The integral role of PTEN in brain function: from neurogenesis to synaptic plasticity and social behavior
Open accessAbstract
The phosphatase and tensin homolog deleted on chromosome 10 (PTEN) gene is a critical tumor suppressor that plays an essential role in the development and functionality of the central nervous system. Located on chromosome 10 in humans and chromosome 19 in mice, PTEN encodes a protein that regulates cellular processes such as division, proliferation, growth, and survival by antagonizing the PI3K‑Akt‑mTOR signaling pathway. In neurons, PTEN dephosphorylates phosphatidylinositol‑3,4,5‑trisphosphate (PIP3) to PIP2, thereby modulating key signaling cascades involved in neurogenesis, neuronal migration, and synaptic plasticity. PTEN is crucial for embryonic neurogenesis, controlling the proliferation of neural progenitor cells and guiding the migration and proper lamination of neurons in cortical and hippocampal structures. It also regulates dendritic growth and axon guidance, ensuring correct neuronal connectivity. In postnatal neurogenesis, PTEN maintains the balance of stem cell proliferation and integration of new neurons into existing circuits, particularly in the hippocampal dentate gyrus. Animal models with PTEN deletion or mutation exhibit significant structural and functional neuronal abnormalities, including enlarged soma and dendritic hypertrophy, increased synaptic density, and altered synaptic plasticity mechanisms such as long‑term potentiation and long‑term depression. These changes lead to deficits in learning and memory tasks, as well as impairments in social behaviors. PTEN mutations are associated with neurodevelopmental disorders like intellectual disability, epilepsy, and autism spectrum disorders accompanied by macrocephaly. Understanding PTEN’s mechanisms offers valuable insights into its contributions to neurodevelopmental disorders and presents potential therapeutic targets for cognitive impairments and neurodegenerative diseases. Future research should focus on elucidating PTEN’s functions in mature neurons and its influence on established neuronal networks, which may have significant implications for memory enhancement and behavioral modifications.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
PTEN upstream regulators affect both mTOR and INS pathways.
“PTEN upstream regulators affect both mTOR and INS pathways. 41”
From Disruption of hippocampal upstream regulators of mTOR and insulin pathways in Down syndrome with Alzheimer's disease neuropathology: Preliminary observations (2026) · cites this paper as [41]
The “Intracellular signaling cascade of PTEN/PI3K-Akt-mTOR pathway” section says PTEN inhibits signaling through PI3K, Akt, and mTOR. It also describes feedback from mTORC1 to insulin receptor substrate-1 (IRS-1), but does not say that upstream regulators of PTEN affect both the mTOR and INS pathways. (LLM, conf=0.78)
Experimental — accuracy not yet measuredPTEN is important for regulation of neurogenesis.
“and is important for regulation of neurogenesis. 41”
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
mTOR Signaling in Growth, Metabolism, and Disease
Saxton, R. A., & Sabatini, D. M. (2017) · Cell · doi:10.1016/j.cell.2017.02.004 · Cited by 7,555 · see citing works
Phosphorylation and regulation of Akt/PKB by the rictor-mTOR complex
Sarbassov, D. D., Guertin, D. A., Ali, S. M., & Sabatini, D. M. (2005) · Science · doi:10.1126/science.1106148 · Cited by 6,216 · see citing works
TOR signaling in growth and metabolism
Wullschleger, S., Loewith, R., & Hall, M. N. (2006) · Cell · doi:10.1016/j.cell.2006.01.016 · Cited by 5,787 · see citing works
Upstream and downstream of mTOR
Hay, N., & Sonenberg, N. (2004) · Genes & Development · doi:10.1101/gad.1212704 · Cited by 4,181 · see citing works
AKT/PKB Signaling: Navigating the Network
Manning, B. D., & Toker, A. (2017) · Cell · doi:10.1016/j.cell.2017.04.001 · Cited by 3,772 · see citing works
Negative regulation of PKB/Akt-dependent cell survival by the tumor suppressor PTEN
Stambolic, V., Suzuki, A., de la Pompa, J. L., Brothers, G. M., Mirtsos, C., Sasaki, T., Ruland, J., Penninger, J. M., Siderovski, D. P., & Mak, T. W. (1998) · Cell · doi:10.1016/s0092-8674(00)81780-8 · Cited by 2,551 · see citing works
The functions and regulation of the PTEN tumour suppressor
Song, M. S., Salmena, L., & Pandolfi, P. P. (2012) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3330 · Cited by 1,926 · see citing works
Cancer Research Communications
Calura, E., Fruscio, R., Paracchini, L., Bignotti, E., Martini, P., Sales, G., Beltrame, L., Clivio, L., Ceppi, L., Di Marino, M., et al. (2021) · doi:10.1158/1078-0432 · Cited by 1,537 · see citing works
Pten is essential for embryonic development and tumour suppression
Cristofano, A. D., Pesce, B., Cordon‐Cardo, C., & Pandolfi, P. P. (1998) · Nature Genetics · doi:10.1038/1235 · Cited by 1,518 · see citing works
mTOR signaling: At the crossroads of plasticity, memory and disease
Hoeffer, C. A., & Klann, E. (2010) · Trends in Neurosciences · doi:10.1016/j.tins.2009.11.003 · Cited by 1,128 · see citing works
Evidence of Brain Overgrowth in the First Year of Life in Autism
Courchesne, E. (2003) · JAMA · doi:10.1001/jama.290.3.337 · Cited by 1,120 · see citing works
Excitotoxicity and stroke: Identifying novel targets for neuroprotection
Lai, T. W., Zhang, S., & Wang, Y. T. (2014) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2013.11.006 · Cited by 1,106 · see citing works
Pten Regulates Neuronal Arborization and Social Interaction in Mice
Kwon, C.-H., Luikart, B. W., Powell, C. M., Zhou, J., Matheny, S. A., Zhang, W., Li, Y., Baker, S. J., & Parada, L. F. (2006) · Neuron · doi:10.1016/j.neuron.2006.03.023 · Cited by 970 · see citing works
Lifetime Cancer Risks in Individuals with GermlinePTENMutations
Tan, M.-H., Mester, J. L., Ngeow, J. Y. Y., Rybicki, L. A., Orloff, M. S., & Eng, C. (2012) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-11-2283 · Cited by 892 · see citing works
Fingar, D. C., Richardson, C. J., Tee, A. R., Cheatham, L. A., Tsou, C., & Blenis, J. (2003) · Molecular and Cellular Biology · doi:10.1128/mcb.24.1.200-216.2004 · Cited by 865 · see citing works
Butler, M. G., Dasouki, M. J., Zhou, X.-P., Talebizadeh, Z., Brown, M., Takahashi, T. N., Miles, J. H., Wang, C. H., Stratton, R., Pilarski, R., et al. (2005) · Journal of Medical Genetics · doi:10.1136/jmg.2004.024646 · Cited by 778 · see citing works
Backman, S. A., Stambolic, V., Suzuki, A., Haight, J., Elia, A., Pretorius, J. K., Tsao, M., Shannon, P. T., Bolon, B. N., Ivy, G. O., et al. (2001) · Nature Genetics · doi:10.1038/ng782 · Cited by 511 · see citing works
Pten regulates neuronal soma size: a mouse model of Lhermitte-Duclos disease
Kwon, C.-H., Zhu, X., Zhang, J., Knoop, L. L., Tharp, R., Smeyne, R. J., Eberhart, C. G., Burger, P. C., & Baker, S. J. (2001) · Nature Genetics · doi:10.1038/ng781 · Cited by 478 · see citing works
Protean PTEN: Form and Function
Waite, K. A., & Eng, C. (2002) · The American Journal of Human Genetics · doi:10.1086/340026 · Cited by 457 · see citing works
Nuclear PTEN controls DNA repair and sensitivity to genotoxic stress
Bassi, C., Ho, J., Srikumar, T., Dowling, R. J. O., Gorrini, C., Miller, S. J., Mak, T. W., Neel, B. G., Raught, B., & Stambolic, V. (2013) · Science · doi:10.1126/science.1236188 · Cited by 403 · see citing works
Hippocampus development and generation of dentate gyrus granule cells is regulated by LEF1
Galcerán, J., Miyashita-Lin, E. M., Devaney, E. J., Rubenstein, J. L. R., & Grosschedl, R. (2000) · Development · doi:10.1242/dev.127.3.469 · Cited by 399 · see citing works
High cumulative risks of cancer in patients with PTEN hamartoma tumour syndrome
Bubien, V., Bonnet, F., Brouste, V., Hoppe, S., Barouk-Simonet, E., David, A., Edery, P., Bottani, A., Layet, V., Caron, O., et al. (2013) · Journal of Medical Genetics · doi:10.1136/jmedgenet-2012-101339 · Cited by 374 · see citing works
Pleasure, S. J., Anderson, S. A., Hevner, R. F., Bagri, A., Marín, Ó., Lowenstein, D. H., & Rubenstein, J. L. R. (2000) · Neuron · doi:10.1016/s0896-6273(00)00149-5 · Cited by 356 · see citing works
Bajenaru, M. L., Zhu, Y., Hedrick, N. M., Donahoe, J. S., Parada, L. F., & Gutmann, D. H. (2002) · Molecular and Cellular Biology · doi:10.1128/mcb.22.14.5100-5113.2002 · Cited by 322 · see citing works
PTEN function: the long and the short of it
Hopkins, B. D., Hodakoski, C., Barrows, D., Mense, S. M., & Parsons, R. E. (2014) · Trends in Biochemical Sciences · doi:10.1016/j.tibs.2014.02.006 · Cited by 309 · see citing works
mTORC2 controls actin polymerization required for consolidation of long-term memory
Huang, W., Zhu, P. J., Zhang, S., Zhou, H., Stoica, L., Galiano, M., Krnjević, K., Roman, G., & Costa-Mattioli, M. (2013) · Nature Neuroscience · doi:10.1038/nn.3351 · Cited by 307 · see citing works
Rac1 Regulates the Activity of mTORC1 and mTORC2 and Controls Cellular Size
Saci, A., Cantley, L. C., & Carpenter, C. L. (2011) · Molecular Cell · doi:10.1016/j.molcel.2011.03.017 · Cited by 275 · see citing works
mTor is required for hypertrophy of Pten-deficient neuronal soma in vivo
Kwon, C.-H., Zhu, X., Zhang, J., & Baker, S. J. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2132711100 · Cited by 256 · see citing works
PI3K/AKT signaling pathway: Molecular mechanisms and therapeutic potential in depression
Guo, N., Wang, X., Xu, M., Bai, J., Yu, H., & Zhang, L. (2024) · Pharmacological Research · doi:10.1016/j.phrs.2024.107300 · Cited by 232 · see citing works
McBride, K. L., Varga, E. A., Pastore, M., Prior, T. W., Manickam, K., Atkin, J., & Herman, G. E. (2010) · Autism Research · doi:10.1002/aur.132 · Cited by 231 · see citing works
A Role for Nuclear PTEN in Neuronal Differentiation
Lachyankar, M. B., Sultana, N. A., Schonhoff, C. M., Mitra, P., Poluha, W., Lambert, S., Quesenberry, P. J., Litofsky, N. S., Recht, L. D., Nabi, R. R., et al. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-04-01404.2000 · Cited by 231 · see citing works
PTEN signaling in brain: neuropathology and tumorigenesis
Endersby, R., & Baker, S. J. (2008) · Oncogene · doi:10.1038/onc.2008.239 · Cited by 222 · see citing works
Stocker, H., Andjelković, M., Oldham, S., Laffargue, M., Wymann, M. P., Hemmings, B. A., & Hafen, E. (2002) · Science · doi:10.1126/science.1068094 · Cited by 198 · see citing works
LaSarge, C. L., & Danzer, S. C. (2014) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2014.00018 · Cited by 193 · see citing works
Shah, O. J., & Hunter, T. R. (2006) · Molecular and Cellular Biology · doi:10.1128/mcb.01254-05 · Cited by 178 · see citing works
Amiri, A., Cho, W., Zhou, J., Birnbaum, S. G., Sinton, C. M., McKay, R. M., & Parada, L. F. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.5462-11.2012 · Cited by 172 · see citing works
Deletion of PTEN produces autism-like behavioral deficits and alterations in synaptic proteins
Lugo, J. N., Smith, G. D., Arbuckle, E. P., White, J., Holley, A. J., Floruta, C. M., Ahmed, N., Gomez, M. C., & Okonkwo, O. (2014) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2014.00027 · Cited by 159 · see citing works
Page, D. T., Kuti, O. J., Prestia, C., & Sur, M. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0804428106 · Cited by 149 · see citing works
Urbańska, M., Góźdź, A., Swiech, L. J., & Jaworski, J. (2012) · Journal of Biological Chemistry · doi:10.1074/jbc.m112.374405 · Cited by 149 · see citing works
Pten KnockdownIn VivoIncreases Excitatory Drive onto Dentate Granule Cells
Luikart, B. W., Schnell, E., Washburn, E. K., Bensen, A. L., Tovar, K. R., & Westbrook, G. L. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.0061-11.2011 · Cited by 141 · see citing works
Hyperactivity of Newborn Pten Knock-out Neurons Results from Increased Excitatory Synaptic Drive
Williams, M. R., DeSpenza, T., Li, M., Gulledge, A. T., & Luikart, B. W. (2015) · The Journal of Neuroscience · doi:10.1523/jneurosci.3144-14.2015 · Cited by 140 · see citing works
A recollection of mTOR signaling in learning and memoryPreprint
Graber, T. E., McCamphill, P. K., & Sossin, W. S. (2013) · Learning & Memory · doi:10.1101/lm.027664.112 · Cited by 135 · see citing works
Clipperton‐Allen, A. E., & Page, D. T. (2014) · Human Molecular Genetics · doi:10.1093/hmg/ddu057 · Cited by 134 · see citing works
Takeuchi, K., Gertner, M. J., Zhou, J., Parada, L. F., Bennett, M. V. L., & Zukin, R. S. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1222803110 · Cited by 119 · see citing works
The mTORC2 signaling network: targets and cross-talks
Ragupathi, A., Kim, C., & Jacinto, E. (2024) · Biochemical Journal · doi:10.1042/bcj20220325 · Cited by 113 · see citing works
PTEN in Autism and Neurodevelopmental Disorders.Preprint
Rademacher, S., & Eickholt, B. (2019) · Cold Spring Harbor Perspectives in Medicine · doi:10.1101/cshperspect.a036780 · Cited by 106 · see citing works
Sperow, M., Berry, R. B., Bayazitov, I. T., Zhu, G. G., Baker, S. J., & Zakharenko, S. S. (2011) · The Journal of Physiology · doi:10.1113/jphysiol.2011.220236 · Cited by 103 · see citing works
McCabe, M. P., Cullen, E. R., Barrows, C. M. L., Shore, A. N., Tooke, K. I., Laprade, K. A., Stafford, J. M., & Weston, M. C. (2020) · eLife · doi:10.7554/elife.51440 · Cited by 93 · see citing works
Kreis, P., Leondaritis, G., Lieberam, I., & Eickholt, B. J. (2014) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2014.00023 · Cited by 85 · see citing works
Cellular dynamics of neuronal migration in the hippocampus
Hayashi, K., Kubo, K., Kitazawa, A., & Nakajima, K. (2015) · Frontiers in Neuroscience · doi:10.3389/fnins.2015.00135 · Cited by 74 · see citing works
Stacho, M., & Manahan‐Vaughan, D. (2022) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2022.806356 · Cited by 70 · see citing works
Sun, J., Liu, Y., Tran, J., O’Neal, P., Baudry, M., & Bi, X. (2016) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-016-2269-z · Cited by 69 · see citing works
PTEN Nuclear FunctionsPreprint
Ho, J., Cruise, E. S., Dowling, R. J. O., & Stambolic, V. (2019) · Cold Spring Harbor Perspectives in Medicine · doi:10.1101/cshperspect.a036079 · Cited by 68 · see citing works
Retrograde Changes in Presynaptic Function Driven by Dendritic mTORC1
Henry, F. E., McCartney, A. J., Neely, R., Perez, A. S., Carruthers, C. J. L., Stuenkel, E. L., Inoki, K., & Sutton, M. A. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.2149-12.2012 · Cited by 67 · see citing works
García‐Junco‐Clemente, P., & Golshani, P. (2014) · Communicative & Integrative Biology · doi:10.4161/cib.28358 · Cited by 57 · see citing works
Bond, A. M., Berg, D. A., Lee, S., Garcia-Epelboim, A., Adusumilli, V. S., Ming, G., & Song, H. (2020) · Brain Sciences · doi:10.3390/brainsci10120909 · Cited by 57 · see citing works
Timing of mTOR activation affects tuberous sclerosis complex neuropathology in mouse models
Magri, L., Cominelli, M., Cambiaghi, M., Cursi, M., Leocani, L., Minicucci, F., Poliani, P. L., & Galli, R. (2013) · Disease Models & Mechanisms · doi:10.1242/dmm.012096 · Cited by 51 · see citing works
Zhu, G. G., Chow, L. M. L., Bayazitov, I. T., Tong, Y., Gilbertson, R. J., Zakharenko, S. S., Solecki, D. J., & Baker, S. J. (2012) · Development · doi:10.1242/dev.083154 · Cited by 46 · see citing works
LaSarge, C. L., Santos, V. R., & Danzer, S. C. (2015) · Neurobiology of Disease · doi:10.1016/j.nbd.2014.12.029 · Cited by 40 · see citing works
PTEN suppresses axon outgrowth by down-regulating the level of detyrosinated microtubules
Kath, C., Goñi‐Oliver, P., Müller, R., Schultz, C., Haucke, V., Eickholt, B. J., & Schmoranzer, J. (2018) · PLoS ONE · doi:10.1371/journal.pone.0193257 · Cited by 37 · see citing works
Radial Glia, the Keystone of the Development of the Hippocampal Dentate Gyrus
Xu, L., Tang, X., Wang, Y., Xu, H., & Fan, X. (2014) · Molecular Neurobiology · doi:10.1007/s12035-014-8692-y · Cited by 31 · see citing works
Nuclear trafficking of Pten after brain injury leads to neuron survival not death
Goh, C., Putz, U., Howitt, J. A., Low, L., Gunnersen, J. M., Bye, N., Morganti-Kossmann, M. C., & Tan, S. (2013) · Experimental Neurology · doi:10.1016/j.expneurol.2013.11.017 · Cited by 30 · see citing works
Analysis of the role of GSK3 in the mitotic checkpoint
Rashid, M. S., Mazur, T. M., Ji, W., Liu, S. T., & Taylor, W. R. (2018) · Scientific Reports · doi:10.1038/s41598-018-32435-w · Cited by 30 · see citing works
Lugo, J. N., Smith, G. D., Morrison, J. B., & White, J. (2013) · Learning & Memory · doi:10.1101/lm.032839.113 · Cited by 29 · see citing works
What Is the Relationship Between Hippocampal Neurogenesis Across Different Stages of the Lifespan?
Bond, A. M., Ming, G., & Song, H. (2022) · Frontiers in Neuroscience · doi:10.3389/fnins.2022.891713 · Cited by 27 · see citing works
PTENα Modulates CaMKII Signaling and Controls Contextual Fear Memory and Spatial Learning
Wang, P., Mei, F., Hu, J., Zhu, M., Qi, H., Chen, X., Li, R., McNutt, M. A., & Yin, Y. (2017) · Cell Reports · doi:10.1016/j.celrep.2017.05.088 · Cited by 26 · see citing works
Smith, G. D., White, J., & Lugo, J. N. (2016) · Scientific Reports · doi:10.1038/srep36559 · Cited by 24 · see citing works
Seo, M. K., Hiền, L. T. T., Park, M. K., Choi, A. J., Seog, D., Kim, S. H., Park, S. W., & Lee, J. G. (2020) · Scientific Reports · doi:10.1038/s41598-020-58017-3 · Cited by 23 · see citing works
Luan, Y., Zhang, H., Ma, K., Liu, Y., Lü, H., Chen, X., Liu, Y., & Zhang, Z. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241210324 · Cited by 18 · see citing works
Neuronal subset-specific deletion of Pten results in aberrant Wnt signaling and memory impairments
Hodges, S. L., Reynolds, C. D., Smith, G. D., Jefferson, T. S., Gao, N., Morrison, J. B., White, J., Nolan, S. O., & Lugo, J. N. (2018) · Brain Research · doi:10.1016/j.brainres.2018.08.007 · Cited by 13 · see citing works
PTEN isoforms with dual and opposing function
Taylor, J., & Abdel-Wahab, O. I. (2019) · Nature Cell Biology · doi:10.1038/s41556-019-0405-3 · Cited by 8 · see citing works
Pten, a candidate tumor suppressor gene, maps to mouse Chromosome 19
Hansen, G. M., & Justice, M. J. (1998) · Mammalian Genome · doi:10.1007/s003359900690 · Cited by 8 · see citing works
Latchney, S. E., Lopez, B. R. R., Womble, P. D., Blandin, K. J., & Lugo, J. N. (2023) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2023.1308066 · Cited by 5 · see citing works
Fiuji, H., & Nassiri, M. (2020) · Gene Reports · doi:10.1016/j.genrep.2020.100895 · Cited by 1 · see citing works
Flagged first, then by citations
Research works printed but not linked: 2
- Kitazawa, A., Kubo, K., Hayashi, K., Matsunaga, Y., Ishii, K., & Nakajima, K. (2014). Hippocampal pyramidal neurons switch from a multipolar mi- gration mode to a novel "climbing" migration mode during develop- ment. J Neurosci, 34(4), 1115-1126. https://doi.org/10.1523/JNEUROS- CI.2254-13.2014 · DOI
- Singh, S., & Singh, T. G. (2020). Role of Nuclear Factor Kappa B (NF-kappaB) Signalling in Neurodegenerative Diseases: An Mechanistic Approach. Curr Neuropharmacol, 18(10), 918-935. https://doi.org/10.2174/157015 · DOI
Cited by
Sorted by citations
Nordbeck, A. J., Martá‐Ariza, M., Ek Olofsson, H., Kanshin, E., Ueberheide, B., Jones, K., Sanford, B., Hamlett, E. D., Head, E., Mufson, E. J., et al. (2026) · Alzheimer's & Dementia · doi:10.1002/alz.71776
Heterozygous Mutations of PTEN in Macrocephaly Patient With Epilepsy: A Case Report
Wang, L., Su, Y., & Mo, M. (2025) · Case Reports in Medicine · doi:10.1155/carm/5190615
Analysis of PTEN Antagonistic Peptides (PAPs) in Neuronal Growth and Traumatic Brain Injury (TBI)
Rivera, K. K., Tsai, Y., Song, J., Gu, H., Gutt, A.-S., Sinske, D., Klugmann, C., Pagliarini, M., Roselli, F., Synatschke, C. V., et al. (2026) · Biomacromolecules · doi:10.1021/acs.biomac.6c00695
Ranjbar, M., Ghiasvand, K., Rastegari, B., Khorsand, M., & Takhshid, M. A. (2026) · Histochemistry and Cell Biology · doi:10.1007/s00418-026-02515-4
- Authors
- Chwin, N., & Kiryk, A.
- Affiliations
- Instytut Biologii Doświadczalnej im. Marcelego Nenckiego (PL)
- ORCID
- Kiryk, Anna
- Venue
- Acta Neurobiologiae Experimentalis
- Published
- 2024-12-11
- Volume
- 84
- Issue
- 4
- Pages
- 309-318
- ISSN
- 0065-1400 (ISSN-L)
- 1689-0035
- OpenAlex
- W4405256446
- Cited by
- 3
- References
- 74
- Citations by year
- 2026: 2 · 2025: 1
- FWCI
- 0.21
- Type
- journal article
- Language
- en
- Open access
- diamond
- doi.org
- Locations
- Acta Neurobiologiae Experimentalis (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetics and Neurodevelopmental Disorders
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › PI3K/AKT/mTOR signaling in cancer
- Keywords
- PTEN, neurogenesis, synaptic plasticity, social behavior, PI3K/AKT/mTOR pathway, neuronal migration, neural progenitor proliferation, dentate gyrus, dendritic growth, axon guidance, long-term potentiation, long-term depression, learning and memory, neurodevelopmental disorders, intellectual disability, epilepsy, autism spectrum disorder, macrocephaly, tumor suppressor
- MeSH terms
- Animals, Brain, Humans, Neuronal Plasticity, Neurons, Social Behavior, PTEN Phosphohydrolase, Neurogenesis
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review