Cargando…
New therapeutic targets in rare genetic skeletal diseases
Introduction: Genetic skeletal diseases (GSDs) are a diverse and complex group of rare genetic conditions that affect the development and homeostasis of the skeleton. Although individually rare, as a group of related diseases, GSDs have an overall prevalence of at least 1 per 4,000 children. There a...
Autores principales: | Briggs, Michael D, Bell, Peter A, Wright, Michael J, Pirog, Katarzyna A |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Informa Healthcare
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4643203/ https://www.ncbi.nlm.nih.gov/pubmed/26635999 http://dx.doi.org/10.1517/21678707.2015.1083853 |
Ejemplares similares
-
The utility of mouse models to provide information regarding the pathomolecular mechanisms in human genetic skeletal diseases: The emerging role of endoplasmic reticulum stress (Review)
por: BRIGGS, MICHAEL D., et al.
Publicado: (2015) -
Skeletal Dysplasias Associated with Mild Myopathy—A Clinical and Molecular Review
por: Piróg, Katarzyna A., et al.
Publicado: (2010) -
Mild Myopathy Is Associated with COMP but Not MATN3 Mutations in Mouse Models of Genetic Skeletal Diseases
por: Piróg, Katarzyna A., et al.
Publicado: (2013) -
New developments in chondrocyte ER stress and related diseases
por: Briggs, Michael D., et al.
Publicado: (2020) -
Animal models and systems biology approaches for the functional validation of genetic determinants of skeletal diseases
por: Bell, Peter A, et al.
Publicado: (2015)