Development and application of neural stem cells for treating various human neurological diseases in animal models
Identifieur interne : 000E09 ( Main/Exploration ); précédent : 000E08; suivant : 000E10Development and application of neural stem cells for treating various human neurological diseases in animal models
Auteurs : Bo-Rim Yi [Corée du Sud] ; Seung U. Kim [Canada, Corée du Sud] ; Kyung-Chul Choi [Corée du Sud]Source :
- Laboratory Animal Research [ 1738-6055 ] ; 2013.
Abstract
Stem cells derived from adult tissues or the inner cell mass (ICM) of embryos in the mammalian blastocyst (BL) stage are capable of self-renewal and have remarkable potential for undergoing lineage-specific differentiation under
Url:
DOI: 10.5625/lar.2013.29.3.131
PubMed: 24106507
PubMed Central: 3791346
Affiliations:
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Le document en format XML
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<front><div type="abstract" xml:lang="en"><p>Stem cells derived from adult tissues or the inner cell mass (ICM) of embryos in the mammalian blastocyst (BL) stage are capable of self-renewal and have remarkable potential for undergoing lineage-specific differentiation under <italic>in vitro</italic>
culturing conditions. In particular, neural stem cells (NSCs) that self-renew and differentiate into major cell types of the brain exist in the developing and adult central nervous system (CNS). The exact function and distribution of NSCs has been assessed, and they represent an interesting population that includes astrocytes, oligodendrocytes, and neurons. Many researchers have demonstrated functional recovery in animal models of various neurological diseases such as stroke, Parkinson's disease (PD), brain tumors, and metastatic tumors. The safety and efficacy of stem cell-based therapies (SCTs) are also being evaluated in humans. The therapeutic efficacy of NSCs has been shown in the brain disorder-induced animal models, and animal models may be well established to perform the test before clinical stage. Taken together, data from the literature have indicated that therapeutic NSCs may be useful for selectively treating diverse types of human brain diseases without incurring adverse effects.</p>
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<biblStruct><analytic><author><name sortKey="Tang, Y" uniqKey="Tang Y">Y Tang</name>
</author>
<author><name sortKey="Shah, K" uniqKey="Shah K">K Shah</name>
</author>
<author><name sortKey="Messerli, Sm" uniqKey="Messerli S">SM Messerli</name>
</author>
<author><name sortKey="Snyder, E" uniqKey="Snyder E">E Snyder</name>
</author>
<author><name sortKey="Breakefield, X" uniqKey="Breakefield X">X Breakefield</name>
</author>
<author><name sortKey="Weissleder, R" uniqKey="Weissleder R">R Weissleder</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Vermes, A" uniqKey="Vermes A">A Vermes</name>
</author>
<author><name sortKey="Guchelaar, Hj" uniqKey="Guchelaar H">HJ Guchelaar</name>
</author>
<author><name sortKey="Dankert, J" uniqKey="Dankert J">J Dankert</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Okano, H" uniqKey="Okano H">H Okano</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Gage, Fh" uniqKey="Gage F">FH Gage</name>
</author>
</analytic>
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</listBibl>
</div1>
</back>
</TEI>
<affiliations><list><country><li>Canada</li>
<li>Corée du Sud</li>
</country>
<settlement><li>Séoul</li>
</settlement>
</list>
<tree><country name="Corée du Sud"><noRegion><name sortKey="Yi, Bo Rim" sort="Yi, Bo Rim" uniqKey="Yi B" first="Bo-Rim" last="Yi">Bo-Rim Yi</name>
</noRegion>
<name sortKey="Choi, Kyung Chul" sort="Choi, Kyung Chul" uniqKey="Choi K" first="Kyung-Chul" last="Choi">Kyung-Chul Choi</name>
<name sortKey="Kim, Seung U" sort="Kim, Seung U" uniqKey="Kim S" first="Seung U." last="Kim">Seung U. Kim</name>
</country>
<country name="Canada"><noRegion><name sortKey="Kim, Seung U" sort="Kim, Seung U" uniqKey="Kim S" first="Seung U." last="Kim">Seung U. Kim</name>
</noRegion>
</country>
</tree>
</affiliations>
</record>
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