Experimental Models of CNS Deficits in Lysosomal Storage Diseases
- Авторлар: Lebedev A.1,2,3, Kotova M.2, Kolesnikova T.2, Galstyan D.1,3,4, Kalueff A.1,2,3,4,5,6
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Мекемелер:
- World-class Scientific Research Center “Center of Personalized Medicine”, Almazov National Medical Research Center, Ministry of Healthcare of Russian Federation
- Neurobiology Department, Research Center for Genetics and Life Sciences, Sirius University of Science and Technology
- Institute of Translational Biomedicine, St. Petersburg State University
- Granov Russian Scientific Center for Radiology and Surgical Technologies, Ministry of Healthcare of Russian Federation
- Ural Federal University
- Scientific Research Institute of Neurosciences and Medicine
- Шығарылым: Том 109, № 11 (2023)
- Беттер: 1567-1583
- Бөлім: ОБЗОРНЫЕ И ПРОБЛЕМНЫЕ СТАТЬИ
- URL: https://journals.rcsi.science/0869-8139/article/view/232272
- DOI: https://doi.org/10.31857/S0869813923110080
- EDN: https://elibrary.ru/GNDEZV
- ID: 232272
Дәйексөз келтіру
Аннотация
Lysosomal storage diseases are characterized by enzyme deficiency in the lysosomal appar-atus of the cell, triggering a pathological accumulation of undigested cellular material (proteins, lipids or carbohydrates) and tissue damage. Clinically and etiologically dive-rse, this group includes over 70 presently recognized hereditary conditions with no known effective therapy. Thus, the search for therapeutic strategies directed at these disorders represents an urgent unmet biomedical task, also necessitating the use of appropriate and valid experimental (animal) models. Here, we discuss the existing models of lysosomal storage diseases and the applicability of rodent and zebrafish as model organisms for probing these diseases.
Негізгі сөздер
Авторлар туралы
A. Lebedev
World-class Scientific Research Center “Center of Personalized Medicine”,Almazov National Medical Research Center, Ministry of Healthcare of Russian Federation; Neurobiology Department, Research Center for Genetics and Life Sciences,
Sirius University of Science and Technology; Institute of Translational Biomedicine, St. Petersburg State University
Email: avkalueff@gmail.com
Russia, St. Petersburg; Russia, Sirius Federal Territory; Russia, St. Petersburg
M. Kotova
Neurobiology Department, Research Center for Genetics and Life Sciences,Sirius University of Science and Technology
Email: avkalueff@gmail.com
Russia, Sirius Federal Territory
T. Kolesnikova
Neurobiology Department, Research Center for Genetics and Life Sciences,Sirius University of Science and Technology
Email: avkalueff@gmail.com
Russia, Sirius Federal Territory
D. Galstyan
World-class Scientific Research Center “Center of Personalized Medicine”,Almazov National Medical Research Center, Ministry of Healthcare of Russian Federation; Institute of Translational Biomedicine, St. Petersburg State University; Granov Russian Scientific Center for Radiology and Surgical Technologies,
Ministry of Healthcare of Russian Federation
Email: avkalueff@gmail.com
Russia, St. Petersburg; Russia, St. Petersburg; Russia, St. Petersburg
A. Kalueff
World-class Scientific Research Center “Center of Personalized Medicine”,Almazov National Medical Research Center, Ministry of Healthcare of Russian Federation; Neurobiology Department, Research Center for Genetics and Life Sciences,
Sirius University of Science and Technology; Institute of Translational Biomedicine, St. Petersburg State University; Granov Russian Scientific Center for Radiology and Surgical Technologies,
Ministry of Healthcare of Russian Federation; Ural Federal University; Scientific Research Institute of Neurosciences and Medicine
Хат алмасуға жауапты Автор.
Email: avkalueff@gmail.com
Russia, St. Petersburg; Russia, Sirius Federal Territory; Russia, St. Petersburg; Russia, St. Petersburg; Russia, Yekaterinburg; Russia, Novosibirsk
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