Cargando…
Analysis of RNA-Seq datasets reveals enrichment of tissue-specific splice variants for nuclear envelope proteins
Laminopathies yield tissue-specific pathologies, yet arise from mutation of ubiquitously-expressed genes. A little investigated hypothesis to explain this is that the mutated proteins or their partners have tissue-specific splice variants. To test this, we analyzed RNA-Seq datasets, finding novel is...
Autores principales: | Capitanchik, Charlotte, Dixon, Charles R., Swanson, Selene K., Florens, Laurence, Kerr, Alastair R. W., Schirmer, Eric C. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7000147/ https://www.ncbi.nlm.nih.gov/pubmed/29912636 http://dx.doi.org/10.1080/19491034.2018.1469351 |
Ejemplares similares
-
Mechanotransduction, nuclear architecture and epigenetics in Emery Dreifuss Muscular Dystrophy: tous pour un, un pour tous
por: Bianchi, Andrea, et al.
Publicado: (2018) -
An overview of treatment strategies for Hutchinson-Gilford Progeria syndrome
por: Harhouri, Karim, et al.
Publicado: (2018) -
Lipodystrophic syndromes due to LMNA mutations: recent developments on biomolecular aspects, pathophysiological hypotheses and therapeutic perspectives
por: Vigouroux, Corinne, et al.
Publicado: (2018) -
Clinical aspects of Emery-Dreifuss muscular dystrophy
por: Madej-Pilarczyk, Agnieszka
Publicado: (2018) -
Invertebrate models of lamin diseases
por: Rzepecki, Ryszard, et al.
Publicado: (2018)