TRF1 is a stem cell marker and is essential for the generation of induced pluripotent stem cells (Q34348666)

1 August 2017

title

TRF1 is a stem cell marker and is essential for the generation of induced pluripotent stem cells (English)

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Erratum: TRF1 is a stem cell marker and is essential for the generation of induced pluripotent stem cells

1 August 2017

corrigendum / erratum

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Miguel Foronda

3

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Ignacio Flores

object named as

Ignacio Flores

6

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Maria A Blasco

object named as

Maria A Blasco

8

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author name string

Ralph P Schneider

1

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1 August 2017

Ianire Garrobo

2

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1 August 2017

Jose A Palacios

4

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1 August 2017

Rosa M Marión

5

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1 August 2017

Sagrario Ortega

7

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1 August 2017

language of work or name

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1 January 2013

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1 August 2017

published in

Nature Communications

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1 August 2017

volume

4

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1 August 2017

page(s)

1946

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Switching and signaling at the telomere

1 August 2017

cites work

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Targeted deletion reveals an essential function for the telomere length regulator Trf1.

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Conditional TRF1 knockout in the hematopoietic compartment leads to bone marrow failure and recapitulates clinical features of dyskeratosis congenita

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Increased telomere fragility and fusions resulting from TRF1 deficiency lead to degenerative pathologies and increased cancer in mice

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Analysis of human and mouse reprogramming of somatic cells to induced pluripotent stem cells. What is in the plate?

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A p53-mediated DNA damage response limits reprogramming to ensure iPS cell genomic integrity

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Telomeres acquire embryonic stem cell characteristics in induced pluripotent stem cells

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TPP1 is required for TERT recruitment, telomere elongation during nuclear reprogramming, and normal skin development in mice

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Mammalian telomeres resemble fragile sites and require TRF1 for efficient replication

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Lrig1 expression defines a distinct multipotent stem cell population in mammalian epidermis

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SnapShot: Hair Follicle Stem Cells

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The cell-surface marker MTS24 identifies a novel population of follicular keratinocytes with characteristics of progenitor cells

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Blimp1 defines a progenitor population that governs cellular input to the sebaceous gland

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Keratin 15 promoter targets putative epithelial stem cells in the hair follicle bulge.

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Lgr5 intestinal stem cells have high telomerase activity and randomly segregate their chromosomes

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Paneth cells constitute the niche for Lgr5 stem cells in intestinal crypts

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A reserve stem cell population in small intestine renders Lgr5-positive cells dispensable

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Targeted expression of oncogenic K-ras in intestinal epithelium causes spontaneous tumorigenesis in mice

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Nanog safeguards pluripotency and mediates germline development

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Epigenetic regulation of Nanog expression by Ezh2 in pluripotent stem cells.

21 January 2018

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Telomere elongation in induced pluripotent stem cells from dyskeratosis congenita patients

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TINF2, a component of the shelterin telomere protection complex, is mutated in dyskeratosis congenita

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Epigenetic regulation of telomere length in mammalian cells by the Suv39h1 and Suv39h2 histone methyltransferases

21 January 2018

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XPF nuclease-dependent telomere loss and increased DNA damage in mice overexpressing TRF2 result in premature aging and cancer.

21 January 2018

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The Ink4/Arf locus is a barrier for iPS cell reprogramming

21 January 2018

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Lgr6 Marks Stem Cells in the Hair Follicle That Generate All Cell Lineages of the Skin

21 January 2018

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inferred from DOI database lookup

7 January 2021

based on heuristic

Regulatory sequences of the mouse villin gene that efficiently drive transgenic expression in immature and differentiated epithelial cells of small and large intestines

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS2946

inferred from DOI database lookup

7 January 2021

based on heuristic

Sequence analysis of the shelterin telomere protection complex genes in dyskeratosis congenita

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS2946

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1038/NCOMMS2946

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Dimensions Publication ID

1 August 2017

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1022584013

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