(Q50480011)

English

Sequential introduction of reprogramming factors reveals a time-sensitive requirement for individual factors and a sequential EMT-MET mechanism for optimal reprogramming.

scientific article published on 26 May 2013

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/23708003

Sequential introduction of reprogramming factors reveals a time-sensitive requirement for individual factors and a sequential EMT-MET mechanism for optimal reprogramming. (English)

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/23708003

15

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/23708003

14

object named as

Duanqing Pei

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Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/23708003

12

object named as

Guangjin Pan

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/23708003

7

object named as

Chengqian Feng

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/23708003

10

object named as

Yunqian Guo

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/23708003

13

object named as

Jiekai Chen

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/23708003

11

object named as

Dajiang Qin

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/23708003

author name string

Xiaopeng Liu

1

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/23708003

Hao Sun

2

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/23708003

Jing Qi

3

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/23708003

Linli Wang

4

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/23708003

Songwei He

5

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/23708003

Jing Liu

6

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/23708003

Chunlan Chen

8

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/23708003

Wen Li

9

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/23708003

publication date

26 May 2013

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/23708003

Nature Cell Biology

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/23708003

15

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/23708003

7

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/23708003

829-838

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/23708003

https://scigraph.springernature.com/pub.10.1038/ncb2765

0 references

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Generation of human induced pluripotent stem cells by direct delivery of reprogramming proteins

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Generation of mouse induced pluripotent stem cells without viral vectors

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Generation of induced pluripotent stem cells using recombinant proteins

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Copy number variation and selection during reprogramming to pluripotency

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Background mutations in parental cells account for most of the genetic heterogeneity of induced pluripotent stem cells

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Vitamin C enhances the generation of mouse and human induced pluripotent stem cells

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The histone demethylases Jhdm1a/1b enhance somatic cell reprogramming in a vitamin-C-dependent manner.

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H3K9 methylation is a barrier during somatic cell reprogramming into iPSCs

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A mesenchymal-to-epithelial transition initiates and is required for the nuclear reprogramming of mouse fibroblasts

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Direct cell reprogramming is a stochastic process amenable to acceleration

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Single-cell expression analyses during cellular reprogramming reveal an early stochastic and a late hierarchic phase

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Reprogramming of murine and human somatic cells using a single polycistronic vector

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A negative feedback loop of transcription factors that controls stem cell pluripotency and self-renewal

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A high proliferation rate is required for cell reprogramming and maintenance of human embryonic stem cell identity

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Functional genomics reveals a BMP-driven mesenchymal-to-epithelial transition in the initiation of somatic cell reprogramming

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Autoregulation of E-cadherin expression by cadherin-cadherin interactions: the roles of beta-catenin signaling, Slug, and MAPK

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Cadherin switching: essential for behavioral but not morphological changes during an epithelium-to-mesenchyme transition.

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The EMT regulator slug and lung carcinogenesis

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Role of the epithelial-mesenchymal transition regulator Slug in primary human cancers

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Transcriptional activation of ZEB1 by Slug leads to cooperative regulation of the epithelial-mesenchymal transition-like phenotype in melanoma

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Coexpression of Oct4 and Nanog enhances malignancy in lung adenocarcinoma by inducing cancer stem cell-like properties and epithelial-mesenchymal transdifferentiation.

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Critical and reciprocal regulation of KLF4 and SLUG in transforming growth factor β-initiated prostate cancer epithelial-mesenchymal transition

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A small-molecule inhibitor of tgf-Beta signaling replaces sox2 in reprogramming by inducing nanog

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Facilitators and impediments of the pluripotency reprogramming factors' initial engagement with the genome

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Cancer invasion and the microenvironment: plasticity and reciprocity

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Epithelial-mesenchymal transitions in tumour progression

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A switch from E-cadherin to N-cadherin expression indicates epithelial to mesenchymal transition and is of strong and independent importance for the progress of prostate cancer

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Transitions between epithelial and mesenchymal states in development and disease

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Mesenchymal-epithelial transition during somitic segmentation is regulated by differential roles of Cdc42 and Rac1.

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Evidence for mesenchymal-epithelial transition associated with mouse hepatic stem cell differentiation

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MET signalling: principles and functions in development, organ regeneration and cancer

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Promotion of reprogramming to ground state pluripotency by signal inhibition

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Mouse meningiocytes express Sox2 and yield high efficiency of chimeras after nuclear reprogramming with exogenous factors

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Rational optimization of reprogramming culture conditions for the generation of induced pluripotent stem cells with ultra-high efficiency and fast kinetics

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12 December 2020

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Expression of the E-cadherin repressors Snail, Slug and Zeb1 in urothelial carcinoma of the urinary bladder: relation to stromal fibroblast activation and invasive behaviour of carcinoma cells

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12 December 2020

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Generation of induced pluripotent stem cell lines from adult rat cells

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Vitamin C improves the quality of somatic cell reprogramming

1 reference

https://pubmed.ncbi.nlm.nih.gov/23708003

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Mesenchyme to epithelium transition during development of the mammalian kidney tubule

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12 December 2020

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Identifiers

10.1038/NCB2765

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/23708003

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/23708003

ResearchGate publication ID

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