TY - JOUR
T1 - From cloned frogs to patient matched stem cells
T2 - Induced pluripotency or somatic cell nuclear transfer?
AU - Yamada, Mitsutoshi
AU - Byrne, James
AU - Egli, Dieter
N1 - Funding Information:
This work was supported by the New York Stem Cell Foundation. D.E. is a NYSCF-Robertson Investigator.
Publisher Copyright:
© 2015 Elsevier Ltd.
Copyright:
Copyright 2015 Elsevier B.V., All rights reserved.
PY - 2015/10/1
Y1 - 2015/10/1
N2 - Nuclear transfer has seen a remarkable comeback in the past few years. Three groups have independently reported the derivation of stem cell lines by somatic cell nuclear transfer, from either adult, neonatal or fetal cells. Though the ability of human oocytes to reprogram somatic cells to stem cells had long been anticipated, success did not arrive on a straightforward path. Little was known about human oocyte biology, and nuclear transfer protocols developed in animals required key changes to become effective with human eggs. By overcoming these challenges, human nuclear transfer research has contributed to a greater understanding of oocyte biology, provided a point of reference for the comparison of induced pluripotent stem cells, and delivered a method for the generation of personalized stem cells with therapeutic potential.
AB - Nuclear transfer has seen a remarkable comeback in the past few years. Three groups have independently reported the derivation of stem cell lines by somatic cell nuclear transfer, from either adult, neonatal or fetal cells. Though the ability of human oocytes to reprogram somatic cells to stem cells had long been anticipated, success did not arrive on a straightforward path. Little was known about human oocyte biology, and nuclear transfer protocols developed in animals required key changes to become effective with human eggs. By overcoming these challenges, human nuclear transfer research has contributed to a greater understanding of oocyte biology, provided a point of reference for the comparison of induced pluripotent stem cells, and delivered a method for the generation of personalized stem cells with therapeutic potential.
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U2 - 10.1016/j.gde.2015.06.007
DO - 10.1016/j.gde.2015.06.007
M3 - Review article
C2 - 26282611
AN - SCOPUS:84939531078
SN - 0959-437X
VL - 34
SP - 29
EP - 34
JO - Current Opinion in Genetics and Development
JF - Current Opinion in Genetics and Development
ER -