CERKL, a retinal disease gene, encodes an mRNA-binding protein that localizes in compact and untranslated mRNPs associated with microtubules.
The function of CERKL (CERamide Kinase Like), a causative gene of retinitis pigmentosa and cone-rod dystrophy, still awaits characterization. To approach its cellular role we have investigated the subcellular localization and interaction partners of the full length CERKL isoform, CERKLa of 532 amino...
Guardado en:
Autores principales: | Alihamze Fathinajafabadi, Eva Pérez-Jiménez, Marina Riera, Erwin Knecht, Roser Gonzàlez-Duarte |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
Public Library of Science (PLoS)
2014
|
Materias: | |
Acceso en línea: | https://doaj.org/article/137b022134104c63822854c025b0a0c2 |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
Ejemplares similares
-
SWI/SNF associates with nascent pre-mRNPs and regulates alternative pre-mRNA processing.
por: Anu Tyagi, et al.
Publicado: (2009) -
Tau Modulates mRNA Transcription, Alternative Polyadenylation Profiles of hnRNPs, Chromatin Remodeling and Spliceosome Complexes
por: Mauro Montalbano, et al.
Publicado: (2021) -
The HILDA complex coordinates a conditional switch in the 3'-untranslated region of the VEGFA mRNA.
por: Peng Yao, et al.
Publicado: (2013) -
Enhanced mRNA FISH with compact quantum dots
por: Yang Liu, et al.
Publicado: (2018) -
Intradermal delivery of modified mRNA encoding VEGF-A in patients with type 2 diabetes
por: Li-Ming Gan, et al.
Publicado: (2019)