Amenable epigenetic traits of dental pulp stem cells underlie high capability of xeno-free episomal reprogramming

10.1186/s13287-018-0796-2

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Main Authors:	Thekkeparambil Chandrabose, S, Sriram, S, Subramanian, S, Cheng, S, Ong, W.K, Rozen, S, Kasim, N.H.A, Sugii, S
Other Authors:	DUKE-NUS MEDICAL SCHOOL
Format:	Article
Published:	2020
Subjects:	Article cell differentiation cell line cell maturation controlled study dental pulp stem cell DNA methylation embryonic stem cell epigenetics gene gene expression gene knockdown genetic trait genome-wide association study HERV FRD gene human human cell induced pluripotent stem cell neural crest cell nuclear reprogramming PAX9 gene priority journal animal cell culture cell reprogramming technique cytology genetic epigenesis genetics mesenchymal stem cell metabolism mouse nonobese diabetic mouse plasmid primary cell culture procedures SCID mouse tooth pulp Animals Cells, Cultured Cellular Reprogramming Cellular Reprogramming Techniques Dental Pulp Epigenesis, Genetic Humans Mesenchymal Stem Cells Mice Mice, Inbred NOD Mice, SCID Plasmids Primary Cell Culture
Online Access:	https://scholarbank.nus.edu.sg/handle/10635/178098
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Institution:	National University of Singapore

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spelling	sg-nus-scholar.10635-1780982023-10-31T09:20:25Z Amenable epigenetic traits of dental pulp stem cells underlie high capability of xeno-free episomal reprogramming Thekkeparambil Chandrabose, S Sriram, S Subramanian, S Cheng, S Ong, W.K Rozen, S Kasim, N.H.A Sugii, S DUKE-NUS MEDICAL SCHOOL Article cell differentiation cell line cell maturation controlled study dental pulp stem cell DNA methylation embryonic stem cell epigenetics gene gene expression gene knockdown genetic trait genome-wide association study HERV FRD gene human human cell induced pluripotent stem cell neural crest cell nuclear reprogramming PAX9 gene priority journal animal cell culture cell reprogramming technique cytology genetic epigenesis genetics mesenchymal stem cell metabolism mouse nonobese diabetic mouse plasmid primary cell culture procedures SCID mouse tooth pulp Animals Cells, Cultured Cellular Reprogramming Cellular Reprogramming Techniques Dental Pulp Epigenesis, Genetic Humans Mesenchymal Stem Cells Mice Mice, Inbred NOD Mice, SCID Plasmids Primary Cell Culture 10.1186/s13287-018-0796-2 Stem Cell Research and Therapy 9 1 68 2020-10-20T05:05:32Z 2020-10-20T05:05:32Z 2018 Article Thekkeparambil Chandrabose, S, Sriram, S, Subramanian, S, Cheng, S, Ong, W.K, Rozen, S, Kasim, N.H.A, Sugii, S (2018). Amenable epigenetic traits of dental pulp stem cells underlie high capability of xeno-free episomal reprogramming. Stem Cell Research and Therapy 9 (1) : 68. ScholarBank@NUS Repository. https://doi.org/10.1186/s13287-018-0796-2 17576512 https://scholarbank.nus.edu.sg/handle/10635/178098 Attribution 4.0 International http://creativecommons.org/licenses/by/4.0/ Unpaywall 20201031
institution	National University of Singapore
building	NUS Library
continent	Asia
country	Singapore Singapore
content_provider	NUS Library
collection	ScholarBank@NUS
topic	Article cell differentiation cell line cell maturation controlled study dental pulp stem cell DNA methylation embryonic stem cell epigenetics gene gene expression gene knockdown genetic trait genome-wide association study HERV FRD gene human human cell induced pluripotent stem cell neural crest cell nuclear reprogramming PAX9 gene priority journal animal cell culture cell reprogramming technique cytology genetic epigenesis genetics mesenchymal stem cell metabolism mouse nonobese diabetic mouse plasmid primary cell culture procedures SCID mouse tooth pulp Animals Cells, Cultured Cellular Reprogramming Cellular Reprogramming Techniques Dental Pulp Epigenesis, Genetic Humans Mesenchymal Stem Cells Mice Mice, Inbred NOD Mice, SCID Plasmids Primary Cell Culture
spellingShingle	Article cell differentiation cell line cell maturation controlled study dental pulp stem cell DNA methylation embryonic stem cell epigenetics gene gene expression gene knockdown genetic trait genome-wide association study HERV FRD gene human human cell induced pluripotent stem cell neural crest cell nuclear reprogramming PAX9 gene priority journal animal cell culture cell reprogramming technique cytology genetic epigenesis genetics mesenchymal stem cell metabolism mouse nonobese diabetic mouse plasmid primary cell culture procedures SCID mouse tooth pulp Animals Cells, Cultured Cellular Reprogramming Cellular Reprogramming Techniques Dental Pulp Epigenesis, Genetic Humans Mesenchymal Stem Cells Mice Mice, Inbred NOD Mice, SCID Plasmids Primary Cell Culture Thekkeparambil Chandrabose, S Sriram, S Subramanian, S Cheng, S Ong, W.K Rozen, S Kasim, N.H.A Sugii, S Amenable epigenetic traits of dental pulp stem cells underlie high capability of xeno-free episomal reprogramming
description	10.1186/s13287-018-0796-2
author2	DUKE-NUS MEDICAL SCHOOL
author_facet	DUKE-NUS MEDICAL SCHOOL Thekkeparambil Chandrabose, S Sriram, S Subramanian, S Cheng, S Ong, W.K Rozen, S Kasim, N.H.A Sugii, S
format	Article
author	Thekkeparambil Chandrabose, S Sriram, S Subramanian, S Cheng, S Ong, W.K Rozen, S Kasim, N.H.A Sugii, S
author_sort	Thekkeparambil Chandrabose, S
title	Amenable epigenetic traits of dental pulp stem cells underlie high capability of xeno-free episomal reprogramming
title_short	Amenable epigenetic traits of dental pulp stem cells underlie high capability of xeno-free episomal reprogramming
title_full	Amenable epigenetic traits of dental pulp stem cells underlie high capability of xeno-free episomal reprogramming
title_fullStr	Amenable epigenetic traits of dental pulp stem cells underlie high capability of xeno-free episomal reprogramming
title_full_unstemmed	Amenable epigenetic traits of dental pulp stem cells underlie high capability of xeno-free episomal reprogramming
title_sort	amenable epigenetic traits of dental pulp stem cells underlie high capability of xeno-free episomal reprogramming
publishDate	2020
url	https://scholarbank.nus.edu.sg/handle/10635/178098
_version_	1781792280882970624

Amenable epigenetic traits of dental pulp stem cells underlie high capability of xeno-free episomal reprogramming

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