Somatic mosaicism: implications for the cardiovascular system-Reference-Cited by-同舟云学术

Somatic mosaicism: implications for the cardiovascular system

Published:2019-12-26 Issue:30 Volume:41 Page:2904-2907
ISSN:0195-668X
Container-title:European Heart Journal
language:en
Short-container-title:

Author:

Sano Soichi¹,Wang Ying¹,Walsh Kenneth¹

Affiliation:

1. Hematovascular Biology Center, Robert M. Berne Cardiovascular Research Center, University of Virginia School of Medicine, 415 Lane Road, Box 801394, Suite 1010, Charlottesville, VA 22908, USA

Funder

National Institutes of Health

American Heart Association Postdoctoral Fellowship

Kanae Foundation for the Promotion of Medical Science

Publisher

Oxford University Press (OUP)

Subject

Cardiology and Cardiovascular Medicine

Link

http://academic.oup.com/eurheartj/article-pdf/41/30/2904/33643425/ehz907.pdf

Reference20 articles.

1. Somatic mutation in single human neurons tracks developmental and transcriptional history;Lodato;Science,2015

2. Aging and neurodegeneration are associated with increased mutations in single human neurons;Lodato;Science,2018

3. Tumor evolution. High burden and pervasive positive selection of somatic mutations in normal human skin;Martincorena;Science,2015

4. Somatic mutant clones colonize the human esophagus with age;Martincorena;Science,2018

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