Cargando…
Skeletal Muscle, but not Cardiovascular Function, Is Altered in a Mouse Model of Autosomal Recessive Hypophosphatemic Rickets
Autosomal recessive hypophosphatemic rickets (ARHR) is a heritable disorder characterized by hypophosphatemia, osteomalacia, and poor bone development. ARHR results from inactivating mutations in the DMP1 gene with the human phenotype being recapitulated in the Dmp1 null mouse model which displays e...
Autores principales: | Wacker, Michael J., Touchberry, Chad D., Silswal, Neerupma, Brotto, Leticia, Elmore, Chris J., Bonewald, Lynda F., Andresen, Jon, Brotto, Marco |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4866514/ https://www.ncbi.nlm.nih.gov/pubmed/27242547 http://dx.doi.org/10.3389/fphys.2016.00173 |
Ejemplares similares
-
Hypophosphatemic rickets
por: Jagtap, Varsha S., et al.
Publicado: (2012) -
Approach to Hypophosphatemic Rickets
por: Ackah, Sarah A, et al.
Publicado: (2022) -
Autosomal Dominant Hypophosphatemic Rickets: A Case Report and Review of the Literature
por: Mameli, Chiara, et al.
Publicado: (2021) -
Cardiac thromboxane A2 receptor activation does not directly induce cardiomyocyte hypertrophy but does cause cell death that is prevented with gentamicin and 2-APB
por: Touchberry, Chad D, et al.
Publicado: (2014) -
Restoration of Endothelial Function in Pparα
(−/−) Mice by Tempol
por: Silswal, Neerupma, et al.
Publicado: (2015)