Contemporary retrotransposition of a novel non-coding gene induces exon-skipping in dystrophin mRNA-Reference-Cited by-同舟云学术

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Contemporary retrotransposition of a novel non-coding gene induces exon-skipping in dystrophin mRNA

Published:2010-09-09 Issue:12 Volume:55 Page:785-790
ISSN:1434-5161
Container-title:Journal of Human Genetics
language:en
Short-container-title:J Hum Genet

Author:

Awano Hiroyuki,Malueka Rusdy Ghazali,Yagi Mariko,Okizuka Yo,Takeshima Yasuhiro,Matsuo Masafumi

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://www.nature.com/articles/jhg2010111.pdf

Reference22 articles.

1. Deininger, P. L. & Batzer, M. A. Mammalian retroelements. Genome Res. 12, 1455–1465 (2002).

2. Goodier, J. L. & Kazazian, Jr. H. H. Retrotransposons revisited: the restraint and rehabilitation of parasites. Cell 135, 23–35 (2008).

3. Chen, J. M., Stenson, P. D., Cooper, D. N. & Ferec, C. A systematic analysis of LINE-1 endonuclease-dependent retrotranspositional events causing human genetic disease. Hum. Genet. 117, 411–427 (2005).

4. Callinan, P. A. & Batzer, M. A. Retrotransposable elements and human disease. Genome Dyn. 1, 104–115 (2006).

5. Belancio, V. P., Deininger, P. L. & Roy-Engel, A M. LINE dancing in the human genome: transposable elements and disease. Genome Med. 1, 97 (2009).

Cited by 15 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. Transposable element insertions in 1000 Swedish individuals;PLOS ONE;2023-07-28

2. Exonization of a deep intronic long interspersed nuclear element in Becker muscular dystrophy;Frontiers in Genetics;2022-08-25

3. Long‐read whole‐genome sequencing for the genetic diagnosis of dystrophinopathies;Annals of Clinical and Translational Neurology;2020-09-20

4. Human Genomic Variants and Inherited Disease;Emery and Rimoin's Principles and Practice of Medical Genetics and Genomics;2019

5. Exonization of an Intronic LINE-1 Element Causing Becker Muscular Dystrophy as a Novel Mutational Mechanism in Dystrophin Gene;Genes;2017-10-03

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