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https://elar.urfu.ru/handle/10995/144208| Title: | Developing Novel Experimental Models of m-TORopathic Epilepsy and Related Neuropathologies: Translational Insights from Zebrafish |
| Authors: | de, Abreu, M. S. Demin, K. A. Kotova, M. M. Mirzaei, F. Shariff, S. Kantawala, B. Zakharchenko, K. V. Kolesnikova, T. O. Dilbaryan, K. Grigoryan, A. Yenkoyan, K. B. Kalueff, A. V. |
| Issue Date: | 2023 |
| Publisher: | MDPI |
| Citation: | De Abreu, M. S., Demin, K. A., Kotova, M. M., Mirzaei, F., Shariff, S., Kantawala, B., Zakharchenko, K. V., Kolesnikova, T. O., Dilbaryan, K., Grigoryan, A., Yenkoyan, K. B., & Kalueff, A. V. (2023). Developing Novel Experimental Models of m-TORopathic Epilepsy and Related Neuropathologies: Translational Insights from Zebrafish. International Journal of Molecular Sciences, 24(2), [1530]. https://doi.org/10.3390/ijms24021530 De Abreu, MS, Demin, KA, Kotova, MM, Mirzaei, F, Shariff, S, Kantawala, B, Zakharchenko, KV, Kolesnikova, TO, Dilbaryan, K, Grigoryan, A, Yenkoyan, KB & Kalueff, AV 2023, 'Developing Novel Experimental Models of m-TORopathic Epilepsy and Related Neuropathologies: Translational Insights from Zebrafish', International Journal of Molecular Sciences, Том. 24, № 2, 1530. https://doi.org/10.3390/ijms24021530 |
| Abstract: | The mammalian target of rapamycin (mTOR) is an important molecular regulator of cell growth and proliferation. Brain mTOR activity plays a crucial role in synaptic plasticity, cell development, migration and proliferation, as well as memory storage, protein synthesis, autophagy, ion channel expression and axonal regeneration. Aberrant mTOR signaling causes a diverse group of neurological disorders, termed ‘mTORopathies’. Typically arising from mutations within the mTOR signaling pathway, these disorders are characterized by cortical malformations and other neuromorphological abnormalities that usually co-occur with severe, often treatment-resistant, epilepsy. Here, we discuss recent advances and current challenges in developing experimental models of mTOR-dependent epilepsy and other related mTORopathies, including using zebrafish models for studying these disorders, as well as outline future directions of research in this field. |
| Keywords: | ANIMAL MODEL MTOR MTOROPATHY SIGNALING PATHWAY ZEBRAFISH ANIMALS DISEASE MODELS, ANIMAL EPILEPSY MAMMALS SIGNAL TRANSDUCTION TOR SERINE-THREONINE KINASES ZEBRAFISH ION CHANNEL MAMMALIAN TARGET OF RAPAMYCIN TARGET OF RAPAMYCIN KINASE ANIMAL MODEL AUTOPHAGY (CELLULAR) BEHAVIOR DISORDER CELL DIFFERENTIATION EXPERIMENTAL MODEL HUMAN MTOR SIGNALING MTOROPATHY MYELINATION NERVE CELL DIFFERENTIATION NERVE CELL PLASTICITY NERVE SPROUTING NERVOUS SYSTEM NERVOUS SYSTEM DEVELOPMENT NEUROPATHOLOGY NONHUMAN PROTEIN FUNCTION RECURRENT DISEASE REGULATORY MECHANISM REVIEW RODENT MODEL ZEBRA FISH ANIMAL DISEASE MODEL EPILEPSY GENETICS MAMMAL METABOLISM SIGNAL TRANSDUCTION ZEBRA FISH |
| URI: | https://elar.urfu.ru/handle/10995/144208 |
| Access: | info:eu-repo/semantics/openAccess cc-by |
| License text: | https://creativecommons.org/licenses/by/4.0/ |
| SCOPUS ID: | 85146776820 |
| WOS ID: | 000917726400001 |
| PURE ID: | 33342459 |
| ISSN: | 1422-0067 1661-6596 |
| DOI: | 10.3390/ijms24021530 |
| Sponsorship: | YSMU; Ministry of Education and Science of the Russian Federation, Minobrnauka; European Union-funded H2020; Horizon 2020 Framework Programme, H2020, (857600); State Committee of Science, SCS, (20TTCG-3A012, N10-14/I-1) Funding text 1: The study was performed by selected students and staff of YSMU COBRAIN Scientific-Educational Center for Fundamental Brain Research with support from the Republic of Armenia State Committee of Science (20TTCG-3A012 and N10-14/I-1) and the European Union-funded H2020 COBRAIN project (857600). ; Funding text 2: The publication research was supported by the Ministry of Science and Higher Education of the Russian Federation (Ural Federal University Program of Development within the Priority-2030 Program). |
| Appears in Collections: | Научные публикации ученых УрФУ, проиндексированные в SCOPUS и WoS CC |
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