iPSC line derived from a Bloom syndrome patient retains an increased disease-specific sister-chromatid exchange activity.
Author:
Funder
Montpellier public hospital
National Infrastructure in Biology and Health
Publisher
Elsevier BV
Subject
Cell Biology,Developmental Biology,General Medicine
Reference4 articles.
1. Bloom's syndrome: clinical spectrum, molecular pathogenesis, and cancer predisposition;Cunniff;Mol. Syndromol. Janv.,2017
2. Chromatin structure and gene expression programs of human embryonic and induced pluripotent stem cells;Guenther;Cell Stem Cell,2015
3. Rejuvenating senescent and centenarian human cells by reprogramming through the pluripotent state;Lapasset;Genes Dev.,2011
4. Reprogramming of Human Peripheral Blood Mononuclear Cell (PBMC) from a patient suffering of a Werner syndrome resulting in iPSC line (REGUi003-A) maintaining a short telomere length;Gatinois;Stem Cell Res.,2019
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3. Reprogramming: Emerging Strategies to Rejuvenate Aging Cells and Tissues;International Journal of Molecular Sciences;2021-04-13
4. Generation of human pluripotent stem cell lines (iPSCs) from mesenchymal stem cells (MSCs) from three elderly patients with osteoarthritis;Stem Cell Research;2020-04
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