Cargando…
Structural Variation of Alu Element and Human Disease
Transposable elements are one of major sources to cause genomic instability through various mechanisms including de novo insertion, insertion-mediated genomic deletion, and recombination-associated genomic deletion. Among them is Alu element which is the most abundant element, composing ~10% of the...
Autores principales: | Kim, Songmi, Cho, Chun-Sung, Han, Kyudong, Lee, Jungnam |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korea Genome Organization
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5056899/ https://www.ncbi.nlm.nih.gov/pubmed/27729835 http://dx.doi.org/10.5808/GI.2016.14.3.70 |
Ejemplares similares
-
Alu Recombination-Mediated Structural Deletions in the Chimpanzee Genome
por: Han, Kyudong, et al.
Publicado: (2007) -
Transposable Elements: No More 'Junk DNA'
por: Kim, Yun-Ji, et al.
Publicado: (2012) -
A study of transposable element-associated structural variations (TASVs) using a de novo-assembled Korean genome
por: Mun, Seyoung, et al.
Publicado: (2021) -
Alu pair exclusions in the human genome
por: Cook, George W, et al.
Publicado: (2011) -
Alu elements: know the SINEs
por: Deininger, Prescott
Publicado: (2011)