Cargando…
A Genome-Wide Screen for the Exonisation of Reference SINE-VNTR-Alus and Their Expression in CNS Tissues of Individuals with Amyotrophic Lateral Sclerosis
The hominid-specific retrotransposon SINE-VNTR-Alu (SVA) is a composite element that has contributed to the genetic variation between individuals and influenced genomic structure and function. SVAs are involved in modulating gene expression and splicing patterns, altering mRNA levels and sequences,...
Autores principales: | Pfaff, Abigail L., Bubb, Vivien J., Quinn, John P., Koks, Sulev |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10380656/ https://www.ncbi.nlm.nih.gov/pubmed/37511314 http://dx.doi.org/10.3390/ijms241411548 |
Ejemplares similares
-
Characterisation of the Function of a SINE-VNTR-Alu Retrotransposon to Modulate Isoform Expression at the MAPT Locus
por: Fröhlich, Alexander, et al.
Publicado: (2022) -
Locus specific reduction of L1 expression in the cortices of individuals with amyotrophic lateral sclerosis
por: Pfaff, Abigail L., et al.
Publicado: (2022) -
CRISPR deletion of a SINE-VNTR-Alu (SVA_67) retrotransposon demonstrates its ability to differentially modulate gene expression at the MAPT locus
por: Fröhlich, Alexander, et al.
Publicado: (2023) -
The Role of SINE-VNTR-Alu (SVA) Retrotransposons in Shaping the Human Genome
por: Gianfrancesco, Olympia, et al.
Publicado: (2019) -
Reference SVA insertion polymorphisms are associated with Parkinson’s Disease progression and differential gene expression
por: Pfaff, Abigail L., et al.
Publicado: (2021)