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Article: Establishment of human-embryonic-stem-cell line from mosaic trisomy 9 embryo

TitleEstablishment of human-embryonic-stem-cell line from mosaic trisomy 9 embryo
Authors
KeywordsEuploid recovery
Human embryonic stem cells
Mosaic trisomy 9
Issue Date2015
Citation
Taiwanese Journal of Obstetrics and Gynecology, 2015, v. 54, n. 5, p. 505-511 How to Cite?
AbstractObjective: Human-embryonic-stem-cell (hESC) lines derived from chromosomally or genetically abnormal embryos obtained following preimplantation genetic diagnosis are valuable in investigating genetic disorders. Materials and methods: In this study, a new hESC line, Center of Clinical Reproductive Medicine 8 (CCRM8) was established by isolation, culture, and passaging of the inner cell mass of mosaic trisomy 9 embryos. Results: A karyotype analysis showed that the hESC line possessed a euploid (46 chromosomes). The undifferentiated hESCs exhibited long-term proliferation capacity and expressed typical markers of OCT4, TRA-1-60, and TRA-1-81. In vitro embryoid-body (EB) formation, differentiation, and in vivo teratoma production confirmed the pluripotency of the hESC line. The data represented here are the first detailed report on the characterization and differentiation of one Chinese hESC line generated from mosaic trisomy 9 embryos. Conclusion: Our study showed that chromosomally aberrant embryos could generate a normal hESC line, which would be useful in investigating gene function and embryo development.
Persistent Identifierhttp://hdl.handle.net/10722/365577
ISSN
2023 Impact Factor: 2.0
2023 SCImago Journal Rankings: 0.632

 

DC FieldValueLanguage
dc.contributor.authorHuang, Boxian-
dc.contributor.authorJiang, Chunyan-
dc.contributor.authorChen, Aiqin-
dc.contributor.authorCui, Yugui-
dc.contributor.authorXie, Jiazi-
dc.contributor.authorShen, Jiandong-
dc.contributor.authorChen, Juan-
dc.contributor.authorCai, Lingbo-
dc.contributor.authorLiao, Tingting-
dc.contributor.authorNing, Song-
dc.contributor.authorJiang, Shi Wen-
dc.contributor.authorFan, Guoping-
dc.contributor.authorQin, Lianju-
dc.contributor.authorLiu, Jiayin-
dc.date.accessioned2025-11-05T09:46:09Z-
dc.date.available2025-11-05T09:46:09Z-
dc.date.issued2015-
dc.identifier.citationTaiwanese Journal of Obstetrics and Gynecology, 2015, v. 54, n. 5, p. 505-511-
dc.identifier.issn1028-4559-
dc.identifier.urihttp://hdl.handle.net/10722/365577-
dc.description.abstractObjective: Human-embryonic-stem-cell (hESC) lines derived from chromosomally or genetically abnormal embryos obtained following preimplantation genetic diagnosis are valuable in investigating genetic disorders. Materials and methods: In this study, a new hESC line, Center of Clinical Reproductive Medicine 8 (CCRM8) was established by isolation, culture, and passaging of the inner cell mass of mosaic trisomy 9 embryos. Results: A karyotype analysis showed that the hESC line possessed a euploid (46 chromosomes). The undifferentiated hESCs exhibited long-term proliferation capacity and expressed typical markers of OCT4, TRA-1-60, and TRA-1-81. In vitro embryoid-body (EB) formation, differentiation, and in vivo teratoma production confirmed the pluripotency of the hESC line. The data represented here are the first detailed report on the characterization and differentiation of one Chinese hESC line generated from mosaic trisomy 9 embryos. Conclusion: Our study showed that chromosomally aberrant embryos could generate a normal hESC line, which would be useful in investigating gene function and embryo development.-
dc.languageeng-
dc.relation.ispartofTaiwanese Journal of Obstetrics and Gynecology-
dc.subjectEuploid recovery-
dc.subjectHuman embryonic stem cells-
dc.subjectMosaic trisomy 9-
dc.titleEstablishment of human-embryonic-stem-cell line from mosaic trisomy 9 embryo-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1016/j.tjog.2015.08.003-
dc.identifier.pmid26522100-
dc.identifier.scopuseid_2-s2.0-84984570563-
dc.identifier.volume54-
dc.identifier.issue5-
dc.identifier.spage505-
dc.identifier.epage511-
dc.identifier.eissn1875-6263-

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