Activity-dependent synaptic Wnt release regulates hippocampal long term potentiation

The Wnt Signaling Pathway in Development and Disease

Logan, C. Y., & Nusse, R. (2004) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.20.010403.113126 · Cited by 5,325 · see citing works

Convergence of Wnt, ß-Catenin, and Cadherin Pathways

Nelson, W. J., & Nusse, R. (2004) · Science · doi:10.1126/science.1094291 · Cited by 2,515 · see citing works

Structural basis of long-term potentiation in single dendritic spines

Matsuzaki, M., Honkura, N., Ellis-Davies, G. C. R., & Kasai, H. (2004) · Nature · doi:10.1038/nature02617 · Cited by 2,500 · see citing works

A molecular mechanism for the effect of lithium on development.

Klein, P. S., & Melton, D. A. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.16.8455 · Cited by 2,305 · see citing works

WNT and β-catenin signalling: diseases and therapies

Moon, R. T., Kohn, A. D., Ferrari, G. V. D., & Kaykas, A. (2004) · Nature Reviews Genetics · doi:10.1038/nrg1427 · Cited by 1,763 · see citing works

Morphological Changes in Dendritic Spines Associated with Long-Term Synaptic Plasticity

Yuste, R., & Bonhoeffer, T. (2001) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.24.1.1071 · Cited by 1,269 · see citing works

Actin-based plasticity in dendritic spines

Matus, A. (2000) · Science · doi:10.1126/science.290.5492.754 · Cited by 815 · see citing works

Mapping Wnt/β-catenin signaling during mouse development and in colorectal tumors

Maretto, S., Cordenonsi, M., Dupont, S., Braghetta, P., Broccoli, V., Hassan, A. B., Volpin, D., Bressan, G. M., & Piccolo, S. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0434590100 · Cited by 759 · see citing works

Axonal Remodeling and Synaptic Differentiation in the Cerebellum Is Regulated by WNT-7a Signaling

Hall, A. C., Lucas, F. R., & Salinas, P. C. (2000) · Cell · doi:10.1016/s0092-8674(00)80689-3 · Cited by 687 · see citing works

A local Wnt-3a signal is required for development of the mammalian hippocampus

Lee, S. M. K., Tole, S., Grove, E. A., & McMahon, A. P. (2000) · Development · doi:10.1242/dev.127.3.457 · Cited by 636 · see citing works

WNTS in the vertebrate nervous system: from patterning to neuronal connectivity

Ciani, L., & Salinas, P. C. (2005) · Nature reviews. Neuroscience · doi:10.1038/nrn1665 · Cited by 631 · see citing works

Anterior-Posterior Guidance of Commissural Axons by Wnt-Frizzled Signaling

Lyuksyutova, A. I., Lu, C.-C., Milanesio, N., King, L. A., Guo, N., Wang, Y., Nathans, J., Tessier‐Lavigne, M., & Zou, Y. (2003) · Science · doi:10.1126/science.1089610 · Cited by 557 · see citing works

Expression of CD44 in Apc and TcfMutant Mice Implies Regulation by the WNT Pathway

Wielenga, V. T., Smits, R., Kořínek, V., Smit, L., Kielman, M. F., Fodde, R., Clevers, H. C., & Pals, S. T. (1999) · American Journal Of Pathology · doi:10.1016/s0002-9440(10)65297-2 · Cited by 512 · see citing works

Destabilization of β-catenin by mutations in presenilin-1 potentiates neuronal apoptosis

Zhang, Z., Hartmann, H., Do, V. M., Abramowski, D., Sturchler, C., Staufenbiel, M., Sommer, B., van de Wetering, M., Clevers, H. C., Säftig, P., et al. (1998) · Nature · doi:10.1038/27208 · Cited by 511 · see citing works

Cadherin Regulates Dendritic Spine Morphogenesis

Togashi, H., Abe, K., Mizoguchi, A., Takaoka, K., Chisaka, O., & Takeichi, M. (2002) · Neuron · doi:10.1016/s0896-6273(02)00748-1 · Cited by 485 · see citing works

Wnt signaling through Dishevelled, Rac and JNK regulates dendritic development

Rosso, S. B., Sussman, D., Wynshaw-Boris, A., & Salinas, P. C. (2005) · Nature Neuroscience · doi:10.1038/nn1374 · Cited by 485 · see citing works

Social interaction and sensorimotor gating abnormalities in mice lacking Dvl1

Lijam, N., Paylor, R., McDonald, M. P., Crawley, J. N., Deng, C.-X., Herrup, K., Stevens, K. E., Maccaferri, G., McBain, C. J., Sussman, D. J., et al. (1997) · Cell · doi:10.1016/s0092-8674(00)80354-2 · Cited by 470 · see citing works

Mammalian Ryk Is a Wnt Coreceptor Required for Stimulation of Neurite Outgrowth

Lu, W., Yamamoto, V. N., Ortega, B., & Baltimore, D. (2004) · Cell · doi:10.1016/j.cell.2004.09.019 · Cited by 466 · see citing works

Expression of multiple novel Wnt-1/int-1-related genes during fetal and adult mouse development.Preprint

Gavin, B. J., McMahon, J. A., & McMahon, A. P. (1990) · Genes & Development · doi:10.1101/gad.4.12b.2319 · Cited by 455 · see citing works

β-catenin is critical for dendritic morphogenesis

Yu, X., & Malenka, R. C. (2003) · Nature Neuroscience · doi:10.1038/nn1132 · Cited by 454 · see citing works

Wnt-mediated axon guidance via the Drosophila Derailed receptor

Yoshikawa, S., McKinnon, R. D., Kokel, M., & Thomas, J. B. (2003) · Nature · doi:10.1038/nature01522 · Cited by 416 · see citing works

The Drosophila Wnt, Wingless, Provides an Essential Signal for Pre- and Postsynaptic Differentiation

Packard, M. C., Koo, E. S., Gorczyca, M. G., Sharpe, J., Cumberledge, S., & Budnik, V. (2002) · Cell · doi:10.1016/s0092-8674(02)01047-4 · Cited by 410 · 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

Induction of Dickkopf-1, a Negative Modulator of the Wnt Pathway, Is Associated with Neuronal Degeneration in Alzheimer's Brain

Caricasole, A., Copani, A., Caraci, F., Aronica, E., Rozemüller, A. J. M., Caruso, A., Storto, M., Gaviraghi, G., Terstappen, G. C., & Nicoletti, F. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.1381-04.2004 · Cited by 394 · see citing works

Biochemical characterization of Wnt-Frizzled interactions using a soluble, biologically active vertebrate Wnt protein

Hsieh, J.-C., Rattner, A., Smallwood, P. M., & Nathans, J. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.7.3546 · Cited by 349 · see citing works

Depolarization Drives β-Catenin into Neuronal Spines Promoting Changes in Synaptic Structure and Function

Murase, S., Mosser, E. A., & Schuman, E. M. (2002) · Neuron · doi:10.1016/s0896-6273(02)00764-x · Cited by 337 · see citing works

Activation of Wnt signaling rescues neurodegeneration and behavioral impairments induced by β-amyloid fibrils

Ferrari, G. V. D., Chacón, M. A., Barría, M. I., Garrido, J., Godoy, J. A., Olivares, G. H., Reyes, A. E., Alvarez, A. R., Bronfman, M., & Inestrosa, N. C. (2003) · Molecular Psychiatry · doi:10.1038/sj.mp.4001208 · Cited by 331 · see citing works

Role of β-Catenin in Synaptic Vesicle Localization and Presynaptic Assembly

Bamji, S. X., Shimazu, K., Kimes, N. E., Huelsken, J., Birchmeier, W., Lu, B., & Reichardt, L. F. (2003) · Neuron · doi:10.1016/s0896-6273(03)00718-9 · Cited by 310 · see citing works

Involvement of Claudin-1 in the β-Catenin/Tcf Signaling Pathway and its Frequent Upregulation in Human Colorectal Cancers

Miwa, N., Furuse, M., Tsukita, S., et al. (2001) · Oncology Research Featuring Preclinical and Clinical Cancer Therapeutics · doi:10.3727/096504001108747477 · Cited by 299 · see citing works

Wnt–Ryk signalling mediates medial–lateral retinotectal topographic mapping

Schmitt, A. M., Shi, J., Wolf, A. M., Lu, C.-C., King, L. A., & Zou, Y. (2006) · Nature · doi:10.1038/nature04334 · Cited by 292 · see citing works

Ryk-mediated Wnt repulsion regulates posterior-directed growth of corticospinal tract

Liu, Y., Shi, J., Lu, C.-C., Wang, Z.-B., Lyuksyutova, A. I., Song, X., & Zou, Y. (2005) · Nature Neuroscience · doi:10.1038/nn1520 · Cited by 264 · see citing works

Presenilin mutations associated with Alzheimer disease cause defective intracellular trafficking of β-catenin,a component of the presenilin protein complex

Nishimura, M., Yu, G., Lévesque, G., Zhang, D. M., Ruel, L., Chen, F., Milman, P., Holmes, E., Liang, Y., Kawarai, T., et al. (1999) · Nature Medicine · doi:10.1038/5526 · Cited by 218 · see citing works

Wnt Signaling Protects 3T3-L1 Preadipocytes from Apoptosis through Induction of Insulin-like Growth Factors

Longo, K. A., Kennell, J. A., Ochocinska, M. J., Ross, S. E., Hahn, W. S., & MacDougald, O. A. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m206402200 · Cited by 212 · see citing works

Wnt-3a overcomes β-amyloid toxicity in rat hippocampal neurons

Alvarez, A. R., Godoy, J. A., Müllendorff, K., Olivares, G. H., Bronfman, M., & Inestrosa, N. C. (2004) · Experimental Cell Research · doi:10.1016/j.yexcr.2004.02.028 · Cited by 211 · see citing works

WNT-3, Expressed by Motoneurons, Regulates Terminal Arborization of Neurotrophin-3-Responsive Spinal Sensory Neurons

Krylova, O. Y., Herreros, J., Cleverley, K., Ehler, E., Henríquez, J. P., Hughes, S. M., & Salinas, P. C. (2002) · Neuron · doi:10.1016/s0896-6273(02)00860-7 · Cited by 199 · see citing works

Wnt Signaling Mutants Have Decreased Dentate Granule Cell Production and Radial Glial Scaffolding Abnormalities

Zhou, C. J., Zhao, C., & Pleasure, S. J. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.4071-03.2004 · Cited by 196 · see citing works

Antipsychotics alter the protein expression levels of β-catenin and GSK-3 in the rat medial prefrontal cortex and striatum

Alimohamad, H., Rajakumar, N., Seah, Y.-H., & Rushlow, W. J. (2005) · Biological Psychiatry · doi:10.1016/j.biopsych.2004.11.036 · Cited by 187 · see citing works

Wnt-3, a gene activated by proviral insertion in mouse mammary tumors, is homologous to int-1/Wnt-1 and is normally expressed in mouse embryos and adult brain.

Roelink, H., Wagenaar, E., da Silva, S. L., & Nusse, R. (1990) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.87.12.4519 · Cited by 187 · see citing works

LEF1-mediated regulation of Delta-like1 links Wnt and Notch signaling in somitogenesisPreprint

Galcerán, J., Sustmann, C., Hsu, S.-C., Roessler, S. K., & Grosschedl, R. (2004) · Genes & Development · doi:10.1101/gad.1249504 · Cited by 184 · see citing works

WNT signaling, in synergy with T/TBX6, controls Notch signaling by regulating Dll1 expression in the presomitic mesoderm of mouse embryosPreprint

Hofmann, M., Schuster-Gossler, K., Watabe‐Rudolph, M., Aulehla, A., Herrmann, B. G., & Gossler, A. (2004) · Genes & Development · doi:10.1101/gad.1248604 · Cited by 175 · see citing works

Increased expression of Wnt-1 in schizophrenic brains

Miyaoka, T., Seno, H., & Ishino, H. (1999) · Schizophrenia Research · doi:10.1016/s0920-9964(98)00179-0 · Cited by 161 · see citing works

Abnormalities of Wnt signalling in schizophrenia – evidence for neurodevelopmental abnormality

Cotter, D., Kerwin, R. W., Al-Sarraji, S., Brion, J., Chadwich, A., Lovestone, S., Anderton, B. H., & Everall, I. (1998) · Neuroreport · doi:10.1097/00001756-199805110-00024 · Cited by 152 · see citing works

IDENTIFICATION OF LINOTTE , A NEW GENE AFFECTING LEARNING AND MEMORY IN DROSOPHILA MELANOGASTER

Dura, J., Préat, T., & Tully, T. (2007) · Journal of Neurogenetics · doi:10.1080/01677060701693479 · Cited by 132 · see citing works

Signal transduction during amyloid-β-peptide neurotoxicity: role in Alzheimer disease

Fuentealba, R. A., Farı́as, G. G., Scheu, J., Bronfman, M., Marzolo, M., & Inestrosa, N. C. (2004) · Brain Research Reviews · doi:10.1016/j.brainresrev.2004.07.018 · Cited by 126 · see citing works

Identification ofLinotte, a New Gene Affecting Learning and Memory inDrosophila Melanogaster

Dura, J., Préat, T., & Tully, T. (1993) · Journal of Neurogenetics · doi:10.3109/01677069309167272 · Cited by 121 · see citing works

LIN-23-Mediated Degradation of β-Catenin Regulates the Abundance of GLR-1 Glutamate Receptors in the Ventral Nerve Cord of C. elegans

Dreier, L., Burbea, M., & Kaplan, J. M. (2005) · Neuron · doi:10.1016/j.neuron.2004.12.058 · Cited by 94 · see citing works

Reduced GSK-3? mRNA levels in postmortem dorsolateral prefrontal cortex of schizophrenic patients

Kozlovsky, N., Weickert, C. S., Tomaskovic‐Crook, E., Kleinman, J. E., Belmaker, R. H., & Agam, G. (2004) · Journal of Neural Transmission · doi:10.1007/s00702-004-0166-3 · Cited by 90 · see citing works

The human frizzled-3 (FZD3) gene on chromosome 8p21, a receptor gene for Wnt ligands, is associated with the susceptibility to schizophrenia

Katsu, T., Ujike, H., Nakano, T., Tanaka, Y., Nomura, A., Nakata, K., Takaki, M., Sakai, A., Uchida, N., Imamura, T., et al. (2003) · Neuroscience Letters · doi:10.1016/j.neulet.2003.09.017 · Cited by 80 · see citing works

Association study of the human FZD3 locus with schizophrenia

Yang, J., Si, T., Ling, Y., Ruan, Y., Han, Y., Wang, X., Zhang, H., Kong, Q., Li, X., Liu, C., et al. (2003) · Biological Psychiatry · doi:10.1016/s0006-3223(03)00291-9 · Cited by 66 · see citing works

Direct interaction of Frizzled‐1, ‐2, ‐4, and ‐7 with PDZ domains of PSD‐95

Hering, H., & Sheng, M. (2002) · FEBS Letters · doi:10.1016/s0014-5793(02)02831-4 · Cited by 65 · see citing works

The Drosophila learning and memory gene linotte encodes a putative receptor tyrosine kinase homologous to the human RYK gene product

Dura, J., Taillebourg, E., & Préat, T. (1995) · FEBS Letters · doi:10.1016/0014-5793(95)00847-3 · Cited by 64 · see citing works

Cadherins Communicate Structural Plasticity of Presynaptic and Postsynaptic Terminals

Goda, Y. (2002) · Neuron · doi:10.1016/s0896-6273(02)00765-1 · Cited by 60 · see citing works

Down‐regulation of Dickkopf 3, a regulator of the Wnt signalling pathway, in elderly schizophrenic subjects

Ftouh, S., Akbar, M. T., Hirsch, S. R., & de Belleroche, J. (2005) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2005.03239.x · Cited by 49 · see citing works

Novel target genes of the Wnt pathway and statistical insights into Wnt target promoter regulation

Ziegler, S., Röhrs, S., Tickenbrock, L., et al. (2005) · FEBS Journal · doi:10.1111/j.1742-4658.2005.04581.x · Cited by 46 · see citing works

Inhibitory effect of a presenilin 1 mutation on the Wnt signalling pathway by enhancement of β‐catenin phosphorylation

Kawamura, Y., Kikuchi, A., Takada, R., Takada, S., Sudoh, S., Shibamoto, S., Yanagisawa, K., & Komano, H. (2001) · European Journal of Biochemistry · doi:10.1046/j.1432-1327.2001.02197.x · Cited by 36 · see citing works

Presenilin function: connections to Alzheimer's disease and signal transduction

Fraser, P. E., Yu, G., Lévesque, L., et al. (2001) · Biochemical Society Symposia · doi:10.1042/bss0670089 · Cited by 29 · see citing works

Neuropathology of the cerebral cortex observed in a range of animal models of prenatal cocaine exposure may reflect alterations in genes involved in the Wnt and cadherin systems

Novikova, S. I., He, F., Bai, J., & Lidow, M. S. (2005) · Synapse · doi:10.1002/syn.20134 · Cited by 24 · see citing works

Wnt Signaling in Development

Wehrle, C., Lickert, H., & Kemler, R. (2003) · Elsevier eBooks · doi:10.1016/b978-012124546-7/50613-6 · Cited by 23 · see citing works

The GSK3 hypothesis of Alzheimer’s disease

Hooper, C., Killick, R., & Lovestone, S. (2008) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2007.05194.x · Cited by 1,191 · see citing works

Dentate gyrus-specific knockdown of adult neurogenesis impairs spatial and object recognition memory in adult rats

Jessberger, S., Clark, R. E., Broadbent, N. J., Clemenson, G. D., Consiglio, A., Lie, D. C., Squire, L. R., & Gage, F. H. (2009) · Learning & Memory · doi:10.1101/lm.1172609 · Cited by 654 · see citing works

The Aβ oligomer hypothesis for synapse failure and memory loss in Alzheimer’s disease

Ferreira, S. T., & Klein, W. L. (2011) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2011.08.003 · Cited by 442 · see citing works

Wnt signaling in the nervous system and in Alzheimer's disease

Inestrosa, N. C., & Varela-Nallar, L. (2014) · Journal of Molecular Cell Biology · doi:10.1093/jmcb/mjt051 · Cited by 324 · see citing works

Restoring Wnt/β-catenin signaling is a promising therapeutic strategy for Alzheimer’s disease

Jia, L., Piña-Crespo, J., & Li, Y. (2019) · Molecular Brain · doi:10.1186/s13041-019-0525-5 · Cited by 288 · see citing works

Wnt signaling in neural circuit assembly

Salinas, P. C., & Zou, Y. (2008) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.31.060407.125649 · Cited by 274 · see citing works

WNT signaling in neuronal maturation and synaptogenesis

Rosso, S. B., & Inestrosa, N. C. (2013) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2013.00103 · Cited by 272 · see citing works

Wingless-type family member 5A (Wnt-5a) stimulates synaptic differentiation and function of glutamatergic synapses

Varela-Nallar, L., Alfaro, I. E., Serrano, F. G., Parodi, J., & Inestrosa, N. C. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1010011107 · Cited by 197 · see citing works

Wnts in adult brain: from synaptic plasticity to cognitive deficiencies

Oliva, C. A., Vargas, J. Y., & Inestrosa, N. C. (2013) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2013.00224 · Cited by 162 · see citing works

GSK3: a key target for the development of novel treatments for type 2 diabetes mellitus and Alzheimer disease

Gao, C., Hölscher, C., Liu, Y., & Li, L. (2012) · revneuro · doi:10.1515/rns.2011.061 · Cited by 164 · see citing works

A review of the evidence for the canonical Wnt pathway in autism spectrum disorders

Kalkman, H. (2012) · Molecular Autism · doi:10.1186/2040-2392-3-10 · Cited by 142 · see citing works

Modulation of Wnt/β-catenin signaling promotes blood-brain barrier phenotype in cultured brain endothelial cells

Laksitorini, M. D., Yathindranath, V., Xiong, W., Hombach-Klonisch, S., & Miller, D. W. (2019) · Scientific Reports · doi:10.1038/s41598-019-56075-w · Cited by 105 · see citing works

Wnt/β-Catenin Signaling in Alzheimer’s Disease

Ferrari, G., Avila, M., Medina, M., Perez-Palma, E., Bustos, B., & Alarcon, M. (2014) · CNS & Neurological Disorders - Drug Targets · doi:10.2174/1871527312666131223113900 · Cited by 95 · see citing works

Role of the Wnt receptor Frizzled-1 in presynaptic differentiation and function

Varela-Nallar, L., Grabowski, C. P., Alfaro, I. E., Alvarez, A. R., & Inestrosa, N. C. (2009) · Neural Development · doi:10.1186/1749-8104-4-41 · Cited by 97 · see citing works

Reactivation of cocaine reward memory engages the Akt/GSK3/mTOR signaling pathway and can be disrupted by GSK3 inhibition

Shi, X., Miller, J. S., Harper, L. J., Poole, R. L., Gould, T. J., & Unterwald, E. M. (2014) · Psychopharmacology · doi:10.1007/s00213-014-3491-8 · Cited by 79 · see citing works

Dysregulated Wnt Signalling in the Alzheimer’s Brain

Aghaizu, N. D., Jin, H., & Whiting, P. J. (2020) · Brain Sciences · doi:10.3390/brainsci10120902 · Cited by 70 · see citing works

Aberrant Wnt signaling pathway in medial temporal lobe structures of Alzheimer’s disease

Riise, J., Plath, N., Pakkenberg, B., & Parachikova, A. (2015) · Journal of Neural Transmission · doi:10.1007/s00702-015-1375-7 · Cited by 66 · see citing works

Hippocampal Deficits in Amyloid-β-Related Rodent Models of Alzheimer’s Disease

Vyas, Y., Montgomery, J. M., & Cheyne, J. E. (2020) · Frontiers in Neuroscience · doi:10.3389/fnins.2020.00266 · Cited by 66 · see citing works

LEF1/β-Catenin Complex Regulates Transcription of the Cav3.1 Calcium Channel Gene (<i>Cacna1g</i>) in Thalamic Neurons of the Adult Brain

Wisniewska, M. B., Misztal, K., Michowski, W., Szczot, M., Purta, E., Lesniak, W., Klejman, M. E., Dabrowski, M., Filipkowski, R. K., Nagalski, A., et al. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.1425-09.2010 · Cited by 64 · see citing works

Neuron activity–induced Wnt signaling up-regulates expression of brain-derived neurotrophic factor in the pain neural circuit

Zhang, W., Shi, Y., Peng, Y., Zhong, L., Zhu, S., Zhang, W., & Tang, S.-J. (2018) · Journal of Biological Chemistry · doi:10.1074/jbc.ra118.002840 · Cited by 59 · see citing works

ФОРМИРОВAНИЕ ГОТОВНОСТИ БУДУЩИХ ПЕДAГОГОВ К ОРГAНИЗAЦИИ РAБОТЫ ПО РAЗВИТИЮ ВAЛЕОЛОГИЧЕСКОЙ КУЛЬТУРЫ ШКОЛЬНИКОВ

БАЗАРБАЕВА, Ә. А., Майгельдиева, Ш. М., & ЖҮНДІБАЕВА, Т. Н. (2023) · Pedagogy and Psychology · doi:10.51889/2077-6861.2023.1.30.016

Коммуникaтивно- прaгмaтический aнaлиз дипломaтических бумaг (нa основе вербaльных нот)

Кaмирдиновa, Н., & Кaлиевa, Ш. С. (2018) · DOAJ (DOAJ: Directory of Open Access Journals)

Susquehanna Chorale Spring Concert "Roots and Wings"

Hawkins, D. (2017)

A GEOMETRIC MEAN IN THE FURUTA INEQUALITY

Fujii, M., & Nakamoto, R. (2002) · Scientiae mathematicae Japonicae · Cited by 15 · see citing works

ИСПОЛЬЗОВAНИЕ ПОТЕНЦИAЛA СОЦИAЛЬНЫХ ПAРТНЕРОВ В ПОДГОТОВКЕ БУДУЩИХ ПЕДAГОГОВ

Атабекова, Б. Б. (2024) · Habaršy. Pedagogika ġylymdary seriâsy · doi:10.51889/2959-5762.2023.80.4.019