2025) · APL Materials · doi:10.1063/5.0284305 · Cited by 2 · see citing works

New routes to the neuroendocrine hypothalamus: the extracellular space

Nicolas, J. C., Huwart, S. J. P., Ziemens, D., Freire-Agulleiro, Ó., Lee, T. H.-Y., Mattot, V., & Quarta, C. (2025) · European Journal of Endocrinology · doi:10.1093/ejendo/lvaf197 · Cited by 2 · see citing works

Das Gehirn. Wie ein Organ unsere Essensentscheidungsteuert Die physiologische Kontrolle des Essverhaltens verstehen

Lippert, R. N. (2023) · doi:10.5771/9783987400087-15 · Cited by 1 · see citing works

Global Clock Coordination by the Brain Clock in the Suprachiasmatic Nucleus Through Relay and Amplification of Diffusible and Neural Signaling

Silver, R., Yao, Y., & Myung, J. (2025) · European Journal of Neuroscience · doi:10.1111/ejn.70097 · Cited by 2 · see citing works

Spatial and single-cell transcriptomics on SSPO PTV mutant mice reveals SCO-spondin’s function in mood regulation through brain barriersPreprint

Gao, Y., Xu, J., Li, S., Yi, W., Xiao, L., Feng, F., Zhang, B., Li, J., & Yang, X. (2024) · medRxiv · doi:10.1101/2024.04.09.24305433 · Cited by 2 · see citing works

Kcnb1-Kcng4 axis regulates Scospondin secretion and Reissner fiber developmentPreprint

Amini, R. R., Jain, R. P., & Korzh, V. P. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.12.20.629661 · Cited by 2 · see citing works

Morphofunctional Organization of the Subfornical Organ

Соколов, Д. А., Alexeeva, N. Т., Nikityuk, D. B., Клочкова, С. В., & Lushnikova, E. L. (2023) · Journal of Anatomy and Histopathology · doi:10.18499/2225-7357-2023-12-1-9-19 · Cited by 1 · see citing works

Perspective: rheostasis revisited—hibernation and tanycytes

Wood, S. H. (2025) · Journal of Comparative Physiology B · doi:10.1007/s00360-025-01636-x · Cited by 1 · see citing works

Kv2.1 negatively regulates Reissner fiber development

Amini, R. R., Jain, R., Jędrychowska, J., & Korzh, V. P. (2026) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2025.1720752 · Cited by 1 · see citing works

Early Regressive Development of the Subcommissural Organ of Two Human Fetuses with Non-Communicating Hydrocephalus

Carmona-Calero, E. M., González-Toledo, J. M., Hernández-Abad, L. G., Castañeyra-Perdomo, A., & González-Marrero, I. (2022) · Children · doi:10.3390/children9121966 · Cited by 1 · see citing works

CSF Physiology

Bubeníková, A., Skalický, P., Whitley, H., & Bradáč, O. (2023) · Springer eBooks · doi:10.1007/978-3-031-36522-5_5 · Cited by 1 · see citing works

Rhythmic patterns in microglial cells within the circadian pineal gland from male rats

Freites, C. L., Avila, M., Amiotti, J. B., & Muñoz, E. M. (2025) · The Anatomical Record · doi:10.1002/ar.70099

Melatonina como fator regulador do perfil de ativação de microglias no cerebelo de ratos

de Souza, E. D. S. (2021) · doi:10.11606/d.41.2021.tde-16072021-164107

NEUROSURGERY OF THE PINEAL REGION TUMOURS: ROLE OF MICROSURGERY

Dizdarević, K. (2021) · doi:10.5644/pi2021.197.05

Tumori centralnog nervnog sistema

(2021) · doi:10.5644/pi2021.197.00

Alterations in morphology and barrier function of tanycytes in an APP/PS1 transgenic mouse model of Alzheimer’s diseasePreprint

Qi, G., Gong, P., Liu, Y., Hu, J., Kang, S., Tang, H., & Qin, S. (2023) · Research Square · doi:10.21203/rs.3.rs-2895842/v1

Neurotoxic Effects of Polycyclic Aromatic Hydrocarbons in Vertebrates, from Behavioral to Cellular Levels

Dunton, A. D. (2023) · doi:10.12794/metadc2179285

Морфологічні структури циркумвентрикулярного комплексу (Morphological structures of the circumvetricular complex)

Пикалюк, В., Романюк, А., Антонюк, О. П., Слободян, О., & Апончук, Л. С. (2024) · Notes in Current Biology · doi:10.29038/ncbio.24.1-2

LPS mediated neuronal c-Fos activation: whole-brain mapping, site and time effect in intoxicated mice

Hussein, M. N. A., Alotaibi, K. S., Althobaiti, S. A., Albattal, S. B., Xiao, K., Dai, J., Cao, G., & Soliman, M. M. (2025) · Toxicology Research · doi:10.1093/toxres/tfaf131

Neurobiological mechanisms of postoperative delirium at neural molecular and cellular levels

Lu, X., Yan, R., & Song, S. (2025) · Academia Medicine and Health · doi:10.20935/acadmedhealth7977

Signal Amplification in the HPT Axis—Evidence for Its Existence, Location, Significance, and Molecular Mechanisms

Li, J., Moyd, S. A., & Zhang, Q. (2026) · Acta Physiologica · doi:10.1111/apha.70202

Caractérisation et modulation du microbiote intestinal dans le contexte de la maladie d’Alzheimer : vers une nouvelle piste thérapeutique

Ismeurt, C. (2021) · theses.fr (ABES) · doi:10.70675/159d4638zb5f8z4580zb26fzd0419dba4d37

Ependymomas are cancers of the pre-neural crest/roof plate lineagePreprint

Balin, P., Kumar, S. A., Galton, R., Delaidelli, A., Orisme, W., Haldipur, P., Mankahla, N., Saadeldin, A. M., von Krosigk, N., Vladoiu, M. C., et al. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.07.13.736818

Iba-1-ИММУНОПОЛОЖИТЕЛЬНЫЕ КЛЕТКИ ШИШКОВИДНОЙ ЖЕЛЕЗЫ КРЫСЫ

Yakovlev, V. S., Суфиева, Д. А., Grigor’ev, I. P., Гусельникова, В. В., & Korzhevsky, D. E. (2026) · Успехи геронтологии · doi:10.34922/ae.2026.39.3.015

Hypothalamic supraoptic and paraventricular nuclei

Krabichler, Q., & Grinevich, V. (2026) · Elsevier eBooks · doi:10.1016/b978-0-443-24078-2.00012-7

Hypothalamic neuroimmune remodeling as an immunometabolic bridge between childhood obesity and earlier pubertal onset

Liu, P., Chen, Y., Zhang, Y. F., Peng, Y., Lei, E., & Liu, J. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2026.1932785

Exercise-related brain remodeling through bidirectional brain-body crosstalk: an integrative narrative review

Yin, D., Luo, C., Hu, J., & Bi, S.-Z. (2026) · Frontiers in Integrative Neuroscience · doi:10.3389/fnint.2026.1954740

Origin and development of circumventricular organs in living vertebrate

Korzh, V. P., & Kondrychyn, I. (2019) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2019.10.010 · Cited by 13 · see citing works

Cerebrospinal fluid and central nervous system development

Bueno, D. (2020) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2019.12.014 · Cited by 3 · see citing works

Circumventricular Organs

McKinley, M. J., Clarke, I. J., & Oldfield, B. J. (2004) · Elsevier eBooks · doi:10.1016/b978-012547626-3/50020-x · Cited by 22 · see citing works

Introduction

McKinley, M. J., McAllen, R. M., Davern, P. J., Giles, M., Penschow, J., Sunn, N., Uschakov, A., & Oldfield, B. J. (2003) · Advances in anatomy, embryology and cell biology · doi:10.1007/978-3-642-55532-9_1 · Cited by 134 · see citing works

The circumventricular organs.

Kaur, C., & Ling, E.-A. (2017) · PubMed · doi:10.14670/hh-11-881 · Cited by 61 · see citing works