Glutamate and GABA receptor signalling in the developing brain

Excitatory actions of gaba during development: the nature of the nurture

Ben-Ari, Y. (2002) · Nature Reviews Neuroscience · doi:10.1038/nrn920 · Cited by 2,448

The caudal ganglionic eminence is a source of distinct cortical and subcortical cell populations

Nery, S., Fishell, G., & Corbin, J. G. (2002) · Nature Neuroscience · doi:10.1038/nn971 · Cited by 558

Selective acquisition of AMPA receptors over postnatal development suggests a molecular basis for silent synapses

Petralia, R. S., Esteban, J. A., Wang, Y. –., Partridge, J. G., Zhao, H. –., Wenthold, R. J., & Malinow, R. (1999) · Nature Neuroscience · doi:10.1038/4532 · Cited by 496

NMDA Receptor Content of Synapses in Stratum Radiatum of the Hippocampal CA1 Area

Racca, C., Stephenson, F. A., Streit, P., Roberts, J. D. B., & Somogyi, P. (2000) · The Journal of Neuroscience · doi:10.1523/jneurosci.20-07-02512.2000 · Cited by 304

Role of reelin in the control of brain development1Published on the World Wide Web on 21 October 1997.1

Curran, T., & D'Arcangelo, G. (1998) · Brain Research Reviews · doi:10.1016/s0165-0173(97)00035-0 · Cited by 246

Distribution and synaptic localisation of the metabotropic glutamate receptor 4 (mGluR4) in the rodent CNS

Corti, C., Aldegheri, L., Somogyi, P., & Ferraguti, F. (2002) · Neuroscience · doi:10.1016/s0306-4522(01)00591-7 · Cited by 243

GABA receptor antagonists modulate postmitotic cell migration in slice cultures of embryonic rat cortex

Behar, T. N. (2000) · Cerebral Cortex · doi:10.1093/cercor/10.9.899 · Cited by 218

GABA: A Pioneer Transmitter That Excites Immature Neurons and Generates Primitive Oscillations

Ben-Ari, Y., Gaiarsa, J.-L., Tyzio, R., & Khazipov, R. (2007) · Physiological Reviews · doi:10.1152/physrev.00017.2006 · Cited by 1,304

Structure, Function, and Pharmacology of Glutamate Receptor Ion Channels

Hansen, K. B., Wollmuth, L. P., Bowie, D., Furukawa, H., Menniti, F. S., Sobolevsky, A. I., Swanson, G. T., Swanger, S. A., Greger, I. H., Nakagawa, T., et al. (2021) · Pharmacological Reviews · doi:10.1124/pharmrev.120.000131 · Cited by 686

Cerebral plasticity: windows of opportunity in the developing brain

Ismail, F. Y., Fatemi, A., & Johnston, M. V. (2017) · European Journal of Paediatric Neurology · doi:10.1016/j.ejpn.2016.07.007 · Cited by 572

KCC2 Expression Promotes the Termination of Cortical Interneuron Migration in a Voltage-Sensitive Calcium-Dependent Manner

Bortone, D., & Polleux, F. (2009) · Neuron · doi:10.1016/j.neuron.2009.01.034 · Cited by 387

Synaptopathies: synaptic dysfunction in neurological disorders – A review from students to students

Lepeta, K., Lourenco, M. V., Schweitzer, B. C., Martino Adami, P. V., Banerjee, P., Catuara‐Solarz, S., de La Fuente Revenga, M., Guillem, A. M., Haidar, M., Ijomone, O. M., et al. (2016) · Journal of Neurochemistry · doi:10.1111/jnc.13713 · Cited by 386

Cannabis and adolescent brain development.

Lubman, D. I., Cheetham, A., & Yücel, M. (2015) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2014.11.009 · Cited by 360

Genes related to sex steroids, neural growth, and social-emotional behavior are associated with autistic traits, empathy, and Asperger syndrome

Chakrabarti, B., Dudbridge, F., Kent, L., Wheelwright, S., Hill‐Cawthorne, G., Allison, C., Banerjee‐Basu, S., & Baron‐Cohen, S. (2009) · Autism Research · doi:10.1002/aur.80 · Cited by 295

Towards a Better Understanding of GABAergic Remodeling in Alzheimer’s Disease

Govindpani, K., Calvo-Flores Guzmán, B., Vinnakota, C., Waldvogel, H., Faull, R., & Kwakowsky, A. (2017) · International Journal of Molecular Sciences · doi:10.3390/ijms18081813 · Cited by 208

Neural basis of psychosis-related behaviour in the infection model of schizophrenia

Meyer, U., & Feldon, J. (2009) · Behavioural Brain Research · doi:10.1016/j.bbr.2008.12.022 · Cited by 158

Minireview: Recent Progress in Gonadotropin-Releasing Hormone Neuronal Migration

Tobet, S. A., & Schwarting, G. A. (2006) · Endocrinology · doi:10.1210/en.2005-1275 · Cited by 123

Single-cell transcriptomics analyses of neural stem cell heterogeneity and contextual plasticity in a zebrafish brain model of amyloid toxicity

Cosacak, M. I., Bhattarai, P., Reinhardt, S., Petzold, A., Dahl, A., Zhang, Y., & Kizil, C. (2019) · Cell Reports · doi:10.1016/j.celrep.2019.03.090 · Cited by 116

Metabotropic Glutamate Receptors in Glial Cells: A New Potential Target for Neuroprotection?

Spampinato, S. F., Copani, A., Nicoletti, F., Sortino, M. A., & Caraci, F. (2018) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2018.00414 · Cited by 105

Defects During Mecp2 Null Embryonic Cortex Development Precede the Onset of Overt Neurological Symptoms

Bedogni, F., Cobolli Gigli, C., Pozzi, D., Rossi, R. L., Scaramuzza, L., Rossetti, G., Pagani, M., Kilstrup-Nielsen, C., Matteoli, M., & Landsberger, N. (2016) · Cerebral Cortex · doi:10.1093/cercor/bhv078 · Cited by 84

A psychobiological framework of the substrates that mediate nicotine use during adolescence

O'Dell, L. E. (2009) · Neuropharmacology · doi:10.1016/j.neuropharm.2008.07.039 · Cited by 81

Integrative system biology analyses of CRISPR-edited iPSC-derived neurons and human brains reveal deficiencies of presynaptic signaling in FTLD and PSP

Jiang, S., Wen, N., Li, Z., Dube, U., Del Aguila, J., Budde, J., Martinez, R., Hsu, S., Fernandez, M. V., Cairns, N. J., et al. (2018) · Translational Psychiatry · doi:10.1038/s41398-018-0319-z · Cited by 73

Neuropeptides as neuroprotective agents: oxytocin a forefront developmental player in the mammalian brain

Vargas-Martínez, F., Uvnäs-Moberg, K., Petersson, M., Olausson, H. A., & Jiménez-Estrada, I. (2014) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2014.10.001 · Cited by 51

Theanine, r-glutamylethylamide, increases neurotransmission concentrations and neurotrophin mRNA levels in the brain during lactation

Yamada, T., Terashima, T., Wada, K., Ueda, S., Ito, M., Okubo, T., Juneja, L. R., & Yokogoshi, H. (2007) · Life Sciences · doi:10.1016/j.lfs.2007.08.023 · Cited by 47

Isochronic development of cortical synapses in primates and mice

Wildenberg, G., Li, H., Sampathkumar, V., Sorokina, A., & Kasthuri, N. (2023) · Nature Communications · doi:10.1038/s41467-023-43088-3 · Cited by 31

Polarised localisation of the voltage-gated sodium channel NaV1. 2 in cerebellar granule cells

Martínez-Hernández, J., Ballesteros-Merino, C., Fernández-Alacid, L., Nicolau, J. C., Aguado, C., & Luján, R. (2013) · The Cerebellum · doi:10.1007/s12311-012-0387-1 · Cited by 27

The interplay between glutamatergic circuits and oxytocin neurons in the hypothalamus and its relevance to neurodevelopmental disorders

Leithead, A. B., Tasker, J. G., & Harony‐Nicolas, H. (2021) · Journal of Neuroendocrinology · doi:10.1111/jne.13061 · Cited by 26

Persistent gene expression changes in ventral tegmental area of adolescent but not adult rats in response to chronic nicotine

Doura, M. B., Luu, T. V., Lee, N. H., & Perry, D. C. (2010) · Neuroscience · doi:10.1016/j.neuroscience.2010.06.071 · Cited by 24

Laminar distribution of neurotransmitter receptors in different reeler mouse brain regions

Cremer, C. M., Lübke, J. H. R., Palomero-Gallagher, N., & Zilles, K. (2011) · Brain Structure and Function · doi:10.1007/s00429-011-0303-3 · Cited by 17

Macromolecular complexes at active zones: integrated nano-machineries for neurotransmitter release

Chua, J. J. E. (2014) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-014-1657-5 · Cited by 9