Decoding pluripotency: Genetic screens to interrogate the acquisition, maintenance, and exit of pluripotency-Reference-Cited by-同舟云学术

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Decoding pluripotency: Genetic screens to interrogate the acquisition, maintenance, and exit of pluripotency

Published:2019-08-13 Issue:1 Volume:12 Page:
ISSN:1939-5094
Container-title:WIREs Systems Biology and Medicine
language:en
Short-container-title:WIREs Syst Biol Med

Author:

Li Qing V.¹²^ORCID,Rosen Bess P.¹³^ORCID,Huangfu Danwei¹^ORCID

Affiliation:

1. Sloan Kettering Institute New York New York

2. Louis V. Gerstner Jr. Graduate School of Biomedical Sciences Memorial Sloan Kettering Cancer Center New York New York

3. Weill Graduate School of Medical Sciences at Cornell University New York New York

Funder

National Institute of Diabetes and Digestive and Kidney Diseases

American Diabetes Association

Juvenile Diabetes Research Foundation International

New York State Stem Cell Science

Publisher

Wiley

Subject

Biochemistry, Genetics and Molecular Biology (miscellaneous),Medicine (miscellaneous)

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/wsbm.1464

Reference191 articles.

1. Coupling shRNA screens with single-cell RNA-seq identifies a dual role for mTOR in reprogramming-induced senescence

2. ENU Mutagenesis, a Way Forward to Understand Gene Function

3. A Multiplexed Single-Cell CRISPR Screening Platform Enables Systematic Dissection of the Unfolded Protein Response

4. Characterization of human embryonic stem cell lines by the International Stem Cell Initiative

5. The CRISPR tool kit for genome editing and beyond

Cited by 11 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. 3D Enhancer–promoter networks provide predictive features for gene expression and coregulation in early embryonic lineages;Nature Structural & Molecular Biology;2023-12-05

2. Systematic mapping and modeling of 3D enhancer-promoter interactions in early mouse embryonic lineages reveal regulatory principles that determine the levels and cell-type specificity of gene expression;2023-07-19

3. A critical role for heme synthesis and succinate in the regulation of pluripotent states transitions;eLife;2023-07-10

4. Genetically Engineered Triple MAPT-Mutant Human-Induced Pluripotent Stem Cells (N279K, P301L, and E10+16 Mutations) Exhibit Impairments in Mitochondrial Bioenergetics and Dynamics;Cells;2023-05-13

5. Parallel genome-scale CRISPR screens distinguish pluripotency and self-renewal;2023-05-03

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