Cargando…
Mutations in spliceosomal proteins and retina degeneration
A majority of human genes contain non-coding intervening sequences – introns that must be precisely excised from the pre-mRNA molecule. This event requires the coordinated action of five major small nuclear ribonucleoprotein particles (snRNPs) along with additional non-snRNP splicing proteins. Intro...
Autores principales: | Růžičková, Šárka, Staněk, David |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5449078/ https://www.ncbi.nlm.nih.gov/pubmed/27302685 http://dx.doi.org/10.1080/15476286.2016.1191735 |
Ejemplares similares
-
Spliceosome Mutations in Uveal Melanoma
por: Nguyen, Josephine Q.N., et al.
Publicado: (2020) -
Chromatin-Spliceosome Mutations in Acute Myeloid Leukemia
por: Ochi, Yotaro, et al.
Publicado: (2021) -
The impact of spliceosome mutations in MDS
por: Boultwood, Jacqueline, et al.
Publicado: (2019) -
Spliceosome mutations in myelodysplastic syndromes and chronic myelomonocytic leukemia
por: Chesnais, Virginie, et al.
Publicado: (2012) -
Mutations in spliceosome genes and therapeutic opportunities in myeloid malignancies
por: Taylor, Justin, et al.
Publicado: (2019)