Genomic instability in iPS: time for a break-Reference-Cited by-同舟云学术

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Genomic instability in iPS: time for a break

Published:2011-03-16 Issue:6 Volume:30 Page:991-993
ISSN:0261-4189
Container-title:The EMBO Journal
language:en
Short-container-title:

Author:

Blasco Maria A¹,Serrano Manuel²,Fernandez-Capetillo Oscar³

Affiliation:

1. Telomeres and Telomerase Group, Spanish National Cancer Research Centre (CNIO); Madrid Spain

2. Tumor Suppression Group, Spanish National Cancer Research Centre (CNIO); Madrid Spain

3. Genomic Instability Group, Spanish National Cancer Research Centre (CNIO); Madrid Spain

Publisher

Wiley

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,Molecular Biology,General Neuroscience

Reference12 articles.

1. Somatic coding mutations in human induced pluripotent stem cells;Gore;Nature,2011

2. An oncogene-induced DNA damage model for cancer development;Halazonetis;Science,2008

3. Copy number variation and selection during reprogramming to pluripotency;Hussein;Nature,2011

4. Dynamic changes in the copy number of pluripotency and cell proliferation genes in human ESCs and iPSCs during reprogramming and time in culture;Laurent;Cell Stem Cell,2011

5. Improved efficiency and pace of generating induced pluripotent stem cells from human adult and fetal fibroblasts;Mali;Stem Cells,2008

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3. Intrinsic deletion at 10q23.31, including thePTENgene locus, is aggravated upon CRISPR-Cas9–mediated genome engineering in HAP1 cells mimicking cancer profiles;Life Science Alliance;2023-11-20

4. CRISPR-Cas9-mediated genome engineering exaggerates genomic deletion at 10q23.31 including thePTENgene locus mimicking cancer profiles;2023-04-06

5. Generation of developmentally competent oocytes and fertile mice from parthenogenetic embryonic stem cells;Protein & Cell;2021-11-30

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