Dendritic arbor development and synaptogenesis

Rho GTPases and the Actin Cytoskeleton

Hall, A. (1998) · Science · doi:10.1126/science.279.5350.509 · Cited by 6,138

Synaptic Activity and the Construction of Cortical Circuits

Katz, L. C., & Shatz, C. J. (1996) · Science · doi:10.1126/science.274.5290.1133 · Cited by 3,048

Driving AMPA receptors into synapses by LTP and CaMKII: requirement for GluR1 and PDZ domain interaction

Hayashi, Y., Shi, S.-H., Esteban, J. A., Piccini, A., Poncer, J.-C., & Malinow, R. (2000) · Science · doi:10.1126/science.287.5461.2262 · Cited by 1,524

Activation of postsynaptically silent synapses during pairing-induced LTP in CA1 region of hippocampal slice

Liao, D., Hessler, N. A., & Malinow, R. (1995) · Nature · doi:10.1038/375400a0 · Cited by 1,365

Inhibition of Postsynaptic PKC or CaMKII Blocks Induction But Not Expression of LTP

Malinow, R., Schulman, H., & Tsien, R. W. (1989) · Science · doi:10.1126/science.2549638 · Cited by 1,325

Rapid Spine Delivery and Redistribution of AMPA Receptors After Synaptic NMDA Receptor Activation

Shi, S.-H., Hayashi, Y., Petralia, R. S., Zaman, S. H., Wenthold, R. J., Svoboda, K., & Malinow, R. (1999) · Science · doi:10.1126/science.284.5421.1811 · Cited by 1,276

Influence of dendritic structure on firing pattern in model neocortical neurons

Mainen, Z. F., & Sejnowski, T. J. (1996) · Nature · doi:10.1038/382363a0 · Cited by 1,231

An essential role for postsynaptic calmodulin and protein kinase activity in long-term potentiation

Malenka, R. C., Kauer, J. A., Perkel, D. J., Mauk, M. D., Kelly, P. T., Nicoll, R. A., & Waxham, M. N. (1989) · Nature · doi:10.1038/340554a0 · Cited by 1,025

Rapid Dendritic Morphogenesis in CA1 Hippocampal Dendrites Induced by Synaptic Activity

Maletic-Savatic, M., Malinow, R., & Svoboda, K. (1999) · Science · doi:10.1126/science.283.5409.1923 · Cited by 1,009

LTP promotes formation of multiple spine synapses between a single axon terminal and a dendrite

Toni, N., Buchs, P.-A., Nikonenko, I., Bron, C. R., & Muller, D. (1999) · Nature · doi:10.1038/46574 · Cited by 949

Spatiotemporal Mapping and Molecular Basis of Whole-brain Circuit MaturationPreprint

Xue, J., Brawner, A. T., Thompson, J. R., Yelhekar, T. D., Newmaster, K. T., Qiu, Q., Cooper, Y. A., Yu, C. R., Ahmed-Braima, Y. H., Kim, Y., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.01.03.572456 · Cited by 5

DSCAM is differentially patterned along the optic axon pathway in the developing Xenopus visual system and guides axon termination at the target

Santos, R. A., Rio, R. D., Alvarez, A. D., Romero, G., Vo, B. Z., & Cohen‐Cory, S. (2022) · Neural Development · doi:10.1186/s13064-022-00161-9 · Cited by 4

Ryanodine receptor-dependent mechanisms of PCB developmental neurotoxicity

Lein, P. J. (2023) · Advances in neurotoxicology · doi:10.1016/bs.ant.2023.09.003 · Cited by 5

Neurite density of the hippocampus is associated with trace eyeblink conditioning latency in 4‐ to 6‐year‐olds

Vieites, V., Ralph, Y. K., Reeb‐Sutherland, B. C., Dick, A. S., Mattfeld, A. T., & Pruden, S. M. (2023) · European Journal of Neuroscience · doi:10.1111/ejn.16217 · Cited by 4

Monensin Sensitive 1 Regulates Dendritic Arborization in Drosophila by Modulating Endocytic Flux

Harish, R. K., Tendulkar, S., Deivasigamani, S., Ratnaparkhi, A., & Ratnaparkhi, G. S. (2019) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2019.00145 · Cited by 4

Linking Motoneuron PIC Location to Motor Function in Closed-Loop Motor Unit System Including Afferent Feedback: A Computational Investigation

Kim, H. (2020) · eNeuro · doi:10.1523/eneuro.0014-20.2020 · Cited by 4

Characterization of synaptic dysfunction in an in vitro corticostriatal model system of Huntington’s disease

Artamonov, D. N., Korzhova, V., Wu, J., Rybalchenko, P. D., Im, K., Krasnoborova, V. A., Власова, О. Л., & Борисович, Б. И. (2013) · Biochemistry (Moscow) Supplement Series A Membrane and Cell Biology · doi:10.1134/s1990747813040028 · Cited by 4

Morfología Neuronal en el Trastorno del Espectro Autista

Vásquez, B., & del Sol, M. (2020) · International Journal of Morphology · doi:10.4067/s0717-95022020000501513 · Cited by 11

Cajals achievements in the field of the development of dendritic arbors

García-López, P., García‐Marín, V., Martínez‐Murillo, R., & Freire, M. (2010) · The International Journal of Developmental Biology · doi:10.1387/ijdb.093001pg · Cited by 5

Calcium and CREST for Healthy Dendrites

Jefferis, G. S. X. E., Komiyama, T., & Luo, L. (2004) · Science · doi:10.1126/science.1093472 · Cited by 4

Insights into GABA functions in the developing cerebellum

Fiszman, M. L. (2005) · International review of neurobiology · doi:10.1016/s0074-7742(05)71004-7 · Cited by 4

Brain-derived neurotrophic factor : generation and characterization of adult mice lacking BDNF in the adult brain

Rauskolb, S. (2008) · edoc (University of Basel) · doi:10.5451/unibas-004587325 · Cited by 4

The Molecular Basis of Experience-Dependent Motor System Development

Kalb, R. G., Zhou, W., & Zhang, L. (2013) · Advances in experimental medicine and biology · doi:10.1007/978-1-4614-5465-6_2 · Cited by 3

Time windows for postnatal changes in morphology and membrane excitability of genioglossal and oculomotor motoneurons

Carrascal, L. (2015) · World Journal of Neurology · doi:10.5316/wjn.v5.i4.113 · Cited by 3

Wiring Up the Brain: Axon Navigation

Sanes, D. H., Reh, T. A., Harris, W. A., & Landgraf, M. (2019) · Elsevier eBooks · doi:10.1016/b978-0-12-803996-0.00005-8 · Cited by 3

From the periphery to the brain: Wiring the olfactory system

Blanchart, A., & López‐Mascaraque, L. (2011) · Translational Neuroscience · doi:10.2478/s13380-011-0038-x · Cited by 3

Dysregulation of TrkB phosphorylation and proBDNF protein in adenylyl cyclase 1 and 8 knockout mice in a model of fetal alcohol spectrum disorder

Susick, L. L., Chrumka, A. C., Hool, S. M., & Conti, A. C. (2016) · Alcohol · doi:10.1016/j.alcohol.2015.11.008 · Cited by 3

Neuronal Development

Kempermann, G. (2010) · Oxford University Press eBooks · doi:10.1093/med/9780199729692.003.0004 · Cited by 4

THE VON ECONOMO NEURONS: FROM CELLS TO BEHAVIOR

Watson, K. K. (2006) · doi:10.7907/fz94-dw76 · Cited by 3

Dendrite Development, Synapse Formation and Elimination

Cline, H. T. (2009) · Elsevier eBooks · doi:10.1016/b978-008045046-9.00347-8 · Cited by 5

Mitral Cell Dendritic Morphology in the Adult Zebrafish Olfactory Bulb following Growth, Injury and Recovery

Rozofsky, J. P., Pozzuto, J. M., & Byrd-Jacobs, C. A. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25095030 · Cited by 2

Wnt Signaling in Neurite Development

Rosso, S. B., & Salinas, P. C. (2007) · Springer eBooks · doi:10.1007/978-0-387-68561-8_10 · Cited by 2

Synaptic Dialogue: Substrate for Protein-Synthesis-Independent Long-Term Memory

Holahan, M. R., & Routtenberg, A. (2006) · Springer eBooks · doi:10.1007/0-387-25443-9_24 · Cited by 2

Learning by structural remodeling in a class of single cell models

Kelleher, K. J., Hajdik, V., Colbert, C. M., & Josić́, K. (2008) · Journal of Computational Neuroscience · doi:10.1007/s10827-008-0078-6 · Cited by 2

Cell adhesion and synaptogenesis.

Chen, G., Wu, X., & Tuncdemir, S. N. (2007) · PubMed · Cited by 2

Quantitative Geometric Three-Dimensional Reconstruction of Neuronal Architecture and Mapping of Labeled Proteins from Confocal Image Stacks

Evers, J. F., & Duch, C. (2014) · Neuromethods · doi:10.1007/978-1-4939-0381-8_10 · Cited by 2

Potential roles of polyunsaturated fatty acid-enriched diets in modulating social stress-like features

Chakraborty, N., Gautam, A., Muhie, S. Y., Miller, S., Meyerhoff, J. L., Sowe, B., Jett, M., & Hammamieh, R. (2023) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2023.109309 · Cited by 2

Evidence that Astroglia Influence Dendrite Morphogenesis and Synaptogenesis Independently in the Vertebrate Central Nervous System

Wallace, C. S., & Withers, G. S. (2018) · InTech eBooks · doi:10.5772/intechopen.73891 · Cited by 3

Creation of long-term mental representations using the dimension of fractal dendrites

Gagne, R., & Gagné, S. (2006) · International Joint Conference on Neural Networks (IJCNN) · doi:10.1109/ijcnn.2005.1556229 · Cited by 2

Using G-CaMP 1.6 to Monitor Visually-Evoked Synaptic Activity in Tectal Neurons in vivo

Naumann, E. A. (2005) · KOPS (University of Konstanz) · Cited by 2

Bilirubin impairs neuritogenesis and synaptogenesis in NSPCs by downregulating NMDAR-CREB-BDNF signaling

Zhang, Y., Li, S., Li, L., Huang, H., Fu, Z., & Hua, Z. (2024) · In Vitro Cellular & Developmental Biology - Animal · doi:10.1007/s11626-023-00844-5 · Cited by 1

An effective framework to study signal transmission due to non-homogeneous extracellular space in neuron

Das, B., Baruah, S. M. B., Roy, S., & Bhattacharyya, D. K. (2025) · Journal of Biological Physics · doi:10.1007/s10867-025-09689-3 · Cited by 1

A systematic review of the effect of pulse parameters of next-generation TMS devices on corticospinal excitability and neuroplasticity

Agboada, D., Rethwilm, R., Kuder, M., Mack, W., & Seiberl, W. (2025) · Brain Research · doi:10.1016/j.brainres.2025.150120 · Cited by 1

Dendritic learning-based gravitational waves prediction model

Jia, D., Xu, W., Zhong, Z., Sun, J., Hirobayashi, S., Lei, Z., & Gao, S. (2026) · Information Sciences · doi:10.1016/j.ins.2026.123218 · Cited by 1

NFE2L2 suppresses microglia-mediated neuroinflammation to preserve neuronal dendritic architecture from cadmium-induced damage

Li, S., Wang, X., Ma, X., Ding, R., Cai, B., Song, H., Chen, Y., Yao, D., Chen, Y., Zhang, X., et al. (2026) · Cell Biology and Toxicology · doi:10.1007/s10565-026-10178-z · Cited by 1

In Vivo Imaging of Brain Development: Technologies, Models, Applications, and Impact on Understanding the Etiology of Mental Retardation

Glunčić, V. (2009) · Humana Press eBooks · doi:10.1007/978-1-60761-287-2_9 · Cited by 1

DEVELOPMENTAL REGULATION AND FUNCTION OF AMPA RECEPTOR SUBUNITS IN CHICKEN LUMBAR MOTONEURONS

Ni, X. (2009) · ScholarWorks -A service of University of Vermont Libraries (University of Vermont) · Cited by 1

Membrane Trafficking Mechanisms: Exocytosis and Endocytosis in Dendrites

Winckler, B. (2016) · Springer eBooks · doi:10.1007/978-4-431-56050-0_4 · Cited by 1

Impact of Structural Plasticity on Memory Capacity

Bozelos, P., & Poirazi, P. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-803784-3.00015-9 · Cited by 1

Dendritic Development

Cline, H. T., Ghosh, A., Jan, Y. N., & Sanes, J. (2013) · Elsevier eBooks · doi:10.1016/b978-0-12-385870-2.00020-2 · Cited by 1

Docosahexaenoic Acid and Its Metabolites in Brain

(2006) · Springer eBooks · doi:10.1007/978-0-387-49931-4_6 · Cited by 1

Dynamic structural remodeling of the human visual system prompted by bilateral retinal gene therapy

Ashtari, M., Cook, P. A., Lipin, M. Y., Yu, Y., Ying, G., Maguire, A. M., Bennett, J., Gee, J. C., & Zhang, H. G. (2023) · Current Research in Neurobiology · doi:10.1016/j.crneur.2023.100089 · Cited by 1

Morphological changes in motoneurons of the oculomotor nucleus of mice after a 30-day space flight and through a 7-day period of readaptation to earth gravity

Mikheeva, I. B., Zhujkova, N., Mikhailova, G. Z., Shtanchaev, R. S., Pavlik, L. L., & Arkhipov, V. (2023) · Brain Structure and Function · doi:10.1007/s00429-023-02704-0 · Cited by 1

Role of Synaptogenesis in Morphologic Stabilization of Developing Dendrites

Haas, K. Z. (2006) · Springer eBooks · doi:10.1007/978-0-387-32562-0_21 · Cited by 1

Synaptogenesis

Kayser, M. S., & Dalva, M. B. (2014) · Cambridge University Press eBooks · doi:10.1017/cbo9780511995583.024 · Cited by 2

Single dendrite seeks stable relationship

Morgan, J., & Wong, R. (2004) · Nature Neuroscience · doi:10.1038/nn0304-205 · Cited by 1

Co-expression of Argonaute2 enhances short hairpin RNA-induced RNA interference in Xenopus CNS neurons in vivo

Chen, C.-M. (2009) · Frontiers in Neural Circuits · doi:10.3389/neuro.04.025.2009 · Cited by 1

Concordant transcriptional and morphological remodeling revealed by in vivo Perturb-CLEARPreprint

Wu, B., Simmons, S., Kim, S., Li, J., Akram, M. A., Park, C. S., Zheng, X., Mendez, I., Patel, S., Chau, A., et al. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.04.06.716787 · Cited by 2

Adult Neurogenesis Controls Excitatory-Inhibitory Balance in the Olfactory Bulb

Lledo, P., Saghatelyan, A., & Gheusi, G. (2003) · Springer eBooks · doi:10.1007/978-1-4615-0039-1_13

Genetic dissection of sex differences in human brain and behaviour

Tan, G. C.-Y. (2011) · UCL Discovery (University College London)

CHARACTERIZATION AND TREATMENT OF A NOVEL MOUSE MODEL OF TSC-ASSOCIATED AUTISM

Reith, R. M. (2012) · Digital Commons-TMC (Texas Medical Center)

Pre-synaptic terminal dynamics in the hippocampus

Paola, V. D. (2003) · edoc (University of Basel) · doi:10.5451/unibas-003686969

Assembly of sensory-motor connectivity in the spinal cord of mice

Pecho‐Vrieseling, E. (2007) · edoc (University of Basel) · doi:10.5451/unibas-004355201

Ontogênese de conexinas no cerebelo.

Guedes, V. D. A. (2012) · doi:10.11606/t.42.2012.tde-13112012-090209

BDNF in developing aortic baroreceptors & its role in the dendritic morphogenesis of neurons from the Nucleus Tractus Solitarius

Martin, J. L. (2010)

Morphological relationship between axon and dendritic arborizations as revealed by Minkowski functionalsPreprint

Costa, L. D. F., & Barbosa, M. (2007) · arXiv (Cornell University) · doi:10.48550/arxiv.q-bio/0703036

Neural repair: basic cellular and molecular processes

Selzer, M. E., Clarke, S., Cohen, L. G., Kwakkel, G., & Miller, R. H. (2014) · Cambridge University Press eBooks · doi:10.1017/cbo9780511995583.020

Membrane trafficking in neurons regulated by new syntaxin 13-interacting proteins

Steiner, P. (2004) · PubMed · doi:10.5075/epfl-thesis-3091

Addressing the role of the cytoskeletal molecules Diaphanous and Profilin in dendritic morphogenesis in Drosophila melanogaster

Shivalkar, M. (2007) · Elektronische Hochschulschriften der LMU München (Ludwig-Maximilians-Universität München) · doi:10.5282/edoc.7427

"Role of the neuronal protein Cap23 in the maturation and maintenance of dendritic arbors in-vivo"

Sadhu, A. (2006) · edoc (University of Basel) · doi:10.5451/unibas-003850369

The fine scale structure of synaptic inputs in developing hippocampal neurons

Kleindienst, T. (2010) · Electronic Theses of LMU Munich (Ludwig-Maximilians-Universität München) · doi:10.5282/edoc.12662

Differentiation of dendrites and the analysis of spine- like structures on Lobula Plate Tangential Cells in Drosophila melanogaster

Koper, E. (2007) · Electronic Theses of LMU Munich (Ludwig-Maximilians-Universität München) · doi:10.5282/edoc.6924

Role of sensory input in structural plasticity of dendrites in adult neuronal networks

Chakrabarty, A. (2013) · Electronic Theses of LMU Munich (Ludwig-Maximilians-Universität München) · doi:10.5282/edoc.15524

Mechanisms of Depolarization Induced Dendritic Growth of Drosophila Motor Neurons

Cherry, C. (2006) · UA Campus Repository (The University of Arizona)

Calcium and cAMP homeostasis determine network organisation of respiratory pre-Bötzinger neurons in Mecp2 null mice in vitro.

Skorova, E. (2013) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-3913

CELLULAR MECHANISMS UNDERLYING GLUTAMATERGIC CALCIUM RESPONSES IN DEVELOPING AUDITORY BRAINSTEM NEURONS

Negoita, F. A. (2003) · D-Scholarship@Pitt (University of Pittsburgh)

Mitral Cell Dendritic Development in the Mouse Main Olfactory Bulb

Diede, M. R. (2008) · Europe PMC (PubMed Central)

Aus der Klinik und Poliklinik für Psychiatrie und Psychotherapie der Ludwig-Maximilians-Universität München

Möller, H. (2004)

Optical Recording and Photo Modulation in the Study of Dynamics in Neural Circuits

Xu, H. (2010) · doi:10.7301/z0db8025

Regeneration and plasticity of descending propriospinal neurons after transplantation of Schwann cells overexpressing glial cell line-derived neurotrophic factor following thoracic spinal cord injury in adult rats

Deng, L. (2015) · IUScholarWorks (Indiana University) · doi:10.7912/c2/2100

Involvement of neuroligins and associated proteins in synapse development

Levinson, J. N. (2010) · cIRcle (University of British Columbia) · doi:10.14288/1.0071424

The role of adenylyl cyclase signaling pathways in developmental dendritogenesis in vivo

Duncan, B. (2012) · cIRcle (University of British Columbia) · doi:10.14288/1.0072699

Activity-Regulated Genes and Synaptic Plasticity

Leslie, J. H., & Nedivi, E. (2013) · Elsevier eBooks · doi:10.1016/b978-0-12-397266-8.00105-8

Role of EPAC in axon determination

Muñoz-LLancao, P. (2015)

The intrinsic and synaptic properties of inverted pyramidal cells within the neocortex

Steger, R. (2015) · CUNY Academic Works (City University of New York)

Alterations to hippocampal neuroplasticity across the lifespan in a rodent model of FASD

Boschen, K. E. (2024) · Library, Museums and Press - UDSpace (University of Delaware) · doi:10.58088/hr7w-ee44

Glutamate receptors potentiate single K-ATP channels through intracellular ATP changes

Mollajew, R. (2013) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-4292

A new organotypic model of synaptic competition reveals activity-dependent localization of C1qPreprint

Koyama, R., Wu, Y., Bialas, A. R., Thompson, A. D., Welsh, C. A., Frouin, A., Chen, C., & Stevens, B. (2017) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/118646

Molecular Mechanisms Regulating Neurite Growth, Innervation and Survival

Park, K. (2011) · TSpace (University of Toronto)

BK current contributions to action potentials across the first postnatal week reflect age dependent changes in BK current kinetics in rat hippocampal neuronsPreprint

Hunsberger, M., & Mynlieff, M. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/839233

In Vivo and In Vitro analysis of retinal ganglion cell death during development of the rodent retinofugal pathway

Beros, J. L. (2020) · UWA Profiles and Research Repository (UWA) · doi:10.26182/5f641ba971915

Novel roles of cell cycle regulator E2F1 in the CNS: Implications for synaptic damage in HIV-associated neurocognitive disorders

Ting, J. H. (2014) · ScholarlyCommons (University of Pennsylvania)

Towards a Molecular and Cellular Understanding of Remote Memory

Wiltgen, B. J., Brown, R. A. M., Talton, L. E., & Silva, A. J. (2007) · Research and perspectives in neurosciences · doi:10.1007/978-3-540-45702-2_4

Analyses of GWAS and sub-threshold loci lead to the discovery of dendrite development and morphology dysfunction underlying schizophrenia genetic riskPreprint

Chen, R., Wang, Q., Xu, C., Wei, Q., Yang, H., Sutcliffe, J. S., Jiang, Y. W., Ji, Y., Cheng, F., Cook, E. H., et al. (2021) · Research Square · doi:10.21203/rs.3.rs-240477/v1

Structure, Expression and Function of the novel KIND Domain Family Protein very-KIND

Bedrossian, A. (2008)

Modelling Dendrite Shape from Wiring Principles

Cuntz, H. (2013) · Springer series in computational neuroscience · doi:10.1007/978-1-4614-8094-5_6

Differential Expression of DSCAM Guides the Patterning of Retinal Axons Along Their Path and at Their Target in the Developing Xenopus Visual SystemPreprint

Santos, R. A., Rio, R. D., Alvarez, A. D., Romero, G., Vo, B. Z., & Cohen‐Cory, S. (2021) · Research Square · doi:10.21203/rs.3.rs-1175024/v1

Basic Neurophysiology

Strominger, N. L., Demarest, R. J., & Laemle, L. B. (2012) · Humana Press eBooks · doi:10.1007/978-1-61779-779-8_3

Basic Neurophysiology

(2007) · Humana Press eBooks · doi:10.1007/978-1-59259-730-7_3

Bilirubin impairs neuritogenesis and synaptogenesis through NMDAR-CREB-BDNF signalingPreprint

Zhang, Y., Li, S., Li, L., Huang, H., Fu, Z., & Hua, Z. (2023) · Research Square · doi:10.21203/rs.3.rs-2935311/v1

Understanding the Mechanisms of Dendritic Arbor Development: Integrated Experimental and Computational Approaches

Nanda, S., Das, R., Lottes, E. N., Cox, D. N., & Ascoli, G. A. (2023) · Contemporary clinical neuroscience · doi:10.1007/978-3-031-24930-3_1

Alpha-synuclein-associated alterations at the synapse in models of Parkinson’s disease

Santos, P. I. (2023) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-10050

Analyses of GWAS and Sub‐Threshold Loci Lead to the Discovery of Dendrite Development and Morphology Dysfunction Underlying Schizophrenia Genetic Risk

Chen, R., Siciliano, B., Wang, Q., Xu, C., Wei, Q., Yang, H., Sutcliffe, J. S., Jiang, Y. W., Ji, Y., Liu, C., et al. (2025) · Advanced Science · doi:10.1002/advs.202508519

Developmental, Neuroanatomical and Cellular Expression of Genes Causing Dystonia

Cameron, D., Clifton, N. E., de la Fuente, D. C., Holmans, P., Bray, N. J., & Peall, K. J. (2025) · Annals of Clinical and Translational Neurology · doi:10.1002/acn3.70285

Heparin-binding growth-associated molecule (HB-GAM) in activity-dependent neuronal plasticity in hippocampus

Pavlov, I. (2006) · Työväentutkimus Vuosikirja

Studies on palmitoyl-protein thioesterase 1 : Implications for synaptic functions

Suopanki, J. (2002) · Työväentutkimus Vuosikirja

Distinct NMDA Receptor Pools Determine Diverse Forms of Cortical PlasticityPreprint

Rannio, S., Lubembele, K., Ko, C. B., Cherepacha, N., Li, V., Moffat, G. L., Alageswaran, S., Thomazeau, A., Luján, R., & Sjöström, P. J. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.02.14.705915

Canalization of neural dynamics by δ-protocadherins in the developing zebrafish optic tectum

Biswas, S., Emond, M. R., Philip, G. S., & Jontes, J. D. (2026) · PLoS Genetics · doi:10.1371/journal.pgen.1012171

Same Fractal Geometry, Different Canvas: Pollock's Paintings and Golgi-Stained Neural Tissue ComparedPreprint

Petrosini, L., & Panuccio, A. (2026) · Research Square · doi:10.21203/rs.3.rs-10592251/v1

Dendritic growth and synaptic organization from activity-independent cues and local activity-dependent plasticity

Kirchner, J. H., Euler, L., Fritz, I., Castro, A. F., & Gjorgjieva, J. (2023) · eLife · doi:10.7554/elife.87527.3 · Cited by 23

Structural plasticity of dendritic spines: The underlying mechanisms and its dysregulation in brain disorders

Lai, K., & Ip, N. Y. (2013) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2013.08.012 · Cited by 182

Experience-Dependent Dendritic Arbor Development

Cline, H. T. (2016) · Springer eBooks · doi:10.1007/978-4-431-56050-0_13 · Cited by 5

NMDA Receptor as a Mediator of Activity-dependent Synaptogenesis in the Developing BrainPreprint

Constantine‐Paton, M. (1990) · Cold Spring Harbor Symposia on Quantitative Biology · doi:10.1101/sqb.1990.055.01.043 · Cited by 74

Activity-Regulated Genes and Synaptic Plasticity

Leslie, J. H., & Nedivi, E. (2013) · Elsevier eBooks · doi:10.1016/b978-0-12-397266-8.00105-8