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Advances in Genetic Reprogramming: Prospects from Developmental Biology to Regenerative Medicine

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216305%3A26620%2F24%3APU151616" target="_blank" >RIV/00216305:26620/24:PU151616 - isvavai.cz</a>

  • Alternative codes found

    RIV/62156489:43210/24:43924829 RIV/62690094:18470/24:50021307 RIV/00179906:_____/24:10481310

  • Result on the web

    <a href="https://www.eurekaselect.com/article/131443" target="_blank" >https://www.eurekaselect.com/article/131443</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.2174/0929867330666230503144619" target="_blank" >10.2174/0929867330666230503144619</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Advances in Genetic Reprogramming: Prospects from Developmental Biology to Regenerative Medicine

  • Original language description

    The foundations of cell reprogramming were laid by Yamanaka and co-workers, who showed that somatic cells can be reprogrammed into pluripotent cells (induced pluripotency). Since this discovery, the field of regenerative medicine has seen advancements. For example, because they can differentiate into multiple cell types, pluripotent stem cells are considered vital components in regenerative medicine aimed at the functional restoration of damaged tissue. Despite years of research, both replacement and restoration of failed organs/ tissues have remained elusive scientific feats. However, with the inception of cell engineering and nuclear reprogramming, useful solutions have been identified to counter the need for compatible and sustainable organs. By combining the science underlying genetic engineering and nuclear reprogramming with regenerative medicine, scientists have engineered cells to make gene and stem cell therapies applicable and effective. These approaches have enabled the targeting of various pathways to reprogramme cells, i.e., make them behave in beneficial ways in a patient-specific manner. Technological advancements have clearly supported the concept and realization of regenerative medicine. Genetic engineering is used for tissue engineering and nuclear reprogramming and has led to advances in regenerative medicine. Targeted therapies and replacement of traumatized , damaged, or aged organs can be realized through genetic engineering. Furthermore, the success of these therapies has been validated through thousands of clinical trials. Scientists are currently evaluating induced tissue-specific stem cells (iTSCs), which may lead to tumour-free applications of pluripotency induction. In this review, we present state-of-the-art genetic engineering that has been used in regenerative medicine. We also focus on ways that genetic engineering and nuclear reprogramming have transformed regenerative medicine and have become unique therapeutic niches.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    10609 - Biochemical research methods

Result continuities

  • Project

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2024

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    CURRENT MEDICINAL CHEMISTRY

  • ISSN

    0929-8673

  • e-ISSN

    1875-533X

  • Volume of the periodical

    31

  • Issue of the periodical within the volume

    13

  • Country of publishing house

    AE - UNITED ARAB EMIRATES

  • Number of pages

    45

  • Pages from-to

    1646-1690

  • UT code for WoS article

    001229291300009

  • EID of the result in the Scopus database

    2-s2.0-85184227820