Cargando…
Genome-wide identification of tandem repeats associated with splicing variation across 49 tissues in humans
Tandem repeats (TRs) are one of the largest sources of polymorphism, and their length is associated with gene regulation. Although previous studies reported several tandem repeats regulating gene splicing in cis (spl-TRs), no large-scale study has been conducted. In this study, we established a geno...
Autores principales: | Hamanaka, Kohei, Yamauchi, Daisuke, Koshimizu, Eriko, Watase, Kei, Mogushi, Kaoru, Ishikawa, Kinya, Mizusawa, Hidehiro, Tsuchida, Naomi, Uchiyama, Yuri, Fujita, Atsushi, Misawa, Kazuharu, Mizuguchi, Takeshi, Miyatake, Satoko, Matsumoto, Naomichi |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory Press
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10078293/ https://www.ncbi.nlm.nih.gov/pubmed/37307504 http://dx.doi.org/10.1101/gr.277335.122 |
Ejemplares similares
-
Loss of MyD88 alters neuroinflammatory response and attenuates early Purkinje cell loss in a spinocerebellar ataxia type 6 mouse model
por: Aikawa, Tomonori, et al.
Publicado: (2015) -
A novel NONO variant that causes developmental delay and cardiac phenotypes
por: Itai, Toshiyuki, et al.
Publicado: (2023) -
Publisher Correction: A novel NONO variant that causes developmental delay and cardiac phenotypes
por: Itai, Toshiyuki, et al.
Publicado: (2023) -
A missense variant at the RAC1-PAK1 binding site of RAC1 inactivates downstream signaling in VACTERL association
por: Seyama, Rie, et al.
Publicado: (2023) -
Biallelic structural variations within FGF12 detected by long-read sequencing in epilepsy
por: Ohori, Sachiko, et al.
Publicado: (2023)