Telomere elongation in induced pluripotent stem cells from dyskeratosis congenita patients - Wikidata - awgldk - TriplyDB

Telomere elongation in induced pluripotent stem cells from dyskeratosis congenita patients

Telomere elongation in induced pluripotent stem cells from dyskeratosis congenita patients

http://www.wikidata.org/entity/Q24595997

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Telomere shortening and loss of self-renewal in dyskeratosis congenita induced pluripotent stem cells Amniotic Fluid Stem Cells: A Novel Source for Modeling of Human Genetic Diseases An Overview of Direct Somatic Reprogramming: The Ins and Outs of iPSCs Telomere regulation in pluripotent stem cells Molecular therapeutics for heritable skin diseases The genomic stability of induced pluripotent stem cells Programming and Reprogramming Cellular Age in the Era of Induced Pluripotency Stem cell sources for vascular tissue engineering and regeneration Modeling Human Bone Marrow Failure Syndromes Using Pluripotent Stem Cells and Genome Engineering Mitochondrial rejuvenation after induced pluripotency Mitochondrial-associated cell death mechanisms are reset to an embryonic-like state in aged donor-derived iPS cells harboring chromosomal aberrations A balance between elongation and trimming regulates telomere stability in stem cells Current Knowledge and Priorities for Future Research in Late Effects after Hematopoietic Cell Transplantation for Inherited Bone Marrow Failure Syndromes: Consensus Statement from the Second Pediatric Blood and Marrow Transplant Consortium Internati Digital genome-wide ncRNA expression, including SnoRNAs, across 11 human tissues using polyA-neutral amplification.A common variant in the telomerase RNA component is associated with short telomere length.The LARGE principle of cellular reprogramming: lost, acquired and retained gene expression in foreskin and amniotic fluid-derived human iPS cells Induced Pluripotent Stem Cells-A New Foundation in Medicine Effect of a qigong intervention program on telomerase activity and psychological stress in abused Chinese women: a randomized, wait-list controlled trial.Telomerase reverse transcriptase has an extratelomeric function in somatic cell reprogramming.The diagnosis and treatment of dyskeratosis congenita: a review.Female human iPSCs retain an inactive X chromosome.Generation of induced pluripotent stem cells from human kidney mesangial cells Therapeutic opportunities: telomere maintenance in inducible pluripotent stem cells.Induced pluripotent stem cells--opportunities for disease modelling and drug discovery.The promise of induced pluripotent stem cells in research and therapy Aging, rejuvenation, and epigenetic reprogramming: resetting the aging clock.Comparative angiogenic activities of induced pluripotent stem cells derived from young and old mice.TRF1 is a stem cell marker and is essential for the generation of induced pluripotent stem cells.The aging signature: a hallmark of induced pluripotent stem cells?Induced pluripotent stem cells in dermatology: potentials, advances, and limitations Neuronopathic Gaucher's disease: induced pluripotent stem cells for disease modelling and testing chaperone activity of small compounds.Telomere elongation and naive pluripotent stem cells achieved from telomerase haplo-insufficient cells by somatic cell nuclear transfer.The dyskerin ribonucleoprotein complex as an OCT4/SOX2 coactivator in embryonic stem cells.Aged iPSCs display an uncommon mitochondrial appearance and fail to undergo in vitro neurogenesis.Telomere reprogramming and maintenance in porcine iPS cells.Induced pluripotent stem cells for modelling human diseases Human endometrial cells express elevated levels of pluripotent factors and are more amenable to reprogramming into induced pluripotent stem cells.Association of telomere length with authentic pluripotency of ES/iPS cells De novo generation of HSCs from somatic and pluripotent stem cell sources.Telomere dynamics in induced pluripotent stem cells: Potentials for human disease modeling.

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P2860

Telomere elongation in induced pluripotent stem cells from dyskeratosis congenita patients

http://www.wikidata.org/entity/Q24595997

description

2010 nî lūn-bûn

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2010 թուականի Մարտին հրատարակուած գիտական յօդուած

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2010 թվականի մարտին հրատարակված գիտական հոդված

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2010年の論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年论文

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Telomere elongation in induced ...... yskeratosis congenita patients

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Telomere elongation in induced ...... yskeratosis congenita patients

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David L Keefe

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Erin M McLoughlin

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Frederick D Goldman

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Hongguang Huo

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In-Hyun Park

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Justine D Miller

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Lin Liu

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Maja Okuka

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Sabine Loewer

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Suneet Agarwal

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P2860

A telomerase component is defective in the human disease dyskeratosis congenita

X-linked dyskeratosis congenita is caused by mutations in a highly conserved gene with putative nucleolar functions

Extension of life-span by introduction of telomerase into normal human cells

Telomere measurement by quantitative PCR

Telomere elongation in immortal human cells without detectable telomerase activity

Disease-specific induced pluripotent stem cells

Dyskeratosis congenita mutations in the H/ACA domain of human telomerase RNA affect its assembly into a pre-RNP

Telomerase RNA level limits telomere maintenance in X-linked dyskeratosis congenita

Induced pluripotent stem cell lines derived from human somatic cells

Induction of pluripotent stem cells from adult human fibroblasts by defined factors

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10.1038/NATURE08792

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Rosana Maria dos Reis

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41466377

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1005411330

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20164838

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