Cargando…
Cardiac Hypertrophy in Mice with Long-Chain Acyl-CoA Dehydrogenase (LCAD) or Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency
Cardiac hypertrophy is a common finding in human patients with inborn errors of long-chain fatty acid oxidation. Mice with either very long-chain acyl-CoA dehydrogenase deficiency (VLCAD−/−) or long-chain acyl-CoA dehydrogenase deficiency (LCAD−/−) develop cardiac hypertrophy. Cardiac hypertrophy, i...
Autores principales: | Cox, Keith B., Liu, Jian, Tian, Liqun, Barnes, Stephen, Yang, Qinglin, Wood, Philip A. |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
2009
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2787798/ https://www.ncbi.nlm.nih.gov/pubmed/19736549 http://dx.doi.org/10.1038/labinvest.2009.86 |
Ejemplares similares
-
Renal response to short- and long-term exercise in very-long-chain acyl-CoA dehydrogenase-deficient (VLCAD(−/−)) mice
por: Tucci, Sara, et al.
Publicado: (2014) -
Metabolic Outcomes of Anaplerotic Dodecanedioic Acid Supplementation in Very Long Chain Acyl-CoA Dehydrogenase (VLCAD) Deficient Fibroblasts
por: Radzikh, Igor, et al.
Publicado: (2021) -
Postmortem diagnosis of very long chain acyl‐CoA dehydrogenase (VLCAD) deficiency in a neonate with sudden cardiac death
por: Singh, Prapti, et al.
Publicado: (2023) -
Two siblings with very long-chain acyl-CoA dehydrogenase (VLCAD) deficiency suffered from rhabdomyolysis after l-carnitine supplementation
por: Watanabe, Kenji, et al.
Publicado: (2018) -
Very-Long-Chain Acyl-CoA Dehydrogenase Deficiency: Family Impact and Perspectives
por: Crawford, Sarah, et al.
Publicado: (2023)