Cargando…
WWOX-Related Neurodevelopmental Disorders: Models and Future Perspectives
The WW domain-containing oxidoreductase (WWOX) gene was originally discovered as a putative tumor suppressor spanning the common fragile site FRA16D, but as time has progressed the extent of its pleiotropic function has become apparent. At present, WWOX is a major source of interest in the context o...
Autores principales: | Steinberg, Daniel J., Aqeilan, Rami I. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8623516/ https://www.ncbi.nlm.nih.gov/pubmed/34831305 http://dx.doi.org/10.3390/cells10113082 |
Ejemplares similares
-
Neurological Disorders Associated with WWOX Germline Mutations—A Comprehensive Overview
por: Banne, Ehud, et al.
Publicado: (2021) -
Neonatal neuronal WWOX gene therapy rescues Wwox null phenotypes
por: Repudi, Srinivasarao, et al.
Publicado: (2021) -
WWOX Loss of Function in Neurodevelopmental and Neurodegenerative Disorders
por: Aldaz, C. Marcelo, et al.
Publicado: (2020) -
Modeling WWOX Loss of Function in vivo: What Have We Learned?
por: Tanna, Mayur, et al.
Publicado: (2018) -
WWOX loss activates aerobic glycolysis
por: Abu-Remaileh, Muhannad, et al.
Publicado: (2014)