Trophic Interactions Between Astroglial Cells and Hippocampal Neurons in Culture

Growth of a rat neuroblastoma cell line in serum-free supplemented medium.

Bottenstein, J. E., & SATO, G. H. (1979) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.76.1.514 · Cited by 2,268

Rat hippocampal neurons in dispersed cell culture.

Banker, G. A., & Cowan, W. M. (1977) · Brain Research · doi:10.1016/0006-8993(77)90594-7 · Cited by 1,110

Growth and cultivation of dissociated neurons and glial cells from embryonic chick, rat and human brain in flask cultures.

Booher, J., & Sensenbrenner, M. (1972) · PubMed · Cited by 760

Adult rat brain astrocytes support survival of both NGF-dependent and NGF-insensitive neurones

Lindsay, R. M. (1979) · Nature · doi:10.1038/282080a0 · Cited by 373

Trophic Mechanisms in the Peripheral Nervous System

Varon, S. S., & Bunge, R. P. (1978) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.01.030178.001551 · Cited by 326

Further observations on hippocampal neurons in dispersed cell culture

Banker, G. A., & Cowan, W. M. (1979) · Journal of Comparative Neurology · doi:10.1002/cne.901870302 · Cited by 285

Nerve Growth Factor

Bradshaw, R. A. (1978) · Annual Review of Biochemistry · doi:10.1146/annurev.bi.47.070178.001203 · Cited by 246

Neuron-glia interactions.

Varon, S. S., & Gg, S. (1979) · PubMed · Cited by 244

Induction of neurite outgrowth by a conditioned-medium factor bound to the culture substratum

Collins, F. (1978) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.75.10.5210 · Cited by 241

Survival and development in culture of dissociated parasympathetic neurons from ciliary ganglia

Helfand, S. L., Smith, G. A., & Wessells, N. K. (1976) · Developmental Biology · doi:10.1016/0012-1606(76)90174-3 · Cited by 177

Motoneurone survival is induced by immature astrocytes from developing avian spinal cord

Eagleson, K. L., Raju, T. R., & Bennett, M. R. (1985) · Developmental Brain Research · doi:10.1016/0165-3806(85)90135-x · Cited by 64

Novel neuroglial and glioglial relationships mediated by L-serine metabolism

Furuya, S., & Watanabe, M. (2003) · Archivum histologicum japonicum · doi:10.1679/aohc.66.109 · Cited by 63

Substance P and somatostatin coexist within neuritic plaques: Implications for the pathogenesis of Alzheimer's disease

Armstrong, D. M., Benzing, W. C., Evans, J. A., Terry, R. D., Shields, D., & Hansen, L. A. (1989) · Neuroscience · doi:10.1016/0306-4522(89)90431-4 · Cited by 63

Neurotropic influence of mesenchymal limb target tissue on spinal cord neurite growth in vitro

Pollack, E. D., Muhlach, W. L., & Liebig, V. (1981) · The Journal of Comparative Neurology · doi:10.1002/cne.902000308 · Cited by 63

Gliotoxic effects of α-aminoadipic acid on monolayer cultures of dissociated postnatal mouse cerebellum

Huck, S., Grass, F., & Hatten, M. E. (1984) · Neuroscience · doi:10.1016/0306-4522(84)90170-2 · Cited by 62

Small-Molecule-Based Lineage Reprogramming Creates Functional Astrocytes

Tian, E., Sun, G., Sun, G., Chao, J., Ye, P., Warden, C., Riggs, A. D., & Shi, Y. (2016) · Cell Reports · doi:10.1016/j.celrep.2016.06.042 · Cited by 61

Endothelins Stimulate c‐fos and Nerve Growth Factor Expression in Astrocytes and Astrocytoma

Ladenheim, R. G., Lacroix, I., Chaverot, N., Strosberg, A. D., & Couraud, P. (1993) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1993.tb05846.x · Cited by 61

Astroglia—Neuron interactions that promote long-term neuronal survival

Schmalenbach, C., & Müller, H. W. (1993) · Journal of Chemical Neuroanatomy · doi:10.1016/0891-0618(93)90044-5 · Cited by 60

Regeneration of axons in the optic nerve of the adult Browman-Wyse (BW) mutant rat

Berry, M., Hall, S. M., Rees, L., Carlile, J., & Wyse, J. P. H. (1992) · Journal of Neurocytology · doi:10.1007/bf01191507 · Cited by 60

Interferon induces astrocyte maturation causing an increase in cholinergic properties of cultured human spinal cord cells

Erkman, L., Wuarin, L., Cadelli, D., & Kato, A. C. (1989) · Developmental Biology · doi:10.1016/0012-1606(89)90234-0 · Cited by 60

ERK-mediated production of neurotrophic factors by astrocytes promotes neuronal stem cell differentiation by erythropoietin

Park, M. H., Lee, S. M., Lee, J. W., Son, D. J., Moon, D. C., Yoon, D. Y., & Hong, J. T. (2005) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2005.10.218 · Cited by 59

Synaptogenesis in hippocampal cultures

Verderio, C., Coco, S., Pravettoni, E., Bacci, A., & Matteoli, M. (1999) · Cellular and Molecular Life Sciences · doi:10.1007/s000180050384 · Cited by 60

Humoral and contact interactions in astroglia/stem cell co‐cultures in the course of glia‐induced neurogenesis

Környei, Z., Szlávik, V., Szabó, B., Gócza, E., Czirók, A., & Madarász, E. (2004) · Glia · doi:10.1002/glia.20123 · Cited by 59

Progress in Facilitating the Recovery of Function after Central Nervous System Trauma

Cotman, C. W., & Nieto‐Sampedro, M. (1985) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1985.tb20800.x · Cited by 59

Reduced synaptic activity and dysregulated extracellular matrix pathways in midbrain neurons from Parkinson’s disease patients

Stern, S., Lau, S., Manole, A., Rosh, I., Percia, M. M., Ezer, R. B., Shokhirev, M. N., Qiu, F., Schafer, S. T., Mansour, A. A., et al. (2022) · npj Parkinson s Disease · doi:10.1038/s41531-022-00366-z · Cited by 60

Neurotrophin‐3 enhances neurite outgrowth in cultured hippocampal pyramidal neurons

Morfini, G. A., Ditella, M. C., Feiguin, F. M., Carri, N. G., & Cáceres, A. (1994) · Journal of Neuroscience Research · doi:10.1002/jnr.490390212 · Cited by 58

Extracellular matrix derived from astrocytes stimulates neuritic outgrowth from PC12 cells in vitro

Wujek, J. R., & Akeson, R. A. (1987) · Developmental Brain Research · doi:10.1016/0165-3806(87)90198-2 · Cited by 58

Region‐specifi neuro‐astroglial interactions: Ultrastructural study of the in vitro expression of neuronal polarity

Autillo‐Touati, A., Chamak, B., Araud, D., Vuillet, J., Seite, R., & Prochiantz, A. (1988) · Journal of Neuroscience Research · doi:10.1002/jnr.490190308 · Cited by 58

Calsyntenins Mediate TGN Exit of APP in a Kinesin‐1‐Dependent Manner

Ludwig, A., Blume, J., Diep, T., Yuan, J. X., Mateos, J. M., Leuthäuser, K., Steuble, M., Streit, P., & Sonderegger, P. (2009) · Traffic · doi:10.1111/j.1600-0854.2009.00886.x · Cited by 57

Enhanced cell survival in fetal hippocampal suspension transplants grafted to adult rat hippocampus following kainate lesions: A three-dimensional graft reconstruction study

Shetty, A. K., & Turner, D. A. (1995) · Neuroscience · doi:10.1016/0306-4522(95)00025-e · Cited by 57

Neuronal cell death, nerve growth factor and neurotrophic models: 50 years on

Bennett, M. R., Gibson, W. G., & Lemon, G. (2002) · Autonomic Neuroscience · doi:10.1016/s1566-0702(01)00358-7 · Cited by 57

Postnatal changes in the number of astrocytes, oligodendrocytes, and microglia in the visual cortex (area 17) of the macaque monkey: A stereological analysis in normal and monocularly deprived animals

OʼKusky, J. R., & Colonnier, M. (1982) · The Journal of Comparative Neurology · doi:10.1002/cne.902100309 · Cited by 57

Testosterone and progesterone metabolism in the central nervous system: Cellular localization and mechanism of control of the enzymes involved

Martini, L., Celotti, F., & Melcangi, R. C. (1996) · Cellular and Molecular Neurobiology · doi:10.1007/bf02088095 · Cited by 58

Isolation of a protein from bovine brain which promotes neurite extension from chick embryo cerebral cortex neurons in defined medium

KLIGMAN, D. E. (1982) · Brain Research · doi:10.1016/0006-8993(82)90955-6 · Cited by 57

Trophic effects of brain areas on the developing cerebral cortex: I. Growth and histological organization of intraocular grafts

Björklund, H., Seiger, Å., Hoffer, B. J., & Olson, L. (1983) · Developmental Brain Research · doi:10.1016/0165-3806(83)90091-3 · Cited by 57

Expression of Lysophosphatidic Acid Receptor in Rat Astrocytes: Mitogenic Effect and Expression of Neurotrophic Genes

Tabuchi, S., Kume, K., Aihara, M., & Shimizu, T. (2000) · Neurochemical Research · doi:10.1023/a:1007542532395 · Cited by 56

Action of a trophic factor(s) from rabbit corneal epithelial culture on dissociated trigeminal neurons

Chan, K., & Haschke, R. H. (1981) · Journal of Neuroscience · doi:10.1523/jneurosci.01-10-01155.1981 · Cited by 56

Patterns of glial proliferation during formation of olfactory glomeruli in an insect

Oland, L. A., & Tolbert, L. P. (1989) · Glia · doi:10.1002/glia.440020103 · Cited by 56

NILE/L1 and NCAM‐polysialic acid expression on growing axons of isolated neurons

van den Pol, A. N., & Kim, W. T. (1993) · The Journal of Comparative Neurology · doi:10.1002/cne.903320208 · Cited by 56

Interneurons versus efferent neurons: Heterogeneity in their neurite outgrowth response to glia from several brain regions

Denis‐Donini, S., & Estenoz, M. (1988) · Developmental Biology · doi:10.1016/0012-1606(88)90430-7 · Cited by 56

Astroglial modulation of transient potassium current development in cultured mouse hippocampal neurons

Wu, R., & Barish, M. (1994) · Journal of Neuroscience · doi:10.1523/jneurosci.14-03-01677.1994 · Cited by 56

Insulin and Neuroparsin Promote Neurite Outgrowth in Cultured Locust CNS

Vanhems, E., Delbos, M., & Girardie, J. (1990) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1990.tb00468.x · Cited by 55

Signaling by N- and C-terminal sequences of parathyroid hormone-related protein in hippocampal neurons.

Fukayama, S., Tashjian, A. H., Davis, J. N., & Chisholm, J. C. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.22.10182 · Cited by 55

N-methyl-d-aspartate (NMDA) receptors are inactivated by trypsin

Allen, C. N., Brady, R. J., Swann, J. W., Hori, N., & Carpenter, D. O. (1988) · Brain Research · doi:10.1016/0006-8993(88)90507-0 · Cited by 55

Purification of a human red blood cell protein supporting the survival of cultured CNS neurons, and its identification as catalase

Walicke, P. A., Varon, S. S., & Manthrope, M. (1986) · Journal of Neuroscience · doi:10.1523/jneurosci.06-04-01114.1986 · Cited by 54

NEURONAL–GLIAL INTERACTIONS

Lauder, J. M., & McCarthy, K. L. (1986) · Elsevier eBooks · doi:10.1016/b978-0-12-250452-5.50016-4 · Cited by 54

Neuronotrophic Factors Released by C6 Glioma Cells

Westermann, R., Hardung, M., Meyer, D., Ehrhard, P. B., Otten, U., & Unsicker, K. (1988) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1988.tb02474.x · Cited by 54

Nigral type I astrocytes release a soluble factor that increases dopaminergic neuron survival through mechanisms distinct from basic fibroblast growth factor

O'Malley, E. K., Sieber, B.-A., Morrison, R. S., Black, I. B., & Dreyfus, C. F. (1994) · Brain Research · doi:10.1016/0006-8993(94)91401-x · Cited by 53

Loss of Calcium/Calmodulin-dependent Protein Kinase II Activity in Cortical Astrocytes Decreases Glutamate Uptake and Induces Neurotoxic Release of ATP

Ashpole, N. M., Chawla, A., Martin, M. P., Brustovetsky, T., Brustovetsky, N., & Hudmon, A. (2013) · Journal of Biological Chemistry · doi:10.1074/jbc.m113.466235 · Cited by 52

Upregulation of GABAACurrent by Astrocytes in Cultured Embryonic Rat Hippocampal Neurons

Liu, Q., Schaffner, A. E., Li, Y., Dunlap, V., & Barker, J. L. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-09-02912.1996 · Cited by 52

NLRP6 expressed in astrocytes aggravates neurons injury after OGD/R through activating the inflammasome and inducing pyroptosis

Zhang, J., Jiang, N., Zhang, L., Meng, C., Zhao, J., & Wu, J. (2020) · International Immunopharmacology · doi:10.1016/j.intimp.2019.106183 · Cited by 51

Rapid laminar-dependent changes in GFAP immunoreactive astrocytes in the visual cortex of rats reared in a complex environment

Jones, T. A., Hawrylak, N., & Greenough, W. T. (1996) · Psychoneuroendocrinology · doi:10.1016/0306-4530(95)00041-0 · Cited by 51

Human Astrocytes Exhibit Tumor Microenvironment-, Age-, and Sex-Related Transcriptomic Signatures

Krawczyk, M. C., Haney, J. R., Pan, L., Caneda, C., Khankan, R. R., Reyes, S. D., Chang, J. W., Morselli, M., Vinters, H. V., Wang, A., et al. (2022) · Journal of Neuroscience · doi:10.1523/jneurosci.0407-21.2021 · Cited by 51

Tissue inhibitor of metalloproteinase-2 (TIMP-2) regulates myogenesis and β1 integrin expression in vitro

Lluri, G., Langlois, G. D., Soloway, P. D., & Jaworski, D. M. (2007) · Experimental Cell Research · doi:10.1016/j.yexcr.2007.06.007 · Cited by 50

Melanocortins stimulate proliferation and induce morphological changes in cultured rat astrocytes by distinct transducing mechanisms

Zohar, M., & Salomon, Y. (1992) · Brain Research · doi:10.1016/0006-8993(92)90608-c · Cited by 50

Peptide t sequences prevent neuronal cell death produced by the envelope protein (gp 120) of the human immunodeficiency virus

Brenneman, D. E., Buzy, J. M., Ruff, M. R., & Pert, C. B. (1988) · Drug Development Research · doi:10.1002/ddr.430150403 · Cited by 50

Age-related changes of VIP, NPY and somatostatin-immunoreactive neurons in the cerebral cortex of aged rats

Ik, C., Lee, Y. I., Lee, E. Y., Park, K. H., & Baik, S. H. (1997) · Brain Research · doi:10.1016/s0006-8993(97)00009-7 · Cited by 50

Characterization of Epidermal Growth Factor Receptors in Astrocytic Glial and Neuronal Cells in Primary Culture*

Wang, S. L., Shiverick, K. T., OGILVIE, S., Dunn, W. A., & Raizada, M. K. (1989) · Endocrinology · doi:10.1210/endo-124-1-240 · Cited by 49

Changing interactions between astrocytes and neurons during CNS maturation

Geisert, E. E., & Stewart, A. M. (1991) · Developmental Biology · doi:10.1016/0012-1606(91)90084-g · Cited by 49

An essential role for de novo biosynthesis of L-serine in CNS development.

Furuya, S. (2008) · PubMed · Cited by 48

Effect of DJ-1 on the neuroprotection of astrocytes subjected to cerebral ischemia/reperfusion injury

Li, P., Zhao, Y., Li, Y., Zhou, Y., Lei, S., Lei, S., Yu, S., & Zhao, Y. (2018) · Journal of Molecular Medicine · doi:10.1007/s00109-018-1719-5 · Cited by 48

Co-culture with astrocytes or microglia protects metabolically impaired neurons

Park, L. C. H., Zhang, H., & Gibson, G. E. (2001) · Mechanisms of Ageing and Development · doi:10.1016/s0047-6374(01)00336-0 · Cited by 48

[2] Generation and culturing of precursor cells and neuroblasts from embryonic and adult central nervous system

Ray, J., Raymon, H. K., & Gage, F. H. (1995) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/0076-6879(95)54004-0 · Cited by 48

Neurite promoting activity of insulin, insulin-like growth factor I and nerve growth factor on spinal motoneurons is astrocyte dependent

Ang, L. C., Bhaumick, B., & Juurlink, B. H. J. (1993) · Developmental Brain Research · doi:10.1016/0165-3806(93)90086-p · Cited by 48

Roles of neuroligins in central nervous system development: focus on glial neuroligins and neuron neuroligins

Liu, X., Hua, F., Yang, D., Lin, Y., Zhang, L., Ying, J., Sheng, H., & Wang, X. (2022) · Journal of Translational Medicine · doi:10.1186/s12967-022-03625-y · Cited by 50

Dexamethasone regulates basic fibroblast growth factor, nerve growth factor and S100β expression in cultured hippocampal astrocytes

Niu, H., Hinkle, D. A., & Wise, P. M. (1997) · Molecular Brain Research · doi:10.1016/s0169-328x(97)00221-0 · Cited by 47

Novel Expression of Functional Luteinizing Hormone/Chorionic Gonadotropin Receptors in Cultured Glial Cells From Neonatal Rat Brains1

Alhader, A. A., Lei, Z. M., & Rao, C. V. (1997) · Biology of Reproduction · doi:10.1095/biolreprod56.2.501 · Cited by 47

Proliferation of cerebellar neurons induced by astrocytes treated with thyroid hormone is mediated by a cooperation between cell contact and soluble factors and involves the epidermal growth factor‐protein kinase a pathway

Martinez, R., & Gomes, F. C. A. (2005) · Journal of Neuroscience Research · doi:10.1002/jnr.20463 · Cited by 46

Retinal ganglion cell survival requirements: A major but transient dependence on Mu¨ller glia during development

Raju, T. R., & Bennett, M. R. (1986) · Brain Research · doi:10.1016/0006-8993(86)90017-x · Cited by 46

Production, regulation and role of nitric oxide in glial cells

Vincent, V. A. M., Tilders, F. J. H., & van Dam, A.-M. (1998) · Mediators of Inflammation · doi:10.1080/09629359890929 · Cited by 45

Radial glia in the neocortex of adult rats: effects of neonatal brain injury

Rosen, G. D., Sherman, G. F., & Galaburda, A. M. (1994) · Developmental Brain Research · doi:10.1016/0165-3806(94)90155-4 · Cited by 44

Intercellular signaling in neuronal-glial networks

Cooper, M. S. (1995) · Biosystems · doi:10.1016/0303-2647(94)01450-l · Cited by 44

Spatial and Temporal Regulation of Ca2+/Calmodulin-Dependent Protein Kinase II Activity in Developing Neurons

Menegon, A., Verderio, C., Leoni, C., Benfenati, F., Czernik, A. J., Greengard, P., Matteoli, M., & Valtorta, F. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-16-07016.2002 · Cited by 44

Chapter 26 NGF-dependent sprouting and regeneration in the hippocampus

Gage, F. H., Buzsáki, G., & Armstrong, D. M. (1990) · Progress in brain research · doi:10.1016/s0079-6123(08)61262-5 · Cited by 44

What distinguishes axons from dendrites? Neurons know more than we do

Sargent, P. B. (1989) · Trends in Neurosciences · doi:10.1016/0166-2236(89)90121-5 · Cited by 44

Organotypic cultures of neural retina: Neurite outgrowth stimulated by brain extracts

Carri, N. G., & Ebendal, T. (1983) · Developmental Brain Research · doi:10.1016/0165-3806(83)90061-5 · Cited by 44

AXON REACTION AND CENTRAL NERVOUS SYSTEM REGENERATION

Barron, K. D. (1983) · Elsevier eBooks · doi:10.1016/b978-0-12-635120-0.50007-2 · Cited by 44

Long-Term Culture of Rat Hippocampal Neurons at Low Density in Serum-Free Medium: Combination of the Sandwich Culture Technique with the Three-Dimensional Nanofibrous Hydrogel PuraMatrix

Kaneko, A., & Sankai, Y. (2014) · PLoS ONE · doi:10.1371/journal.pone.0102703 · Cited by 43

Calsyntenin-1 shelters APP from proteolytic processing during anterograde axonal transport

Steuble, M., Diep, T., Schätzle, P., Ludwig, A., Tagaya, M., Kunz, B., & Sonderegger, P. (2012) · Biology Open · doi:10.1242/bio.20121578 · Cited by 45

Thyroid hormone treated astrocytes induce maturation of cerebral cortical neurons through modulation of proteoglycan levels

Dezonne, R. S., Stipursky, J., Araújo, A. P. B., Nones, J., Pavão, M. S. G., Porcionatto, M. A., & Gomes, F. C. A. (2013) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2013.00125 · Cited by 42

Cellular composition of a cerebral hemisphere primary culture

Hansson, E. (1984) · Neurochemical Research · doi:10.1007/bf00964164 · Cited by 42

Adult and embryonic frontal cortex transplants after frontal cortex ablation enhance recovery on a reinforced alternation task

Kesslak, J. P., Brown, L., Steichen, C., & Cotman, C. W. (1986) · Experimental Neurology · doi:10.1016/0014-4886(86)90241-4 · Cited by 42

α2-Macroglobulin is an astroglia-derived neurite-promoting factor for cultured neurons from rat central nervous system

Mori, T., Iijima, N., Kitabatake, K., & Kohsaka, S. (1990) · Brain Research · doi:10.1016/0006-8993(90)91059-p · Cited by 42

Survival and neurite growth of chick embryo spinal cord cells in serum-free culture

Tanaka, H., & Obata, K. (1982) · Developmental Brain Research · doi:10.1016/0165-3806(82)90143-2 · Cited by 42

A P arkinson's disease gene, DJ ‐1, repairs brain injury through S ox9 stabilization and astrogliosis

Choi, D., Eun, J., Kim, B. G., Jou, I., Park, S. M., & Joe, E.-H. (2017) · Glia · doi:10.1002/glia.23258 · Cited by 41

Astrocytes are crucial for survival and maturation of embryonic hippocampal neurons in a neuron‐glia cell‐insert coculture assay

Pyka, M., Busse, C., Seidenbecher, C. I., Gundelfinger, E. D., & Faissner, A. (2010) · Synapse · doi:10.1002/syn.20816 · Cited by 41

Cultured astrocytes express biglycan, a chondroitin/dermatan sulfate proteoglycan supporting the survival of neocortical neurons

Koops, A., Kappler, J., Junghans, U., Kuhn, H. G., Kresse, H., & Müller, H. W. (1996) · Molecular Brain Research · doi:10.1016/0169-328x(96)00067-8 · Cited by 41

Regenerative and other responses to injury in the retinal stump of the optic nerve in adult albino rats: transection of the intracranial optic nerve.

Zeng, B., Anderson, P. N., Campbell, G., & Lieberman, A. R. (1994) · Europe PMC (PubMed Central) · Cited by 41

Selegiline is neuroprotective in primary brain cultures treated with 1-methyl-4-phenylpyridinium

Koutsilieri, E., Chen, T.-S., Rausch, W., & Riederer, P. F. (1996) · European Journal of Pharmacology · doi:10.1016/0014-2999(96)00184-7 · Cited by 41

Cortical astrocytes activated by basic fibroblast growth factor secrete molecules that stimulate differentiation of mesencephalic dopaminergic neurons

Gaul, G., & Lübbert, H. (1992) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.1992.0083 · Cited by 41

Cell Death in Neuronal Development

Berg, D. K. (1982) · Springer eBooks · doi:10.1007/978-1-4684-1131-7_9 · Cited by 40

Endogenous and exogenous factors support neuronal survival and choline acetyltransferase activity in embryonic spinal cord cultures

Manthorpe, M., Luyten, W. H. M. L., Longo, F. M., & Varon, S. S. (1983) · Brain Research · doi:10.1016/0006-8993(83)91039-9 · Cited by 40

Heads‐up: New roles for the fragile X mental retardation protein in neural stem and progenitor cells

Callan, M. A., & Zarnescu, D. C. (2011) · genesis · doi:10.1002/dvg.20745 · Cited by 39

Circulating plasma factors involved in rejuvenation

Kang, J. S., & Yang, Y. R. (2020) · Aging · doi:10.18632/aging.103933 · Cited by 39

Development and Maintenance of the Neuronal Cytoskeleton in Aggregated Cell Cultures of Fetal Rat Telencephalon and Influence of Elevated K+ Concentrations

Riederer, B. M., Monnet‐Tschudi, F., & Honegger, P. (1992) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1992.tb09767.x · Cited by 39

Effects of serum, tissue extract, conditioned medium, and culture substrata on neurite appearance from spinal cord explants of chick embryo

Tanaka, H., Sakai, M., & Obata, K. (1982) · Developmental Brain Research · doi:10.1016/0165-3806(82)90142-0 · Cited by 39

Specific neurotrophic interactions between cortical and subcortical visual structures in developing rat: in vitro studies

Repka, A., & Cunningham, T. J. (1987) · The Journal of Comparative Neurology · doi:10.1002/cne.902560407 · Cited by 39

Astrocytes in neuroendocrine systems: An overview

MacDonald, A. J., Robb, J. L., Morrissey, N. A., Beall, C., & Ellacott, K. L. J. (2019) · Journal of Neuroendocrinology · doi:10.1111/jne.12726 · Cited by 41

Dopaminergic neuroprotective effects of rotigotine via 5-HT1A receptors: Possibly involvement of metallothionein expression in astrocytes

Isooka, N., Miyazaki, I., Kikuoka, R., Wada, K., Nakayama, E., Shin, K., Yamamoto, D., Kitamura, Y., & Asanuma, M. (2019) · Neurochemistry International · doi:10.1016/j.neuint.2019.104608 · Cited by 38

Looking for a Treatment for the Early Stage of Alzheimer’s Disease: Preclinical Evidence with Co-Ultramicronized Palmitoylethanolamide and Luteolin

Facchinetti, R., Valenza, M., Bronzuoli, M. R., Menegoni, G., Ratano, P., Steardo, L., Campolongo, P., & Scuderi, C. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21113802 · Cited by 38

Possible neuroprotective property of nicotinic acetylcholine receptors in association with predominant upregulation of glial cell line‐derived neurotrophic factor in astrocytes

Takarada, T., Nakamichi, N., Kawagoe, H., Ogura, M., Fukumori, R., Nakazato, R., Fujikawa, K., Kou, M., & Yoneda, Y. (2012) · Journal of Neuroscience Research · doi:10.1002/jnr.23101 · Cited by 38

Nerve Growth Factor Function in the Central Nervous System

Gage, F. H., Tuszynski, M. H., Chen, K. S., Fagan, A. M., & Higgins, G. A. (1991) · Current topics in microbiology and immunology · doi:10.1007/978-3-642-75747-1_5 · Cited by 38

Branching enhancement by basic fibroblast growth factor in cut neurite of hippocampal neurons

Miyagawa, T., Saito, H., & Nishiyama, N. (1993) · Neuroscience Letters · doi:10.1016/0304-3940(93)90069-w · Cited by 38

Comparative features of spinal neuronotrophic factors in fluids collected in vitro and in vivo

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Oorschot, D. E., Peterson, D. A., & Jones, D. G. (1991) · Progress in Neurobiology · doi:10.1016/0301-0082(91)90007-n · Cited by 37

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