Phosphokinome Analysis of Barth Syndrome Lymphoblasts Identify Novel Targets in the Pathophysiology of the Disease

Barth Syndrome (BTHS) is a rare X-linked genetic disease in which the specific biochemical deficit is a reduction in the mitochondrial phospholipid cardiolipin (CL) as a result of a mutation in the CL transacylase tafazzin. We compared the phosphokinome profile in Epstein-Barr-virus-transformed lymp...

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Detalles Bibliográficos
Autores principales: Agarwal, Prasoon, Cole, Laura K., Chandrakumar, Abin, Hauff, Kristin D., Ravandi, Amir, Dolinsky, Vernon W., Hatch, Grant M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6073761/
https://www.ncbi.nlm.nih.gov/pubmed/30002286
http://dx.doi.org/10.3390/ijms19072026

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6073761/
https://www.ncbi.nlm.nih.gov/pubmed/30002286
http://dx.doi.org/10.3390/ijms19072026

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