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Electrophysiological Abnormalities in VLCAD Deficient hiPSC-Cardiomyocytes Can Be Improved by Lowering Accumulation of Fatty Acid Oxidation Intermediates

Patients with very long-chain acyl-CoA dehydrogenase deficiency (VLCADD) can present with life-threatening cardiac arrhythmias. The pathophysiological mechanism is unknown. We reprogrammed fibroblasts from one mildly and one severely affected VLCADD patient, into human induced pluripotent stem cells...

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Detalles Bibliográficos
Publicado en:Int J Mol Sci
Main Authors: Knottnerus, Suzan J. G., Mengarelli, Isabella, Wüst, Rob C. I., Baartscheer, Antonius, Bleeker, Jeannette C., Coronel, Ruben, Ferdinandusse, Sacha, Guan, Kaomei, IJlst, Lodewijk, Li, Wener, Luo, Xiaojing, Portero, Vincent M., Ulbricht, Ying, Visser, Gepke, Wanders, Ronald J. A., Wijburg, Frits A., Verkerk, Arie O., Houtkooper, Riekelt H., Bezzina, Connie R.
Formato: Artigo
Idioma:Inglês
Publicado: MDPI 2020
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Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC7177397/
https://ncbi.nlm.nih.gov/pubmed/32276429
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ijms21072589
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